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  • Articles  (38,778)
  • Chemistry  (38,741)
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  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    The @Journal of Supercritical Fluids 7 (1994), S. 265-274 
    ISSN: 0896-8446
    Keywords: PAH ; adsorption ; carbon dioxide ; contaminated soil ; solubility ; supercritical-fluid extraction
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics , Process Engineering, Biotechnology, Nutrition Technology
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Bioresource Technology 48 (1994), S. 251-255 
    ISSN: 0960-8524
    Keywords: Pinus pinaster bark ; adsorption ; cation exchange ; metal cations ; water treatment
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Process Engineering, Biotechnology, Nutrition Technology
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  • 3
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Bioresource Technology 48 (1994), S. 79-81 
    ISSN: 0960-8524
    Keywords: Dyeing wastewater ; adsorption ; carbonised coirpith waste ; pH effect
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Process Engineering, Biotechnology, Nutrition Technology
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  • 4
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    The @Journal of Supercritical Fluids 3 (1990), S. 71-77 
    ISSN: 0896-8446
    Keywords: adsorption ; molecular separations ; near-critical phenomena ; supercritical fluid chromatography
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics , Process Engineering, Biotechnology, Nutrition Technology
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  • 5
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    The @Journal of Supercritical Fluids 7 (1994), S. 289-292 
    ISSN: 0896-8446
    Keywords: adsorption ; quartz crystal microbalance ; resonance frequency
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics , Process Engineering, Biotechnology, Nutrition Technology
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  • 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.
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  • 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.
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  • 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.
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  • 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.
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  • 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.
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  • 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 ).
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  • 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.
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  • 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.
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  • 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.
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  • 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.
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  • 16
    Electronic Resource
    Electronic Resource
    Springer
    Adsorption 6 (2000), S. 169-174 
    ISSN: 1572-8757
    Keywords: adsorption ; WS2 ; nanotubes and fullerenes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract Adsorption-desorption cycles were measured for methane on non-irradiated WS2, and on irradiated WS2 (which contained, in part, WS2 fullerenes and nanotubes). Both types of samples were further subdivided into three sets: one set received no further treatment, another set was heated under vacuum, and the last set was acid-treated and heated. The specific surface area was determined for each set; so was the presence or absence of a hysteresis loop in the adsorption-desorption cycles. The results of these two groups of measurements were correlated with the space available for adsorption. The implications of the results for the experimental determination of the dimensionality of gas adsorbed at the interior of nanotubes are discussed.
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  • 17
    Electronic Resource
    Electronic Resource
    Springer
    Adsorption 6 (2000), S. 137-147 
    ISSN: 1572-8757
    Keywords: adsorption ; kinetics ; linear driving force model ; process design
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract The Linear Driving Force (LDF) model for gas adsorption kinetics is frequently and successfully used for analysis of adsorption column dynamic data and for adsorptive process designs because it is simple, analytic, and physically consistent. Yet, there is a substantial difference in the characteristics of isothermal batch uptake curves on adsorbent particles by the LDF and the more rigorous Fickian Diffusion (FD) model. It is demonstrated by using simple model systems that the characteristics of the adsorption kinetics at the single pore or the adsorbent particle level are lost in (a) evaluating overall uptake on a heterogeneous porous solid, (b) calculating breakthrough curves from a packed adsorbent column, and (c) establishing the efficiency of separation by an adsorptive process due to repeated averaging of the base kinetic property. That is why the LDF model works in practice.
