ALBERT

Description: 〈p〉Publication date: 10 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Electrochimica Acta, Volume 296〈/p〉 〈p〉Author(s): Saheed Bukola, Stephen E. Creager〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Transmission rates for protons and deuterons across single-layer graphene embedded in Nafion | graphene | Nafion sandwich structures are measured as a function of temperature in electrochemical hydrogen pump cells. Rates of ion transmission through graphene are obtained in the form of area-normalized ion-transfer resistances, and are interpreted in terms of ion-exchange current densities and standard heterogeneous ion-transfer rate constants. An encounter pre-equilibrium model for the ion-transfer step is then used to provide rate constants for the fundamental microscopic step of ion (proton or deuteron) transmission across graphene. Application of this rate model to interpret variable-temperature data on proton and deuteron transmission rates provides values for the activation energy and pre-exponential factor for the fundamental ion transmission step across graphene. Activation energies obtained from the Arrhenius plots for proton and deuteron transmission are as follows; for proton, E〈sub〉act〈/sub〉 = 48 ± 2 kJ/mole (0.50 ± 0.02 eV) and for deuteron, E〈sub〉act〈/sub〉 = 53 ± 5 kJ/mole (0.55 ± 0.05 eV). The difference between these two values of approximately 5 kJ/mole is in good agreement with the expected difference in vibrational zero-point energies for O〈img src="https://sdfestaticassets-eu-west-1.sciencedirectassets.com/shared-assets/16/entities/sbnd"〉H and O-D bonds, albeit with some uncertainty given the uncertainties in the activation energy values. Pre-exponential frequency factor values of 8.3 ± 0.4 × 10〈sup〉13〈/sup〉 s〈sup〉−1〈/sup〉 and is 4.7 ± 0.5 × 10〈sup〉13〈/sup〉 s〈sup〉−1〈/sup〉 were obtained for proton and deuteron transmission respectively across graphene. These pre-factor values are both quite large, on the order of the values predicted from the Eyring – Polanyi equation with a transmission coefficient near one. The ratio of 1.8 for the rate pre-factors (H/D) is in reasonable agreement with the value of 1.3 for the ratio of bond vibrational frequencies for O〈img src="https://sdfestaticassets-eu-west-1.sciencedirectassets.com/shared-assets/16/entities/sbnd"〉H and O-D stretching, respectively. Taken together, these data support a model in which proton and deuteron transmission across graphene are largely adiabatic processes for which the differences in transmission rate at room temperature are due largely to differences in activation energies.〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: 1 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Electrochimica Acta, Volume 295〈/p〉 〈p〉Author(s): Kaili Jin, Man Zhou, Hong Zhao, Shixiong Zhai, Fengyan Ge, Yaping Zhao, Zaisheng Cai〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉With the large theoretical capacity and environmental benignity, copper sulfide (CuS) becomes a prospective candidate electrode material for supercapacitors. In this work, electroconductive mesoporous carbonized clothes (Cc) was obtained by carbonizing the waste cotton fabrics. Then the CuS was galvanostatic electrodeposited on 〈em〉Cc〈/em〉 to prepare the binder-free 〈em〉g〈/em〉-CuS/Cc electrode. In the galvanostatic electrodeposition process, CuS grew along the crystal surface to form regular nanosheets, and a part of Cu〈sup〉2+〈/sup〉 were reduced to Cu〈sup〉1.1+〈/sup〉. In addition, on account of the synergistic effect of electrochemical double layer capacitance with pseudocapacitance and the high specific surface area (450.76 m〈sup〉2〈/sup〉 g〈sup〉−1〈/sup〉), the 〈em〉g〈/em〉-CuS/Cc composite displayed not only outstanding areal specific capacitance (4676 mF cm〈sup〉−2〈/sup〉 at 2 mA cm〈sup〉−2〈/sup〉) but also excellent cycling performance (89.8% retention after 10000 cycles). Meanwhile, the symmetrical flexible supercapacitor (SC) based on 〈em〉g〈/em〉-CuS/Cc electrodes with PVA-KOH gel electrolyte (〈em〉g〈/em〉-CuS/Cc-SC) accomplished a high specific capacitance of 1333 mF cm〈sup〉−2〈/sup〉 at 2 mA cm〈sup〉−2〈/sup〉 as well as ultrahigh energy density of 0.96 Wh cm〈sup〉−2〈/sup〉 at the power density of 4.36 W cm〈sup〉−2〈/sup〉. Therefore, 〈em〉g〈/em〉-CuS/Cc shows a great potential for applications in the next generation of flexible energy storage devices.〈/p〉〈/div〉 〈/div〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0013468618324447-fx1.jpg" width="384" alt="Image 1" title="Image 1"〉〈/figure〉〈/p〉〈/div〉

Description: 〈p〉Publication date: 1 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Electrochimica Acta, Volume 295〈/p〉 〈p〉Author(s): Kang Li, Zhanwei Xu, Xuetao Shen, Kai Yao, Jianshe Zhao, Ronglan Zhang, Jun Zhang, Li Wang, Jianfeng Zhu〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Commercial lithium/thionyl chloride (Li/SOCl〈sub〉2〈/sub〉) batteries cannot meet the 3.15 V platform required for most instruments. A 〈em〉hovenia acerba〈/em〉-like assembly constructed with cobalt tetrapyridinoporphyrazine of thickness of 5–15 nm is anchored on acid-functionalized multi-walled carbon nanotubes (CoTAP/MWCNTs), which were prepared using an 〈em〉in situ〈/em〉 solid synthesis process. The discharge time of Li/SOCl〈sub〉2〈/sub〉 batteries with a voltage greater than 3.15 V catalyzed by CoTAP/MWCNTs is found to be 11 min longer than batteries without catalysts and 4 min longer than those catalyzed by CoTAP alone. The energy of Li/SOCl〈sub〉2〈/sub〉 batteries with a voltage greater than 3.15 V catalyzed by CoTAP/MWCNTs is discovered to be 11.44-times higher than batteries with AF-MWCNTs and 6.17-times higher than those catalyzed by bulk CoTAP. This is due to the fact that more CoTAP ultrafine nanoparticulates are anchored on the AF-MWCNTs. These nanoparticulates provide more active sites for the catalytic reaction of SOCl〈sub〉2〈/sub〉. The assemblies are shown to have an adsorption-coordination effect on Li ions and to delay the deposition of lithium chloride passive films enhancing battery voltage platforms.〈/p〉〈/div〉 〈/div〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉A 〈em〉hovenia acerba〈/em〉-like assembly constructed with cobalt tetrapyridinoporphyrazine of thickness of 5–15 nm is anchored on acid-functionalized multi-walled carbon nanotubes (CoTAP/MWCNTs), which were prepared using an 〈em〉in situ〈/em〉 solid synthesis process. The discharge time of Li/SOCl〈sub〉2〈/sub〉 batteries with a voltage greater than 3.15 V catalyzed by CoTAP/MWCNTs is found to be 11 min longer than batteries without catalysts and 4 min longer than those catalyzed by CoTAP alone.〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0013468618324319-fx1.jpg" width="270" alt="Image 1" title="Image 1"〉〈/figure〉〈/p〉〈/div〉

Description: 〈p〉Publication date: February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Chemosphere, Volume 216〈/p〉 〈p〉Author(s): Xinjiang Hu, Weixuan Wang, Guangyu Xie, Hui Wang, Xiaofei Tan, Qi Jin, Daixi Zhou, Yunlin Zhao〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉A novel ternary composite of graphitic carbon nitride (g-C〈sub〉3〈/sub〉N〈sub〉4〈/sub〉)/graphene oxide (GO) sheets/BiFeO〈sub〉3〈/sub〉 (CNGB) with highly enhanced visible-light photocatalytic activity toward Cr(VI) photoreduction is prepared and characterized. The characterization and photocatalysis experiments corroborate its reasonable band gap, efficient charge separation and transfer, widened visible-light adsorption, easy solid-liquid separation, good stability and superior catalytic activity of CNGB. Three CNGB samples with different ratios of g-C〈sub〉3〈/sub〉N〈sub〉4〈/sub〉 and BiFeO〈sub〉3〈/sub〉 (CNGB-1, -2, -3 with 2:4, 3:3, and 4:2, respectively), though possessing different adsorption ability, eventually remove all Cr(VI) ions via photocatalysis within 90 min. The catalytic efficiency of the composite is the highest at pH 2; increases in pH decrease the catalytic ability. The inorganic anions such as SO〈sub〉4〈/sub〉〈sup〉−〈/sup〉, Cl〈sup〉−〈/sup〉, and NO〈sub〉3〈/sub〉〈sup〉−〈/sup〉 only slightly affects the photocatalytic process. The matching of the band structure between BiFeO〈sub〉3〈/sub〉 and g-C〈sub〉3〈/sub〉N〈sub〉4〈/sub〉 generates efficient photogenerated electron migration from the conduction band of g-C〈sub〉3〈/sub〉N〈sub〉4〈/sub〉 to that of BiFeO〈sub〉3〈/sub〉, which is also facilitated by the electron bridging and collecting effects of GO, and holes transfer from the valence band of BiFeO〈sub〉3〈/sub〉 to that of g-C〈sub〉3〈/sub〉N〈sub〉4〈/sub〉, yielding the efficient separation of photogenerated electron-hole pairs and the subsequent enhancement of photocatalytic activity. The research provides a theoretical basis and technical support for the development of photocatalytic technologies for effective application in wastewater treatment and Cr-contaminated water restoration.〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Chemosphere, Volume 216〈/p〉 〈p〉Author(s): F. Faghihzadeh, N.M. Anaya, H. Hadjeres, T.B. Boving, V. Oyanedel-Craver〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉 〈p〉This study present assessed the effect of UV pulsed light (PL) on microbial and organic pollutants using two spiral lamps were used, i.e., PL1 and PL2 lamps, with wavelength cut-offs of 190 and 240 nm, respectively. Overall, our study demonstrated that pulsed UV light impacts several microbial biomolecules and degrades polycyclic aromatic hydrocarbons (PAHs) in aqueous solution. In microbial inactivation by PL2, temporary changes of bacterial cellular components, specifically proteins, were observed, but the compositional changes of bacteria that were exposed to PL1 were permanent due to ozonolysis. PL1 irradiation caused greater deactivation of the bacteria than PL2 irradiation due to the generation of ozone. The higher efficacy of PL1 in terms of membrane disruption, reduction of respiration rate, and reduction of growth rate was due to the production of ozone during the irradiation period. The bacteria that were irradiated with both PL lamps regrew due to photoreactivation, such as an enzymatic DNA-repair mechanism.〈/p〉 〈p〉The PAH degradation kinetics indicate that higher molecular weights degraded faster than those with lower molecular weights. For both lamps, the degradation of naphthalene and fluorene was first order, whereas second order for pyrene and anthracene. Any effect of ozonolysis on the PAH degradation rates was not apparent, which indicated that photolysis was the primary degradation pathway. PAH solutions treated with both pulsed UV lamps did not result in a toxicity effect on the bacteria.〈/p〉 〈/div〉 〈/div〉

Description: 〈p〉Publication date: 15 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 536〈/p〉 〈p〉Author(s): Gang Yuan, Xiao Zhao, Yeru Liang, Lin Peng, Hanwu Dong, Yong Xiao, Chaofan Hu, Hang Hu, Yingliang Liu, Mingtao Zheng〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉As a new class of zero-dimensional carbon nanomaterials, carbon dots have triggered intensive research interest in various fields. However, the low surface area, hydrophilicity, and agglomeration characteristics limit their applications in energy storage fields. Herein, we demonstrate that nitrogen-doped carbon dots can be employed as efficient nanoenhancer to boost the electrochemical performance of three-dimensional graphene. The as-prepared materials exhibit an interconnected framework with abundant oxygen- and nitrogen-containing functional groups, which enable fast penetration and transport of electrolyte ions and provide more active sites and electric conductivity. Employed as binder-free electrode for supercapacitors, the resultant materials present high specific capacitance (338 F g〈sup〉−1〈/sup〉) and areal capacitance (604 μF cm〈sup〉−2〈/sup〉) at a current density of 0.5 A g〈sup〉−1〈/sup〉, which is much higher than that of pristine three-dimensional graphene (190 F g〈sup〉−1〈/sup〉, and 114 μF cm〈sup〉−2〈/sup〉), with an enhancement of 78% and 430%, respectively. Moreover, superior long-term cycling stability (94% of capacitance retention after 20 000 charging/discharging cycles at 10 A g〈sup〉−1〈/sup〉) as well as improved electric conductivity can also be achieved. These results certify that nitrogen-doped carbon dots can be applied as nanobooster to comprehensively improve the performance of graphene for high-performance electrochemical energy storage.〈/p〉〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉 〈p〉Small nitrogen-doped carbon dots (〈em〉N〈/em〉-CDs) are employed as efficient nanoenhancer to significantly boost the electrochemical performances of three-dimensional graphene (3DG) for supercapacitors.〈/p〉 〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0021979718312931-ga1.jpg" width="500" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉 〈/div〉 〈/div〉

Description: 〈p〉Publication date: 15 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 536〈/p〉 〈p〉Author(s): Yuanyuan Zhang, Lili Wang, Fengying Dong, Qiao Chen, Haiyan Jiang, Mei Xu, Jinsheng Shi〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Bi〈sub〉2〈/sub〉O〈sub〉2〈/sub〉CO〈sub〉3〈/sub〉-based ternary composite materials are generally synthesized by two- or multi-step method and special precursor of CO〈sub〉3〈/sub〉〈sup〉2−〈/sup〉 is usually utilized in synthesis of Bi〈sub〉2〈/sub〉O〈sub〉2〈/sub〉CO〈sub〉3〈/sub〉, which are time-consuming, laborious and relatively costly. In this paper, for the first time, a facile one-step solvothermal method is used to fabricate Z-scheme Bi〈sub〉2〈/sub〉O〈sub〉2〈/sub〉CO〈sub〉3〈/sub〉/Bi/Bi〈sub〉2〈/sub〉WO〈sub〉6〈/sub〉 ternary composites. Interestingly, ethylene glycol not only acts as solvent for the reaction system, but also reduced Bi〈sup〉3+〈/sup〉 into metallic Bi and itself is oxidized to CO〈sub〉3〈/sub〉〈sup〉2−〈/sup〉, which could construct Bi〈sub〉2〈/sub〉O〈sub〉2〈/sub〉CO〈sub〉3〈/sub〉. On this occasion, Bi〈sub〉2〈/sub〉O〈sub〉2〈/sub〉CO〈sub〉3〈/sub〉/Bi/Bi〈sub〉2〈/sub〉WO〈sub〉6〈/sub〉 ternary composites are obtained after one-step method. High resolution transmission electron microscopy clearly reveals each component in composites. The as-prepared samples could be applied in various photocatalytic activities. Under solar light irradiation, Bi〈sub〉2〈/sub〉O〈sub〉2〈/sub〉CO〈sub〉3〈/sub〉/Bi/Bi〈sub〉2〈/sub〉WO〈sub〉6〈/sub〉 composites exhibited prominent photodegradation performances for both ciprofloxacin and bisphenol A. Meanwhile, these composites could also be used in efficient photoreduction of CO〈sub〉2〈/sub〉. The efficient photocatalytic activity could be mainly ascribed to Z-scheme electron transfer mechanism in ternary composites, which is determined by surface redox reactions, active species trapping experiment, electron spin resonance spectrum.〈/p〉〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0021979718312918-ga1.jpg" width="425" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: 15 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 536〈/p〉 〈p〉Author(s): Hua Guo, Ya Su, Yanling Shen, Yumei Long, Weifeng Li〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Optimizing heterostructure of nanocomposites holds great potential for making full use of their ability. Herein, gold nanoparticles (AuNPs) were in situ synthesized over the surface of graphitic carbon nitride (g-C〈sub〉3〈/sub〉N〈sub〉4〈/sub〉) via one-step pyrolyzation route using a single source precursor. The precursor of melamine chloroauric (C〈sub〉3〈/sub〉H〈sub〉6〈/sub〉N〈sub〉6〈/sub〉H〈sup〉+〈/sup〉⋅AuCl〈sub〉4〈/sub〉〈sup〉−〈/sup〉) was obtained through chemical precipitation reaction between melamine and chloroauric acid. The morphological analysis confirmed the compact contact between Au nanoparticles and g-C〈sub〉3〈/sub〉N〈sub〉4〈/sub〉. Then, the Au-g-C〈sub〉3〈/sub〉N〈sub〉4〈/sub〉 nanocomposites were employed to fabricate electrochemical sensor by modifying glassy carbon electrode (GCE). Electrochemical experiments showed that the Au-g-C〈sub〉3〈/sub〉N〈sub〉4〈/sub〉 exhibited enhanced electrocatalytic activity towards tetracycline oxidation as compared with either pure g-C〈sub〉3〈/sub〉N〈sub〉4〈/sub〉 or Au nanoparticles. Based on cyclic voltammetry (CV) method, the sensor was applied in the detection of tetracycline with a low detection limit of 0.03 μM (S/N = 3) and the linear range of concentration were 0.1–20 μM and 20–200 μM, respectively. Moreover, such an electrochemical sensor demonstrated high stability and good selectivity. Finally, the electrochemical sensor was applied to drug assays and exhibited sufficient precision and accuracy. Therefore, this work paves a new way of preparing g-C〈sub〉3〈/sub〉N〈sub〉4〈/sub〉–based heterostructures and provides an efficient method for the detection of tetracycline in clinical analysis and quality control.〈/p〉〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0021979718313018-ga1.jpg" width="419" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: 15 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 536〈/p〉 〈p〉Author(s): Mingmei Zhang, Hong Liu, Ying Wang, Tianjiao Ma〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Three-dimensional (3D) flower center/petal nanostructure exhibits excellent electrochemical performance because of their unique unfold ultra-thin multi-layer structure benefit to the rapid transmission of electrons and the full infiltration of the electrolyte. A three-phase Fe〈sub〉5〈/sub〉Ni〈sub〉4〈/sub〉S〈sub〉8〈/sub〉 nanosflower is constructed by one step alcohothermal technique using a mixture solvent of glycerol, diethylene glycol and ethylenediamine. Ethylenediamine successfully functions as the complexing agent of metal ions to slowly release the metal ions in the process of reaction, which encourage the flower petal nanostructure formation. Interestingly, when the proportion of iron increased, a novel Fe〈sub〉7〈/sub〉S〈sub〉8〈/sub〉@Fe〈sub〉5〈/sub〉Ni〈sub〉4〈/sub〉S〈sub〉8〈/sub〉 flower center/petal nanostructure come into being. Benefiting from the interconnected structure of the multi-layer shell, the Fe〈sub〉7〈/sub〉S〈sub〉8〈/sub〉@ Fe〈sub〉5〈/sub〉Ni〈sub〉4〈/sub〉S〈sub〉8〈/sub〉 nanosflower displays high specific capacitance of 670.4C g〈sup〉−1〈/sup〉 at 1 A g〈sup〉−1〈/sup〉, excellent rate capability of 79.2% (531.0C g〈sup〉−1〈/sup〉 at 20 A g〈sup〉−1〈/sup〉), and longer cycling stability of 92.1% retained capacitance after 5000 cycles. Furthermore, the assembled hybrid supercapacitor demonstrates high energy density of 49.9 Wh kg〈sup〉−1〈/sup〉 at power density of 770.0 W kg〈sup〉−1〈/sup〉. Our results provide a new strategy to design metal sulfides with special structure for application to asymmetrical supercapacitor cathode material.〈/p〉〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉 〈p〉A three-phase core/shell flower-like Fe〈sub〉7〈/sub〉S〈sub〉8〈/sub〉@Fe〈sub〉5〈/sub〉Ni〈sub〉4〈/sub〉S〈sub〉8〈/sub〉 is successfully constructed by one step alcohothermal technique using a mixture solvent of glycerol, diethylene glycol and ethylenediamine. The as-obtained composites become a promising electrode material for the next generation energy storage devices with high specific capacitance (670.4C g〈sup〉−1〈/sup〉 at 1 A g〈sup〉−1〈/sup〉), excellent energy density (49.9 Wh kg〈sup〉−1〈/sup〉 at power density of 770.0 W kg〈sup〉−1〈/sup〉), as well as good long-term cycling stability (almost 88.9% retention after 10,000 cycles).〈/p〉 〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0021979718312906-ga1.jpg" width="496" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉 〈/div〉 〈/div〉

Description: 〈p〉Publication date: February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Chemosphere, Volume 216〈/p〉 〈p〉Author(s): Yaquan Liu, Xinyue Pang, Jiarui Song, Xinhe Liu, Juanjuan Song, Yongna Yuan, Chunyan Zhao〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Decabromodiphenyl ethane (DBDPE) is widely used in industry as an alternative to the decabromodiphenyl ether (BDEs). The large-scale use of DBDPE could lead to rapid growth of the human accumulation level of DBDPE. However, the biophysics of accumulation of DBDPE in cell membranes, as one of determinants of DBDPE metabolism is not clear. In the present study, detailed observations of cell lactate dehydrogenase (LDH) and reactive oxygen species (ROS) levels measurements proved that the DBDPE exposure to cell could result in significant cell membrane damage by concentration-dependent manners. The fluorescence anisotropy analysis supported the evidence that high concentration DBDPE bound decreased membrane fluidity significantly. Besides it, a detailed molecular dynamic (MD) simulation was approached to investigate the effects of DBDPE on the DPPC (dipalmitoyl phosphatidylcholine) phospholipid bilayer, which was constructed as the model of cell membrane. The molecular dynamic simulation revealed that DBDPE molecules can easily enter the membrane from the aqueous phase. Under the concentration of a threshold, the DBDPE molecules tended to aggregate inside the DPPC bilayer and caused pore formation. The bound of high concentration of DBDPE could result in significant variations in DPPC bilayer with a less dense, more disorder and rougher layer. The knowledge about DBDPEs interactions with lipid membranes is fundamentally essential to understand the in vivo process of DBDPE and the physical basis for the toxicity of DBDPE in cell membranes.〈/p〉〈/div〉 〈/div〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0045653518320010-fx1.jpg" width="457" alt="Image 1" title="Image 1"〉〈/figure〉〈/p〉〈/div〉

