Kinetics and Modeling of Solution ARGET ATRP of Styrene, Butyl Acrylate, and Methyl Methacrylate

被引:53
|
作者
Li, Xiaohui [1 ]
Wang, Wen-Jun [1 ]
Li, Bo-Geng [1 ]
Zhu, Shiping [2 ]
机构
[1] Zhejiang Univ, State Key Lab Chem Engn, Inst Polymerizat & Polymer Engn, Dept Chem & Biol Engn, Hangzhou 310027, Peoples R China
[2] McMaster Univ, Dept Chem Engn, Hamilton, ON L8S 4L7, Canada
基金
中国国家自然科学基金;
关键词
acrylates; atom transfer radical polymerization (ATRP); modeling; solution ARGET ATRP; styrene; TRANSFER RADICAL POLYMERIZATION; DIFFUSION-CONTROLLED REACTIONS; PROPAGATION RATE COEFFICIENTS; ACTIVATION RATE CONSTANTS; SILICA-GEL; ELECTRON-TRANSFER; EQUILIBRIUM-CONSTANTS; SIMULTANEOUS REVERSE; SUPPORTED CATALYST; NORMAL INITIATION;
D O I
10.1002/mren.201100024
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
This work reports a kinetic model for the activator-regenerated-by-electron-transfer atom-transfer radical polymerization (ARGET ATRP) and its verification by the experimental data of solution ARGET ATRP of styrene, methyl methacrylate, and butyl arylate from literatures. The effects of ATRP equilibrium constant K and apparent reducing rate coefficient k(r) on the ARGET ATRP kinetics are investigated. A highly active initiation/catalyst system with a large K results in a poor control of the polymerization while an increased k(r) promotes the polymerization rate but the formation of dead polymer chains. Reducing agent with a moderate k(r) gives good control over ARGET ATRP. It is not feasible to use a moderate catalyst system for the ARGET ATRP of highly active monomers.
引用
收藏
页码:467 / 478
页数:12
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