ALBERT

Description: Ferulic acid (FA), an important phenolic acid, is widely distributed in higher plants and presents many pharmacological effects. Therefore, sensitive determination of FA in complex matrix is necessary. Molecularly imprinted polymers-coated CdTe quantum dots (CdTe-QDs@MIPs) exhibited incomparable advantages because of their combination of excellent selectivity of MIPs and high sensitivity of QDs. Here, a fluorescent probe based on CdTe-QDs@MIPs was successfully fabricated for selective and sensitive determination of FA. MIPs shell was obtained by the reverse microemulsion method using FA, 3-(aminopropyl) triethoxysilane (APTES), and tetraethyl orthosilicate (TEOS), as template, functional monomer, and crosslinker. In optimal conditions, the fluorescence CdTe-QDs@MIPs sensor exhibited fast response (within only 3 min), high sensitivity (limit of detection, LOD at 0.85 μg/l), excellent linear ranges (2–100 μg/l) with a correlation coefficient of 0.9996, and distinguished selectivity for FA. Satisfactory recoveries from 91.8% to 110.3% were achieved with precisions below 6.6% for FA analysis in real pineapple juice and apple juice by developed CdTe-QDs@MIPs. The fluorescence results coincided well with those obtained by high-performance liquid chromatography (HPLC). It could be concluded that the resultant CdTe-QDs@MIPs offered a new way for rapid and sensitive analysis of FA in the complex matrix.

Description: Tianwang Buxin pill (TWBXP) is an ancient Chinese classic prescription. Liquiritin, deoxyschizandrin, and tanshinone II A are three bioactive components in TWBXP, which have been proven to be closely related to the therapy effect of neurodegenerative disease. Their contents are very low in TWBXP. In this study, we used a diode array detector (DAD) to perform a full wavelength scanning in order to choose a most suitable detection wavelength to establish an HPLC method for the simultaneous determination of these three components in TWBXP. Various chromatographic conditions were investigated to verify its applicability. Finally, a Kromasil C18 column (250 × 4.6 mm, 5 μm) thermostated at 30°C, mobile phase as 0.2% phosphoric acid solution (eluent A), and 0.1% phosphoric acid-acetonitrile solution (eluent B) were used. Both external standard method and internal standard method were used for quantification. The results showed that both methods were simple and convenient in operation without special pretreatment and exhibits excellent precision, repeatability (RSD  0.9990), and good recoveries (recovery value between 95% and 105%). Because of the low contents in samples, the internal standard method provided a better accurate result than the external standard method. The stability results showed the sample became stable within 24 hours at room temperature. The method provides a convenient and effective way for the quality control of TWBXP, and it can help the research about AD in the future.

Description: In this work, gas chromatography-ion mobility spectrometry (GC-IMS) was used to analyze the volatile organic compound changes of rapeseed oil with different refined grades, the odor fingerprints of refined rapeseed oil were constructed, and a nonlinear model was built to realize rapid and accurate discrimination of rapeseed oil with different refined grades. 124 rapeseed oil samples with different refined grades were collected and analyzed by GC-IMS and chemometric tools, and 34 characteristic peaks were selected by the colorized difference method as variables to characterize the internal quality in rapeseed oil of different refined grades. The principal component analysis algorithm was used to further reduce dimensionality and extract the most relevant information. The k-nearest neighbor algorithm was applied to build a discriminant model. All the samples were recognized accurately without errors, and the results show the potential of this method to discriminate different refined grades of vegetable oil.

Description: The quantitative analysis of multicomponents by the single-marker (QAMS) method was established and the relationship between F value (the ratio of the sum of the contents of emodin-8-O-β-D-glucopyranoside and physcion-8-O-β-D-glucopyranoside to the sum of the contents of emodin and physcion) and the steaming time was found to identify and differentiate Polygonum multiflorum Radix and its processed product. Emodin was considered as the control substance, and the correction factors of physcion, emodin-8-O-β-D-glucopyranoside, and physcion-8-O-β-D-glucopyranoside were computed. In addition, the contents of the four components were determined. When the F value is greater than or equal to 1.0, the sample was identified as Polygonum multiflorum Radix, and if the F value was between 0.6 and 1.0, the sample of Polygoni multiflori Radix Preaparata was processed incompletely. The F value of the qualified Radix Polygonum multiflorum should be no more than 0.6. However, the influence of different sample injection volumes and the chromatographic columns and instruments used on the durability of the correction factors and RSD ≤3% hindered accurate identification; therefore, a QAMS method using an external standard value with methodological verification was developed. We redefined the “Polygonum multiflorum rules.” The method using “Polygonum multiflorum rules” revised after optimization of the determination results was used, as it was accurate and led to convenient operation and low inspection costs, and moreover, the method could differentiate Polygoni multiflori Radix Preaparata and Polygonum multiflorum Radix medicinal samples and precisely identify samples that were different from the completely processed product Polygoni multiflori Radix Preaparata.

Description: A modified multiobjective self-adaptive differential evolution algorithm (MMOSADE) is presented in this paper to improve the accuracy of multiobjective optimization design in the nuclear power system. The performance of the MMOSADE is tested by the ZDT test function set and compared with classical evolutionary algorithms. The results indicate that MMOSADE has a better performance in convergence and diversity. Based on the MMOSADE, a multiobjective optimization design platform for the nuclear power system is proposed, and the application of which is carried out. The evaluation program of the PRHR-HX in AP1000 is developed, and its reliability is verified. The optimal design schemes of PHHR-HX are obtained by utilizing the multiobjective optimization design platform. The results show that the optimal design schemes can envelop the prototype design scheme. This conclusion proves that the optimization design platform proposed in this paper is effective and feasible.

Description: COMSOL Multiphysics has been used to conduct thermal-hydraulic analysis in multiple nuclear applications. The aim of this study is to benchmark the prediction accuracy of COMSOL Multiphysics in performing thermal-hydraulic analysis of TRIGA (Training, Research, Isotopes, General Atomics) reactors such as the Geological Survey TRIGA Reactor (GSTR) by comparing its predictions with RELAP5 (a widely used code in nuclear thermal-hydraulic analysis) results and experimental data. The GSTR type is Mark I with a full thermal power of 1 MW, and it resides at the Denver Federal Center (DFC) in Colorado. The numerical investigation of the present work is carried out by developing single-subchannel thermal-hydraulic models of the GSTR utilizing RELAP5 and COMSOL codes. The models estimate the temperatures (fuel, outer clad, and coolant) and water flow patterns in the core as well as fuel element powers at which void starts to form within the coolant subchannels. Then, these models’ predictions are quantitatively evaluated and compared with the measured data.

Description: A practical scale mechanical decladder that can slit spent nuclear fuel rod-cuts (hulls + pellets) of several tens of kg HM/batch is being developed to supply UO2 pellets to a voloxidation process. The mechanical decladder is an apparatus for separating and recovering fuel material and cladding tubes by horizontally slitting the cladding tube of a fuel rod and a defective irradiated fuel rod. In this study, we address the engineering design of the mechanical decladder for the pretesting of rod-cut slitting. To obtain the requirements of the mechanical decladder, we first manufactured a slitter for testing based on the decladding and shearing conditions of hulls and pellets. The performance test of the testing device for decladding was carried out using a 2-CUT blade module and a 3-CUT blade module. We evaluated the decladding methods for the mechanical decladder and selected the 3-CUT blade module based on the results. A buckling measurement instrument was used to perform a buckling verification test according to the length of a rod-cut and to determine decladder dimensions. The optimum decladding rod-cut length for buckling prevention was calculated. Furthermore, we analyzed the decladding mechanism for various slitting methods. Design/fabrication and preliminary tests of the practical scale mechanical decladder were also performed. For this purpose, we constructed the main mechanism by utilizing the SolidWorks modeling and analysis program and fabricated a new mechanical decladder. Based on the derived requirements, a mechanical decladder with three main modules was designed and fabricated for testing. Simulated rod-cuts of zircaloy were also manufactured to test the basic performance of the decladder, and a data acquisition system was constructed using RSC 232 to measure decladding force and velocity. In the basic test, the rod-cut was completely sectioned into three evenly spaced locations by the new mechanical decladder.

Description: A simple and economic high-performance liquid chromatography (HPLC-UV-Vis) analytical method was validated for the quantitation of specific Bisphenol-A migration from baby feeding bottles. Overall and specific migration assays were done with different food simulating matrices using the filling method. Good linearity was obtained over the concentration range of 0.01–0.6 mg/kg. The limit of detection (LOD) and limit of quantification (LOQ) were 0.004 and 0.010 mg/kg, respectively. The repeatability of the method (%RSD, ) was between 89.5 and 99.0%, while recovery ranged from 83.2 to 98.4%. The method was applied to specific migration assays from baby feeding bottles purchased from different plastic producers in Colombia. The results show that, in a first migration assay, Bisphenol-A was not detectable in all samples. In a second migration test, Bisphenol-A concentrations were higher than the most restricted limit (0.05 mg/kg) with ethanol 95% and isooctane as food simulants.

Description: An efficient, sensitive, and low-cost method has been developed for turn-on fluorescence sensing of dopamine (DA). The method relies on the rapid reaction of DA and 3-Hydroxyphenylboronic acid (3-HPBA) via specific recognition between boronic acids and cis-diol of DA in alkaline solution. The reaction product shows an excitation wavelength of 417 nm and the maximum emission peak at 470 nm. The proposed method allows the determination of DA in the range of 50 nM–25 μM, and the whole detection can be completed within 5 minutes. Furthermore, the presented approach has good selectivity and has been successfully applied to DA sensing in human serum samples, showing great potential in clinical diagnosis.

Description: CIPS is a shift in the axial power towards the bottom half of the core, also known as axial offset anomaly (AOA), which results from the deposited of corrosion products during an operation. The main reason of CIPS is the solute particles especially boron compounds concentrated inside the porous deposit. The impact of CIPS is that the axial power distribution control may be more difficult and the shutdown margin can be decreased simultaneously. Besides, it also requires estimated critical condition (ECC) calculations to account for the effects of AOA. In this article, thermal-hydraulic subchannel code and boron deposit model have been combined to analyze the CIPS risk. The neutronics codes deal with the generation of homogenized neutron cross section as well as the calculation of local power factor. A simple rod assembly is analyzed with this combined method and simulation results are presented. Simulation results provide the boron hideout amount inside crud deposits and power shapes. The obtained results clearly show the power shape suppression in regions where crud deposits exist, which is a clear indication of CIPS phenomenon. And the CIPS effects on CHF have also been investigated. Result shows a margin of DNBR decrease in the crud case.

Description: After the severe accident (SA) occurred at the Three-Miles Island Nuclear Power Plant (NPP), important efforts on the investigation of the different phenomena during this kind of accidents have been started. Several experimental campaigns investigating one phenomenon at time or the combination of two or more phenomena have been performed. Today, the Phébus experimental campaign is probably the most important activity on the evaluation of the coupling among different phenomena. Four out of five tests investigated the degradation of an intact Pressurized Water Reactor (PWR) fuel bundle and the subsequent transport of Fission Products (FP) and Structural Materials (SM) through the primary circuit and into the containment, while the fifth test was only the degradation of a bed of PWR fuel bundle debris. These tests were performed between 1990 and 2010 at the CEA Cadarache laboratories (France) in a 5000:1 scaled facility. The main four tests varied the employed control rod materials, the fuel burn-up, and the oxidizing conditions of the atmosphere (strongly or weakly). The outcomes of this experimental campaign created a solid base for the understanding of the involved phenomena and allowed the development of models and software codes capable of simulating the evolution of a SA in a real NPP. ASTEC and MELCOR were two of the main SA codes profiting from the results of this Phébus campaign. These two codes were further improved in the latest years to account for the findings obtained in more recent experimental campaigns. A continuous verification and validation work is then necessary to check how the newer code’s versions reproduce the tests performed in these older experimental campaigns such as Phébus one. The present work is intended to be the final step of a series of publications covering the activities carried out at University of Pisa with the ASTEC and the MELCOR SA codes on the four Phébus tests employing an intact PWR fuel bundle. Because of the complexity and the extent of these tests, only the containment aspects were considered in the precedent works, i.e., only the thermal-hydraulics transient and its coupling with the FP and SM behavior. Then, general conclusions based on the outcomes of these precedent works are summarized in this work.

Description: For sequentially collected data, this paper introduces a lag-one differencing method to estimate the random error standard deviation and then uses the estimate to calculate a change detection threshold in a moving window method to detect shifts in the short-term systematic error. Performance results on simulated and real data are presented. Fortunately, the impact of having to perform change detection on the estimated short-term systematic and random error variances is anticipated to be modest or small. The motivating example arises from facilities under nuclear safeguards agreements, where inspector data collected during International Atomic Energy Agency (IAEA) verifications are compared to corresponding operator data. The differences between the operator and inspector values are evaluated using an application of analysis of variance (ANOVA). Typically, it is assumed that short-term systematic errors change across inspection periods, so inspection periods form the groups used in the ANOVA. In some data sets, it appears that the short-term errors have changed at other times, so change detection methods could be used to detect the actual change times.

