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  • 1994  (14)
  • 1991  (8)
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  • Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics  (16)
  • Process Engineering, Biotechnology, Nutrition Technology  (8)
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  • Articles  (24)
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  • 1990-1994  (24)
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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of polymers and the environment 2 (1994), S. 225-236 
    ISSN: 1572-8900
    Keywords: Polyanion ; dispersant ; detergent ; poly(acrylic acid) ; adsorption ; 14C-polyaspartate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Polyaspartate synthesized using thermal methods (thermal polyaspartate; TPA) has been shown to have dispersant and crystallization inhibition activities. These activities suggest that the polymer may be used in water treatment and paper processing and as a detergent and paint additive. The commercial potential for TPA is enhanced by the fact that it may be synthesized on a large scale. Therefore, a study of the biodegradation of the polymer was undertaken. TPA was produced by hydrolysis of a polysuccinimide synthesized by dry thermal polymerization of aspartic acid. The resulting polymer was a poly(α,β-dl-aspartate) having a 70% β structure and containing a racemic mixture of aspartic acid. TPA was incubated with both dilute effluent and activated sludge from a wastewater treatment plant. Low-biomass effluent experiments showed changes in molecular size of TPA concomitant with oxygen demand induced by the polymer, suggesting susceptibility of TPA to at least partial biodegradation. Low-biomass sludge experiments (SCAS, modified Sturm) yielded approximately 70% mineralization of 20 mg L−1 TPA by 28 days, suggesting that a significant portion of the polymer was labile. High-biomass sludge experiments using14C-TPA at 1 mg L−1 revealed approximately 30% mineralization and 95% total removal of TPA carbon from solution in 23 days, with most of the mineralization and removal taking place in less than 5 days. Additional short-term studies using a variety of particulate substrates, including activated sludge, confirmed that TPA is subject to removal from solution by adsorption. From these studies with labeled TPA, it was concluded that TPA is subject to rapid removal and at least partial degradation in a wastewaster treatment plant. Using gel and thin-layer chromatography, it was determined that at least part of the unmineralized residue from the high biomass assays was polyaspartate. It is speculated that the unusual structure of TPA compared to natural proteins may limit the rate of proteolysis of the polymer and thus its overall degradation rate.
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  • 2
    Electronic Resource
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    Springer
    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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  • 3
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    Springer
    Colloid & polymer science 272 (1994), S. 196-203 
    ISSN: 1435-1536
    Keywords: Colloid ; polymer ; adsorption ; rheology
    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 flocculation properties have been investigated for a well-characterized aqueous system of precipitated nanometric silicabeads in the presence of a high molecular-weight poly(ethylene oxide). Particular attention was given to the evolution of these properties with increasing concentration. In addition, the corresponding consequences on the rheological behavior in the homogeneous domains of the phase diagram of the systems were studied. Important rheological effects can actually be obtained with such systems, even at moderate values of the volume fraction of the dispersed phase (5·10−3≦Φ≦5·10−2). According to the adsorption level, the number of particles per macromolecular chain, and the free polymer equilibrium concentration, quite different phenomena were observed such as rheopectic shear-induced gelation, Newtonian flow or thixotropic shear-thinning.
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  • 4
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    Springer
    Colloid & polymer science 272 (1994), S. 1620-1626 
    ISSN: 1435-1536
    Keywords: Zeolite ; modification ; chloroform ; 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 chloroform from its aqueous solution on Na−Y and Li−Na−Y modified by SiCl4 were measured and compared with those on Na−ZSM-5 and Na-Mordenite. No adsorption occurred on Na−Y with high hydrophilicity, while the siliceous faujasites became capable of adsorption and its amount increased with increase in the Si/A1 ratio. Adsorption isotherms are of Langmuir type, suggesting that adsorption proceeds by pore filling. The adsorption amounts expressed in volume on Na−Y with high hydrophobicity corresponded to their pore volumes. Adsorption characteristics of chloroform from gaseous phase on Na−Y with different Si/A1 ratio were also measured. The adsorption capability decreased with increasing Si/A1 ratio. Immersional heats of zeolites into water or chloroform were measured in order to evaluate the surface affinity to both solvents. Immersional heats into water were almost constant (about 500 mJ·m−2) for zeolites with their Si/A1 ratio below 10. The heats decreased with an increase in the Si/A1 ratio above 10, then became almost constant (about 120 mJ·m−2) over 30 in their ratio. Heats of immersion of Na−Y series into chloroform were almost constant irrespective of their Si/A1 ratio, but decreased slightly when the ratio exceeded 20. Adsorption characteristics of chloroform could be well related to immersional heats into both solvents.
