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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 264 (1986), S. 56-64 
    ISSN: 1435-1536
    Keywords: Polymeric antiredeposition agents ; adsorption ; hydrophilization ; steric repulsion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Description / Table of Contents: Abstract In laundering, oily soils are detached from textile surfaces and dispersed. In addition, the washing solution should reduce the redeposition of free suspended soil particles onto the textile fibres. In the case of a recommended predetermined dosage of a detergent the main part of the required stabilizing effect is due to the surfactants, complexing agents, builders and zeolites. Polymeric antiredeposition agents cause only gradual additional improvements. In the case of a weak dosage the stabilizing effects of the surfactants and builders rapidly decrease and the effects of the polymeric antiredeposition agents increase. The mechanism of these effects is characterized by high selectivity of the textile substrates. In the case of polar textiles (for instance cotton) carboxy methyl cellulose is often successfully used. In this case the mode of action is mostly due to steric repulsion of the adsorbed layer. In the case of hydrophobic polyester fibres cellulose ethers with hydrophobic sidechains (for instance hydroxy propyl cellulose) show very good effects. In this case the steric component of the polymeric repulsion is supported by the decrease of the driving force of the heterocoagulation (hydrophilization of all hydrophobic interfaces). For this reason combinations of several antiredeposition agents are often used for mixed fabrics. The performenace of the polymeric agents for polyesters can be characterized by their ability to cause strong effective irreversible hydrophilization effects despite the competitive influences of the residual detergent ingrediences.
    Notes: Zusammenfassung Im Waschprozeß werden ölige Anschmutzungen von textilen Oberflächen abgelöst und dispergiert. Die Flotte soll darüber hinaus das Wideraufziehen (Redeposition) frei schwebender Schmutzanteile auf Textilfasern vermindern. Bei empfohlener Solldosierung eines Waschmittels entfalten Tenside, Komplexbildner, Builder und Zeolithe den größten Teil der erforderlichen Stabilisierungswirkung. Polymere Vergrauungsinhibitoren bewirken nur graduelle zusätzliche Verbesserungen. Mit fortschreitender Unterdosierung nimmt die stabilisierende Tensid-und Builder-Wirkung schnell ab und die Bedeutung polymerer Vergrauungsinhibitoren steigt. Der Wirkungsmechanismus weist ein hohes Maß an Selektivität gegenüber textilen Substraten auf. Auf polarem Gut (z. B. Baumwolle) wird oft mit Erfolg Carboxymethylcellulose eingesetzt. Die Wirkungsweise beruht in diesem Falle weitgehend auf der sterischen Polymerschutzwirkung adsorbierter Schichten. Auf hydrophoberen Polyesterfasern zeigen Celluloseether mit hydrophoben Seitenketten (z. B. Hydroxypropylcellulose) sehr gute Effekte. Dabei wird die sterische Komponente der Polymerschutzwirkung durch Erniedrigung der treibenden Kraft der Heterokoagulation (Hydrophilierung sämtlicher hydrophober Grenzflächen) verstärkt. An Mischgeweben werden daher oft Kombinationen mehrerer Vergrauungsinhibitoren genutzt. Die vergrauungsinhibierende Wirksamkeit polymerer Substanzen für Polyester kann durch deren Fähigkeit, ungeachtet der Konkurrenz mit restlichen Inhaltsstoffen des Waschmittels möglichst starke effektiv irreversible Hydrophilierungseffekte hervorzurufen, charakterisiert werden.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 263 (1985), S. 141-146 
    ISSN: 1435-1536
    Keywords: Bovine serum albumin ; soap-free ; acrylic acid-copolymerized latex ; 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 The adsorbability of bovine serum albumin (BSA) onto styrene/acrylic acid copolymer (PS/PAA) latex prepared without emulsifier was investigated as a function of pH and ionic strength. Polystyrene (PS) latex was used as a reference sample. The adsorption isotherms of BSA onto PS/PAA latices showed a stepwise nature. The thickness of the adsorbed BSA monolayer suggested that BSA molecules adsorbed onto PS/PAA2 latex (here, the subscript, i. e., 2, represents the mol % of acrylic acid used in copolymerization) in a “side-on” mode near the isoelectric point (IEP) of this protein. However, in the case of PS/PAA5 latex, a portion of the BSA molecules probably adsorbed in a “loop” or an “end-on” mode. The amount of BSA adsorbed onto PS/PAA latices greatly depended on pH and ionic strength; its value showed a maximum in the neighborhood of the IEP of BSA as in PS latex. The amount adsorbed onto PS/PAA latices except in the alkaline pH region was greater than that onto PS latex. Moreover, the amount adsorbed onto PS/PAA5 latex was greater than that onto PS/PAA2 latex. Both these results are probably attributed to hydrogen bonding between BSA molecule and PS/PAA latex. It was found that the adsorbability of BSA especially at a high ionic strength greatly depended on the surface properties of polymer latices.
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  • 3
    ISSN: 1435-1536
    Keywords: adsorption ; calcium carbonate ; neutron scattering ; nonaqueous dispersions ; surface active agent
    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 Colloidal dispersions of calcium carbonate in toluene, with the particles stabilised by an alkyl aryl sulphonic acid, have been examined by small angle neutron scattering. On the basis of the assumption that the adsorbed layer of stabilising surface active agent formed a concentric shell around a spherical calcium carbonate core particle, a method was developed to determine both the radius of the core particle and the thickness of the adsorbed layer. For the two series of particles examined the calcium carbonate core particles were found to have radii of 22 and 67 å respectively and in both cases the adsorbed layer thickness was found to be 19.0±1 å. The method provides a means of obtaining adsorbed layer thicknesses under conditions where particle and layer cannot be separated.
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  • 4
    ISSN: 1435-1536
    Keywords: Keratin fibers ; adsorption ; cationic polyelectrolytes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Adsorption of the cationic polymers poly(methacrylamidopropyltrimethyl ammonium chloride) (PMAPTAC) and poly(1,1-dimethylpiperidinium-3,5-diallylmethylene chloride) (PDMPDAMC) on human hair was studied by measurements of the amount of polymer adsorbed and by the streaming potential method. Results reflect the amphoteric nature of the keratin surface and show that the excess of anionic sites at pH values above 4 is the main driving force for the adsorption of cationic polyelectrolytes. Lowering the pH below 4 or addition of neutral salt (KCl) reduces the amount of adsorbed polymer. It was shown that the adsorption of cationic polymer in the concentration range 0.01 to 0.1 % and at neutral pH reverses the overall character of the surface from anionic to cationic. Keratin fibers modified in this manner do not exhibit amphoteric character and bear excess positive charge in the pH range 2–9.5. The value of the amount of the polymer adsorbed at saturation concentration (∼2 mg/g) as well as the lack of molecular weight effect in the range (5 · 104 − 106) on the amount of polymer adsorbed suggest that polymer chains adopt a rather extended conformation on the fiber surface. Some data concerning the formation of a complex between adsorbed cationic polymer and anionic detergents or polyelectrolytes are also presented.
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  • 5
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    Springer
    Colloid & polymer science 263 (1985), S. 933-934 
    ISSN: 1435-1536
    Keywords: Gelatin ; emulsion ; gel ; shear modulus ; 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 The incorporation of emulsion oil droplets into a gelatin gel leads to an initial increase in shear modulus at 25 °C for a gelatin concentration of 8 wt % but an initialdecrease for a concentration of 5 wt %. The latter result is consistent with a net lowering of the gelatin concentration available for gelation in the aqueous phase due to adsorption at the oil-water interface.
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  • 6
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    Colloid & polymer science 263 (1985), S. 720-725 
    ISSN: 1435-1536
    Keywords: Kinetics ; adsorption ; cellulose ; polyamideamine ; exponential kinetic equation
    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 kinetic dependences have been investigated of the adsorption process of polyamideamine on monocarboxyl cellulose, bleached sulphate cellulose pulp of softwood and bleached sulphite cellulose pulp of hardwood. It has been found that the process kinetics can be described by means of the Elovich-Tyomkin exponential kinetic equation; the influence of the entropy factors plays a decisive role in changing the process speed; the activation energy is of the order of 6.5–8.0 kJ/mol.
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  • 7
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    Colloid & polymer science 105 (1997), S. 6-10 
    ISSN: 1435-1536
    Keywords: Colloidal aqueous suspensions ; adsorption ; rheology ; polyethylene oxide ; phosphonate ; calcium carbonate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract New polymeric dispersing agents designed to stabilize and lower the viscosity of aqueous mineral suspensions have been synthesized and studied. These dispersants are made of a non-ionic hydrosoluble polymer (polyethylene oxide) with a functional group (diphosphonate) having a strong affinity for the mineral surfaces attached at one end of the macromolecular chains. This molecular architecture allows a brush-like adsorption at the solid surface which differs from conventional homopolymer dispersants such as polyacrylates. The adsorption of these dispersants onto calcium carbonate as a model mineral and the rheological behavior of concentrated aqueous colloidal dispersions of CaCO3 particles were studied. Strong adsorption by the polymer chain-end provides an enhanced colloidal stability of the suspensions of CaCO3 particles. The addition of the dispersing polymer causes a deaggregation of the initially flocculated CaCO3 particles, which results in a drastic reduction of the viscosity of the concentrated suspensions. Thus, the viscosity of a 20 wt% CaCO3 suspension in water at pH=11 is lowered to 2 mPa s upon the addition of a low concentration of polymer. Comparison with polyacrylate dispersants shows the advantages of such a diblock macromolecular structure with a non-ionic polymeric part at high solid contents and high ionic strengths.