Description: The drying process of Uncariae Ramulus Cum Uncis (URCU), a kind of traditional Chinese medicine, was studied in a scale dryer in laboratory at 65°C. It was observed that the alkaloids content of URCU firstly showed a tendency of increasing and then decreasing after reaching the peak at the 570th minute in the process of constant temperature drying. Moreover, the coagulation time of rabbit determined by test tubes has been adopted to study the effect imposed by the content of alkaloids on the anticoagulating activity of URCU. In addition, the software of Minitab was also utilized to fit the correlation between the content of alkaloids and the anticoagulating activity of URCU. The results obtained demonstrated that anticoagulant activities were available in both rhynchophylline and isorhynchophylline, among which the latter was the stronger one, while procoagulant activity was shown in corynoxeine. The case study can provide a useful reference for the research on drying other Chinese herbal medicines (CHMs) and further study on URCU.

Description: This study presents the time-dependent analyses of transmutations of long-lived fission products (LLFPs) and medium-lived fission products (MLFPs) occurring in thermal reactors in a conceptual helium gas-cooled accelerator-driven system (ADS). In accordance with this purpose, the CANDU-37 and PWR 15 × 15 spent fuels are separately considered. The ADS consists of LBE-spallation neutron target, subcritical fuel zone, and graphite reflector zone. While the considered ADS is fueled with the spent nuclear fuels extracted from each thermal reactor without the use of additional fuel, fission products extracted from same thermal reactor are also placed into transmutation zone in graphite reflector zone. The LLFP transmutation performance of the modified ADS is analyzed by considering three different spent fuels extracted from the thermal reactors. Spent fuels are extracted from CANDU-37 in case A, from PWR-15 × 15 in case B, and from CANDU-37 fueled with mixture of PWR 15 × 15 spent fuel and 46% ThO2 in case C. The LBE target is bombard with protons of 1000 MeV. The proton beam power is assumed as 20 MW, which corresponds to 1.24828·1017 protons per second. MCNPX 2.7 and CINDER 90 computer codes are used for the time-dependent burn calculations. The ADS is operated under subcritical mode until the value of keff increases to 0.984, and the maximum operation times are obtained as 3400, 3270, and 5040 days according to the spent fuel cases of A, B, and C, respectively. The calculations bring out that in the modified ADS, LLFPs and MLFPs, which are extracted from thermal reactors, can be transformed to stable isotopes in significant amounts along with energy production.

Description: Ischemia/reperfusion cerebral injury can cause serious damage to nerve cells. The injured organelles are cleared by autophagy eventually, which is critical for cell survival. Dexmedetomidine is neuroprotective in various ischemia/reperfusion models. Mitochondrial calcium uniporter (MCU) is the most important channel of mitochondrial Ca2+ influx into mitochondria, where Ca2+ has a potential effect on mitochondrial autophagy. However, the role of MCU in the changes of mitophagy and autophagy caused by dexmedetomidine is unknown. In this study, we constructed an in vitro I/R model by subjecting the oxygen and glucose deprivation/reperfusion model to SH-SY5Y cells to mimic the cerebral I/R injury. We found that postconditioning with dexmedetomidine and 3-methyladenine (3MA, an autophagy inhibitor) increased the cell survival meanwhile reduced the production of autophagic vesicles and the expression of LC3 and Beclin 1. This process also increased the expression of BCL-2, P62, and TOM20. After applied with spermine (MCU-specific agonist), the expression of autophagy proteins by dexmedetomidine was reversed, and the same changes were also observed in immunofluorescence. The results of our study suggested that dexmedetomidine can inhibit MCU and reduce excessive mitophagy and autophagy for conferring protection against I/R injury.

Description: Thermal reactors have been considered as interim solution for transmutation of minor actinides recycled from spent nuclear fuel. Various studies have been performed in recent decades to realize this possibility. This paper presents the neutronic feasibility study on transmutation of minor actinides as burnable poison in the VVER-1000 LEU (low enriched uranium) fuel assembly. The VVER-1000 LEU fuel assembly was modeled using the SRAC code system, and the SRAC calculation model was verified against the MCNP6 calculations and the available published benchmark data. Two models of minor actinide loading in the LEU fuel assembly have been investigated: homogeneous mixing in the UGD (Uranium-Gadolinium) pins and coating a thin layer to the UGD pins. The consequent negative reactivity insertion by minor actinides was compensated by reducing the gadolinium content and boron concentration. The reactivity of the LEU assembly versus burnup and the transmutation of minor actinide nuclides were examined in comparison with the reference case. The results demonstrate that transmutation of minor actinides as burnable poison in the VVER-1000 reactor is feasible as minor actinides could partially replace the functions of gadolinium and boric acid for excess reactivity control.

Description: As key equipment in nuclear power plant, the reactor power control system is adopted to strictly control and regulate the reactor power of a PWR (pressurized water reactor) in a nuclear power plant. A well-optimized predictive control algorithm based on SDMC (stepped dynamic matrix controller) is developed and introduced in this paper and applied to the power regulation of a reactor power model. In addition, the test and verification of this application is conducted by two different methods and devices: the virtual verification platform and the physical DCS (digital control system). The result of the verification suggests that the application of SDMC gains a better performance in the maximum dynamic deviation, adjustment time, overshoot, and so on.

Description: The electrochemical behaviour of auramine O on the hanging mercury drop electrode has been investigated by cyclic and square wave voltammetry method. Reduction peak of auramine O was irreversible and adsorptive on the hanging mercury drop electrode. The optimal conditions were chosen to be Briton–Robinson buffer pH 9.0, accumulation potential −0.5 V vs. Ag/AgCl/KCl, accumulation time 60 s, pulse amplitude 250 mV·s−1, and frequency 50 Hz. At the optimum experimental conditions, the peak of the target analyte was sharp and asymmetric. The linearity of the peak current depending on the concentration ranged from 4.0 × 10−8 to 6.4 × 10−7 mol L−1. The limit of detection and limit of quantitation were 2.46 × 10−8 mol L−1 and 8.21 × 10−8 mol L−1, respectively. The recovery and relative standard deviation were 94.9% and 2.0% (n = 5). The developed method was successfully applied to determine auramine O in chicken samples with an appropriate sample preparation.

Description: By-products (phenyl salicylate, phenyl 4-hydroxybenzoate, and xanthone) from transesterification between phenol and dimethyl carbonate (DMC) were qualitatively analyzed by gas chromatography-mass spectrometry, and a gas chromatographic method with directed injection for simultaneous quantitative analysis of the product (DPC) and by-products of the transesterification has been established. Based on the results of qualitative and quantitative analyses, the mechanism of the by-products generation was preliminarily deduced. The sample for quantitative analysis was directly diluted in acetone, and related compounds were separated on an HP-5 capillary column and detected by a hydrogen flame ionization detector (FID). The product and by-products were well separated, the correlation coefficients (r) within the concentration range of 1.0 μg/mL–100 μg/mL were ≥0.9997, the relative standard deviations were between 0.5% and 4.4%, spiked recoveries were between 91.5% and 105.6%, and detection limits were between 0.11 and 0.18 μg/mL. The established method is simple, rapid, accurate, sensitive, and highly specific. It is suitable for simultaneous qualitative and quantitative analyses of the product and by-products of transesterification between phenol and DMC.

Description: A novel HPLC method was developed and validated for simultaneous determination of potassium guaiacolsulfonate and sodium benzoate in pediatric oral powder. In this method, an analytical C8 column maintained at 25°C was used for chromatographic separation with a mixture of methanol and 0.02 M solution of tetrabutylammonium sulfate as the mobile phase. The composition of mobile phase was varied using a gradient program including an initial hold time of 7 minutes with methanol content maintained at 20% (v/v), followed by a linear gradient in 5.5 minutes in which methanol content was increased from 20% (v/v) to 50% (v/v) and a final hold time of 2.5 minutes with methanol content maintained at 20% (v/v). The total flow rate of mobile phase was maintained at 1.0 mL per minute. The UV detection was performed at 280 nm. Injection volume was set at 20 µl. The method was fully validated in terms of specificity, linearity, precision, accuracy, and robustness according to requirements of current guidelines and was proved as reliable and suitable for the intended application.

Description: The aim of this study was to develop an ultraperformance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method to assess the concentration of jervine in rat plasma and its pharmacokinetics. Diazepam was used as internal standard (IS). The chromatographic separation of jervine and IS was carried out on an UPLC BEH C18 column (2.1 mm × 50 mm, 1.7 μm) with a flow rate of 0.4 mL/min. A mixture of acetonitrile and water (0.1% formic acid) was used as a mobile phase. The UPLC-MS/MS was equipped with an electrospray ionization (ESI), adopting multiple reactive monitoring mode to determine jervine in rat plasma. The retention times of jervine and the internal standard were 1.71 and 2.13 min, respectively. The calibration curve of jervine ranged between 1 and 1000 ng/mL. The lower limit of quantitation (LLOQ) was 1 ng/mL, and the lower limit of determination (LLOD) was 0.2 ng/mL. The accuracy was ±6%; the interday precision and intraday precision were no more than 9%. The recovery was higher than 90.3%, and the matrix effect was lower than 10%. The UPLC-MS/MS method was successfully developed and used for the application of the pharmacokinetic study. The primary pharmacokinetic parameters of jervine in this study were as follows: the AUC(0–∞) was 969.3 ± 277.7 ng/mL·h, the Cmax was 506.6 ± 192.8 ng/mL, the CL/F was 1.7 ± 0.5 L/h/kg, and the t1/2 was 3.4 ± 1.2 h.

Description: The development of a reliable electrochemical sensor using a hybrid nanocomposite consisting of ionic liquid (1-butyl-3-methylimidazolium hexafluorophosphate) functionalized graphene oxide (GrO-IL) and gold nanoparticles (AuNPs) stabilized by chitosan (Chit) was described. The new sensor, labelled as GrO-IL-AuNPs-Chit/CSE, exhibited an improved electrocatalytic response to cancer drugs such as purine antimetabolites (6-thioguanine, 6-mercaptopurine, and azathioprine) in a wide concentration range with a low detection limit (20–40 nmol·L−1, S/N = 3), and satisfactory recoveries (97.1–103.0%). The sensor has been also successfully used for cyclic voltammetric study of a salmon sperm double-stranded DNA degradation and DNA-6-mercaptopurine interaction in aqueous solutions (pH 7.4).

Description: The aim of this study was to estimate the influence of different chromatographic conditions on the limits of detection and limits of quantitation (LODs and LOQs) of spironolactone by means of TLC-densitometry under different chromatographic conditions. A comparison of results obtained showed that the choice of appropriate chromatographic conditions for NP-TLC and RP-TLC analysis with densitometry could effectively decrease the LODs and LOQs of spironolactone. Of all chromatographic systems tested, the best was the one comprising chromatographic plates precoated with a mixture of silica gel 60, kieselguhr F254, and mobile phase A (n-hexane-ethyl acetate-glacial acetic acid, 24.5 : 24.5 : 1, v/v/v). The estimated average LOD and LOQ values were 0.034 and 0.103 μg/spot, respectively. This indicates that the described procedure is sufficiently sensitive for the identification and quantification of spironolactone alone. Thereby, the simple and cost-effective TLC-densitometric method can be utilized for the routine quality control of spironolactone in bulk drugs as well as in simple pharmaceutical formulations.

Description: Plicosepalus is an important genus of the Loranthaceae family, and it is a semiparasitic plant grown in Saudi Arabia, traditionally used as a cure for diabetes and cancer in human and for increasing lactation in cattle. A flavonoid quercetin (P1), (-)-catechin (P2), and a flavane gallate 2S,3R-3,3′,4′,5,7-pentahydroxyflavane-5-O-gallate (P3) were isolated from the methanol extract of the aerial parts of P. curviflorus (PCME). The PCME and the isolated compounds were subjected to pharmacological assays to estimate peroxisome proliferator-activated receptors PPARα and PPARγ agonistic, anti-inflammatory, cytotoxic, and antimicrobial activities. Results proved for the first time the dual PPAR activation effect of the PCME and catechin (P2), in addition to the promising anti-inflammatory activity of the flavonoid quercetin (P1). Interestingly, both PCME and isolated compounds showed potent antioxidant activities while no antimicrobial effect against certain microbial strains had been reported from the extract and the isolated compounds. Based on the pharmacological importance of these compounds, an HPTLC validated method was developed for the simultaneous estimation of these compounds in PCME. It was found to furnish a compact and sharp band of compounds P1, P2, and P3 at Rf = 0.34, 0.47, and 0.65, respectively, using dichloromethane, methanol, and formic acid (90 : 9.5 : 0.5, (v/v/v)) as the mobile phase. Compounds P1, P2, and P3 were found to be 11.06, 10.9, 6.96 μg/mg, respectively, in PCME. The proposed HPTLC method offers a sensitive, precise, and specific analytical tool for the quantification of quercetin, catechin, and flavane gallates in P. curviflorus.

Description: The quality of strawberry powder depends on the freshness of the fruit that produces the powder. Therefore, identifying whether the strawberry powder is made from freshly available, short-term stored, or long-term stored strawberries is important to provide consumers with quality-assured strawberry powder. Nevertheless, such identification is difficult by naked eyes, as the powder colours are very close. In this work, based on the measurement of near-infrared (NIR) spectroscopy and mid-infrared (MIR) spectra of strawberry powered, good classification results of 100.00% correct rates to distinguish whether the strawberry powder was made from freshly available or stored fruit was obtained. Furthermore, partial least squares regression and least squares support vector machines (LS-SVM) models were established based on NIR, MIR, and combination of NIR and MIR data with full variables or optimal variables of strawberry powder to predict the storage days of strawberries that produced the powder. Optimal variables were selected by successive projections algorithm (SPA), uninformation variable elimination, and competitive adaptive reweighted sampling, respectively. The best model was determined as the SPA-LS-SVM model based on MIR spectra, which had the residual prediction deviation (RPD) value of 11.198 and the absolute difference between root-mean-square error of calibration and prediction (AB_RMSE) value of 0.505. The results of this work confirmed the feasibility of using NIR and MIR spectroscopic techniques for rapid identification of strawberry powder made from freshly available and stored strawberry.