Description: 〈p〉Publication date: February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Chemosphere, Volume 216〈/p〉 〈p〉Author(s): Yangke Long, Sifan Bu, Yixuan Huang, Yueqi Shao, Ling Xiao, Xiaowen Shi〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Metal-free carbo-catalyst has recently emerged as a promising candidate as a substituent for tradition-metal based heterogeneous catalyst for catalytic activation of peroxymonosulfate (PMS). However, most reported carbo-catalysts suffer from low catalytic efficiency and poor stability, thus a high-performance catalyst is urgently desired. In this study, a novel carbo-catalyst (NHPC-800), prepared by using tannic acid and dicyandiamide as renewable carbon/nitrogen feedstocks via a simple pyrolysis route, is reported as an activator of PMS with highly efficient catalytic ability and stability. The as-prepared NHPC-800 possesses as high as 22.4 atom% of nitrogen dopants and a hierarchically porous structure with abundant meso/macropores, accompanied by the abundant edges and wrinkles, which supply sufficient exposed catalytically active centers and fast electrons/mass transportations. Using rhodamine B as a model pollutant, the NHPC-800 shows a highly efficient catalytic ability which is superior to most reported carbo-catalysts and even some state-of-the-art metal catalysts. Based on competitive quenching experiments and electron paramagnetic resonance (EPR) results, a non-radical pathway involving the generation of 〈sup〉1〈/sup〉O〈sub〉2〈/sub〉 is responsible for the degradation of pollutants. Given that the NHPC-800 shows good recycling performance and strong resistance to adventitious interference such as anions and natural organic matters, we believe NHPC-800 can be a promising candidate for practical applications, and this study can provide inspirations for the further development of highly efficient carbo-catalysts.〈/p〉〈/div〉 〈/div〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0045653518320460-fx1.jpg" width="343" alt="Image 1" title="Image 1"〉〈/figure〉〈/p〉〈/div〉

Description: 〈p〉Publication date: 15 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 536〈/p〉 〈p〉Author(s): Ngoc-Hanh Cao-Luu, Quoc-Thai Pham, Zong-Han Yao, Fu-Ming Wang, Chorng-Shyan Chern〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉 〈h6〉Hypothesis〈/h6〉 〈p〉How to encapsulate poly(N-isopropylacrylamide) (PNIPAM) mesoglobule cores by silica shells greatly affects the resultant nanoparticle structures. Incorporation of acrylamide (AM) unit into PNIPAM in combination with 3-glycidyloxypropyltrimethoxysilane (GLYMO, as a coupling agent) effectively induces nucleation and growth of silica on PNIPAM core surfaces, where the –NH〈sub〉2〈/sub〉 of acrylamide reacts with the epoxide of GLYMO while GLYMO further participates in subsequent sol-gel reaction of tetraethyl orthosilicate (TEOS), thereby leading to desirable particle morphology.〈/p〉 〈/div〉 〈div〉 〈h6〉Experiments〈/h6〉 〈p〉PNIPAM-based core–silica shell nanoparticles were prepared by sol〈em〉-〈/em〉gel reaction of TEOS and GLYMO in the presence of polymeric core particles. The major parameters investigated in a systematic fashion include acrylamide concentration and weight ratio of polymer:GLYMO:TEOS. GPC, DLS, DSC, FE-SEM, TEM, FTIR and TGA were then used to characterize polymeric cores and hybrid nanoparticles.〈/p〉 〈/div〉 〈div〉 〈h6〉Findings〈/h6〉 〈p〉The particle morphology was governed primarily by the acrylamide content and the weight ratio of PNIPAM/AM:GLYMO:TEOS, and desirable hybrid nanoparticles with narrow particle size distribution were achieved. The LCST of PNIPAM-based mesoglobules increases with increasing acrylamide content. Encapsulation of PNIPAM-based mesoglobules with silica also reduces their thermo-sensitivity. This is the first report of developing a novel approach to prepare PNIPAM-based mesoglobule core–silica shell nanoparticles with controllable particle morphologies.〈/p〉 〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0021979718312888-ga1.jpg" width="500" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: 15 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 536〈/p〉 〈p〉Author(s): Patryk Wąsik, Annela M. Seddon, Hua Wu, Wuge H. Briscoe〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉We present a box counting fractal dimension (FD) analysis of the dendritic patterns obtained under conditions far from equilibrium 〈em〉via〈/em〉 rapid evaporation of a sessile drop containing 〈em〉reactive〈/em〉 ZnO nanoparticles. These dendrites were manifestations of solidified Bénard-Marangoni (BM) instability convection cells, and we previously noted that their complex hierarchical morphologies were superficially analogous to the foliage of red algae, Spanish dagger, or spider plant. The fractal dimension of the Bénard-Marangoni dendrites was found to vary in the range of 1.77–1.89 and also depend on the size of the Bénard-Marangoni cells. These fractal dimension results were correlated with the morphological details of the Bénard-Marangoni cells and ZnO particle characteristics, providing a quantitative description of such complex surface patterns emerging from the dynamic process of the Bénard-Marangoni instability.〈/p〉〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0021979718312773-ga1.jpg" width="498" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: 15 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 536〈/p〉 〈p〉Author(s): Bin Fang, Xingchang Lu, Junyi Hu, Geng Zhang, Xinsheng Zheng, Limin He, Jianbo Cao, Jiangjiang Gu, Feifei Cao〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Emerging carbon dots (CDs) are widely used as fluorescent probes in biological and environmental fields, nevertheless, the control of CDs based on different detection mechanisms is rarely reported. In this paper, green luminescent CDs (G-CDs) were prepared by a facile hydrothermal treatment of benzoxazine monomers (BZM). The obtained G-CDs showed pH dependent photoluminescence, which could be designed as fluorescence turn-on and turn-off sensors. The G-CDs exhibited weak photoluminescence at pH = 7.0 and could be turned on by Zn(II) selectively with the limitation of 0.32 μM in the concentration range from 1 to 100 μM. When pH = 10.0, Cr(VI) could quench the strong fluorescence of G-CDs efficiently, and the limit of detection was 0.99 μM with a linear range of 1–50 μM. Furthermore, the fluorescence turn-on and turn-off performance of G-CDs was attributed to the intramolecular charge transfer (ICT) of Zn(II) and the inner filter effect (IFE) of Cr(VI), respectively. The excellent probes were successfully applied for the detection of Zn(II) in biological system and Cr(VI) in environment.〈/p〉〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0021979718312839-ga1.jpg" width="463" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: 1 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Electrochimica Acta, Volume 295〈/p〉 〈p〉Author(s): Shuxing Wu, Hengzhi Guo, Kwan San Hui, Kwun Nam Hui〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Rational electrode architectural design, favorable electrode composition, and versatile synthesis approach play a significant role in developing advanced electrodes for high-performance supercapacitor. In this work, we report a facile approach for fabricating 1D hierarchical CuO@Co〈sub〉〈em〉x〈/em〉〈/sub〉Ni〈sub〉〈em〉1−x〈/em〉〈/sub〉(OH)〈sub〉2〈/sub〉 nanowire arrays grown on 3D highly conductive copper foam. The optimized CuO@Co〈sub〉0.2〈/sub〉Ni〈sub〉0.8〈/sub〉(OH)〈sub〉2〈/sub〉 electrode delivers an ultrahigh specific capacity of 374.7 mAh g〈sup〉−1〈/sup〉 at 2 A g〈sup〉−1〈/sup〉 with exceptional rate capability (301.7 mAh g〈sup〉−1〈/sup〉 at 50 A g〈sup〉−1〈/sup〉) and remarkable cycling stability (95.9% after 10 000 cycles at 50 A g〈sup〉−1〈/sup〉). A flexible asymmetric solid-state supercapacitor (ASC) is fabricated using the optimized CuO@Co〈sub〉0.2〈/sub〉Ni〈sub〉0.8〈/sub〉(OH)〈sub〉2〈/sub〉 as the positive electrode, activated carbon-coated nickel foam as the negative electrode, and polyvinyl alcohol/KOH gel as electrolyte. The flexible ASC operating with a potential window of 0–1.6 V delivers an energy density of 46.5 Wh kg〈sup〉−1〈/sup〉 with a power density of 526.9 W kg〈sup〉−1〈/sup〉. The ASC also exhibits excellent cycling stability with a capacity retention of 84.3% after 10 000 cycles at a current density of 7 A g〈sup〉−1〈/sup〉.〈/p〉〈/div〉 〈/div〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0013468618324459-fx1.jpg" width="325" alt="Image 1" title="Image 1"〉〈/figure〉〈/p〉〈/div〉

Description: 〈p〉Publication date: 1 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Electrochimica Acta, Volume 295〈/p〉 〈p〉Author(s): Krishnan Shanmugam Anuratha, Hsiao-Shan Peng, Yaoming Xiao, Tzu-Sen Su, Tzu-Chien Wei, Jeng-Yu Lin〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉In this current work, a bifunctional TiO〈sub〉2〈/sub〉 thin film with reduced pin-hole effect and enhanced light trapping capability was successfully fabricated by using a facile galvanostatic anodic deposition route in the presence of Brij-58 soft template (ST). The surface morphology of electrodeposited TiO〈sub〉2〈/sub〉 thin film using ST confirmed the formation of nano-sized TiO〈sub〉2〈/sub〉 particles with improved porous nature than that of TiO〈sub〉2〈/sub〉 thin film electrodeposited in the absence of ST. Compared with the conventional scaffold porous layer (PL) fabricated from commercial mesoporous TiO〈sub〉2〈/sub〉 composed of ∼30 nm nanoparticles, the electrodeposited TiO〈sub〉2〈/sub〉 film using ST demonstrated the reduced pinhole effect and improved light trapping feature. Owing to the bifunctional behavior of electrodeposited TiO〈sub〉2〈/sub〉 using ST, the cell efficiency of the perovskite solar cell was achieved up to 17.06% which was ca.10% higher than those with commercial TiO〈sub〉2〈/sub〉 nanoparticles.〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Chemosphere, Volume 216〈/p〉 〈p〉Author(s): Nicole S.M. Vieira, Joana C. Bastos, Luís P.N. Rebelo, Ana Matias, João M.M. Araújo, Ana B. Pereiro〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉The use of fluorinated ionic liquids (FILs) as novel materials in biological and pharmaceutical applications is an emerging research field. The knowledge of their cytotoxicity and that of 1-octanol/water partition coefficients are essential to assess their environmental risks, to estimate their toxicity and activity, or the hydrophilic/lipophilic balance, as well as to explore their properties as solvents in extraction processes or for successful drug design. The study of the cytotoxicity in four different human cell lines and the experimental measurement of the partition coefficient between 1-octanol and water (P〈sub〉〈em〉o/w〈/em〉〈/sub〉), using the slow-stirring method, were carried out for several FILs. In both studies, the effect of the cation ([C〈sub〉2〈/sub〉C〈sub〉1〈/sub〉Im]〈sup〉+〈/sup〉, [C〈sub〉2〈/sub〉C〈sub〉1〈/sub〉py]〈sup〉+〈/sup〉, [C〈sub〉4〈/sub〉C〈sub〉1〈/sub〉pyr]〈sup〉+〈/sup〉, [N〈sub〉1112(OH)〈/sub〉]〈sup〉+〈/sup〉, or [N〈sub〉4444〈/sub〉]〈sup〉+〈/sup〉), the cationic alkyl side-chain length ([C〈sub〉n〈/sub〉C〈sub〉1〈/sub〉Im]〈sup〉+〈/sup〉, with n = 2, 6, 8 or 12), and the anionic fluorinated chain length/anionic fluorinated domain size ([C〈sub〉4〈/sub〉F〈sub〉9〈/sub〉SO〈sub〉3〈/sub〉]¯, [C〈sub〉8〈/sub〉F〈sub〉17〈/sub〉SO〈sub〉3〈/sub〉]¯, or [N(C〈sub〉4〈/sub〉F〈sub〉9〈/sub〉SO〈sub〉3〈/sub〉)〈sub〉2〈/sub〉]¯) were analysed. The results reveal that both toxicity and partition properties are mainly influenced by the size of the cationic hydrogenated alkyl side-chain and that of the anionic fluorinated domain. The intrinsic tuneability of the FILs allows for their selection according to the lipophilic or hydrophilic character of the target biological system under consideration. The toxicity studies corroborate the biocompatible nature of some FILs tested in this work. Along, for all the FILs under study P〈sub〉〈em〉o/w〈/em〉〈/sub〉 〈 1.00. Accordingly, a decadic logarithm of the bioconcentration factor in fish of 0.5 would be estimated, which is below the regulatory endpoint used by regulatory agencies.〈/p〉〈/div〉 〈/div〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0045653518320204-fx1.jpg" width="500" alt="Image 1" title="Image 1"〉〈/figure〉〈/p〉〈/div〉

Description: 〈p〉Publication date: February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Chemosphere, Volume 216〈/p〉 〈p〉Author(s): Yasir Aziz, Ghulam Abbas Shah, Muhammad Imtiaz Rashid〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Recently, there is a growing interest among agriculturists to use nanotechnology for the development of nutrient-use efficient fertilizers. However, its sustainable use for the synthesis of mineral or organic nano-fertilizers requires a thoughtful of the mechanism as well as the fate of nutrients and their interaction with soil-plant systems. Therefore, the aim of current study was to investigate the mixing of three different application rates of zinc oxide nanoparticles (ZNPs: 1.4, 2.8 and 3.6 mg kg〈sup〉−1〈/sup〉 soil) as well as zeolite (141, 282 and 423 mg kg〈sup〉−1〈/sup〉 soil) with biogas slurry (AS) on soil nutrient availability and herbage nitrogen (N) and zinc (Zn) uptake in a standard pot experiment. We found that both ZNPs and zeolite significantly increased mineral N content in soil compared to AS alone (P 〈 0.05). On the other hand, plant available phosphorus or potassium and microbial biomass carbon (C) in the soil were neither significantly affected by any application rate of ZNPs nor zeolite mixed AS. Soil microbial biomass N was significantly higher in second and third application rates of both ZNPs and zeolite amended AS treatments compared to AS alone. However, this increment in mineral N did not influence shoot uptake and herbage apparent recovery of this nutrient from AS. Similarly, co-mixing of both ZNPs and zeolite in AS did not influence shoot N uptake but Zn uptake was significantly higher in this treatment compared to AS alone. Therefore, this combination would be considered for improving crop Zn uptake under such fertilizer management regimes.〈/p〉〈/div〉 〈/div〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0045653518319805-fx1.jpg" width="357" alt="Image 1" title="Image 1"〉〈/figure〉〈/p〉〈/div〉

Description: 〈p〉Publication date: February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Chemosphere, Volume 216〈/p〉 〈p〉Author(s): Roya Nazari, Ljiljana Rajić, Ali Ciblak, Sebastián Hernández, Ibrahim E. Mousa, Wei Zhou, Dibakar Bhattacharyya, Akram N. Alshawabkeh〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉This study investigates the effect of palladium (Pd) form on the electrochemical degradation of chlorobenzene in groundwater by palladium-catalyzed electro-Fenton (EF) reaction. In batch and flow-through column reactors, EF was initiated via in-situ electrochemical formation of hydrogen peroxide (H〈sub〉2〈/sub〉O〈sub〉2〈/sub〉) supported by Pd on alumina powder or by palladized polyacrylic acid (PAA) in a polyvinylidene fluoride (PVDF) membrane (Pd-PVDF/PAA). In a mixed batch reactor containing 10 mg L〈sup〉−1〈/sup〉 Fe〈sup〉2+〈/sup〉, 2 g L〈sup〉−1〈/sup〉 of catalyst in powder form (1% Pd, 20 mg L〈sup〉−1〈/sup〉 of Pd) and an initial pH of 3, chlorobenzene was degraded under 120 mA current following a first-order decay rate showing 96% removal within 60 min. Under the same conditions, a rotating Pd-PVDF/PAA disk produced 88% of chlorobenzene degradation. In the column experiment with automatic pH adjustment, 71% of chlorobenzene was removed within 120 min with 10 mg L〈sup〉−1〈/sup〉 Fe〈sup〉2+〈/sup〉, and 2 g L〈sup〉−1〈/sup〉 catalyst in pellet form (0.5% Pd, 10 mg L〈sup〉−1〈/sup〉 of Pd) under 60 mA. The EF reaction can be achieved under flow, without external pH adjustment and H〈sub〉2〈/sub〉O〈sub〉2〈/sub〉 addition, and can be applied for in-situ groundwater treatment. Furthermore, the rotating PVDF-PAA membrane with immobilized Pd-catalyst showed an effective and low maintenance option for employing Pd catalyst for water treatment.〈/p〉〈/div〉 〈/div〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0045653518320046-fx1.jpg" width="341" alt="Image 1" title="Image 1"〉〈/figure〉〈/p〉〈/div〉

Description: 〈p〉Publication date: February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Chemosphere, Volume 217〈/p〉 〈p〉Author(s): Mengmeng Liu, Min Zhang, Rongjie Hao, Tingting Du, Tong Li, Yao Li〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Graphene oxide (GO) is a structural analog of graphene and contains numerous O-containing functional groups. As rapidly increasing production and usage of GO, it is inevitable to flow into the water and wastewater treatment system and finally oxidized by disinfectants to form DBPs. Meanwhile, as GO is a nano sized carbon material, it may also break the human digestion system when it was absorbed by human body. This study explored the DBP formation when only GO was present. Effects of Br〈sup〉−〈/sup〉 were also considered during the DBP formation. Both trihalomethanes (THMs) and haloacetic acids (HAAs) were formed during the chlorination and chloramination procedure, but the total concentration of THMs was at least three times higher than that of HAAs. Irradiation can significantly enhance the DBP formation via the formation of radicals. The wrinkled appearance and decomposition of aromatic ring may both be effective on the DBP formation via chlorination or bromination. The findings of this study advance knowledge on the DBP formation of GO in water treatment systems and provide insight on the toxic effects of the transformation products of GO.〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Chemosphere, Volume 216〈/p〉 〈p〉Author(s): Bo Liu, Jing Wu, Cheng Cheng, Jiukai Tang, Muhammad Farooq Saleem Khan, Jian Shen〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract:〈/h5〉 〈div〉〈p〉Identifying the causes of water body pollution is critical because of the serious water contamination in developing countries. The textile industry is a major contributor to severe water pollution due to its high discharge of wastewater with high concentrations of organic and inorganic pollutants. In this study, fluorescence excitation emission matrix–parallel factor (EEM-PARAFAC) analysis was applied to characterize textile industry wastewater and trace its presence in water bodies. The EEM spectra of textile wastewater samples collected from 12 wastewater treatment plants (WWTPs) revealed two characteristic peaks: Peak T1 (tryptophan-like region) and Peak B (tyrosine-like region). Two protein-like components (C1 and C2) were identified in the textile wastewater by PARAFAC analysis. The components identified from different textile WWTPs were considered identical (similarity 〉0.95). C1 and C2 were not sensitive to changes in pH, ionic strength, or low humic acid concentration (TOC 〈 4 mg/L). Therefore, C1 combined with C2 was proposed as a source-specific indicator of textile wastewater, which was further demonstrated by conducting high-performance size exclusion chromatography analysis. These results suggested that EEM-PARAFAC analysis is a reliable means of identifying textile wastewater pollution in water bodies and may also enable the identification of other industrial wastewater.〈/p〉〈/div〉 〈/div〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0045653518320162-fx1.jpg" width="500" alt="Image 1" title="Image 1"〉〈/figure〉〈/p〉〈/div〉

Description: 〈p〉Publication date: February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Chemosphere, Volume 216〈/p〉 〈p〉Author(s): Bo Chen, Sijiang Chen, Huinan Zhao, Yang Liu, Fengxia Long, Xuejun Pan〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Ascribing to their significant differences in physicochemical properties, it is extremely challenging to treat complex wastewater containing more than one class of pollutants via one-step treatment. Here, we focused on disposal of complex wastewater bearing organic dye and heavy metal by using adsorptive method. Thus, by combining the advantages of polyethyleneimine (PEI), β-cyclodextrin (β-CD) as well as Fe〈sub〉3〈/sub〉O〈sub〉4〈/sub〉 magnetic nanoparticles, a versatile β-CD and PEI bi-functionalized magnetic nanoadsorbent (Fe〈sub〉3〈/sub〉O〈sub〉4〈/sub〉-PEI/β-CD) with spatially separated sorption sites was successfully constructed for simultaneous capture of methyl orange (MO) and Pb(II) in complex wastewater. In this setting, β-CD cavities and positively charged N-containing groups of PEI were mainly responsible for removal of MO via host-guest inclusion and electrostatic attraction, respectively, and oxygen-bearing groups on the edge of β-CD as well as the free amino moieties in PEI acted as the active sites for Pb(II) uptake. In their individual mono-pollutant system, the adsorption processes can be better described via applying pseudo-second-order kinetic and Langmuir isotherm models. Interestingly, presence of MO in Pb(II)-MO binary system significantly promoted the uptake of Pb(II). But the coexisting Pb(II) had almost no effects on MO uptake. Such results demonstrated that both MO and Pb(II) could be simultaneously and synergistically removed by Fe〈sub〉3〈/sub〉O〈sub〉4〈/sub〉-PEI/β-CD through multiple mechanisms (such as electrostatic attraction, host-guest inclusion, chelating, etc.). Particularly, the excellent regeneration and stability make Fe〈sub〉3〈/sub〉O〈sub〉4〈/sub〉-PEI/β-CD an ideal integrative adsorbent for purification of actual wastewater contaminated by MO and Pb(II). Thus, this study provides some insights into designing a well-performed and easily recyclable adsorbent for simultaneous and synergetic capture of both organic and inorganic contaminants in complex wastewater.〈/p〉〈/div〉 〈/div〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉A versatile β-CD and PEI bi-functionalized magnetic nanoadsorbent with spatially separated sorption sites (denoted as Fe3O4-PEI/β-CD) was successfully constructed for simultaneous removal of methyl orange (MO) and Pb(II) from complex wastewater through multiple mechanisms (such as electrostatic attraction, host-guest inclusion, chelating, etc.).〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0045653518320198-fx1.jpg" width="444" alt="Image 1" title="Image 1"〉〈/figure〉〈/p〉〈/div〉

