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受限空间内聚苯乙烯微粒的制备

     

摘要

以(N,N-二甲氨基-4-吡啶)五氰合铁(Ⅱ)封端的聚氧丙烯聚氧乙烯共聚物(EPE—Fe)与苯乙烯在水中自组装形成纳米体系(EPE-Fe-St),在纳米尺度受限空间内进行了苯乙烯自由基聚合,制备了聚苯乙烯微球(EPE—Fe—PS).用Fe^3+对自组装体系的纳米球壳进行固化后形成Fe—EPE—Fe-St体系,聚合后也制备了聚苯乙烯微球(Fe—EPE-Fe—PS).研究结果表明,制备了粒径为60-200nm的不同粒径单分散聚苯乙烯微球,聚合温度对纳米Fe—EPE—Fe-St体系粒径影响较小,而对EPE—Fe-St体系较大.在受限空间内苯乙烯的自由基聚合可得到数均分子量超过70万的聚苯乙烯;自组装体系中引发剂量增多使聚苯乙烯分子量下降,聚合温度上升也使分子量下降,而增加自组装的EPE—Fe用量可增加聚苯乙烯的分子量.两种受限条件下的聚苯乙烯微球的玻璃化转变温度(Tg)在90~135℃之间,纳米反应器壳层的硬化提高了聚苯乙烯微球的Tg.%The poly(ethylene glycol)-b-poly(propylene glycol)-b-poly(ethylene glycol) terminated with pentacyano(4-(dimethylamino)-pyridine) ferrate (EPE-Fe) complex surfactant was synthesized and was used to be self-assembled with styrene (St) in water to form a nano-reactor (EPE-Fe-St). The free radical polymerization of styrene occurred in the confined space in nanosize. And the polystyrene nanospheres (EPE-Fe-PS) were prepared in the nano-reactor. Furthermore, ferric ion was used to cure the shell of the EPE-Fe-St to form a hardened nano-reactor (Fe-EPE-Fe-St). The styrene polymerization was also arisen in the nano-reactor to form polystyrene nanospheres (Fe-EPE-Fe-PS) with a hardened shell. The results of molecular weight and morphology of polystyrene nanospheres show that the various size of monodispersed polystyrene nanospheres in 60--200 nm have been obtained in the confined nanospace. The effect of polymerization temperature on the size of self-assembled EPE-Fe-St is remarkable, and on the size of the Fe-EPE-Fe-St is slight. The higher molecular weight of the polystyrene has achieved more than 700000 in the confined space. In the self-assembled nano-reactor, the molecular weight of PS decreases with increase of initiator content in St solution and enhancement of polymerization temperature, and increases with augment of EPE-Fe content in water. The glass transition temperature (Tg) of the polystyrene nanospheres prepared in two kinds of the confined space are in the range of 90- 135 ℃. The Tg of polystyrene nanosphere is enhanced obviously after hardening the shell of nano-reactor whether the hardening shell arises before or after the polymerization.

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