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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 58 (1995), S. 1317-1323 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Suspension copolymerization and modification of pentaerythritol triacrylate (PENTA)-butyl acrylate (BA) matrices with ethylenediamine (EtDA) are discussed. It is shown that aminolysis in water solution offers gel structure carriers with small pore radii (about 3 nm). These carriers are characterized by the high swelling and sharp correlation between the pH value and the specific volume. The enzymes (acylase, glucoamylase, and peroxydase) are immobilized by means of the glutaraldehyde method. The best matrix seems to be copolymers modified in a 95% solution of ethylenediamine in water. Preparations do not lose activity after 1 month storage at 4°C. © 1995 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 56 (1995), S. 433-439 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Structures of copolymers of styrene and divinylbenzene (50% crosslinking degree) prepared in suspension polymerization in the presence of mixtures of nonsol (heptane or decane) and sol (toluene or tetralin) diluents were investigated. The studies showed that the diluents enriched with nonsol solvents resulted in an increase of pore volumes and posities for the prepared copolymers. The sol diluents affected mainly the gel regions of the polymer matrices. Isotropic swelling of the matrices prepared in the presence of toluene is the opposite of the effect observed for tetralin family copolymers. The virtual difference of both kind of matrices was demonstrated in the sorption of phenol. The tetralin family copolymers were characterized by a prolonged time for column breakthrough. © 1995 John Wiley & Sons, Inc.
    Additional Material: 4 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 27 (1982), S. 277-288 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The stress-stain and ultimate behavior in compression of homogeneous and macroporous beads of styrene-divinylbenzene copolymers has been investigated in the dry state or in equilibrium with toluene, acetone, methanol, and water. The penetration modulus A indicates sensitively the transition from the glassy into the rubbery state induced by an increase in temperature or swelling. For macroporous copolymers, A of the glassy polymers is mainly determined by the porosity P, while in the rubbery region it primarily depends on the matrix structure (degree of crosslinking and concentration and composition of the diluent). The high value of the slope s of the A vs. P dependence (s ∼ -3) for macroporous copolymers is evidence of the complex deformation mechanism (bucking of pore walls). The relative compression at break, εb=0.3-0.4, is independent of the composition, and the compressive strength is roughly proportional to the penetration modulus.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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