By Henry Warson (auth.), Mohamed S. El-Aasser, John W. Vanderhoff (eds.)
It is very acceptable that this symposium at the emulsion polymeriza tion of vinyl acetate used to be held in popularity of the commercial value of poly(vinyl acetate) and vinyl acetate copolymers, and their really targeted houses between emulsion polymers as a rule. Poly( vinyl acetate) latexes have been the 1st man made polymer latexes to be made on a advertisement scale: their creation utilizing polyvinyl alcohol as emulsifier begun in Germany throughout the mid-1930s and has endured to the current day, transforming into gradually with the years. certainly, poly(vinyl acetate) latexes ready with polyvinyl alcohol are nonetheless one of many mainstays of the adhesives undefined. With the passing of time, despite the fact that, vinyl acetate copolymers were constructed: copolymers with maleate esters akin to dibutyl maleate, acrylate esters similar to ethyl acrylate and butyl acrylate, versatic acid esters, and, extra lately, ethylene. those flexible copolymers have chanced on expanding use in additional refined adhesives with really good homes, adhesives for clay coatings on paper, carpet backing, and inside and external paints. hence greater than forty five years after the 1st advertisement construction of vinyl acetate latexes, their use remains to be turning out to be, either in genuine amounts and assorted functions. the commercial value of vinyl acetate latexes makes the mechanism and kinetics in their emulsion polymerization of functional in addition to medical interest.
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It truly is relatively applicable that this symposium at the emulsion polymeriza tion of vinyl acetate was once held in reputation of the economic significance of poly(vinyl acetate) and vinyl acetate copolymers, and their really detailed houses between emulsion polymers commonly. Poly( vinyl acetate) latexes have been the 1st artificial polymer latexes to be made on a advertisement scale: their creation utilizing polyvinyl alcohol as emulsifier begun in Germany in the course of the mid-1930s and has persevered to the current day, turning out to be progressively with the years.
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Gardon,J. Polym. , A-i, 6,643 (1968). 10. J. Uge1stad, P. C. M¢rk and 1. O. Aasen, J. Polym. , A-J, 5, 2281 (1967). 11. K. H. S. Chang, M. H. Litt and M. Nomura, this volume, Chapt. 6. 12. A. R. Berens, Angew. Makromol. , 47,97 (1975). 13. F. W. Waite, ICI Ltd (Paints Division), Slough, private communication. 14. W. J. Priest, J. Phys. , 56,1077 (1952). 15. R. N. Haward,J' Polym. , 4, 273 (1949). 16. A. S. Dunn and P. A. Taylor, Makromol. , 83,207 (1965). 17. D. H. Napper and A. G. Parts, J. Polym.
S. DUNN 0·95. However, the ratio obtained for the linear sample could be raised to 0·99 by modifying the operating conditions. The ratios for GH-17 and B differed from each other and were both lower than for the linear sample. In general, secondary hydrogen atoms have a lower bond dissociation energy than primary hydrogen atoms and are therefore more reactive in transfer reactions. Transfer to the secondary hydrogen atom of the me thine group transforms it into a quaternary carbon atom which has a long relaxation time and is difficult to detect in low concentration by 13C NMR spectroscopy.
M. Kolthoff and I. K. Miller,J. A mer. Chem. , 73,3055 (1951). 26. 1. A. Phelisse and C. A. Quiby (Rhone-Pou1enc), US Patent 3161630, 1964. 27. C. H. Bamford, A. D. Jenkins and R. P. Wayne, Trans. , 56, 930 (1960). 28. -J. Liu and I. M. Krieger, in Emulsions, Latices, and Dispersions, P. Becher and M. N. ), New York, Dekker, 1979, p. 344. 29. (a) B. V. Derjaguin and J. D. -chim. USSR, 14,633 (1941). (b) E. J. W. Verwey and J. Th. G. Overbeek, Theory of the Stability of Lyophobic Colloids, Elsevier, Amsterdam, 1948.