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出 处:《功能高分子学报》2010年第4期317-322,共6页Journal of Functional Polymers
基 金:山西省自然科学基金资助项目(2008021013)
摘 要:采用过氧化氢-硫酸亚铁的氧化还原引发体系,首先使苯乙烯(St)在乳液聚合体系中进行均聚合,制得了端羟基聚苯乙烯(PSt-OH),然后将PSt-OH增溶于十二烷基硫酸钠的胶束溶液中,在硫酸铈铵的引发作用下,使水溶液中的N-乙烯基吡咯烷酮(NVP)在PSt-OH端羟基部位发生嵌段共聚合,制得了双亲嵌段共聚物PSt-b-PVP。采用红外光谱(FT-IR)、核磁共振氢谱(1H-NMR)、凝胶渗透色谱(GPC)、差示扫描量热(DSC)等手段对嵌段共聚物的组成与结构进行了表征。结果表明:在Ce(Ⅳ)盐的氧化作用下,增溶于胶束中的端羟基聚苯乙烯端会在端基产生自由基,顺利地实现NVP的嵌段共聚合反应。随着共聚合时间的延长,共聚物PSt-b-PVP大分子链中亲水嵌段PVP的比例不断增大。The emulsion polymerization of styrene(St) was firstly carried out by initiating of H2O2-Fe^2+ redox initiation system.PSt-OH was obtained with hydroxyl group as end group in polystyrene.Subsequently,the macromolecules PSt-OH were solubilizated in the micellar solution of sodium dodecylsulfate(SDS),and the block polymerization of N-vinylpyrrolidone(NVP) in the aqueous solution at the end group of PSt-OH was initiated by cerium ammonium sulfate,resulting in the amphiphilic block copolymer PSt-b-PVP.Several means were adopted to characterize the chemical composition and structure of PSt-b-PVP,such as FT-IR,^1H-NMR,GPC and DSC.Results show that by the oxidation action of cerium(Ⅳ) salt,free radicals can be produced at the sites of the hydroxyl groups of PSt-OH,which are solubilized in the micellar solution of SDS,and the block copolymerization of NVP can be favorably realized.With the(increasing) of copolymerization time,the content of PVP block is increased.
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