Description: 〈p〉Publication date: February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Chemosphere, Volume 216〈/p〉 〈p〉Author(s): Xian Cao, Shuai Zhang, Hui Wang, Xianning Li〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉In general, refractory organics were hardly used as co-substrate in bioelectrochemical system. This study established a coupled bioelectrochemical system composed of a biofilm electrode reactor and a microbial fuel cell for using the azo dye X-3B as part of co-substrate. The two units degraded the azo dye X-3B stepwise while using it as part of co-substrate. Our results indicated that the removal efficiency of X-3B increased 28.5% using the coupled system compared with a control system. Moreover, the addition of the co-substrate glucose, which was necessary for MFC electricity generation, was reduced on the premise of stable removal efficiency in the coupled system to prevent resource waste due to using X-3B as part of co-substrate. The intermediate products of X-3B degradation were further explored using gas chromatography–mass spectrometry and a X-3B degradation pathway was proposed at the same time. Microbial communities were analyzed, illustrating that the mechanism of X-3B degradation was dependent on bioelectrochemistry rather than on microbial degradation.〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Chemosphere, Volume 216〈/p〉 〈p〉Author(s): Nikita Bakanov, Matthias V. Wieczorek, Ralf Schulz〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Understanding fate and transport of plant protection products (PPPs) that enter vegetated streams from agricultural fields is important for both exposure assessment and risk attenuation, yet limited knowledge is available. The present laboratory study investigated sorption processes governing mass transfer of three common PPPs between water and aquatic plant phases at flow-through exposure conditions (transient aqueous-phase PPP-peak of 4 h 25 min) using three temperature regimes. The exposure produced rapid sorption of PPPs to plants, followed by a gradual depuration from plants. Dynamic sorption kinetics depended on temperature, plant species, and physicochemical properties of the PPPs. Sorption to plants contributed to a 10% reduction of the water-phase peak concentrations of the PPPs. However, being reversible, the attenuation effect was limited to the residence time of the PPPs in the systems. Results of the present study highlight that effectivity of aquatic plants in the attenuation of PPP loads may vary greatly depending on hydrodynamic properties of aquatic systems.〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Chemosphere, Volume 217〈/p〉 〈p〉Author(s): Huihui Wang, Hui Ma, Min Zhang, Tingting Du, Rongjie Hao, Mengmeng Liu, Yao Li〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Disinfection byproducts (DBPs) can be formed from many different kinds of carbon- and nitrogen-based organic materials. This study investigated DBP formation in the presence of two types of polybrominated diphenyl ethers (PBDEs), 2,2′,4,4′-tetrabromodiphenyl ether (BDE 47) and 2,2′,3,3′,4,4′,5,5′,6,6′-decabromodiphenyl ether (BDE 209). The effects of PBDEs on the formation of DBPs upon the chlorination (or chloramination) of Suwannee River humic acid (SRHA) were also evaluated. Results indicated that the chlorination of BDE 47 and BDE 209 resulted in the formation of DBPs, with 1,1,1-trichloro-2-propanone (1,1,1-TCP) being the major DBP type formed. When PBDEs were present in the SRHA solution, a lower amount of CHCl〈sub〉3〈/sub〉 was formed, and more 1,1,1-TCP was produced. However, the effects of PBDEs on the formation of DBPs in the real surface water were insignificant because of the complicated water chemistry.〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Chemosphere, Volume 217〈/p〉 〈p〉Author(s): Jiena Yun, Chang Zhu, Qian Wang, Qiaoli Hu, Gang Yang〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Sulfur dioxide (SO〈sub〉2〈/sub〉) ranks as a major air pollutant and is likely to generate acid rain. When molecular oxygen is the oxygen source, the regular surfaces of gibbsite (one of the most abundant mineral dusts) show no reactivity for SO〈sub〉2〈/sub〉 conversions to H〈sub〉2〈/sub〉SO〈sub〉4〈/sub〉, while the partially dehydrated (100) surface with coordination-unsaturated Al sites becomes catalytically effective. Because of the easy availability of molecular oxygen, results manifest that acid rain can form under all atmospheric conditions and may account for the high conversion ratio of atmospheric SO〈sub〉2〈/sub〉. The (100) and (001) surfaces show divergent catalytic effects, and hydrolysis is always the rate-limiting step. Path A (hydrolysis and then oxidation) is preferred for (100) surface, whereas a third path with obviously lower activation barriers is presented for (001) surface, which is non-existent for (100) surface. Atomic oxygen originating from the dissociation of molecular oxygen is catalytically active for (100) surface, while the active site of (001) surface fails to be recovered, suggesting that SO〈sub〉2〈/sub〉 conversions over gibbsite surfaces are facet-controlled. This work also offers an environmentally friendly route for production of H〈sub〉2〈/sub〉SO〈sub〉4〈/sub〉 (one of the essential compounds in chemical industry), directly using molecular oxygen as the oxygen source.〈/p〉〈/div〉 〈/div〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0045653518320769-fx1.jpg" width="326" alt="Image 1" title="Image 1"〉〈/figure〉〈/p〉〈/div〉

Description: 〈p〉Publication date: February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Chemosphere, Volume 216〈/p〉 〈p〉Author(s): Guanghui Wang, Wenzhe Fan, Qin Li, Nansheng Deng〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉In this work, aspartic acid-β-cyclodextrin (ACD) was synthesized by the reaction of β-cyclodextrin with aspartic acid and epichlorohydrin, and graphene oxide-TiO〈sub〉2〈/sub〉 (GO-TiO〈sub〉2〈/sub〉) composite catalyst was prepared by a hydrothermal method. The complexation of ACD with New Coccine (NC) and Pb〈sup〉2+〈/sup〉 was characterized with FT-IR and XPS, respectively, the results show that ACD can simultaneously complex NC and Pb〈sup〉2+〈/sup〉. XRD analysis and SEM images of GO-TiO〈sub〉2〈/sub〉 show that TiO〈sub〉2〈/sub〉 platelets are well distributed on both sides of the graphene oxide sheets, and display a similar XRD pattern to the pure TiO〈sub〉2〈/sub〉 nanoparticles with the typical diffraction peak of anatase phase. The effects of ACD on the photocatalytic degradation of NC and photocatalytic reduction of Pb〈sup〉2+〈/sup〉 were investigated in the single pollution system, and the synergistic effects on the simultaneous photocatalytic NC degradation and Pb〈sup〉2+〈/sup〉 reduction in the presence of ACD were also evaluated. The results showed that the presence of ACD was favorable to the acceleration of photocatalytic oxidation of NC and photocatalytic reduction of Pb〈sup〉2+〈/sup〉 in the single pollution system, and the photocatalytic reaction rate constants of NC and Pb〈sup〉2+〈/sup〉 in the presence of ACD increased 58% and 42%, respectively. For the combined pollution system, the synergistic effects on the simultaneous conversion of NC and Pb〈sup〉2+〈/sup〉 in aqueous solutions were also further enhanced. ACD enhanced photocatalytic activity was attributed to the improvement of the electron transfer and mass transfer at the GO-TiO〈sub〉2〈/sub〉 interface.〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Chemosphere, Volume 216〈/p〉 〈p〉Author(s): Xinbo Wang, Hong Cheng, Peiying Hong, Xixiang Zhang, Zhiping Lai〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Despite advanced materials and techniques to reduce the fouling issue of membranes, 10–30% of the cost of ultrafiltration (UF) processes have been spent on membrane cleaning. Particularly in water treatment, the traditional heavy metal-based method is challenged due to its environmental pollution risk and increasing public health awareness. Here, we report the synthesis of a metal-free contact-active antifouling and antimicrobial membrane by covalently functionalizing a commercial polyacrylonitrile (PAN) UF membrane with 2,4-diamino-1,3,5-triazine (DAT) via a one-step catalyst-free hydrothermal [4 + 2] cyclization of dicyandiamide reaction. The proposed mechanism of the antimicrobial activity of the DAT-functionalized membrane is through strong attraction between the DAT groups and the microbial membrane protein via strong hydrogen bonding, leading to microbial membrane disruption and thus microbe death. A high water flux and good reusability of the membrane against protein in a UF experiment were achieved. The low cost, easy availability of the compounds, as well as the facile reaction offer a high potential of the membrane for real applications in ultrafiltration.〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Chemosphere, Volume 217〈/p〉 〈p〉Author(s): Jalil Jaafari, Kamyar Yaghmaeian〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉In this study, the interaction of the initial metal concentration, time of reaction and 〈em〉Chlorella coloniales〈/em〉 algae dose were taken for the biosorption of Cr, Cd, Co, Fe and As from aqueous solutions using the Box–Behnken design. The regression equation coefficients were calculated and the data confirmed the validity of second-order polynomial equation for the removal of Cr, Cd, Co, Fe and As with 〈em〉Chlorella coloniales〈/em〉 algae. Analysis of variance (ANOVA) showed a high coefficient of determination value (R〈sup〉2〈/sup〉) for Cr, Cd, Co, Fe, and As, being respectively 0.998, 0.998, 0.995, 0.998 and 0.994. Heavy metal biosorption increased with the increase in time of reaction from 30 h to 100 h then smoothly steadily decreased. The biosorption capacity of 〈em〉Chlorella coloniales〈/em〉 increased when initial Cd concentration was increased from 5 to 12 mg/L, and then no change was seen with further increasing in initial Cd concentration. At low concentrations of heavy metal, 〈em〉Chlorella coloniales〈/em〉 showed its effectiveness for Cr, Co, Fe and As bioaccumulation, but at high concentrations of heavy metal bioaccumulation efficiency decreased Under optimal value of process parameters, maximum efficiencies for the removal of Cr, Cd, Co, Fe, and As were 97.8, 97.05, 95.15, 98.6 and 96.5% respectively. The results of the present study suggest that use of 〈em〉C. Coloniales〈/em〉 algae can be a good alternative to the current expensive methods of removing heavy metals from aqueous solution.〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Chemosphere, Volume 216〈/p〉 〈p〉Author(s): Khalid Rehman Hakeem, Hesham F. Alharby, Reiazul Rehman〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉The effect of lead (Pb)-induced oxidative stress was investigated in 〈em〉Fagopyrum kashmirianum〈/em〉. The seedlings absorbed the Pb readily by showing time (15 and 30 days) and concentration (0, 100, 200 and 300 μM) dependent effects. Pb caused reduction in both root and shoot lengths but its accumulation was more in roots (22.32 mg g〈sup〉−1〈/sup〉 DW) than shoots (8.86 mg g〈sup〉−1〈/sup〉 DW) at the highest concentration (300 μM) resulting in translocation factor (TF) 〈 1 at all concentrations. Thus the uptake and translocation of Pb between roots and shoots showed a positive correlation indicating the plant as root accumulator. Amongst the photosynthetic pigments, chlorophyll content showed a decline while the carotenoid and anthocyanin levels were elevated. The fresh mass and biomass showed a non-significant decrease at both the sampling times. The osmolyte and antioxidative enzymes (SOD, CAT, APX. POD, GR and GST) were positively correlated with Pb treatments except proline and CAT, which showed decline in 30-day-old plants. The alleviation of Pb-stress is an indication for existence of strong detoxification mechanism in 〈em〉F. kashmirianum, which〈/em〉 suggest that it could be cultivated in Pb-contaminated soils.〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Chemosphere, Volume 216〈/p〉 〈p〉Author(s): Celestina E. Sobral – Souza, Ana R.P. Silva, Nadghia F. Leite, Janaina E. Rocha, Amanda K. Sousa, José G.M. Costa, Irwin R.A. Menezes, Francisco A.B. Cunha, Larissa A. Rolim, Henrique D.M. Coutinho〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉The present study had as its objective to verify the 〈em〉Psidium guajava〈/em〉 var. Pomifera L. chelating, antioxidant and cytoprotective effects against mercury and aluminum. The ethanolic extract, tannic and flavonoid fractions were subjected to LC-MS analysis. The Ferric Reducing Antioxidant Power (FRAP) and ferric ion reduction demonstrated a present antioxidant activity. The fungicidal and bactericidal activity of these metals were established. After determining the sub-allelopathic doses, germination tests using 〈em〉Lactuca sativa〈/em〉 were performed. Quercetin and its derivatives were the main compounds identified in the extract and the fractions. Mercury chloride significantly reduced the bactericidal effect of the flavonoid fraction (p 〈 0.001). None of the fractions were cytoprotective against mercury or aluminum in the fungal model assays. Using a sub-allelopathic concentration (64 μg/mL), the ethanolic extract, flavonoid and tannic fractions were found to be cytoprotective against aluminum for radicles, however only the tannic fraction was cytoprotective for caulicles. These data suggest that natural 〈em〉P. guajava〈/em〉 products are promising cytoprotective compound sources. This activity may be related to the antioxidant effect of secondary metabolites, mainly flavonoids. Our results point to a potential for environmental intervention product and technique development aimed at mitigating contamination by toxic metals such as mercury and aluminum.〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Chemosphere, Volume 216〈/p〉 〈p〉Author(s): Jie Luo, Xinli Xing, Shihua Qi, Jian Wu, X.W. Sophie Gu〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Hyperaccumulators can mobilize all metals in soil through secreting exudates to form soluble compounds but only hyperaccumulate part of them. Metals that cannot be accumulated are defined as non-hyperaccumulated metals and can increase the leaching risk in phytoremediation. Cd and Zn hyperaccumulator 〈em〉Noccaea caerulescens〈/em〉 (formerly 〈em〉Thlaspi caerulescens〈/em〉) was utilized to remediate multi-metal polluted soil in the present study, and the leaching risk of non-hyperaccumulated metals including Cu and Pb was investigated during the phytoremediation process. Comparing with 〈em〉Thlaspi arvense〈/em〉, a non-hyperaccumulator, 〈em〉N. caerulescens〈/em〉 significantly decreased the concentrations of Cd and Zn in leachate gathered from precipitation simulation experiments without electric field, but meanwhile dramatically increased the concentrations of Cu and Pb in soil solution. Electric field with low (2 V) and moderate (4 V) voltages increased the biomass yield and metal uptake capacity of 〈em〉N. caerulescens〈/em〉 simultaneously and therefore further reduced the concentrations of Cd and Zn in the leachate. Although the volume of leachate decreased significantly in pots with electric field, the leaching risk of Pb and Cu was deteriorated. Thus, decontaminating multi-metal polluted soil with electric field and hyperaccumulator should be conducted with caution due to potential secondary environmental risk caused by activated non-hyperaccumulated metals.〈/p〉〈/div〉 〈/div〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0045653518320320-egi10NH7JS1ZHN.jpg" width="286" alt="Image" title="Image"〉〈/figure〉〈/p〉〈/div〉

Description: 〈p〉Publication date: February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Chemosphere, Volume 217〈/p〉 〈p〉Author(s): Haitao Shen, Weiwei Li, Stephen E. Graham, James M. Starr〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Ingestion of soils and house dusts is an important pathway for children's exposure to sorbed organic pollutants such as polychlorinated biphenyls (PCBs). To reduce the uncertainty of the exposure estimates, it is important to understand the extent to which chemicals desorb and become bioaccessible following ingestion. In this study we use a three compartment in vitro digestive system to model the role of soil and house dust physicochemical properties on the post ingestion bioaccessibility of PCBs. Matched pairs (n = 37) of soil and dust were characterized for percent carbon and nitrogen, pH, moisture content, and particle size distribution. They were then fortified with a mixture of 18 PCBs and processed through the assay. The percent bioaccessibility of each PCB was calculated, then modeled using individual PCB log K〈sub〉ow〈/sub〉 values and the soil and dust properties. The bioaccessibility of the PCBs in soil (x̄ = 65 ± 16%) was greater (p 〈 0.001) than that of the PCBs in house dust (x̄ = 36 ± 14%). In the soil model, carbon was the sole statistically significant predictive (p ≤ 0.05) variable, while in house dust, both carbon and clay content were statistically significant (p ≤ 0.05) predictors.〈/p〉〈/div〉 〈/div〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0045653518320666-fx1.jpg" width="355" alt="Image 1" title="Image 1"〉〈/figure〉〈/p〉〈/div〉

Description: 〈p〉Publication date: February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Chemosphere, Volume 216〈/p〉 〈p〉Author(s): Xue Wu, Zheng Bo Zhu, Jia Hui Chen, Yi Fan Huang, Zi Li Liu, Jian Wen Zou, Ya Hua Chen, Na Na Su, Jin Cui〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Hydrogen-rich water (HRW) has been widely used in research on plant resistance to Cd. However, the underlying molecular mechanism of HRW in ameliorating cadmium stress in vegetables is largely unknown. In this study, the RNA-sequencing analyses were used to characterize the role of HRW in the alleviation of Cd toxicity in Chinese cabbage seedlings. Based on the obtained results, two genes encoding metal ionic transporters, 〈em〉BcIRT1〈/em〉 and 〈em〉BcZIP2〈/em〉 were ultimately selected out. Then, a systematic validation of the metal ion transport function of these two ZIP-encoding genes of pak choi were performed via a yeast transformation system. The results showed that 〈em〉BcIRT1〈/em〉 and 〈em〉BcZIP2〈/em〉 increased the sensitivity of different yeast mutant strains to relative metal ionic stresses and facilitated the accumulation of metal ions (Cd〈sup〉2+〈/sup〉, Mn〈sup〉2+〈/sup〉, Zn〈sup〉2+〈/sup〉, and Fe〈sup〉2+〈/sup〉) in yeast; thus, it suggests that 〈em〉BcIRT1〈/em〉 and 〈em〉BcZIP2〈/em〉 probably have the ability to transport Cd〈sup〉2+〈/sup〉, Mn〈sup〉2+〈/sup〉, Zn〈sup〉2+〈/sup〉 and Fe〈sup〉2+〈/sup〉 in pak choi. The time-course and concentration-dependent expression profiles of 〈em〉BcIRT1〈/em〉 and 〈em〉BcZIP2〈/em〉 showed that as time with HRW increased, the effectiveness of the repression on the expression of 〈em〉BcIRT1〈/em〉 and 〈em〉BcZIP2〈/em〉 increased, and as the seedlings were exposed to increased Cd concentrations, the inhibition of 〈em〉BcIRT1〈/em〉 and 〈em〉BcZIP2〈/em〉 by HRW was also increased. Over all, these findings provide new insights into the genome-wide transcriptome profiles in pak choi and show that HRW reduced Cd uptake probably through inhibiting the expression of transporters related to Cd absorption, 〈em〉BcIRT1〈/em〉 and 〈em〉BcZIP2〈/em〉.〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Chemosphere, Volume 217〈/p〉 〈p〉Author(s): Peter Butcherine, Kirsten Benkendorff, Brendan Kelaher, Bronwyn J. Barkla〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Widespread agricultural use of systemic neonicotinoid insecticides has resulted in the unintended contamination of aquatic environments. Water quality surveys regularly detect neonicotinoids in rivers and waterways at concentrations that could impact aquaculture stock. The toxicity of neonicotinoids to non-target aquatic insect and crustacean species has been recognised, however, there is a paucity of information on their effect on commercial shrimp aquaculture. Here, we show that commercially produced shrimp are likely to be exposed to dietary, sediment and waterborne sources of neonicotinoids; increasing the risks of disease and accidental human consumption. This review examines indicators of sublethal neonicotinoid exposure in non-target species and analyses their potential usefulness for ecotoxicology assessment in shrimp. The identification of rapid, reliable responses to neonicotinoid exposure in shrimp will result in better decision making in aquaculture management.〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Chemosphere, Volume 216〈/p〉 〈p〉Author(s): Maqusood Ahamed, Mohd Javed Akhtar, M.A. Majeed Khan, Salman A. Alrokayan, Hisham A. Alhadlaq〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Bismuth oxide nanoparticles (Bi〈sub〉2〈/sub〉O〈sub〉3〈/sub〉 NPs) have shown great potential for several applications including cosmetics and biomedicine. However, there is paucity of research on toxicity of Bi〈sub〉2〈/sub〉O〈sub〉3〈/sub〉 NPs. In this study, we first examined dose-dependent cytotoxicity and apoptosis response of Bi〈sub〉2〈/sub〉O〈sub〉3〈/sub〉 NPs in human breast cancer (MCF-7) cells. We further explored the potential mechanisms of cytotoxicity of Bi〈sub〉2〈/sub〉O〈sub〉3〈/sub〉 NPs through oxidative stress. Physicochemical study demonstrated that Bi〈sub〉2〈/sub〉O〈sub〉3〈/sub〉 NPs have crystalline structure and spherical shape with mean size of 97 nm. Toxicity studies have shown that Bi〈sub〉2〈/sub〉O〈sub〉3〈/sub〉 NPs reduce cell viability and induce membrane damage dose-dependently in the concentration range of 50–300 μg/ml. Bi〈sub〉2〈/sub〉O〈sub〉3〈/sub〉 NPs also disturbed cell cycle of MCF-7 cells. Oxidative stress response of Bi〈sub〉2〈/sub〉O〈sub〉3〈/sub〉 NPs was evident by generation of reactive oxygen species (ROS), higher lipid peroxidation, reduction of glutathione (GSH) and low superoxide dismutase (SOD) enzyme activity. Interestingly, supplementation of external antioxidant N-acetyl-cysteine almost negated the effect of Bi〈sub〉2〈/sub〉O〈sub〉3〈/sub〉 NPs induced oxidative stress and cell death. We also found that exposure of Bi〈sub〉2〈/sub〉O〈sub〉3〈/sub〉 NPs induced apoptotic response in MCF-7 cells suggested by impaired regulation of Bcl-2, Bax and caspase-3 genes. Altogether, we found that Bi〈sub〉2〈/sub〉O〈sub〉3〈/sub〉 NPs induced cytotoxicity in MCF-7 cells through modulating the redox homeostasis 〈em〉via〈/em〉 Bax/Bcl-2 pathway. This study warranted further research to delineate the underlying mechanism of Bi〈sub〉2〈/sub〉O〈sub〉3〈/sub〉 NPs induced toxicity at 〈em〉in vivo〈/em〉 level.〈/p〉〈/div〉 〈/div〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0045653518320897-fx1.jpg" width="492" alt="Image 1" title="Image 1"〉〈/figure〉〈/p〉〈/div〉

Description: 〈p〉Publication date: February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Chemosphere, Volume 216〈/p〉 〈p〉Author(s): Xingdong Wang, Qiaoqiao Chi, Xuejiao Liu, Yin Wang〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉A novel approach was used to prepare sewage sludge (SS)-derived biochar via coupling of hydrothermal pretreatment with pyrolysis (HTP) process at 300–700 °C. The influence of the pyrolysis temperature on the characteristics and environmental risk of heavy metals (HMs) in biochar derived from SS were investigated. The HTP process at higher pyrolysis temperature (≥500 °C) resulting in a higher quality of SS-derived biochar and in HMs of lower toxicity and environmental risk, compared with direct SS pyrolysis. Surface characterization and micromorphology analysis indicate that the N〈sub〉2〈/sub〉 adsorption capacity and BET surface area in biochar (SRC〈sub〉220〈/sub〉-500) obtained from hydrothermally treated SS at 220 °C (SR〈sub〉220〈/sub〉) pyrolysis at 500 °C, significantly increased the BET surface area and achieved its maximum value (47.04 m〈sup〉2〈/sup〉/g). Moreover, the HTP process can promote the HMs in SS be transformed from bioavailable fractions to more stable fractions. This increases with the pyrolysis temperature, resulting in a remarkable reduction in the potential environmental risk of HMs from the biochar obtained from the HTP process.〈/p〉〈/div〉 〈/div〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0045653518320605-fx1.jpg" width="340" alt="Image 1" title="Image 1"〉〈/figure〉〈/p〉〈/div〉

