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作 者:陈志军[1] 王振保[1] 周思凯[1] 路文忠[1] 马亚洲[2]
机构地区:[1]郑州轻工业学院材料与化工学院,河南郑州450002 [2]中国神马集团神马实业有限公司,河南平顶山467000
出 处:《塑料工业》2005年第10期9-11,30,共4页China Plastics Industry
摘 要:将含有双键的N,N二甲氨基甲基丙烯酸乙酯化学锚接在交联聚苯乙烯(PS)微球表面,再用过氧化苯甲酰引发甲基丙烯酸乙酯(EMA)氮氧调控自由基原位接枝聚合反应,将聚甲基丙烯酸乙酯(PEMA)接枝在交联PS微球表面,制备了PEMA刷子层;研究了聚合反应机理,并对所合成交联PS接枝PEMA共聚物进行了表征。结果表明,在2,2,6,6四甲基哌啶1氧自由基存在下,EMA的聚合反应为”活性”自由基聚合,所得到的PEMA摩尔质量分布在1.18~1.3范围,摩尔质量随聚合时间的延长而增大(9000~57000g/mol);红外光谱显示PEMA被接枝到了交联PS微球表面,交联PS微球粒径在0.5~1.2μm之间。Poly(ethyl methacrylate)was prepared by means of in-situ grafting of ethyl methacrylate on a crosslinked PS microsphere backbone initiated by BPO in the presence of 2,2,6, 6-tetramethyl-1-piperidinoxyl (TEMPO). The mechanism of the controlled free radical polymerization was studied and the grafted product was characterized. The experimental results showed that the grafting polymerization of ethyl methacrylate in-situ of crosslinked PS microsphere surface initiated by BPO in the presence of 2,2,6,6 -tetramethyl-1-piperidinoxyl (TEM- PO)was living free radical polymerization, the synthesized poly(ethyl methacrylate)had lower polydispersities (1.18 - 1.3), the molecular weight could be controlled in the range of 9 000-57 000 g/mol.The FTIR result showed the poly (ethyl methacrylate)was grafted onto the crosslinked PS microsphere surface, and the particle diameter of the crosslinked PS rnicrospheres was in the range of 0.5-1.2μm.
关 键 词:交联聚苯乙烯微球 聚合物刷子 氮氧调控自由基接枝聚合 聚甲基丙烯酸乙酯
分 类 号:TQ325.2[化学工程—合成树脂塑料工业]
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