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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 31 (1993), S. 3453-3464 
    ISSN: 0887-624X
    Keywords: quaternization ; poly(vinylpyridines) ; alkyl halide ; kinetics ; steric hindrance ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Quaternization reactions of poly(vinylpyridines) with alkyl halides show retardation in excess of that predicted by the classical second-order kinetics. Based on the classical collision and transition state theories, a kinetic model has been developed to quantify such retardation, in which the overall reaction rate is characterized by a rate constant k0 of the intrinsic reactivity between a pyridyl group and an alkyl halide group, and by a steric hindrance effect parameter α. The latter accounts for the degree to which the rate of collisions of reactants is reduced, or to which the freedom of movement of the reactants in the transition state is restricted as the reaction proceeds. The resulting kinetic expression has been validated using experimental results reported in the literature and those of our own. The functional dependence of k0 and α values on the nature of poly(vinylpyridines) and that of alkyl halides is explained. Other factors affecting k0 and α, including changes in macromolecular dimensions and/or in the distribution of residue environment, quality of solvent, and reaction temperature, are discussed. © 1993 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 2153-2163 
    ISSN: 0887-6266
    Keywords: reactive blending ; kinetics ; interface ; mixing ; coalescence ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: We present an experimental study of polymer-polymer reaction kinetics at the interfaces between two immiscible polymer phases under flow in a batch mixer of type Haake Rheocord. To that end, we have developed a model chemical system that is composed of a mixture of polystyrene (PS) and poly(methyl methacrylate) (PMMA). A small fraction of PS bear hydroxyl terminal group (PS-OH) and that of PMMA contain nonclassical isocyanate moieties that are randomly distributed along the PMMA chains (PMMA-r-NCO). This reactive system is particularly pertinent to modeling practical reactive blending processes because the amount and rate of copolymer formation can be determined with great accuracy (on the order of ppm). This study shows that the overall reaction rate is controlled primarily by interfacial generation through convective mixing. Most reaction and morphological development are accomplished within a very short period of time (1-3 min). For a PS/PMMA (60/40) reactive blend, the ultimate size of the PMMA particles is as small as 0.2 μm and is reached within 2 to 3 min. A surface coverage of about 0.5 of the PMMA particles by a monolayer of the copolymer is enough to prevent dynamic coalescence, whereas a much higher surface coverage is needed to eliminate static coalescence. In the nonentangled regime (Mn of the PS-OH = 7800 g/mol), temperature has a significant effect on the reaction rate, while it has little effect in the entangled regime (Mn of the PS-OH = 53,200 g/mol). © 1998 John Wiley & Sons, Inc. J. Polym. Sci. B Polym. Phys. 36: 2153-2163, 1998
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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