Kinetics and modeling of methyl methacrylate graft copolymerization in the presence of natural rubber latex

被引:12
|
作者
Sirirat, Tanita [1 ]
Vatanatham, Terdthai [1 ]
Hansupalak, Nanthiya [1 ]
Rempel, Garry Llewellyn [2 ]
Arayapranee, Wanvimon [3 ]
机构
[1] Kasetsart Univ, Dept Chem Engn, Bangkok 10900, Thailand
[2] Univ Waterloo, Dept Chem Engn, Waterloo, ON N2L 3G1, Canada
[3] Rangsit Univ, Dept Chem & Mat Engn, Pathum Thani 12000, Thailand
基金
加拿大自然科学与工程研究理事会;
关键词
Core-shell Particle; Graft Copolymerization; Methyl Methacrylate; Modeling; Natural Rubber Latex; MOLECULAR-WEIGHT DISTRIBUTIONS; FREE-RADICAL POLYMERIZATIONS; HIGH-IMPACT POLYSTYRENE; EMULSION POLYMERIZATION; REDOX INITIATOR; CHAIN TRANSFER; STYRENE; PARTICLES; ACRYLONITRILE; POLYBUTADIENE;
D O I
10.1007/s11814-014-0274-1
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A graft copolymerization model for using cumene hydroperoxide/tetraethylenepentamine (CHPO/TEPA) as a redox initiator was developed to describe the grafting of methyl methacrylate onto natural rubber latex as a core-shell particle. The model allows estimating the effects of the initiator concentration, monomer-rubber weight ratio, and temperature on the properties of graft product, e.g., % grafting efficiency and the % monomer composition in the graft copolymer and free polymer. The rate expressions of polymer chain formation are developed by taking into account a reduction of CHPO by TEPA and a population event of radicals between core/shell phases. The parameter estimation is performed to find the kinetic parameters. Validation with experimental results demonstrates a good applicability of the proposed model. The model results reveal that the formation of grafted polymer chains rather form by the chain transfer reaction to rubber chains from homopolymer radicals and the initiation reaction of cumyloxy radicals to rubber chains.
引用
收藏
页码:980 / 992
页数:13
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