ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • Articles  (129)
  • Other Sources
  • adsorption  (129)
  • Springer  (129)
  • American Geophysical Union
  • American Physical Society
  • 1995-1999  (129)
  • 1945-1949
  • 1940-1944
  • Chemistry and Pharmacology  (129)
  • Electrical Engineering, Measurement and Control Technology  (5)
  • Medicine
Collection
  • Articles  (129)
  • Other Sources
Publisher
  • Springer  (129)
  • American Geophysical Union
  • American Physical Society
  • Wiley-Blackwell  (20)
Years
Year
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 105 (1997), S. 6-10 
    ISSN: 1435-1536
    Keywords: Colloidal aqueous suspensions ; adsorption ; rheology ; polyethylene oxide ; phosphonate ; calcium carbonate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract New polymeric dispersing agents designed to stabilize and lower the viscosity of aqueous mineral suspensions have been synthesized and studied. These dispersants are made of a non-ionic hydrosoluble polymer (polyethylene oxide) with a functional group (diphosphonate) having a strong affinity for the mineral surfaces attached at one end of the macromolecular chains. This molecular architecture allows a brush-like adsorption at the solid surface which differs from conventional homopolymer dispersants such as polyacrylates. The adsorption of these dispersants onto calcium carbonate as a model mineral and the rheological behavior of concentrated aqueous colloidal dispersions of CaCO3 particles were studied. Strong adsorption by the polymer chain-end provides an enhanced colloidal stability of the suspensions of CaCO3 particles. The addition of the dispersing polymer causes a deaggregation of the initially flocculated CaCO3 particles, which results in a drastic reduction of the viscosity of the concentrated suspensions. Thus, the viscosity of a 20 wt% CaCO3 suspension in water at pH=11 is lowered to 2 mPa s upon the addition of a low concentration of polymer. Comparison with polyacrylate dispersants shows the advantages of such a diblock macromolecular structure with a non-ionic polymeric part at high solid contents and high ionic strengths.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of applied electrochemistry 28 (1998), S. 993-998 
    ISSN: 1572-8838
    Keywords: thiosulfate ; silver ; adsorption ; differential capacitance
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Electrical Engineering, Measurement and Control Technology
    Notes: Abstract The differential capacitance of a polycrystalline Ag electrode was measured in a NaClO4 electrolyte containing Na2S2O3 at concentrations ranging from 0.1 to 20mm and at electrode potentials ranging from −0.9 to −0.3V vs SCE. The differential capacitance measurements were analysed to obtain the surface coverage of specifically adsorbed thiosulfate (S2O32−) as a function of both electrode potential and bulk concentration. The various forms for the adsorption isotherm at an electrochemical interface which are commonly employed are reviewed and discussed. The adsorption behaviour is best explained by the formation of image dipoles by the specifically adsorbed ions, whose energetic interactions are then dominated by repulsion of like dipoles. The adsorption data is quantitatively fit to an adsorption isotherm for interacting dipoles, yielding an effective dipole moment of 0.72D for the system S2O32−/Ag.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of applied electrochemistry 28 (1998), S. 819-825 
    ISSN: 1572-8838
    Keywords: adsorption ; experimental design ; metal electrodeposition ; modelling ; voltammetry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Electrical Engineering, Measurement and Control Technology
    Notes: Abstract Chromium deposition on an inert electrode is a complex process. To gain a better understanding of phenomena involved in multistep reactions we have studied such a mechanism and developed Voltasim, a new software that simulates cyclic voltammograms for a two-step metal deposition with adsorption. In addition, Voltasim is suitable for either reversible or quasi-reversible or irreversible reactions. The software was validated with experimental results obtained for the chromium deposition case. Data fitting was achieved using a screening design of experiments involving 12␣parameters.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 4
    ISSN: 1572-8838
    Keywords: adsorption ; dye photooxidation ; titanium dioxide
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Electrical Engineering, Measurement and Control Technology
    Notes: Abstract A two-part study was undertaken to examine the feasibility of combining a batch-recirculated photoreactor with a hollow-fibre membrane based ultrafiltration unit for heterogeneous photocatalysis applications. Methylene Blue (MB) and titanium dioxide (Degussa, P-25) were used as the test substrate and photocatalyst respectively for this study. This paper, which forms Part I of this study, describes the influence of MB concentration, recirculation flow rate, TiO2 dose, solution volume in the reservoir and solution pH on the photocatalytic reaction rate. The dark adsorption of MB on the TiO2 particle surface was also analysed. The combination of the reservoir and the annular reaction vessel could be modelled as a continuous flow stirred tank in series with a plug-flow reactor. This model predicts that the reaction rate should increase with a decrease of solution volume in the reservoir, both in the low and high substrate concentration regimes of the Langmuir–Hinshelwood kinetics formalism. This prediction was borne out by the experimental data for the low concentration regime. Part II of this series will describe experiments and modelling of the UF unit, and the operation of the combined system, respectively.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 5
    ISSN: 1572-8838
    Keywords: acidic media ; adsorption ; corrosion inhibitors ; electrochemical impedance spectroscopy ; mild steel ; triazoles
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Electrical Engineering, Measurement and Control Technology
    Notes: Abstract A new class of corrosion inhibitors, namely, 3,5-bis(n-hydroxyphenyl)-4-amino-1,2,4-triazoles and 3,5-bis(n-aminophenyl)-4-amino-1,2,4-triazoles which have been labelled n-HPAT and n-APAT has been synthesized. The influence of aminotriazoles on the corrosion of mild steel in 1m HCl has been studied using weight loss and electrochemical impedance spectroscopy. Results obtained show that these compounds are very good anodic inhibitors. The adsorption of these aminotriazoles is found to obey Langmuir adsorption isotherm.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Adsorption 1 (1995), S. 103-112 
    ISSN: 1572-8757
    Keywords: adsorption ; mixtures ; activity coefficients ; zeolites
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract Experimental and simulated data for adsorption of gas mixtures on energetically heterogeneous surfaces like activated carbon and zeolites exhibit negative deviations from ideality. The deviations are large in some cases, with activity coefficients at infinite dilution equal to 0.1 or less. Similar molecules form ideal mixtures, but molecules of different size or polarity are nonideal. Equations for bulk liquid mixtures (Wilson, Margules, etc.) do not apply to isobars for adsorbed mixtures. A two-constant equation for activity coefficients as a function of composition and spreading pressure is in good agreement with theory, simulation, and experiment.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Adsorption 2 (1996), S. 23-32 
    ISSN: 1572-8757
    Keywords: GCMC ; DFT ; adsorption ; MCM-41 ; buckytube ; simulation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract MCM-41 and buckytubes are novel porous materials with controllable pore sizes and narrow pore size distributions. Buckytubes are carbon tubes with internal diameters in the range 1–5 urn. The structure of each tube is thought to be similar to one or more graphite sheets rolled up in a helical manner. MCM-41 is one member of a new family of highly uniform mesoporous silicate materials produced by Mobil, whose pore size can be accurately controlled in the range 1.5–10 nm. We present grand canonical Monte Carlo (GCMC) simulations of single fluid and binary mixture adsorption in a model buckytube, and nonlocal density functional theory (DFT) calculations of trace pollutant separation in a range of buckytubes and MCM-41 pores. Three adsorbed fluids are considered; methane, nitrogen and propane. The GCMC studies show that the more strongly adsorbed pure fluid is adsorbed preferentially from an equimolar binary mixture. Ideal adsorbed solution theory (IAST) is shown to give good qualitative agreement with GCMC when predicting binary mixture separations. The DFT results demonstrate the very large increases in trace pollutant separation that can be achieved by tuning the pore size, structure, temperature and pressure of the MCM-41 and buckytube adsorbent systems to their optimal values.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 8
    ISSN: 1572-8757
    Keywords: Monte Carlo simulation ; Gibbs-Duhem integration ; adsorption ; liquid mixtures ; faujasite
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract Grand canonical Monte Carlo simulations of adsorption of N2 and O2 and their mixtures in a model zeolitic cavity 14 Å in diameter were performed at 77.5 K for pressures ranging from zero up to saturation, where the adsorbed phase is in equilibrium with coexisting vapor and liquid phases. The same intermolecular potential functions were employed for gas-gas interactions in the vapor, liquid, and adsorbed phases. The gas-solid interaction potential includes dispersion-repulsion energy, induced electrostatic energy, and an ion-quadrupole term to model the interaction of the electric field in zeolites like NaX with polar molecules like N2. The simulation of the coexisting vapor and liquid phases reproduces the saturation properties of pure liquid oxygen and nitrogen at 77.5 K. Activity coefficients in the adsorbed phase derived from simulations as a function of cavity filling and composition show negative deviations from Raoult's law, even though the non-idealities in the bulk liquid phase have the opposite sign. The simulation of the surface excess isotherm for adsorption from liquid mixtures exhibits preferential adsorption of N2 and has the commonly-observed quadratic shape skewed toward the more strongly adsorbed component. Micropore condensation is observed for oxygen but not for nitrogen. The condensation of oxygen is similar to a first order phase transition but because of the small number of molecules that can fit into a micropore, coexistence of the two phases is replaced by oscillations between gas- and liquid-like densities.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Adsorption 2 (1996), S. 95-101 
    ISSN: 1572-8757
    Keywords: osmosis ; reverse osmosis ; adsorption ; diffusion ; molecular dynamics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract Computer simulation studies using the method of molecular dynamics have been carried out to investigate osmosis and reverse osmosis in solutions separated by semi-permeable membranes. The method has been used to study the dynamic approach to equilibrium in such systems from their initial nonequilibrium state. In addition density profiles of both the solute and solvent molecules have been investigated, especially near the walls for adsorption effects. Finally the diffusion coefficients and osmotic pressure have also been measured. Our results show both osmosis and reverse osmosis, as well as a smooth transition between the two when either the solution concentration is changed, or the density (pressure) difference between the solvent and solution compartments is varied. We believe this new method can be used to improve our understanding of these two important phenomena at the molecular level.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Adsorption 2 (1996), S. 227-235 
    ISSN: 1572-8757
    Keywords: pillared clays ; heavy metal ions ; adsorption ; cation exchange capacity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract The effect of base treatment on the cation exchange capacity (CEC) of pillared clays and their adsorption isotherms for Cu2+, Cr3+ and Pb2+ have been investigated. Results indicate that although the CEC of pillared clays are only about 15% of that of the parent clays, a large fraction of the native clays CEC may be recovered by treatment with base. The fraction of the CEC recovered depends upon the base strength, its concentration, and the temperature. Contrary to previous suggestions the mechanism of recovery is related to the destruction of pillars which is accompanied by the loss of surface area. It is possible under conditions specified to prepare these base treated pillared clays as a new class of useful, regenerable adsorbent for heavy metal adsorption from aqueous solution.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 11
    Electronic Resource
    Electronic Resource
    Springer
    Adsorption 3 (1996), S. 107-115 
    ISSN: 1572-8757
    Keywords: adsorption ; molecular simulation ; isosteric heat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract Experimental measurements of adsorption yield the surface excess. The Gibbs surface excess is the actual or absolute amount of gas contained in the pores less the amount of gas that would be present in the pores in the absence of gas-solid intermolecular forces. Molecular simulation of adsorption yields the absolute amount adsorbed. Comparison of simulated adsorption isotherms and heats of adsorption with experiment requires a conversion from absolute to excess variables. Molecular simulations of adsorption of methane in slit pores at room temperature show large differences between absolute and excess adsorption. The difference between absolute and excess adsorption may be ignored when the pore volume of the adsorbent is negligible compared to the adsorption second virial coefficient (V≪B 1s ).