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  • 8
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    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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  • 9
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    Journal of polymers and the environment 8 (2000), S. 67-79 
    ISSN: 1572-8900
    Keywords: Polyvinyl alcohol ; biodegradation ; soil, clay ; adsorption
    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 The rates and extents of absorption and desorption of polyvinyl alcohol (PVA) samples on different solid substrates comprising montmorillonite, quartz sand, and farm soil, as well as humic acid mixture are reported. The uptake of PVA by the substrates was analyzed as a function of PVA hydrolysis (72–98%), molecular weight, and molecular weight distribution. Higher adsorption was detected on montmorillonite followed by farm soil, whereas the quartz sand did not display any specific adsorption affinity for the PVA. An increase in the hydrolysis degree of PVA increased the adsorption rate and extent whereas this feature was reversed by an increase in PVA molecular weight. The desorption of PVA samples from the different substrates was performed both under various pH conditions and in the presence of concentrated HF that was used to dissolve the silicon derivatives present in the substrates. Biodegradation experiments carried out in liquid cultures of PVA adsorbed on montmorillonite showed that the mineralization of the adsorbed PVA was much lower than that detected for the nonadsorbed PVA. This investigation suggests that irreversible adsorption of PVA on the clay component occurs in soil, thus substantially inhibiting PVA biodegradation.
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  • 10
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    Oxidation of metals 47 (1997), S. 495-506 
    ISSN: 1573-4889
    Keywords: chromia-forming alloys ; nonmetallic-element effects ; segregation ; adsorption ; surface compounds ; nucleation ; oxide grain boundaries
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The effect of S, N, and C on the oxidation of Ni 20%Cr and Fe-20%Cr was investigated by two approaches (i) using AES and LEED following oxide nucleation and growth under UHV conditions and (ii) by thermogravimetry and subsequent SEM analysis, under conditions where only adsorption/segregation of these elements and congregation of Cr occurred. Sulfur retards nucleation, inhibits lateral growth, and leads to a coarse-grained oxide with a wide network of ridges at the grain boundaries—the growth rate decreases with increasing sulfur activity. Nitrogen and carbon or rather the cosegregated Cr promote the nucleation of C2O3, which leads to many grains and grain boundaries in the oxide layer, accelerated growth and a sponge-like morphology.
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  • 11
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    Journal of computer-aided materials design 6 (1999), S. 69-80 
    ISSN: 1573-4900
    Keywords: adsorption ; friction ; lubrication ; tribological system
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract A molecular dynamics simulation study of friction in boundary lubrication was conducted in order to investigate the atomic-scale behavior of lubricant molecules during sliding motion. The simulated system consisted of two silicon (001) semi-infinite substrates lubricated by a three-layer film of dodecane. Silicon was modeled using the Stillinger–Weber potential, and the dodecane with the Consistent Force Field function; a novel scheme was used to generate the silicon–dodecane interaction potentials. The simulations show that dodecane molecules strongly prefer to adsorb into the ledges on the silicon surface. The orientation of the adsorbed molecules depends, however, on the concentration of the lubricant at the surface, showing a tendency to stand up at high lubricant concentrations. In sliding, the dodecane layers adsorbed on the surfaces behave as a solid, whereas the middle layer exhibits liquid-like characteristics. The friction coefficient of this well-lubricated case was calculated to be 0.08.
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  • 12
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    Oxidation of metals 12 (1978), S. 183-190 
    ISSN: 1573-4889
    Keywords: NiO ; electrical conductivity ; adsorption ; gas-solid equilibria
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The electrical conductivity of NiO was measured at 740°C in an oxygen pressure range of 10−2 −1.3 Torr. By means of continuous recording, longtime experiments were performed. The results show that for any admittance of oxygen, the electrical conductivity initially increased and then decreased to its initial value. For pressures higher than 0.1 Torr the decrease of the signal was reduced and the time required to attain the initial value sometimes reached several days. These results suggest that the electrical conductivity changes may be considered as a transitory phenomenon connected to attaining gassolid equilibrium.
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  • 13
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    Oxidation of metals 39 (1993), S. 353-370 
    ISSN: 1573-4889
    Keywords: Sulfur ; chromia ; tracer ; sulfur solubility ; adsorption ; pores
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The solubility of sulfur in chromia has been studied in H2-H2O-H2S tagged with35S at 973 and 1173 K at low oxygen and sulfur partial pressures typical for coal gasification-systems. For monocrystalline samples, it has been shown that sulfur-containing species are only present adsorbed on the surface of the specimens and can be removed by ultrasonic cleaning in acetone. The surface coverage after 4 weeks of exposure to H2-H2O-H2S was between 2.8 and 19.3% of a monolayer. In polycrystalline chromia, sulfur was located only in pores and cracks of the sample. In dense, compact areas of the specimens the solubility of sulfur was below the detection limit of autoradiography, which was estimated to be better than 0.17 ppm.
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  • 14
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    Oxidation of metals 10 (1976), S. 135-148 
    ISSN: 1573-4889
    Keywords: adsorption ; steel ; oxygen ; Auger spectroscopy ; ellipsometry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract A study of the adsorption of oxygen on steel at room temperature has been performed in an ultra-high-vacuum system with oxygen in the pressure range from 10−9 to 10−4 Torr. Ellipsometry, surface potential difference, and Auger spectroscopy were the surface techniques used. The surface of the steel was cleaned by Cs+ and Ar+ bombardment. The mechanism of the adsorption process is postulated to involve adsorption of molecular oxygen, followed by dissociation and chemisorption of atomic oxygen to form one monolayer. Further adsorption on top of this monolayer is associated with a place-exchange process to produce multilayers of oxide.
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  • 15
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    Journal of porous materials 4 (1997), S. 5-15 
    ISSN: 1573-4854
    Keywords: pillared clay ; pore size modification ; adsorption ; cracking ; carbon
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract To enhance the adsorption selectivity of pillared clays an attempt is made to modify the initial pore size by a controlled deposition of carbon. Cracking of hydrocarbons in the pores of the pillared clay results in coke deposits which can alter the pore size. Based on the evaluation of the amount of coke, the coke density, the decrease in micropore volume, changes in the micropore size distribution and the acidity it was possible to distinguish between pore-blocking, pore-filling and pore-narrowing effects. The modification mechanisms strongly depend on the initial porous structure, the acidity (Brönsted/Lewis), the cracking conditions (static or flow) and the hydrocarbons used. The carbon deposition results in a decrease in pore volume due to pore-filling (Ti-PILC) and pore-blocking (Al-PILC) without achieving a controlled pore-narrowing but some indications for pore-entrance narrowing were found.
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  • 16
    ISSN: 1573-4854
    Keywords: relative permeability ; pore structure characterisation ; adsorption
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract A novel design for the application of a simplified experimental procedure, capable of providing satisfactory relative permeability data for porous media at low relative pressures, is presented. The technique avoids the two-component mixing complications as well as the problems arising from the sample macroscopic inhomogeneity. The latter has been reduced with the aid of a variable pressure compaction procedure. Thus, it becomes easier to utilise the powerful relative permeability technique for the characterisation of the structure of porous solids. Emphasis is given to the combination of the relative permeability data obtained with an analytical approach based on Effective Medium Theory for the calculation of pore connectivity.
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  • 17
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    Journal of porous materials 2 (1995), S. 191-199 
    ISSN: 1573-4854
    Keywords: adsorption ; analysis of pore structure ; estimation from sorption pore shape ; from ad-de-sorption surface area ; calculations from sorption
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The interpretation of pore dimensions based on physical ad-desorption analyses is central to the characterization of pore network structure. Several approaches have been proposed and are commonly employed in the analysis of physical adsorption and/or desorption to deduce the dimensions of the porous network. These approaches assume either theoretical (e.g., BET, the Halsey equation as interpreted by Pierce et al., or the more recent analyses of microporosity) or “standard” isotherms as model(s) for the sequential calculations required in estimating the pore network dimensions. Subsequent representation of the pore dimensions and the relationship between these distributions in dimension and other experimental parameters (such as catalytic activity, adsorptivity or transport); thus, depend explicitly on the model employed in the analyses. Each instrument currently available for the measurement of porous solid structure by sorption employs the same specific models for the relationship between the volume ad-desorbed and the dimensions of the porous network that is being characterized. This paper analyzes the interpretation of porous dimensions based on the sequential calculations required in the analyses. A new approach is proposed which is based on a modification to current practices reflecting Halsey's original theory for the thickness of the adsorbed layer (as a function of P/P 0). Further, the calculations of the incremental changes in the exposed surface area are discussed as they relate to pore network structure. A method is proposed to infer the differences in pore shape. Sorption data are analyzed by these new approaches, and these analyses will be compared with those approaches currently employed. Analyses based on these modified approaches provide a dramatically more consistent interpretation of the sorption data and the corresponding pore network structures.
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  • 18
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    Journal of porous materials 3 (1996), S. 5-16 
    ISSN: 1573-4854
    Keywords: carbon molecular sieve ; adsorption ; adsorption kinetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Equilibrium and kinetics of oxygen and nitrogen sorption in two different carbon molecular sieves (CMS) have been modeled. In both CMS materials, equilibrium characteristics are adequately described by the Langmuir model. However, for kinetics of sorption, one CMS followed classic Fickian diffusion, while the other sample did not. A mathematical model was developed which accurately describes both pure component as well as binary uptakes in both materials. Simple manipulation of the boundary condition of the diffusion process allows the model to accurately predict both Fickian and surface barrier diffusion. All parameters needed to estimate binary uptake rates are obtained from pure component uptakes and isotherms. In addition, the model predicts both pure component and binary diffusion rates with diffusion coefficients which are not concentration dependent.