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  • 18
    ISSN: 1572-8757
    Keywords: silical glasses ; CPG ; Vycor ; adsorption ; capillary condensation ; molecular simulation ; Monte-Carlo ; SANS ; SAXS ; fractals ; surface roughness ; Porod's law ; Gurvitch rule ; hysteresis loop
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract We have performed atomistic Grand Canonical Monte-Carlo (GCMC) simulations of adsorption of xenon in a Vycor-like matrix at 195 K. The disordered mesoporous network is obtained by applying a numerical 3D off-lattice reconstruction procedure to a simulation box originally containing silicon and oxygen atoms of a non-porous silica solid. In order to reduce the computational cost, we have applied a homothetic decrease of the simulation box dimensions which preserves the morphology and the topology of the pore network (the average pore dimension is then around 30 Å). The surface chemistry is obtained in a realistic fashion by saturating all dangling bonds with hydrogen atoms. Small angle scattering spectra calculated on different numerical samples have evidenced a departure from Porod's law due to surface roughness. The simulated isotherms calculated on such disordered connected porous networks, show the capillary condensation phenomenon. The shape of the adsorption curves differs from that obtained for simple pore geometries. The analysis of the adsorbed quantity distribution indicates partial molecular-film formation depending on the local surface curvature and roughness.
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  • 19
    ISSN: 1572-8757
    Keywords: adsorption ; zeolite ; chlorodifluoromethane ; adsorption structure ; H and F NMR ; chemicalshift ; relaxation time ; adsorbate mobility
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract The adsorption of CHClF2 on NaY5.6 zeolite has been studied by measuring the H and F NMR of the adsorbed CHClF2, focusing in particular on the measurements of the chemical shift and longitudinal relaxation time, as well as the adsorption isotherm measurements. It is possible to determine the coordination structure of the CHClF2 adsorbed on NaY5.6 zeolite by measuring the adsorption amount dependence of the chemical shift. In addition, the motional activity of the adsorbed molecules in the super cage of the zeolite is discussed on the basis of observed longitudinal relaxation times for various adsorption amounts.
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  • 20
    ISSN: 1572-8757
    Keywords: adsorption ; EPR ; mordenite ; MOR ; NO ; zeolite
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract Adsorption isotherms of nitrogen monoxide (NO) and in situ EPR spectra of adsorbed NO on mordenite zeolites (MOR) of different cation types (HM, NaM and CaM) are measured at different temperatures to elucidate the effect of the strong adsorption promoted by the enhancement of potential field in micropore of MOR (micropore filling) as well as the electrostatic interaction in MOR on NO adsorption. The NO molecules adsorb irreversibly and fill up the micropore of MOR at 201 K, above the critical temperature of NO, regardless of the kind of cation species. The NO adsorption takes place even at 273 K. In the adsorption at 273 K, the strength of electrostatic field formed by cation sites affects the adsorptivity and the order of saturation amount of adsorption (V s) corresponds to that of the electrostatic field strength. EPR results show that NO molecules strongly interact with cation sites in MOR and disproponation reaction of NO take place on CaM.
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  • 21
    ISSN: 1572-882X
    Keywords: cellulase ; cottonfibres ; electron microscopy ; biopolishing ; adsorption ; colloidalgold labeling
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract Because cellulases are finding more applications in the textile and detergent industries, their effect on cotton fibres must be evaluated. For this purpose, the action of a recombinant cellulase, endoglucanase V from the fungus Humicola insolens, has been followed by scanning electron microscopy (SEM) in classical longitudinal views as well as in cross-sections of cotton fibres. The experiments were conducted at large enzyme dilution typical of conditions where cellulases are used for biopolishing, i.e. for the removal of defects created by mechanical abrasion. Endoglucanase V appears to restrict its action to the hydrolysis of the loose fibrils created at the surface of the fibres and no indication of extensive enzyme penetration and damage to the interior of the fibres could be detected by SEM. The adsorption sites for endoglucanase V on cotton fibres were examined by transmission electron microscopy (TEM) on ultrathin cross-sections after immuno-gold labeling of the enzyme. This approach showed that the enzymes did not penetrate the fibres but remained at their surface. The use of an immuno-gold labeled cellulase provides a new way to probe the surface features of cotton fibres
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  • 22
    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.