Description: Coking coal was extracted with tetrahydrofuran solvent using ultrasonic and microwave-assisted method at 50°C and atmospheric pressure. Wettability of raw coal and its residue (residual coal) was tested with capillary penetration method. The raw and residual coals were studied by Fourier transform infrared spectroscopy (FTIR) with curve-fitting analysis. The variation of main surface functional groups of coking coal before and after extraction and its effect on wettability were analyzed. The results were obtained as the following: after extraction with tetrahydrofuran, hydroxyl, ether oxygen, and carbonyl in the coal structure were dissolved, the content of hydrophilic functional groups reduced, and then the hydrophobicity of coal enhanced. At the same time, part of aliphatic hydrocarbon dissolved, the length of aliphatic chains () decreased from 3.961 of raw coal to 3.636 of residual coal, the length of aliphatic chains became shorter, aliphatic CH2 side-chains decreased and aliphatic CH3 side-chains increased, and hydrophobic functional groups content increased. In the aromatic structure, four hydrogens per ring increased and two, three, and five hydrogens per ring decreased. Reduction of substitution functional groups and aliphatic hydrocarbon decreased with the side-chains breakage produce more active sites, which increases the degree of condensation of the aromatic ring (). The combined action of the decrease of the hydrophilic functional groups and the increase of the hydrophobic functional groups made the wettability of the coking coal become weak.

Description: Using the standard colors provided in the instructions, PackTest products can approximate and quickly estimate the chemical characteristics of liquid samples. The combination of PackTest products and deep learning was examined for its accuracy and precision in quantifying chemical oxygen demand, ammonium ion, and phosphate ion using a pseudocolor imaging method. Each PackTest product underwent reactions with standard solutions. The generated color was scanner-read. From the color image, ten grayscale images representing the intensity values of red, green, blue, cyan, magenta, yellow, key black, and , and the values of and were generated. Using the grayscale images representing the red, green, and blue intensity values, 73 other grayscale images were generated. The grayscale intensity values were used to prepare datasets for the ten and 83 (=10 + 73) images. For both datasets, chemical oxygen demand quantification was successful, resulting in values of normalized mean absolute error of less than 0.4% and coefficients of determination that were greater than 0.9996. However, the quantification of ammonium and phosphate ions commonly provided false positive results for the standard solution that contained no ammonium ion/phosphate ion. For ammonium ion, multiple regression markedly improved the accuracy using the pseudocolor method. Phosphate ion quantification was also improved by avoiding the use of an estimated value for the reference solution that contained no phosphate ion. Real details of the measurements and the perspectives were discussed.

Description: In this study, we first examined the sorption of Pd on MX-80 in Na-Ca-ClO4 solution as a function of (3–9) and ionic strength (0.1 M–4 M) and confirmed that the experimentally derived values could be fitted by a 2-site protolysis nonelectrostatic surface complexation and cation exchange (2SPNE SC/CE) model using three binary surface complexation constants previously estimated. Then, we investigated the sorption of Pd on MX-80 in Na-Ca-Cl-ClO4 solution as a function of (3–9) and molar concentration ratio (0–∞) at the ionic strength = 4 M. We found that the sorption of Pd on MX-80 in Na-Ca-Cl-ClO4 solution could be simulated only by the three binary and one ternary surface complexations (). This suggests that the contribution of other ternary surface complexations such as ≡S-OH ≡ ( = 1, 2 and 3) to Pd sorption in Na-Ca-Cl-ClO4 solution with ionic strength = 4 M was negligibly small.

Description: To ensure that the outside dose rate of waste package is below the limitation of national laws and regulations, based on the standard 200L drum, a new drum with inner shielding was proposed for intermediate-level radioactive waste (ILW) storage. For comparison, FLUKA and QAD-CGA were used to verify the shielding design of the ILW storage drums produced in INET with multiple inner shielding layers. The flux and dose were calculated and analyzed for four different cases. In QAD-CGA calculation, it was found that different buildup factors can lead to the considerably different results. A weighted algorithm was proposed to correct QAD-CGA for multilayer shielding cases. In FLUKA calculation, parameter optimization and tailored variance reduction technique (VRT) were used. Quantitative efficiency evaluation of different FLUKA settings using the FOM factor was carried out. The differences in the calculated dose rates results between the FLUKA and QAD-CGA programs are within one order of magnitude. The results of QAD-CGA are generally higher than those of FLUKA. The analysis shows that appropriate corrections in QAD-CGA can make the trend of the calculation results more consistent with the theory. In FLUKA calculation, with optimized setting and VRT adopted, the calculation efficiency can be improved more than 20 times. The results of this study provide not only suggestions for the design of the ILW storage drums but also useful references for other similar work.

Description: The most important experimental parameters of the flow potentiometric stripping analysis (PSA) with oxygen as an oxidant were investigated and optimised. A simple, homemade flow system consisting of glassy carbon tubes, which served as a working and auxiliary electrode, was used. By applying a rest period before the stripping step (the flow stop mode) and by imposing a constant reductive current simultaneously with the interruption of potentiostatic control, significant increase of the flow PSA sensitivity was achieved. In the determination of cadmium and lead, quantitation limits of 0.11 and 0.82 μg/L were obtained. The precision of the method was evaluated in terms of repeatability and reproducibility, with values of relative standard deviation lower than 4.0% for cadmium and 4.2% for lead. This modified technique was applied for simultaneous determination of cadmium and lead in milk, after a simple pretreatment of the samples by dilution and acidification. The method accuracy was confirmed by analysing the certified reference material of skimmed milk powder (ERM-BD151).

Description: Combination therapy is opted as a potential therapeutic strategy for cancer treatment. Astragalus membranaceus combined with pemetrexed disodium or gemcitabine could reinforce the overall effects and alleviate the adverse effects. To investigate the effects of Astragalus membranaceus on the pharmacokinetics of pemetrexed disodium and gemcitabine, a HPLC method for simultaneous determination of pemetrexed disodium and gemcitabine in rat plasma was developed and validated. Chromatographic separation was achieved on a C18 column using a gradient mode containing water (containing 20 mM NaH2PO4 and 0.1% FA) and methanol at a flow rate of 0.8 mL/min. The specificity, linearity, recovery, stability, precision, and accuracy of the HPLC method were all validated. The rats were pretreated with Astragalus extract at the dosage of 3 g/kg for 20 consecutive days until we commence studying the pharmacokinetics of pemetrexed disodium or gemcitabine. There were no significant differences in pharmacokinetic parameters of pemetrexed disodium between the Astragalus extract treatment group and the control group. However, AUC, MRT, and Cl of gemcitabine were changed dramatically after treating with Astragalus extract (). The AUC(0−t), AUC(0−∞), and MRT of gemcitabine decreased from 15747.12 ± 497.11 to 12312.41 ± 594.21 mg/L·min, 15976.18 ± 511.33 to 12489.59 ± 682.01 mg/L·min, and 97.83 ± 5.82 to 84.37 ± 2.79 min, respectively. The Cl of gemcitabine increased from 0.019 ± 0.0067 to 0.024 ± 0.0013 L/min/kg. The results showed that the pretreatment of Astragalus extract could exert an influence on the pharmacokinetic characteristics of gemcitabine in rats.

Description: The effects of six ionic liquids with surfactant property (1-hydroxyethyl-3-methyl imidazolium bis(trifluoromethylsulfonyl)imide ([HOEtMIm][NTf2]), 1-hydroxyethyl-3-methyl imidazolium tetrafluoroborate ([HOEtMIm][BF4]), 1-dodecyl-3- methyl imidazolium bromide ([C12MIm]Br), 1-tetradecyl-3- methyl imidazolium bromide ([C14MIm]Br), trioctyl methyl ammonium chloride ([N8,8,8,1])Cl, and tetraethyl ammonium chloride ([N2,2,2,2]Cl)) on the oxidation characteristics and functional groups of coal were studied by means of critical micelle concentration, surface tension, thermogravimetric analysis, temperature-programmed oxidation, and Fourier transform infrared spectroscopy (FTIR) measurements. The lower critical micelle concentration for the ionic liquids except the [N2,2,2,2]Cl suggests the favorable surface activity of these ionic liquids. The surface activities of [N8,8,8,1]Cl, [C14MIm]Br, [C12MIm]Br, and [HOEtMIm][NTf2] were high, while that of [N2,2,2,2]Cl was relatively lower. The thermal stabilities of [HOEtMIm][NTf2] and [HOEtMIm][BF4] were high, while those of [N8,8,8,1]Cl and [N2,2,2,2]Cl were lower. The oxidation activities of ionic liquid-mixed coals were weakened to different degrees except [N8,8,8,1]Cl-mixed coal, because of the poor thermal stability and decomposition of [N8,8,8,1]Cl accelerating the coal oxidation. The other five ionic liquids were suitable for inhibiting coal oxidation, particularly the [HOEtMIm][BF4] and [HOEtMIm][NTf2] with higher inhibition rate, longer inhibition time, and also better thermal stabilities. The activation energy results further confirmed such inhibition effect. The functional group results showed that treatment of ionic liquids on coal can change the contents of hydrogen bonds, aliphatic groups, and aromatic groups in coal. It was inferred that the [HOEtMIm][BF4], [HOEtMIm][NTf2], and [C14MIm]Br were more effectively to affect coal structure and decrease coal oxidation activity.

Description: Reactor pressure vessel (RPV) support is a key safety facility which is categorized as Class 1 in the ASME nuclear safety design. The temperature distribution of RPV support is one of the key considerations for the concrete safety contacting with the bottom of the support. So it is necessary for accurate evaluation on the temperature field characteristics of RPV support, especially the bottom of support. This paper investigates the temperature field characteristics of modified RPV support which will be applied to a large advanced pressurized water reactor. A support entity is manufactured in a ratio of 1:1, and its temperature distribution is measured under simulated reactor operating conditions. Numerical simulation is also used to validate the results by the developed CFD model. The results show that under the operating conditions, of which the inlet cooling air temperature is 35.35°C and the velocity is 6.25 m/s, the temperature distribution of modified RPV support bottom is uneven, and the highest temperature is around 38°C, which is much lower than the demanding design temperature 93.3°C. Therefore, the design of the modified RPV support is reliable. In addition, the results of numerical simulation agree well with the experimental results with the error less than ±4°C, which ensures the reliability of the conclusion. The effects of inlet cooling air temperature and velocity on the RPV support temperature distribution are further studied. Both the temperature decrease and velocity increase can reduce the RPV support temperature. But the effect of inlet cooling air temperature is more obvious than inlet cooling air velocity. So the best way to improve air cooling capacity is to decrease the support inlet cooling air temperature. The results can provide a good guidance to the design of RPV support for the subsequent large advanced pressurized water reactor.

Description: Dendranthema indicum var. aromaticum is a new species with strong fragrance and is used as a herbal medicine by Chinese folks. The abundant flavonoids play important roles in its pharmacological activities. In this study, an ultrasound-assisted method was used to extract total flavonoids (TF) from D. indicum var. aromaticum by response surface methodology. A quadratic model was developed to optimize the extraction conditions, whose accuracy was verified by statistic analysis. Ethanol and acetic acid at the volume ratio of 70% : 2% were selected as the extract solvent. The optimized extraction conditions were as follows: extraction time, 40 min; solid/liquid ratio, 1 : 23 g/mL; and temperature, 60°C. This is the first report of an efficient and easy-operating method for TF extraction from D. indicum var. aromaticum. Besides, this study provides reference for future pharmacological research on D. indicum var. aromaticum and extraction of bioactive components from other herbs.

Description: For most of the remote maintenance activities of equipment in a hot cell, replacing breakdown modules is preferred over in situ repair because of insufficient space in the cell and the limited operability of remote handling tools. In such cases, the maintenance operation can be decomposed into transport of the new modules to the failed equipment, replacement of the broken modules with new ones, and then transport of the broken parts to the reserved space for further repair or disposal. In this respect, transfer is the most basic operation during remote maintenance, which is also true for the maintenance of pyroprocessing equipment. Hence, this paper proposes a maintenance automation framework for automated pyroprocessing equipment from the standpoint of module transfer. For the maintenance automation framework, maintenance-related functions and events are defined, and they are integrated with the pyroprocess automation framework. The proposed framework is verified by a case study on the maintenance of a large module through a hardware-in-the-loop simulation.

Description: Sample pretreatment is important for chemical phase analysis of elements. In this study, the geological samples of the Laozuoshan gold mine are chosen to pretreat by ultrasonic centrifugation and cyclotron oscillation, and the content of gold in eight chemical phases (water-soluble, ion exchange and clay adsorption, organic matter bound, iron-manganese oxide bound, naked or seminaked, carbonate bound, sulfide bound, and insoluble silicate states) is determined by atomic absorption spectrometry. The results show that the gold content of water-soluble, ion exchange and clay adsorption, iron-manganese oxide, and naked or seminaked states in the rock and ore samples is low, and some samples have high gold content of insoluble silicate states in the two methods. However, the gold content of organic matter bound, carbonate bound, and sulfide bound states obtained by ultrasonic centrifugation and cyclotron oscillation methods is significantly different. According to the X-ray fluorescence spectrometry data and the actual geological condition, the result given by the cyclotron oscillation method is more reasonable. The gold content of sulfide bound state in sediment samples is the highest and consistent with the mineral information, which could be applied to preliminarily predict the rock and ore conditions in the corresponding mining areas. In contrast with ultrasonic centrifugation, the cyclotron oscillation method has the advantages of simplicity, high efficiency, practicality, and environmental protection, and it can be better used for the determination of gold chemical phase state in geological samples by atomic absorption spectrometry.