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  • 19
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    Journal of porous materials 5 (1998), S. 275-287 
    ISSN: 1573-4854
    Keywords: activated carbons ; adsorption ; characterization ; Dubinin-Radushkevich ; carbon dioxide
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract In this paper we present adsorption isotherms of carbon dioxide on five different activated carbons from CHEMVIRON CARBON Belgium (Centaur HSV, BPL 410, F30-470, WS 42, Reactivated) and on a carbon molecular sieve from BERGBAU FORSCHUNG Gmbh (CMS II). The temperature is 303 K and the pressure ranges from 100 kPa up to 4000 kPa. Such conditions correspond to relative pressures ranging from 0.01 to 0.5. We also provide, for the same six sorbents, the nitrogen isotherms at 77 K (pressure: 0.001 to 100 kPa, relative pressure: 10-5 to 1). A theoretical treatment based on the Dubinin-Radushkevich and Stoeckli concept is presented and applied to the experimental results in order to obtain the micropore size distribution function (considered as Gaussian) of each sorbent. Using the CO2 data, it is possible to point out important structural differences between the six carbons. The theoretical treatment provides micropore size distribution functions in agreement with what is physically expected. Using N2 data, the structural differences are not so well marked. As a consequence, the structural parameters provided by the theoretical treatment are not reliable: except for the total micropore volume, they fluctuate strongly when changing the relative pressure domain of the used data.
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  • 20
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    Journal of porous materials 3 (1996), S. 257-266 
    ISSN: 1573-4854
    Keywords: pillared clay ; pore size modification ; adsorption ; polymers ; carbon
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract In order to use pillared clays (PILC) for selective adsorption, further modifications of the porous structure are necessary. The deposition of carbon residues onto the porous structure of pillared clays by the carbonization of polymers (polyvinylalcohol) was proposed to achieve a controlled modification of the pore size. Ti and Al-pillared clays (calcined and non-calcined) were impregnated with PVA (different grades and different concentrations and subsequently carbonized to form carbon phases. The effect of the carbon deposits on the porosity of Ti- and Al-PILC is discussed in terms of pore-blocking, pore-filling and pore-narrowing. The deposition of carbon using PVA resulted in a complete pore-blocking for Al-PILC and in a narrowing of the pore size distribution for Ti-PILC, without achieving a controlled pore-narrowing.
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  • 21
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    Journal of porous materials 4 (1997), S. 277-280 
    ISSN: 1573-4854
    Keywords: woodceramics ; porous carbon ; adsorption ; humidity sensor
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The humidity sensor characteristics of Woodceramics were investigated. The Woodceramics used in this experiment were prepared at 650–900°C. The size of specimens selected was 1 × 1 × 10 mm . One was used as-cut and the other was polished. Above 700°C, the resistance of the specimen was below 50 Ω and the decrease of resistance with increasing relative humidity was small. The specimen prepared at 650°C had a resistance of about 1 kΩ. The resistance of as-cut specimens decreased with increase in relative humidity, but that of the polished specimen did not change significantly. The difference between as-cut and polished samples was explained by the differences in surface micro-structure.
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  • 22
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    Colloid & polymer science 265 (1987), S. 1018-1026 
    ISSN: 1435-1536
    Keywords: NO ; α-FeOOH ; carbon fiber ; adsorption ; micropore filling
    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 isotherms of NO, SO2, NH3, and CO2 onα-FeOOH dispersed activated carbon fibers at 303 K were examined to determine the role of surface modification in micropore filling. The parameters on micropore structures were obtained from both nitrogen adsorption at 77 K and benzene adsorption at 303 K; both isotherms were of BDDTI type and gave the same micropore volume. The preoxidation conditions of ACF, prior to the deposition ofα-FeOOH against the NO adsorptivity were examined. The dispersion ofα-FeOOH on ACF was effective in enhancement of micropore filling, irrespective of the adsorbate molecule. We determined the degree of volume filling for each gas by the use of a DR plot. The modified DR plot for an NO gas, of which the critical temperature was much lower than 303 K, was proposed. The degree of volume filling for various gases was correlated with the deviation of each boiling point from 303 K and with the van der Waalsa constant.
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  • 23
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    Colloid & polymer science 268 (1990), S. 476-483 
    ISSN: 1435-1536
    Keywords: Silicasuspensions ; polyelectrolytes ; adsorption ; flocculation ; peptization
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    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
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    Colloid & polymer science 265 (1987), S. 1085-1089 
    ISSN: 1435-1536
    Keywords: Wetting ; advancingcontact angle ; surfactant transfer ; amine ; adsorption
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    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The structure of the adsorption layer at the solid/gas interface is characterized, as a function of conditioning concentration, by the measurement of preceding contact angles. The contact angles were determined tensiometrically (plate method) and cinema tographically (capillary rise method) in the system glass or mercury/n-dodecyl ammonium chloride solution/air, respectively. In the dependence of contact angle on concentration, four regions are provable. These regions correlate with the surfactants, which are bound to adsorption in a heteropolar mode or by van der Waals forces of interaction, with the formation of layer-like coverage and with bilayers. Special attention was given to the fact that loosely bound surfactants are transferred from the solid/gas interface to the liquid/gas interface and cause a reduction of the preceding contact angle.
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  • 25
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    Colloid & polymer science 271 (1993), S. 56-62 
    ISSN: 1435-1536
    Keywords: Alumina ; phosphate ester dispersants ; flow calorimetry ; adsorption
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    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The interaction of two commercially available phosphate ester dispersants with calcined alumina has been investigated using the techniques of flow calorimetry and electrophoresis. Flow calorimetric experiments have shown that these dispersants chemically interact with the surface of calcined alumina. The electrical charging of alumina particles in an iso-octane solution containing a phosphate ester indicates that an acid-base interaction mechanism is operative in this system.
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  • 26
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    Colloid & polymer science 272 (1994), S. 196-203 
    ISSN: 1435-1536
    Keywords: Colloid ; polymer ; adsorption ; rheology
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    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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  • 27
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    Colloid & polymer science 271 (1993), S. 236-240 
    ISSN: 1435-1536
    Keywords: PVC plastisol ; adsorption ; plastification
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    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The significant phenomenological analogy between physical adsorption from liquid solutions on microporous adsorbents and plastification of PVC has been observed. This justified the use of the solution analog of the adsorption isotherm equations of the theory of volume filling of micropores as being adequate to describe the process of plastification of PVC by the composition of plasticizer and modifying agent. The qualitative agreement between isotherm predicted by model and experimental data allowed to formulate the mechanism of the process of interest.
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  • 28
    ISSN: 1435-1536
    Keywords: Cotton fibers ; dye ; adsorption ; calorimetry ; zeta potential ; fluorescence ; degree of whiteness
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    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Fluorescent whitening agents (FWA) are used to improve the whiteness of cellulose fabrics. It is well known but not completely understood that the fluorescence decreases (chemical and physical mechanisms of distinguishing) above a certain FWA concentrationc crit. This reduction of fluorescence correlates very well with the alteration of the adsorption process studied by calorimetry and zeta potential measurements. The results obtained by these methods indicate that the adsorption mechanism is different at concentrations below and abovec crit. The reduction of the intensity of fluorescence, the degree of whiteness and the zeta potential are caused by the adsorption of a second layer of fluorescent whitening agents. This second layer reduces the zeta potential due to a shielding effect and reduces the whiteness and fluorescence by a bathochromic shift of the reflection curves. The final effect is a reduction of the total reflection.
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  • 29
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    Colloid & polymer science 274 (1996), S. 548-554 
    ISSN: 1435-1536
    Keywords: Polyacrylic acid ; γ-Al2O3 ; mercury surface ; adsorption ; voltammetry
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    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract In this paper the adsorption of polyacrylic acid (MW=5000) on the hydrophobic mercury surface and on the hydrophilic γ-Al2O3 surface at pH=3–4 in 0.55 M sodium chloride solution was investigated. Measurements of change of the double layer capacitance by phase selective a.c. voltammetry were used for determination of the adsorption of polyacrylic acid on the mercury electrode. The same method was used for the determination of the polyacrylic acid remaining in the solution after the adsorption on hydrophilic particles (γ-Al2O3 particles). The results obtained for adsorption of polyacrylic acid were compared to the results of the adsorption of humic substance of similar molecular weight under similar experimental conditions. The study has shown that polyacrylic acid in acidic solution is strongly adsorbed on the mercury surface, which is comparable to the adsorption of humic substance on the mercury surface. At the same time, the adsorption/deposition of polyacrylic acid on the γ-Al2O3 surface is weaker compared to humic acid, indicating at a smaller degree of interaction of polyacrylic acid with aluminium ions and with hydrophilic surface.
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  • 30
    ISSN: 1435-1536
    Keywords: Key words Polyelectrolyte ; adsorption ; latex ; surface charge
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    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract  Adsorption of a well-characterized cationic polyacrylamide (CPAM) onto the surface of a model colloid (monodisperse polystyrene latex with carboxylic functional groups) was studied over a wide range of pH (4–9) and KCl concentration (c s =10-3–0.3 M). The surface charge density of the latex particles with and without adsorbed CPAM was also measured over the same range of electrolyte compositions. The adsorbed amount of CPAM increases with increase in c s and pH. The polyelectrolyte adsorption alters substantially the surface charge density of the latex particles as compared to the polymer-free case. A large overcompensation of the surface charge by the adsorbed polyelectrolyte is established at high c s and low pH. A qualitative explanation of the observed features is put forward.
