Miniemulsion and conventional emulsion copolymerization of styrene and butadiene: A comparative kinetic study

被引:8
|
作者
Li, Donghong
Sudol, E. David
El-Aasser, Mohamed S. [1 ]
机构
[1] Lehigh Univ, Inst Emuls Polymers, Bethlehem, PA 18015 USA
[2] Lehigh Univ, Dept Chem Engn, Bethlehem, PA 18015 USA
关键词
styrene-butadiene; miniemulsion; copolymerization; polymer kinetics; calorimetry;
D O I
10.1002/app.23746
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The kinetics of conventional and miniemulsion copolymerizations of styrene and butadiene were compared using the Mettler RC1 calorimeter. A two-step homogenization procedure was applied to obtain miniemulsions of these monomers with hexadecane as the costabilizer. The results indicated that the miniemulsion polymerizations proceeded mainly by nucleation in the monomer droplets, while in the conventional emulsion polymerizations, particle formation occurred by a combination of micellar and homogeneous nucleation. The overall rate of miniemulsion polymerization was faster than the corresponding conventional emulsion system if the surfactant concentration was below the critical micelle concentration (cmc) and slower if the surfactant concentration was above the cmc. The homogenization process is important for making stable miniemulsion systems, but had no effect on the conventional emulsion system (without hexadecane), most likely because of the second stage addition of the butadiene monomer. The dependencies of the rate of polymerization (heat of reaction) and number of particles on the surfactant concentration differed for the two types of polymerization systems. (c) 2006 Wiley Periodicals, Inc.
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页码:2304 / 2312
页数:9
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