Description: A simple, rapid, and reliable method based on dispersive solid-phase extraction (d-SPE) and gas chromatography-mass spectrometry (GC-MS) was developed for quantitating polychlorinated biphenyls (PCBs) in vegetable samples. Parameters affecting both the extraction yields and cleanup efficiency, including the type and volume of extraction solvent, extraction time, type and volume of cleanup sorbent, and cleanup time, were optimized. Matrix effects were evaluated, and matrix-matched calibration was recommended. Under the optimized conditions, carboxylated multiwalled carbon nanotubes (MWCNTs-COOH), which exhibit excellent adsorption capabilities due to large surface area and unique structure, were employed as d-SPE sorbent to remove interfering substances, rather than the analytes, from vegetable samples. Satisfactory linear relationship was observed for all PCBs across a concentration range of 5–500 μg/kg with correlation coefficients no less than 0.9993. Four representative vegetables (cucumber, tomato, lettuce, and cabbage) were selected as matrices for method validation. Each matrix was spiked at concentrations of 5, 10, and 100 μg/kg to evaluate recoveries, which ranged from 84.5% to 116.5% with relative standard deviations () between 0.6% and 17.6%. The limits of detection and the limits of quantification ranged from 0.3 to 1.4 μg/kg and 0.8 to 4.5 μg/kg, respectively. Twelve real vegetable samples were analyzed using the proposed method. Three of the target PCBs were detected in one lettuce sample with the total concentration of 17.9 μg/kg.

Description: Nata de coco, a bacterial cellulose as a result of coconut water fermentation, is a conductive polymer with a electrical conductivity of 553 μS/cm and has high mechanical stability. In this study, nata de coco was used as a supporting membrane for the development of phenol sensors in potentiometry. Nata de coco membrane containing phenol is coated on the surface of the printed carbon electrode (screen-printed carbon electrode). The cross-sectional area of the carbon electrode coated with the membrane is 1.5 × 3 mm2, while the reference electrode is Ag/AgCl. The thickness of the electrode membrane affects the Nernstian factor. The optimum Nernstian factor is produced by 100 μm membrane thickness containing 117.5 μg of phenol. Measurement of phenol solution was carried out at pH 11, in the concentration range of 10−8 to 10−2 mol/L, resulting in a Nernstian factor of 41.8 ± 1.3 mV/decade. The Nernstian factor increased to 55.7 ± 0.4 mV/decade if the membrane of the electrode contained 0.1% Fe3O4 nanoparticles. This sensor has been applied in the real sample of river water, resulting in good accuracy and precision.

Description: Rhizoma Alismatis (RA), widely known as “Ze-Xie” in China, is the tuber of Alisma orientale (Sam.) Juzep (Alismaceae), a Chinese herbal medicine that has been used to treat hyperlipidemia, diabetes, hypertension, dysuria, and inflammation. In this study, a sensitive and reliable method based on an ultra-performance liquid chromatography (UPLC) couple with two ionisation modes, including electrospray ionisation (ESI) and atmospheric pressure chemical ionisation (APCI) tandem mass spectrometry (MS), namely, UPLC-ESI/APCI-MS/MS was developed and validated to simultaneously determine 8 triterpenoids (ESI mode) and 2 sesquiterpenoids (APCI mode) in RA. Ten marker compounds were analysed with a Waters’ CORTECS UPLC C18 column (200 mm × 2.1 m, 1.6 μm) and gradient elution with water (contained 0.1% formic) and acetonitrile within 7 min. The established method was validated for linearity, intra- and interday precisions, accuracy, recovery, and stability. The calibration curve for 10 marker compounds showed good linear regression (r 〉 0.9971). The limits of detection and quantification for analytes were 0.14–1.67 ng/mL and 0.44–5.65 ng/mL, respectively. The relative standard deviations (RSD, %) and accuracy (RE, %) of intra- and interday precisions were less than 3.83% and 1.21% and 3.22% and 1.46%, repeatability and stability for real samples were less than 2.78% and 3.19%, respectively. All recoveries of the 10 marker compounds ranged from 97.24% to 102.49% with RSDs less than 4.05%. The developed method efficiently determined the 10 marker compounds in RA and was subsequently applied to optimise harvest time and crude processing temperature. The result indicated the 90% wilted phase and 70°C (or lower) may be the best harvest time and the processing temperature of RA.

Description: The feasibility of combining elemental fingerprints and chemical pattern recognition methods for authentication of the geographical origins of a Chinese herb, Gastrodia elata BI. (GE), was studied in this paper. A total of 210 GE samples were collected from 7 different producing areas. The levels of 15 mineral elements in GE, including Zn, Cd, Co, Cr, Cu, Ca, Mg, Mn, Mo, Ni, Pb, Sr, Fe, Na, and K, were determined using inductively coupled plasma mass spectrometry (ICP-MS). Using the autoscaled data of elemental fingerprints and partial least-squares discriminant analysis (PLSDA), two chemometrics strategies for multiclass classifications, One-Versus-Rest (OVR) and One-Versus-One (OVO), were studied and compared in discrimination of GE geographical origins. As a result, OVR-PLSDA and OVO-PLSDA could achieve the classification accuracy of 0.672 and 0.925, respectively. The results indicate that mineral elemental fingerprints coupled with chemometrics can provide a useful alternative method for simultaneous discrimination of multiple GE geographical origins.

Description: The stability of W against U, rare-earth (RE) elements, Cd, and various chlorides was evaluated by melting and distillation testing. Three runs were performed with a W crucible to examine its reactivity: (i) RE melting by induction heating, (ii) salt distillation test of U-dendrite and various chlorides, and (iii) Cd distillation test from U–Cd alloy. The W crucible remained stable after the RE melting test using induction melting, exhibiting its applicability for induction heating systems. The salt distillation test with the W crucible at 1050°C exhibited the stability of W against U and various chlorides, showing no interaction. The Cd distillation test with the W crucible at 500°C showed that the crucible was very stable against Cd, maintaining a shiny surface. These results reveal that the W crucible is stable under operation conditions for both salt and Cd distillation, suggesting the high potential utility of W as a crucible material for application in cathode processes in pyroprocessing.

Description: A novel method was developed for the simultaneous determination of Pb(II), Cd(II), and Zn(II) based on the cathodic stripping response at a bismuth film electrode associated with oxine as a chelating agent. The developed method provided a high and sharp electrochemical response compared with the method without oxine. A linear response of peak currents was observed for Pb(II), Cd(II), and Zn(II) concentration in the range from 2 ppb to 110 ppb. The detection limits of Pb(II), Cd(II), and Zn(II) were 0.45, 0.17, and 0.78 ppb, respectively. This method was successfully applied to the determination of Pb(II), Cd(II), and Zn(II) in lake-water and river-water samples. The metals were detected at the ultratrace level, showing the feasibility of the proposed method for environmental applications.

Description: The Critical Heat Flux (CHF) prediction under high pressure condition, even close to the vicinity of the critical pressure of water, is an important issue. Although there are many empirical CHF correlations, most of them have covered the pressure under 15MPa. In this study, based on the CHF experiment database of upflow boiling in vertical round tube from 15MPa to the vicinity of the critical pressure of water, the Katto, Bowring, Hall-Mudawar, Alekseev correlations, and Groeneveld LUT-2006 are comparatively studied. With an error analysis of the predicted CHF to the experiment database, the prediction capability and the applicability of these correlations are evaluated and the parametric trends of CHF varying with pressure from 15MPa to critical pressure are proposed. Simultaneously, according to the characteristics of Departure from Nucleate Boiling (DNB) type CHF under high pressure condition, the constitutive correlations of Weisman & Pei model are proposed. The prediction results of three entrainment and deposition correlations of Kataoka, Celata, and Hewitt corresponding to the Dry-Out (DO) type CHF are analyzed. Based on the two improved models above, a comprehensive CHF mechanistic model under high pressure condition combining the DNB and DO type CHF is established. The verification based on the experiment database of upflow boiling in vertical round tube and the parametric trends analysis of CHF varying with thermal-hydraulic and geometric parameters are carried out. Findings of this study have a positive effect on further development of CHF prediction method for universal CHF mechanism, especially under high pressure region.

Description: In this work, SiO2 nanoparticles were prepared by the sol-gel method after sodium silicate was extracted from rice husk ash (RHA) under various experimental conditions such as types of acids, NaOH concentration, dissolved time, and temperature and used for removal of Fe2+ ions from aqueous solutions. The extracted SiO2 was morphologically and chemically characterized and showed a surface area of 78 m2/g and uniform pores of 2.71 nm, offering high adsorption capacity for Fe2+ ions. The influence of pH, contact time, and amount of adsorbent was studied in order to establish the best conditions for the Fe2+ adsorption and removal. Furthermore, the adsorption data were fitted with an exponential shape curve for all the three variable parameters that affect the adsorption process. The best results were obtained for pH 5, 20 min contact time, and 0.5 g adsorbent dose. The loading adsorption capacity was 9 mg of Fe2+ ions/g SiO2 in the concentration range 0.1–1.0 mgL−1. In addition, the synthesized SiO2 with the size of around 50 nm can be used for specific heavy metal removal and drug delivery, after modification of the SiO2 surface with various functional groups.

Description: The pepper tree Schinus molle L. is an evergreen ornamental plant belonging to the Anacardiaceae family, native to South America and widespread throughout the world. It has biological activities and is used in folk medicine. This paper aims to contribute to a deeper knowledge of its chemical composition and biological properties. S. molle leaf extracts were obtained by sequential extraction with solvents of different polarities and subsequently tested on the HL-60 human leukaemia cell line to define a possible cytotoxic activity. Among the investigated extracts, the petroleum ether extract revealed a high cytotoxic activity, and its chemical composition was further investigated. By a silica column chromatography, eight fractions were obtained, and their compositions were determined by GC-MS analysis. Compounds and relative abundance differed widely among the fractions; sesquiterpenes resulted the main component and alcoholic sesquiterpenes the most abundant.

Description: Folic acid (FA) is an important vitamin for human growth, especially for pregnant women. FA deficiency is associated with megaloblastic anemia, neural tube defects, cardiovascular diseases, irritability, diarrhea, and psychiatric disorders. Normally, FA molecules bind to folate-binding protein (FBP) in the serum as complex. Before quantify the FA concentration, a releasing procedure should be conducted. Alkaline condition and tris(2-carboxyethyl)phosphine (TCEP) are used to release binding FA to freeing state. In this work, a chemiluminescence immunoassay (CLIA) for human serum FA was established by competition model. Streptavidin (SA) was labeled to magnetic beads by an 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide/N-hydroxysuccinimide (EDAC/NHS) method. Activated biotin molecules were labeled to FBP molecules purified from milk. FA was labeled to horseradish peroxidase (HRP) by EDAC to activate the FA molecules. The pretreated samples or standards were added into the reaction tube with biotin-FBP and FA-horseradish peroxidase (HRP), FA in the sample compete with FA-HRP for binding to biotin-FBP, the signal is inversely proportional to the FA concentration. The method established shows good thermostability and performance. The limitation of detection (LOD) is 0.44 ng/mL. The intra-assay coefficient of variation (CV) is 3.6%–7.1%, the interassay CV is 4.2%–7.5%, and the recovery rate is 92.1%–103.5%. Cross reactivity (CR) was remarkably low with aminopterin, folinic acid, and methotrexate. The method shows good correlation with the FA CLIA product from Beckman Coulter; the equation is y = 0.9618x−0.1434 while the R2 value is 0.9224. The established method is sensitive, rapid, and accurate which can fully satisfy for the clinical requirement.

Description: Because a pool scrubbing is important for reducing radioactive aerosols to the environment for a nuclear reactor in a severe accident situation, many researches have been performed. However, decontamination factor (DF) dependence on aerosol concentration was seldom considered in an aerosol number concentration with limited aerosol coagulation. To investigate an existence of DF dependence on the concentration, DF in a pool scrubbing with 2.4 m water submergence was derived from aerosol measurements by light scattering aerosol spectrometers. It was observed that DF increased monotonically with decreasing particle number concentration in a constant thermohydraulic condition: a gradual increase from 10 to 32 in the range of 1.3×1011 - 8.0×1011/m3 at the inlet and a significant increase from 32 to 77 in the range of 3.6×1010 - 1.3×1011/m3. Two validation experiments were conducted in the range with the gradual DF increase to confirm whether the DF dependence is a real pool scrubbing phenomenon. In addition, characteristics of the DF dependence in different water submergences were investigated experimentally. It was found that the DF dependence became more significant in higher water submergence. Significant DF dependence was observed in the condition of the water submergence higher than 1.6 m and the inlet particle number concentration less than around 1×1011 /m3. It is recommended to perform further analysis for the DF dependence mainly in such condition since it could make a difference to both experiment and model of the pool scrubbing.