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  • 5
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    Springer
    Colloid & polymer science 272 (1994), S. 324-331 
    ISSN: 1435-1536
    Keywords: Surfactants ; silicates ; adsorption ; calorimetry ; x-ray diffraction
    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 Nonionic surfactants were adsorbed on low-charged layer silicates in the interlayers. After drying, the surfactants were arranged in densely packed double layers. However, in suspension considerably higher basal spacings are measured by x-ray diffraction which indicate that large quantities of non-ionic surfactants are adsorbed. With the aid of calorimetry, enthalpies of displacement were recorded which suggest strong interactions of the non-ionic surfactants with smectites. In analogy to tests on hydrophilic SiO2, the adsorption of smectites is found to depend on the degree of ethoxylation of the non-ionic surfactant. The adsorption declines with increasing EO content.
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  • 6
    ISSN: 1435-1536
    Keywords: Parallel plate flow chamber ; adsorption ; desorption ; blocked area ; image analysis
    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 and desorption rates of 736 nm diameter polystyrene particles on glass were studiedin situ using a parallel plate flow chamber and automated image analysis. Adsorption and desorption rates were measured simultaneously during deposition, enabling the determination of initial deposition rates, blocked areas per particle, desorption rate coefficients, and the number of adhering particles in the stationary state. Deposition experiments were done from suspensions with different potassium nitrate concentrations (1, 10 and 50 mM) and at varying shear rates (15 to 200 s−1). The initial deposition rate, the desorption rate, the blocked area per particle and the number of adhering particles in the stationary state showed major variations with the shear rate and the ionic strength of the suspension. At low ionic strength, the number of adhering particles showed an oscillatory behavior in time, presumably due to a varying interaction between particle and collector surface. Blocked areas, determined from deposition kinetics, ranged 705 to 2374 cross-sections at low ionic strength, and from 10 to 564 at high ionic strength and corresponded well with those estimated from local pair distribution functions which were obtained from an analysis of the spatial arrangement of the adhering particles.
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  • 7
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    Colloid & polymer science 272 (1994), S. 830-836 
    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 Hydrophobic faujasite-type zeolites were prepared by the treatment of hydrophilic Na-Y4.6 with silicon tetrachloride (SiCl4) by way of dealumination-silicon exchange reaction. Hydrophilic-hydrophobic characters of these zeolite surfaces were evaluated by measurements of immersional heats into water orn-hexane. Adsorption rates of sodium dodecylsulfate (SDoS) on these zeolites from its aqueous solution and their adsorption characteristics were investigated, and compared with those on ZSM-5 with various Si/Al ratios. The adsorption ability of SDoS into zeolite micropores developed on the zeolite only when it was modified to some extent. The adsorption rates of SDoS were very slow and proved to be affected by molecular diffusion in zeolite pores. They depended on hydrophilic-hydrophobic character of zeolites as well as on pore structures. Adsorption isotherms of SDoS were of Langmuir type, which indicates that the adsorption occurred typically into zeolite pores. Adsorbed amount of SDoS depended on the balance of hydrophilic-hydrophobic character and number of cation site of zeolite surfaces, and had a maximum in case of ZSM-5 zeolites.
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  • 8
    ISSN: 1435-1536
    Keywords: Protein ; adsorption ; surface modification ; hydrophilization
    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 Chemical modifications of mineral surfaces were performed in order to gain insight into what surface properties are decisive of the accumulation of dental plaque. A non-charged, hydrophilic surface was made by two consecutive plasma polymerizations, firstly with allyl alcohol, secondly with acrylic acid, followed by adsorption of a poly(ethylene glycol)-poly(ethylene imine) adduct. A strongly hydrophobic surface was obtained by plasma polymerization of hexamethyldisiloxane. Ellipsometry was used to monitor protein interaction with the surfaces. The hydrophilic surface gave very little adsorption of both a model protein, IgG, and of saliva proteins. The hydrophobic surface, on the other hand, adsorbed high amounts of both types of proteins. In vitro adhesion of an oral bacterium,S. mutans, as well as in vivo studies, gave the opposite result, the hydrophobic surface giving less adhesion and less plaque accumulation than the hydrophilic surface. A tentative explanation of this behavior is that the saliva proteins that bind to the hydrophobic surface adsorb in an unnatural conformation which does not favor bacteria adherence.
