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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 114 (2001), S. 4696-4701 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: In this paper we return to the problem of adsorption of correlated random copolymers at a liquid–liquid interface. We explain our particular interest in the exponentially decaying sequential correlations, which are obtained by a specially developed "coloring" procedure. In comparison with our previous work [N. A. Denesyuk and I. Y. Erukhimovich, J. Chem. Phys. 113, 3894 (2000)], we present an improved analytical analysis, based on the full Green functions of the chains under consideration. Calculating the interfacial tension enables us to introduce a new definition of the adsorption point and to compare it with that applied within the ground state dominance approximation. Bearing in mind the possible practical applications, we additionally consider the case of diblock copolymer. We show that, for equal selectivities and mean compositions, adsorption is always deeper for the chains of diblock copolymers. Nevertheless, for a wide range of identified parameters correlated random copolymers can still serve as effective compatibilizers, comparable with diblock copolymers and polyblock chains. © 2001 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 113 (2000), S. 3894-3900 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Theoretical study of adsorption of an ideal correlated random copolymer chain at a liquid-liquid interface (ICRC-LL) is presented in this paper. Introduction of a certain referent system (a homopolymer chain in external attracting field) allows us to develop a principle of free energy calculation for ICRC-LL and to construct its phase diagram. Exponentially decaying (short-range) and oscillating correlations are considered in parallel that reveals easier adsorption for the first type of correlations. It is shown that chains with short-range and oscillating correlations undergo continuous (second-order) adsorption transition. For both types of correlations the transition temperature diverges when composition of a chain becomes symmetric. © 2000 American Institute of Physics.
    Type of Medium: Electronic Resource
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