Description: The present work reports the distribution of pollutants in the Madrid city and province from 22 monitoring stations during 2010 to 2017. Statistical tools were used to interpret and model air pollution data. The data include the annual average concentrations of nitrogen oxides, ozone, and particulate matter (PM10), collected in Madrid and its suburbs, which is one of the largest metropolitan places in Europe, and its air quality has not been studied sufficiently. A mapping of the distribution of these pollutants was done, in order to reveal the relationship between them and also with the demography of the region. The multivariate analysis employing correlation analysis, principal component analysis (PCA), and cluster analysis (CA) resulted in establishing a correlation between different pollutants. The results obtained allowed classification of different monitoring stations on the basis of each of the four pollutants, revealing information about their sources and mechanisms, visualizing their spatial distribution, and monitoring their levels according to the average annual limits established in the legislation. The elaboration of contour maps by the geostatistical method, ordinary kriging, also supported the interpretation derived from the multivariate analysis demonstrating the levels of NO2 exceeding the annual limit in the centre, south, and east of the Madrid province.

Description: A free-of-dust pollution extraction method combined-homogenate and ultrasonic cavitation system, namely, homogenate-combined ultrasonic cavitation synergistic extraction (HUCSE), was proposed for the efficient extraction of flavonoids from Cinnamomum camphora leaves. Response surface methodology of Box–Behnken design was employed to optimize the HUCSE process, and the optimum operation conditions attained with an extraction yield of 7.95 ± 0.27 mg/g were ethanol concentration 76%, homogenate/ultrasonic time 25 min, solvent-to-solid ratio 22 mL/g, and ultrasonic power 240 W. A second-order kinetic mathematical methodology was performed to depict the behaviors of HUCSE and heat reflux extraction method. The results suggested that the developed HUCSE is an efficient and green method for the extraction of C. camphora flavonoids or other plant natural products, where the obvious higher parameters of extraction capacity at saturation, second-order extraction rate constant, and original extraction rate were obtained when compared to the heat reflux method. The antioxidant activity assays in vitro showed that the C. camphora flavonoids possessed strong antioxidant activity and are promising to be applied as a natural alternative antioxidant.

Description: Patulin (PAT) is a highly genotoxic mycotoxin still found as the common contaminant of various kinds of spoiled fruits and related commodities which are often endorsed as the health-enhancing products. Thus, a fast and convenient liquid-solid extraction followed by a solid-phase cleanup with the MycoSep®228 AflaPat multifunctional column was used for the highly efficient isolation of PAT with an average recovery of 112.7% from commercial dietary supplements and herbal blends formulated with dried hawberry. Analysis of the PAT content was carried out using gradient elution with a Synergi Polar C18 column (150 × 2 mm, 4 μm) and UHPLC system equipped with a mass spectrometer. PAT was detected in all () commercial single-component dietary supplements formulated with dried hawberry belonging to Crataegus monogyna and/or Crataegus laevigata. Similarly, PAT was detected in 67% of the studied multicomponent commercial herbal blends () that contained—in addition to hawberry—different amounts of apple, chokeberry, elderberry, hibiscus, or mallow. Moreover, the PAT content was determined in the hawberry collected from the mature wild hawthorn trees belonging to three botanical species, Crataegus monogyna Jacq., Crataegus laevigata (Poiret) DC, and Crataegus rhipidophylla Gand, growing in the recreational forest areas and in the law-protected state national forest park in Poland. In conclusion, to prevent PAT accumulation and reduce the health risk of consumers in globalizing markets, the implementation of improved cultivation/processing practices of hawthorn trees and hawberry as well as increased analytical control related to the presence of PAT in dietary supplements and herbal blends formulated with fresh, dried, or frozen hawberry should be urgently recommended.

Description: UV-Vis absorption spectra of tannic acid were gained at pH 1.0∼9.0. Due to the pH value dependence of complex, the stoichiometry of tannic acid with iron ions was tested in buffer solution by the mole ratio method. The result suggests that the complex ratio of tannic acid to Fe(III) is 1 : 1 and to Fe(II) 3 : 1 in the carbonate buffer solution, and the complex ratio of iron-tannic complexes is 1 : 1 at pH 2.2. Due to the different color changes of tannic acid with iron ions in the coordination reactions, a tannic acid test paper was designed. The concentrations of Fe(III) more than 5.000 × 10−6 mol/L and the concentrations of Fe(II) more than 1.000 × 10−5 mol/L in aqueous solution can be detected by this test paper.

Description: For the proposed novel procedure of immobilizing HLW with magnesium potassium phosphate cement (MKPC), Fe2O3 was added as a modifying agent to verify its effect on the solidification form and the immobilization of the radioactive nuclide. The results show that Fe2O3 is inert during the hydration reaction. It slows down the hydration reaction and lowers the heat release rate of the MKPC system, leading to a 3°C-5°C drop in the mixture temperature during hydration. Early comprehensive strength of Fe2O3 containing samples decreased slightly while the long-term strength remained unchanged. For the sintering process, Fe2O3 played a positive role, lowering the melting point and aiding the formation of ceramic structure. CsFe(PO4)2, or CsFePO4, was generated by sintering at 900°C. These products together with the ceramic structure and absorption benefit the immobilization of Cs+. The optimal sintering temperature for heat treatment is 900°C; it makes the solidification form a fired ceramic-like structure.

Description: A competitive fluorescence immunoassay for the identification and quantification of morphine has been developed on the basis of hapten-coated plate format. Hapten was prepared through covalent conjugating a morphine derivative with albumin bovine. In the immunoassay, the hapten was inoculated on a 96-well plate and then bound with monoclonal antibodies labeled with a signal indicating dye, fluorescein isothiocyanate (FITC). Unbound FITC-antibodies were rinsed off from the plate. The fluorescein intensity decreases in the presence of morphine molecules due to the competitively binding to antibodies against hapten. The intensity is inversely correlated with the concentration of morphine. In quantitative analysis for urine samples, we obtained a linearity range of 0.2 μg/mL∼2.5 μg/mL, along with a detection limit of c.a. 1 ng/mL. The fluorescence immunoassay shows low cross-reactivity (below 10%) to 6-acetylmorphine, 3-acetylmorphine, and heroine. The developed method produced comparable results to the standard GC-MS/MS method. In conclusion, a rapid and efficient screening tool for morphine in clinical human urine has been established.

Description: The theory of using dilute organic acid solutions to leach the carbonaceous part from low-grade carbonaceous phosphate ore has been proposed by researchers as an effective approach to increase the proportion of P and to utilize the abundant low-grade resource. In this paper, a comprehensive experimental study was carried out to confirm the feasibility of organic acid leaching and investigate the optimized leaching conditions. Utilizing the low-grade carbonaceous phosphate ore produced in Zhijin, southwest of China, the effects of different types of acid, acid concentrations, reaction temperatures, reaction times, and liquid-solid ratios on leaching rate of P2O5 were evaluated using single-factor experiments and orthogonal experiments. The reaction mechanism, examined by SEM technique and the reaction thermodynamic analysis suggested that the leaching of P2O5 mainly resulted from the process of dissolution of dolomite (the main gangue mineral) in organic acid, consequently enriching the phosphate rock (the mineral of value). The effectiveness and impacts of different types of acid and reaction conditions were also studied. To conclude, this study first confirmed the viability of enriching P2O5 from low-grade ores through organic acid leaching the carbonaceous part by experimental data, and the experimental results will provide an essential scientific support for further upgrade of the technology to commercial scale utilization.

Description: Evaluation of aerosol deposition in the containment vessel is an important step for the assessment of radioactive material release to the environment. ART Mod 2 is a calculation code that is used for evaluation of aerosol deposition in the containment vessel. The authors modified aerosol deposition models of ART Mod 2, namely, gravitational settling model, Brownian diffusion model, diffusiophoresis model, and thermophoresis model in order to increase potential of capturing the deposition phenomena. This study aims to compare the simulated results of modified ART Mod 2 with aerosol deposition of cesium compounds in the containment vessel of Phébus FPT3 experiment, in order to validate modified ART Mod 2 code. It is found that aerosol deposition using modified ART Mod 2 agrees with Phébus FPT3. Prediction of Brownian diffusion is significantly improved due to the consideration of turbulent damping process. Cesium mass flow rate and aerosol size are factors that can significantly influence the uncertainty of the results. When conditions of single volumes are carefully selected to match those of the Phébus FPT3 experiment, modified ART Mod 2 can predict aerosol deposition in Phébus FPT3 with relative accuracy.

Description: A rapid and sensitive quantitative analytical method was established for the simultaneous determination of five chromones (prim-O-glucosylcimifugin, cimifugin, 4′-O-β-D-glucosyl-5-O-methylvisamminol, 5-O-methylvisammiol, and sec-o-glucosylhamaudol) in the plasma of RS-treated rats for the first time using ultra performance liquid chromatography- (UPLC-) tandem mass spectrometry. The Waters Acquity UPLC BEH C18 (50 mm × 2.1 mm, 1.7 μm) was used as the chromatographic column, 0.1% formic acid water and 0.1% formic acid acetonitrile comprised the mobile phases, and all samples were determined under positive ion mode. The results showed that all analytes had good linearity (), between-day and within-day precisions less than 15%, accuracy between −5.50% and 5.53%, and extraction recovery between 88.26% and 97.65%. Both the matrix effect and stability met the requirements. This method was successfully applied for the comparative pharmacokinetics of five active components of RS in normal and febrile rats. The results showed that the pharmacokinetic behavior of RS extract significantly differed between the two types of rats.

Description: Recent studies have detected different antimicrobial residues in broiler chicken feathers, where they persisted for longer periods of time and at greater concentrations than in edible tissues. However, until today, lincomycin behaviour in this nonedible tissue has not been assessed yet. Considering this, an analytical methodology to detect and quantify this antibiotic concentration in feathers, muscle, and liver tissues from broiler chickens was implemented and in-house validated. The methodology will allow the determination of the bioaccumulation of this highly persistent antibiotic in feathers of treated birds. For this purpose, 98% lincomycin and 95% lincomycin D3 standards were used. Methanol was selected as the extraction solvent, and Chromabond® Florisil® cartridges were used for the clean-up stage. The separation of analytes was performed through the analytical column SunFire C18 with a running time of 4 minutes, and the instrumental analysis was performed through an LC-MS/MS, with a liquid chromatograph Agilent® 1290 Infinity, coupled to an AB SCIEX® API 5500 mass spectrometer. An internal protocol for an in-house validation was designed based on recommendations from Commission Decision 2002/657/EC and the Guidance document on the estimation of limit of detection and limit of quantification for measurements in the field of contaminants in feed and food. The average retention time for lincomycin was 2.255 min (for quantifier ion, 126.0). The calibration curves showed a coefficient of determination (r2) greater than 0.99 for all matrices, while recovery levels ranged between 98% and 101%. The limit of detection (LOD) calculated was of 19, 22, and 10 μg·kg−1, and the limit of quantification (LOQ) was of 62, 73, and 34 μg·kg−1 in feathers, muscle, and liver, respectively. This method detects lincomycin in the studied matrices, confidently and accurately, as it is required for designing analytical studies of drug residues in edible and nonedible tissues, such as feathers.

Description: Nanosized adsorbents when used in potentiometric methods of analysis usually show better performance rather than the traditional potentiometric approach; this is attributed to the high specific surface area of the nanomaterial used in addition to the lack of internal diffusion resistance, thus improving their adsorption capacity. In the presented work, a rapid and sensitive potentiometric determination of chlorpheniramine maleate (CPM) and pseudoephedrine hydrochloride (PSE) in pure form, in pharmaceutical preparation, and in biological fluid was developed based on functionalized magnetic nanoparticles (Fe3O4). This strategy was compared with the classical potentiometric strategy. Three types of sensors were constructed using phosphotungstic acid (PTA), β-cyclodextrin (β-CD), and β-cyclodextrin-conjugated Fe3O4 magnetic nanoparticles for the potentiometric determination of each of CPM and PSE. The prepared sensors were characterized in regards to their composition, life duration, working pH range, and response time. The sensors have demonstrated promising selectivity to CPM and PSE in the presence of pharmaceutical formulation excipients, plasma matrix, and a diversity of both organic and inorganic interfering materials. The developed sensors have displayed good responses. Statistical comparison of the achieved results with a reported method has revealed no significant difference regarding both accuracy and precision.

Description: The essential oils (EO) of R. officinalis and L. dentata have been widely used due to their antioxidant activity. However, due to their high volatility, the loading of EO into polymeric nanocapsules (NC) represents an efficient way of retaining their effect in future topical administration. In this way, the quantitative determination of EO incorporated into NC is necessary for simultaneous monitoring of the main components of the EO during the nanoencapsulation process as well as for precise and exact dosing of the components used during the performance of in vitro and in vivo biological tests. In this study, EO were isolated by hydrodistillation in a Clevenger-type apparatus and characterized by GC-MS and GC-FID analyses. The major constituents of EO-R. officinalis were camphor (39.46%) and 1,8-cineole (14.63%), and for EO-L. dentata were 1,8-cineole (68.59%) and β-pinene (11.53%). A new analytical method based on GC-FID for quantification of free and encapsulated EO was developed and validated according to ICH. Linearity, limit of detection and quantification, and intra- and interday precision parameters were determined. The methods were linear and precise for the quantification of the main components of EO. The EO were encapsulated by nanoprecipitation and were analyzed by the GC-FID method validated for their direct quantification. The NC size was 200 nm with homogeneous size distribution. The quantification of the incorporated EO within a NC is an important step in NC characterization. In this way, an encapsulation efficiency of at least 59.03% and 41.15% of total EO-R. officinalis and EO-L. dentata, respectively, was obtained. Simple, repeatable, and reproducible methods were developed as an analytical tool for the simultaneous quantification of the main components of EO loaded in polymeric nanocapsules as well as their monitoring in biological assays.

