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Redox polymerization: Kinetics of polymerization of acrylonitrile initiated by the system 2,2′‐thiodiethanol/trichloroaquobipyridylmanganese(III) in dilute sulfuric acid

机译:氧化还原聚合:2,2′-硫代二乙醇/三氯夸联吡啶基锰(III)在稀硫酸中引发的丙烯腈聚合动力学

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AbstractThe kinetics of polymerization of acrylonitrile and methyl methacrylate initiated by the redox system 2,2′‐thiodiethanol/trichloroaquobipyridylmanganese(III) have been investigated in the temperature range 20–35°C in dilute sulfuric acid. The oxidation of the substrate in the absence of monomer has also been studied. A third‐order reaction involving the complex, the substrate, and H+leads to the production of primary radicals which initiate polymerization of the monomers. The primary radicals are more reactive towards methyl methacrylate than towards acrylonitrile. The termination of polymerization with both monomers is by mutual interaction between the growing radicals. A suitable kinetic scheme has been proposed, and the rate constants e
机译:摘要研究了在20–35°C的温度范围内,在20–35°C的稀硫酸中,丙烯腈和甲基丙烯酸甲酯聚合动力学。还研究了在没有单体的情况下基底的氧化。涉及络合物、底物和 H+ 的三级反应导致初级自由基的产生,从而引发单体的聚合。伯自由基对甲基丙烯酸甲酯的反应性高于对丙烯腈的反应性。与两种单体的聚合终止是通过生长的自由基之间的相互相互作用。提出了一种合适的动力学方案,速率常数为

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