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 12
    Electronic Resource
    Electronic Resource
    Springer
    Adsorption 3 (1997), S. 189-195 
    ISSN: 1572-8757
    Keywords: Dubinin-Radushkevitch equation ; Dubinin-Astakhov equation ; adsorption ; micropore adsorption
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract The Dubinin-Radushkevitch (D-R) equation, which was originally proposed as an empirical adaptation The Polanyi adsorption potential theory, has been the fundamental equation to quantitatively describe the adsorption gases and vapors by microporous sorbents. The equation, based on the postulate that the mechanism for adsorption in micropores is that of pore-filling rather than layer-by-layer surface coverage, generally applies well to adsorption systems involving only van der Waals forces and is especially useful to describe adsorption on activated ???. The ability of the D-R equation to describe gas adsorption on porous materials has inspired many to undertake studies, both experimental and theoretical, to explain the source of the success of the D-R equation in ??? of molecular properties at the gas-solid interface. In many cases, these studies have led to extensions or modifications of the original D-R equation. Many of these attempts and the resulting extensions are reviewed and discussed here. Recently, an isotherm equation was derived for adsorption of gases and vapors on microporous ??? from statistical mechanical principles. It was shown that the D-R equation is an approximated form of this potential theory isotherm. This development is also reviewed and discussed.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 13
    Electronic Resource
    Electronic Resource
    Springer
    Adsorption 4 (1998), S. 25-33 
    ISSN: 1572-8757
    Keywords: hydrophobic zeolites ; breakthrough curves ; adsorption ; binary mixtures ; modeling ; overall mass transfer ; roll-up
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract Breakthrough curve measurements of SO2 and water vapor were carried out on a number of selected mordenite and pentasil zeolites from their binary and ternary mixtures with CO2 at 50 and 100°C. SO2 capacities of these samples were found to be significantly reduced by the presence of water. Competitive adsorption led to unusually high overshoot peaks of SO2 breakthrough curves. On the other hand, SO2 was found to displace water on the samples with very high silica to alumina ratio. A linear driving force, isothermal model was used to predict the breakthrough curves. Langmuir and extended Langmuir equilibrium models were used to describe the equilibrium properties of water and SO2, respectively. The overall mass transfer resistance obtained from the model was compared to the values calculated from a simplified biporous adsorbent model to shed some light on the adsorption kinetics.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 14
    Electronic Resource
    Electronic Resource
    Springer
    Adsorption 5 (1999), S. 183-192 
    ISSN: 1572-8757
    Keywords: adsorption ; activated carbon ; neural network ; ideal adsorption solution theory
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract Three neural network models were used for prediction of adsorption equilibria of binary vapour mixtures on an activated carbon. The predictions were compared both with published experimental data and calculated values from the Ideal Adsorption Solution (IAS) model. The neural network was trained using both binary and single component experimental adsorption data. Even for a limited number of data points (about 60) the network models were capable of approximating experimental data very precisely.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 15
    Electronic Resource
    Electronic Resource
    Springer
    Adsorption 5 (1999), S. 261-278 
    ISSN: 1572-8757
    Keywords: adsorption ; concentrated systems ; pressure transients ; flow transients
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract A study of the occurrence of large pressure and flow transients when a strongly adsorbed gas is fed to a column which is initially loaded with a lightly adsorbed gas is presented here. Under certain conditions, these transients can cause premature breakthrough and change the shape of the breakthrough curve. This will result in improper estimation of adsorption parameters by the dynamic column loading method and lower apparent adsorption capacity in a full scale unit. A data acquisition system was used to record the pressure and flow transients. An isothermal PDE model developed to study these transients agreed reasonably well with the nonisothermal experimental results. The PDE model predicts that pressure and flow transients will occur during step and pulse~tests conducted to obtain adsorption and mass transfer parameters by the chromatographic method. For instance, lower adsorption capacity will be realized during step tests due to lowering in column pressure. Oscillations were observed when columns are connected in series. The PDE model also predicts these oscillations. Simulations indicate that the extent of oscillations is dependent on the dead volume between columns.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 16
    ISSN: 1572-879X
    Keywords: methane ; adsorption ; hydroxyl groups ; H-D exchange reaction
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Infrared investigations on the interaction of methane with silica, aluminas (η,γ and α) and HZSM-5 zeolite have been carried out. At low temperature (173 K), methane adsorption was observed over these oxides and HZSM-5 zeolite. Our findings featured that the infrared inactiveΝ 1 band (2917 cm−1) of a gaseous methane molecule became active and shifted to lower frequencies (2900 and 2890 cm−1) when it adsorbed on the surfaces of these adsorbents. Our results also demonstrate that hydroxyl groups played a very important role in methane adsorption over the acidic oxides and the HZSM-5 zeolite. When interaction between the hydroxyl groups and methane took place, the band shift of the hydroxyl groups varied with different oxides. The strength of the interaction decreased according to the following sequence, Si-OH-Al〉Al-OH〉Si-OH, which is in accordance with the order of their acidities. At higher temperatures, methane interacted quite differently with various oxides and HZSM-5 zeolite. It has been observed that the hydroxyl groups of silica, γ-alumina and HZSM-5 zeolite could exchange with CD4 at temperatures higher than 773K, while those on η-alumina could exchange at a temperature as low as 573 K. Another interesting observation was the formation of formate species over Al2O3 (both η and γ) at temperatures higher than 473 K. The formate species would decompose to CO2, or produce carbonate at much higher temperatures. Formation of formate species was not observed over silica and HZSM-5 under similar conditions, α-Al2O3 did not adsorb or react with methane in any case.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 17
    ISSN: 1572-879X
    Keywords: carbon dioxide ; adsorption ; reduction ; dissociation ; 12-tungstophosphoric acid ; 12-molybdophosphoric acid
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract 12-tungstophosphoric and 12-molybdophosphoric acids are capable of sorbing and reducing CO2 without the presence of added reductants. The adsorbed CO2 (physisorbed as CO2) desorbs from the acids and salts at low temperatures (50–200°C). Carbon dioxide also desorbs only from the acids at high temperatures (500–600°C), suggesting the direct or indirect involvement of the protons in the process and the importance of the Keggin unit as well. Raman and DRIFTS results show that the species responsible for the evolution of CO2 (at high temperatures) are carbonaceous in nature. Carbon deposits extract the anionic oxygen atoms from the Keggin units during the high-temperature desorption process. The extraction of anionic oxygen atoms by carbon is confirmed using labeled carbon dioxide. The spectroscopic data imply that carbon exists on the surface as such but, additionally, as either carbon or CO2 bound to the terminal oxygen atoms of the Keggin anion.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 18
    Electronic Resource
    Electronic Resource
    Springer
    Catalysis letters 53 (1998), S. 215-220 
    ISSN: 1572-879X
    Keywords: FT‐IR ; adsorption ; butene ; ZSM‐5 ; mordenite
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Reactions of cis‐ and trans‐2‐butene adsorbed on deuterated ZSM‐5 and mordenite were studied by IR spectroscopy below 300 K. 2‐butene molecules hydrogen‐bonding to Brønsted acid sites (OD) reacted when the temperature was increased above 250 and 230 K on D‐ZSM‐5 and D‐mordenite, respectively. H/D isotope exchange reaction of Brønsted acidic hydroxy groups accompanied the isomerization of cis‐ to trans‐2‐butene, and then dimerization of trans‐2‐butene followed on ZSM‐5, while rapid formation of paraffinic alkoxy groups was dominantly observed on mordenite.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 19
    Electronic Resource
    Electronic Resource
    Springer
    BioMetals 9 (1996), S. 169-175 
    ISSN: 1572-8773
    Keywords: bacteria ; adsorption ; uptake ; metals
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Passive and active accumulation of zinc and cadmium by a common soil and freshwater bacterium, Cytophaga johnsonae, was studied using a radio-tracer batch distribution technique. The effects of variation of pH (3–10), as well as of ionic strength (0.007 and 0.07 m) on passive accumulation of the metals were examined. For both zinc and cadmium, accumulation was mainly due to passive processes, such as surface adsorption and/or diffusion into the periplasm. However, at low zinc concentrations, accumulation increased when glucose was added, suggesting an active uptake; at higher zinc concentrations such uptake was not detected, probably because it was masked by the stronger sorption properties of the cell wall. Adsorption of the metals was pH dependent: at higher ionic strength, accumulation was enhanced at pH values above 7; at lower ionic strength, adsorption differed and was markedly higher, with increased accumulation between pH 5 and 8.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 20
    ISSN: 1572-879X
    Keywords: Brønsted acidity ; FTIR ; 1 H MAS NMR ; adsorption ; zeolites
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The influence of the Si/Al ratio, of the nature of the T-atom and of the pore size on the acidic strength of Brønsted sites in zeolites has been investigated using changes of the vibrational properties of Brønsted OH(OD) groups and a shift change of Brønsted protons in nuclear magnetic resonance upon adsorption of weak bases. Deuterated acetonitrile and trichloro-acetonitrile have been chosen to probe the acidic strengths of ZSM-5, FeZSM-5, mordenite and zeolite Y, which are often used as catalysts. From the results of the FTIR and 1 H MAS NMR studies it can be concluded that the chemical composition of the lattice dominates the acidic strength of the Brønsted sites in zeolites. Differences in structure or pore size play a much smaller role.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 21
    ISSN: 1572-879X
    Keywords: solid oxide fuel cells ; fuel reforming anodes ; steam reforming ; methane ; nickel ; yttria-stabilised zirconia ; temperature-programmed oxidation ; adsorption ; surface carbon
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The activation energy for the removal of surface carbon formed by methane decomposition following high-temperature reforming, from a nickel/zirconia solid oxide fuel cell (SOFC) anode has been calculated using two methods based on temperature-programmed oxidation. It is found that there is a fairly good agreement between the two methods. In addition, it was observed that the addition of small quantities of lithium to the anode resulted in a significant lowering of the activation energy for surface carbon removal by about 50 kJ mol-1.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 22
    ISSN: 1572-8838
    Keywords: photovoltaic cells ; photoelectrochemical cells ; vapour-deposited electrodes ; PcZn thin films ; MePTCDI thin films ; electrode kinetics ; adsorption
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Electrical Engineering, Measurement and Control Technology
    Notes: Abstract As a direct comparison to all-solid state photovoltaic cells, photoelectrochemical cells consisting of n-type N,N′-dimethyl-3,4,9,10-perylenetetracarboxylic acid diimide (MePTCDI) and p-type phthalocyaninatozinc(ii) (PcZn) thin film electrodes vapour-deposited onto ITO have been investigated in aqueous ferri/ferrocyanide, p-benzoquinone/hydroquinone or I3−/I− electrolytes. The ferri/ferrocyanide cell has been studied in more detail, and the results are discussed with regard to the HOMO-, LUMO- and Fermi-energies of the materials used. A setup of the electrodes in a tandem cell could increase the efficiency of the cell due to improved light harvesting. Saturation of the photocurrent with increasing ferri/ferrocyanide electrolyte concentration at single PcZn or MePTCDI electrodes is discussed using a model of reactant adsorption prior to the charge transfer step. In addition, a decrease observed for the open-circuit voltage of the entire cell with increasing ferri/ferrocyanide concentration leads to an optimum concentration of 10−3 moldm−3.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 23
    Electronic Resource
    Electronic Resource
    Springer
    Topics in catalysis 3 (1996), S. 169-194 
    ISSN: 1572-9028
    Keywords: density functional theory ; zeolites ; adsorption ; hydrogen bonding ; water ; methanol ; ammonia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Non-local density functional theory has been used to investigate the adsorption of water, methanol and ammonia on cluster representations for zeolites. Only in the case of ammonia is the chemisorbed ion pair complex found to be a minimum, while binding energies are close to the lower bounds of experimental values. Large frequency shifts are found for hydroxyl stretching modes, particularly as the loading of adsorbate is increased.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 24
    ISSN: 1572-8757
    Keywords: micropore size distribution ; activated carbon ; adsorption ; desorption ; equilibrium ; kinetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract This paper deals with the prediction of adsorption equilibrium and kinetics of hydrocarbons onto activated carbon samples having different micropore size distribution (MPSD). The microporous structure of activated carbon is characterised by the distribution of slit-shaped micropores, which is assumed to be the sole source of surface heterogeneity. The interaction between adsorbate molecule and pore walls is described by the Lennard-Jones potential theory. Different adsorbates have access to different pore size range of activated carbon due to the size exclusion, a phenomenon could have a significant influence on both multicomponent equilibria and kinetics. Activated carbons with three different MPSDs are studied with ethane and propane as the two model adsorbates. The Heterogeneous Macropore Surface Diffusion model (HMSD) is employed to simulate adsorption kinetics. The simulation results show that the MPSD is an important factor affecting both the multicomponent equilibria and kinetics.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 25