Description: The management of spent nuclear fuel assemblies of nuclear reactors is a priority subject among member states of the International Atomic Energy Agency. For the majority of these countries, the destination of such fuel assemblies is a decision that is yet to be made and the “wait-and-see” policy is thus adopted by them. In this case, the irradiated fuel is stored in on-site spent fuel pools until the power plant is decommissioned or, when there is no more racking space in the pool, they are stored in intermediate storage facilities, which can be another pool or dry storage systems, until the final decision is made. The objective of this study is to propose a methodology that, using optimization algorithms, determines the ideal time for removal of the fuel assemblies from the spent fuel pool and to place them into dry casks for intermediate storage. In this scenario, the methodology allows for the optimal dimensioning of the designed spent fuel pools and the casks’ characteristics, thus reducing the final costs for purchasing new Nuclear Power Plants (NPP), as the size and safety features of the pool could be reduced and dry casks, that would be needed anyway after the decommissioning of the plant, could be purchased with optimal costs. To demonstrate the steps involved in the proposed methodology, an example is given, one which uses the Monte Carlo N-Particle code (MCNP) to calculate the shielding requirements for a simplified model of a concrete dry cask. From the given example, it is possible to see that, using real-life data, the proposed methodology can become a valuable tool to help making nuclear energy a more attractive choice costwise.

Description: Xylitol, a sugar substitute frequently used in sugar-free gum, is generally considered harmless to humans but it can be extremely toxic to dogs. Dog-owning customers are becoming increasingly aware of the risks associated with xylitol-containing chewing gums. However, there remains some uncertainty if these chewing gums are still dangerous to dogs after they have been partially consumed. In this work, a reliable low-cost analytical method has been developed to quantify the xylitol in sugar-free gum samples. Xylitol was extracted from gum samples using water as a solvent. Extractions were analyzed by GC-MS with direct aqueous injection (DAI). This method was successfully applied to over 120 samples including fresh gum and 5 min, 15 min, and 30 min chewed gum samples.

Description: Several spectrophotometric approaches utilize different functions of the iso-absorptivity coefficient in zero-order absorption signals and its manipulated spectra. This work introduced an investigation concerning the efficiency power of recent methods based on iso-absorptivity coefficient in different spectral signals. These methods were as follows: absorptivity centering method (a-Centering), absorbance subtraction method (AS), amplitude modulation method (AM,) and amplitude summation method (A-Sum). These methods were applied to determine the binary mixture of ofloxacin (OFX) and dexamethasone (DXM). Linearity of the proposed methods was investigated in the range of 1.0–10.0 μg/ml for both drugs. The proposed methods were validated as per ICH guidelines and were successfully applied for the simultaneous determination of OFX and DXM in their pharmaceutical preparation without interference from additives. Statistical analysis of the results obtained by the proposed spectrophotometric methods compared with a reported method revealed no significant difference between the proposed and reported methods, confirming accuracy and precision at 95% confidence limit.

Description: We report a detailed analysis of singlet oxygen generated from the photofunctional polymer film (PFPF) matrix which is the silicone polymer film (PDMS) embedded with a photosensitizer. Activation and deactivation dynamics of singlet oxygen generated from PFPFs were investigated with time-resolved phosphorescence spectroscopy. The singlet oxygen generated from PFPFs was dissipated into three different regions of the polymer matrix; the inside (component A), the surface (component B), and the outside (component C). According to the deactivation dynamics of singlet oxygen in the polymer matrix, the components B and C are expected to be more important for various applications.

Description: A comparative study of chemical stability of terfenadine (TER) and its in vivo metabolite fexofenadine (FEX) was performed. Both TER and FEX were subjected to high temperature at different pH and UV/VIS light at different pH and then quantitatively analyzed using new validated LC-UV methods. These methods were used to monitor the degradation processes and to determine the kinetics of degradation for both the compounds. As far as the effects of temperature and pH were concerned, FEX occurred more sensitive to degradation than TER. As far as the effects of UV/VIS light and pH were concerned, the both drugs were similarly sensitive to high doses of light. Using all stress conditions, the processes of degradation of TER and FEX followed the first-order kinetics. The results obtained for these two antihistaminic drugs could be helpful in developing their new derivatives with higher activity and stability at the same time.

Description: The objective of the experiment was to investigate the stability of the composition of selected essential oils in the model systems containing methanol and hexane solutions which were treated with ultrasound. Solutions of the oils, with a concentration of 90 mg/ml, were subjected to the effect of ultrasounds with a frequency of 20 kHz and an output power of 200 W for periods of 2 min and 10 min at 50% and 80% power. The experiment has shown no significant effect on the composition of the essential oils resulting from the applied parameters of the process in the tested model systems. The study indicates that the sonication parameters adopted in the experiment can be applied in the case of analogous systems containing essential oils in their composition.

Description: In this work, high-performance liquid chromatography in combination with inductively coupled plasma dynamic reaction cell quadrupole mass spectrometry was introduced and optimized for speciation analysis of five major arsenic species including arsenobetain (AsB), arsenite (As(III)), monomethylarsonic (MMA), dimethylarsenonic acid (DMA), and arsenate (As(V)) in rice samples. Five arsenic compounds were separated on a Hamilton PRP X100 strong anion-exchange column employed with the mobile phase that is compatible with mass spectrometry, containing ammonium carbonate, methanol, and disodium ethylenediaminetetraacetic acid. Arsenic compounds were detected online by inductively coupled plasma dynamic reaction cell quadrupole mass spectrometry utilizing oxygen as the reaction gas at a flow rate of 0.7 mL·min−1. Five selected arsenic species were baseline separated at the optimum experimental conditions. The excellent LOD and LOQ values of the developed method were achieved in the range of 0.5 to 2.9 μg·kg−1 and 1.7 to 9.6 μg·kg−1 for all species of arsenic, respectively. The ionization effect in plasma during chromatographic gradient elution was systematically investigated by using postcolumn injector. Arsenic compounds in rice samples were extracted by diluted nitric acid at elevated temperature. The extraction efficiency and the interconversion of target compounds during sample preparation were also assessed. The full validation of the developed method was performed by using certified reference material, BRC 211, from European Institute of Reference and Standard for speciation analysis. The recovery of all selected arsenic species was in the range of 70 to 135.5%. The validated method was also applied to analyze rice samples collected from some contaminated rice fields. The results showed that As(III), DMA, and As(V) were found in all rice samples. Average concentration (range) of inorganic arsenic and DMA in all rice samples were 130.3 (65.5–228.1) and 32 (8.2–133.01) μg·kg−1, respectively. However, total concentration of inorganic arsenic in most of investigated rice samples was below the maximum residual level according to US-FDA and European Union standards.

Description: Nordic Boiling Water Reactors (BWRs) employ ex-vessel debris coolability as a severe accident management strategy (SAM). Core melt is released into a deep pool of water where formation of noncoolable debris bed and ex-vessel steam explosion can pose credible threats to containment integrity. Success of the strategy depends on the scenario of melt release from the vessel that determines the melt-coolant interaction phenomena. The melt release conditions are determined by the in-vessel phase of severe accident progression. Specifically, properties of debris relocated into the lower plenum have influence on the vessel failure and melt release mode. In this work we use MELCOR code for prediction of the relocated debris. Over the years, many code modifications have been made to improve prediction of severe accident progression in light-water reactors. The main objective of this work is to evaluate the effect of models and best practices in different versions of MELCOR code on the in-vessel phase of different accident progression scenarios in Nordic BWR. The results of the analysis show that the MELCOR code versions 1.86 and 2.1 generate qualitatively similar results. Significant discrepancy in the timing of the core support failure and relocated debris mass in the MELCOR 2.2 compared to the MELCOR 1.86 and 2.1 has been found for a domain of scenarios with delayed time of depressurization. The discrepancies in the results can be explained by the changes in the modeling of degradation of the core components and changes in the Lipinski dryout model in MELCOR 2.2.

Description: The present work describes a novel, simple, and fast electroanalytical methodology for naproxen (NAP) determination in pharmaceutical formulations and biological fluids in the presence of its degradation products. Carbon paste electrodes (CPEs) modified with different carbon nanomaterials, namely, glassy carbon powder (GCE), multiwall carbon nanotubes (MWCNTs), single-walled carbon nanotubes (SWCNTs), graphene nanosheets (Gr), and graphene oxides (GO) were tested. Comprehensive studies were performed on the electrode matrix composition including the nature of the pasting liquids, pH, carbon nanomaterials, and mode of electrode modification. Two anodic oxidation peaks were recorded at 0.890 and 1.18 V in 1 × 10−1 mol·L−1 phosphate buffer solution at pH 6. Oxidation of naproxen (NAP) is an irreversible diffusion-controlled process. Calibration plots were rectilinear in the concentration ranging from 0.067 to 1.0 µg·mL−1 with correlation coefficient 0.9979. Photodegradation of NAP resulted in disappearance of the oxidation peak at 1.18 V, allowing simultaneous determination of NAP in presence of its degradation product. The achieved high sensitivity and selectivity suggest the application of the proposed protocol for naproxen determination in pharmaceutical preparations and human blood plasma.

Description: The analysis of the thermal condition of spent FA (fuel assembly) of BN-350 reactor in a six-place cask for dry storage is presented. Simulation of the thermal condition of the cask is conducted with finite elements method using ANSYS software. Calculations of fuel temperature, fuel cladding, and assembly structural elements are the part of the safety analysis for storage of spent FA. In conclusion, the results of the thermal calculations in the cases of filling cask with argon and atmospheric air are given when the thickness of the insulation cask with concrete is 0.5 and 1 m. As a result of the calculated studies, the parameters of SNF (spent nuclear fuel) storage are determined, under which the fuel temperatures will have minimum and maximum values.

Description: A stability-indicating LC method was developed for quantification of linagliptin (LGT) and three synthetic impurities. The method utilizes a Thermo Scientific® RP-8 column (100 mm × 4.6 mm; 5 μm) with the PDA detector for quantitation of impurities. A mixture of 0.1% formic acid with pH 3.5 (A) and acetonitrile (B) was used as the mobile phase at a flow rate of 0.6 mL·min−1 with gradient elution. The percentage of mobile phase B increases from 30% to 70% over 5 min and decreases from 70% to 30% between 5 and 8 min. The method was validated according to International Council for Harmonization (ICH) guidelines. The LOD values obtained were 0.0171 μg·mL−1 and 0.015 μg·mL−1 for LGT and impurities, respectively. The LOQ values were 0.06 μg·mL−1 for LGT and impurities. In all cases, the correlation coefficients of LGT and impurities were 〉0.999, showing the linearity of the method. The % recovery of the LGT and added impurity were in the range of 92.92–99.79%. The precision of the method showed values less than 1.47% for LGT and less than 4.63% for impurities. The robustness was also demonstrated by small modifications in the chromatographic conditions. The selectivity was evidenced because the degradation products formed in stress conditions did not interfere in the determination of LGT and impurities. Toxicity prediction studies suggested toxicity potential of the impurities, which was confirmed using biological safety studies in vitro.

Description: TOF-ND elastic scattering of thermal neutrons offers some important advantages over X-ray diffraction (XRD), X-ray fluorescence (XRF), and metallography for the study of archaeological and numismatic problems. Traditional analytical methods are usually destructive and often probe only the surface. Neutrons deeply penetrate samples, simultaneously giving nondestructive bulk information about the crystal structure, composition, and texture (alignment of crystallites) from which thermomechanical manufacturing processes (e.g., cast, struck, or rolled) may be inferred. An analysis of the metal composition and minting processes used for making ancient Judaean bronze and leaded bronze coins from first century BCE and CE is used as a case study. One of the first ND analyses of the temperature used for striking bronze coins is also presented.

Description: A C-Ag+-C structure-based fluorescence biosensor with novel combination design of exonuclease III (Exo III) dual-recycling amplification is proposed for the application of silver ions (Ag+) detection. Since oligo-1 involves C-C mismatches, the presence of Ag+ can be captured to form C-Ag+-C base pairs, which results in a double-helix structure with a blunt terminus. The double-helix structure can be cleaved by EXO III to release short mononucleotide fragments (trigger DNA) and Ag+. Released Ag+ can form new bindings with oligo-1, and other trigger DNA can be produced in the digestion cycles. Hybridization with the signal DNA (oligo-2) transforms a trigger DNA into double-stranded DNA with blunt terminus which can be cleaved by Exo III to reproduce the trigger DNA and form guanine- (G-) quadruplex DNA. The trigger DNA returns free to the solution and hybridizes with another signal DNA, which realizes the dual-recycling amplification. The G-quadruplex DNA can be reported by N-methylmesoporphyrin IX (NMM), a specific G-quadruplex DNA fluorochrome. This method allows Ag+ to be determined in the 5 to 1500 pmol/L concentration range, with a 2 pmol/L detection limit, and it has been successfully applied to the detection of Ag+ in real samples.

Description: There are results of long-term thermal aging of samples of irradiated and nonirradiated FA jacket and nonirradiated fuel element cladding at a temperature range from 300 to 550°C in argon, to 600°C in air. Materials have been studied before and after thermal tests. The forecast estimation of expected corrosion damage of barrier material at the radionuclide release from spent fuel assemblies of BN-350 reactor into environment during dry storage for 50 years was carried out.

