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  • 1
    ISSN: 0887-624X
    Keywords: emulsion polymerization ; isotachophoresis ; oligomer ; free radical ; aqueous phase ; styrene ; termination ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The concentrations and probable nature of charged oligomers formed by aqueous-phase termination in the persulfate-initiated emulsion polymerization of styrene were measured by isotachophoresis. Isotachophoresis has some advantages over other techniques (e.g., GPC, UV spectroscopy) in that it separates species according to their molecular weight, geometry, and charge. The charged water-soluble oligomeric species were detected in experiments in which particles were nucleated in a surfactant-free environment. Identification of the moieties present was made by comparison with model compounds. Evidence was found for bimolecular combination as a major mechanism of termination in the aqueous phase, although the possibility of disproportionation could not be ruled out. The species formed in the aqueous phase under saturated monomer conditions were found to be subject to further reaction towards the end of polymerization. The surface adsorption characteristics of the compounds formed were compared with those of known surfactants and showed good agreement with the assumptions in the model of Maxwell et. al. [Macromolecules, 24, 1629 (1991)] for initiator efficiencies in emulsion polymerization. The relatively large concentrations of nonradical aqueous-soluble oligomeric compounds demonstrate conclusively that initiator efficiencies are not 100%, as is often assumed in such systems. © 1993 John Wiley & Sons, Inc.
    Additional Material: 18 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 32 (1994), S. 605-630 
    ISSN: 0887-624X
    Keywords: free radical ; exit ; emulsion ; polymerization ; model ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The exit or desorption of free radicals from latex particles is an important kinetic process in an emulsion polymerization. This article unites a successful theory of radical absorption (i.e., initiator efficiency), based on propagation in the aqueous phase being the rate determining step for entry of charged free radicals, with a detailed model of radical desorption. The result is a kinetic scheme applicable to true “zero-one” systems (i.e., where entry of a radical into a latex particle already containing a radical results in instantaneous termination), which is still, with a number of generally applicable assumptions, relatively simple. Indeed, in many physically reasonable limits, the kinetic representation reduces to a single rate equation. Specific experimental techniques of particular significance and methods of analysis of kinetic data are detailed and discussed. A methodology for both assessing the applicability of the model and its more probable limits, via use of known rate coefficients and theoretical predictions, is outlined and then applied to the representative monomers, styrene and methyl methacrylate. A detailed application of the theory and illustration of the methodology of model discrimination via experiment is contained in the second article of this series. © 1994 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 32 (1994), S. 631-649 
    ISSN: 0887-624X
    Keywords: free radical ; exit ; emulsion ; polymerization ; experiment ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In emulsion polymerizations, desorption (exit) from latex particles of monomeric radical species that arise from transfer can be an important determinant of the overall kinetics. An examination of various methodologies for the testing of postulated free radical exit mechanisms is made. These utilize the model descriptions for the exit process presented in the accompanying article of Casey et al., employing data consisting of conversion as a function of time for the approach to steady state polymerization conditions. Experimental data are presented on the exit rate coefficients as a function of such experimental parameters as: particle size, monomer concentration, and aqueous-phase free-radical concentration for a series of styrene polymerizations at 50°C, where the average number of free radicals per particle (n̄) never exceeds 0.5. It is demonstrated for these systems that while the conversion/time dependence from a single run, under conditions sensitive to exit, is insensitive to mechanistic assumptions as to the fate of desorbed free radicals, the variation of the exit rate coefficient with particle size so obtained suggests a second order dependence on n̄, implying complete re-entry of desorbed free radicals under all conditions studied. Once the monomeric radicals have re-entered, they are more likely to remain inside the particle where they will either propagate or undergo termination rather than re-escape. The article also presents an estimate for the rate coefficient at 50°C of the first propagation step of the monomeric radical subsequent to transfer. The conclusions drawn here for seeded systems should prove useful for study of particle nucleation mechanisms, when exit is particularly likely in small, newly formed, particles. © 1994 John Wiley & Sons, Inc.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
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