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Synthesis and polymerization kinetics of copolymer styrene-vinyltrimethoxysilane by emulsifier-free emulsion polymerization

机译:通过无乳化剂乳液聚合的共聚物苯乙烯 - 乙烯基三甲氧基硅烷合成和聚合动力学

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Copolymers of styrene (St) and vinyltrimethoxysilane (VTMS) have been synthesized by emulsifier-free emulsion copolymerization using ammonium persulfate (APS) as initiator. Acrylic acid used as functional monomer was also added into the emulsion. The effects of varying the concentrations of initiator and VTMS as well as the polymerization temperature on the polymerization conversion and rate were investigated in detail. The copolymer was characterized by Fourier transform infrared spectrometer (FTIR). Copolymerization of VTMS with St was confirmed by the appearance of an absorption peak between 1000 cm~(-1) to 1200 cm~(-1) (due to Si-O-C bonds) in the IR spectrum. The siloxane segments in the copolymer chain underwent hydrolysis and self-condensation, resulting in a change in the structure of the copolymers from linear into a cross-linked network. As a result, the organic and inorganic hybrid materials were formed. The polymerization rate increased with increasing polymerization temperature, molar concentration of initiator and decreased with increasing molar concentration of VTMS. The apparent activation energy and kinetic features of the polymerization system were also obtained.
机译:通过使用过硫酸铵(APS)作为引发剂,通过乳化剂 - 无乳化乳液共聚合合成苯乙烯(ST)和乙烯基三甲氧基氧硅烷(VTMS)的共聚物。也将用作官能单体的丙烯酸也加入乳液中。详细研究了改变引发剂和VTM浓度的影响以及聚合温度对聚合转化率和速率。共聚物的特征在于傅里叶变换红外光谱仪(FTIR)。通过IR光谱中的1000cm〜(-1)至1200cm〜(-1)(由于Si-O-C键)的吸收峰的外观确认VTM与ST的共聚。共聚物链中的硅氧烷段介入水解和自缩,导致共聚物的结构变化从线性到交联网络中。结果,形成有机和无机杂化材料。聚合速率随着聚合温度的增加,引发剂的摩尔浓度而增加,随着VTM的摩尔浓度的增加而降低。还得到了聚合体系的表观活化能量和动力学特征。

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