Description: Two-phase flow instability may occur in nuclear reactor systems, which is often accompanied by periodic fluctuation in fluid flow rate. In this study, bubble rising and coalescence characteristics under inlet flow pulsation condition are analyzed based on the MPS-MAFL method. To begin with, the single bubble rising behavior under flow pulsation condition was simulated. The simulation results show that the bubble shape and rising velocity fluctuate periodically as same as the inlet flow rate. Additionally, the bubble pairs’ coalescence behavior under flow pulsation condition was simulated and compared with static condition results. It is found that the coalescence time of bubble pairs slightly increased under the pulsation condition, and then the bubbles will continue to pulsate with almost the same period as the inlet flow rate after coalescence. In view of these facts, this study could offer theory support and method basis to a better understanding of the two-phase flow configuration under flow pulsation condition.

Description: To perform accurate and synchronous detection of the soluble solid contents (SSC) in fresh jujubes at different stages of maturity, hyperspectral imaging was used to establish robust models. The combined data constituting four maturation stages were used to build the grid-search least squares support vector machine (GS-LS-SVM) model. The determination coefficient (Rp2), the root-mean-square error (RMSEP), and the residual predictive deviation (RPD) of the prediction set for samples of the overall stages were 0.98, 1.10%, and 7.85, respectively. Furthermore, a successive projections algorithm (SPA) was used to extract the characteristic wavelengths of the combined data. An artificial bee colony (ABC) algorithm (for the prediction set, Rp2 = 0.98, RMSEP = 1.19%, RPD = 7.25) was used to improve the SPA-LS-SVM model, which was better than the SPA-GS-LS-SVM model (for the prediction set, Rp2 = 0.98, RMSEP = 1.24%, RPD = 6.96). Lastly, visualization of the SSC distribution map was performed based on the SPA-ABC-LS-SVM model, which clearly showed that the SSC gradually increased during maturation. The results indicated that it was realistic to construct a detection model of the multimaturity stage. This research also demonstrated that the combination of hyperspectral imaging and the ABC had good application values in the testing of agricultural products.

Description: In the present study, we developed and validated a rapid and simple liquid chromatography-tandem mass spectrometry (LC-MS/MS) method for the determination of lorlatinib in mouse serum and tissue samples, and such a method was successfully applied to investigate the pharmacokinetic study and tissue distribution of lorlatinib after oral administration. Samples were processed with methanol to precipitate protein and extract drugs, and Afatinib-d6 was used as the internal standard (IS). For LC-MS/MS analysis, compounds were separated on a C18 column by gradient elution (0.1% of formic acid and methanol) at 0.5 mL/min in the positive-ion mode with m/z 407.28 [M + H]+ for lorlatinib and m/z 492.10 [M + H]+ for IS. Good linearity was observed within the calibration ranges. Selectivity, accuracy (−6.42% to 8.84%), precision (1.69% to 10.98%), recoveries (91.4% to 115.0%), and matrix effect (84.2% to 110.6%) were all within the acceptable ranges. After oral administration, serum concentration of lorlatinib quickly achieved the maximal concentration (2,705.683 ± 539.779 μg/L) at 0.625 ± 0.231 h. The highest concentration was detected in the liver (3,153.93 ng/100 mg), followed by the stomach (2,159.92 ng/100 mg) and the kidney (548.83 ng/100 mg). In conclusion, a simple and rapid detection method was established and validated for determination of lorlatinib in blood and tissue samples of mouse. The pharmacokinetic study and tissue distribution of lorlatinib were successfully investigated using this method.

Description: The Nuclear Material Accounting (NMA) system is one of the main safeguards measures to detect the existence of nuclear material diversion. It has become more important for large reprocessing facilities to apply Near Real Time Accountancy (NRTA) system based on NMA and statistical techniques to meet quantitative and timeliness goals. It is also important to quantitatively evaluate the performance of NMA system including NRTA from the standpoints of Safeguards and Security by Design (SSBD) prior to construction of nuclear-material-handling facilities. Such evaluation improves safeguards effectiveness and efficiency. Modeling and Simulation (M&S) work is a good way to evaluate performance for various NMA systems and to determine the optimal one among different options. For these purposes, in the present study, the PYroprocessing Material flow and MUF Uncertainty Simulation+ (PYMUS+) code, which uses evaluation algorithms to calculate many safeguards factors such as MUF uncertainty, detection probability, and others, was developed. According to a previous report, the PYMUS code, the predecessor of PYMUS+, can calculate MUF uncertainties only for a fixed model having 10 tHM/year, whereas the PYMUS+ code can additionally calculate detection probabilities according to diverse nuclear diversion scenarios as well as MUF uncertainties. The most important feature of the PYMUS+ code is its capability to evaluate many process and NMA system model options that a user wants to evaluate. Furthermore, a user can make a static process model having simplicity and a matching NMA model based on the PYMUS+ code regardless of facility throughput and is not even required to have professional programming knowledge. In the present work, some intercomparative studies were conducted to verify the M&S techniques applied in this code. It is expected that this code will be a useful tool for evaluation of NRTA system of pyroprocessing and other reprocessing facilities.

Description: In this paper, mid- and near-infrared spectroscopy fingerprints were combined to simultaneously discriminate 12 famous green teas and quantitatively characterize their antioxidant activities using chemometrics. A supervised pattern recognition method based on partial least square discriminant analysis (PLSDA) was adopted to classify the 12 famous green teas with different species and quality grades, and then optimized sample-weighted least-squares support vector machine (OSWLS-SVM) based on particle swarm optimization was employed to investigate the quantitative relationship between their antioxidant activities and the spectral fingerprints. As a result, 12 famous green teas can be discriminated with a recognition rate of 100% by MIR or NIR data. However, compared with individual instrumental data, data fusion was more adequate for modeling the antioxidant activities of samples with RMSEP of 0.0065. Finally, the performance of the proposed method was evaluated and validated by some statistical parameters and the elliptical joint confidence region (EJCR) test. The results indicate that fusion of mid- and near-infrared spectroscopy suggests a new avenue to discriminate the species and grades of green teas. Moreover, the proposed method also implies other promising applications with more accurate multivariate calibration of antioxidant activities.

Description: Gold nanoclusters (AuNCs) are one of metal nanoclusters, which play a pivotal role in the recent advances in the research of fluorescent probes for their fluorescence effect. They are favored by most researchers due to their strong stability in fluorescence and adjustability in fluorescence wavelength when compared to traditional organic fluorescent dyes. In this review, we introduce various synthesis strategies of gold-nanocluster-based fluorescent probes and summarize their application for environmental analysis and biological sensing. The use of gold-nanocluster-based fluorescent probes for the analysis of heavy metals and inorganic and organic pollutants is covered in the environmental analysis while biological labeling, imaging, and detection are presented in biological sensing.

Description: In this study, an ultrasensitive detection method for aqueous Pb2+ based on digital polymerase chain reaction (dPCR) technology and a Pb2+-dependent DNAzyme was developed. In the presence of Pb2+, the Gr-5 DNAzyme was activated and catalyzed the hydrolytic cleavage of the substrate strand, resulting in an increase in the amount of template DNA available for dPCR and a resultant change in the number of droplets showing a positive signal. Moreover, the detection system was found to be sensitive and stable in environmental sample detection. In summary, an ultrasensitive quantitative detection method for Pb2+ within environmental substrates was established.

Description: To improve essential oil quality, especially to reserve the thermal instability of compounds, supercritical CO2 extraction (SFE) was applied to recover essential oil from Cymbopogon citronella leaves. A response surface methodology was applied to optimize the extraction process. The highest essential oil yield was predicted at extraction time 120  min, extraction pressure 25  MPa, extraction temperature 35°C, and CO2 flow 18  L/h for the SFE processing. Under these experimental conditions, the mean essential oil yield is 4.40%. In addition, the chemical compositions of SFE were compared with those obtained by hydrodistillation extraction (HD). There were 41 compounds obtained of SFE, while 35 compounds of HD. Alcohols and aldehydes were the main compositions in the essential oils. Furthermore, the antioxidant activities and antimicrobial of essential oils obtained by HD and the evaluated condition of SFE were compared. Results showed that the antioxidant activities of SFE oil are better than those of HD. Minimum inhibitory concentrations (MICs) were determined by the microdilution method. Essential oil obtained from SFE and HD exhibited a significant antimicrobial activity against all tested microorganisms. It is confirmed that the SFE method can be an alternative processing method to extract essential oils from Cymbopogon citronella leaves.

Description: Tiliroside exhibits a wide spectrum of effects on the human body; considering expensive synthesis of tiliroside, linden trees seem to be a good source of this compound. For the first time, 46 various extraction methods were developed to receive tiliroside from Tilia L., including ultrasound-assisted extraction, maceration, maceration with stirring, accelerated solvent extraction, and extraction under reflux. The effects of extraction techniques, solvents, additives, and temperature on the content of tiliroside were studied using analytical and statistical methods. A new, rapid, simple, sensitive, and selective liquid chromatography-electrospray ionization-tandem mass spectrometry (LC-ESI-MS/MS) method was developed to determine the content of tiliroside in Tilia L. flowers. The LC-ESI-MS/MS analysis demonstrated the highest content of tiliroside in Tilia L. flowers obtained using accelerated solvent extraction (ASE) where 70% ethanol with addition of 1% acetic acid was used as a solvent (7.400 ± 0.019 mg of tiliroside per g dry extract).The results showed that the extracts of Tiliae inflorescentia contained large amounts of tiliroside; therefore, they are good sources of this compound. Moreover, ASE was found to be superior to other extraction techniques due to its high efficiency as well as considerable saving of time and solvent.

Description: A rapid and simple ultra-high-performance supercritical fluid chromatography (UHPSFC) with photodiode array (PDA) method was developed and validated for simultaneous determination of eight Sudan dyes in chili oil. In particular, a pair of isomer, Sudan red B and Sudan IV, was included in the analysis. After being diluted with dichloromethane, the analytes were separated on an Acquity UPC2 HSS C18 SB column with gradient elution using CO2 as the mobile phase and acetonitrile/methanol (v/v, 45/55, containing 0.1% formic acid) as the organic modifier. Analytes were quantified by external calibration curves over ranges of 0.5–50 mg/L, with correlation coefficients above 0.999. The method gave recoveries of the target compounds (spiked at levels of 1, 5, and 25 mg/kg) ranging from 82.6 to 108.3%, with intraday and interday relative standard deviations of less than 8.0% and 8.6%, respectively. The limits of detection (LODs) and the limits of quantification (LOQs) for eight dyes were from 0.10 to 0.30 mg/kg and 0.30–1.00 mg/kg, respectively. This method was applied for the analysis of chili oil samples collected from the supermarket in Beijing. This validated that the UHPSFC-PDA method provides a useful strategy for the simultaneous determination of Sudan dyes in chili oil for routine analysis.

Description: Colorectal cancer is the most common critical disease both in the developed and developing countries. Capecitabine, which has served in clinical practice at least for 10 years, is a first-line antidigestive tract cancer drug for its better efficacy, patient compliance, and lower side effects. An ultra-high-performance liquid chromatography tandem mass spectrometry (UHPLC-MS/MS) method has been developed and completely validated for simultaneous determination of capecitabine and its five metabolites in human plasma from colorectal cancer patients after administration of capecitabine tablet. One-step liquid-liquid extraction was successfully applied using ethyl acetate and isopropanol (19 : 1, V : V) for sample pretreatment. Chromatographic separation was achieved within 5 min based on an Atlantis T3-C18 column (3.0 µm, 2.1 × 100 mm) with gradient elution using mobile phases consisting of 0.0075% formic acid in water (pH 4) and in acetonitrile, and the flow rate was 0.3 mL/min. Linear range was approximately 20.0–5000.0 ng/mL for all analytes. Linear correlation coefficients were 〉0.99 for all regression curves. The intraday and interday accuracy and precision of the method were within ±15.0% and less than 15.0%, respectively. The mean recovery and matrix effect as well as stability of all the analytes ranged from 59.27% to 90.15% and from 74.84% to 114.48% as well as within ±15.0%. This simple, rapid, and sensitive method was successfully applied in 42 sparse clinical samples to verify its practicability.

Description: This work presents a reliable approach to trace teas’ geographical origins despite changes in teas caused by different harvest years. A total of 1447 tea samples collected from various areas in 2014 (660 samples) and 2015 (787 samples) were detected by FT-NIR. Seven classifiers trained on the 2014 dataset all succeeded to trace origins of samples collected in 2014; however, they all failed to predict origins for the 2015 samples due to different data distributions and imbalanced dataset. Three outlier detection based undersampling approaches—one-class SVM (OC-SVM), isolation forest and elliptic envelope—were then proposed; as a result, the highest macro average recall (MAR) for the 2015 dataset was improved from 56.86% to 73.95% (by SVM). A model updating approach was also applied, and the prediction MAR was significantly improved with increase in the updating rate. The best MAR (90.31%) was first achieved by the OC-SVM combined SVM classifier at a 50% rate.

Description: In this paper, a valid evaluation method for the quality control of Danggui Kushen pills (DKP) has been established based on quantitative analysis of multicomponents by single marker (QAMS). Gallic acid, matrine, oxymatrine, catechin, ferulic acid, and rutin were selected as the indexes for quality evaluation of DKP. The analysis was achieved on an Agilent ZORBAX SB-C18 column (250  mm × 4.6  mm, 5 μm) via gradient elution. Gallic acid was used as internal standard to determine the relative correction factors (RCF) between gallic acid and other five constituents in DKP. The contents of those components were calculated at the same time. The accuracy of QAMS method was verified by comparing the contents of six components calculated by external standard (ES) method with those of the QAMS method. It turned out that there was no significant difference between the quantitative results of QAMS method and external standard method. The proposed QAMS method was proved to be accurate and feasible according to methodological experiments, which provided an accurate, efficient, and economical approach for quality evaluation of DKP.