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  • 23
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    Adsorption 6 (2000), S. 159-167 
    ISSN: 1572-8757
    Keywords: silicalite-1 ; adsorption ; TEOM ; alkanes ; isosteric heat ; adsorption entropy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract The equilibrium adsorption of the light alkanes methane, ethane, propane, n-butane, and i-butane in silicalite-1 has been investigated using the TEOM technique. Either a conventional or a dual-site Langmuir isotherm appropriately describes the equilibrium data. Good agreement with the literature data determined by other techniques indicates the TEOM is a reliable technique. The adsorption of i-butane in silicalite-1 reveals the discrete preferential molecular siting, implying a discrete-dual-structural heterogeneity for light alkanes in silicalite-1.
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  • 24
    Electronic Resource
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    Adsorption 6 (2000), S. 325-335 
    ISSN: 1572-8757
    Keywords: copper ; ca-koalinite ; adsorption ; desorption ; thermodynamics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract The temperature effect on Cu adsorption and desorption on kaolinite has been investigated at four temperatures (8°C, 25°C, 30°C and 40°C). The clay sample was saturated with Ca. Copper was sorbed from solutions containing eleven Cu concentrations between 0.0010 and 0.0211 M, equilibrated for 2 days. Cu adsorption decreased, but desorption increased with increasing temperature, indicating that adsorption is an exothermic process while desorption is endothermic. These conclusions are confirmed by the values of ΔH 0 estimated for adsorption and desorption. The initial copper concentration is a significant factor influencing mainly the adsorption process, which is spontaneous (ΔG 0 〈 0) only for low initial Cu concentrations. The desorption process is spontaneous for all Cu concentrations. ΔS 0 values have also been calculated. Experimental adsorption data were successfully fitted to the Freundlich isotherm and to the Gouy-Chapman model in order to express the process quantitatively.
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  • 25
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    Adsorption 6 (2000), S. 349-357 
    ISSN: 1572-8757
    Keywords: sulfadiazene ; adsorption ; kinetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract To investigate the nature of interactive forces between sulfadiazene molecules and alumina surface the experiments were performed for the adsorption of sulfadiazene (SD) from its aqueous sulution onto the alumina surfaces at 25 ± 0.2°C and the influence of factors such as increasing concentration of SD (4.0–20.0 × 10−3 mol cm−3), the time required for adsorption equilibrium, pH (2.0–12.0) and temperature (5–45°C) of the adsorption medium, the presence of ions like Cl−, SO2− 4 and PO3− 4 (0.01–0.30 M) and organic solvents (5% v/v) were observed on the course of adsorption of SD. Various adsorption and kinetic parameters such as adsorption coefficient, the rate constants for adsorption and desorption were also evaluated. The results of the above cited studies facilitated to formulate the mechanisms of interaction between SD and alumina surfaces. From application view point the present work may be a potential tool for an effective chromatographic separation of sulfa drugs from industrial effluents.
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  • 26
    ISSN: 1572-882X
    Keywords: biotechnology ; cellulase ; endoglucanase ; cellobiohydrolase ; adsorption
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract Cellulases can be used to modify pulp fibres. For the development of biotechnical applications, a better understanding of the adsorption of cellulases onto commercial wood fibres is needed. In this work, the adsorption behaviour of purified CBH I and EG II on bleached Kraft fibres was investigated. Three variables were studied with respect to their effect on adsorption: fibre type (hardwood or softwood), fibre history (never-dried or once-dried), and ionic strength. The results showed that fibre history had the largest influence on the extent of adsorption of each enzyme. The effect of ionic strength was shown to be dependent on the enzyme and fibre type. At high ionic strength, CBH I exhibited a higher affinity for both once-dried and never-dried fibres at low enzyme concentrations; however, salt was shown to decrease the extent of adsorption at higher enzyme dosages. In contrast, salt increased the maximum adsorption of EG II, most notably on the once-dried hardwood fibres. Fibre type was also shown to affect adsorption behaviour. CBH I had a higher affinity for softwood fibres than for hardwood fibres at low enzyme concentrations. The maximum adsorption of EG II onto once-dried softwood fibres increased by 80% compared to the once-dried hardwood fibres. Interestingly, this did not correlate to in creased fibre hydrolysis.