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  • 9
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    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 43 (1994), S. 874-880 
    ISSN: 0006-3592
    Keywords: sludge ; sorption ; precipitation ; metals ; adsorption ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A conceptual model describing the relative roles of sorption and precipitation processes for metals in solid-solution suspensions is presented. The model performance is demonstrated using experimental data on sorption and precipitation of metals in samples of activated sludge mixed liquor. Based on the experimental results presented here, it appears that, at total metal and mixed liquor suspended solids concentrations and pH values generally encountered in full-scale municipal (or combined municipal/industrial) activated sludge systems, metals are primarily removed by sorption processes.
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  • 10
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    Biotechnology and Bioengineering 43 (1994), S. 1087-1093 
    ISSN: 0006-3592
    Keywords: adsorption ; ion exchange ; chitosan ; equilibrium ; BSA ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Equilibrium isotherms for adsorption of bovine serum albumin (BSA) on a new adsorbent, a strongly basic crosslinked chitosan (Chitopearl 2503), which is hard and is not compressed by pressure in a column, have been presented and compared with diethylaminoethyl (DEAE) Sepharose Fast Flow (hard gel). In Chitopearl 2503, when only buffer existed in the BSA solution, the isotherm was not affected by the initial concentration of BSA but it was affected by pH considerably. The isotherm was favorable when pH ≥ pl (≅ 4.8). When NaCl existed in the BSA solution, the amount of BSA absorbed on the resin decreased with increasing concentration of NaCl. When the concentration of NaCl was 200 mol/m3, the resin did not adsorb BSA at all. The equilibrium data were correlated by the Langmuir equation reasonably well. The BSA may be adsorbed mainly by electrostatic attraction between negatively charged BSA and positively charged quanternary ammonium groups at pH 〉 pl and by protonation reaction of the primary ammonium groups by weak acid groups of BSA at pH = pl. These are confirmed by measuring the amount of inorganic ion exchanged for BSA. In DEAE Sepharose Fast Flow, the isotherm was favorable when pH 〉 pl but unfavorable ar pH = pl. The saturation capacity of BSA on Chitopearl 2503 is about 1.3 to 2.2 times larger than that on DEAE Sepharose Fast Flow. © 1994 John Wiley & Sons, Inc.
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  • 11
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    Biotechnology and Bioengineering 44 (1994), S. 961-966 
    ISSN: 0006-3592
    Keywords: cellobiohydrolase ; endoglucanase ; adsorption ; hydrolytic efficiency ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Specific quantifications of the major cellulolytic components of the Trichoderma reesei enzyme complex, i.e., endoglucanases I and III and cellobiohydrolases I and II, are described and, employing a defined mixture of these four cellulases reconstituted according to the composition of the native Trichoderma cellulase complex, used to determine the binding of each individual component onto filter paper. During substrate degradation by this enzyme mixture, the specific adsorption of each individual cellulase gradually increases and no preferential binding of one enzyme component in any particular phase of cellulose hydrolysis is found. T. reesei cellobiohydrolases I and II admixed with endoglucanases I and III represent a “full-value” cellulase system that is capable of degrading semicrystalline cellulose efficiently. In comparison with the crude Trichoderma enzyme complex, almost identical adsorption properties and similar hydrolytic efficiency are found for the reconstituted mixture. © 1994 John Wiley & Sons, Inc.