Description: Caffeine is widely present in food and drinks, such as teas and coffees, being also part of some currently commercialized medicines, but despite its enhancement on several functions of human body, its exceeding use can promote many health problems. In order to develop new fast approaches for the caffeine sensing, graphite-epoxy composite electrodes (GECE) were used as substrate, being modified by different diazonium salts, synthetized as their tetraflouroborate salts. An analytical method for caffeine quantification was developed, using sware wave voltammetry (SWV) in Britton–Robinson buffer pH 2.0. Detection limits for bare electrode and 4-benzenesulfonic modified electrode were observed circa 145 µmol·L−1 and 1.3 µmol·L−1, respectively. The results have shown that the modification shifts the oxidation peaks to lower potential. Kinetics of the reaction limited by diffusion was more expressive when caffeine was added to the solution, resulting in decreases of impedance, characterized by lower Rct. All results for caffeine determination were compared to a reference chromatographic procedure (HPLC), showing no statistical difference. Analytical parameters for validation were suitably determined according to local legislation, leading to a linear behaviour from 5 to 150 µmol·L−1; precision of 4.09% was evaluated based on the RDC 166/17, and accuracy was evaluated in comparison with the reference method, with recovery of 98.37 ± 2.58%.

Description: SY0916 has been proven to be a potent treatment agent against rheumatoid arthritis in preclinical studies and has been shown to be safe in phase I clinical trials. However, SY0916 is unstable in water, which is frequently used in pharmaceutical development processes. The degradation behaviour and stability of SY0916 in aqueous solutions were investigated at different pH levels, periods of time, and temperatures. Two degradation products (DPs) were successfully separated and characterized by liquid chromatography coupled to high-resolution tandem mass spectrometry (LC-HRMS/MS), liquid chromatography coupled to nuclear magnetic resonance with solid phase extraction (LC-SPE-NMR), and nuclear magnetic resonance (NMR). SY0916 decomposed to its α,β-unsaturated ketone in protonic solvents, and the α,β-unsaturated ketone further transformed into its alcohol form through a conjugate addition reaction in aqueous media. The results of this study indicate that the pH of the buffer solutions should be maintained between 3.0 and 3.6 for maximum SY0916 stability. Factors that affect degradation should be carefully controlled to mitigate or avoid drug decay.

Description: The present study aims at building a miniature mass method for the simultaneous determination of 12 phenols including the subtypes of bibenzyl, phenanthrene, and fluorenone, which was used to evaluate the quality of Dendrobium chrysotoxum. Through the full scan mode, new compounds were elucidated. The new compounds were quantified by carrying out the analysis of the ratio of the standard solution areas to new compound areas versus analyte concentration. The limit of detection (LOD) and limit of quantification (LOQ) for phenols were 0.5 µg/mL–1 µg/mL and 1 µg/mL–2 µg/mL, respectively. Average recoveries of phenols were ranged from 83.2% to 97.5%. Reproducibility represented by the RSD percentage was from 2.3% to 8.7%. The average content of the four analytes, erianin, chrysotobibenzyl, confusarin, and moscatilin, were more than 200 mg/kg, and the content of bibenzyl compounds was found to be the highest in Dendrobium chrysotoxum. Among these bibenzyl compounds, erianin was determined as the typical chemical marker from Dendrobium chrysotoxum. The newly established UPLC with a miniature mass detector method was found to be an appropriate tool for the quality assessment of Dendrobium chrysotoxum.

Description: In a fast reactor, we evaluated a new core concept that prevents severe recriticality after whole-scale molten formation in a severe accident. A core concept in which Duplex pellets including neutron absorber are loaded in the outer core has been proposed. Analysis by the continuous energy model Monte Carlo code MVP using the JENDL-4.0 nuclear data library revealed that this fast reactor core has large negative reactivity due to fuel melting at the time of a severe accident, so that the core prevents recriticality. Regarding the core nuclear and thermal characteristics, the loading of Duplex pellets including neutron absorber in the outer core caused no significant differences from the normal core without Duplex pellets.

Description: Every year, over 200 million adults are undergoing noncardiac surgery. These noncardiac surgery patients may face the risk of cardiac mortality and morbidity during the perioperative and recovery periods. Around ten million patients who underwent noncardiac surgery experience cardiac complications within the first 30 days of the postoperative period; the complications are myocardial infarction, cardiac death, and cardiac arrest. This cardiovascular risk is mostly faced by the patients having cerebrovascular or cardiac disease and the patients with the age greater than 50 years. Monitoring and treating cardiac diseases with a suitable biomarker during the perioperative period is necessary for the early recovery of noncardiac surgery patients. This review discussed the risk factors and the key guidelines to avoid the cardiovascular risks during the perioperative period of noncardiac surgery patients. In addition, the biomarkers and identification strategies for cardiac diseases are discussed.

Description: Interest in evaluation of severe accidents induced by extended station blackout (ESBO) has significantly increased after Fukushima. In this paper, the severe accident process under the high and low pressure induced by an ESBO for a small integrated pressurized water reactor (IPWR)-IP200 is simulated with the SCDAP/RELAP5 code. For both types of selected scenarios, the IP200 thermal hydraulic behavior and core meltdown are analyzed without operator actions. Core degradation studies firstly focus on the changes in the core water level and temperature. Then, the inhibition of natural circulation in the reactor pressure vessel (RPV) on core temperature rise is studied. In addition, the phenomena of core oxidation and hydrogen generation and the reaction mechanism of zirconium with the water and steam during core degradation are analyzed. The temperature distribution and time point of the core melting process are obtained. And the IP200 severe accident management guideline (SAMG) entry condition is determined. Finally, it is compared with other core degradation studies of large distributed reactors to discuss the influence of the inherent design characteristics of IP200. Furthermore, through the comparison of four sets of scenarios, the effects of the passive safety system (PSS) on the mitigation of severe accidents are evaluated. Detailed results show that, for the quantitative conclusions, the low coolant storage of IP200 makes the core degradation very fast. The duration from core oxidation to corium relocation in the lower-pressure scenario is 53% faster than that of in the high-pressure scenario. The maximum temperature of liquid corium in the lower-pressure scenario is 134 K higher than that of the high-pressure scenario. Besides, the core forms a molten pool 2.8 h earlier in the lower-pressure scenario. The hydrogen generated in the high-pressure scenario is higher when compared to the low-pressure scenario due to the slower degradation of the core. After the reactor reaches the SAMG entry conditions, the PSS input can effectively alleviate the accident and prevent the core from being damaged and melted. There is more time to alleviate the accident. This study is aimed at providing a reference to improve the existing IPWR SAMGs.

Description: In a fast spectrum reactor, the fuel rod bundle is mainly positioned radially by the wire which can make contact with the adjacent fuel rods, and then it is inevitable that flow-induced vibration (FIV) will cause fretting wear and vibration fatigue of the fuel cladding at the contact position. Therefore, the computational model of fretting wear and fatigue life about the fuel rod bundle caused by FIV will be studied in this paper. Based on the random vibration model of the fuel rod bundle, Hertz contact theory, and Archard wear theory, the fretting wear life computational model and the fatigue life computational model of the wire-to-adjacent fuel rod (WAFR) contact have been established. Finally, taking CEFR design parameters as an example, the fretting wear life and vibration fatigue life of the cladding are calculated, and it is found that fatigue affects the service life of the fuel rod more seriously than fretting wear. The calculation model and method lay a foundation for further accurate prediction and analysis of the fuel rod life.

Description: For the new nuclear power plants, the hazard of liquefaction due to earthquakes should be excluded by appropriate site selection or eliminated by engineering measures. An important question is how to define a quantitative criterion for negligibility of the liquefaction hazard. In the case of operating plants, liquefaction can be revealed as a beyond-design-basis event. It is important to learn whether the liquefaction hazard has a safety relevance and whether there is a sufficient margin to the onset of liquefaction. The use of pseudoprobabilistic method would be practicable for the definition of probability of liquefaction, but it could result in overconservative results. In this paper, the applicability of the pseudoprobabilistic procedure is demonstrated for the sites in diffuse seismicity environment and for low hazard levels that are typical for nuclear safety considerations. Use of the procedure is demonstrated in a case study with realistic site-plant parameters.

Description: The electrophoretic deposition (EPD) technique was used to create a uniform SiO2 thin film coating on boiling plates, 4 mm in width and 9 mm in length. Significant enhancement in critical heat flux (CHF), for the hydrophilic surfaces generated by this anodic EPD method, has been observed. In order to increase the coating strength, the plates were sintered at various temperatures. To find the thickness and uniformity of the coatings, the SEM images were captured. The captured images showed that the coating thickness uniformly increased up to 90 nm for 0.5% nanofluid percentage by the EPD method. The results show that the hydrophilic and super-hydrophilic surfaces have different boiling heat transfer (BHT) coefficients and CHF behaviors. Also, the results showed an increase of 160% in the CHF value by sintering compared to a bare surface. However, because of the setup simplicity, the shape independency, the particle-coating uniformity, and thickness controllability, the EPD technique can be an appropriate option for modification of the surface and coating on the nuclear fuel cladding.

Description: To implement EU REACH- (Registration, Evaluation, and Authorization of Chemicals-) like chemical legislations in various countries of which the purpose is human and environment safety, the first step is substance identification followed by the hazard and risk assessments. Although both structural and composition identifications are required, the latter can more importantly result in the essential data to fill out the required substance information such as purity and concentrations of constituents, as well as impurities. With fatty acid zinc salts (FAZSs) as an exemplary industrial chemical of which chromatographic and nuclear magnetic resonance (NMR) analyses were impossible due to their insolubility in water and any organic solvents, the composition characterization was tried by preparing their fatty acid methyl esters (FAMEs) using the conc. HCl/methanol/toluene method. This acid-catalyzed methyl esterification was optimized with zinc stearate as a surrogate substance. Gas chromatography-mass spectrometry (GC-MS) and NMR analyses on methyl-esterified products revealed that the optimum conditions were at 90°C for 10 min or 45°C for 30 min with two equivalent HCl as well as at 45°C for 10 min with five equivalent HCl. Almost all zinc stearates were converted into the corresponding fatty acids with 97–99% conversion rates. Free fatty acids (FFAs) were detected in extracted ion chromatograms of pyrolysis-gas chromatography-mass spectrometry (Py-GC-MS) in the methyl-esterified products with incomplete conversions of 73∼79%. The optimized conc. HCl/methanol/toluene method of direct one-step reaction from FAZSs was compared with the two-step NaOH saponification/BF3-methanol method after acidic hydrolysis of FAZSs. The mechanism of fatty acid zinc salts into free fatty acids and fatty acid methyl esters was suggested with the evidence of the formation of Zn(OH)2.

Description: In order to improve the strength and resistance of ordinary nonel tubes, calcium sulfate whiskers (CSW, treated with silane coupling agent) and maleic anhydride grafted polyethylene (PE-g-MAH) are used to control the wall material of the nonel tube that the blending of the low-density polyethylene was enhanced. The effects of mass fraction of CSW or PE-g-MAH on the tensile properties, interfacial structure, melting and crystallization characteristics, and thermal decomposition behavior of the composite system were studied, and the thermal decomposition kinetics were calculated. The results show that, relative to pure LDPE, the strength of LDPE/CSW (85/15) is increased by 7.58%, and the strength of LDPE/CSW/PE-g-MAH (84/15/1) is increased by 7.58%. The addition of CSW or PE-g-MAH has gradually changed the fracture mode of the LDPE matrix. Thermal analysis shows that CSW can reduce the crystallinity of LDPE. The melting and crystallization characteristics of LDPE/CSW/PE-g-MAH composites have little effect, but the thermal decomposition stability is improved. The kinetic analysis showed that the reaction order (n) was around 1, CSW could improve LDPE/CSW thermal decomposition activation energy, and PE-g-MAH increased the thermal decomposition activation energy of LDPE/CSW/PE-g-MAH.

Description: A new data-driven sampling-based framework was developed for uncertainty quantification (UQ) of the homogenized kinetic parameters calculated by lattice physics codes such as TRITON and Polaris. In this study, extension of the database for the delayed neutron data (DND) is performed by exploring more delayed neutron experiments and adding additional isotopes/actinides to the data libraries. Afterwards, the framework is utilized to obtain a deeper knowledge of the kinetic parameters’ sensitivity and uncertainty. The kinetic parameters include precursor-group-wise delayed neutron fraction (DNF) and decay constant. Input uncertainties include nuclear data (i.e., cross-sections) and DND (i.e., precursor group parameters and fractional delayed neutron yield). It is found that kinetic parameters, especially DNFs, have large uncertainties. The DNF uncertainty is driven by the cross-section uncertainties for LWR designs, while decay constant uncertainty is dominated by the DND uncertainties. The usage of correlated U-235 thermal DND in the UQ process significantly reduces the DND uncertainty contribution on the kinetic parameters. Large void fraction and presence of neutron absorber (e.g., control rod) increase the DNF uncertainty due to the hardening of neutron spectrum. High correlation between the DNF groups () is observed, while the decay constant groups () show weak correlation to each other and also to DNF groups. The DNF uncertainties of the dominant precursor group 4 for PWR, BWR, and VVER are about 7.5%, 9.4%, and 7.6%, respectively. The DNF uncertainty grows to larger values after fuel burnup. Kinetic parameters’ values and uncertainties provided here can be efficiently used in subsequent core calculations, point reactor kinetics, and other applications.