Description: 〈p〉Publication date: 15 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 536〈/p〉 〈p〉Author(s): Huihui Sun, Katarzyna Zielinska, Marina Resmini, Ali Zarbakhsh〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉In dermal drug delivery, the influence of the chemical structure of the carriers on their penetration mechanisms is not yet fully understood. This is a key requirement in order to design highly efficient delivery systems. In this study, neutron reflectivity is used to provide insights into the interactions between thermoresponsive 〈em〉N〈/em〉-isopropylacrylamide based nanogels, cross-linked with 10%, 20% and 30% 〈em〉N,N'〈/em〉-methylenebisacrylamide, and skin lipid multi-bilayers models. Ceramide lipid multi-bilayers and ceramide/cholesterol/behenic acid mixed lipid multi-bilayers were used for this work. The results indicated that in both multi-bilayers the lipids were depleted by the nanogels mainly through hydrophobic interactions. The ability of nanogels to associate with skin lipids to form water-dispersible complexes was found to be a function of the percentage cross-linker. An enhanced depletion of lipids was further observed in the presence of benzyl alcohol, a well-known skin penetration enhancer.〈/p〉〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0021979718312840-ga1.jpg" width="294" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: 15 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 536〈/p〉 〈p〉Author(s): Zexing Wu, Min Song, Zijin Zhang, Jie Wang, Xien Liu〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Investigation of non-precious, highly-active and durable catalysts is an essential criteria for the development of electrocatalytic hydrogen evolution reaction (HER). In this work, reduced graphene oxide coupled with molybdenum phosphide (MoP-RGO) is prepared through a facile and scalable one-step strategy. Three strategies are developed to tune the electrocatalytic performance of MoP-RGO including optimize the pyrolysis temperature, add NaCl template and introduction of sulfur atoms. After the optimization, the overpotentials at 10 mA cm〈sup〉−2〈/sup〉 reduced from 238 to 152 mV (alkaline electrolyte) and 232 to 144 mV (acid medium), respectively. This work mainly focus on exploiting various strategies to tune the electrocatalytic performance of non-precious catalysts for HER which can provide multiple avenues to develop efficient electrocatalysts.〈/p〉〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉 〈p〉Pyrolysis temperature, NaCl template and sulfur atom are used to tune the electrocatalytic performance of MoP-RGO. After the optimized process, the overpotentials needed to deliver 10 mA cm〈sup〉−2〈/sup〉 reduced from 238 to 152 mV (alkaline electrolyte) and 232 to 144 mV (acid medium), respectively.〈/p〉 〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0021979718312657-ga1.jpg" width="353" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉 〈/div〉 〈/div〉

Description: 〈p〉Publication date: 15 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 536〈/p〉 〈p〉Author(s): Prakhar Sengar, Karelid Garcia-Tapia, Kanchan Chauhan, Akhil Jain, Karla Juarez-Moreno, Hugo A. Borbón-Nuñez, Hugo Tiznado, Oscar E. Contreras, Gustavo A. Hirata〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉The current photodynamic therapy (PDT) is majorly hindered by the shallow penetration depth and oxygen dependency, limiting its application to deep-seated solid hypoxic tumors. Thus, it is meaningful to develop efficient X-ray mediated PDT system capable of generating reactive oxygen species (ROS) under both the normoxic and hypoxic conditions. Herein, we report the synthesis and characterization of nanocomposite, YAG:Pr@ZnO@PpIX with an amalgamation of UV-emitting Y〈sub〉2.99〈/sub〉Pr〈sub〉0.01〈/sub〉Al〈sub〉5〈/sub〉O〈sub〉12〈/sub〉 (YAG:Pr) nanoscintillator, and zinc oxide (ZnO) and protoporphyrin IX (PpIX) as photosensitizers. YAG:Pr surface was coated with a ZnO layer (∼10 nm) by atomic layer deposition, and then PpIX was covalently conjugated via a linker to give YAG:Pr@ZnO@PpIX. The photo- and cathodoluminescence analyses gave the evidences of efficient energy transfer from YAG:Pr to ZnO at ∼320 nm, and YAG:Pr@ZnO to PpIX at Soret region (350–450 nm). The nanohybrid was able to produce both, Type I and Type II ROS upon direct and indirect photoactivation with UV〈sub〉365nm〈/sub〉 and UV〈sub〉290nm〈/sub〉, respectively. In vitro cytotoxicity of non-activated YAG:Pr@ZnO@PpIX in mouse melanoma cells revealed low toxicity, which significantly enhanced upon photoactivation with UV〈sub〉365nm〈/sub〉 indicating the photokilling property of the nanohybrid. Overall, our preliminary studies successfully demonstrate the potential of YAG:Pr@ZnO@PpIX to overcome the limited penetration and oxygen-dependency of traditional PDT.〈/p〉〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0021979718312876-ga1.jpg" width="287" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Chemosphere, Volume 216〈/p〉 〈p〉Author(s): Yan Wang, Qiaonan Zhang, Yuwei Zhang, Hongxia Zhao, Feng Tan, Xiaowei Wu, Jingwen Chen〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Concentrations and temporal variations of priority polycyclic aromatic hydrocarbons (PAHs) in the air from a suburban area of Dalian, China were investigated for a 1-year period to assess their sources and potential correlations with six criteria air pollutants and meteorological parameters. The total concentrations of PAHs were in the range of 4.32–112.2 ng/m〈sup〉3〈/sup〉 (Mean = 52.37 ± 23.99 ng/m〈sup〉3〈/sup〉). Seasonality was discovered with the PAHs following an order of winter 〉 spring 〉 summer 〉 autumn. The impacts of meteorological parameters on PAH levels were season-dependent. High temperature may increase the air concentrations of 4-ring PAHs during the non-heating period, whereas high relative humidity may raise the concentrations of 3- and 4-ring PAHs during the heating period. Correlations of PAHs with criteria air pollutants, such as SO〈sub〉2〈/sub〉, NO〈sub〉2〈/sub〉, and O〈sub〉3〈/sub〉, indicated that both fossil fuel combustion and photochemical oxidation influenced the air concentrations of PAHs. According to the source apportionment by diagnostic ratios and PMF model, coal combustion and traffic emission were estimated to be the main sources of PAHs in Dalian, followed by petroleum release and biomass burning. It was worth noting that the contribution of coal combustion to the PAH burdens increased from 26% to 45% due to the emission from domestic heating in winter. This extra emission needs a continuous concern in the future.〈/p〉〈/div〉 〈/div〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0045653518320551-fx1.jpg" width="500" alt="Image 1" title="Image 1"〉〈/figure〉〈/p〉〈/div〉

Description: 〈p〉Publication date: February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Chemosphere, Volume 216〈/p〉 〈p〉Author(s): Min Liu, Shenglan Jia, Ting Dong, Yuan Han, Jingchuan Xue, Elvy Riani Wanjaya, Mingliang Fang〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Bisphenol A diglycidy ether (BADGE) and its derivatives are epoxy resins and widely used as emerging plasticizers in food packages and material coating. Though known as endocrine disruptors, little information is available on their occurrence, exposure routes and toxicity. Besides, the analysis of BADGE and its derivatives has always been a challenge due to their reactive chemical properties and the background contamination. Therefore, we firstly developed a novel water-free method to analyze BADGE and its derivatives in dust samples together with other two typical plasticizers bisphenol A (BPA) and bisphenol S (BPS). In order to investigate the levels in paired dust and urine samples, 33 paired samples were collected from Singapore. In both dust and urine samples, the predominant compounds were BPA, BADGE-2H〈sub〉2〈/sub〉O and BPS. A significantly positive correlation of BPA levels in paired dust and urine samples was observed in this small-scale study. To tentatively explore the human health effect from exposure to these bisphenol plasticizers, we assessed the correlation between the urinary concentrations of these compounds and oxo-2’-deoxyguanosine (8-OHdG), an oxidative stress biomarker. The result showed that 8-OHdG levels in urine samples was positively correlated with urinary BPA level and body mass index (BMI), suggesting that elevated oxidative stress might be associated with BPA exposure and obesity. In the future, a larger scale study is warranted due to the limited sample size in this study.〈/p〉〈/div〉 〈/div〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0045653518319453-fx1.jpg" width="300" alt="Image 1" title="Image 1"〉〈/figure〉〈/p〉〈/div〉

Description: 〈p〉Publication date: February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Chemosphere, Volume 216〈/p〉 〈p〉Author(s): Tao Cui, Chenyang Shen, Anlin Xu, Weiqing Han, Jiansheng Li, Xiuyun Sun, Jinyou Shen, Lianjun Wang〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉In this work, a novel coupled-oxidation tubular reactor (COTR)/non-thermal dielectric barrier discharge (NTP-DBD) catalytic plasma in a synergistic electro-catalysis system was investigated for odorous mercaptans decomposition. In order to enhance the degradation efficiency of electro-oxidation, a novel enhanced Ti/PbO〈sub〉2〈/sub〉 electro-catalytic tubular reactor prepared by using flow dynamic electrodeposition was designed and applied as pretreatment process for CH〈sub〉3〈/sub〉SNa wastewater. The results indicated that the optimal condition was 7 mA cm〈sup〉−2〈/sup〉 of current density, 10 g L〈sup〉−1〈/sup〉 of initial concentration of CH〈sub〉3〈/sub〉SNa, 9.0 of pH and 5.0 g L〈sup〉−1〈/sup〉 of electrolyte concentration. Addition of Fe〈sup〉2+〈/sup〉 and H〈sub〉2〈/sub〉O〈sub〉2〈/sub〉 and mechanism of COTR system were first put forward. The target species CH〈sub〉3〈/sub〉SNa were removed over 90% by this process. In order to treat the CH〈sub〉3〈/sub〉SH effusion which was co-produced with CH〈sub〉3〈/sub〉SNa aqueous solution, the technology of NTP-DBD catalytic plasma reactor followed by a chemical absorption has been developed. MSH could be removed over 95% under the condition of 2 s of residence time, 15 kV of output voltage with oxygen concentration of 9%. Moreover, the synthetic Ni-doped AC catalyst had the best performance under 0.7 mmol g〈sup〉−1〈/sup〉 of nickel loading. The conclusion was the energetic electrons generated in the DBD reactor played a key role on the removal of MSH, and the major decomposition products of MSH were detected as CH〈sub〉3〈/sub〉SSCH〈sub〉3〈/sub〉, SO〈sub〉2〈/sub〉 and NO〈sub〉2〈/sub〉. Moreover, the gaseous products in the plasma exhaust could be absorbed and fixed by the subsequent aqueous NaOH solution.〈/p〉〈/div〉 〈/div〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0045653518320411-fx1.jpg" width="359" alt="Image 1" title="Image 1"〉〈/figure〉〈/p〉〈/div〉

Description: 〈p〉Publication date: February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Chemosphere, Volume 216〈/p〉 〈p〉Author(s): Changlong Wei, Xin Song, Qing Wang, Yun Liu, Na Lin〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉6:2 chlorinated polyfluorinated ether sulfonate (trade name F-53B), a perfluorooctane sulfonate alternative used as a mist suppressant in the chromium plating industry, is environmentally persistent and bioaccumulative. In this study, the kinetic and equilibrium data of F-53B sorption onto soils were obtained to investigate the relationship between sorption parameters and soil attributes. The effects of potential coexisting Cu(II), anionic Cr(VI) and sulfate on F-53B sorption by soils were explored. This is the first report of the effects of F-53B sorption behavior on soils with coexisting contaminants of Cu(II) and Cr(VI). The results showed that sorption kinetics of F-53B on soils could be well-fitted by the pseudo-second-order model. The maximum F-53B sorption capacity ranged from 22.71 to 92.36 mg/kg on six different soils, and the correlation analysis indicated a positive relationship between the maximum sorption capacity and the soil organic content, Al〈sub〉2〈/sub〉O〈sub〉3〈/sub〉, and Fe〈sub〉2〈/sub〉O〈sub〉3〈/sub〉. The desorption percentages of F-53B in this study, defined as the proportion of sorbed F-53B on soils that was recovered upon desorption, were lower than 8.2%. Moreover, F-53B sorption capacities generally decreased in the presence of Cu(II), Cr(VI), and sulfate, indicating that these ions can facilitate the F-53B mobility in the subsurface. Taken together, these findings suggest that electrostatic interaction, hydrophobic interaction, ligand exchange, and surface complexation contributed to the F-53B sorption on soils.〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: 10 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Electrochimica Acta, Volume 296〈/p〉 〈p〉Author(s): Kadir Tuna, Arnd Kilian, Thorsten Ressler〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Electroless plating of tin layers with thicknesses of more than 3 μm is becoming an important process in the production of circuit boards and semiconductor. Phosphonates constitute promising complexing agents for autocatalytic tin electrolytes. However, detailed time-resolved investigations or electrochemical impedance spectroscopy (EIS) measurements of tin deposition in this system are lacking. Here, deposition of tin was investigated by electrochemical quartz microbalance (EQCM) and electrochemical impedance spectroscopy. EQCM investigations showed a strong drop in deposition rate within the first ten minutes. Bath parameters had a significant effect on the drop of deposition rate. The results indicated an inhibitive pyrophosphate adsorption on the tin electrode surface which caused the observed drop of deposition rate. Impedance measurements confirmed this assumption. The equivalent circuit applied for the analysis of EIS data, included an increasing adsorbate resistance Rp, which can be related to the thickness of an adsorbed permeable pyrophosphate layer. Impedance measurements at selected frequencies revealed a linear relation between deposition rate and conductance 1/Rp. Subsequently, gluconate substituting for pyrophosphate was tested as complexing agent. Combined EQCM and EIS measurements during deposition using a gluconate containing electrolyte showed a stable rate with an invariant conductance.〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: 1 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Electrochimica Acta, Volume 295〈/p〉 〈p〉Author(s): Tao Liu, Xiaolin Sun, Shimei Sun, Quanhai Niu, Hui Liu, Wei Song, Fengting Cao, Xichao Li, Takeo Ohsaka, Jianfei Wu〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Lithium-sulfur batteries were investigated as promising next-generation energy storage devices owing to their high capacity in comparison to conventional lithium-ion batteries. Nevertheless, the serious shuttle effect and sluggish redox kinetics originated from dissolution of polysulfides and insulating property of sulfur and lithium sulfide, restricted their practical applications. To overcome these stubborn problems, a robust and environment-friendly biomass carbon fiber interlayer anchored with uniformly-distributed SiO〈sub〉2〈/sub〉 nanoparticles was demonstrated. Benefiting from the excellent conductivity of carbon fiber, together with the stable chemical adsorption of SiO〈sub〉2〈/sub〉 for soluble polysulfides, this low-cost and lightweight interlayer could not only remarkably enhance sulfur utilization, but also efficiently capture the polysulfides by chemical entrapment strategies. With this biomass carbon fiber@SiO〈sub〉2〈/sub〉 interlayer, the batteries delivered a high reversible capacity of 1352.8 mAh g〈sup〉−1〈/sup〉 at 0.1 C and enhanced capacity of 618.4 mAh g〈sup〉−1〈/sup〉 after 500 cycles at 1.0 C. Even up to 4.2 mg cm〈sup〉−2〈/sup〉 sulfur loading, high cycling stability was also achieved by this interlayer. We believe this robust and low-cost interlayer has a great potential for practical applications of Li–S batteries.〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Chemosphere, Volume 216〈/p〉 〈p〉Author(s): Jaime Rodríguez-Estival, Marta I. Sánchez, Cristina Ramo, Nico Varo, Juan A. Amat, Juan Garrido-Fernández, Dámaso Hornero-Méndez, Manuel E. Ortiz-Santaliestra, Mark A. Taggart, Mónica Martinez-Haro, Andy J. Green, Rafael Mateo〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉European populations of black-necked grebes (〈em〉Podiceps nigricollis〈/em〉) congregate every year to moult at the salt ponds of the Odiel Marshes (SW Spain). However, the Odiel Marshes are part of one of the most metal-polluted coastal estuaries in the world, which may pose risks to wildlife. We assessed the exposure of grebes to metal pollution during the critical moulting period in the Odiel Marshes and its potential to cause adverse health effects. Levels of metals in red blood pellet (as a biomarker of exposure), plasma carotenoids, eye redness, and body condition (as biomarkers of effects) were studied. Metal content was also analyzed in the brine shrimp 〈em〉Artemia parthenogenetica〈/em〉, the most important food for grebes in this hypersaline ecosystem during the moulting period. Results showed that, in comparison to toxicity thresholds, grebes had relatively high blood levels of arsenic (As), mercury (Hg) and zinc (Zn). The high loads found in 〈em〉Artemia〈/em〉 and the way blood levels vary during the moulting period indicate that shrimp consumption may be the main route of metal exposure for grebes. Plasma carotenoids and body condition showed a positive association with exposure to As, while the relationship of lutein-like carotenoids with Hg accumulation was negative at the beginning of the moulting period to become positive afterwards. Moreover, eye redness was negatively affected by As accumulation. Factors including food resource availability, seasonal fluctuations in physiological status, and interannual variations in the degree of environmental contamination should be considered in monitoring efforts when using moult migrant waterbirds as sentinel species.〈/p〉〈/div〉 〈/div〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S004565351832006X-egi108SW54GQSP.jpg" width="355" alt="Image" title="Image"〉〈/figure〉〈/p〉〈/div〉

Description: 〈p〉Publication date: February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Chemosphere, Volume 216〈/p〉 〈p〉Author(s): Hong Wang, Zhiqiu Gao, Jingzheng Ren, Yibo Liu, Lisa Tzu-Chi Chang, Kevin Cheung, Yun Feng, Yubin Li〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉This study investigates the urban-rural and sex differences in the increased risks of the ten most common cancers in China related to high PM〈sub〉2.5〈/sub〉 concentration in the southeastern side of Hu line. Pearson correlation coefficient is estimated to reveal how the cancers closely associated with PM〈sub〉2.5〈/sub〉 long-term exposure. Then linear regression is conducted to evaluate sex- and area-specific increased risks of those cancers from high level PM〈sub〉2.5〈/sub〉 long-term exposure. The major finding is with the increase of every 10 μg/m〈sup〉3〈/sup〉 of annual mean PM〈sub〉2.5〈/sub〉 concentration, the increase of relative risks for lung cancer incidence and mortality are 15% and 23% for males, and 22% and 24% for females in rural area. For urban area, the increase of relative risk for ovarian cancer incidence is 9% for females, while that for prostatic cancer increases 17% for males. For leukemia, the increase of relative risks for incidence and mortality are 22% and 19% for females in rural area, while in urban area the increase of relative risk for mortality is 9% for males and for incidence is 6% for females. It is also found that with increased PM〈sub〉2.5〈/sub〉 exposure, the risks for ovarian and prostatic cancer rise significantly in urban area, while risks for lung cancer and leukemia rise significantly in rural area. The results demonstrate the higher risks for lung cancer and leukemia with increased PM〈sub〉2.5〈/sub〉 exposure are more significant for female. This study also suggests that the carcinogenic effects of PM〈sub〉2.5〈/sub〉 have obvious sex and urban-rural differences.〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Chemosphere, Volume 216〈/p〉 〈p〉Author(s): Yanju Liu, Jianhua Du, Zhaomin Dong, Mohammad Mahmudur Rahman, Yongchao Gao, Kaihong Yan, Ravi Naidu〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉There is increasing concern about the use of chromated copper arsenate (CCA) treated timber due to the possible leaching of toxic metals or metalloids. CCA-treated timber waste are currently stockpiled across Australia with limited information about their risks to the environment or human health. In this study, the treatment and utilisation of CCA-treated timber waste as garden mulch, garden retaining walls, and soil additive were investigated. Iron materials were used as immobilising agents. The bioavailability of Cr, Cu and As to 〈em〉Spinacia oleracea〈/em〉 from CCA-treated timber, before and after treatment, was determined in the context of human health risk assessment. The results showed that the iron-based treatments resulted in significant decreases in the concentrations of Cu and As in spinach grown in CCA-treated timber in soil. Analyses of CCA derived Cu and As in spinach showed that they accumulated in the roots rather than in the leaves. The risks of toxicity to humans varied for different utilisation scenarios and the immobilisation amendments were shown to reduce carcinogenic and non-carcinogenic risks. The information obtained in this study can inform development of utilisation options for CCA-treated timber wastes.〈/p〉〈/div〉 〈/div〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0045653518320022-fx1.jpg" width="307" alt="Image 1" title="Image 1"〉〈/figure〉〈/p〉〈/div〉

Description: 〈p〉Publication date: February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Chemosphere, Volume 216〈/p〉 〈p〉Author(s): Han Chen, Tao Lin, Wei Chen, Hui Tao, Hang Xu〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉The variations of disinfection byproduct (DBP) precursors and DBPs-associated toxic potencies were evaluated by ozonation, followed by a up-flow biological activated carbon (O〈sub〉3〈/sub〉/UBAC) filter treating two reconstituted water samples, featuring either high bromide (105.3 μg/L) or dissolved organic nitrogen (0.73 mg N/L) concentration, respectively. Ozonation contributed to ∼20% decrease in dissolved organic carbon (DOC) concentration at a dosage of 0.7 mg of O〈sub〉3〈/sub〉/mg of DOC, but no further reduction in DOC level was observed with an increased dose of 1.0 mg of O〈sub〉3〈/sub〉/mg of DOC. When chlorine or preformed monochloramine was used as a disinfectant, UBAC process led to ∼40% reduction in the sum of detected DBP formation potential (FP) due to the removal of precursors at a feasible empty bed contact time of 15 min. The integrated effect of ozonation and UBAC biofiltration decreased the sum of DBP FP by ∼50% including halonitromethanes (THNMs), N-nitrosamines (NAs), and bromate, which increased in the effluent of ozonation. Chloramination produced less DBPs by weight as well as DBPs-associated additive toxic potencies than chlorination. The reduction in additive toxic potencies was generally lower than the removal efficiency of DBP FP after chlor(am)ination of treated waters by O〈sub〉3〈/sub〉/UBAC, indicating that the removal of DBPs-associated additive toxic potencies should be focused to better understand on the residual risk to public health in controlling DBP precursors.〈/p〉〈/div〉 〈/div〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0045653518319064-fx1.jpg" width="273" alt="Image 1" title="Image 1"〉〈/figure〉〈/p〉〈/div〉