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  • 12
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    Biotechnology and Bioengineering 44 (1994), S. 1064-1073 
    ISSN: 0006-3592
    Keywords: Trichoderma reesei ; cellulase ; cellulose hydrolysis ; adsorption ; synergism ; FPLC ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Hydrolysis of microcrystalline cellulose (Avicel) by cellobiohydrolase I and II (CBH I and II) from Trichoderma reesei has been studied. Adsorption and synergism of the enzymes were investigated. Experiments were performed at different temperatures and enzyme/substrate ratios using CBH I and CBH II alone and in reconstituted equimolar mixtures. Fast protein liquid chromatography (FPLC) analysis was found to be an accurate and reproducible method to follow the enzyme adsorption. A linear correlation was found between the conversion and the amount of adsorbed enzyme when Avicel was hydrolyzed by increasing amounts of CBH I and/or CBH II. CBH I had lower specific activity compared to CBH II although, over a wide concentration range, more CBH I was adsorbed than CBH II. Synergism between the cellobiohy-drolases during hydrolysis of the amorphous fraction of Avicel showed a maximum as a function of total enzyme concentration. Synergism measured as a function of bound enzyme showed a continuous increase, which indicates that by decreasing the distance between the two enzymes the synergism is enhanced. The adsorption process for both enzymes was slow. Depending on the enzyme/substrate ratio it took 30-90 min to reach 95% of the equilibrium binding. The amount of bound enzyme decreased with increasing temperature. The two enzymes compete for the adsorption sites but also bind to specific sites. Stronger competition for adsorption sites was shown by CBH I. © 1994 John Wiley & Sons, Inc.
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  • 13
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    Polymer International 35 (1994), S. 379-387 
    ISSN: 0959-8103
    Keywords: electrolyte ; latex ; particle size ; rate of polymerisation ; polydispersity ; adsorption ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The effects of adding potassium chloride in concentrations below that required to coagulate the latex to recips of emulsion polymerisation of styrene have been investigated using different concentrations of potassium octadecanoate, which has a low critical micelle concentration (CMC), and potassium dodecanoate, which has a moderately high CMC. At relatively high concentration of octadecanoate the final particle size is significantly increased; the rate of polymerisation is initially increased but later retarded. The effects of increasing micelle size and increased rate of coalescence are dominant. At lower concentration of this emulsifier, the rate is reduced from the onset of interval II.With dodecanoate, concentrations of electrolyte up to 0.3 M accelerate the rate. No significant change in the particle size was observed up to 0.2M electrolyte, thereafter it slightly increased. The increase in micellar concentration can only partially account for these effects. It is believed that the increase in the amount of solubilised monomer inside the micelles, and later inside the latex particles, and the resistance to coalescence (because of the favourable adsorption mechanism of this emulsifier) may account for these observations.With both emulsifiers, electrolyte reduces the induction period and latices with narrow particle size distributions are produced.
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  • 14
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    Polymer International 33 (1994), S. 315-319 
    ISSN: 0959-8103
    Keywords: gelatin ; adsorption ; silica ; kinetics ; solid-liquid interface ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The kinetics of adsorption of gelatin from its aqueous solution on to silica has been studied at room temperature. The adsorption isotherms were found to be of the Langmuir type. From the adsorption isotherms, the adsorption coefficient, surface coverage and rate constants for adsorption and desorption were evaluated. The rate of adsorption was found to be maximum at the isoelectric point of gelatin and decreased with increase in pH of the adsorption medium. The increased ionic strength of the medium also caused an increase in the rate and amount of adsorption.
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  • 15
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    Colloid & polymer science 269 (1991), S. 70-76 
    ISSN: 1435-1536
    Keywords: Illuminationeffect ; adsorption ; diffusion ; cellulosemembrane ; directdye
    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 effect of illumination on transport of sulfonated bisazo direct dyes, CI Direct Yellow 12, and CI Direct Yellow 4, into a cellulose membrane has been studied at various temperatures. Transport of CI Direct Yellow 12, which exhibits photoinduced reversible trans-cis isomerism in aqueous solution into a cellulose membrane, was influenced by illumination. It is likely that the transport was influenced by transisomerization of the photoisomeric dye and the diffusivity was controlled by surface diffusion rather than by pore diffusion under both light and dark conditions.
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  • 16
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    Colloid & polymer science 269 (1991), S. 1077-1085 
    ISSN: 1435-1536
    Keywords: Aluminum oxide ; adsorption ; light scattering ; fish oil ; poly(vinylbutyral)
    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 effects of added poly(vinylbutyral) (PVB) and oxidized Menhaden fish oil (O-FO) on dilute suspensions of Al2O3 in the azeotropic solvent mixture 73/27 Wt.-% trichloroethylene/ethanol were studied by static (SLS) and dynamic light-scattering (DLS). The DLS correlation function consisted of four terms from: 1) interdiffusion of the two solvents, 2) diffusion of Al2O3, 3) diffusion of added O-FO and/or PVB, and 4) an induced velocity of particles through the scattering volume due to “laser pressure.” The amplitude and relaxation time of all terms could be determined. Addition of PVB to the Al2O3 suspension resulted in an increase in particle size corresponding to the adsorption of a monolayer of coils. Addition of O-FO to the Al2O3 suspension did not produce a significant increase in particle size, indicating either no adsorption or a compact conformation of O-FO molecules on the Al2O3 surface.
