On the Termination Mechanism in the Radical Polymerization of Acrylates

被引:32
作者
Ballard, Nicholas [1 ]
Hamzehlou, Shaghayegh [1 ]
Ruiperez, Fernando [1 ]
Asua, Jose M. [1 ]
机构
[1] Univ Basque Country UPV EHU, POLYMAT & Kimika Aplikatua Saila, Tolosa Etorbidea 72, Donostia San Sebastian 20018, Spain
关键词
acrylates; emulsion polymerization; gelation; radical polymerization; termination reactions; N-BUTYL ACRYLATE; SEMIBATCH EMULSION POLYMERIZATION; INTRAMOLECULAR CHAIN TRANSFER; IONIZATION MASS-SPECTROMETRY; PULSED-LASER POLYMERIZATION; STRUCTURAL-PROPERTIES; RAFT POLYMERIZATION; RATE COEFFICIENTS; ALKYL ACRYLATES; KINETICS;
D O I
10.1002/marc.201600278
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
In a recent publication, Nakamura and co-workers studied the termination mechanism in the radical polymerization of acrylates. Contrary to conventional thinking, their conclusion is that termination is overwhelmingly by disproportionation. This finding impacts on a large body of the previous work in the polymerization of acrylic monomers which this work seeks to address. Analysis of the molecular weight distribution of acrylic polymers obtained under different polymerization conditions shows that termination by combination is the more probable mechanism for mutual termination of secondary radicals. It is proposed that in the experiments conducted by Nakamura and co-workers, backbiting plays a key role and their experimental data are reinterpreted, showing that they are more revealing with respect to the mode of termination of the midchain radical produced by backbiting, than to bimolecular termination of secondary radicals.
引用
收藏
页码:1364 / 1368
页数:5
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