Description: 〈p〉Publication date: February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Chemosphere, Volume 217〈/p〉 〈p〉Author(s): Brooke K. Mayer, Carlan Johnson, Yu Yang, Nicole Wellenstein, Emily Maher, Patrick J. McNamara〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉This study evaluated strategies targeting macro- and micro-organic contaminant mitigation using low-energy titanium dioxide photocatalysis. Energy inputs of 1, 2, and 5 kWh m〈sup〉−3〈/sup〉 resulted in incomplete oxidation of macro-organic natural organic matter, signified by greater reductions of UV〈sub〉254〈/sub〉 and specific ultraviolet UV absorbance (SUVA) in comparison to dissolved organic carbon (DOC). The rate of UV〈sub〉254〈/sub〉 removal was 3 orders of magnitude greater than the rate of DOC degradation. Incomplete oxidation improved operation of downstream filtration processes. Photocatalysis at 2 kWh m〈sup〉−3〈/sup〉 increased the bed life of downstream granular activated carbon (GAC) filtration by 340% relative to direct filtration pretreatment. Likewise, photocatalysis operated ahead of microfiltration decreased fouling, resulting in longer filter run times. Using 2 kWh m〈sup〉−3〈/sup〉 photocatalysis increased filter run time by 36 times in comparison to direct filtration. Furthermore, levels of DOC and UV〈sub〉254〈/sub〉 in the membrane permeate improved (with no change in removal across the membrane) using low-energy photocatalysis pretreatments. While high-energy UV inputs provided high levels of removal of the estrogenic micro-organics estrone (E1), 17β-estradiol (E2), estriol (E3), and 17α-ethynlestradiol (EE2), low-energy photocatalysis did not enhance removal of estrogens beyond levels achieved by photolysis alone. In the cases of E1 and E3, the addition of TiO〈sub〉2〈/sub〉 as a photocatalyst reduced degradation rates of estrogens compared to UV photolysis. Overall, process electrical energy per order magnitude reductions (EEOs) greatly improved using photocatalysis, versus photolysis, for the macro-organics DOC, UV〈sub〉254〈/sub〉, and SUVA; however, energy required for removal of estrogens was similar between photolysis and photocatalysis.〈/p〉〈/div〉 〈/div〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0045653518320885-fx1.jpg" width="500" alt="Image 1" title="Image 1"〉〈/figure〉〈/p〉〈/div〉

Description: 〈p〉Publication date: February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Chemosphere, Volume 216〈/p〉 〈p〉Author(s): Rahat Riaz, Usman Ali, Jun Li, Gan Zhang, Khan Alam, Andrew James Sweetman, Kevin C. Jones, Riffat Naseem Malik〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Lesser Himalayan Region (LHR) is an important mountain ecosystem which supports a wide range of biodiversity for native flora and fauna. Human population in this region is largely dependent upon local sources for their livelihood. Surface soil (n = 32) and sediment (n = 32) were collected from four different altitudinal ranges of LHR and analyzed for priority Polycyclic Aromatic Hydrocarbons (PAHs) recommended by USEPA. Level, sources and distribution pattern of PAHs were assessed in soil and sediments samples collected from four altitudinal zones in LHR. Total PAHs concentration level of PAHs in soil and sediments ranged from 62.79 to 1080 ng g〈sup〉−1〈/sup〉 and 14.54–437.43 ng g〈sup〉−1〈/sup〉, respectively. Compositional profile of PAHs in both soil and sediment were dominated by low and medium molecular weight PAHs, ranged from 18.02 to 402.18 ng g〈sup〉−1〈/sup〉in soil and 0.32–96.34 ng g〈sup〉−1〈/sup〉in sediments. In the context of spatial distribution trend, highest mean concentrations of PAHs in soil were recorded in zone D (sites from the rural region) and for sediments highest concentrations were detected at zone A, which includes dam sites. In all four zones, no altitudinal trend of PAHs in soil and sediments was observed. Source apportionment through receptor modelling by positive matrix factorization (PMF) revealed that local sources such as biomass combustion and vehicular emissions are important sources of PAHs in this region. The prevalence of monsoon atmospheric circulation system in LHR implicated that this region is also influenced by medium and long range atmospheric transportation of PAHs from neighboring countries where potential sources and high level of PAHs has been reported.〈/p〉〈/div〉 〈/div〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0045653518320009-fx1.jpg" width="357" alt="Image 1" title="Image 1"〉〈/figure〉〈/p〉〈/div〉

Description: 〈p〉Publication date: February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Chemosphere, Volume 217〈/p〉 〈p〉Author(s): Xiaohui Zhang, Song Tang, Mao Wang, Weimin Sun, Yuwei Xie, Hui Peng, Aimin Zhong, Hongling Liu, Xiaowei Zhang, Hongxia Yu, John P. Giesy, Markus Hecker〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Acid mine drainage (AMD) is one of the most hazardous byproducts of some types of mining. However, research on how AMD affects the bacterial community structure of downstream riverine ecosystems and the distribution of metal resistance genes (MRGs) along pollution gradient is limited. Comprehensive geochemical and high-throughput next-generation sequencing analyses can be integrated to characterize spatial distributions and MRG profiles of sediment bacteria communities along the AMD-contaminated Hengshi River. We found that (1) diversities of bacterial communities significantly and gradually increased along the river with decreasing contamination, suggesting community composition reflected changes in geochemical conditions; (2) relative abundances of phyla 〈em〉Proteobacteria〈/em〉 and genus 〈em〉Halomonas〈/em〉 and 〈em〉Planococcaceae〈/em〉 that function in metal reduction decreased along the AMD gradient; (3) low levels of sediment salinity, sulfate, aquatic lead (Pb), and cadmium (Cd) were negatively correlated with bacterial diversity despite pH was in a positive manner with diversity; and (4) arsenic (As) and copper (Cu) resistance genes corresponded to sediment concentrations of As and Cu, respectively. Altogether, our findings offer initial insight into the distribution patterns of sediment bacterial community structure, diversity and MRGs along a lotic ecosystem contaminated by AMD, and the factors that affect them.〈/p〉〈/div〉 〈/div〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S004565351832085X-fx1.jpg" width="437" alt="Image 1" title="Image 1"〉〈/figure〉〈/p〉〈/div〉

Description: 〈p〉Publication date: February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Chemosphere, Volume 217〈/p〉 〈p〉Author(s): Kenneth Brezinski, Beata Gorczyca〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Natural organic matter (NOM) constitutes the terrestrial and aquatic sources of organic plant like material found in water bodies. As of recently, an ever-increasing amount of effort is being put towards developing better ways of unraveling the heterogeneous nature of NOM. This is important as NOM is responsible for a wide variety of both direct and indirect effects: ranging from aesthetic concerns related to taste and odor, to issues related to disinfection by-product formation and metal mobility. A better understanding of NOM can also provide a better appreciation for treatment design; lending a further understanding of potable water treatment impacts on specific fractions and constituents of NOM. The use of high performance size-exclusion chromatography has shown a growing promise in its various applications for NOM characterization, through the ability to partition ultraviolet absorbing moieties into ill-defined groups of humic acids, hydrolysates of humics, and low molecular weight acids. HPSEC also has the ability of simultaneously measuring absorbance in the UV–visible range (200–350 nm); further providing a spectroscopic fingerprint that is simply unavailable using surrogate measurements of NOM, such as total organic carbon (TOC), ultraviolet absorbance at 254 nm (UV〈sub〉254〈/sub〉), excitation-emission matrices (EEM), and specific ultraviolet absorbance at 254 nm (SUVA〈sub〉254〈/sub〉). This review mainly focuses on the use of HPSEC in the characterization of NOM in a potable water setting, with an additional focus on strong-base ion-exchangers specifically targeted for NOM constituents.〈/p〉〈/div〉 〈/div〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0045653518318824-fx1.jpg" width="474" alt="Image 1" title="Image 1"〉〈/figure〉〈/p〉〈/div〉

Description: 〈p〉Publication date: February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Chemosphere, Volume 216〈/p〉 〈p〉Author(s): John Pierce Wise, James T.F. Wise, Catherine F. Wise, Sandra S. Wise, Cairong Zhu, Cynthia L. Browning, Tongzhang Zheng, Christopher Perkins, Christy Gianios, Hong Xie, John Pierce Wise〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉One Environmental Health has emerged as an important area of research that considers the interconnectedness of human, animal and ecosystem health with a focus on toxicology. The great whales in the Gulf of Maine are important species for ecosystem health, for the economies of the Eastern seaboard of the United States, and as sentinels for human health. The Gulf of Maine is an area with heavy coastal development, industry, and marine traffic, all of which contribute chronic exposures to environmental chemicals that can bioaccumulate in tissues and may gradually diminish an individual whale's or a population's fitness. We biopsied whales for three seasons (2010–2012) and measured the levels of 25 metals and selenium in skin biopsies collected from three species: humpback whales (〈em〉Megaptera novaeangliae〈/em〉), fin whales (〈em〉Balaenoptera physalus〈/em〉), and a minke whale (〈em〉Balaenoptera acutorostrata〈/em〉). We established baseline levels for humpback and fin whales. Comparisons with similar species from other regions indicate humpback whales have elevated levels of aluminum, chromium, iron, magnesium, nickel and zinc. Contextualizing the data with a One Environmental Health approach finds these levels to be of potential concern for whale health. While much remains to understand what threats these metal levels may pose to the fitness and survival of these whale populations, these data serve as a useful and pertinent start to understanding the threat of pollution.〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Chemosphere, Volume 216〈/p〉 〈p〉Author(s): Han Wang, Guangjing Xu, Zheng Qiu, Yan Zhou, Yu Liu〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉The high energy consumption associated with biological treatment of municipal wastewater is posing a serious impact and challenge on the current global wastewater industry and is also inevitably linked to the issue of global climate change. To tackle such an emerging situation, this study aimed to develop strategies to effectively suppress nitrite oxidizing bacteria (NOB) in pilot-scale mainstream nitritation-denitritation system coupled with MBR for municipal wastewater treatment. The results showed that stable nitrite shunt was achieved, while more than 90% of COD and NH〈sub〉4〈/sub〉〈sup〉+〈/sup〉-N removal were obtained via nitritation-denitritation in the pilot plant fed with real municipal wastewater. Through adjusting aeration intensity in MBR in combination with the integrated control of dissolved oxygen (DO), sludge retention time (SRT) and sludge return ratio, NOB was successfully suppressed with a nitrite accumulation rate (NAR) of more than 80%.〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Chemosphere, Volume 217〈/p〉 〈p〉Author(s): Dong Chen, Zhong-wen Meng, Yi-ping Chen〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Large quantities of molybdenum (Mo) slag are generated as a by-product during mining and smelting, which not only occupy huge stretches of arable land and natural habitats but also threaten the local ecosystem and environment. How to recycle this Mo slag is becoming an urgent issue. Here, we reported the toxicity assessment of Mo slag as a mineral fertilizer for slag recycling in agricultural practices. The results showed the following: (1) Lower rates of slag (1.0%, 2.5%, and 5.0%) fertilization, especially 5.0% slag, increased the activities of antioxidant enzymes (superoxide dismutase, catalase, and peroxidase), the contents of chlorophyll, and both the maximum quantum yield and quantum efficiency of photosystem II; decreased the content of malondialdehyde and the non-photochemical quenching of photosystem II; and eventually increased the height, leaf area, and biomass of pakchoi seedlings; (2) Higher rates (7.5% and 10.0%) of Mo slag application resulted in a reduction in the aforementioned physiological and morphological parameters (except for peroxidase activity) of pakchoi seedlings; and (3) Although fertilization with 5.0% slag increased the accumulation of the non-essential elements arsenic (As), lead (Pb), and cadmium (Cd) in pakchoi seedlings, their contents were still lower than the maximum levels of the Codex Alimentarius Commission, European Union, and standards of China. From the perspectives of plant nutrition and food safety, our results showed that Mo slag fertilization at rates lower than 5.0% can be applied as a mineral fertilizer for pakchoi grown on calcareous soils.〈/p〉〈/div〉 〈/div〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0045653518320915-fx1.jpg" width="399" alt="Image 1" title="Image 1"〉〈/figure〉〈/p〉〈/div〉

Description: 〈p〉Publication date: February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Chemosphere, Volume 217〈/p〉 〈p〉Author(s): Rui Qu, Shu-Shen Liu, Tong Li, Hai-Ling Liu〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉In the field of computational toxicology, predicting toxicological interaction or hormesis effect of a mixture from individuals is still a challenge. The two most frequently used model concentration addition (CA) and independent action (IA) also cannot solve these challenges perfectly. In this paper, we used IDV〈sub〉equ〈/sub〉 (an interpolation method based on the Delaunay triangulation and Voronoi tessellation as well as the training set of direct equipartition ray design (EquRay) mixtures) to predict the toxicities of binary mixtures composed of hormetic ionic liquids (ILs). One of the purposes is to verify the predictive ability of IDV〈sub〉equ〈/sub〉. The other one is to improve the risk assessment of ILs mixtures especial hormetic ILs, because the toxicity reports of ILs mixtures are rarely reported in particular the toxicity of the hormetic ILs mixtures. Hence, we determined time-dependent toxicities of four ILs and their binary mixtures (designed by EquRay) to 〈em〉Vibrio qinghaiensis〈/em〉 sp.-Q67 at first. Then, mixture toxicities were predicted and compared using the IDV〈sub〉equ〈/sub〉 and CA. The results show that, the accuracy of IDV〈sub〉equ〈/sub〉 is higher than the accuracy of CA. And, more important, to some mixtures out of the CA application, IDV〈sub〉equ〈/sub〉 also can predict the mixture effects accurately. It showed that IDV〈sub〉equ〈/sub〉 can be applied to predict the toxicity of any binary mixture regardless of the type of concentration-response curve of the components. These toxicity data provided useful information for researching the prediction of hormesis or toxicological interaction of the mixture and toxicities of ILs mixtures.〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Chemosphere, Volume 217〈/p〉 〈p〉Author(s): Gaël Le Croizier, Camille Lacroix, Sébastien Artigaud, Stéphane Le Floch, Jean-Marie Munaron, Jean Raffray, Virginie Penicaud, Marie-Laure Rouget, Raymond Laë, Luis Tito De Morais〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Subcellular cadmium (Cd) partitioning was investigated in the liver of two marine fish species, the European sea bass 〈em〉Dicentrarchus labrax〈/em〉 and the Senegalese sole 〈em〉Solea senegalensis〈/em〉, dietary exposed to an environmentally realistic Cd dose for two months followed by a two-month depuration. The two species displayed different handling strategies during the depuration period. Cd was largely bound to detoxifying fractions such as heat stable proteins (HSP) including metallothioneins (MT) in sea bass, while Cd was more linked to sensitive fractions such as organelles in sole. Whole liver concentrations and subcellular partitioning were also determined for essential elements. The greatest impairment of essential metal homeostasis due to Cd exposure was found in sole. These elements followed the Cd partitioning pattern, suggesting that they are involved in antioxidant responses against Cd toxicity. Cd consumption diminished sole growth in terms of body weight, probably due to lipid storage impairment. The contrasting partitioning patterns showed by the two species might imply different pathways for Cd elimination from the liver. In sea bass, MT-bound Cd would be excreted through bile or released into blood, crossing the cell membrane via a protein transporter. In sole, MRG-bound Cd would be sequestered by organelles before being released into the blood via vesicular exocytosis. These distinct strategies in cellular Cd handling in the liver might account for differential sensitivity to Cd toxicity and differential Cd excretion pathways between the two marine fish species.〈/p〉〈/div〉 〈/div〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0045653518320873-fx1.jpg" width="496" alt="Image 1" title="Image 1"〉〈/figure〉〈/p〉〈/div〉

Description: 〈p〉Publication date: 1 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Electrochimica Acta, Volume 295〈/p〉 〈p〉Author(s): Lei Lu, Xinyan Jiao, Jiawei Fan, Wu Lei, Yu Ouyang, Xifeng Xia, Zhixin Xue, Qingli Hao〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Oxygen reduction reaction (ORR) and Lithium storage both play the key roles in energy conversion and storage devices. Here, we report a honeycomb-like nitrogen-doped carbon derived from enteromorpha algae (N-EA), using a one-step pyrolysis process at only 600 °C to simultaneously achieve doping, carbonization and activation. After anchoring CoFe〈sub〉2〈/sub〉O〈sub〉4〈/sub〉 on N-EA, CoFe〈sub〉2〈/sub〉O〈sub〉4〈/sub〉/N-EA, not only inherits the high surface area, porous structure, active nitrogen species from N-EA, but also benefits from the active sites and high theoretical specific capacity of Li storage from CoFe〈sub〉2〈/sub〉O〈sub〉4〈/sub〉. The synergistic effect makes CoFe〈sub〉2〈/sub〉O〈sub〉4〈/sub〉/N-EA an alternative catalyst to commercial Pt/C for ORR with superior activity and stability. Moreover, CoFe〈sub〉2〈/sub〉O〈sub〉4〈/sub〉/N-EA exhibits a remarkable cycle performance with a 100% capacity retention (∼900 mAh g〈sup〉−1〈/sup〉) after 500 cycles at 0.5 A g〈sup〉−1〈/sup〉. Green preparation, waste utilization, good ORR performance and Li storage property of CoFe〈sub〉2〈/sub〉O〈sub〉4〈/sub〉/N-EA could make it a promising candidate for fuel cells and LIBs.〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: 15 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 536〈/p〉 〈p〉Author(s): Xueyi Guo, Weijia Wang, Xiuhong Yuan, Ying Yang, Qinghua Tian, Yang Xiang, Yan Sun, Zhiming Bai〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Magnetic nano capture agent (MNCA)-based magnetic separation is considered as a promising approach to rapidly isolate heavy metals from blood. Limited removal efficiency and potential biosafety risks are the major challenges for the clinical use of MNCA-based magnetic separation. Here, we report a highly-efficient MNCA-based magnetic separation of heavy metals from blood in continuous multi-stage adsorption mode. The interactions between MNCA and blood components (〈em〉e.g.〈/em〉 blood cells and plasma proteins) and the MNCA-induced cellular immune responses are studied in detail. The distribution and redistribution of heavy metals in blood are quantitatively analyzed. It demonstrates that concentration dependent redistribution can increase the contact between heavy metals and MNCA, leading to improvement on heavy metal removal efficiency. The removal performance is tested in batch mode and in continuous mode. Results show that 97.97% of Pb and 96.53% of Cd are removed from blood in 120 min using continuous multi-stage adsorption mode, and the residual concentrations of Pb and Cd in blood decrease from 400 μg L〈sup〉−1〈/sup〉 to 8.11 μg L〈sup〉−1〈/sup〉 and 13.84 μg L〈sup〉−1〈/sup〉, respectively. This study paves an effective way for heavy metal intoxication therapy by MNCA-based magnetic separation.〈/p〉〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S002197971831292X-ga1.jpg" width="500" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: 1 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 535〈/p〉 〈p〉Author(s): Hélène Labie, Adeline Perro, Véronique Lapeyre, Bertrand Goudeau, Bogdan Catargi, Rachel Auzély, Valérie Ravaine〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉A simple route to deliver on demand hydrosoluble molecules such as peptides, packaged in biocompatible and biodegradable microgels, is presented. Hyaluronic acid hydrogel particles with a controlled structure are prepared using a microfluidic approach. Their porosity and their rigidity can be tuned by changing the crosslinking density. These negatively-charged polyelectrolytes interact strongly with positively-charged linear peptides such as poly-〈span〉l〈/span〉-lysine (PLL). Their interactions induce microgel deswelling and inhibit microgel enzymatic degradability by hyaluronidase. While small PLL penetrate the whole volume of the microgel, PLL larger than the mesh size of the network remain confined at its periphery. They make a complexed layer with reduced pore size, which insulates the microgel inner core from the outer medium. Consequently, enzymatic degradation of the matrix is fully inhibited and non-affinity hydrophilic species can be trapped in the core. Indeed, negatively-charged or small neutral peptides, without interactions with the network, usually diffuse freely across the network. By simple addition of large PLL, they are packaged in the core and can be released on demand, upon introduction of an enzyme that degrades selectively the capping agent. Single polyelectrolyte layer appears as a simple generic method to coat hydrogel-based materials of various scales for encapsulation and controlled delivery of hydrosoluble molecules.〈/p〉〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0021979718311238-ga1.jpg" width="395" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: 15 January 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 534〈/p〉 〈p〉Author(s): Pengfei Chen, Pingxing Xing, Zhiqiang Chen, Xin Hu, Hongjun Lin, Leihong Zhao, Yiming He〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉This paper is designed for elevating the photocatalytic H〈sub〉2〈/sub〉-evoultion performance of g-C〈sub〉3〈/sub〉N〈sub〉4〈/sub〉 through the modification of AgNbO〈sub〉3〈/sub〉 nanocubes. Via the microwave heating method, g-C〈sub〉3〈/sub〉N〈sub〉4〈/sub〉 was in-situ formed on AgNbO〈sub〉3〈/sub〉 surface to fabricate a close contact between the two semiconductors in forty minutes. X-ray diffraction (XRD), Fourier transform-infrared (FT-IR), X-ray photoelectron spectroscopy (XPS) experiments were performed to confirm the binary structure of the synthesized AgNbO〈sub〉3〈/sub〉/g-C〈sub〉3〈/sub〉N〈sub〉4〈/sub〉 composite. N〈sub〉2〈/sub〉-adsorption and visible diffuse reflection spectroscopy (DRS) analyses indicated that the addition of AgNbO〈sub〉3〈/sub〉 to g-C〈sub〉3〈/sub〉N〈sub〉4〈/sub〉 showed nearly negligible influence on the specific surface area and the optical property. Photoluminescence (PL) spectroscopy experiment suggested that the AgNbO〈sub〉3〈/sub〉/g-C〈sub〉3〈/sub〉N〈sub〉4〈/sub〉 displayed reduced PL emission and longer lifetime of photoexcited charge carriers than g-C〈sub〉3〈/sub〉N〈sub〉4〈/sub〉, which could be ascribed to the suitable band potential and the intimate contact of g-C〈sub〉3〈/sub〉N〈sub〉4〈/sub〉 and AgNbO〈sub〉3〈/sub〉. This result was also confirmed by the transient photocurrent response experiment. The influence of the enhanced charge separation was displayed in their photocatalytic reaction. AgNbO〈sub〉3〈/sub〉/g-C〈sub〉3〈/sub〉N〈sub〉4〈/sub〉 sample showed enhanced performance in photocatalytic H〈sub〉2〈/sub〉-generation under visible light illumination. The H〈sub〉2〈/sub〉-evolution rate is determined to be 88 μmol·g〈sup〉−1〈/sup〉·h〈sup〉−1〈/sup〉, which reaches 2.0 times of g-C〈sub〉3〈/sub〉N〈sub〉4〈/sub〉. This study provides a feasible and rapid approach to fabricate g-C〈sub〉3〈/sub〉N〈sub〉4〈/sub〉 based composite.〈/p〉〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0021979718311007-ga1.jpg" width="500" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: 15 January 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 534〈/p〉 〈p〉Author(s): Jie Yang, Liujie Wang, Zhihua Ma, Mingdeng Wei〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉A newly self-supported electrode composed of Mn〈sub〉3〈/sub〉O〈sub〉4〈/sub〉 on Ni foam/graphene (NF/graphene/Mn〈sub〉3〈/sub〉O〈sub〉4〈/sub〉) was synthesized in situ by electrodeposition, and was used as a supercapacitor electrode for the first time. An ultrahigh specific capacitance of 630 Fg〈sup〉−1〈/sup〉 can be achieved at a current density of 0.5 Ag〈sup〉−1〈/sup〉. The maximum energy density of 94.4 Wh kg〈sup〉−1〈/sup〉 can be achieved, and the capacitance retention can be maintained about 97% after 20,000 cycles at 10 Ag〈sup〉−1〈/sup〉. The electrochemical properties, including specific capacitance, energy density and cycling performance, were better than those in previous reports on Mn〈sub〉3〈/sub〉O〈sub〉4〈/sub〉-graphene electrodes. Such an outstanding property may be attributed to its unique characteristics, such as self-supported structure, favorable electric conductivity and cellular-like porous morphology.〈/p〉〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉 〈p〉A self-supported electrode composed of Mn〈sub〉3〈/sub〉O〈sub〉4〈/sub〉 on Ni foam/graphene was firstly synthesized and exhibited an ultra-high specific capacitance of 630 Fg〈sup〉−1〈/sup〉 at 0.5 Ag〈sup〉−1.〈/sup〉〈/p〉 〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0021979718311536-ga1.jpg" width="337" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉 〈/div〉 〈/div〉