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  • 31
    ISSN: 1435-1536
    Keywords: Key words poly(ethylene oxide) ; silica-tethered poly(methyl methacrylate) ; adsorption ; spin-label ; molecular motion
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    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract  The spin-label method was used to study the structure and molecular motion of poly(ethylene oxide) (PEO) chains adsorbed on a silica-tethered poly(methyl methacrylate) (PMMA). Spin-labelled PEO with a narrow molecular weight distribution, having number averaged molecular weight (M N)=6.0×103, was adsorbed on the surface of the silica-tethered PMMA with various grafting ratios in carbon tetrachloride solution at 35 °C. ESR spectra were measured at various temperatures after the samples were completely dried. The ESR spectra are composed of two spectra arising from spin-labels attached to “train” and “tail” segments, which are strongly and weakly interacted with the silica surface, respectively. The fractional amount of the “tail” segments increases extremely with the grafting ratio of PMMA. Molecular mobility of the PEO chains estimated from the temperature dependence of the ESR spectra also decreases significantly with the grafting ratio of PMMA. Structure and molecular motion of the PMMA chains tethered on the silica were also studied using the spin-labelled PMMA. Consequently, parts of the PEO segments penetrate into the PMMA chains and is adsorbed on the silica surface (“train” segments), whereas parts of the PMMA segments protrude from the surface. The other PEO segments are entangled with the tethered PMMA chains (“tail” segments).
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  • 32
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    Colloid & polymer science 265 (1987), S. 312-317 
    ISSN: 1435-1536
    Keywords: Cellulose ; thermodynamics ; adsorption ; polyelectrolyte ; hydrolyzed modifiedpolyacrylnitrile
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    Notes: Abstract The thermodynamics of adsorption has been studied of hydrolyzed modified polyacrylnitrile (HMP) in water solutions with a concentration ranging from 0.25 g/l to 2.00 g/l on bleached sulphate and unbleached and bleached sulphite celluloses at temperatures of 0, 20, 40, and 60
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  • 33
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    Colloid & polymer science 267 (1989), S. 371-375 
    ISSN: 1435-1536
    Keywords: Bridgingflocculation ; adsorption ; collisionefficiencyfactor
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    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The collision efficiency approach to flocculation is analyzed on the basis of a model describing the probability of aggregation by polymer bridging. The model allows for the effect of the randomness of distribution of polymer over particles as well as the effect of simultaneous coagulation and weak flocculation. It is argued that the collision efficiency approach is applicable to a rather limited range of experimental systems and provides a qualitative understanding rather than a quantitative theory of the relationship between flocculation and adsorption.
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  • 34
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    Colloid & polymer science 264 (1986), S. 260-266 
    ISSN: 1435-1536
    Keywords: Flotation ; adsorption ; carboxylic acid ; amine ; associate
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    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The flotation and adsorption properties of two ionic collectors (n-dodecylamine andn-dodecanoic acid) are compared on the bases of results of mercury flotation in the model flotation apparatus and electrochemical measurements of the double layer capacity. The flotation recovery and the adsorption parameters (standard free enthalpyΔG° A, the interaction coefficient of Frumkin's isotherm, the surface area per molecule) have been determined within the pH range 2.5–12 in solutions of various collector concentrations containing 0.1 N KCl. The maxima of flotation recovery and surface excess have been found at pHs corresponding to pK values for both substances. The influence of the electrolyte on flotation recovery and the gas bubble size distribution dependent upon the pH of the solution is presented forn-dodecanoic acid. The maxima of flotation recovery are involved through the formation of ion-molecule associates (1∶1) as well as an optimum of the bubble size distribution.
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  • 35
    ISSN: 1435-1536
    Keywords: Flow ; adsorption ; entanglements ; apparent-viscosity
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    Notes: Abstract Adsorption-entanglement layers are thick, i.e. multimolecular, layers formed at solid surfaces from solutions of high molecular weight polymers in a state of flow. This publication, the second part of a series of four, is concerned with the effect that the chemical nature of the surface has on formation of these layers. It is shown that for the solutions of polyethylene (PE) and polymethylmethacrylate (PMMA) the layers form most readily on carbon surfaces. Further it is shown that in the case of PE, addition of aluminium stearate can prevent formation of the layers along steel surfaces.These and other effects reported in the paper all bear on actual situations encountered in rheological practice and in particular on the measurement of viscosities. It is concluded that the marked dependence of layer formation on the chemical nature and treatment of the surface is responsible for the differences in viscosity measurements featuring in earlier works by different authors.
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  • 36
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    Colloid & polymer science 269 (1991), S. 70-76 
    ISSN: 1435-1536
    Keywords: Illuminationeffect ; adsorption ; diffusion ; cellulosemembrane ; directdye
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    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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  • 37
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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)
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    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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  • 38
    ISSN: 1435-1536
    Keywords: Polymers ; adsorption ; networks ; swelling ; macroreticular resins
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    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Two groups of polymer networks (polymer resins) are investigated by selective liquid sorption fromn-propanol-water mixtures. Group 1 consists of gel polymerized polar (hydrophilic) ion exchangers which swell in the binary liquid mixture. Group 2 consists of non-polar, non-swelling, macroporous resins. The free energy isotherms accompanying the sorption processes are calculated from the excess isotherms and the bulk activities. The adsorption excess free energies reveal the differences in polarity of the polymer network.
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  • 39
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    Colloid & polymer science 270 (1992), S. 113-127 
    ISSN: 1435-1536
    Keywords: Polypropylene ; filler ; surfactant ; composite ; thermally stimulatedcurrent ; adsorption
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    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Thermally stimulated polarization (TSP) and depolarization (TSD) experiments have been performed with two grades of polypropylene and some respective CaCO3-filled composites containing small amounts of nonionic surfactant (0–2 wt%). The effects of electrode blocking, electrode materials on the thermally stimulated currents, and reproducibility of the measurements have been studied. The effect of water vapor adsorbed from the ambient air on the AC dielectric properties and on the thermally stimulated polarization behavior has been determined. The addition of either CaCO3 or surfactant to PP decreases the intensity of the αc depolarization current peak in the pre-melting region, while the presence of both components increases the current. Partial discharges are present in poly propylene/CaCO3 composites under high voltages if neither water vapor nor a coherent surfactant layer is present at the matrix/filler interface. A short literature survey is presented on the TSC studies of polyolefins and their composites, and various mechanisms responsible for the observed changes are discussed, including interfacial polarization, trap redistribution through nucleation, and oriented adsorption.
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  • 40
    ISSN: 1435-1536
    Keywords: Liposomes ; adsorption ; spreading ; surfacefilm ; monolayer
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    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Liposomes from pure dipalmitoylphosphatidylcholine (DPPC) and mixed DPPC: distearoylphosphatidylcholine (DSPC): soybean lecithin (SL) prepared by the Bangham method with sonication were dispersed into solution or spread at the interface and the kinetics of the surface film formation was studied by measuring and recording the evolution of superficial tension, surface potential, and superficial (14C labeled) DPPC density. A simple theoretical approach can describe these kinetics by two processes: irreversible diffusion of closed vesicles into or from the bulk phase, and irrevers ible transformation of closed spherical vesicles into destroyed ones which form the surface film. Diffusion controls the phenomenon for small initial amounts of liposomes. Transformation controls the phenomenon for important initial amounts of liposomes. The kinetic constant of the transformation,K, does not depend on the technique used to form the surface film (spreading or adsorption). The equilibrium and rheological properties of surface films formed after liposome spreading are compared to those of monolayers
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  • 41
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    Colloid & polymer science 271 (1993), S. 1157-1164 
    ISSN: 1435-1536
    Keywords: Polymer emulsion ; albumin ; fibrinogen ; protein ; adsorption ; surface hydrophilicity ; surface heterogeneity ; microsphere
    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 competitive adsorption of bovine fibrinogen (BFb) and bovine serum albumin onto polymer microspheres from the mixture solution was examined under various protein-to-microsphere ratios using various homopolymer microspheres and poly(2-hydroxyethyl methacrylate)/polystyrene composite microspheres having heterogeneous surface structures consisting of both hydrophilic and hydrophobic parts. They were produced by emulsifier-free (seeded) emulsion polymerizations. The selective adsorption of BFb was not observed for the homopolymer microspheres, but observed for the composite polymer microspheres having optimum compositions.
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  • 42
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    Colloid & polymer science 271 (1993), S. 709-713 
    ISSN: 1435-1536
    Keywords: Water glass ; silica gel ; argon ; adsorption ; microporous
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    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Surface characterization of silica gels prepared at different gelation pH from water glass and sulphuric acid were made by argon adsorption at 77 K using continuous volumetric method. While microporous silica gels prepared in the pH range of 1–3 had BET surface areas of 504–571 m2 g−1, total pore volumes of 0.26–0.31 cm3 g−1 and micropore volumes of 0.16–0.23 cm3 g−1, mesoporous silica gels prepared in the pH range of 3.36–0.65 had BET surface areas of 374–530 m2 g−1 and pore volumes of 0.61–0.79 cm3 g−1.
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  • 43
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    Colloid & polymer science 272 (1994), S. 1620-1626 
    ISSN: 1435-1536
    Keywords: Zeolite ; modification ; chloroform ; adsorption
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    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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  • 44
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    Colloid & polymer science 272 (1994), S. 324-331 
    ISSN: 1435-1536
    Keywords: Surfactants ; silicates ; adsorption ; calorimetry ; x-ray diffraction
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    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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  • 45
    ISSN: 1435-1536
    Keywords: Parallel plate flow chamber ; adsorption ; desorption ; blocked area ; image analysis
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    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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  • 46
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    Colloid & polymer science 271 (1993), S. 307-309 
    ISSN: 1435-1536
    Keywords: Silica ; TiO2 ; adsorption ; ionic surfactant ; surface modified
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    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Colloidal silica and titanium dioxide were surface-modified by chemisorption of octadecyl dimethylmethoxy silane. The surface density of these alkyl silane groups was adjusted to less than 7% of the available surface hydroxyls, leaving the adsorbents hydrophilic and electrically charged in aqueous solution. Ionic surfactants (tetradecylpyridinium chloride and sodium lauryl sulfate) are adsorbed onto the surface-modified silica and titanium dioxide from aqueous solution, even in the case where the surface of the adsorbents exhibits the same sign of electrical charge as the surfactant ionic head groups. According to the adsorption model of Gu the chemiadsorbed alkyl chains are supposed to serve as anchors for small surface aggregates of the ionic surfactants.