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  • 27
    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.
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  • 28
    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.
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    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.
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    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).
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    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.
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    Cellulose 1 (1994), S. 169-196 
    ISSN: 1572-882X
    Keywords: cellulases ; hydrolysis ; adsorption ; multidomain structure ; synergy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract Most effective cellulolytic enzymes are made of at least two constitutive domains, a catalytic domain and a non-catalytic cellulose-binding domain linked by a flexible peptide. There are several families of catalytic domains and of cellulose-binding domains resulting in a large number of their possible combinations. Removal of the cellulose-binding domain drastically reduces the binding capacity of cellulases to insoluble cellulose while the catalytic efficiency on soluble substrates is usually maintained. Isolated cellulose-binding domains bear most of the binding properties of cellulases (quasi-irreversibility and dispersive effect) but do not hydrolyse cellulose. The multiple types of synergy that cellulases display when acting in combination on cellulose appear to result from their different activities and selectivity, from the substrate microheterogeneity, and sometimes from both.
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    Enzyme and Microbial Technology 7 (1985), S. 217-219 
    ISSN: 0141-0229
    Keywords: Ethanol ; adsorption ; fermentation ; inhibition ; silicalite ; xylose
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
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    Enzyme and Microbial Technology 16 (1994), S. 18-23 
    ISSN: 0141-0229
    Keywords: Granular starch ; adsorption ; elution ; fusion protein ; starch-binding domain ; β-galactosidase
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
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    ISSN: 0141-0229
    Keywords: Alcoholysis ; adsorption ; interesterification ; lipase ; operational stability ; silica gel
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    Enzyme and Microbial Technology 16 (1994), S. 671-675 
    ISSN: 0141-0229
    Keywords: Rhizopus arrhizus ; adsorption ; isotherms, hard and soft metals ; metal ions
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    ISSN: 0141-0229
    Keywords: Cellulose ; adsorption ; cellulase ; synergism ; thermodynamics
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    Chemie Ingenieur Technik - CIT 21 (1949) 
    ISSN: 0009-286X
    Keywords: Chemistry ; Industrial Chemistry
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    Chemie Ingenieur Technik - CIT 21 (1949), S. 6-8 
    ISSN: 0009-286X
    Keywords: Chemistry ; Industrial Chemistry
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    Notes: Die Anordnung dient zur Messung von Dampfdruckerniedrigungen verdünnter Lösungen (10-3 Mol/l) insbesondere assoziierender Substanzen. Es wurde eine Meßanordnung entwickelt, in der die durch kleine Druckdifferenzen verursachte Ausbuchtung der Wölbung des Meniskus eines Hg-Manometers nach dem Prinzip eines Photometers lichtelektrisch mit einem Vakuumthermoelement gemessen wird. Die Anordnung gestattet unabhängig vom Gesamtdruck noch Druckschwankungen von 10-4 mm Hg zu messen.
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    Keywords: Chemistry ; Industrial Chemistry
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    Notes: Es werden einige Regeleinrichtungen besprochen, die zum Aufbau von im wesentlichen automatisch arbeitenden Destillationskolonnen sowohl für diskontinuierlichen als auch für kontinuierlichen Betrieb führten.