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  • 17
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    Colloid & polymer science 269 (1991), S. 1045-1054 
    ISSN: 1435-1536
    Keywords: Foam formation ; thin liquid films ; surfactant vapors ; adsorption ; dissolution
    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 new possibility of obtaining foams and single thin liquid films by supplying a surfactant through the gaseous phase is presented. Argon saturated with vapors ofn-amyl orn-decyl alcohol was passed through the water phase and formation of the foam was measured as a function of time, gas flow rate, and volume of the water phase. Formation and properties of microscopic thin liquid films were measured as a function of the time of their contact with the surfactant vapors. Two possible mechanisms of foam formation by supplying surfactant via the gaseous phase are discussed. A theoretical model of surfactant dissolution is presented and its predictions are compared with the experimental results. It is shown that foam formation resulted mainly from dissolution of the surfactant vapors in the water phase.
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  • 18
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    Colloid & polymer science 269 (1991), S. 161-165 
    ISSN: 1435-1536
    Keywords: Hydroxyapatite ; phosphoserine ; incongruentdissolution ; adsorption ; ion-exchange
    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 Concentrations of phosphate and calcium ions, liberated from the surface of hydroxyapatite (HAP) during the adsorption of phosphoserine (PSer), were determined at 30°C. HAP showed a marked incongruent dissolution behavior in the presence of PSer. That is, the concentration of phosphate ion in solution increases with the addition of PSer due to the ion-exchange between PSer and phosphate ion on HAP (molar ratio of the former to the latter=3∶2), whereas the concentration of calcium ion decreases with this release of phosphate ion, because the solubility product of HAP restricts the concentrations of both ions in solution (calculated values of — log (Ca2+)10 (PO 4 3− )6 (OH−)2 were 115.8±1.0). The affinity of PSer to HAP was highest at pH 5.8 where the PSer and the HAP surface had the opposite charges. This electrostatic attraction force between PSer and HAP was shielded to some extent by the addition of KCl.
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  • 19
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    Colloid & polymer science 269 (1991), S. 259-263 
    ISSN: 1435-1536
    Keywords: Drug targeting ; polyacrylic ; lattices ; nanoparticles ; electrophoretic mobility ; ζ-potential ; adsorption ; electrolytes ; human serum
    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 ζ-potential of copolymer particles of acrylic amide, acrylic acid, acrylic butyl ester, and styrene were measured in different electrolyte solutions. In an isotonic solution of sodium chloride, they vary with the content of acrylic acid between −36 mV and −49 mV. In the presence of 2∶1-electrolytes, the ζ-potential could be correlated with the logarithm of the electrolyte concentration. The 2∶1-electrolytes predominantly determine the ζ-potential of the particles not only in the solutions of these electrolytes, but also in mixed electrolyte solutions. In the presence of human serum, the electrophoretic mobility increases with increasing acrylic acid content of the polymer.
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  • 20
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    Biotechnology and Bioengineering 37 (1991), S. 537-543 
    ISSN: 0006-3592
    Keywords: colloidal particles ; γ-globulin ; adsorption ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The effect of surface properties on the adsorption of bovine γ-globulin, a model protein for antibody, was studied. Polystyrene latex (PS), hydrophilic copolymer lattices of styrene/2-hydroxyethyl methacrylate [P(S/HEMA)], styrene/ methacrylic acid [P(S/MAA)] and methyl methacrylate/ 2-hydroxyethyl methacrylate [P(MMA/HEMA)], and colloidal silica were used. The adsorption isotherms of γ-globulin on these colloidal particles were measured as a function of pH and ionic strength. The hydrophilic particles showed low affinities for γ-globulin at alkaline pH, while PS showed high affinities for γ-globulin over the whole range of pH and ionic strength. The γ-globulin adsorption on hydrophilic particles was highly reversible with respect to the pH and ionic strength compared with that on PS. These differences indicate that the dominant driving forces of adsorption are related to the hydrophilicity of particles. The adsorption isotherms of all colloidal particles showed the plateau values, and the order of maximum values of plateau adsorption was P(S/MAA) 〉 PS or P(S/HEMA), silica 〉 P(MMA/HEMA). Thus, they were also affected by the charged groups and the hydrophilicity of the surfaces. On the other hand, the plateau values of all colloidal particles were more or less symmetrical with a maximum at around the isoelectric point of γ-globulin at an ionic strength of 0.01. This behavior is attributed to the important role of the lateral interaction between the adsorbed molecules at low ionic strength.