    ISSN: 1572-879X
    Keywords: NO ; adsorption ; Cu-ZSM-5 ; TPD ; nitrosopropane ; N2O
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A surface intermediate with a C/N ratio close to 3 has been shown by TPD to form at co-adsorption of NO and propane as well as NO, propane and O2 on low-exchanged Cu-ZSM-5. The adsorption of NO, propane and oxygen has been studied to evaluate their effect on the formation of this complex. Its formation is accompanied by a decrease in the concentration of surface nitrite–nitrate. The kinetics of nitrite–nitrate adspecies formation as a function of the reagents concentration and temperature has been investigated. Some NO adspecies have been found to decompose yielding N2O.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 26
    ISSN: 1572-879X
    Keywords: microcalorimetry ; carbon monoxide ; adsorption ; platinum ; DFT
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Microcalorimetric measurements were conducted at 573 K of CO adsorption on Pt clusters supported in L-zeolite. The measured heat of CO adsorption is 175 kJ/mol, and the heat decreases to 90 kJ/mol near saturation coverage. Quantum chemical calculations were performed using density functional theory to study the interaction of CO with 10-atom Pt clusters. The heat of CO adsorption on atop-sites is calculated to be 209 kJ/mol, while a lower heat of 142 kJ/mol is calculated for CO on bridge-sites. These values decrease to 197 and 102 kJ/mol for population of two atop-sites and two bridge-sites, respectively, on the same Pt10 cluster. The heat of adsorption decreases to 157 kJ/mol when six CO molecules adsorb on six atop-sites of the cluster. The calculated initial heat of CO adsorption on Pt10 clusters is in agreement with experimental and theoretical values reported for CO adsorption on Pt single-crystal surfaces. The higher heat of CO adsorption at atop-sites may be caused by more σ-donation from CO to sp orbitals of Pt for atop-sites. The heat of CO adsorption on bridge-sites becomes higher on negatively charged platinum clusters. The calculated C-O stretching frequencies for charged and neutral platinum clusters agree with experimental data.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 27
    ISSN: 1572-879X
    Keywords: nitrogen dioxide ; titania ; propene ; selective oxidation ; adsorption
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Titania pretreated with NO2 has been found to catalyze the partial oxidation of propene into oxygenates such as acetone and acrolein at around 623 K, while fresh TiO2 produces only carbon oxides. Temperature‐programmed desorption (TPD) revealed that nitrogen oxides adsorbed on TiO2 are stable at temperatures below 673 K. Even after the propene oxidation at 573 K for 2 h, nitrogen oxides were confirmed still to exist on the TiO2 surface. At temperatures higher than 673 K, however, the desorption and/or the reduction of the adsorbed nitrogen oxides took place, and concomitantly the catalytic ability giving oxygenates disappeared.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 28
    ISSN: 1572-879X
    Keywords: adsorption ; adsorption isotherms ; dinitrogen ; FTIR spectroscopy ; geminal species ; NaY ; nitrogen ; zeolites
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Adsorption of N2 on NaY zeolites at 85 K and equilibrium pressures higher than 1 kPa results in the formation of geminal dinitrogen complexes characterized by an IR band at 2333.5 cm−1 (2255.4 cm−1 after adsorption of 15N2). With decreasing equilibrium pressure the complexes tend to loose one N2 ligand, thus forming linear species characterized by an IR band at 2336.8 cm−1 (2258.7 cm−1 after adsorption of 15N2). All species disappear completely after evacuation. Co-adsorption of N2 and CO revealed that the dinitrogen complexes are formed on Na+ cations. The changes in the concentrations of the linear and geminal N2 species with the changes in the equilibrium pressure are excellently described by equations of adsorption isotherms proposed earlier for mono- and di-carbonyls.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 29
    ISSN: 1572-879X
    Keywords: hydrogen ; copper ; activation energy ; adsorption ; sticking probability
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The coverage-dependent sticking probabilities of molecular hydrogen on polycrystalline copper supported on alumina have been determined in the temperature range 213–273 K by analysis of the hydrogen frontal adsorption line shape. In this temperature range the initial sticking probabilities increase from 8× 10−13 (213 K) to 1.3× 10−10 (273 K). The overall activation energy to adsorption has been found to be 42 kJ mol−1. The application of reactive frontal chromatography for the measurement of hydrogen sticking probabilities on copper is a novel variant of the N2O reactive frontal chromatographic method, developed for the measurement of copper surface areas. Its use here shows that reactive frontal chromatography may be applied generally to any adsorbate/adsorbent system involving activated adsorption and low sticking probabilities.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 30
    Electronic Resource
    Electronic Resource
    Springer
    Catalysis letters 60 (1999), S. 1-9 
    ISSN: 1572-879X
    Keywords: microcalorimetry ; IR ; platinum ; gold ; ethylene ; CO ; adsorption ; quantum chemical calculations ; DFT
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Ethylene adsorption on a Pt/Au/SiO2 catalyst (2 wt% Pt; Au/Pt atomic ratio of 10) was studied using adsorption microcalorimetry and FTIR spectroscopy. Ethylene adsorption at 300 K on Pt/Au/SiO2 produced π‐bonded, di‐σ‐bonded, and ethylidyne species with an initial heat of 140 kJ/mol, compared to a heat of 157 kJ/mol for Pt/SiO2 on which only ethylidyne species formed. At 203 and 263 K, ethylene adsorbed on Pt as well as on Au surface atoms for the Pt/Au/SiO2 catalyst. Quantum chemical, DFT calculations indicate that Au exerts a significantly smaller electronic effect on Pt than does addition of Sn to Pt.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 31
    Electronic Resource
    Electronic Resource
    Springer
    Catalysis letters 61 (1999), S. 7-13 
    ISSN: 1572-879X
    Keywords: sum‐frequency spectroscopy ; Pt(111) ; carbon monoxide ; adsorption ; far‐infrared ; free‐electron laser
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Sum‐frequency spectroscopy (SFS) was used in an attempt to detect the platinum–carbon vibration of CO adsorbed on Pt(111). The international free‐electron laser FELIX at the FOM Institute, Rijnhuizen, provided the required tunable far‐infrared (19–23 µm) source, while complementary measurements in the C–O stretch region (4.7–5.1 µm) were performed at the University of Oxford with a conventional nanosecond laser system. Ordered Pt(111) surfaces were prepared by the H2/O2 flame annealing approach and CO monolayers were produced by exposure of the Pt crystal to gaseous CO in a flow reactor. The monolayers were characterized by sum‐frequency (SF) measurements of the v C-O vibrational frequency. The CO adsorbed primarily in the terminal (atop) configuration, with a v C-O frequency of around 2078 cm−1. In the far‐IR region, the non‐resonant background from the Pt substrate could readily be detected by SFS, but there was no evidence for the v Pt-CO mode. Direct laser‐induced desorption and thermal desorption of CO are unlikely under the experimental conditions. It is therefore probable that the intrinsic cross‐section of the Pt–CO mode is too low for easy detection by SFS. The implications for the use of SFS to detect metal–adsorbate vibrational modes are discussed in light of these findings.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 32
    ISSN: 1572-879X
    Keywords: Fe‐ZSM‐5 ; carbon monoxide ; FTIR spectroscopy ; nitrates ; nitrogen monoxide ; selective catalytic reduction ; adsorption ; zeolites
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Adsorption of NO on Fe‐ZSM‐5 leads to formation of Fen+–NO (n = 2 or 3) species (1880 cm-1), Fe2+(NO)2 complexes (1920 and 1835 cm-1) and NO+ (2133 cm-1). Water strongly suppresses the formation of NO+ and Fen+(NO)2 and more slightly the formation of Fen+ –NO. Introduction of oxygen to NO converts the nitrosyls into surface nitrates (1620 and 1575 cm-1) and this process is almost unaffected by water. The nitrates are thermally stable up to ca. 300°C, but readily interact with propane at 200°C, thus forming surface C–H–N–O deposit (bands in the 1700–1300 cm-1 region). Here again, water does not hinder the process. The C–H–N–O deposit is relatively inert (it does not interact with NO or NO + O2 at ambient temperature) but, at temperatures higher than 250 °C, it is decomposed to NCO- species (bands at 2215 (Fe–NCO) and 2256 cm-1 (Al–NCO)). In the presence of water, however, the Fe–NCO species only are formed. At ambient temperature the NCO- species are inert towards NO and O2, but easily react with a NO + O2 mixture. The mechanism of the selective catalytic reduction of nitrogen oxides on Fe‐ZSM‐5 and the effect of water on the process are discussed.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 33
    ISSN: 1572-8757
    Keywords: wool ; water vapour ; adsorption ; diffusion ; column dynamics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract Adsorption of water vapour on wool provides not only textile comfort, but also convenience in transportation due to increase in its bulk density. The adsorption and desorption isotherms of water vapour for wool were determined by both volumetric technique using a Coulter Omnisorp 100CX instrument and gravimetric method employing a Cahn 2000 electronic microbalance. Adsorption isotherm fitting to B.E.T. model and hysteresis on desorption was observed. The average effective diffusion coefficient of water in wool was found to be 8.4 × 10-14 m2s-1 at 25°C from gravimetric data. The effects of packing height and air velocity on the breakthrough curves were also investigated in the wool packed columns. For pseudo first order model, k values changing between 0.33 × 10-6 − 69 × 10-6 s-1 was obtained for 2.2–6.4 cm s-1 air velocity and 0.05–0.20 m packing height ranges.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 34
    ISSN: 1572-8757
    Keywords: adsorption ; molecular simulation ; activated carbon ; surface oxygen ; alkaloids
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract The influence of the density and the type of surface oxygen on the adsorption of berberine alkaloid onto activated carbon was investigated using the molecular dynamics simulation method in vacuum. The carbon surface consisted of a basal plane of graphite and surface oxygen groups which were bonded on the graphite plane in a regular square array with various densities. Two types of surface oxygen groups, =O and —OH, were employed. The simulation results showed that the berberine alkaloids were favorable to be adsorbed on the negative charged carbon surfaces. It was indicated that the vdw attraction of the carbon surface to the alkaloid molecule dominates the adsorption only at the lower surface density of oxygen. It is also indicated that a good adsorptive selectivity for a certain berberine alkaloid can be obtained by controlling the density of surface oxygen. The adsorption simulation of berberine alkaloids onto activated carbon in the presence of water was also carried out by using a dome-shape molecular model for presenting the alkaloid/water/carbon system. It was found that the adsorption of berberine alkaloids on the activated carbon which has a higher density of surface oxygen was strongly inhibited by the presence of water.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 35
    ISSN: 1572-8757
    Keywords: kinetics ; isotope-exchange ; nitrogen ; adsorption ; methane ; zeolite ; equilibria
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract The Isotope Exchange Technique (IET) was used to simultaneously measure pure and binary gas adsorption equilibria and kinetics (self-diffusivities) of CH4 and N2 on pelletized 4A zeolite. The experiment was carried out isothermally without disturbing the adsorbed phase. CH4 was selectively adsorbed over N2 by the zeolite because of its higher polarizability. The multi-site Langmuir model described the pure gas and binary adsorption equilibria fairly well at three different temperatures. The selectivity of adsorption of CH4 over N2 increased with increasing pressure at constant gas phase composition and temperature. This curious behavior was caused by the differences in the sizes of the adsorbates. The diffusion of CH4 and N2 into the zeolite was an activated process and the Fickian diffusion model described the uptake of both pure gases and their mixtures. The self-diffusivity of N2 was an order of magnitude larger than that for CH4. The pure gas self-diffusivities for both components were constants over a large range of surface coverages (0 〈 θ 〈 0.5). The self-diffusivities of CH4 and N2 from their binary mixtures were not affected by the presence of each other, compared to their pure gas self-diffusivities at identical surface coverages.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 36
    Electronic Resource
    Electronic Resource
    Springer
    Adsorption 5 (1999), S. 159-167 
    ISSN: 1572-8757
    Keywords: impedance spectroscopy ; uptake curve ; adsorption ; polarization of adsorbate ; dielectric properties of adsorbed phases
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract Physisorption equilibria of gases on inert porous solids like activated carbon or molecular sieves can be characterized by measuring the (frequency dependent) capacitance of a capacitor filled with a sample adsorbent. This quantity strongly depends not only on the physico-chemical structure of the empty adsorbent in vacuum, but also on the permanent or induced dipole moments of the molecules adsorbed and of the fluid phase. Consequently, it should be possible to determine the excess mass being adsorbed on the internal surface of a highly porous solid by measurements of the dielectric constant. The aim of this work is to show for various pure gases and adsorbents that the change of the capacitance of an adsorption system depends on the adsorbed mass. Therefore, this effect can be used to characterize porous solids and their adsorbates and, for example, to check the state or the quality of industrial adsorbents during a process on site if calibration measurements have been taken (Staudt et al., 1994, 1998).