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    Chemie Ingenieur Technik - CIT 21 (1949), S. 1-6 
    ISSN: 0009-286X
    Keywords: Chemistry ; Industrial Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: Unsere wichtigsten chemischen Großsynthesen gehen von Acetylen bzw. vom Kohlenoxyd-Wasserstoff-Gemisch aus. Die Arbeiten im letzten Jahrzehnt bezweckten, diese Rohstoffe unmittelbar aus dem Ferngas zu gewinnen. Von den entwickelten Verfahren verdient insbesondere das Sauerstoff-Verfahren Beachtung. Es liefert ein Synthesegas mit nur noch 0,2% Methan und ist unempfindlich gegen den im Ferngas vorhandenen organischen Schwefel. Eine etwa folgende Umsetzung des Kohlenoxydes mit Wasserdampf zu CO2 und Wasserstoff kann in unmittelbarem Ánschluß an der Kohlenwasserstoff-Spaltung vorgenommen werden, so daß kein neuer Dampfverbrauch auftritt. Während in der folgenden Arbeit über das Verfahren zur Verarbeitung des gesamten Ferngases auf Kohlenoxyd und Wasserstoff berichtet wird, wird in einer weiteren Arbeit die chemische Verwertung der einzelnen Bestandteile des Ferngases behandelt.
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    Chemie Ingenieur Technik - CIT 21 (1949), S. 19-24 
    ISSN: 0009-286X
    Keywords: Chemistry ; Industrial Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Nach den verfügbaren amerikanischen Quellen wird zusammenfassend über die seit etwa 1940 in Amerika erreichten Fortschritte auf dem Gebiet der Sauerstoff-Erzeugung und -Anwendung berichtet, besonders über Versuche an Austauschböden und Trennkolonnen für kleinere, meist leichtbewegliche Anlagen, über die Mittel zur Kälteerzeugung, über die Herstellung und den Versand von flüssigem Sauerstoff sowie über die unmittelbare Erzeugung von hochkomprimiertem Sauerstoff für die Flaschenfüllung durch Verdampfung des flüssigen Sauerstoffs im Zerlegungsapparat. Weiter wird ein neuer Austauschertyp besprochen und auf neu erschlossene Anwendungsgebiete für billigen, mäßig reinen Sauerstoff hingewiesen.
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    Chemie Ingenieur Technik - CIT 21 (1949), S. 15-18 
    ISSN: 0009-286X
    Keywords: Chemistry ; Industrial Chemistry
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    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Bei Kohlenoxyd-Hydrierungen unter Drucken zwischen 300 und 1000 at und Temperaturen über 400° erwiesen sich z. T. sog. „kohlenoxydfeste“ metallische Werkstoffe, insbesondere Stähle mit mehr als 13% Chrom, für den praktischen Betrieb als ungeeignet, obwohl sie anscheinend von Kohlenoxyd nicht abgebaut wurden. Es wurden daher 20 derartige Stähle und 6 eisenfreie Metallproben gegenüber Wassergas bei 1000 at und Temperaturen zwischen 300 und 450° untersucht und aus den Ergebnissen Folgerungen für die praktische Verwendungsmöglichkeit im Apparafebau gezogen.
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    Chemie Ingenieur Technik - CIT 21 (1949), S. 24-30 
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    Keywords: Chemistry ; Industrial Chemistry
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    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
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    Chemie Ingenieur Technik - CIT 21 (1949), S. 31-31 
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    Keywords: Chemistry ; Industrial Chemistry
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    Chemie Ingenieur Technik - CIT 21 (1949), S. 33-37 
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    Keywords: Chemistry ; Industrial Chemistry
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    Notes: Die Angabe, daß sich die Ausscheidung von Härtebildern mit Orthophosphaten in wässeriger Lösung unter Bildung von Tricalciumphosphat vollziehe, ist unzutreffend. Der Niederschlag dürfte vielmehr die Formel des Hydroxylapatits haben.