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  • 21
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    Biotechnology and Bioengineering 37 (1991), S. 955-959 
    ISSN: 0006-3592
    Keywords: flotation ; Streptomyces pilosus ; lead ; adsorption ; sodium dodecylsulfate ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The flotation of Streptomyces pilosus was studied in the absence and presence of adsorbed Pb(II) ions on the cell walls and with and without using sodium dodecylsulfate (SDS) as collector. Adsorption of SDS onto the organism in the absence and presence of Pb(II) ions was also investigated. It was found that in the absence of adsorbed Pb(II), very little flotation took place with or without the presence of SDS although SDS adsorbed to some extent on the organism. The presence of Pb(II) on the bacterium's cell walls significantly increased flotation even in the absence of the collector. Addition of SDS, however, further increased both flotation rate and recovery.
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  • 22
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    Biotechnology and Bioengineering 38 (1991), S. 273-279 
    ISSN: 0006-3592
    Keywords: coimmobilization ; Phanerochaete chrysosporium ; pentachlorophenol ; biodegradation ; adsorption ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The concept of coimmobilizing cell mass (and/or enzyme) and adsorbent in a hydrogel matrix for biodegradation of toxic organic chemicals was introduced. Under defined experimental conditions, the coimmobilized system using activated carbon and Phanerochaete chrysosporium was compared with nonimmobilized systems for the degradation of pentachlorophenol (PCP). It was demonstrated that the coimmobilized system degraded PCP more effectively than the nonimmobilized system. A solid substrate included in the coimmobilized system could support the biodegradation. Isolation of the degrading agents from a model interrupting microorganism by the coimmobilized capsule membrane reduced the interference on the biodegradation. In simulated contaminated soil extract and sand, the coimmobilized system also exhibited higher degradative ability and stability than the nonimmobilized systems.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 23
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 268 (1990), S. 476-483 
    ISSN: 1435-1536
    Keywords: Silicasuspensions ; polyelectrolytes ; adsorption ; flocculation ; peptization
    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 possibility to concentrate, then redisperse colloidal suspensions is not only of great theoretical interest, but is also relevant to the industrial process of solid-liquid separation, which must often be followed by a redispersion stage. Up to now, these consecutive operations were unrealizable in the presence of polymers, since flocculation and adsorption were generally considered irreversible in this case. Previous studies have pointed out the occurrence of two main flocculation mechanisms: charge neutralization and interparticle bridging. The use of copolymers makes it possible to take into account these two different mechanisms together. Using this fact we prepared new copolymers of acrylamide with N-vinylimidazole via radical polymerization and characterized them by light scattering, viscometry, potentiometric titrations, and UV studies. One peculiarity of the chosen system is its dependence on pH: actually the degree of neutralization of such cationic polyelectrolytes does vary with pH, especially near the pK value. This paper shows that these copolymers may induce reversible flocculation of negatively charged suspensions, e.g., silica suspensions, by simple pH adjustment. Performances of the system were followed by various physico-chemical methods. The observed results are explained in terms of flocculation mechanisms as a function of pH.
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  • 24
    ISSN: 1435-1536
    Keywords: Poly-vinylalcohol ; proteins ; polysaccharides ; mixture ; inerface ; adsorption ; ultrathinfilm
    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 Ultra-thin films of syndiotactic-rich poly-vinyl alcohol (s-PVA) with several proteins and polysaccharides were prepared by the bubble and frame methods using a mixed dilute aqueous solution (1.5g/dL).The mixed amount ofΒ-cyclodextrin (Β-CD) was the largest among these proteins and polysaccharides giving a weight ratio (Β-CD/s-PVA) of 1. The ratios of silk fibroin(SF), lysozyme, pepsin, and pectin tos- PVA were 0.58, 0.40, 0.35, and 0.35, respectively. For theΒ-CD/s-PVA and SF/s-PVA blend thin films, the phase separation was observed.
    Type of Medium: Electronic Resource
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