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 37
    ISSN: 1572-8757
    Keywords: zeolites ; polar compounds ; adsorption ; adsorption isotherms ; equilibrium ; liquid phase ; breakthrough curves ; acetonitrile ; acrylonitrile ; dioxane ; ZSM-5 ; MCM-22 ; Na-X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract The liquid phase removal of low concentrations of polar compounds (acetonitrile, acrylonitrile and dioxane) from toluene by adsorption on zeolites reveals very high selectivity factors. Kinetic selectivity factors as high as 16,100 are observed. The selection of the zeolites (MFI, MWW and FAU type) allowed the study of the effects of varying aluminum content, the presence and absence of acidic centers and varying pore volumes. To assess the relative effectiveness of each adsorbent, both equilibrium and continuous flow, pseudo equilibrium, breakthrough experiments were conducted. The continuous flow experiments were carried out at 25 and 75°C. The zeolites H-ZSM-5, H-MCM-22 and Na-X are highly effective in removing the polar compounds from toluene to a concentration level down to less than 20 ppm (detection limit). The results obtained with the equilibrium batch experiments are confirmed by the continuous flow breakthrough experiments.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 38
    Electronic Resource
    Electronic Resource
    Springer
    Microchimica acta 126 (1997), S. 159-166 
    ISSN: 1436-5073
    Keywords: polyethylene ; adsorption ; preconcentration ; aluminium ; thallium ; beryllium ; chrome azurol S ; rhodamine B
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Polyethylene powder has been shown to function effectively as an adsorbent for the preconcentration of complexing agents and their metal complexes. The adsorbed trace compound can easily be eluted from the polyethylene by use of polar organic solvents and subsequently be determined by AAS or spectrophotometry. In this paper, the adsorptivity of chrome azurol S and rhodamine B and their complexes with aluminium, beryllium and thallium (as [Tl Br4]−) on polyethylene was investigated. The influence of the pH and the effect of the saline concentration of the solution were studied. From the preconcentration of aluminium and beryllium with chrome azurol S, enrichment factors up to 10 and 20, respectively, could be achieved. For thallium with rhodamine B the factor was 50. With this analytical procedure, recoveries of 92–110%, 94–103% and 96–104% with relative standard deviations of 3.4–5.4%, 2.6–5.3 and 1.6–7.2% for aluminium, beryllium and thallium respectively, were achieved. The method was used for the preconcentration of trace amounts of the metals from tap water, dialysis solutions and solid salts.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 39
    ISSN: 1436-5073
    Keywords: porphyrin ; adsorption ; quartz ; piezoelectric ; sensor
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The adsorption behavior of 5,10,15,20-tetrakis (4-N-methylpyridiniumyl)-porphyrin (H2TMPyP) from aqueous solutions onto a quartz crystal interface was investigated in situ using an electrode-separated piezoelectric sensor (ESPS). With H2TMPyP adsorbed onto quartz crystal surface of the ESPS, its oscillating frequency decreases linearly with increasing adsorption amount. The adsorption densities obtained in the ESPS method were greater than those determined in a solution depletion method. The influence of surface roughness of quartz crystal and bulk solution properties on the measurement of adsorption density in the ESPS method was discussed.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 40
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular modeling 3 (1997), S. 315-320 
    ISSN: 0948-5023
    Keywords: Keywords: Molecular Dynamics simulation ; adsorption ; isotherm ; hydrocarbon ; graphite
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract We perform Molecular Dynamics simulations of thin hydrocarbon films adsorbed on the basal plane of graphite to determine structural and thermodynamic properties. Specifically we study the behaviour of liquid benzene/n-heptane mixtures. The intra adsorbate and the adsorbate-substrate interactions are described using a phenomenological force field whose careful parameterization will be reported in a following paper. The foremost quantity we calculate is the adsorption isotherm, i.e. the surface excess concentration as a function of the benzene bulk mole fraction at T = 283 K, which is in quite reasonable agreement with the experiment. Along with the isotherm we compare the surface induced ordering of the two components in terms of order parameter profiles.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 41
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular modeling 3 (1997), S. 347-354 
    ISSN: 0948-5023
    Keywords: Keywords: Molecular dynamics ; Monte Carlo ; adsorption ; water ; sodium chloride ; calcium carbonate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The intention of this work is to aid the construction of a water model capable of describing bulk water in contact with ionic surfaces. The model should be sufficiently simple to be useful for simulating large systems. Here, the extended simple point charge (SPC/E) water model, which is one of the most commonly used descriptions of bulk water, was tested in a strongly heterogeneous system. Simulations were carried out on the NaCl(100) and the calcite(10¯14) surfaces, described in terms of Lennard-Jones and Coulomb potentials. On the NaCl surface Molecular Dynamics simulations show that SPC/E water forms clusters due to its high permanent dipole moment. Better agreement with the experimental adsorbate structure was achieved by reducing the water dipole moment to its gas phase value. On the calcite surface adsorption isotherms were simulated using a Molecular Dynamics-Monte Carlo hybrid technique, which consists of a normal Molecular Dynamic simulation with randomly chosen insertion and removal Monte Carlo steps repeated after a constant time period. The method is tested by calculating adsorption isotherms for two Lennard-Jones systems, i.e. methane in contact with the graphite basal plane and with the zeolite silicalite (ZSM5), for which we obtain excellent agreement with the experimental isotherms. For calcite, however, the simulated adsorption isotherms again show a strong dependence on the choice of the dipole moment. The SPC/E value yields a strongly exaggerated coverage, whereas the gas phase value severely underestimates the coverage in comparison with the experiment. From our results we draw the conclusion that a fixed charged model is not recommendable for the simulation on ionic surfaces, and that it is highly desirable to include variable polarization.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 42
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 48 (1997), S. 741-754 
    ISSN: 1572-8943
    Keywords: adsorption ; calorimetry ; differential heat ; micropore ; xylenes ; Y faujasites
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The differential enthalpies of adsorption ofp-xylene andm-xylene on NaY, KY and BaY zeolites were measured by isothermal calorimetry coupled with isothermal volumetry at 25
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 43
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 46 (1996), S. 417-429 
    ISSN: 1572-8943
    Keywords: adsorption ; aluminium oxide ; silica gel ; ternary mixtures
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Formation of mixed adsorbed layers was tested for ternary liquid mixtures containing methanol or acetone and the binary solvent benzene+n — heptane. The specific excess adsorption isotherms from the liquid phase were measured on silica gel, silanized silica gel and aluminium oxide. The experimental adsorption data are discussed on the basis of the changes in the mixed solvent composition.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 44
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 49 (1997), S. 541-552 
    ISSN: 1572-8943
    Keywords: adsorption ; bimetallic ; catalyst ; microcalorimetry ; particle structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Microcalorimetric studies of oxygen and hydrogen chemisorption during the last decade improved the understanding of the structure and structural dynamics of supported bimetallic catalyst particles. For example, it was found that on graphitic supports two different reduced surface compositions/structures can be created for base metal/noble metal particles. Appropriate treatments “switch” the surface from almost pure reduced base metal to true alloy. Calorimetric studies also indicate support interactions play a major role in controlling bimetallic particle surface structure. In contrast to behaviour found on graphitic supports, iron/noble metal particles supported on refractory oxides apparently do not form alloy surfaces. The reduced surface is dominated by the noble metal. Several studies indicate the value of the models of surface composition/structure developed using microcalorimetry for predicting the activity/selectivity of bimetallic particles.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 45
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 50 (1997), S. 215-227 
    ISSN: 1572-8943
    Keywords: adsorption ; herbicide ; IR-spectroscopy ; montmorillonite ; soil ; s-triazine ; terbuthylazine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Adsorption of the herbicide terbuthylazine by a soil from the Jezreel Valley was investigated by thermo-IR-spectroscopy. The adsorption took place mainly by the clay mineral montmorillonite. The adsorbed molecule was hydrogen bonded via the aniline groups to water molecules which were coordinated to the exchangeable metallic cations. When the sample was thermally treated at 115°C interlayer water was evolved, part of the herbicide decomposed and the other part became directly coordinated to the exchangeable metallic cations. The decomposition product contained a CO group.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 46
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 50 (1997), S. 257-268 
    ISSN: 1572-8943
    Keywords: adsorption ; alachlor ; degradation ; montmorillonite
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The adsorption of the tertiary aromatic amide alachlor by Na-montmorillonite and Al-polyhydroxy-montmorillonite was investigated by DTA, XRD, SEM and Thermo-FTIR Spectroscopy. This molecule is adsorbed into the interlayer space of the montmorillonite, replacing interlayer water. In this organo-clay complex the interlayer water forms hydrogen bonds with N or O atoms of the tertiary amide group. Samples which were aged during six months degraded by hydrolysis to give mainly secondary amide. This reaction was catalysed by Al-polyhydroxy-montmorillonite more than by Na-montmorillonite.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 47
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 55 (1999), S. 1011-1020 
    ISSN: 1572-8943
    Keywords: adsorption ; adsorption calorimetry ; microporous carbon ; porosity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The fundamental empirical relationships that correlate the adsorption energy with physicochemical parameters of adsorbates are discussed. Based on the experimental data of the adsorption enthalpy of different organic adsorbates on microporous activated carbons some new correlations between adsorption enthalpy and entropy at zero surface coverage and physicochemical parameters of adsorbed molecules are proposed. It is shown that they can be applied for the calculation of carbon porosity. The influence of carbon surface oxidation on its energetic heterogeneity is also discussed.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 48
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 57 (1999), S. 643-651 
    ISSN: 1572-8943
    Keywords: adsorption ; heat capacity ; solid-liquidinterface ; solid monolayer
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Heat capacity measurements have been made to investigate the formation of two solid monolayers each of n-pentane, n-heptane and n-dodecane adsorbed on graphite, one at submonolayer coverages and the other coexisting with the liquid. At submonolayer coverages the monolayers are found to melt respectively at 99.8, 151.6, and 217.3 K, well below the bulk melting points. The monolayers coexisting with the liquid melted at 205.6 for heptane and at 287.8 K for dodecane, whereas no evidence was obtained for pentane on the formation of such solid monolayer above the bulk melting point. The order persisting in the liquid near the interface depends upon the length of the molecules. The dodecane monolayers showed another transitions below the melting points both at submonolayer and multilayer coverages.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 49
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 54 (1998), S. 333-342 
    ISSN: 1572-8943
    Keywords: active carbon ; adsorption ; enthalpies of wetting ; isothermal calorimetry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Enthalpies of wetting of two active carbons and one brown coal coke by several pure liquids (mainly homologous series) were measured at 298.15 K with two quasi-isothermal microcalorimeters. Different measuring cells with cavities of about 0.5 and 15 cm3 were used. The advantage of the larger measuring cell with three independent 15 cm3 cavities is the higher mass of active carbon, leading to a high reproducibility with standard deviations below 1% and a reduced measuring time. Experiments were carried out with n-alkanes, l-alkanols, cycloalkanes and isomers thereof, i.e. 2-propanol, methylcyclohexane, 2,2,4-trimethylpentane (isooctane and 2-ethyl-1-hexanol, and water. Like the polarity, the size and the three-dimensional expansion of the molecules, the energetic and geometric heterogeneity of the adsorbent influences the enthalpy of wetting.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 50
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 56 (1999), S. 323-330 
    ISSN: 1572-8943
    Keywords: adsorption ; balance ; gravimetry ; sorption ; thermoporometry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The results of surface structure investigations involving the use of thermoporometry and gas-sorptometry on porous glass, silica and a zeolite were compared. The most frequent and the mean pore width were found to be in accordance, but major differences in specific surface were observed. These two measuring methods complement each other, because with gas adsorption a dry sample is investigated, while with thermoporometry a sample immersed in a liquid is investigated. The probe molecules (nitrogen or noble gas and water or benzene, respectively) differ in size. The features of the two methods are discussed.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 51
