Li Hui, Wang Wenwen, Li Chunmei, Tan Jiaojun, Yin Dezhong, Zhang Hepeng, Zhang Baoliang, Yin Changjie, Zhang Qiuyu
Key Laboratory of Applied Physics and Chemistry in Space of Ministry of Education, School of Science, Northwestern Polytechnical University, Xi'an 710072, China.
School of Materials Science and Engineering, Wuhan Textile University, Wuhan 430200, China.
J Colloid Interface Sci. 2015 Sep 1;453:226-236. doi: 10.1016/j.jcis.2015.04.051. Epub 2015 May 7.
In this paper, poly(n-butyl acrylate)-g-poly(methyl methacrylate) multigraft copolymers were synthesized by macromonomer technique and miniemulsion copolymerization. The PMMA macromonomers were obtained by an activator generated by electron transfer atom transfer radical polymerization (AGET ATRP) in emulsion system and subsequent allylation. Then the copolymerization of different macromonomers with nBA was carried out in miniemulsion system, obtaining multigraft copolymers with high molecular weight. The latex particles and distribution of emulsion AGET ATRP and miniemulsion copolymerization were characterized using laser light scattering. The molecular weight and polydispersity indices of macromonomers and multigraft copolymers were analyzed by gel permeation chromatography, and the number-average molecular weight range is 187,600-554,800 g/mol for PnBA-g-PMMA copolymers. In addition, the structural characteristics of macromonomer and brush-like copolymers were determined by infrared spectra and (1)H nuclear magnetic resonance spectroscopy. The thermal performance of brush-like copolymers were characterized by differential scanning calorimetry and thermogravimetric analysis. Atomic force microscopy results showed that the degree of microphase separation was varying with increasing PMMA content in PnBA-g-PMMA. The dynamic rheometer analysis revealed that multigraft copolymer with PMMA content of 31.4% exhibited good elastomeric properties to function as a TPE. These multigraft copolymers show a promising low cost and environmental friendly thermoplastic elastomer.
本文采用大分子单体技术和微乳液共聚法合成了聚(丙烯酸正丁酯)-g-聚(甲基丙烯酸甲酯)多接枝共聚物。通过乳液体系中的电子转移原子转移自由基聚合(AGET ATRP)产生的活化剂以及随后的烯丙基化反应得到聚甲基丙烯酸甲酯大分子单体。然后在微乳液体系中使不同的大分子单体与丙烯酸正丁酯进行共聚反应,得到高分子量的多接枝共聚物。利用激光光散射对乳液AGET ATRP和微乳液共聚反应的乳胶粒及其分布进行了表征。通过凝胶渗透色谱法分析了大分子单体和多接枝共聚物的分子量及多分散指数,对于聚(丙烯酸正丁酯)-g-聚(甲基丙烯酸甲酯)共聚物,其数均分子量范围为187,600 - 554,800 g/mol。此外,通过红外光谱和氢核磁共振光谱确定了大分子单体和刷状共聚物的结构特征。用差示扫描量热法和热重分析法对刷状共聚物的热性能进行了表征。原子力显微镜结果表明,在聚(丙烯酸正丁酯)-g-聚(甲基丙烯酸甲酯)中,随着聚甲基丙烯酸甲酯含量的增加,微相分离程度发生变化。动态流变仪分析表明,聚甲基丙烯酸甲酯含量为31.4%的多接枝共聚物表现出良好的弹性体性能,可作为热塑性弹性体使用。这些多接枝共聚物显示出一种有前景的低成本且环保的热塑性弹性体。