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

机译:苯乙烯,丙烯酸丁酯和甲基丙烯酸甲酯溶液ARGET ATRP的动力学和建模

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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 fer on the ARGET ATRP kinetics are investigated. A highly active initiation/catalyst system with a large if resultsin 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 kI_gives good control over ARGET ATRP. It is not feasible to use a moderate catalyst system for the ARGET ATRP of highly active monomers.
机译:这项工作报告了活化剂通过电子转移原子转移自由基聚合(ARGET ATRP)的动力学模型,并通过文献中苯乙烯,甲基丙烯酸甲酯和芳基丁酸丁酯的ARGET ATRP溶液的实验数据进行了验证。研究了ATRP平衡常数K和表观还原速率系数fer对ARGET ATRP动力学的影响。如果活化活性/引发剂体系较大,则引发聚合反应的控制较差,而增大的k_r则促进了聚合速率,但形成了失效的聚合物链。具有适度kI的还原剂可很好地控制ARGET ATRP。对于高活性单体的ARGET ATRP使用适度的催化剂体系是不可行的。

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  • 来源
    《Macromolecular reaction engineering》 |2011年第10期|p.467-478|共12页
  • 作者单位

    Biological Engineering, Zhejiang University, Hangzhou, Zhejiang 310027, P.R. China;

    Biological Engineering, Zhejiang University, Hangzhou, Zhejiang 310027, P.R. China;

    Biological Engineering, Zhejiang University, Hangzhou, Zhejiang 310027, P.R. China;

    Department of Chemical Engineering, McMaster University, Hamilton, Ontario, Canada L8S 4L7;

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