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    Colloid & polymer science 272 (1994), S. 830-836 
    ISSN: 1435-1536
    Keywords: Zeolite ; modification ; surfactant ; adsorption
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    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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  • 48
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    Keywords: Protein ; adsorption ; surface modification ; hydrophilization
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    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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  • 49
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    Colloid & polymer science 273 (1995), S. 787-792 
    ISSN: 1435-1536
    Keywords: Zeolite ; modification ; surfactant ; adsorption
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    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Adsorption characteristics of anion-, cation- and nonion-type surfactants and phenol from their aqueous solution on Na-Y zeolites modified by SiCl4 treatment and NA-ZSM-5 zeolites with several Si/Al ratios were measured. Surfactants used were sodium dodecylbenzenesulfonte (DBS), laurylpyridinium chloride (LPC), polyoxyethylenenonylphenylether (POENPE) and phenol. Adsorption of surfactants was enhanced by SiCl4 treatment of Na-Y, which indicates an important role of the hydrophilic-hydrophobic character in the adsorption. Adsorption isotherms were in general of Langmuir type and adsorbed amount depended on the Al/(Si+Al) or Si/Al ratio of zeolite frameworks. In case of DBS adsorption of Na-ZSM-5 series, adsorption occurred only on the outer surface due to steric hindrance. LPC adsorption abilities were observed on even hydrophilic zeolites and were ascribed to ion exchange effect. In case of phenol adsorption on hydrophobic Na-Y, the adsorption isotherm was of Type V according to BDDT classification.
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  • 50
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    Colloid & polymer science 273 (1995), S. 817-821 
    ISSN: 1435-1536
    Keywords: Composite particle ; temperature-sensitive ; biomolecules ; adsorption ; surface
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    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Temperature-sensitive composite polymer particles were prepared by seeded emulsion copolymerization of dimethylaminoethyl methacrylate and ethylene glycol dimethacrylate with 0.17 μm-sized monodispersed polystyrene seed particles. The adsorption and desorption behaviors of low molecular weight cationic emulsifier as well as albumin were examined to determine the variation of surface properties as a function of temperature below and above 35°C.
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  • 51
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    Colloid & polymer science 274 (1996), S. 779-787 
    ISSN: 1435-1536
    Keywords: Silica particles ; colloid stability ; Hamaker constant ; van der Waals potential ; adsorption ; rheology ; SAXS
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Hydrophilic Stöber silica particles are stable in ethanol, but flocculation may be induced by the addition of sufficient cyclohexane. Low-shear rheological measurements indicated non-Newtonian behaviour beyond the critical cyclohexane concentration. The thickness and composition of the solvation layer around the particles were calculated from the adsorption excess isotherm on the basis of a multilayer adsorption model. The composition dependences of the Hamaker constants of the dispersion medium and the adsorption layer were obtained from optical dispersion measurements. A single-sheet, hard-sphere model predicted a weak van der Waals attraction in the ethanolic regime, but a strong attraction in the cyclohexane-rich region, in good accordance with the rheological properties of the dispersions and visual observations.
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  • 52
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    Colloid & polymer science 74 (1987), S. 64-68 
    ISSN: 1435-1536
    Keywords: Wetting ; adsorption ; contact angle ; surfactants ; monolayers
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    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract When a liquid containing surface active molecules advances on a hydrophilic solid surface, specific instabilities are observed. They are due to the diffusion of the surface active molecules which adsorb on the surface, increasing the contact angle. These instabilities appear as waves travelling along the contact line and are visible only in a limited range of liquid edge velocities.
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  • 53
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    Colloid & polymer science 263 (1985), S. 778-781 
    ISSN: 1435-1536
    Keywords: Gelatin ; ionic surfactants ; adsorption ; surface rheology ; octadecanoic acid
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    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Surface rheological measurements of octandecanoic acid monolayers spread on gelatin solutions were performed. The interaction of the spread monolayer with the gelatin involves a strong rise of the solidity of the surface structure with distinct viscoelastic properties and is comparable with the experimental findings looking into the interaction between gelatin and an ionic surfactant. The results found by the addition of sodium-dodecylsulfate to the gelatin solution are discussed, assuming the formation of a multilayer consisting of octadecanoic acid molecules interacting to a negligible degree with the gelatin-surfactant complexes displaced from the surface. The surface rheological parameters are influenced by both layers in opposition to the dynamic behaviour at compression and dilation described in the first part of this paper. An analogous effect is found if the cationic hexadecyltrimethylammoniurn-bromide is added to the gelatin solution. The influence of CTAB is interpreted as the consequence of a steric hindrance, caused by the concentration of groups with opposite charges on the small polar ranges of the gelatin molecules. As a particular interaction of octadecanoic acid with the complexes is possible, a mixed adsorption layer is formed and the high solidity of the surface layer is prevented by the presence of molecules not interacting with the complexes.
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  • 54
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    Colloid & polymer science 267 (1989), S. 899-906 
    ISSN: 1435-1536
    Keywords: Claymineral ; montmorillonite ; adsorption ; polyethyleneglycol ; watertreatment
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    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Adsorption rates and capacities of polyethylene glycol (PEG) were investigated for five montmorillonite clays. The adsorption of PEG for all the montmorillonite clays was rapid, and equilibrium was attained within 30 min. The adsorption isotherms of PEG for all the montmorillonites conformed to the Freundlich equation. The adsorption heats were 7.3 and 11.6 kJ · mol−1(mw.:2000), and 8.7 and 14.2 kJ · mol−1(mw.:20000) for the montmorillonite and the bentonite II-Ca, respectively. Adsorption capacities for all the clay samples approached constants for the molecular weight of PEG over 2000, though they increased with the increase of molecular weight under 2000. The adsorption capacities were slightly influenced by a nearly neutral pH. The montmorillonite clays which had different interlayer cations showed quite different adsorption capacities. The bentonite II-Ca, the acid clay, and the activated clay showed large adsorption capacities that were 30–50 % of that of an activated carbon.
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  • 55
    ISSN: 1435-1536
    Keywords: Poly-vinylalcohol ; proteins ; polysaccharides ; mixture ; inerface ; adsorption ; ultrathinfilm
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    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.
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  • 56
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    Colloid & polymer science 265 (1987), S. 889-896 
    ISSN: 1435-1536
    Keywords: Polyacrylamide ; kaolinite ; clay-polymercomplex ; adsorption
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    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The variation in polyacrylamide adsorption on Na-kaolinite as a function of the electrolyte concentration of the clay suspension, was determined under three pH conditions, where the clays display varying charge characteristics. Interpretation of the results is based on two arguments: non-charged polyacrylamide adsorption is restricted to the edge faces of the colloidal platelets and hydrogen bonding between the amide groups of the polymer and the “isolated” hydroxyl sites of these faces is the mode of surface attachment. At constant pH, when Na-kaolinite bears charged surface groups, the polymer adsorption, which is related to the density of the anchoring sites, parallels the state of ionization of the edge surface. The mechanism by which the salt modifies the adsorption properties of the kaolinite in neutral medium is not established with certainty. Nevertheless, no polymer-clay association occurs if the surface is entirely uncharged. This result is in line with the fact that while hydroxyl groups are engaged in internal hydrogen bonds, they cannot hydrogen-bond to the polyacrylamide. Variations in the clay-polymer affinity are attributed to a modification of the interfacial structure of the adsorbed polymer, associated with changes in the surface density of the anchoring groups.
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  • 57
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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
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    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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  • 58
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    Colloid & polymer science 269 (1991), S. 161-165 
    ISSN: 1435-1536
    Keywords: Hydroxyapatite ; phosphoserine ; incongruentdissolution ; adsorption ; ion-exchange
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    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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  • 59
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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
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    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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  • 60
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    Colloid & polymer science 270 (1992), S. 1027-1034 
    ISSN: 1435-1536
    Keywords: Solid liquid interface ; multilayer ; adsorption ; enthalpy of displacement ; layer silicate
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    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The adsorption from methanol/water and the enthalpy of displacement of methanol by water were studied on K-60 silica gel, on graphitized PRINTEX-80, and onn-alkylammonium vermiculites. The adsorption between the hydrophobized silicate layers was followed by x-ray measurements. The excess isotherms of alkylammonium vermiculites in methanol/water exhibit two maxima corresponding to the two steps of the individual isotherm. The equilibrium constant of the exchange of water by methanol is calculated. For calculating the adsorption capacities and molar adsorption potentials, a new equation is proposed which combines the adsorption excess quantities with free energy and enthalpy functions.
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  • 61
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    Colloid & polymer science 270 (1992), S. 609-616 
    ISSN: 1435-1536
    Keywords: Anionic surfactants ; crystalline silicic acids ; delamination ; intercalation ; silica ; surfactant ; adsorption
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    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Lamellar crystalline silicas (crystalline silicic acids, chemical composition SiO2·xH2O; examples: H4Si14O30·xH2O, H4Si20O42·xH2O) are distinguished from the amorphous forms by their layered structure and exceptional adsorption properties. One outstanding example is the reaction with anionic surfactants. Several types of crystalline silicas (typical H4Si20O42·xH2O) can intercalate ionic pairs consisting of surfactant anion and gegen ion into the interlayer space. The saturation value of SDS adsorption is 0.475 mmol SDS/g H4Si20O42·3H2O. The acid H4Si14O30·xH2O adsorbs anionic surfactants at the external surfaces only (saturation value 0.04 mmol/g H4Si14O30·0.8 H2O). When anionic surfactants are adsorbed in the interlayer space, the layer separation increases to such an extent that the crystals disarticulate in a fan-like manner or delaminate into thinner packets of layers or smaller aggregates. Washing-out the SDS ionic pairs or drying reconstitutes the parallel layer orientation and leads to re-aggregation of the packets and fragments.