Description: 〈p〉Publication date: 1 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 535〈/p〉 〈p〉Author(s): Jianhui Li, Haiting Yan, Dongfeng Dang, Wei Wei, Lingjie Meng〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Graphene has attracted enormous attention due to its unique physical properties and attractive applications in many fields. However, it is an ongoing challenge to develop a facile and low-cost method for the large scale preparation of high-quality graphene (HQGr). In this work, we have developed an improved liquid-phase exfoliation method to mass produce HQGr. This method is quite simple but efficient by exfoliation of graphite in organic solvent with the co-assistance of sodium citrate and water. Remarkably, the concentration of as-exfoliated HQGr was as high as 0.71 mg/mL under optimal conditions, while the oxygen content in HQGr was only 2.39%. After annealing at 500 °C for 2 h in argon atmosphere, the mean conductivity of annealed HQGr was as high as 1.4 × 10〈sup〉4〈/sup〉 S m〈sup〉−1〈/sup〉. Therefore, this facile method for liquid-phase exfoliation of graphite has excellent potential in the industrial-scale production of HQGr for numerous applications in energy storage, optical and electronic fields.〈/p〉〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉 〈p〉High-quality graphene (HQGr) was efficiently prepared by exfoliation of graphite in organic solvent with the co-assistance of sodium citrate and water. The effects of alkali metal species, solvent type and the volume ratio of NMP/water in co-solvent on the exfoliation efficiency of graphite were studied systematically. HQGr have great potential for numerous applications in optical and electronic fields, such as anode material of lithium ion batteries.〈/p〉 〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0021979718311755-ga1.jpg" width="500" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉 〈/div〉 〈/div〉

Description: 〈p〉Publication date: 1 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 535〈/p〉 〈p〉Author(s): Jingwen Wang, Min Zheng, Zhigang Xie〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Carrier-free nanodrugs named BCNPs were prepared by the coassembly of 2,5-bis(4-(diethylamino)benzylidene)cyclopentanone (BDBC) and curcumin (CCM) in the absence of surfactants. The as-synthesized BCNPs possess high dispersity and stability in aqueous media, along with favorable photostability and good biocompatibility. Comparing with their counterparts BDBC and CCM, BCNPs exhibit higher singlet oxygen yield and better two-photon photodynamic therapy (PDT) efficacy. Moreover, BCNPs display dramatically enhanced ability for inhibiting the growth of HeLa cells, which benefits from the synergistic treatment of BDBC and CCM under the irradiation of 450/808 nm. This work highlights the potential of using simple coassembly strategy to codelivery of multiple drugs in one single formulation for cancer therapy.〈/p〉〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0021979718311767-ga1.jpg" width="500" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: 1 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 535〈/p〉 〈p〉Author(s): Rui Zhang, Xiupeng Liu, Tingting Zhou, Tong Zhang〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Hollow metal oxide semiconductor (MOS) materials with controllable shells have attracted increasing attention because of their interesting properties and potential applications in sensors, catalysis, biology, etc. Cuprous oxide (Cu〈sub〉2〈/sub〉O), which is a typical p-type semiconductor material, has four kinds of nanostructures (i.e., single-, double-, triple-, and quadruple-shelled spheres) and was successfully synthesized by the simple regulation of hexadecyl trimethyl ammonium bromide (CTAB) concentration. All as-obtained samples were at the nanometer level, and the hollow layers were also located between the two shells of the Cu〈sub〉2〈/sub〉O nanostructures. The structural evolution and formation mechanism of the core-in-hollow multishelled nanostructure were also studied in this work. Moreover, the gas sensing performance of four kinds of materials was measured. The performance of the quadruple-shelled Cu〈sub〉2〈/sub〉O-based formaldehyde (HCHO) sensor was greater than that of other sensors. The results indicated that the well-defined multishelled structure may significantly enhance HCHO detection by facilitating the gas adsorption quantity and transport rate.〈/p〉〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉 〈p〉A controllable multishelled Cu〈sub〉2〈/sub〉O nanoparticles-based sensing platform exhibits an excellent response/recovery formaldehyde behavior at a working temperature of 120 °C.〈/p〉 〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0021979718311573-ga1.jpg" width="329" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉 〈/div〉 〈/div〉

Description: 〈p〉Publication date: 1 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 535〈/p〉 〈p〉Author(s): Liang Wang, Ji He, Lingli Zhu, Yilei Wang, Xuequan Feng, Binge Chang, H. Enis Karahan, Yuan Chen〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Graphene hydrogels hold great potential for the disinfection of bacteria-contaminated water. However, the intrinsic antibacterial activity of graphene hydrogels is not satisfactory, and the incorporation of other antibacterial agents often results in their unwanted releases. Here, we present a new strategy to improve the antibacterial activities of graphene hydrogels. We first synthesized a new pi-conjugated molecule containing five aromatic rings and two side-linked quaternary ammonium (QA) groups, denoted as piQA. Next, we fabricated composite gravity filters by assembling piQA with reduced graphene oxide (rGO) hydrogel. The rGO hydrogel helps to form a sponge-like physical sieve, contributes to the overall antibacterial activity, and provides abundant pi-rich surfaces. The large aromatic cores of piQA allow the formation of collectively strong pi-pi interactions with rGO, resulting in a high piQA mass loading of ∼31 wt%. Due to the sieving effect of rGO hydrogel and the synergistic antibacterial activity of rGO and piQA, the filters prepared based on piQA-rGO assemblies can remove over 99.5% of Gram-negative 〈em〉Escherichia coli〈/em〉 (〈em〉E. coli〈/em〉) and Gram-positive 〈em〉Staphylococcus aureus〈/em〉 (〈em〉S. aureus〈/em〉) cells with a high-water treatment capacity of 10 L g〈sup〉−1〈/sup〉. Furthermore, the piQA-rGO assemblies show low toxicity towards two different mammalian cell lines (L929 and macrophages), and the release of piQA is also negligible. Overall, the new piQA-rGO assembly demonstrates high potential for water disinfection applications.〈/p〉〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0021979718311597-ga1.jpg" width="380" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: 1 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 535〈/p〉 〈p〉Author(s): Yuxi Zhang, Hao Fang, Yanqiao Zhang, Ming Wen, Dandan Wu, Qingsheng Wu〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Tremendous attention has been focused on exploring highly efficient and economical catalysts to the reduction of 〈em〉p〈/em〉-nitrophenol for the purpose of green chemistry. However, it is still a challenge to elevate the catalysts with high activity and desirable recyclability. Herein, Cobalt-Cobalt Ferrite (Co-CoFe〈sub〉2〈/sub〉O〈sub〉4〈/sub〉) nanobrushes have been synthesized by controlled growth-reduction process in one step, which is applied to catalyze the reduction of 〈em〉p〈/em〉-nitrophenol. 〈em〉In situ〈/em〉 generated active Co(0) can induce Co-CoFe〈sub〉2〈/sub〉O〈sub〉4〈/sub〉 nanobrushes to achieve higher catalytic activity with a reaction rate of 0.0457 s〈sup〉−1〈/sup〉 for the reduction of 〈em〉p〈/em〉-nitrophenol due to the synergetic effect between 〈em〉in situ〈/em〉 generated Co(0) and its induced defects on the CoFe〈sub〉2〈/sub〉O〈sub〉4〈/sub〉 support. Compared with other catalysts calculated and gathered in Table S1 in Supporting Information, as-designed Co-CoFe〈sub〉2〈/sub〉O〈sub〉4〈/sub〉 nanobrushes can be employed as a good candidate for the nitro-reduction reaction.〈/p〉〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉 〈p〉Induced by active Co(0), as-designed Co-CoFe〈sub〉2〈/sub〉O〈sub〉4〈/sub〉 complex structures show excellent catalytic performance on the reduction of 〈em〉p〈/em〉-nitrophenol to 〈em〉p〈/em〉-aminophenol, suggesting as a good catalyst candidate for the nitro-reduction reaction in line with the purpose of Green Chemistry.〈/p〉 〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0021979718312104-ga1.jpg" width="312" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉 〈/div〉 〈/div〉

Description: 〈p〉Publication date: 1 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 535〈/p〉 〈p〉Author(s): Yanxiao Li, Congjie Wei, Chenglin Wu〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Silver nanowire graphene (AgNW-GN) composite, as an alternative transparent conductive film (TCF) to conventional indium tin oxide (ITO), has much improved mechanical and electrical properties. These advantages make AgNW-GN an ideal TCF for planar devices. The adhesion of AgNW-GN composite film plays a critical role in these applications. However, the effect of silver nanowire on the adhesion between AgNW-GN and copper substrate remains unexplored. In the present work, AgNW-GN composite films with different AgNW concentrations were prepared and their adhesion with copper substrates was characterized using the double cantilever beam (DCB) experiment and the digital image correlation (DIC). The interfacial failures were characterized using scanning electron microscopy (SEM), Raman spectroscopy, and atomic force microscopy (AFM). The results showed the brittle to ductile interfacial fracture transition with increased amount of AgNW. The interfacial traction separation relations (TSR) were subsequently extracted. The competing interfacial failure mechanism was discovered and modeled between the interfaces of epoxy/composite and composite/copper. The associated transfer criterion was subsequently established combining both experimental and modeling results.〈/p〉〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0021979718312025-ga1.jpg" width="500" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: 1 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 535〈/p〉 〈p〉Author(s): Xuejie Yue, Tao Zhang, Dongya Yang, Fengxian Qiu, Zhangdi Li, Gengyao Wei, Yu Qiao〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉To maintain personal thermal comfort in cold weather, indoor heating consumes large amount of energy and is a primary source of greenhouse gas emission. Traditional clothes are too thick for thermal comfort in cold outdoor environment, resulting the lower wearing comfort. In this work, a multifunctional Ag nanoparticles/cellulose fibers thermal insulation membrane starting from waste paper cellulose fibers was prepared via simple silver mirror reaction and subsequent vacuum filtration process to improve the infrared reflection properties of membranes for human thermal insulation. The sphere-like Ag nanoparticles were tightly anchored on surface of waste paper cellulose fibers, forming an Ag nanoparticles infrared radiation reflection coating with high infrared reflectance, resulting in high thermal insulation capacity of the thermal insulation membrane. In addition, Ag nanoparticles endow the thermo insulation membrane with excellent antibacterial activity, and the thermo insulation membranes can effectively inhibit the growth of both 〈em〉Staphylococcus aureus〈/em〉 and 〈em〉Escherichia coli〈/em〉. In this thermal insulation system, the thermo insulation membranes show superhydrophilicity and porosity, which allow the membranes to be breathable for comfortable wearing feeling. These promising results including high infrared reflection for high thermal insolating, high breathability for wearing comfort, and excellent antibacterial activity make the Ag/cellulose thermo insulation membranes promising candidates for applications in human thermal management, energy regulation and other facilities.〈/p〉〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0021979718311974-ga1.jpg" width="280" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: 1 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 535〈/p〉 〈p〉Author(s): Faisal Rehman, Khalid Mahmood, Arshi Khalid, Muhammad Shahzad Zafar, Madsar Hameed〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉ZnO as an electron transporting material (ETM) in perovskite solar cells has many benefits, including low temperature processability and high mobility. We explore here for the first time, hysteresis-less mesostructured perovskite solar cells with an incredible steady-state efficiency of 20.62% particularly enhancement of the device stability. We anticipated a device structure consisting of a novel fully-solution-processed and low-temperature barium hydroxide hybridized boron-doped ZnO (B:ZnO) bilayer film as electron transport material (ETM). We modify the design of ETMs with reduced trap states density is very crucial to obtain highly stabilized power conversion efficiency (PCE) and adjustable architectures in perovskite solar cells which should produce an impact on emerging highly efficient devices and their future commercialization.〈/p〉〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉 〈p〉A uniquely structured bilayer ETM is studied for the first time, as an electron transporting material in detail for hybrid perovskite solar cells leading to power conversion efficiency above 20.5%.〈/p〉 〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0021979718311998-ga1.jpg" width="251" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉 〈/div〉 〈/div〉

Description: 〈p〉Publication date: 15 January 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 534〈/p〉 〈p〉Author(s): Hui Sun, Tianshu Yao, Xi Xie, Yuxi Lu, Yan Wang, Zirou Xu, Jie Han, Xiaobing Chen〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Bi〈sub〉5−〈/sub〉〈em〉〈sub〉y〈/sub〉〈/em〉Eu〈em〉〈sub〉y〈/sub〉〈/em〉Fe〈sub〉1−〈/sub〉〈em〉〈sub〉x〈/sub〉〈/em〉Ni〈em〉〈sub〉x〈/sub〉〈/em〉Ti〈sub〉3〈/sub〉O〈sub〉15〈/sub〉 (〈em〉x〈/em〉 = 0, 0.05, 0.10, 0.15, 0.20; 〈em〉y〈/em〉 = 0, 0.1, 0.3, 0.5) nanosheet-based nanoflowers as magnetic recyclable visible-light photocatalysts toward Rhodamine B (RhB) degradation were successfully synthesized by a hydrothermal method. As started from Bi〈sub〉5〈/sub〉FeTi〈sub〉3〈/sub〉O〈sub〉15〈/sub〉 (BFTO), Ni was firstly employed to substitute for Fe at B-site to improve the magnetism for magnetic recyclability. After Ni doping (Bi〈sub〉5〈/sub〉Fe〈sub〉1−〈/sub〉〈em〉〈sub〉x〈/sub〉〈/em〉Ni〈em〉〈sub〉x〈/sub〉〈/em〉Ti〈sub〉3〈/sub〉O〈sub〉15〈/sub〉: BFNTO-〈em〉x〈/em〉, 〈em〉x〈/em〉 = 0, 0.05, 0.10, 0.15, 0.20), both the ferromagnetism and photocatalytic activity were obviously improved, where BFNTO-0.1 (Bi〈sub〉5〈/sub〉Fe〈sub〉0.9〈/sub〉Ni〈sub〉0.1〈/sub〉Ti〈sub〉3〈/sub〉O〈sub〉15〈/sub〉) exhibited the maximum remnant and statured magnetization of 0.14 and 0.82 emu/g respectively. To further improve the magnetism and photocatalytic activity, Eu was chosen to substitute for Bi at A-site. Both ferromagnetism and photocatalytic properties of Bi〈sub〉5−〈/sub〉〈em〉〈sub〉y〈/sub〉〈/em〉Eu〈em〉〈sub〉y〈/sub〉〈/em〉Fe〈sub〉0.9〈/sub〉Ni〈sub〉0.1〈/sub〉Ti〈sub〉3〈/sub〉O〈sub〉15〈/sub〉 (BEFNTO-〈em〉y〈/em〉, 〈em〉y〈/em〉 = 0, 0.1, 0.3, 0.5) were further improved by optimizing the doped europium content. The BEFNTO-0.1 (Bi〈sub〉4.9〈/sub〉Eu〈sub〉0.1〈/sub〉Fe〈sub〉0.9〈/sub〉Ni〈sub〉0.1〈/sub〉Ti〈sub〉3〈/sub〉O〈sub〉15〈/sub〉) showed enhanced photocatalytic activity and could be recycled simply by applying a magnet bar. This work may provide a basis for further developing new visible-light photocatalysts because the layer-structured Aurivillius phase has significant potential in elemental doping and further structural engineering applications.〈/p〉〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0021979718311305-ga1.jpg" width="500" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: 1 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 535〈/p〉 〈p〉Author(s): Kairuo Zhu, Changlun Chen, Haiyan Wang, Yi Xie, Muhammad Wakeel, Abdul Wahid, Xiaodong Zhang〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Layered double oxides (LDO) and γ-Fe〈sub〉2〈/sub〉O〈sub〉3〈/sub〉 have been demonstrated to be promising adsorbents to remove radioactive elements from aqueous media. Herein, magnetic γ-Fe〈sub〉2〈/sub〉O〈sub〉3〈/sub〉 nanoparticles decoration onto porous layered double oxides belts (γ-Fe〈sub〉2〈/sub〉O〈sub〉3〈/sub〉/LDO) were fabricated by in situ solid-state thermolysis technique combined with Fe(III)-loaded layered double hydroxides as a precursor. The microstructure, chemical composition, and magnetic properties of γ-Fe〈sub〉2〈/sub〉O〈sub〉3〈/sub〉/LDO were characterized in detail. The as-obtained γ-Fe〈sub〉2〈/sub〉O〈sub〉3〈/sub〉/LDO was employed as an adsorbent for the elimination of U(VI) from water. The adsorption process followed the Langmuir model with the maximal adsorption capacity of U(VI) onto γ-Fe〈sub〉2〈/sub〉O〈sub〉3〈/sub〉/LDO being 526.32 mg·g〈sup〉−1〈/sup〉 at 303 K and pH 5, which surpassed pristine LDO and many other materials. The Fourier transformed infrared spectra and the X-ray photoelectron spectra analysis suggested that the interaction mechanism was mainly controlled by the surface complexation and electrostatic interactions. All in all, the γ-Fe〈sub〉2〈/sub〉O〈sub〉3〈/sub〉/LDO with remarkable adsorption capacity, excellent regeneration, and easy magnetic separation opens a new expectation as a suitable material for the cleanup of U(VI) from contaminated water.〈/p〉〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0021979718311949-ga1.jpg" width="286" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: 1 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 535〈/p〉 〈p〉Author(s): Luping Sha, Qinfu Zhao, Da Wang, Xian Li, Xiudan Wang, Xinyao Guan, Siling Wang〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉“Gate” engineered mesoporous silica nanoparticles (MSN) have been extensively applied in cancer theranostics. Due to the complexity of tumor development and progression, with chemotherapy alone, it has often been difficult to achieve a good therapeutic effect. Currently, it has been shown that the combination with photothermal therapy overcomes the shortcoming of chemotherapy. In most studies, the photothermal effect has proven to accelerate drug release from nanocarriers and ablate malignant cells directly, but the influence on the intracellular fate of nanocarriers remains unknown. Herein, a lipophilic cyanine dye Cypate acting as a photothermal converting agent was conjugated on the external surface of MSN through a disulfide bond (MSN-Cy) and 〈em〉〈span〉d〈/span〉〈/em〉-〈em〉α〈/em〉-tocopherol polyethylene glycol 1000 succinate (TPGS) was coated on the outside of the MSN-Cy via a hydrophobic interaction (TCMSN) to cover the pores, preventing drug preleakage in the circulation. The TCMSN underwent exocytosis through the lysosome-mediated pathway. Moderate heat induced by near-infrared light promoted lysosome disruption, which thus partly inhibited lysosome-mediated particle exocytosis. In the meantime, TPGS, as a P-glycoprotein inhibitor, blocked the drug efflux. This research elaborated the photothermal effect from a new perspective—inhibiting particle exocytosis. The as-designed “gate” engineered MSN realized a double inhibition of drug efflux and particle exocytosis from cancer cells, thus sustaining the drug action time and enhancing the antitumor activity.〈/p〉〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0021979718311640-ga1.jpg" width="482" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: 15 January 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 534〈/p〉 〈p〉Author(s): Zanru Guo, Hongjian Gu, Qiang Chen, Zhanfeng He, Wenyuan Xu, Jiali Zhang, Yongxin Liu, Leyan Xiong, Longzhen Zheng, Yujun Feng〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉 〈h6〉Hypothesis〈/h6〉 〈p〉The effective separation and recovery of oils from water is important for the protections of ecosystems and the environment. Polymeric porous monoliths have been demonstrated as attractive absorbents for oil/water separation. However, the recyclability was mainly realized by squeezing, combustion, or centrifugation, which may restrict in elastic materials, destroy the adsorbates or need special apparatus. Thus it is desirable to developing monoliths with controllable oil absorption and desorption.〈/p〉 〈/div〉 〈div〉 〈h6〉Experiments〈/h6〉 〈p〉A series of “smart” monoliths with pH-induced switchable wettability were fabricated by high internal phase emulsion (HIPE) polymerization and epoxide ring-opening for the incorporation of amine groups. The resultant monoliths and their wettabilities were examined using Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), nitrogen adsorption/desorption and contact angle analysis, respectively. The oil separation efficiency and recyclability were evaluated.〈/p〉 〈/div〉 〈div〉 〈h6〉Findings〈/h6〉 〈p〉The monoliths with macroporous structure can undergo switchable wettability under reversible pH stimulation. As an absorbent, the monoliths not only separated and recovered organic solvents and oils (including crude oil) from aqueous mixtures through a reversible and recyclable absorption and desorption process upon alternating the pH between 7.0 and 1.0, but also continuously expulsed oils from water surfaces in a continuous manner with the aid of external driving pressures. Moreover, the monoliths also allowed the effective separation of surfactant-free and surfactant-stabilized oil-in-water emulsions with high separation efficiency.〈/p〉 〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉 〈p〉Smart macroporous monoliths with pH-induced switchable wettability and reversible oil absorption-desorption ability were developed.〈/p〉 〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0021979718310968-ga1.jpg" width="500" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉 〈/div〉 〈/div〉