    ISSN: 1572-8943
    Keywords: adsorption ; calorimetry ; derivative enthalpy ; prediction ; selectivity ; single xylene ; xylene mixture ; zeolite
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The derivative enthalpies of adsorption of m-xylene and p-xylene onto the NaY and BaY zeolites were measured at 150°C, then compared with those obtained at 25°C, and finally used to predict the selectivity of adsorption of xylene mixtures. Significant differences were observed as the temperature was elevated: for the NaY zeolite, the adsorbate-adsorbate interactions became prevalent, in contrast with the BaY zeolite, between zeolite and derivative interactions were stronger. The difference between the adsorption derivative enthalpies of the two xylenes displayed an abrupt variation from 2 molec. α−1 for both zeolites, the filling from which selectivity towards m-xylene for the NaY zeolite and towards p-xylene for the BaY zeolite appeared. The preferentially adsorbed xylene was closely connected with the sense of this difference, which changed with the zeolite.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 52
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 49 (1997), S. 1399-1408 
    ISSN: 1572-8943
    Keywords: activated carbon ; adsorption ; sodium ethyl xanthate ; thermal decomposition
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The thermal decomposition of SEX in a nitrogen atmosphere was studied by coupled thermogravimetry-Fourier transform infrared spectroscopy (TG-FTIR), and by pyrolysis-gas chromatography-mass spectrometry (py-GC-MS). The TG curve exhibited two discrete mass losses of 45.8% and 17.8% respectively, at 200 and 257–364°C. The evolved gases identified as a result of the first mass loss were carbonyl sulfide (COS), ethanol (C2H5OH), ethanethiol (C2H5SH), carbon disulfide (CS2), diethyl sulfide ((C2H5)2S), diethyl carbonate ((C2H5O)2CO), diethyl disulfide ((C2H5)2S2), and carbonothioic acid, O, S, diethyl ester ((C2H5S)(C2H5O)CO). The gases identified as a result of the second mass loss were carbonyl sulfide, ethanethiol, and carbon disulfide. Hydrogen sulfide was detected in both mass losses by py-GC-MS, but not detected by FTIR. The solid residue was sodium hydrogen sulfide (NaSH). SEX was adsorbed onto activated carbon, and heated in nitrogen. Two discrete mass losses were still observed, but in the temperature ranges 100–186°C (7.8%) and 186–279°C (11.8%). Carbonyl sulfide and carbon disulfide were now the dominant gases evolved in each of the mass losses, and the other gaseous products were relatively minor. It was demonstrated that water adsorbed on the carbon hydrolysed the xanthate to cause the first mass loss, and any unhydrolysed material decomposed to give the second mass loss.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 53
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 54 (1998), S. 351-361 
    ISSN: 1572-8943
    Keywords: active carbon ; adsorption ; adsorption thermodynamics ; fractal dimension ; microporosity ; pore diameter ; potential theory
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A new adsorption isotherm equation based on the extension of the potential theory of adsorption on microporous fractal solids and corresponding thermodynamic functions were formulated and applied for description of the experimental data of adsorption on a microporous carbon. The comparison of the obtained results with the original Dubinin-Astakhov equation is presented. In this paper the dependence of thermodynamic functions (the differential molar enthalpy of adsorption ΔH and the differential molar entropy of adsorption ΔS) on the fractal dimension D are discussed, as well.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 54
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 58 (1999), S. 67-76 
    ISSN: 1572-8943
    Keywords: adsorption ; DRIFT spectroscopy ; elemental analysis ; γ-aminopropyl-trimethoxysilane ; thermogravimetric analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A comparative method based on thermogravimetry is applied in order to characterise chemically functionalised surfaces. The mass loss of silica modified with γ-aminopropyl-trimethoxysilane (γ-APS) adsorbed from a range of solvents is interpreted by considering the physically adsorbed water, the silanol groups and the organic solvent. DRIFT spectroscopy is used to analyse the binding structure and adsorption mechanism. The mass loss calculated from thermogravimetric analysis is found to be in agreement with the values obtained by classical elemental analysis. Thermogravimetric analysis is found to be a quick and reproducible method, which only requires a few milligram sample. The amount adsorbed seems to be primarily dependent on the solvation of the γ-aminopropyl-trimethoxysilane by the solvent. A good solvent prevents adsorption as shown when comparing the magnitude of the mass loss with the difference between the solubility parameters of the γ-APS and the solvents. Ethanol seems to influence the structure of the adsorbed γ-aminopropyl-trimethoxysilane film.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 55
    Electronic Resource
    Electronic Resource
    Springer
    Journal of sol gel science and technology 11 (1998), S. 185-195 
    ISSN: 1573-4846
    Keywords: cuprous chloride ; gamma-alumina ; adsorption ; ethylene ; carbon monoxide
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Cuprous chloride (CuCl) modified unsupported γ-alumina membranes and adsorbent granules were synthesized by sol-gel processing followed by wet-impregnation of CuCl. The CuCl coated γ-alumina remains mesoporous with a uniform pore size distribution and a large surface area. The mesoporous alumina granules, prepared by a sol-gel oil-drop process, exhibit excellent mechanical strength and attrition resistance. The CuCl modified γ-alumina preferentially adsorbs ethylene and carbon monoxide, with a saturated adsorption capacity of 0.67 and 0.78 mmol/g, respectively. Both equilibrium capacity and kinetic rate for adsorption of ethylene and carbon monoxide on the CuCl modified γ-alumina are much larger than those for ethane and carbon dioxide. These results indicate the potential use of the sol-gel derived CuCl modified γ-alumina for separation of ethylene or carbon monoxide from its gas mixture containing ethane or carbon dioxide.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 56
    Electronic Resource
    Electronic Resource
    Springer
    Journal of sol gel science and technology 7 (1996), S. 69-76 
    ISSN: 1573-4846
    Keywords: sol-gel ; bioactive ; protein ; adsorption
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Recent theories suggest that the local adsorption of biologically active peptide growth factors onto the surface of an implant may contribute to the unique osteogenic nature of silica-containing bioactive ceramics. A sol-gel derived glass is used as a model of the in-vivo reaction product of 45S5 bioactive glass at relatively short times (〈48 hrs.) to investigate protein adsorption/desorption behavior. The adsorption kinetics of three heme-class proteins (cytochrome c, myoglobin, and hemoglobin) are measured spectroscopically. The rate of adsorption is shown to increase with average pore size, which is determined by the silica content of the gel. Adsorption rate decreases as protein size is increased and as solution pH is decreased. Biological function of an adsorbed peroxidase enzyme on pre-reacted Bioglass® is shown to be retained. Desorption during physiologic conditions is shown to be linear with time and pH dependant, while independent of gel bioactivity.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 57
    Electronic Resource
    Electronic Resource
    Springer
    Topics in catalysis 9 (1999), S. 225-234 
    ISSN: 1572-9028
    Keywords: large pore zeolites ; alkylaromatics ; computations ; adsorption ; diffusion characteristics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Alkylation of aromatics over solid acid catalysts such as zeolites, has emerged in the recent past as a viable alternative to conventional Friedel–Crafts alkylation over environmentally hostile catalysts. We studied the diffusion behaviour of ethylbenzene (EB), isobutylbenzene (IBB), o-, m- and p-isobutylethylbenzene (IBEB) in various zeolites such as offretite (OFF), cancrinite (CAN), ZSM-12 (MTW) and ZSM-18 (MEI) by computational procedures. The periodic variations of interaction energy between the molecules and zeolite framework in the calculated diffusion energy profiles are used to predict the energy barrier for diffusion. We analyzed the results to understand the product selectivity in the formation of IBEB in the transalkylation/disproportionation reaction between IBB and EB. The results indicated that the zeolites with channel-like pores are more suitable than those with cage-like pores to achieve better selectivity. The zeolites with channels whose diameters are close to the dimensions of the molecules and those which do not have intersecting channels are better selective catalysts. The efficiency of shape selective production of p-IBEB in these zeolites will be in the order MEI 〈 OFF ∼ MTW 〈 CAN as predicted from their diffusion energy barriers. The detailed analysis of the configurations of the molecules in the most favourable and unfavourable adsorption location, indicate that the p-IBEB has favourable interaction energy in all the four zeolites with different pore architecture, compared to o- and m-IBEB except for MEI. It could be concluded that the pore architecture plays a dominant role in controlling the adsorption and diffusion characteristics of these molecules. The actual values of interaction energy themselves are indication of their adsorption behaviour inside the pores of the zeolite.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 58
    Electronic Resource
    Electronic Resource
    Springer
    Topics in catalysis 9 (1999), S. 235-250 
    ISSN: 1572-9028
    Keywords: Ziegler–Natta ; density functional theory ; adsorption ; polymerisation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Total energy pseudopotential calculations have been used to examine the adsorption of TiCl4 at both the 110 and 100 surfaces of magnesium chloride. Titanium(IV) chloride is found to bind most strongly on the 100 surface resulting in the formation of a complex with approximately trigonal bipyramidal coordination of titanium, which will dissociate to form TiCl 3 + and Cl− with an energy of 127.7 kJ mol−1. Cluster calculations indicate that this site only weakly binds ethene, but does catalyse the formation of C–C bonds with an activation energy consistent with experimental estimates.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 59
    Electronic Resource
    Electronic Resource
    Springer
    Topics in catalysis 9 (1999), S. 123-133 
    ISSN: 1572-9028
    Keywords: NO/Pd ; adsorption ; clusters ; DFT
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The interaction of NO with Pd clusters has been studied by means of the LCGTO-DF method. Metal cluster models (up to 13 atoms) with different size and geometry have been used to describe the atop, bridge and three-fold sites. The use of different model core potentials to increase the size of the cluster model treated and to save computational time has been discussed. The binding energies of N(1s), 4σ, 5σ and 1π electrons are calculated and compared directly to the experimental XPS and UPS data available. The NO is tilted with respect to the surface normal axis when adsorbed on top and bridge sites by about 52.6 and 46.7 degrees, respectively. On the two types of three-fold sites (hcp and fcc) the NO remains upright. The bending angle is very sensitive to the cluster size and affects the binding energies of N(1s), 4σ, 5σ and 1π orbitals. The NO adsorption energies on the different adsorption sites have been estimated using different cluster models. The vibrational frequencies have been calculated in the harmonic approximation and they are in reasonable agreement with the available experimental values. The cluster model approach is discussed in terms of its reliability to determine the adsorption energies and the favored site of adsorption.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 60
    Electronic Resource
    Electronic Resource
    Springer
    Russian chemical bulletin 45 (1996), S. 321-323 
    ISSN: 1573-9171
    Keywords: adsorption ; zeolite, crystal deformation ; high pressure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The deformation of pellets of crystalline zeofite NaX upon adsorption of Xe at pressures from 0.001 to 7 MPa and temperatures from 252.5 to 333 K was studied. In the temperature range studied, the relative linear deformation of zeolite crystals is negative in the initial adsorption region. When the adsorption of Xe increases, its value passes through a minimum and then increases sharply taking positive values at high adsorption volume filling of micropores.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 61
    Electronic Resource
    Electronic Resource
    Springer
    Russian chemical bulletin 45 (1996), S. 534-538 
    ISSN: 1573-9171
    Keywords: adsorption ; radius of a molecule ; adsorbent ; surface ; pore volume
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Equilibrium adsorption isotherms for Ar, Kr, and N2 on crystalline NaA zeolite were measured in the pressure range of 0.1–160 MPa and temperature range of 305–448 K. The method for determining the inaccessible volume of the adsorption system (free volume + micropore volume) and the micropore volume of a sorbent with the use of such adsorbates as monoatomic Ar and Kr and diatomic N2 was applied. The effective radii of N2 and O2 molecules were calculated from the dependence of micropore volume of the zeolite on the radius of the monoatomic gas used. On the basis of this result, one can determine the orientation of the molecules of nitrogen and oxygen in the pores of the zeolite, caused bysorption forces. The use of Ar and Kr as the adsorbates allows one to determine the total surface area of the zeolite, which was found to be equal to 1458 M2/g.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 62
    ISSN: 1573-9171
    Keywords: active carbons ; oxidation ; surface chemistry ; n-hexane ; water ; methanol ; adsorption
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The influence of oxidation by nitric acid on the character of oxygen-containing functional surface groups and porous structure of active carbons is considered. Adsorption properties of the initial and oxidized carbons are studied using adsorption isotherms of vapor of n-hexane and polar substances (water and methanol).