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  • 62
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    Colloid & polymer science 271 (1993), S. 799-801 
    ISSN: 1435-1536
    Keywords: Surfactant ; adsorption ; surface-micelle ; BET equation
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    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Based on the multi-species surface micelle model, the adsorption isotherm equations are derived which are identical to the BET equations. Some of the surfactant adsorption phenomena are explained on this basis.
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  • 63
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    Colloid & polymer science 273 (1995), S. 1028-1032 
    ISSN: 1435-1536
    Keywords: Hydrolyzed polyacrylamide ; hematite ; adsorption ; kinetics
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    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The adsorption measurements of hydrolyzed polyacrylamide (HPAM) onto hematite suspension are carried out to study the dynamics of the polymer adsorption onto the suspension particles and to investigate the mode of the polymer adsorption. The polymer is found to show much affinity for the adsorption because of the opposite charges possessed by the polymeric flocculant and the suspension particles. Various adsorption parameters such as adsorption coefficient, the rate constants for the adsorption and desorption, are evaluated with the help of a recently proposed kinetic scheme. It is found that the extent of adsorption and the adsorption rate are adequately affected by increasing the pH of the suspension while, unexpectedly, the adsorption is found to show only a marginal increase on addition of Na2SO4. Both the amount of the adsorbed polymer and the adsorption rate are also found to increase with the degree of hydrolysis of the polyelectrolyte.
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  • 64
    ISSN: 1435-1536
    Keywords: Sodium dodecylsulfate ; adsorption ; precipitation ; montmorillonite
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    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The interaction of dodecylsulfate anions (DS−) with homoionic Ca-, Mg-, Ni-, Cu-, Cd-, Pb- and Fe-montmorillonites were investigated. Mg- and Cd-montmorillonite do not adsorb DS−, and an anion exchange at the edges of the clay mineral does not take place. Three different adsorption processes are identified on the other montmorillonites: i) Fe-montmorillonite is covered with amorphous iron hydroxide, and DS−-anions are bound at positively charged sites. ii) On Ca- and Pb-montmorillonite DS− is precipitated as Me(DS)2. iii) On Ni- and Cu-montmorillonite DS− forms ion pairs with the cations on the surface. In all cases DS− is not bound above the CMC but the metal ions are mobilized from the surface either by solubilization of the precipitates or by formation of mixed micelles.
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  • 65
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    Colloid & polymer science 274 (1996), S. 112-116 
    ISSN: 1435-1536
    Keywords: Temperature-sensitive ; emulsifier ; biomolecules ; adsorption ; surface
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    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Adsorption and desorption behaviours of emulsifiers and biomolecules on the two kinds of temperature-sensitive composite polymer particles were compared. One (I) was produced by seeded emulsion copolymerization of dimethylaminoethyl methacrylate and ethylene glycol dimethacrylate with 0.17 μm-sized polystyrene seed particles. The other (II) was produced by seeded emulsion copolymerization of N-isopropylacrylamide (NIPAM) and N,N′-methylenebisacrylamide with 0.36 μm-sized styrene-NIPAM copolymer particles. The amount of adsorption at temperatures above each lower critical solution temperature (LCST) was found to be much higher for I than II. In both cases, at temperatures below the LCST, almost all lactalbumin hydrolysate molecules adsorbed above the LCST were desorbed but the desorptions of adsorbed egg albumin and lysozyme molecules were not so high. The adsorption and desorption were reversible for both particles and the efficiency was better for I than II. From these results, it is concluded that the adsorption/desorption of protein onto the temperature-sensitive polymer particles is controllable by changing the temperature below and above the LCST of the shell layer and the sensitivity is based on the surface property of the composite polymer particles.
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  • 66
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    Colloid & polymer science 276 (1998), S. 52-58 
    ISSN: 1435-1536
    Keywords: Key words Dodecanephosphonic acid ; soluble monolayer ; air/water interface ; evaporation ; adsorption ; ion-selective electrodes
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    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract  The air/water interface of the system n-dodecanephosphonic acid (H2DP)–water was studied by surface tension, ion-selective electrodes and evaporation in an electrobalance. The combination of surface tension and ion-selective electrodes measurements enables to study the adsorption of soluble surfactants above the cmc using the Gibbs’ equation. H2DP formed a nonideal monolayer at the air/water interface with A molec=0.995 nm2 below the cmc. Above the cmc there was a reduction in adsorption giving A molec=6.32 nm2, which remained almost constant in the explored concentration range. This adsorption reduction may be due to a change composition on micellization, or to a thermodynamic advantage of micellization on adsorption. The reduction in the evaporation rate of water was mainly due to the reduction of the water activity, caused by the presence of solutes in bulk. This is because the strong changes in the surface coverage did not have significant influence on the evaporation rate.
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  • 67
    ISSN: 1435-1536
    Keywords: Key words Composite particle ; temperature-sensitive ; biomolecules ; specific activity ; adsorption
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    Notes: Abstract  Temperature-sensitive micron-sized monodispersed composite polymer particles were prepared by seeded copolymerization of dimethylaminoethyl methacrylate and ethylene glycol dimethacrylate with 1.77 μm-sized monodispersed polystyrene seed particles. The change in surface property at temperature above and below 35 °C was examined by differential scanning calorimetry, trypsin activity and the adsorption/ desorption behaviors of low molecular weight cationic emulsifier as well as biomolecules.
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  • 68
    ISSN: 1435-1536
    Keywords: Key words Surface tension ; adsorption ; micelle ; entropy ; energy
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    Notes: Abstract The surface tension of aqueous solutions of tetradecyl-trimethylammonium chloride (TTAC) and decyltrimethylammonium chloride (DeTAC) were measured as a function of temperature at concentrations below and above the critical micelle concentration under atmospheric pressure. The entropy and energy of adsorption from the monomeric state and from the micellar state and also the entropy and energy of micelle formation for TTAC were evaluated and compared with those of dodecyltrimethyl-ammonium chloride (DTAC). The values of ΔM W s and ΔM W u for TTAC and DTAC systems show that the micelle formation is driven by the entropy at low temperatures and by the energy at high temperatures.
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  • 69
    ISSN: 1435-1536
    Keywords: Polyelectrolyte ; bentonite ; flocculation ; adsorption
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    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Description / Table of Contents: Abstract The interactions between tert-ammonium type cationic polyelectrolyte, the polycondensate of ethanolamine and epichlorohydrine (PEE), and bentonite particules in dilute aqueous suspensions are studied in the light of adsorption and flocculation. The extents of both phenomena are significantly influenced by the ionic strength of the medium. The adsorption of PEE on the bentonite particles occurs initially at the sites occupied by the hydrogen ions as counterion and then at the sites previously occupied by calcium ions. As flocculation mechanisms, charge neutralization appears to be principal one whereas polymer bridging effect becomes important only when the ionic strength is significant.
    Notes: Résumé Les intéractions entre un polyélectrolyte cationique de type ammonium tertiaire PEE(polycondensat d'éthanolamine et d'épichlorhydrine) et une suspension aqueuse de bentonite ont été étudiées sous l'angle des phénomènes d'adsorption et de floculation. L'importance de ces deux phénomènes est fortement influencée par la force ionique du milieu. L'adsorption du PEE sur les particules de bentonite se situe d'abord sur les sites occupés par les ions hydrogène comme les ions opposés et ensuite sur les sites occupés par les ions calcium. La neutralisation de charge semble être le principal mécanisme de floculation tandis que l'effet du pontage interparticulaire du polyélectrolyte ne devient notable que pour des forces ioniques du milieu importantes.
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  • 70
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    Colloid & polymer science 105 (1997), S. 72-74 
    ISSN: 1435-1536
    Keywords: Zeta potential ; static electricity ; surfactants ; viscose fibres ; adsorption
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    Notes: Abstract Viscose fibres were finished with a blend of a nonionic fatty acid ethoxylate and a quarternary ammonium derivative. Zeta potential and static charging were investigated as a function of a cationic compound. There is strong evidence that the charging of the viscose fibres depends on the chemical nature of the surfactants side-groups.
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  • 71
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    Colloid & polymer science 105 (1997), S. 91-95 
    ISSN: 1435-1536
    Keywords: Surfactant ; adsorption ; pore ; curvature ; mean field ; lattice
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    Notes: Abstract A mean field lattice (MFL) theory has been used to study the adsorption behaviour of nonionic surfactants in hydrophilic cylindrical pores. The theory predicts that with decreasing pore radius the absorbed amount decreases. Moreover, the step in the adsorption isotherm, which is a first-order phase transition in the mean field approximation, shifts to lower concentrations. Both effects have been observed in experiments. When an adsorbed layer is curved from convex (rod) to concave (pore) at constant area, the volume of the layer decreases. As a consequence, the stability of the layer increases and the adsorbed amount decreases.
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    Colloid & polymer science 105 (1997), S. 118-125 
    ISSN: 1435-1536
    Keywords: Langmuir monolayer ; adsorption ; X-ray reflectivity ; surface potential
    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 We have investigated the interaction between a Langmuir monolayer of C20H41NH2, a long-chain fatty amine and large, multivalent, heteropolyanions (phosphotungstic acid, PTA for short) dissolved in the aqueous subphase. By using X-ray reflectivity, surface pressure and surface potential measurements, we show that the adsorption is controlled by the electrostatic interaction between the PTA molecules and the amine film. At basic pH, the amine groups are not charged and no adsorption occurs. On the contrary, at acidic pH, the amines are positively charged. The surface pressure isotherms are markedly different in presence of PTA and the surface potential measurements reveal a reversal of the surface polarity. X-ray reflectivity gives a microscopic picture of the interfacial layer. The PTA anions are adsorbed onto the charged amine head groups as a monolayer or at most a bilayer. Changing the surface density of amines allows to control the total amount of PTA adsorbed and to vary the inorganic layer thickness.