Description: 〈p〉Publication date: 1 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 535〈/p〉 〈p〉Author(s): Ling-Li Min, Li-Ming Yang, Ren-Xiang Wu, Lu-Bin Zhong, Zhi-Hua Yuan, Yu-Ming Zheng〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉A novel iron-doped chitosan electrospun nanofiber mat (Fe@CTS ENM) was synthesized, which was proven to be effective for the removal of arsenite (As(III)) from water at neutral pH condition. The physiochemical properties and adsorption mechanism were explored by SEM-EDS and X-ray photoelectron spectroscopy (XPS). Batch adsorption experiments were carried out to evaluate the As(III) adsorption performance of the Fe@CTS ENM with various process parameters, such as adsorbent dose, solution pH, initial As(III) concentration, contact time, ionic strength, coexisting anions, and natural organic matter. The experimental results indicated that the maximum adsorption capacity was up to 36.1 mg g〈sup〉−1〈/sup〉. Especially, when the adsorbent dosage was higher than 0.3 g L〈sup〉−1〈/sup〉, the As(III) concentration was reduced from 100 µg L〈sup〉−1〈/sup〉 to less than 10 µg L〈sup〉−1〈/sup〉, which indicated the Fe@CTS ENM could effectively remove trace As(III) from water over a wide pH range (from 3.3 to 7.5). Kinetics study demonstrated that the adsorption equilibrium was achieved within 2.0 h, corresponding to a fast uptake of As(III). The presence of common co-ions and humic acid had little effect on the As(III) adsorption. XPS analysis suggested that the Fe〈img src="https://sdfestaticassets-eu-west-1.sciencedirectassets.com/shared-assets/16/entities/sbnd"〉O, C〈img src="https://sdfestaticassets-eu-west-1.sciencedirectassets.com/shared-assets/16/entities/sbnd"〉OH, C〈img src="https://sdfestaticassets-eu-west-1.sciencedirectassets.com/shared-assets/16/entities/sbnd"〉O〈img src="https://sdfestaticassets-eu-west-1.sciencedirectassets.com/shared-assets/16/entities/sbnd"〉C and C〈img src="https://sdfestaticassets-eu-west-1.sciencedirectassets.com/shared-assets/16/entities/sbnd"〉N groups on the adsorbent surface play dominant roles in the adsorption of As(III). Adsorption-desorption regeneration test further demonstrated that no appreciable loss in the adsorption capacities was observed, which confirmed that the Fe@CTS ENM maintained a desirable life cycle that was free of complex synthesis processes, expensive and toxic materials, qualifying it as an efficient and low-cost As(III) adsorbent.〈/p〉〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0021979718311512-ga1.jpg" width="500" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: 1 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 535〈/p〉 〈p〉Author(s): Wenbo Dong, Dongbo Wang, Hou Wang, Mengke Li, Fei Chen, Feiyue Jia, Qi Yang, Xiaoming Li, Xingzhong Yuan, Jilai Gong, Hailong Li, Jun Ye〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉In this study, a series of In〈sub〉2〈/sub〉S〈sub〉3〈/sub〉/UiO-66 composites were fabricated through a one-step solvothermal method for the first time. The diffraction peaks, composition, morphology, and chemical states of the composites were first characterized through X-ray diffraction, X-ray photoelectron spectroscopy, scanning electron microscope, or transmission electron microscope. Then, the performances of as-obtained In〈sub〉2〈/sub〉S〈sub〉3〈/sub〉/UiO-66 composites were assessed by the removal of tetracycline under 1 h dark condition and 1 h visible-light irradiation. Experimental results showed that all the In〈sub〉2〈/sub〉S〈sub〉3〈/sub〉/UiO-66 composites exhibited greater tetracycline removal, as compared with the two parent materials (i.e., UiO-66 and In〈sub〉2〈/sub〉S〈sub〉3〈/sub〉). The highest tetracycline removal was obtained by the developed In〈sub〉2〈/sub〉S〈sub〉3〈/sub〉/UiO-66 composite with Zr: In molar ratio of (0.37:1), labelled as ISUO-0.37, with the maximal tetracycline removal capacity of 106.3 mg/g being achieved, which was greater than that of UiO-66, In〈sub〉2〈/sub〉S〈sub〉3〈/sub〉, or other photocatalysts documented in the literature. The mechanism investigations revealed that compared with UiO-66 and In〈sub〉2〈/sub〉S〈sub〉3〈/sub〉, ISUO-0.37 had higher adsorption capability and photocatalytic performance. Although the specific surface area of ISUO-0.37 (74.57 m〈sup〉2〈/sup〉/g) was lower than that of either UiO-66 (388.6 m〈sup〉2〈/sup〉/g) or In〈sub〉2〈/sub〉S〈sub〉3〈/sub〉 (76.36 m〈sup〉2〈/sup〉/g), the former possessed greater pore diameter and adsorption sites such as 〈img src="https://sdfestaticassets-us-east-1.sciencedirectassets.com/shared-assets/16/entities/sbnd"〉OH, C〈img src="https://sdfestaticassets-us-east-1.sciencedirectassets.com/shared-assets/16/entities/dbnd"〉O, O〈img src="https://sdfestaticassets-us-east-1.sciencedirectassets.com/shared-assets/16/entities/sbnd"〉C〈img src="https://sdfestaticassets-us-east-1.sciencedirectassets.com/shared-assets/16/entities/sbnd"〉O, C〈img src="https://sdfestaticassets-us-east-1.sciencedirectassets.com/shared-assets/16/entities/dbnd"〉C, and C〈img src="https://sdfestaticassets-us-east-1.sciencedirectassets.com/shared-assets/16/entities/sbnd"〉H, which might be the reason for ISUO-0.37 showing the enhanced adsorption capability. The trapping experiment and electron spin resonance measurements demonstrated that 〈sup〉〈img src="https://sdfestaticassets-us-east-1.sciencedirectassets.com/shared-assets/16/entities/rad"〉〈/sup〉O〈sub〉2〈/sub〉〈sup〉−〈/sup〉 and h〈sup〉+〈/sup〉 were the major contributors to the photo-degradation of tetracycline in this work, and more 〈sup〉〈img src="https://sdfestaticassets-us-east-1.sciencedirectassets.com/shared-assets/16/entities/rad"〉〈/sup〉O〈sub〉2〈/sub〉〈sup〉−〈/sup〉 and h〈sup〉+〈/sup〉 were produced by ISUO-0.37, as compared with In〈sub〉2〈/sub〉S〈sub〉3〈/sub〉. Further investigation with the diffused spectra of reflectance showed that ISUO-0.37 had better visible light absorption than either In〈sub〉2〈/sub〉S〈sub〉3〈/sub〉 or UiO-66, which may be the reason for ISUO-0.37 producing more 〈sup〉〈img src="https://sdfestaticassets-us-east-1.sciencedirectassets.com/shared-assets/16/entities/rad"〉〈/sup〉O〈sub〉2〈/sub〉〈sup〉−〈/sup〉. In addition, photoluminescence emission spectra confirmed that the recombination rate of photoexcited electron-hole pairs of ISUO-0.37 composite is much lower than that of In〈sub〉2〈/sub〉S〈sub〉3〈/sub〉, which may increase h〈sup〉+〈/sup〉. It was also found that ISUO-0.37 showed excellent structural stability and recyclability.〈/p〉〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0021979718311962-ga1.jpg" width="453" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: 1 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 535〈/p〉 〈p〉Author(s): Guangle Li, Jinbo Fei, Youqian Xu, Jong-Dal Hong, Junbai Li〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉At present, photophosphorylation in natural or artificial systems is accomplished by the production of protons or their pumping across the biomembranes. Herein, different from this strategy above, we demonstrate a designed system which can effectively enhance photophosphorylation by photo-induced proton-scavenging through molecular assembly. Upon the introduction of photobase generators, a (photo-) chemical reaction occurs to produce hydroxyl ions. Accompanying the further extramembranous acid-base neutralization reaction, an outbound flow of protons is generated to drive the reconstituted adenosine triphosphate (ATP) synthase to produce ATP. That is, contrary to biochemistry, the proton gradient to drive photophosphorylation derives from the scavenging of protons present in the external medium by hydroxyl ions, produced by the partially photo-induced splitting of photobase generator. Such assembled system holds great potential in ATP-consuming bioapplications.〈/p〉〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉 〈p〉Contrary to biochemistry, a designed system effectively enhances photophosphorylation by photo-induced proton-scavenging through molecular assembly.〈/p〉 〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0021979718311561-ga1.jpg" width="294" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉 〈/div〉 〈/div〉

Description: 〈p〉Publication date: 15 January 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 534〈/p〉 〈p〉Author(s): Junyan Zhang, Yongxin Song, Dongqing Li〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉 〈h6〉Hypothesis〈/h6〉 〈p〉The shape of the liquid film (SLF) between a glass slide and an oil droplet immersed in an aqueous solution is influenced by the direct current (DC) electric field. The liquid film, consisting of the central film region and the meniscus film region, is formed between a floating oil droplet and a glass slide overhead.〈/p〉 〈/div〉 〈div〉 〈h6〉Experiments〈/h6〉 〈p〉The SLF was experimentally studied in aqueous solutions of different ionic concentrations and pH values. After the DC electric fields were applied along the glass slide in horizontal direction, the diameter of central film and the thickness of meniscus film were measured by the interference method with an optical microscope.〈/p〉 〈/div〉 〈div〉 〈h6〉Findings〈/h6〉 〈p〉The diameter of the central film decreases with the increase in the applied electric fields and declines at higher pH values while increases when the ionic concentration increases. The meniscus film becomes thicker with the increase in applied electric fields and is thicker in pH = 11 solution and thinner in pH = 3 and 1 mM NaCl solution. This is the first study of dynamic thin liquid film under DC electric field, which may be attributed to the balance of dielectrophoretic (DEP) force, colloidal force and the deformable characteristic of the oil droplet.〈/p〉 〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0021979718311056-ga1.jpg" width="255" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: 1 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 535〈/p〉 〈p〉Author(s): Shinya Higashimoto, Takuto Nakase, Shun Mukai, Masanari Takahashi〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉The copper-indium-sulfide (CIS) ternary colloids were synthesized in “green” water solvent at room temperature employing mercapto-alkyl carboxylic linker molecules such as thioglycolic acid (TGA), thioacetic acid (TAA), 2-mercaptopropionic acid (2-MPA) and 〈span〉l〈/span〉-cysteine (Cys). The stability of the CIS colloids is strongly influenced by the structures of linker molecules, and short linker molecules induce strong adsorption of the CIS colloids on the TiO〈sub〉2〈/sub〉, exhibiting strong visible-light absorption and high photo-conductivities. Effects of linker molecules capping CIS colloids on the solar cell performances were demonstrated. The solar cell performances for the CIS-TiO〈sub〉2〈/sub〉 improve as an increase of photo-conductivity of the CIS-TiO〈sub〉2〈/sub〉 electrodes. In particular, the CIS(TAA)-TiO〈sub〉2〈/sub〉 photoelectrode employing the shortest linker molecules (TAA) exhibited the highest PCE yielding with 6.33% (short-circuit current: 14.0 mA/cm〈sup〉2〈/sup〉, open-circuit voltage: 0.91 V and fill factor: 48.0%).〈/p〉〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0021979718311731-ga1.jpg" width="478" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: 15 January 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 534〈/p〉 〈p〉Author(s): Muhammad Ali, Sarmad Al-Anssari, Muhammad Arif, Ahmed Barifcani, Mohammad Sarmadivaleh, Linda Stalker, Maxim Lebedev, Stefan Iglauer〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉 〈h6〉Hypothesis〈/h6〉 〈p〉CO〈sub〉2〈/sub〉 geological storage (CGS) involves different mechanisms which can store millions of tonnes of CO〈sub〉2〈/sub〉 per year in depleted hydrocarbon reservoirs and deep saline aquifers. But their storage capacity is influenced by the presence of different carboxylic compounds in the reservoir. These molecules strongly affect the water wetness of the rock, which has a dramatic impact on storage capacities and containment security. However, precise understanding of how these carboxylic acids influence the rock’s CO〈sub〉2〈/sub〉-wettability is lacking.〈/p〉 〈/div〉 〈div〉 〈h6〉Experiments〈/h6〉 〈p〉We thus systematically analysed these relationships as a function of pressure, temperature, storage depth and organic acid concentrations. A particular focus was on identifying organic acid concentration thresholds above which storage efficiency may get influenced significantly.〈/p〉 〈/div〉 〈div〉 〈h6〉Findings〈/h6〉 〈p〉These thresholds (defined for structural trapping as a water contact angle θ 〉 90°; and for capillary trapping when primary drainage is unaffected, i.e. θ 〉 50°) were very low for structural trapping (∼10〈sup〉−3〈/sup〉–10〈sup〉−7〈/sup〉 M organic acid concentration C〈sub〉organic〈/sub〉) and extremely low for capillary trapping (10〈sup〉−7〈/sup〉 M to below 10〈sup〉−10〈/sup〉 M C〈sub〉organic〈/sub〉). Since minute organic acid concentrations are always present in deep saline aquifers and certainly in depleted hydrocarbon reservoirs, significantly lower storage capacities and containment security than previously thought can be predicted in carbonate reservoirs, and reservoir-scale models and evaluation schemes need to account for these effects to de-risk CGS projects.〈/p〉 〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0021979718310257-ga1.jpg" width="451" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: 1 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 535〈/p〉 〈p〉Author(s): Jing Du, Lixin Wang, Lei Bai, Shijia Dang, Li Su, Xiujuan Qin, Guangjie Shao〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Development of highly-active and noble-metal-free electrocatalysts for hydrogen evolution reactions is a challenge, and optimizing the structure and the composition of the relative materials is critical to obtain the high-quality catalysts. Ni-based compounds are being explored as noble-metal-free electrocatalysts in hydrogen evolution reactions but the Ni-based needs to be modified effectively. In this work, we co-electrodeposited Ni nanoparticles, hydrophilic graphene and graphene oxide layers on Ni foam to synthesize Ni-HG-rGO/NF catalysts. It was presented a Datura-like shape allowing for high performance with current densities of −10 and −100 mA cm〈sup〉−2〈/sup〉 for HER at overpotentials of −50 and −132 mV, a low Tafel slope of −48 mV dec〈sup〉−1〈/sup〉 and excellent long-term stability in 1.0 M NaOH solution. These results demonstrate that the Ni-HG-rGO/NF electrode can be a competitive electrode materials for HER in alkaline conditions.〈/p〉〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S002197971831138X-ga1.jpg" width="301" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: 1 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 535〈/p〉 〈p〉Author(s): Xiaowei Cheng, Le Huang, Xuanyu Yang, Ahmed A. Elzatahry, Abdulaziz Alghamdi, Yonghui Deng〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Owing to the high costs and instability of natural enzymes, the development of enzyme mimics based on inorganic nanomaterials has attracted a wide concern in recent years. In this work, a stable nanocomposite composed of highly dispersed CeO〈sub〉2〈/sub〉 nanoparticles decorated on zeolite Y as support (CeO〈sub〉2〈/sub〉/Y) was synthesized by a facile wet impregnation method, and the CeO〈sub〉2〈/sub〉/Y nanocomposite was firstly proposed as an efficient peroxidase-mimicking nanozyme for accurate detection of H〈sub〉2〈/sub〉O〈sub〉2〈/sub〉 and glucose. The best catalyst was the nanocomposite with CeO〈sub〉2〈/sub〉 to zeolite Y mass ratio of 0.20 (denoted as 20CeO〈sub〉2〈/sub〉/Y), showing a better affinity and higher catalytic constant to the substrate of H〈sub〉2〈/sub〉O〈sub〉2〈/sub〉 and 3,3′,5,5′-tetramethylbenzidine (TMB) than horseradish peroxidase (HRP) enzymes by the steady-state kinetic analysis. The enzyme-mimicking catalyst could be used over a wider range of pH and temperature for a long-time reuse in TMB oxidation. A facile colorimetric assay was set up for the accurate detection of H〈sub〉2〈/sub〉O〈sub〉2〈/sub〉 and glucose, with the detection limits of 0.323 μM and 35.4 μM, respectively. The CeO〈sub〉2〈/sub〉/Y-based peroxidase mimic was used to precisely detect the glucose concentration in real blood serum samples, exhibiting a great potential to be constructed as a reliable biosensor for glucose detection in some complex systems. The superior peroxidase-mimicking performance of CeO〈sub〉2〈/sub〉/Y nanocomposite is attributed to the synergistic effects of outstanding activity of highly dispersed CeO〈sub〉2〈/sub〉 nanoparticles (5–10 nm) and adsorption properties of zeolite Y with large surface area (517 m〈sup〉2〈/sup〉·g〈sup〉−1〈/sup〉) and pore volume (0.329 cm〈sup〉3〈/sup〉·g〈sup〉−1〈/sup〉).〈/p〉〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉 〈p〉A facile colorimetric assay was developed for the accurate detection of H〈sub〉2〈/sub〉O〈sub〉2〈/sub〉 and glucose with the CeO〈sub〉2〈/sub〉/Y hybrid nanocomposite as a highly efficient peroxidase-mimicking nanozyme, which shows the synergistic effects of outstanding activity of highly dispersed CeO〈sub〉2〈/sub〉 nanoparticles and high surface area and pore volume of zeolite Y as support.〈/p〉 〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0021979718311858-ga1.jpg" width="253" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉 〈/div〉 〈/div〉

Description: 〈p〉Publication date: 1 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 535〈/p〉 〈p〉Author(s): Michaela Sochorová, Pavla Audrlická, Martina Červená, Andrej Kováčik, Monika Kopečná, Lukáš Opálka, Petra Pullmannová, Kateřina Vávrová〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Cholesterol (Chol) is one of the major skin barrier lipids. The physiological level of Chol in the stratum corneum (SC) appears to exceed its miscibility with other barrier lipids, as some Chol is phase separated. Chol synthesis is essential for epidermal homeostasis, yet the role of these Chol domains in SC permeability is unknown. We investigated the impact of Chol depletion on the permeability properties and microstructure of model membranes and human SC. X-ray powder diffraction of membranes constructed from isolated human skin ceramides or synthetic ceramides confirmed that only approximately half of the normal Chol amount can be incorporated in either long or short periodicity lamellar phases. The long periodicity lipid arrangement persisted even in the absence of Chol. Infrared spectroscopy suggested that Chol had negligible effects on the lipid chain order and packing at physiological skin temperature. Chol depletion of the model membranes or isolated human SC did not compromise the barrier function to water and two model permeants. On the contrary, the membrane with the Chol content reduced to 40% of the normal value, where no separated Chol was observed, was significantly less permeable than the control. Thus, a 0.4:1:1 M ratio of Chol/ceramides/fatty acids appears sufficient for skin lipids to limit water loss and prevent the entry of environmental substances. We speculate that the SC Chol domains may have roles in the skin other than barrier function.〈/p〉〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0021979718311883-ga1.jpg" width="500" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: 15 January 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 534〈/p〉 〈p〉Author(s): Nan Lu, Xi Zhang, Ruiqi Na, Wendi Ma, Chongyang Zhang, Yuchao Luo, Yongfeng Mu, Shuling Zhang, Guibin Wang〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉The synthesis of a nanocomposite gel polymer electrolytes (NGPEs) using Li〈sup〉+〈/sup〉-functionalized SPEEK (SPEEK(Li)) nanofiber membrane as a matrix, cross-linked PVA as a gelled agent and LiClO〈sub〉4〈/sub〉 as an electrolytic salt for electric double layer capacitors (EDLCs) were reported in this work. Compared with conventional PVA based gel electrolyte, the “SO〈sub〉3〈/sub〉〈sup〉−〈/sup〉Li〈sup〉+〈/sup〉” functional groups and the pores structure of the SPEEK(Li) nanofiber membrane improves the ionic conductivity as well as mechanical stability, which made the prepared NGPEs exhibited a high ionic conductivity of 8.9 × 10〈sup〉−3〈/sup〉 S cm〈sup〉−1〈/sup〉 at ambient temperature and a large voltage stability window range from 0 to 2.0 V. The fabricated symmetric EDLCs showed a specific capacitance of 146.96 F g〈sup〉−1〈/sup〉 at a current density of 0.5 A g〈sup〉−1〈/sup〉, with a maximum energy density of 18.26 W h kg〈sup〉−1〈/sup〉. Meanwhile, the EDLCs showed outstanding cyclical stability of 98% specific capacitance retention after 3000 cycles GCD testing, all of these results indicated that the NGPEs should be appropriate to EDLCs and next-generation energy storage systems.〈/p〉〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0021979718311020-ga1.jpg" width="383" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: 1 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 535〈/p〉 〈p〉Author(s): Elisangela P. Da Silva, Manuel E.G. Winkler, Willyan M. Giufrida, Lucio Cardozo-Filho, Christian G. Alonso, Jardel B.O. Lopes, Adley F. Rubira, Rafael Silva〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Photocatalytic activity of TiO〈sub〉2〈/sub〉 nanoparticles is highly dependent on their phase composition. The coexistence of anatase and rutile phases in a single nanoparticle eases the electron transfer process between the phases, and favors the separation of photogenerated pairs. In this work, highly photoactive mixed-phase TiO〈sub〉2〈/sub〉 nanostructures were prepared by supercritical antisolvent precipitation (SAS), an environmentally friendly technology. It is shown here that this methodology has the remarkable ability to produce highly porous (515 m〈sup〉2〈/sup〉/g) and crystalline TiO〈sub〉2〈/sub〉 nanoparticles. The phase composition of as-prepared TiO〈sub〉2〈/sub〉 samples can be tailored through annealing process. Several mixed-phase TiO〈sub〉2〈/sub〉 samples were tested to assess the correlation between photocatalytic activity and phase composition. The photocatalytic performance is strongly affected by the anatase-rutile ratio, since the synergism between phases enhances the charge separation, reducing the recombination effect of the photogenerated pairs (e〈sup〉−〈/sup〉/h〈sup〉+〈/sup〉). It was found that the nanocatalyst composed by 7.0 wt% of rutile phase and 93.0 wt% of anatase phase, named as TiO〈sub〉2〈/sub〉_650, presented the highest photodegradation for both methyl orange (MO) and methylene blue (MB) dyes. Interestingly, TiO〈sub〉2〈/sub〉 samples prepared by SAS have superior photoactivity than the benchmark photocatalyst names as P25, which is a widely used TiO〈sub〉2〈/sub〉 material composed of anatase and rutile phases.〈/p〉〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0021979718311792-ga1.jpg" width="309" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: 15 January 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 534〈/p〉 〈p〉Author(s): Na Zhang, Ying Huang, Mingyue Wang, Xudong Liu, Meng Zong〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉A novel hierarchical composites for coupling thistle-like CoNi with dielectric Ag decorated graphene in paraffin wax as high performance microwave absorber has been synthesized by a facile two-step strategy. The components, particle size, microstructure and morphology of the resulting composites are characterized by X-ray diffraction, X-ray photoelectron spectroscopy, Raman spectra, scanning electron microscope, transmission electron microscopy and energy dispersive X-ray spectroscopy, etc. Due to the unique flower structure and good synergistic effect of dielectric loss and magnetic loss, thistle-like CoNi@dielectric Ag decorated graphene composites have showed glorious microwave absorption intensity and frequency width. The maximum reflection loss of −61.9 dB can be gained at 6.96 GHz, which has rarely been reported yet. In addition, the corresponding effective bandwidth with reflection loss less than −10 dB is 5.6 GHz ranging from 12.4 to 18 GHz at only 1.67 mm thickness. This highly efficient and broad band features endow thistle-like CoNi@dielectric Ag decorated graphene composites with promising applications in microwave absorption, electromagnetic shielding, information safety, direct broadcast satellite and military radar fields.〈/p〉〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉 〈p〉Synthesis and microwave absorption properties schematic diagram.〈/p〉 〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0021979718310877-ga1.jpg" width="273" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉 〈/div〉 〈/div〉