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 63
    Electronic Resource
    Electronic Resource
    Springer
    Russian chemical bulletin 45 (1996), S. 1230-1231 
    ISSN: 1573-9171
    Keywords: helium ; adsorption ; zeolite NaA ; adsorption isotherm ; adsorption heat ; Henry constant
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Isotherms of helium adsorption on zeolite NaA were measured by the volumetric method under static conditions at 23–50 K and pressures from 1 Pa to 65 kPa. The Henry constants and the initial heat of helium adsorption were calculated; the isosteric heat was calculated, and its dependence on the adsorption was determined.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 64
    Electronic Resource
    Electronic Resource
    Springer
    Russian chemical bulletin 45 (1996), S. 1307-1311 
    ISSN: 1573-9171
    Keywords: decationized zcolitcs ; adsorption ; IR spectra
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The IR spectra of decationized zeolites with adsorbed bases have been analyzed. A correlation between the shift Δη(OH) of the center of gravity of the set of bandsA,B, andC (components of the η(OH) vibration) and the strength of the H-bond between the bridging hydroxyl groups and the molecule of a base has been found. This is evidence in support of the Fermi-resonance nature of the perturbations of the η(OH) vibration. Spectral data on the adsorption of H2O and MeOH on decationized zcolitcs that cannot be interpreted in terms of the formation of complexes with strong H-bonds have been obtained. Arguments in favor of the formation of H3O+ and MeOH2 + ions linked to the neighboring oxygen atoms in the zeolitc latticevia two identical hydrogen bridges have been presented.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 65
    ISSN: 1573-9171
    Keywords: palladium hydrolysis ; polynuclear hydroxocomplexes (PHC) ; carbon material ; adsorption ; radial atomic distribution method ; X-ray phase analysis ; electron microscopy ; molecule structure modeling ; synthesis of microscopic images
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Adsorption of polynuclear palladium(ii) hydroxocomplexes (PHC) by carbon materials (CM) was studied. It was found that PHC are adsorbed from aqueous solutions without a change in their chemical composition and are composed of clusters (〈10 A) with metalmetal distances typical of the PdO chain structure. Three-dimensional ordered particles with the PdO structure were formed upon adsorption of PlIC on carbon materials at room temperature or after the PHC suspension was dried in air at 400 °C (the size of the particles was 15 and 25 A, respectively). Calculation of the electron-microscopic images of the adsorbed PHC with atomic resolution based on crystal structure modeling showed that PdO particles containing -100 palladium atoms is the final product after drying of the adsorbed PHC.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 66
    Electronic Resource
    Electronic Resource
    Springer
    Russian chemical bulletin 45 (1996), S. 1844-1848 
    ISSN: 1573-9171
    Keywords: adsorption ; differential heats ; excess adsorption ; absolute adsorption ; high pressures and temperatures
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Thermodynamic principles for the calculation of differential heats of excess and absolute adsorption were considered. A set of isosteres of excess adsorption of krypton on zeolite NaA are presented, from which the coverage and temperature dependences of the heats of excess adsorption are calculated and analyzed. The reasons for infinitely high values of the excess heats at finite values of adsorption are discussed. The problems of recalculation of the excess adsorption to absolute adsorption are considered.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 67
    ISSN: 1573-9171
    Keywords: zeolite-like aluminophosphates ; adsorption ; methanol ; IR spectra
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Electrostatic properties of zeolite-like aluminophosphates are intermediate between those of zeolites and zeolite-like silica modifications. The adsorption measurements and IR spectroscopic investigations of the framework vibrations demonstrate that the number of the adsorption complexes of CH3OH with Al atoms increases in the following order: AlPO4-5 〈 AlPO4-17 ≪ AlPO4-18. The OH vibrations of methanol molecules in the first coordination sphere of the Al atoms are reflected in the IR spectra as an absorption band at 3200 cm−1, which is not observed for the adsorption of CH3OH on zeolites.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 68
    Electronic Resource
    Electronic Resource
    Springer
    Russian chemical bulletin 44 (1995), S. 2073-2078 
    ISSN: 1573-9171
    Keywords: scanning force microscopy ; adsorption ; molecular films
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Adsorption of residual impurities from liquid media on various substrates was studied by scanning force microscopy. A new express method for controlling the purity of liquids was suggested.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 69
    ISSN: 1573-9171
    Keywords: photocatalyst ; adsorption ; surfactant ; kinetics ; colloid ; cadmium sulfide
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Photoreduction of Methyl Orange dye (MOr) by sodium sulfide was studied under steady-state photolysis (λ = 365 nm). The reaction was sensitized by the CdS colloid with the characteristic ∼5-nm particle size. The quantum yield of the reaction is independent of the light intensity when the latter is less than 5 mW cm−2. The form of the dependence of the initial quantum yield of the reaction on [MOr] coincides qualitatively with the adsorption isotherm of the dye on the CdS surface. The reaction kinetics under steady-state irradiation were analyzed. The kinetics in solution as a whole are shown to be adequate to those on a single colloidal particle. On the basis of the experimental data, two types of surfaces of the colloidal particles are suggested (“open” and “covered” with macromolecules of a colloid stabilizer), which significantly differ in the rate at which they establish an adsorption-desorption equilibrium with the solution.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 70
    Electronic Resource
    Electronic Resource
    Springer
    Russian chemical bulletin 44 (1995), S. 416-418 
    ISSN: 1573-9171
    Keywords: adsorption ; interface ; dispersion interactions ; inert gases ; methane ; graphite
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A new approach to the estimation of the extent of the inhomogeneous region during the adsorption of a gas on a planar or slightly curved solid surface is developed. Relationships are derived that enable the corresponding calculations to be made for the case of dispersion interactions of gases with solids. Numerical estimations of the extent of the inhomogeneous region for graphite-helium (neon, argon, krypton, xenon, and methane) systems as a function of temperature are presented.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 71
    Electronic Resource
    Electronic Resource
    Springer
    Journal of porous materials 4 (1997), S. 5-15 
    ISSN: 1573-4854
    Keywords: pillared clay ; pore size modification ; adsorption ; cracking ; carbon
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract To enhance the adsorption selectivity of pillared clays an attempt is made to modify the initial pore size by a controlled deposition of carbon. Cracking of hydrocarbons in the pores of the pillared clay results in coke deposits which can alter the pore size. Based on the evaluation of the amount of coke, the coke density, the decrease in micropore volume, changes in the micropore size distribution and the acidity it was possible to distinguish between pore-blocking, pore-filling and pore-narrowing effects. The modification mechanisms strongly depend on the initial porous structure, the acidity (Brönsted/Lewis), the cracking conditions (static or flow) and the hydrocarbons used. The carbon deposition results in a decrease in pore volume due to pore-filling (Ti-PILC) and pore-blocking (Al-PILC) without achieving a controlled pore-narrowing but some indications for pore-entrance narrowing were found.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 72
    ISSN: 1573-4986
    Keywords: Rhizobium meliloti ; nodulation factors ; fermentation ; ultrafiltration ; adsorption ; reversed phase (RP) chromatography ; fluorescence labelling ; LSIMS ; HAD-assay
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Lipooligosaccharides, synthesized by soil bacteria of the genera Rhizobium, are known to have multifunctional effects on a wide variety of plants as signal substances in symbiosis initiation, cell response elicitation and growth regulation. These so called nodulation (Nod-) factors represent interesting biotechnological products with respect to fundamental studies of symbiotic interactions as well as for potential applications. Therefore, a batch fermentation process on a scale of 30 l has been developed by means of the Rhizobium meliloti strain R.m. 1021 (pEK327) strongly overexpressing the genes for the synthesis of Nod factors. Induction by the flavone luteolin led to growth associated production of the lipooligosaccharides. Ultrafiltration was used for separating the biomass from the filtrate containing the extracellular Nod factors. Simultaneously, ultrafiltration reduced the amount of lipophilic substances, which would otherwise interfere with processes downstream. The second separation step consisted in adsorption on XAD-2, a nonspecific hydrophobic adsorptive resin. Adsorption of Nod factors was carried out by batch operation of a stirred tank. Desorption was performed by elution with methanol in a fixed bed column. A semi-preparative reversed phase HPLC (Polygoprep 100-30 C18) was chosen as the final purification step. The Nod factors were obtained after evaporation and lyophilization. Thus, about 600 mg of Nod factors were produced from 20 l of fermentation broth. The Nod factors produced by Rhizobium meliloti R.m. 1021 (pEK327) were identified by liquid secondary ion mass spectrometry and by reversed-phase HPLC as fluorescent derivatives of 2-aminobenzamide. The biological activity of the products was demonstrated by means of the root hair deformation (HAD-) assay. Abbreviations: ads, adsorption; 2-AB, 2-aminobenzamide; BDA, borane dimethylamine complex; Da, Dalton; DMSO, dimethyl sulfoxid; HAC, root hair curling; HAD, root hair deformation; HPLC, high performance liquid chromatography; LSIMS, liquid secondary ion mass spectrometry; MeOH, methanol; Nod, nodulation; OD, optical density; R.m., Rhizobium meliloti; RP, reversed phase; Tc, tetracycline; TY, trypton-yeast; UF, ultrafiltration; UV-Vis, ultraviolet-visible
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 73
    ISSN: 1573-4986
    Keywords: lectin receptor binding ; adsorption ; integrated optics ; lipid membrane incorporation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A novel integrated optical technique is used to monitor the kinetics of incorporation of glycophorin A (GPA) from solution into a planar dimyristoylphosphatidylcholine-cholesterol bilayer membrane, and the subsequent binding of wheat germ agglutinin (WGA) to the membrane-incorporated GPA. The technique significantly improves the attainable accuracy of kinetic measurements. The number of bound molecules can be determined to a precision of ca ± 80 mol µm−2. Our results show that GPA incorporates spontaneously into the bilayer. Binding of WGA to GPA is optimal in the presence of human serum albumin, and can be reversed byN-acetyl-d-glucosamine. The kinetics of the binding are consistent with the presence of two classes of kinetically distinguishable binding sites with association rates of 2.0×104 and 9.6×102 M−1 s−1, and dissociation rates of 2.7×10−3 s−1 and 〈10−5 s−1, respectively. A stoichiometry of 4 WGA monomers per GPA monomer was determined as characteristic of the overall binding interaction.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 74
    ISSN: 1573-4854
    Keywords: relative permeability ; pore structure characterisation ; adsorption
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract A novel design for the application of a simplified experimental procedure, capable of providing satisfactory relative permeability data for porous media at low relative pressures, is presented. The technique avoids the two-component mixing complications as well as the problems arising from the sample macroscopic inhomogeneity. The latter has been reduced with the aid of a variable pressure compaction procedure. Thus, it becomes easier to utilise the powerful relative permeability technique for the characterisation of the structure of porous solids. Emphasis is given to the combination of the relative permeability data obtained with an analytical approach based on Effective Medium Theory for the calculation of pore connectivity.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 75
    Electronic Resource
    Electronic Resource
    Springer
    Journal of porous materials 2 (1995), S. 191-199 
    ISSN: 1573-4854
    Keywords: adsorption ; analysis of pore structure ; estimation from sorption pore shape ; from ad-de-sorption surface area ; calculations from sorption
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The interpretation of pore dimensions based on physical ad-desorption analyses is central to the characterization of pore network structure. Several approaches have been proposed and are commonly employed in the analysis of physical adsorption and/or desorption to deduce the dimensions of the porous network. These approaches assume either theoretical (e.g., BET, the Halsey equation as interpreted by Pierce et al., or the more recent analyses of microporosity) or “standard” isotherms as model(s) for the sequential calculations required in estimating the pore network dimensions. Subsequent representation of the pore dimensions and the relationship between these distributions in dimension and other experimental parameters (such as catalytic activity, adsorptivity or transport); thus, depend explicitly on the model employed in the analyses. Each instrument currently available for the measurement of porous solid structure by sorption employs the same specific models for the relationship between the volume ad-desorbed and the dimensions of the porous network that is being characterized. This paper analyzes the interpretation of porous dimensions based on the sequential calculations required in the analyses. A new approach is proposed which is based on a modification to current practices reflecting Halsey's original theory for the thickness of the adsorbed layer (as a function of P/P 0). Further, the calculations of the incremental changes in the exposed surface area are discussed as they relate to pore network structure. A method is proposed to infer the differences in pore shape. Sorption data are analyzed by these new approaches, and these analyses will be compared with those approaches currently employed. Analyses based on these modified approaches provide a dramatically more consistent interpretation of the sorption data and the corresponding pore network structures.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 76