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    Notes: Bis 1940 war die Anwendung hoher Vakua fast nur auf das Laboratorium beschränkt, in der Technik evakuierte nur die Röhrenindustrie bis auf Drucke von beinahe 10-7 mm Hg, aber es handelte sich auch hier meist nur um verhältnismäßig kleine Volumina. Die anschließende Entwicklung wurde durch mehrere Ereignisse besonders gefördert: durch die Konstruktion hervorragender Pumpen in Deutschland und Amerika, durch die Schaffung guter Gläser in Jena, durch die Erfolge der Vakuumdestillation von Fetten, Ölen und empfindlichen organischen Substanzen in England, Deutschland und später in USA, und schließlich durch das amerikanische Atombombenprojekt, wo bereits bei der Gasdiffusions- und elektromagnetischen Trennung der Uran-Isotope die ersten großen Vakuum-Probleme auftraten. Heute ist selbst die großtechnische Erzeugung von Hochvakuum zwischen -100° und + 1000° C ein untergeordnetes Problem der Verfahrenstechnik geworden.
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    Chemie Ingenieur Technik - CIT 21 (1949), S. 61-63 
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    Notes: Es wird über Versuche mit zwei Ausführungen von Pilzglocken aus Porzellan berichtet, die in Rektifizierböden eingebaut waren. Wirkung, Druckverlust und Flüssigkeitsinhalt der Sälen wurden ermittelt. Um eine gute Wirkung zu erreichen, müssen die Einzelabmessungen des Bodens entsprechend gewählt werden. Auch der Einbau einer Staurippe erhöht die Bodenwirkung.
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    Notes: Die hier beschriebenen Methoden sollen es dem Schichtarbeiter mit einfachen Mitteln ermöglichen, kurzfristig eine gefährliche Acetylen-Anreicherung zu erkennen. Die Ergebnisse werden mit denen quantitativer Methoden verglichen.
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    Notes: Der im folgenden beschriebene Kolbenverdichter arbeitet mit ungeschmierten Kolben und Stopfbüchsen. Die Abdichtung wird durch Labyrinthdichtungen erreicht. Dadurch behält das verdichtete Medium die ursprüngliche Reinheit, so daß der Verdichter in der chemischen Industrie und der Lebensmittelindustrie da verwendet werden kann, wo völlig reine Druckluft gebraucht wird.
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    Chemie Ingenieur Technik - CIT 21 (1949), S. 71-73 
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    Chemie Ingenieur Technik - CIT 21 (1949), S. 68-68 
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    Notes: In den letzten Jahren hat die Fluorchemie, insbesondere die verschiedener organischer fluorierter Verbindungen, erheblich an praktischer Bedeutung gewonnen. Da in einigen Veröffentlichungenz. B. DECHEMA-Werkstofftabellen 1948; ferner Ind. Engng. Chem. 39, 12a u. 91a [1947]. bereits auf die gute Eignung des Silbers als Apparatebauwerkstoff für technische Reaktionen mit Fluorverbindungen hingewiesen worden ist, seien nachstehend einige quantitative Angaben gemasht, die das Ergebnis einer 1944 laboratoriumsmäßig durchgeführten Korrosionsprüfung darsfellen.
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    Chemie Ingenieur Technik - CIT 21 (1949), S. 74-74 
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    Chemie Ingenieur Technik - CIT 21 (1949), S. 79-81 
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    Chemie Ingenieur Technik - CIT 21 (1949), S. 81-86 
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    Chemie Ingenieur Technik - CIT 21 (1949), S. 87-87 
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    Chemie Ingenieur Technik - CIT 21 (1949), S. 88-88 
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    Chemie Ingenieur Technik - CIT 21 (1949), S. 89-94 
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    Notes: Die technisch-wissenschaftliche Forschung der letzten Jahrzehnte brachte eine Erweiterung und Vertiefung unserer Erkenntnisse über die beim gekoppelten Wärme- und Stoffaustausch sich abspielenden Vorgänge. Trotzdem blieben noch Fragen ungeklärt, deren erschöpfende Behandlung für die rechnerische Erfassung baispielsweise der Trocknungsvorgänge unerläßlich ist. Zu diesen Fragen gehört der Zusammenhang zwischen Luftzustand und Gutstemperatur während des Trocknens bei bestimmten Arten der Gasströmung. Im folgenden werden diese Verhältnisse untersucht, wobei sich eine gute Übereinstimmung zwischen theoretischen und experimentellen Ergebnissen ergibt.