Description: 〈p〉Publication date: 1 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 535〈/p〉 〈p〉Author(s): Jianqiang Wang, Hao Guo, Xiaonan Shi, Zhikan Yao, Weihua Qing, Fu Liu, Chuyang Y. Tang〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉We report a novel membrane surface modification method using a fast polydopamine coating (fPDAc) strategy. Specifically, NaIO〈sub〉4〈/sub〉 was introduced in the coating process to accelerate the polydopamine deposition rate. Surface properties and separation performances of fPDAc-coated reverse osmosis membranes were characterized and compared to those obtained using the conventional slow polydopamine coating (sPDAc) strategy. Quartz crystal microbalance measurements showed greatly increased polydopamine deposition rate using the fPDAc method, resulting in a reduction of 97% coating time to reach an areal mass of 2000 ng/cm〈sup〉2〈/sup〉. Both fPDAc and sPDAc enhanced the surface hydrophilicity and reduced the membrane surface charge. At relatively low areal mass deposition (〈1000 ng/cm〈sup〉2〈/sup〉), fPDAc-coated membranes showed improved NaCl rejection together with only mild loss of pure water flux. Nevertheless, this rejection enhancement effect was not noticeable when extensive polydopamine coating was applied due to the undesirable cake-enhanced concentration polarization effect. The extensive polydopamine coating was further accompanied with severe loss of membrane permeability, suggesting that shorter coating time (e.g., 4 min) is preferred using the fPDAc method. Our study provides a more rapid and effective membrane surface coating method compared to the conventional sPDAc method.〈/p〉〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0021979718312049-ga1.jpg" width="312" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: 15 January 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 534〈/p〉 〈p〉Author(s): Xiaoyan Lu, Wei Jia, Hui Chai, Jindou Hu, Shiqiang Wang, Yali Cao〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Simple solid-state chemical reaction was adopted to synthesize NiMoO〈sub〉4〈/sub〉 nanomaterials with different crystal phase without the use of organic solvent or templating agent. The as-prepared NiMoO〈sub〉4〈/sub〉·xH〈sub〉2〈/sub〉O, α-NiMoO〈sub〉4〈/sub〉 and β-NiMoO〈sub〉4〈/sub〉 nanostructures were investigated as the electrode materials for supercapacitors. The β-NiMoO〈sub〉4〈/sub〉 nanorods were composed of the nanoparticles, which exhibited relatively high specific capacitances about 1415 F g〈sup〉−1〈/sup〉 at a charge density of 1 A g〈sup〉−1〈/sup〉, 80.2% of the initial reversible capacity was maintained after 1000 cycles. The β-NiMoO〈sub〉4〈/sub〉//rGO asymmetric supercapacitor (ASC) system was assembled in serials, which displayed high specific energy density of 29.3 Wh kg〈sup〉−1〈/sup〉 at a high power density of 187 W kg〈sup〉−1〈/sup〉. This ASC system can drive the light-emitting diode (LED) effectively and give out light about 40 min, even easily light two LEDs in serials for 20 min. The remarkable electrochemical performances make the as-prepared NiMoO〈sub〉4〈/sub〉 nanostructures an excellent candidate as electrode materials for advanced supercapacitors.〈/p〉〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉 〈p〉The β-NiMoO〈sub〉4〈/sub〉 nanomrods were successfully fabricated by a green solid-state chemical approach and exhibit high electrochemical performance for supercapacitors.〈/p〉 〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0021979718311172-ga1.jpg" width="272" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉 〈/div〉 〈/div〉

Description: 〈p〉Publication date: 1 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 535〈/p〉 〈p〉Author(s): Harkirat Kaur, Girivyankatesh Hippargi, Girish R. Pophali, Amit Bansiwal〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Triclosan, an antimicrobial micro-pollutant with a high bio-accumulation potential represented by its high octanol-water partition coefficient (log K〈sub〉ow〈/sub〉) of 4.76 is commonly encountered in water and wastewater worldwide. The present study focuses on biomimetic surface modification of commercial activated carbon (PAC) with long chain fatty acid namely docosahexaenoic acid (DHA) resulting in enhanced affinity for the hydrophobic micro-pollutant; triclosan (TCS). The sorption process of the resulting modified lipophilic carbon (PAC〈sub〉M〈/sub〉) was investigated for the effect of various experimental conditions. The Freundlich isotherm and pseudo-second-order kinetic models had a better fit. PAC〈sub〉M〈/sub〉 exhibited the maximum adsorption capacity of 395.2 mg g〈sup〉−1〈/sup〉 in contrast to 71.5 mg g〈sup〉−1〈/sup〉 obtained for PAC. The surface morphology in terms of surface area, surface acidity, pore size, contact angle, etc. and were also evaluated. The contact angle of 134.3° obtained for PAC〈sub〉M〈/sub〉 confirmed its highly hydrophobic nature. The efficacy of PAC〈sub〉M〈/sub〉 was also evaluated using real-world secondary treated effluent containing triclosan confirming its applicability for tertiary treatment of wastewater. The study established that the biomimetic approach of creating lipid-like sites on the carbon surface results in the enhanced removal of lipophilic micro-pollutants. It can also be utilized for the removal and recovery of a wide variety of other organic micro-pollutants.〈/p〉〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0021979718311743-ga1.jpg" width="235" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: 15 January 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 534〈/p〉 〈p〉Author(s): Ahmad Tayyebi, Tayyebeh Soltani, Byeong-Kyu Lee〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Monoclinic bismuth vanadate (c-BVO) was prepared via simple calcination of solvothermally processed tetrahedral BiVO〈sub〉4〈/sub〉. The physicochemical and morphological properties of c-BVO demonstrated the successful synthesis of the photoactive monoclinic phase from the tetrahedral phase, which has low photoactivity properties. The photoactivities of c-BVO were investigated using the photodegradation of methylene blue (MB) and photoelectrochemical (PEC) measurements in acidic (pH = 2.5), neutral (pH = 6.5) and basic (pH = 9.5) media. The photocatalytic activity of c-BVO was increased with increasing pH, achieved 99% MB degradation in the basic condition, compared with 70 and 45% in the neutral and acidic media, respectively. Although the tetrahedral BiVO〈sub〉4〈/sub〉 showed mainly adsorption with negligible photodegradation, c-BVO demonstrated both good adsorption and photodegradation activities. The PEC results indicated that the photocurrent density was affected by both pH and applied voltage. Impedance measurements showed faster charge transfer in the neutral condition than in the acidic and basic electrolytes. The incident photon conversion efficiency (IPCE) showed very low activity for tetrahedral BiVO〈sub〉4〈/sub〉, but in comparison it was enhanced by 20- and 10-fold for c-BVO in the visible and simulated solar light, respectively.〈/p〉〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0021979718310208-ga1.jpg" width="309" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: 15 January 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Journal of Colloid and Interface Science, Volume 534〈/p〉 〈p〉Author(s): Ying Yang, Dehong Zeng, Senjie Yang, Lin Gu, Baijun Liu, Shijie Hao〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Core-shell structured carbon nanofiber@metal oxide is one of the most promising hybrid electrodes as supercapacitors, in which the pseudocapacitive metal oxides can be fully exerted and stabilized on the carbonaceous scaffolds. However, facile fabrication of mesoporous carbon nanofibers and integration of them with metal oxides are challenging. Herein, we report a new type of mesoporous carbon nanofibers (MCNs), derived from zinc-trimesic acid fibers, acting as the scaffolds to anchor nickel cobaltite (NiCo〈sub〉2〈/sub〉O〈sub〉4〈/sub〉) nanosheets after surface O-functionalization. The resultant core-shell OMCN@NiCo〈sub〉2〈/sub〉O〈sub〉4〈/sub〉 nanostructure is demonstrated by scanning electron microscope (SEM), elemental mapping, bright-field/high-resolution transmission electron microscope (TEM), selected area electron diffraction (SAED) studies. The anchored NiCo〈sub〉2〈/sub〉O〈sub〉4〈/sub〉 nanosheets are dense (97.4%), and have a strong interaction with OMCN, as revealed by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), thermogravimetric analysis (TGA) and H〈sub〉2〈/sub〉-temperature programmed reduction (H〈sub〉2〈/sub〉-TPR) techniques. As expected, the OMCN@NiCo〈sub〉2〈/sub〉O〈sub〉4〈/sub〉 is highly efficient, showing a high specific capacitance of 1631 F g〈sup〉–1〈/sup〉 at the current density of 1 A g〈sup〉–1〈/sup〉, excellent rate capability and superior cycling stability up to 5000 cycles within a high capacitance retention ratio of 94.5%. This research opens the avenue to fabricate high-efficiency carbon-metal oxide electrodes using metal-organic framework fiber-derived mesoporous carbon nanofibers and integration of them with NiCo〈sub〉2〈/sub〉O〈sub〉4〈/sub〉 nanosheets by increasing the interfacial interaction.〈/p〉〈/div〉 〈/div〉 〈div xml:lang="en"〉 〈h5〉Graphical abstract〈/h5〉 〈div〉 〈p〉NiCo〈sub〉2〈/sub〉O〈sub〉4〈/sub〉 nanosheets coated on zinic-trimesic acid fiber-derived mesoporous carbon nanofibers within surface O-functionalities as high-performance electrode for supercapacitors.〈/p〉 〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S002197971831110X-ga1.jpg" width="276" alt="Graphical abstract for this article" title=""〉〈/figure〉〈/p〉 〈/div〉 〈/div〉

Description: 〈p〉Publication date: 1 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Electrochimica Acta, Volume 295〈/p〉 〈p〉Author(s): Pablo A. García-Salaberri, Iryna V. Zenyuk, Gisuk Hwang, Marcos Vera, Adam Z. Weber, Jeff T. Gostick〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Thin porous media are present in multiple electrochemical energy devices, where they provide key transport and structural functions. The prototypical example is gas diffusion layers (GDLs) in polymer-electrolyte fuel cells (PEFCs). While modeling has traditionally been used to explore PEFC operation, this is often accomplished using volume-averaged (VA) formulations, where the intrinsic inhomogeneities of the GDL are smoothed out and the lack of defining a representative elementary volume is an ever-present issue. In this work, the predictions of a single-phase VA PEFC model are compared to those of a pore-scale PEFC model using GDL tomograms as a part of the meshed domain to delineate important aspects that VA models cannot address. The results demonstrate that while VA models equipped with suitable effective properties can provide a good average estimate for overall performance, the lack of accounting for real structures limits their predictive power, especially for durability and degradation behavior where large deviations are found in the spatial distributions. Furthermore, interfacial effects between the GDL and the microporous layer are explored with the pore-scale model to understand the implications of the layered geometry. It is shown that the actual microstructure of the GDL/MPL transition region can significantly affect the fluxes across the sandwich, something that VA models cannot easily consider. Interfacial design is recognized as a key quality control parameter for large-scale MEA manufacturing and assembly.〈/p〉〈/div〉 〈/div〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0013468618320759-fx1.jpg" width="331" alt="Image 1" title="Image 1"〉〈/figure〉〈/p〉〈/div〉

Description: 〈p〉Publication date: 10 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Electrochimica Acta, Volume 296〈/p〉 〈p〉Author(s): Jinjun Tian, Yan Xue, Mengmeng Wang, Yuanchao Pei, Hucheng Zhang, Jianji Wang〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉High performances, cost-effectiveness, and facile preparation of electrode materials are of utmost importance for supercapacitors in practical applications. Herein, Ni(HCO〈sub〉3〈/sub〉)〈sub〉2〈/sub〉 nanoparticles (NPs) of low cost and environmental friendliness were embedded into polydopamine-reduced graphene oxide (PDA-RGO) networks via cost-effective hydrothermal route. It is shown the conducting PDA can uniformly distributes and robustly immobilizes Ni(HCO〈sub〉3〈/sub〉)〈sub〉2〈/sub〉 NPs in the nanocomposite while the ionic channels are improved for electrolyte access. Consequently, the as-prepared Ni(HCO〈sub〉3〈/sub〉)〈sub〉2〈/sub〉-PDA-RGO composite offers the high Faradaic capacity of 870 C g〈sup〉−1〈/sup〉 at 0.5 A g〈sup〉−1〈/sup〉 and moderate rate capability. Furthermore, the assembled Ni(HCO〈sub〉3〈/sub〉)〈sub〉2〈/sub〉-PDA-RGO//activated carbon hybrid supercapacitor (HSC) delivers a specific capacity of 192 C g〈sup〉−1〈/sup〉 at 0.5 A g〈sup〉−1〈/sup〉 within operation voltage window of 1.7 V. The maximum energy density of the HSC reaches to 45.3 Wh kg〈sup〉−1〈/sup〉 at a power density of 425 W kg〈sup〉−1〈/sup〉, and the initial specific capacity maintains 90.5% after 3000 successive charge-discharge cycles. The high energy density and good cycleability certify the potential of the ternary Ni(HCO〈sub〉3〈/sub〉)〈sub〉2〈/sub〉-PDA-RGO composite in efficient and long lifetime energy storage systems.〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: 1 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Electrochimica Acta, Volume 295〈/p〉 〈p〉Author(s): Libin Zeng, Xinyong Li, Shiying Fan, Zhifan Yin, Mingmei Zhang, Jincheng Mu, Meichun Qin, Tingting Lian, Moses Tadé, Shaomin Liu〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Structure-controlled visible light driven photo-anode with high catalytic performance, plays important roles in environmental pollutants treatment. In this work, a mild hydrothermal assisted anodization approach has been reported to design an integrated self-assembled 3D flower-like MoS〈sub〉2〈/sub〉/1D TiO〈sub〉2〈/sub〉 nanotube arrays (NTAs) hierarchical electrode. The constructed multidimensional electrode not only broadened the absorption spectrum response range but also promoted rapidly electron-hole pairs separation, exhibiting the excellent photoelectron catalytic (PEC) performance and stability in the degradation of target pollutants, which the photocurrent conversion efficiency was 6.5 times higher than that of pure TiO〈sub〉2〈/sub〉. Furtherly, a comprehensive mechanism was proposed to explain the charge transfer on the interface of intimate integration of 3D/1D hybrid nanostructure towards PEC properties in terms of the energy band structures and DFT. Furthermore, the photo-generated active species (〈img src="https://sdfestaticassets-eu-west-1.sciencedirectassets.com/shared-assets/16/entities/rad"〉OH and 〈img src="https://sdfestaticassets-eu-west-1.sciencedirectassets.com/shared-assets/16/entities/rad"〉O〈sub〉2〈/sub〉〈sup〉−〈/sup〉) have been proved by electron paramagnetic resonance spectroscopy and fluorescence probe over the composites. Thus, this work could provide an effective strategy to design multidimensional coupled heterojunction materials toward solar energy conversion for environmental purification.〈/p〉〈/div〉 〈/div〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0013468618323934-fx1.jpg" width="477" alt="Image 1" title="Image 1"〉〈/figure〉〈/p〉〈/div〉

Description: 〈p〉Publication date: 1 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Electrochimica Acta, Volume 295〈/p〉 〈p〉Author(s): Valentín Briega-Martos, José Solla-Gullón, Marc T.M. Koper, Enrique Herrero, Juan M. Feliu〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉The formic acid oxidation reaction has been studied on Pt(111), Pt(100) and Pt nanoparticles with preferential (111) surface structure in 0.1 M HClO〈sub〉4〈/sub〉 in the presence of different concentrations of acetonitrile. An electrocatalytic enhancement towards the formic acid oxidation has been observed under these conditions, and it is proposed that this enhancement is due to two different effects of the adsorbed acetonitrile species: a third-body effect which hinders the formation of CO and a promoting effect of the direct oxidation of formic acid. This promoting effect is structure sensitive. The different enhancement between Pt(111) and Pt(100) indicates that the ratio of free Pt sites and sites occupied by adsorbed acetonitrile is important in order to have the better electrocatalytic activity. On-line mass spectrometry (OLEMS) measurements confirmed the preference for the direct oxidation of formic acid to CO〈sub〉2〈/sub〉, which is almost complete below 0.3 V vs. RHE for Pt(111). Finally, chronoamperometric studies confirmed the lower poisoning rate in the presence of acetonitrile but they also pointed out a competition of formed CO for the Pt sites occupied by acetonitrile species. This work constitutes an example of electrocatalytic enhancement by using an organic molecule for surface modification, which is not as common as using metallic adlayers.〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: 1 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Electrochimica Acta, Volume 295〈/p〉 〈p〉Author(s): Yu Li, Bo Lu, Bingkun Guo, Yicheng Song, Junqian Zhang〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Partial lithiation strategies for silicon composite electrodes are experimentally investigated in this article. Two types of partial lithiation, i.e. voltage- and capacity-control strategies, are presented. Capacity loss and irreversibility of silicon electrodes are significantly suppressed by either partial lithiation strategy without any complicated modifications or treatments. The capacity of partially lithiated silicon electrodes is even higher than that of fully lithiated one after certain cycles. The images of scanning electron microscope suggest that the mechanical damage generated in partially lithiated electrodes is less than that in fully lithiated one. Furthermore, after dozens of cycles with partial lithiation, capacity decay also slows down in subsequent full charge-discharge cycles. The presented experimental results suggest that the partial lithiation strategy relieves the coupled mechanical-electrochemical degradation and is a promising approach for the long-term use of silicon composite electrodes.〈/p〉〈/div〉 〈/div〉

Description: 〈p〉Publication date: 10 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Electrochimica Acta, Volume 296〈/p〉 〈p〉Author(s): Yu Shi, Haiyan Leng, Liang Wei, Shuanglin Chen, Qian Li〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉The structural characteristics and electrochemical performances of superlattice La〈sub〉5.42〈/sub〉Y〈sub〉18.50〈/sub〉Ni〈sub〉76.08-〈em〉x〈/em〉〈/sub〉Mn〈sub〉〈em〉x〈/em〉〈/sub〉 (〈em〉x〈/em〉 = 0, 2, 4, and 6) metal-hydride electrodes were investigated. La〈sub〉5.42〈/sub〉Y〈sub〉18.50〈/sub〉Ni〈sub〉76.08〈/sub〉 alloy is composed of LaY〈sub〉2〈/sub〉Ni〈sub〉9〈/sub〉, Y〈sub〉2〈/sub〉Ni〈sub〉7〈/sub〉, and La〈sub〉2〈/sub〉Ni〈sub〉7〈/sub〉 phases, while the amount of AB〈sub〉3〈/sub〉-type phase increases due to the increasing substitution amount of Ni by Mn. The mechanisms on the related electrochemical thermodynamics and kinetics were investigated systematically. Compared with La〈sub〉5.42〈/sub〉Y〈sub〉18.50〈/sub〉Ni〈sub〉76.08〈/sub〉 alloy, the maximum discharge capacity of La〈sub〉5.42〈/sub〉Y〈sub〉18.50〈/sub〉Ni〈sub〉70.08〈/sub〉Mn〈sub〉6〈/sub〉 alloy increased from 275.2 mAh g〈sup〉−1〈/sup〉 to 379.6 mAh g〈sup〉−1〈/sup〉 and the discharge capacity after 30 cycles increased from 155.0 mAh g〈sup〉−1〈/sup〉 to 281.1 mAh g〈sup〉−1〈/sup〉, which contribute to the increase of the amount of AB〈sub〉3〈/sub〉-type phase as well as the ameliorated structural stability through the substitution of Mn for Ni.〈/p〉〈/div〉 〈/div〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0013468618324873-egi10F074DV8MS.jpg" width="500" alt="Image" title="Image"〉〈/figure〉〈/p〉〈/div〉

Description: 〈p〉Publication date: 10 February 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Electrochimica Acta, Volume 296〈/p〉 〈p〉Author(s): Na Zhao, Zhaokun Ma, Huaihe Song, Yangen Xie, Man Zhang〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉Enhancing microbial electrocatalysis through novel anode design is essential to the efficient and stable operation of microbial fuel cells. Carbon fibers modified by the vertical carbon nanotubes/polypyrrole composites can give full play to their advantages, exhibiting excellent conductivity of the vertical carbon nanotubes and good biocompatibility of the polypyrrole. The carbon nanotubes are vertically grown on the carbon fibers by the chemical vapor deposition method, increasing the transfer efficiency of extracellular electron transfer. And then pyrrole is in-situ polymerized on the exterior and interior of the vertical carbon nanotubes, which can not only avoid direct contact between the vertical carbon nanotubes and electricigens to reduce the damage of the vertical carbon nanotubes to electricigens, but also enhance the positive electricity of anode. The modification of the vertical carbon nanotubes/polypyrrole for mesophase pitch carbon fibers anode improves the electricity generation performances of the microbial fuel cells. In this study, the obtained maximum power density is 1876.62 mW m〈sup〉−2〈/sup〉, which is approximately 2.63-fold higher than unmodified carbon fiber brush anode. The results show that the vertical carbon nanotubes/polypyrrole composite anode has demonstrated the high potential for the use of microbial fuel cells.〈/p〉〈/div〉 〈/div〉