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  • 73
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    Colloid & polymer science 105 (1997), S. 130-137 
    ISSN: 1435-1536
    Keywords: Phase transition ; adsorption ; isotherm ; Brewster angle microscopy ; Gibbs monolayer ; Langmuir monolayer
    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 layers of aqueous solutions of N-dodecyl-γ-hydroxy-butyric acid amide show a first-order phase transition between a fluid-like low-density phase and a condensed phase. Two-dimensional domains are formed which were visualized by Brewster angle microscopy. Theπ- A isotherms of the Langmuir monolayers show the wellknown plateau region with the critical surface pressure as the starting point for the first-order phase transition in the Langmuir monolayer. The measurements ofπ-t adsorption kinetics revealed a conspicuous inflection point at the same critical surface pressure. This inflection point is also related to the start of a first-order phase transition in the Gibbs monolayer. The results of theσ-logc isotherms are interpreted by the Frumkin's equation of state. Based on the calculated interaction parameters, the formation of a condensed phase in Gibbs monolayers is concluded. Thermodynamic behavior and morphological features of the Langmuir and Gibbs monolayers were compared and the similarities in morphology and thermodynamically properties of spread and of adsorbed molecules at the air-water interface demonstrated.
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  • 74
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    Colloid & polymer science 106 (1997), S. 24-33 
    ISSN: 1435-1536
    Keywords: Polyelectrolyte-surfactant association ; surface forces ; steric forces ; critical association concentration ; 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 Interactions between negatively charged surfaces coated with cationic polyelectrolytes across solutions containing an anionic surfactant, sodium dodecyl sulphate (SDS) have been studied. Polyelectrolytes with charge densities between 100% and 10%, counted per monomer unit, were used. At low ionic strength the polyelectrolytes adsorb in a flat conformation to neutralize the negative mica surface charge. The higher the linear charge density of the polyelectrolyte, the thinner adsorbed layers are obtained. In no case could any desorption be detected when the polyelectrolyte containing solution was replaced with an aqueous polyelectrolyte-free solution. The presence of SDS at concentrations considerably below the critical micellar concentration (cmc) does in all cases result in a recharging and a considerable swelling of the adsorbed layer. This is due to a cooperative association of surfactants in the preadsorbed polyelectrolyte layer. In case of the 100% charged PCMA, the force versus distance profile displays clear oscillations. We interpret these oscillations as being caused by the spatial arrangement of SDS micelles induced by the polyelectrolyte. The oscillations in the force curve remain as the SDS concentration is increased to twice the cmc. No similar oscillations in the force distance curve are observed when the surfaces are precoated with less charged polyelectrolytes. In these cases a strong swelling of the polyelectrolyte layer is observed once the surfactant concentration reaches a critical value (well below the cmc).
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  • 75
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    Colloid & polymer science 106 (1997), S. 180-182 
    ISSN: 1435-1536
    Keywords: Rheology ; suspension ; adsorption ; polystyrene ; depletion flocculation
    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 Storage moduli (G′) of hydrophilic and hydrophobic silica suspensions in trans-decalin and in trans-decalin solutions of polystyrene (PS) have been measured by taking account of PS adsorption. PS were adsorbed on the hydrophilic silica. TheG′ values of the hydrophilic suspensions in the presence of low molecular weight PS are similar to those without PS and they are larger than those in the presence of higher molecular weight PS. On the other hand, any PS chains cannot adsorb on the hydrophobic silica particles. TheG′ values of all hydrophobic suspensions are higher than that in trans-decalin due to depletion flocculation and they are two orders of magnitude larger than those for the hydrophilic silica suspensions.
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  • 76
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    Journal of porous materials 1 (1995), S. 139-153 
    ISSN: 1573-4854
    Keywords: microporous ; sol-gel ; silica ; pore size ; 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 Gas physisorption is a generally used technique for the characterization of porous solids. Microporous solids, however, need a different approach compared to mesoporous solids due to enhanced adsorption in pores of molecular dimensions. Therefore, conventional theories and models can not be used. The application of physisorption for microporous solids, and the interpretation of the isotherms is elucidated. Some models presented in literature for pore size assessment in the micropore range are discussed. Based on a number of criteria, the Horváth-Kawazoe model, modified for cylindrical pore geometry, is selected. N2 adsorption measurments on zeolites were performed to calibrate the method and to show the applicability and physical justification. Typical data obtained from experiments on non-supported microporous silica membrane top-layers show that the pore size distribution of these materials is bimodal, with a strong maximum at an effective diameter of 0.5 nm, and a weaker maximum at 0.75 nm.
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  • 77
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    Journal of porous materials 1 (1995), S. 75-84 
    ISSN: 1573-4854
    Keywords: carbon ; silica ; xerogel ; aerogel ; composite ; 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 High surface area carbon-silica xerogels and aerogels were prepared by adding various amounts of activated carbon particles during gelation of tetramethyoxysilane (TMOS). Surface areas and pore structure of the gels were determined by nitrogen and water adsorption and desorption measurements. Carbon increased the surface area of silica gel and the carbon-silica gel composites were found to be hydrophobic. The pore structure of xerogel composites was dominated by carbon whereas that of aerogel composites was apparently controlled by silica component.
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  • 78
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    Journal of porous materials 1 (1995), S. 55-67 
    ISSN: 1573-4854
    Keywords: zeolite ; porous material ; adsorption ; desiccant ; natural gas ; dehumidification ; gas-fired cooling
    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 This study was aimed at modifying the pore structure and surface chemistry of a zeolite to achieve an ideal material for gas-fired dehumidifying and cooling system application. Zeolite Y was chemically modified with various amounts of ethylenediaminetetraacetic acid (H4EDTA) corresponding to H4EDTA/Al (zeolite) molar ratio, X=0.5, 0.6, 0.75, 0.9 and 1.0 under reflux condition to achieve various degrees of dealumination. Sample treated with X=0.5 remained highly crystalline, but crystallinity of the samples decreased as the X increased. Although the sample treated with X=0.9 was x-ray amorphous, SEM micrographs indicated that the original crystal morphology was largely preserved. Chemical analysis and 29Si showed a progressive extraction of Al and Na with increased X. 27Al MASNMR indicated that AlIV was the only Al species up to X=0.75, whereas the x-ray amorphous phase (X=0.9) exhibited three peaks at 60, 52 and 38 ppm indicating the distortion of and change in AlIV coordination. Adsorption analyses using H2O, N2 or Ar as probe molecules indicated that the X-ray amorphous product remained essentially microporous having a broad micropore size distribution and a reduced hydrophilicity. Consequently, water adsorption isotherm changed from an extreme Type I to a moderate Type I. The moderate Type I isotherm with water is the key for its suitability as a desiccant in gas-fired dehumidifying and cooling system. These materials are also potentially useful in solar heating and cooling applications.
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  • 79
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    Journal of porous materials 2 (1995), S. 19-23 
    ISSN: 1573-4854
    Keywords: carbon molecular sieve ; adsorption ; micropore size distribution ; molecular probe ; DR equation
    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 Nitrogen adsorption at 77 K is the most common technique for defining the surface area and pore volume of a porous material. However it is not adequate to assess the microporosity of carbon molecular sieves (CMS), because of activated diffusion effects. In this paper, a molecular probe technique was used to defining the pore size of CMS materials. Adsorption of gases (vapors) with different molecular sizes, were measured by a gravimetric method using a spring balance. The amount adsorbed at room temperature was recorded over a 24-h period. The following molecular probes were chosen: CO2 (0.33 nm), C2H6 (0.4 nm), n-C4H10 (0.43 nm), i-C5H112 (0.5 nm), and CCl4 (0.6 nm). The micropore volumes were estimated by the Dubinin-Raduhkevich (DR) equation. Assuming that the diameters of the micropores are larger than those of the adsorbed molecules, the micropore volume distribution of each sample was estimated. The results demonstrated that the main pore size of the studied CMSs are less than 0.5 nm. One of the samples had a narrow pore size distribution in the range of 0.33–0.43 nm, which is the critical pore size for kinetic separation of oxygen from nitrogen. It is concluded that the molecular probe technique is an effective mean to assess the CMS adsorbents structure, which is not currently possible using conventional approaches with a single adsorbate, such as nitrogen or argon.
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  • 80
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    Journal of porous materials 2 (1995), S. 9-17 
    ISSN: 1573-4854
    Keywords: adsorption ; isotherm ; characterization ; modeling ; simulation ; pore size ; density functional theory ; argon ; nitrogen
    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 formalism of (nonlocal) density functional theory provides an attractive way to describe the physical adsorption process at the fluid-solid interface. It provides numerical results of analytic precision in a small fraction of the time required by a simulation technique. In particular, the ability to model adsorption in a pore space of slit-like or cylindrical geometry has led to useful methods for extracting pore size distribution information from experimental adsorption isotherms. However, critical comparisons of experimental isotherms with the isotherms predicted by density functional theory have shown important differences when using the usual prescription for the nonlocal free energy density functional. It is clear that these differences would affect the accuracy of such pore size information. We show in this paper how a small modification to the mean field computation of the intermolecular attractive potential results in excellent agreement with experiment for the systems studied.