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    Notes: Die bisherigen Definitionen des Wirkungsgrades von Wärmeaustauschern konnten zwangsläufig nicht in jeder Hinsicht befriedigen. Es wird auch immer schwierig sein, einen Wirkungsgrabegriff auf energetischer Grundlage aufzustellen, solange der Wärmeaustauschapparat allein betrachtet wird, da sich Wärme- und Druckverluste jeweils verschieden auswirken. Daher sollte auch das Arbeitsverfahren, in das der Wärmeaustauscher eingeschaltet ist, mit in Betracht gezogen werden. Im folgenden wird gezeigt, daß sich dann ein auf energetischer Grundlage beruhender Gütegradbegriff schaffen läßt, der zwar von Fall zu Fall neu aufgestellt werden muß, dafür aber eine Reihe von Vorteilen für den Erzeuger und den Abnehmer von Wäreaustauschapparaten bietet.
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    Chemie Ingenieur Technik - CIT 21 (1949), S. 103-105 
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    Notes: Der Auslaufbecher DIN 53211 ist ein einfaches, praktisch leicht zu handhabendes Betriebs-Gerät zur Beurteilung der Konsistenz besonders von Farben und Lacken. Die vorliegende Untersuchung zeigt, innerhalb welcher Grenzen der Auslaufbecher tatsächlich geeignet ist, ein zuverlässiges Maß für die Konsistenz mit ihren Nebenerscheinungen, z. B. für die Viskosität usw., zu sein. Der experimentelle Zusammenhang zwischen Auslaufzeit und Viskosität wird durch Versuche mit 11 Normalflüssigkeiten ermittelt. Die genaue Analyse der Versuchsergebnisse gibt einen interessanten Einblick in die Strömungsvorgänge bei diesem Gerät.
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    Chemie Ingenieur Technik - CIT 21 (1949), S. 100-102 
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    Notes: Die Aufzeichnung polarographischer Kurven in Tintenschrift gestattet einfachstes Modellieren und Auswerten der Kurven. Für den Betrieb normaler Tintenschreiber unter Verstärkung der Elektrodenströme mittels Verstärker in Saugschaltung1 wurde während des Krieges ein vollelektrisch arbeitendes Zusatzgerät durchgebildet, in dem alle erforderlichen Schaltelemente und Verstellorgane zur Kurvenaufnahme untergebracht sind. Die einfach zu bedienende, robuste und universell verwendbare polarographische Meßeinrichtung läßt sich auch in technischen Betrieben zur Durchführung von Serienanalysen verwenden. Seine Wirkungsweise wird im folgenden unter Beifügung einiger charakteristischer Kurven erläutert.
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    Chemie Ingenieur Technik - CIT 21 (1949), S. 110-114 
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    Chemie Ingenieur Technik - CIT 21 (1949), S. 106-110 
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    Notes: Vielen Betrieben steht Kühlwasser zur Verfügung, das reich an Carbonathärte ist und daher leicht Versteinungen der Leitungen hervorruft. Um diese Steinbildung zu verhindern, hat sich der Zusatz geringer Mengen an Natriumhexametaphosphat bewährt. Während man zur Prüfung der Brauchbarkeit von Zusätzen bisher einfache Becherglasversuche angestellt hat, haben die Verfasser ein geeignetes, im Laboratorium durchführbares Prüfverfahren entwickelt, wobei die wesentlichen betrieblichen Faktoren berücksichtigt werden können. Im folgenden wird diese Apparatur beschrieben und dann werden damit erzielte Versuchsergebnisse mitgeteilt, die mit den in der Praxis gemachten Erfahrungen gut übereinstimmen. In einem Anhang wird schließlich über Becherglasversuche mit organischen Zusätzen berichtet.
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    Chemie Ingenieur Technik - CIT 21 (1949), S. 116-116 
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