    Electronic Resource
    Electronic Resource
    Springer
    Journal of porous materials 3 (1996), S. 5-16 
    ISSN: 1573-4854
    Keywords: carbon molecular sieve ; adsorption ; adsorption kinetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Equilibrium and kinetics of oxygen and nitrogen sorption in two different carbon molecular sieves (CMS) have been modeled. In both CMS materials, equilibrium characteristics are adequately described by the Langmuir model. However, for kinetics of sorption, one CMS followed classic Fickian diffusion, while the other sample did not. A mathematical model was developed which accurately describes both pure component as well as binary uptakes in both materials. Simple manipulation of the boundary condition of the diffusion process allows the model to accurately predict both Fickian and surface barrier diffusion. All parameters needed to estimate binary uptake rates are obtained from pure component uptakes and isotherms. In addition, the model predicts both pure component and binary diffusion rates with diffusion coefficients which are not concentration dependent.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 77
    Electronic Resource
    Electronic Resource
    Springer
    Journal of porous materials 5 (1998), S. 275-287 
    ISSN: 1573-4854
    Keywords: activated carbons ; adsorption ; characterization ; Dubinin-Radushkevich ; carbon dioxide
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract In this paper we present adsorption isotherms of carbon dioxide on five different activated carbons from CHEMVIRON CARBON Belgium (Centaur HSV, BPL 410, F30-470, WS 42, Reactivated) and on a carbon molecular sieve from BERGBAU FORSCHUNG Gmbh (CMS II). The temperature is 303 K and the pressure ranges from 100 kPa up to 4000 kPa. Such conditions correspond to relative pressures ranging from 0.01 to 0.5. We also provide, for the same six sorbents, the nitrogen isotherms at 77 K (pressure: 0.001 to 100 kPa, relative pressure: 10-5 to 1). A theoretical treatment based on the Dubinin-Radushkevich and Stoeckli concept is presented and applied to the experimental results in order to obtain the micropore size distribution function (considered as Gaussian) of each sorbent. Using the CO2 data, it is possible to point out important structural differences between the six carbons. The theoretical treatment provides micropore size distribution functions in agreement with what is physically expected. Using N2 data, the structural differences are not so well marked. As a consequence, the structural parameters provided by the theoretical treatment are not reliable: except for the total micropore volume, they fluctuate strongly when changing the relative pressure domain of the used data.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 78
    Electronic Resource
    Electronic Resource
    Springer
    Journal of porous materials 3 (1996), S. 257-266 
    ISSN: 1573-4854
    Keywords: pillared clay ; pore size modification ; adsorption ; polymers ; carbon
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract In order to use pillared clays (PILC) for selective adsorption, further modifications of the porous structure are necessary. The deposition of carbon residues onto the porous structure of pillared clays by the carbonization of polymers (polyvinylalcohol) was proposed to achieve a controlled modification of the pore size. Ti and Al-pillared clays (calcined and non-calcined) were impregnated with PVA (different grades and different concentrations and subsequently carbonized to form carbon phases. The effect of the carbon deposits on the porosity of Ti- and Al-PILC is discussed in terms of pore-blocking, pore-filling and pore-narrowing. The deposition of carbon using PVA resulted in a complete pore-blocking for Al-PILC and in a narrowing of the pore size distribution for Ti-PILC, without achieving a controlled pore-narrowing.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 79
    Electronic Resource
    Electronic Resource
    Springer
    Journal of porous materials 4 (1997), S. 277-280 
    ISSN: 1573-4854
    Keywords: woodceramics ; porous carbon ; adsorption ; humidity sensor
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The humidity sensor characteristics of Woodceramics were investigated. The Woodceramics used in this experiment were prepared at 650–900°C. The size of specimens selected was 1 × 1 × 10 mm . One was used as-cut and the other was polished. Above 700°C, the resistance of the specimen was below 50 Ω and the decrease of resistance with increasing relative humidity was small. The specimen prepared at 650°C had a resistance of about 1 kΩ. The resistance of as-cut specimens decreased with increase in relative humidity, but that of the polished specimen did not change significantly. The difference between as-cut and polished samples was explained by the differences in surface micro-structure.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 80
    Electronic Resource
    Electronic Resource
    Springer
    Pharmaceutical research 12 (1995), S. 715-719 
    ISSN: 1573-904X
    Keywords: salbutamol base drug ; oleic acid ; propellant ; metered-dose inhaler ; stability ; adsorption
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The distribution of oleic acid between Salbutamol base drug and the solvent in metered-dose inhalers (MDI's) has been investigated. The equilibrium surfactant concentration in the drug dispersions has been determined using a colorimetric method. The samples examined contained Salbutamol base drug particles and oleic acid dispersed in different propellant blends of freon 11 and 12. The maximum equilibrium concentration observed depended on the propellant blend used. The propellant blend and the distribution of the surfactant affected the dispersion stability. The effect of the surfactant is illustrated by the adsorption isotherm for oleic acid onto the Salbutamol particles. The results are correlated with zeta-potentials and particle size measurements made on similar systems in order to characterize the properties of surfactant stabilized MDI's.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 81
    ISSN: 1573-1421
    Keywords: Gold ; hematite surface ; surface complexation ; adsorption ; potentiometric titration
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract The acid/base properties of the hematite/water interface and surfacecomplexation with gold has been studied by potentiometric titrations in thefour component system H+ – ≡FeOH –AuCl 4 - – Cl-. Equilibrium measurementswere performed in NaCl media at 298.2 K. In the evaluation of equilibriummodel from experimental data the constant capacitance model was applied. Theacid/base properties were investigated in 0.1 M NaCl in the range 2.6 ≤pH ≤ 7.4. The resulting intrinsic constants for protonation anddeprotonation of hydroxyl groups at the surface were logβ 1,1,0,0(int) s = 7.10 ± 0.06 andlog β -1,1,0,0(int) s = - 7.80 ±0.06. The density of proton active surface sites was 2.85nm-2 and the specific capacitance 2.5 C V-1 m-2. In the investigation of surface complexation of gold, thepotentiometric titrations were performed in the range 2.0 ≤ pH ≤ 10.2.Titration data was supplemented with analysis of Au in the aqueous phase byatomic absorbance spectrometry. The equilibrium model proposed consists ofthe following monodentate surface complexes: ≡FeOHAuCl3(log β 0,1,1,-1 s = 1.45 ± 0.03),≡FeOHAuCl2OH (logβ -1,1,1,-2 s = -3.89 ± 0.02), ≡FeOHAu(OH)3 (logβ -3,1,1,-4 s = -21.94 ± 0.05). Aslightly better fit could be obtained by assuming formation of a bidentatecomplex with the composition(≡FeO)2Au(OH)H2O. However, based onstructural arguments this complex was rejected.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 82
    ISSN: 1573-904X
    Keywords: poloxamer ; surfactant ; adsorption ; targeting ; surface energy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Purpose. To investigate the influence of the temperature at which adsorption takes place and the temperature at which the adsorbed surface is studied on the polarity of Poloxamer adsorbed to a hydrophobic surface. The implication is that changes in surface nature of adsorbed Poloxamer may subsequently be related to functionality, such as changes in opsonisation of Poloxamer coated latex in animals. Methods. The surface energies of Poloxamer surfactant have been calculated following adsorption to silanised glass plates. The adsorption to the plates was undertaken at a range of concentrations and at different controlled temperatures. The contact angles were measured using three different liquids on each surface, at a range of controlled temperatures. The surface energies were calculated using the harmonic mean and the acid-base models, via Wilhelmy plate contact angle measurements. These data were compared with previously published adsorption and hydrophobic interaction chromatography studies. Results. The apolar surface energy term remained consistent, but the polar contribution (which was totally of the electron donor type) changed depending upon the temperature of adsorption (and to a lesser extent the temperature at which the surface energy was measured). The polar nature was most elevated at the critical micelle concentration/ temperature. The data are consistent with estimates of surface hydrophobicity made using hydrophobic interaction chromatography. Conclusions. It is argued that the changes in surface energy, which result from the different adsorption conditions, can be expected to influence the functionality of the adsorbed coat, especially for application such as drug targeting.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 83
    ISSN: 1435-1536
    Keywords: Cotton fibers ; dye ; adsorption ; calorimetry ; zeta potential ; fluorescence ; degree of whiteness
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Fluorescent whitening agents (FWA) are used to improve the whiteness of cellulose fabrics. It is well known but not completely understood that the fluorescence decreases (chemical and physical mechanisms of distinguishing) above a certain FWA concentrationc crit. This reduction of fluorescence correlates very well with the alteration of the adsorption process studied by calorimetry and zeta potential measurements. The results obtained by these methods indicate that the adsorption mechanism is different at concentrations below and abovec crit. The reduction of the intensity of fluorescence, the degree of whiteness and the zeta potential are caused by the adsorption of a second layer of fluorescent whitening agents. This second layer reduces the zeta potential due to a shielding effect and reduces the whiteness and fluorescence by a bathochromic shift of the reflection curves. The final effect is a reduction of the total reflection.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 84
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 274 (1996), S. 548-554 
    ISSN: 1435-1536
    Keywords: Polyacrylic acid ; γ-Al2O3 ; mercury surface ; adsorption ; voltammetry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract In this paper the adsorption of polyacrylic acid (MW=5000) on the hydrophobic mercury surface and on the hydrophilic γ-Al2O3 surface at pH=3–4 in 0.55 M sodium chloride solution was investigated. Measurements of change of the double layer capacitance by phase selective a.c. voltammetry were used for determination of the adsorption of polyacrylic acid on the mercury electrode. The same method was used for the determination of the polyacrylic acid remaining in the solution after the adsorption on hydrophilic particles (γ-Al2O3 particles). The results obtained for adsorption of polyacrylic acid were compared to the results of the adsorption of humic substance of similar molecular weight under similar experimental conditions. The study has shown that polyacrylic acid in acidic solution is strongly adsorbed on the mercury surface, which is comparable to the adsorption of humic substance on the mercury surface. At the same time, the adsorption/deposition of polyacrylic acid on the γ-Al2O3 surface is weaker compared to humic acid, indicating at a smaller degree of interaction of polyacrylic acid with aluminium ions and with hydrophilic surface.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 85
    ISSN: 1435-1536
    Keywords: Key words Polyelectrolyte ; adsorption ; latex ; surface charge
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract  Adsorption of a well-characterized cationic polyacrylamide (CPAM) onto the surface of a model colloid (monodisperse polystyrene latex with carboxylic functional groups) was studied over a wide range of pH (4–9) and KCl concentration (c s =10-3–0.3 M). The surface charge density of the latex particles with and without adsorbed CPAM was also measured over the same range of electrolyte compositions. The adsorbed amount of CPAM increases with increase in c s and pH. The polyelectrolyte adsorption alters substantially the surface charge density of the latex particles as compared to the polymer-free case. A large overcompensation of the surface charge by the adsorbed polyelectrolyte is established at high c s and low pH. A qualitative explanation of the observed features is put forward.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 86
    ISSN: 1435-1536
    Keywords: Key words poly(ethylene oxide) ; silica-tethered poly(methyl methacrylate) ; adsorption ; spin-label ; molecular motion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract  The spin-label method was used to study the structure and molecular motion of poly(ethylene oxide) (PEO) chains adsorbed on a silica-tethered poly(methyl methacrylate) (PMMA). Spin-labelled PEO with a narrow molecular weight distribution, having number averaged molecular weight (M N)=6.0×103, was adsorbed on the surface of the silica-tethered PMMA with various grafting ratios in carbon tetrachloride solution at 35 °C. ESR spectra were measured at various temperatures after the samples were completely dried. The ESR spectra are composed of two spectra arising from spin-labels attached to “train” and “tail” segments, which are strongly and weakly interacted with the silica surface, respectively. The fractional amount of the “tail” segments increases extremely with the grafting ratio of PMMA. Molecular mobility of the PEO chains estimated from the temperature dependence of the ESR spectra also decreases significantly with the grafting ratio of PMMA. Structure and molecular motion of the PMMA chains tethered on the silica were also studied using the spin-labelled PMMA. Consequently, parts of the PEO segments penetrate into the PMMA chains and is adsorbed on the silica surface (“train” segments), whereas parts of the PMMA segments protrude from the surface. The other PEO segments are entangled with the tethered PMMA chains (“tail” segments).
