Poly(styrene-b-butyl acrylate-b-styrene) copolymers prepared by iodine transfer bulk polymerization: Kinetics, structure and properties

被引:0
|
作者
Zhang L. [1 ]
Chang Z. [1 ]
Yu D. [2 ]
Bao Y. [1 ,2 ]
机构
[1] State Key Laboratory of Chemical Engineering, College of Chemical and Biological Engineering, Zhejiang University, Hangzhou
[2] Institute of Zhejiang University-Quzhou, Quzhou
关键词
block copolymer; iodine transfer polymerization; kinetics; poly(butyl acrylate); polystyrene;
D O I
10.3969/j.issn.1003-9015.2024.03.010
中图分类号
学科分类号
摘要
Iodine-terminated poly(butyl acrylate) (I-PBA-I) was prepared by iodine transfer bulk polymerization using iodoform chain transfer agent and azo-initiator, and further applied as a macro-chain transfer agent in the chain extension polymerization of styrene to synthesize poly(styrene-b-butyl acrylate-b-styrene) (PS-b-PBA-b-PS) copolymers. The polymerization kinetics, structure and properties of PS-b-PBA-b-PS were characterized. The results show that both homopolymerization of butyl acrylate and block copolymerization of styrene exhibit the characteristics of "living radical polymerization". The number average molecular weight of I-PBA-I was increased from 15 000 to 134 500 as the feed molar ratio of BA to CHI3 (nBA,0/nCHI3,0) increased from 100/1 to 1 000/1. PS-b-PBA-b-PS copolymers with the number average molecular weight of 46 000, 69 000, 97 500 and 127 000 were obtained at nBA,0/nSt,0 ratios of 1/1, 1/2, 1/3 and 1/4, respectively. Micro-phase separation was observed in PS-b-PBA-b-PS copolymers, and block copolymers exhibited certain transparency and improved toughness. The impact strength of PS-b-PBA-b-PS copolymer with nPS/nPBA of 3.85/1 was similar to that of commercial styrene-butadiene block copolymer prepared by anion living polymerization. © 2024 Zhejiang University. All rights reserved.
引用
收藏
页码:432 / 439
页数:7
相关论文
共 22 条
  • [1] KNOLL K, NIESSNER N., Styrolux<sup>+</sup> and styroflex<sup>+</sup> - from transparent high impact polystyrene to new thermoplastic elastomers: Syntheses, applications and blends with other styrene based polymers, Macromolecular Symposia, 132, 1, pp. 231-243, (1998)
  • [2] YEOW J, CHAPMAN R, GORMLEY A J, Et al., Up in the air: Oxygen tolerance in controlled/living radical polymerisation, Chemical Society Reviews, 47, 12, pp. 4357-4387, (2018)
  • [3] CHERNIKOVA E V, SIVTSOV E V., Reversible addition-fragmentation chain-transfer polymerization: Fundamentals and use in practice, Polymer Science, Series B, 59, 2, pp. 117-146, (2017)
  • [4] LORANDI F, FANTIN M, MATYJASZEWSKI K., Atom transfer radical polymerization: A mechanistic perspective, Journal of the American Chemical Society, 144, 34, pp. 15413-15430, (2022)
  • [5] SHANMUGAM S, XU J T, BOYER C., Photocontrolled living polymerization systems with reversible deactivations through electron and energy transfer, Macromolecular Rapid Communications, 38, 13, (2017)
  • [6] NI Y Y, ZHANG L F, CHENG Z P, Et al., Iodine-mediated reversible-deactivation radical polymerization: A powerful strategy for polymer synthesis, Polymer Chemistry, 10, 20, pp. 2504-2515, (2019)
  • [7] CORRIGAN N, JUNG K, MOAD G, Et al., Reversible-deactivation radical polymerization (controlled/living radical polymerization): From discovery to materials design and applications, Progress in Polymer Science, 111, (2020)
  • [8] TELITEL S, TELITEL S, BOSSON J, Et al., Nitroxide mediated photopolymerization: A versatile tool for the tabrication of complex multilayer polyfunctional copolymer nanostructures, Advanced Materials Interfaces, 1, 5, (2014)
  • [9] JAKUBOWSKI W, MIN K, MATYJASZEWSKI K., Activators regenerated by electron transfer for atom transfer radical polymerization of styrene, Macromolecules, 39, 1, pp. 39-45, (2006)
  • [10] MATYJASZEWSKI K, COCA S, GAYNOR S G, Et al., Controlled radical polymerization in the presence of oxygen, Macromolecules, 31, 17, pp. 5967-5969, (1998)