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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 276 (1998), S. 690-697 
    ISSN: 1435-1536
    Keywords: Key words Electrorheology ; polymer suspensions ; hydrolyzed poly(glycidyl methacrylate)RID=""ID="" 〈E6〉Acknowledgements〈/E6〉 One of the authors (M.J.B.) would like to thank the Grant Agency of the Czech Republic (Grant No. 203/96/1379) for partial financial support of this research.RID=""ID="" 〈E5〉Correspondence to〈/E5〉 O. Quadrat
    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  Electrorheological behavior of silicone oil suspensions of macroporous poly[(glycidyl methacrylate)-co-(ethylene dimethacrylate)]) (0.60 : 0.40 w) hydrolyzed to various degrees was investigated. Polarizability of particles expressed by the particle dipole coefficient and, consequently, pseudoplasticity of the system at low shear rates after application of an external electric field steeply increased with the hydrolysis degree of the copolymer. As the size and shape of particles remain unchanged during hydrolysis, a series of model suspensions with the same hydrodynamic properties (Newtonian or slightly pseudoplastic when no electric field was applied) but with different intensity of the electrorheological effect could be prepared. Under these conditions, the use of Mason number failed to correlate the apparent viscosity of suspensions of particles with different polarizability in the electric field. On the other hand, when polarizability of particles of a suspension system changes due to a higher temperature, a single curve in the plot of apparent viscosity vs. the Mason number could be obtained.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1435-1536
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Chicester [u.a.] : Wiley-Blackwell
    Journal of Molecular Recognition 9 (1996), S. 701-705 
    ISSN: 0952-3499
    Keywords: azo coupling ; affinity sorbents ; affinity ligands ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Immobilization of affinity ligands, proteins, enzymes and other functional groups by azo coupling is based on the high reactivity of the support-carrying diazonium groups towards both low- and high-molecular weight compounds containing certain groupings such as phenols, imidazole and some other heterocycles, thiols and amines.The precursor of diazonium group is a diazotizable amine on the matrix. Remarkable progress in its preparation was achieved by application of (4-amino-phenyl)-(2-sulphatoxyethyl) sulphone-type reagents for functionalization of the matrix. A similar type of amine precursor is prepared by the reaction of monosubstituted sulphanilamide with epoxide-containing matrix. The presence of a SO2 group in the para position to diazonium group of these supports (after diazotization) enhances reactivity in azo coupling.‘Reversed’ azo coupling is the reaction of a matrix containing functional groups capable of reacting with diazonium groups of a ligand. Preparation of a suitable matrix and examples of diazotizable ligands are given.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Es wurden makroporöse, bifunktionelle, quecksilberselektive Adsorbentien mit variablem Gehalt an Thiol- und quarternären Ammoniumgruppen durch nukleophilen Angriff von Kaliumethylxanthogenat auf vernetztes Polyvinylbenzyltrimethylammoniumchlorid (Styrol-Anionenaustauscher des I. Typs) dargestellt. Beide Arten von aktiven Gruppen ergänzen einander durch Erhöhung der Selektivität in verdünnten Systemen, der Kapazität in Gegenwart überschüssiger Alkalichloride und der Regenerierungsfähigkeit in wiederholten Zyklen.
    Notes: Macroporous bifunctional mercury adsorbents containing different portions of thiol and quaternary ammonium groups were prepared by nucleophilic attack of potassium ethylxanthogenate to the crosslinked poly[(vinylbenzyl)trimethylammonium chloride] (type I styrene anion exchanger). Both the active groups complemented each other raising selectivity at high dilutions, capacity in the presence of excessive alkali chlorides and regeneration ability in repeated cycles.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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