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 87
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 273 (1995), S. 787-792 
    ISSN: 1435-1536
    Keywords: Zeolite ; modification ; surfactant ; adsorption
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Adsorption characteristics of anion-, cation- and nonion-type surfactants and phenol from their aqueous solution on Na-Y zeolites modified by SiCl4 treatment and NA-ZSM-5 zeolites with several Si/Al ratios were measured. Surfactants used were sodium dodecylbenzenesulfonte (DBS), laurylpyridinium chloride (LPC), polyoxyethylenenonylphenylether (POENPE) and phenol. Adsorption of surfactants was enhanced by SiCl4 treatment of Na-Y, which indicates an important role of the hydrophilic-hydrophobic character in the adsorption. Adsorption isotherms were in general of Langmuir type and adsorbed amount depended on the Al/(Si+Al) or Si/Al ratio of zeolite frameworks. In case of DBS adsorption of Na-ZSM-5 series, adsorption occurred only on the outer surface due to steric hindrance. LPC adsorption abilities were observed on even hydrophilic zeolites and were ascribed to ion exchange effect. In case of phenol adsorption on hydrophobic Na-Y, the adsorption isotherm was of Type V according to BDDT classification.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 88
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 273 (1995), S. 817-821 
    ISSN: 1435-1536
    Keywords: Composite particle ; temperature-sensitive ; biomolecules ; adsorption ; surface
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Temperature-sensitive composite polymer particles were prepared by seeded emulsion copolymerization of dimethylaminoethyl methacrylate and ethylene glycol dimethacrylate with 0.17 μm-sized monodispersed polystyrene seed particles. The adsorption and desorption behaviors of low molecular weight cationic emulsifier as well as albumin were examined to determine the variation of surface properties as a function of temperature below and above 35°C.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 89
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 274 (1996), S. 779-787 
    ISSN: 1435-1536
    Keywords: Silica particles ; colloid stability ; Hamaker constant ; van der Waals potential ; adsorption ; rheology ; SAXS
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Hydrophilic Stöber silica particles are stable in ethanol, but flocculation may be induced by the addition of sufficient cyclohexane. Low-shear rheological measurements indicated non-Newtonian behaviour beyond the critical cyclohexane concentration. The thickness and composition of the solvation layer around the particles were calculated from the adsorption excess isotherm on the basis of a multilayer adsorption model. The composition dependences of the Hamaker constants of the dispersion medium and the adsorption layer were obtained from optical dispersion measurements. A single-sheet, hard-sphere model predicted a weak van der Waals attraction in the ethanolic regime, but a strong attraction in the cyclohexane-rich region, in good accordance with the rheological properties of the dispersions and visual observations.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 90
    Electronic Resource
    Electronic Resource
    Springer
    Biogeochemistry 35 (1996), S. 339-365 
    ISSN: 1573-515X
    Keywords: adsorption ; CP/MAS13C NMR ; DOC ; forest floor leachates ; hydrophilic acids ; hydrophobic acids
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Organic substances are an integral part of the biogeochemistry of many elements in forest ecosystems. However, our understanding of the composition, chemistry, and reactions of these materials are incomplete and sometimes inconsistent. Therefore, we examined in detail dissolved organic carbon (DOC) in forest floor leachates over a two-year period (1992–1993), soil C, and DOC adsorption by a mineral soil to determine the relationship between soil solid and solution C characteristics in a spruce-fir ecosystem. The structural composition of DOC, DOC fractions (hydrophobic and hydrophilic acids, hydrophilic neutrals), and soil samples from the organic and mineral horizons were also analyzed using13C nuclear magnetic resonance (NMR) spectroscopy. Total DOC in forest floor leachates ranged from 7.8 to 13.8 mmol L−1 with an average of 8.6 mmol L−1. Concentrations were highest in September of both 1992 and 1993. Fractionation of the forest floor DOC indicated these solutions contained high organic acid contents that averaged 92% of the total DOC. Hydrophobic acids were also preferentially adsorbed by the B horizon. The13C NMR data suggested alkyl, carbohydrate, aromatic, and carboxylic C were the primary constituents for organic and mineral soils, DOC, and DOC fractions. Compositional changes of C were observed as aromatic and carbohydrate decreased, whereas alkyl, methoxy, and carbonyl moieties increased with depth. However, C composition changed little among the three organic layers based on the similarity of alkyl/carbohydrates ratios as determined from NMR area integration, suggesting that in this acid soil, decomposition proceeds rather slowly. Hydrophobic acids contained high contents of aromatic C, whereas hydrophilic acids were comprised primarily of carboxylic C. Hydrophilic neutrals were rich in carbohydrate C. Results indicated that these DOC fractions were unaltered during the isolation process. Carboxylic C groups appeared to dissolve easily and were probably the primary contributor to organic acidity in our organic dominate leachates. Results also suggested that DOC materials adsorbed on the B horizon underwent further biodegradation. Several seasonal patterns of C composition were observed in the forest floor leachates and DOC fractions collected between 1992 and 1993. Overall, the evidence from this study suggested that (i) DOC levels were mainly controlled by biological activity, (ii) forest floor DOC was comprised primarily of organic acids, (iii) contact of soil leachates with B horizon material affected DOC quantitatively and qualitatively, (iv) phenolic, carboxylic, and carbonyl C appeared to dissolve readily in the forest Oa horizon, (v) DOC materials adsorbed on the B horizon selectively underwent further decomposition, and (vi) C composition is a function of the extent of decomposition and DOC fractions.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 91
    ISSN: 1573-515X
    Keywords: adsorption ; bacterial dissimilatory sulfate reduction ; dry deposition ; forested catchment ; Lake Gårdsjön ; isotopes ; oxidation of sulfur ; sulfate ; sulfur ; Sweden
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract A small catchment on the Swedish West Coast has been studied over four years to determine S dynamics by using S isotope ratios. A Norway spruce dominated forest covers the catchment, and small peat areas occur in the lower parts of the catchment. The runoff δ34SSO4 values varied both during the year, and from year to year. Over the period from February 1990 to December 1993, the δ34SSO4 values ranged from −1‰ to +11‰. Over the same period, the throughfall δ34SSO4 values ranged from +1‰ to +15‰. There was no correlation (r2 = 0.01; Pr(F) = 0.57) between δ34SSO4 values in throughfall and runoff. Since the only input of S to the catchment is atmospheric deposition, the long-term runoff S mass flux is controlled by the deposition. Therefore, processes in the catchment are responsible for the variation in the runoff δ34SSO4 values. During periods with 34SSO4 enriched runoff, bacterial dissimilatory SO42- reduction occurs in the catchment. After very dry periods, oxidation of this reduced S, which is 32S-enriched, can be traced in runoff. Previous studies of the catchment have not been able to distinguish between: 1) oxidation of reduced S and dry deposition, and 2) reduction and adsorption. From the current study, it can be concluded that adsorption and dry deposition cannot cause the observed variation in runoff δ34SSO4.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 92
    Electronic Resource
    Electronic Resource
    Springer
    Journal of inclusion phenomena and macrocyclic chemistry 29 (1997), S. 1-13 
    ISSN: 1573-1111
    Keywords: Zeolite ; thermal behaviour ; adsorption ; isosteric heats ; XRD ; IR ; TG ; DTA
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Crystals collected from the Ellora valley(Aurangabad, MS, India) of the Deccan traps of India have beencharacterized as a stilbite (St) by X-ray diffraction, IRspectroscopy and chemical analyses. The thermal behaviour was studiedusing TG and DTA techniques. The sample was exchanged at refluxtemperature with NH4Cl and NH4St was prepared. This was furthertransformed to the H-form of stilbite (HSt) by heating at 573 K for 12 h.The samples so prepared were used for adsorption studies. The comparativestudy of sorption of these samples shows an increase in the sorptioncapacity of HSt. The isosteric heat was also computed for these samples.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 93
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 273 (1995), S. 1028-1032 
    ISSN: 1435-1536
    Keywords: Hydrolyzed polyacrylamide ; hematite ; adsorption ; kinetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The adsorption measurements of hydrolyzed polyacrylamide (HPAM) onto hematite suspension are carried out to study the dynamics of the polymer adsorption onto the suspension particles and to investigate the mode of the polymer adsorption. The polymer is found to show much affinity for the adsorption because of the opposite charges possessed by the polymeric flocculant and the suspension particles. Various adsorption parameters such as adsorption coefficient, the rate constants for the adsorption and desorption, are evaluated with the help of a recently proposed kinetic scheme. It is found that the extent of adsorption and the adsorption rate are adequately affected by increasing the pH of the suspension while, unexpectedly, the adsorption is found to show only a marginal increase on addition of Na2SO4. Both the amount of the adsorbed polymer and the adsorption rate are also found to increase with the degree of hydrolysis of the polyelectrolyte.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 94
    ISSN: 1435-1536
    Keywords: Sodium dodecylsulfate ; adsorption ; precipitation ; montmorillonite
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The interaction of dodecylsulfate anions (DS−) with homoionic Ca-, Mg-, Ni-, Cu-, Cd-, Pb- and Fe-montmorillonites were investigated. Mg- and Cd-montmorillonite do not adsorb DS−, and an anion exchange at the edges of the clay mineral does not take place. Three different adsorption processes are identified on the other montmorillonites: i) Fe-montmorillonite is covered with amorphous iron hydroxide, and DS−-anions are bound at positively charged sites. ii) On Ca- and Pb-montmorillonite DS− is precipitated as Me(DS)2. iii) On Ni- and Cu-montmorillonite DS− forms ion pairs with the cations on the surface. In all cases DS− is not bound above the CMC but the metal ions are mobilized from the surface either by solubilization of the precipitates or by formation of mixed micelles.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 95
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 274 (1996), S. 112-116 
    ISSN: 1435-1536
    Keywords: Temperature-sensitive ; emulsifier ; biomolecules ; adsorption ; surface
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Adsorption and desorption behaviours of emulsifiers and biomolecules on the two kinds of temperature-sensitive composite polymer particles were compared. One (I) was produced by seeded emulsion copolymerization of dimethylaminoethyl methacrylate and ethylene glycol dimethacrylate with 0.17 μm-sized polystyrene seed particles. The other (II) was produced by seeded emulsion copolymerization of N-isopropylacrylamide (NIPAM) and N,N′-methylenebisacrylamide with 0.36 μm-sized styrene-NIPAM copolymer particles. The amount of adsorption at temperatures above each lower critical solution temperature (LCST) was found to be much higher for I than II. In both cases, at temperatures below the LCST, almost all lactalbumin hydrolysate molecules adsorbed above the LCST were desorbed but the desorptions of adsorbed egg albumin and lysozyme molecules were not so high. The adsorption and desorption were reversible for both particles and the efficiency was better for I than II. From these results, it is concluded that the adsorption/desorption of protein onto the temperature-sensitive polymer particles is controllable by changing the temperature below and above the LCST of the shell layer and the sensitivity is based on the surface property of the composite polymer particles.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 96
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 276 (1998), S. 52-58 
    ISSN: 1435-1536
    Keywords: Key words Dodecanephosphonic acid ; soluble monolayer ; air/water interface ; evaporation ; adsorption ; ion-selective electrodes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract  The air/water interface of the system n-dodecanephosphonic acid (H2DP)–water was studied by surface tension, ion-selective electrodes and evaporation in an electrobalance. The combination of surface tension and ion-selective electrodes measurements enables to study the adsorption of soluble surfactants above the cmc using the Gibbs’ equation. H2DP formed a nonideal monolayer at the air/water interface with A molec=0.995 nm2 below the cmc. Above the cmc there was a reduction in adsorption giving A molec=6.32 nm2, which remained almost constant in the explored concentration range. This adsorption reduction may be due to a change composition on micellization, or to a thermodynamic advantage of micellization on adsorption. The reduction in the evaporation rate of water was mainly due to the reduction of the water activity, caused by the presence of solutes in bulk. This is because the strong changes in the surface coverage did not have significant influence on the evaporation rate.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 97
    ISSN: 1435-1536
    Keywords: Key words Composite particle ; temperature-sensitive ; biomolecules ; specific activity ; adsorption
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract  Temperature-sensitive micron-sized monodispersed composite polymer particles were prepared by seeded copolymerization of dimethylaminoethyl methacrylate and ethylene glycol dimethacrylate with 1.77 μm-sized monodispersed polystyrene seed particles. The change in surface property at temperature above and below 35 °C was examined by differential scanning calorimetry, trypsin activity and the adsorption/ desorption behaviors of low molecular weight cationic emulsifier as well as biomolecules.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 98
    ISSN: 1435-1536
    Keywords: Key words Surface tension ; adsorption ; micelle ; entropy ; energy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The surface tension of aqueous solutions of tetradecyl-trimethylammonium chloride (TTAC) and decyltrimethylammonium chloride (DeTAC) were measured as a function of temperature at concentrations below and above the critical micelle concentration under atmospheric pressure. The entropy and energy of adsorption from the monomeric state and from the micellar state and also the entropy and energy of micelle formation for TTAC were evaluated and compared with those of dodecyltrimethyl-ammonium chloride (DTAC). The values of ΔM W s and ΔM W u for TTAC and DTAC systems show that the micelle formation is driven by the entropy at low temperatures and by the energy at high temperatures.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 99
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 105 (1997), S. 72-74 
    ISSN: 1435-1536
    Keywords: Zeta potential ; static electricity ; surfactants ; viscose fibres ; adsorption
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Viscose fibres were finished with a blend of a nonionic fatty acid ethoxylate and a quarternary ammonium derivative. Zeta potential and static charging were investigated as a function of a cationic compound. There is strong evidence that the charging of the viscose fibres depends on the chemical nature of the surfactants side-groups.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 100
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 105 (1997), S. 91-95 
    ISSN: 1435-1536
    Keywords: Surfactant ; adsorption ; pore ; curvature ; mean field ; lattice
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract A mean field lattice (MFL) theory has been used to study the adsorption behaviour of nonionic surfactants in hydrophilic cylindrical pores. The theory predicts that with decreasing pore radius the absorbed amount decreases. Moreover, the step in the adsorption isotherm, which is a first-order phase transition in the mean field approximation, shifts to lower concentrations. Both effects have been observed in experiments. When an adsorbed layer is curved from convex (rod) to concave (pore) at constant area, the volume of the layer decreases. As a consequence, the stability of the layer increases and the adsorbed amount decreases.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...