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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 1011-1031 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A model is presented for the simulation of the structuration of polymer particles under conditions in which the new polymer chains are compatible with the polymer previously formed. The model involves the calculation of the monomer concentration gradients within the particles due to discrepancies in thermodynamic interactions between the monomer and the different polymers present in each part of the polymer particle. In addition, the distribution of free radicals in the latex particle is taken into account. This distribution results from the anchoring of the hydrophilic end-group of the growing polymer chain on the surface of the particle. The model was applied to the simulation of the polymerization of vinyl acetate on a butyl acrylate-vinyl acetate copolymer seed. It was found that the development of the particle morphology was mainly due to the profile of concentration of radicals in the particle. On the other hand, the effect of the monomer-polymer thermodynamic interactions on the particle morphology was found to be negligible. However, it has to be pointed out that this is because, for the system studied, the interaction parameters of vinyl acetate with polyvinyl acetate and polybutyl acrylate are nearly identical.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 2
    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: A new approach for the estimation of kinetic parameters in emulsion polymerization systems in which the average number of radicals per particle exceeds 0.5 is presented. The approach uses the time evolution of the conversion in chemically initiated systems and is based on a model that includes fundamental parameters such as the propagation rate constant, kp, the termination rate constant in the polymer particles, kt, the rate coefficient for initiator decomposition, kI, and the entry, ka, and exit, kd, rate coefficients. It was found that kp, kt, kI, ka, and, under some circumstances, kd can be accurately estimated provided that termination in the aqueous phase is significant. When the extent of the aqueous phase termination is negligible, only kp, kt, and kI can be estimated. The effect of both the experimental noise level and the run-to-run irreproducibility on the accuracy of the estimates was studied. In addition, it was found that significant inaccuracies resulted from the poor determination of the exact time when polymerization begins. A method to circumvent this problem was proposed.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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