High-conversion emulsion polymerization
TL;DR: In this paper, theories of emulsion homo-polymerization are considered in an attempt to show the causes of the often slow rate of polymerization at high conversions of monomer.
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Abstract: SUMMARY The four important factors that determine the rate of emulsion polymerization are the propagation rate coefficient, the latex-particle concentration, the monomer concentration in the latex particles, and the free-radical concentration in the latex particles. Both theoretical considerations and experimental evidence suggest that the important factors that may reduce the rate of emulsion polymerization at high conversion are the propagation rate coefficient and the monomer concentration in the latex particles, and not the free-radical concentration in the latex particle, if the initiator is not depleted. Various approaches for increasing the rate of emulsion polymerization at high conversion are suggested. One of the important considerations in any industrial application of the emulsion polymerization process is residual monomer in the final emulsion latex product. Often it is very difficult to remove the last few percent of monomer during the polymerization reaction, since the rate of an emulsion polymerization can become relatively slow at high weight fractions of polymer in the latex particles. It should be noted that the problem of slow rates of emulsion poiymerization at high conversions apply for both continuous and batch processes, since in continuous and semi-continuous reactors residual monomer is normally removed by reaction in a post (batch) reactor. In this paper theories of emulsion polymerization are considered in an attempt to show the causes of the often slow rate of emulsion polymerization at high conversions of monomer. Case studies are presented for the emulsion polymerizations of methyl methacrylate and butadiene. The aim of this paper is to distinguish the effect of high conversion upon those factors that determine the rate of an emulsion polymerization. Specifically, we wish to determine why the rate of emulsion polymerization of a specific system may become (uneconomically) slow at high conversion. Having isolated some of the major difficulties, some techniques for circumventing the slow rates of emulsion polymerization at high conversion are suggested. 2. Theory In the following discussions we consider, for simplicity, emulsion homo-polymerization, i.e. the emulsion polymerization of one monomer. However, most of the theoretical description can be easily extended to account for two or more monomers. The rate of any free-radical polymerization can be written as:
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Citations
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Reduction of residual monomer in latex products by enhanced polymerization and extraction in supercritical carbon dioxide
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TL;DR: A submitted manuscript is the author's version of the article upon submission and before peer-review as discussed by the authors, and the final published version features the final layout of the paper including the volume, issue and page numbers.
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References
Kinetics of Emulsion Polymerization
TL;DR: In this article, the kinetics of free radical reactions in isolated loci are discussed subject to the condition that the free radicals are supplied to the loci from an external source, and three cases of interest are considered: that the average number of free radicals per locus is small compared with unity, that this number approximates one half, and that the number is large.
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Swelling of latex particles
TL;DR: In this article, a theoretical relation has been derived for the equilibrium swelling of latex particles, and the equilibrium amount of solvent imbibed by latex particles is a direct function of the particle diameter and an inverse function of interfacial energy at the surface of the particles.
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High‐conversion polymerization. I. Theory and application to methyl methacrylate
TL;DR: The concept of polymer entanglements has been applied in conjunction with classical free-radical kinetics to describe vinyl polymerizations carried to high conversion as mentioned in this paper. But the model is not suitable for high-conversion polymerization.
205
Chain-length-dependent termination rate processes in free-radical polymerizations. 1. Theory
TL;DR: In this article, a complete set of rate equations describing the kinetics of free-radical polymerization is deduced, in which termination rate coefficients are allowed to depend on chain length.
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