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  • 81
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    Journal of porous materials 3 (1996), S. 247-255 
    ISSN: 1573-4854
    Keywords: adsorption ; micropore characterization ; activated carbon ; Dubinin-Astakhov equation ; Dubinin-Radushkevich equation
    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 characterization of the pore structure of microporous materials is of interest because of the usefulness of these materials in many applications. Of these, the characterization of carbon adsorbents is particularly problematic because of the presence of small pores with size on the order of small molecules (micropores) along with a wide distribution of pore sizes, and their non-crystalline structure. In this paper, we present results obtained using the Dubinin-Astakhov equation to analyze data from high pressure CO2 adsorption at 273 K to characterize two sets of microporous carbons. Our results support the conclusions of previous workers that the Dubinin-Astakhov (DA) equation is able to linearize adsorption data that gives rise to curved Dubinin-Radushkevich plots. However, when applied over different ranges of relative pressure on the adsorption isotherm, the Dubinin-Astakhov plots result in different values of micropore volume and characteristic adsorption potential. Furthermore, DA analysis of CO2 (273 K) adsorption data over a wide range of pressures (10−3–22000 Tort), gives results different from DA analysis of CO2 (273 K) isotherms measured at low pressures only (10−3–830 Tort). It would appear desirable to apply the DA equation to data that reflects the entire range of micropore filling on the adsorption isotherm, as opposed to data over a limited relative pressure range. For CO2 adsorption at 273 K, this would necessitate adsorption studies at high pressures, to about 28 atm. Micropore volumes obtained in this manner, agreed with the total pore volumes determined by nitrogen (77 K) adsorption for all the activated carbons studied.
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  • 82
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    Journal of porous materials 5 (1998), S. 227-239 
    ISSN: 1573-4854
    Keywords: pillared clays ; cation doping ; pore structure tailoring ; 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 Techniques and mechanism of doping controlled amounts of various cations into pillared clays without causing precipitation or damages to the pillared layered structures are reviewed and discussed. Transition metals of great interest in catalysis can be doped in the micropores of pillared clay in ionic forms by a two-step process. The micropore structures and surface nature of pillared clays are altered by the introduced cations, and this results in a significant improvement in adsorption properties of the clays. Adsorption of water, air components and organic vapors on cation-doped pillared clays were studied. The effects of the amount and species of cations on the pore structure and adsorption behavior are discussed. It is demonstrated that the presence of doped Ca2+ ions can effectively aides the control of modification of the pillared clays of large pore openings. Controlled cation doping is a simple and powerful tool for improving the adsorption properties of pillared clay.
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  • 83
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    Journal of porous materials 5 (1998), S. 289-303 
    ISSN: 1573-4854
    Keywords: zeolites ; design ; catalysis ; shape selectivity ; adsorption ; properties ; application
    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 Zeolites and molecular sieves are microporous materials with an increasing number of applications. Established applications of molecular sieves are in the field of oil refining processes, selective adsorption and ion exchange. Nowadays, zeolites come to the fore as clean, selective and recyclable catalysts in petrochemistry, e.g., in aromatic alkylation. Zeolites are considered to have a high potential for the synthesis of commodities and fine chemicals due to their molecular sized pores. Nevertheless, only a few commercial applications in fine chemical synthesis are known. Based on the essential criteria, extracted from the organic reaction under consideration, some of the potential pitfalls in selecting and screening zeolites as potential catalysts are discussed.
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  • 84
    ISSN: 1573-2746
    Keywords: catalysis ; adsorption ; transition metal complexes ; designed dispersions ; metal oxide coatings ; infrared spectroscopy ; thermogravimetric 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 , Physics
    Notes: Abstract In many catalytic reactions, the configuration, dispersion andensemble size of the supported catalytic species have a significant impacton the activity, selectivity and product distribution of the catalyst. Byusing the method of molecular design, it becomes possible to fundamentallyoptimize these catalytic reactions, eliminating side reactions and improvingthe activity or selectivity of the catalyst, provided that the detailedreaction mechanisms and the structural dependencies are known. In thismanuscript, several examples are presented that illustrate the dramaticeffect of the ensemble size of the supported catalytic species on thecatalytic behavior. It is evidenced how supported metal oxides may beprepared to have quite different catalytic properties.
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  • 85
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    Tribology letters 4 (1998), S. 59-66 
    ISSN: 1573-2711
    Keywords: scuffing ; oil oxidation ; base oils ; adsorption ; Fourier transform infrared spectroscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract In this work, the effect of base oil oxidation on scuffing was investigated. It was found that under mixed lubrication conditions there is a direct relationship between the level of base oil oxidation and the onset of scuffing, i.e., the greater the oxidation the lower the likelihood of scuffing. An oxidised base oil forms, among other products, carboxylic acids, which reduce scuffing failure in comparison with the parent oil. This was confirmed by the addition of a carboxylic acid directly to the base oil operating under the same mixed lubrication conditions. The removal of the carboxylic acids from the oxidised oil via column chromatography resulted in a scuffing failure performance equivalent to the parent oil.
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  • 86
    ISSN: 1573-2746
    Keywords: contact angle transition ; wetting ; interfacial energy ; solid pb-Ni/graphite system ; 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 , Physics
    Notes: Abstract The wetting of Pb-Ni crystals on graphite has been observed at 558 K in a Scanning Auger Microprobe. Samples were prepared so as to produce 10 μm crystals of Pb with Ni contents increasing from 0 to 0.3 wt% along one axis of the graphite substrate. In the low Ni region, the contact angle was found to decrease slowly from 119° to 98° with increasing Ni content. In the region of high Ni content, a constant contact angle of 83° was measured. In between, crystals with contact angles of 98° and 83° were observed to coexist, near the limit of solubility of Ni in Pb, indicating the presence of a first order transition in contact angle. The continuous decrease in contact angle, in the low Ni region, is due to Ni adsorption at the Pb-graphite interface, which leads to a decrease in interfacial energy. The constant contact angle in the high Ni region is associated with the precipitation of a Ni-rich phase. Various hypotheses are advanced to account for the first order transition in contact angle as a function of Ni concentration.
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  • 87
    ISSN: 1573-2746
    Keywords: catalysis ; adsorption ; transition metal complexes ; designed dispersions ; metal oxide coatings ; infrared spectroscopy ; thermogravimetric 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 , Physics
    Notes: Abstract One way to design a catalyst begins with a consideration of thereaction mechanism to the desired product so that only the chemistryrequired of that mechanism will be present on the surface. The reactionmechanism will suggest the structure(s) to be developed on the surface whichshould be stabilized against changes during operation. We believe that thisideal may be approached by decorating surfaces or porous powders with amonolayer of metal complexes having the desired structures. These complexesmay be partially decomposed to develop a high dispersion of the supportedmetal oxide.
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  • 88
    ISSN: 1573-2711
    Keywords: microstructure ; lubricious oxides ; engineered ; ZnO ; friction ; wear ; vacuum ; relative humidity ; moisture ; adsorption
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Oxide coatings have the potential to lubricate over a wide range of environmental conditions. However, oxides are typically brittle, form abrasive wear debris, and have high friction. ZnO is no exception; hot-pressed 1–2 µm ZnO has a friction coefficient of about 0.6 and causes extensive wear on steel counterfaces. Microstructural engineering may be used to permit plastic deformation and the formation of lubricious transfer films. The work presented here focuses on controlling the microstructure and chemistry within ZnO to provide low-friction and long-life coatings (e.g., µ=0.1−0.2, 1M+ sliding cycles). Coatings having a (0001) columnar texture with good crystallinity along the c-axis wear quickly and generate substantial wear debris. Depositions that create a (0001) texture with a mosaic substructure within the columns deform plastically. Here, nanocrystalline structures may enhance grain boundary sliding and contribute to plastic deformation and low friction. Dislocation motion within ZnO is enhanced by oxygen adsorption, which may further reduce friction by lowering shear strength. In addition, it is likely that defects arising from oxygen deficiency and the high surface-to-volume ratio of nanostructures, promote adsorption of water and/or oxygen. The adsorbed species can reduce friction through passivation of dangling or strained bonds. The complex interaction of mechanical and surface chemical effects result in millions of dry sliding cycles on nanostructured coatings in 50% RH air. In addition, the coatings have low friction in vacuum. Coating characterization and performance are discussed and a mechanism to explain the tribological properties is proposed.
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  • 89
    ISSN: 1573-2746
    Keywords: 8-hydroxyquinaldine ; electropolymerization ; adsorption ; glassy carbon ; kinetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Abstract The kinetics and thermodynamics of the electropolymerization of the chelating agent 8-hydroxyquinaldine on GCE's (Glassy Carbon Electrodes') surface from aqueous phosphate buffers are reported. Thermodynamic functions related to the adsorption of the monomer on the GCE's surfaces were determinated. No contribution from GCE surface's functional group to the electropolymerization reactions was reported. The effects of monomer concentration, pH, and temperature on the electrochemical growth of poly 8-hydroxyquinaldine were investigated. The results suggest that the propagation of the electropolymerization process takes place via a free radical chain reactions. Furthermore, the results indicate that the electrochemical growth of the polymeric films is dictated by pre-polymerization adsorption on the electrode surface.
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    Interface science 5 (1997), S. 159-167 
    ISSN: 1573-2746
    Keywords: adsorption ; ellipsometry ; opsonins ; PEG ; phospholipids ; polymers ; proteins ; TIRF
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Abstract Ellipsometry and total internal reflection fluorescence spectroscopy(TIRF) were used for investigating adsorption processes of relevance forparenteral administration of colloidal drug carriers. Emphasis is put ondiscussing the effects of both protein and surface properties on theadsorption of serum proteins at phospholipid and other surfaces.Furthermore, the adsorption from multicomponent protein systems, such asblood, is addressed, and both competitive and associative adsorptionphenomena discussed. The correlation between effects of the drug carriersurface properties on the serum protein adsorption and the circulation timeand tissue distribution of colloidal drug carriers is also addressed.Finally, the potential of ellipsometry in another adsorption process ofmajor importance for phagocytosis, i.e., the adsorption of colloidalparticles to macroscopic or mesoscopic surfaces, is indicated byinvestigations of the adsorption of oil-in-water emulsion droplets atsilica.
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