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131.
以THF为溶剂,磺胺嘧啶钠为引发剂,甲基丙烯酰氯为封端剂,阴离子聚合合成了一类含双键端基的聚氧乙烯(PEO)大单体;在此基础上,考察了此类大单体与丙烯酰胺、甲基丙烯酸甲酯的自由基共聚反应,合成了一类新型PMMA—PAM—PEO三元共聚物,此物在常温下易于成膜;大单体及共聚物经纯化后,用IR、^1H—NMR、VPO、GPC等进行了表征,证实了产物有预期结构。 相似文献
132.
醇/水介质对PEG大分子单体与BMA分散共聚反应的影响 总被引:1,自引:0,他引:1
通过端基反应法合成了苯乙烯单封端的聚乙二醇(St- PEG)大分子单体,使其与甲基丙烯酸丁酯(BMA)在乙醇 水混合介质中进行分散共聚,得到了聚乙二醇接枝的聚甲基丙烯酸丁酯(PBMA- g -PEG)高分子微球.PBMA- g -PEG共聚物的亲溶剂 疏溶剂平衡将影响微球的形成,反应结束时,体系随BMA浓度和介质中水含量的变化呈现出4种不同的状态,透明清液、乳液、伴有沉淀或凝胶的乳液和凝胶.用透射电子显微镜(TEM)和激光光散射(LLS)对乳液体系的粒径及其形态进行了表征,表明所得接枝高分子微球形态规整具有较好的单分散性.通过控制介质中水的含量和BMA的浓度可得粒径在4 0~5 0 0nm范围的PBMA -g -PEG微球. 相似文献
133.
Poly (ethyleneglycol monomethylether) methacrylate (PEGMM)was synthesized by means of the reaction of methacrylyl chloride with sodium monomethylpolyethyleneglycoxide and was characterized by FTIR, ~1H-NMR,and ultraviolet spectrometries. A series of poly (vinyl alcohol)-graft-PEGMM (PVA-g-PEGMM )and methyl methacrylate-PEGMM copolymer (PMMA-PEGMM) were prepared and tested for antithrombogenicity in vitro. The results indicate that the antithrombogenicity of the copolymers basically increases with the increasing of the DP of polyoxyethylene (POE) chain and tends to a plateau after the DP around 114,i.e. the long chain structure of POE is favourable to the antithrombogenicityof its copolymers ;moreover, the extent of the improvement ofantithrombogenicity also relates to the PEGMM content of the copolymers and the kind of the matrix that the POE chains are located on. These results are consistent with the anticipation of the hypothesis of maintaining proteins normal conformations for blood compatible bioraaterials. 相似文献
134.
Hiroshi Uyama Yoichiro Honda Shiro Kobayashi 《Journal of polymer science. Part A, Polymer chemistry》1993,31(1):123-128
The present article describes the synthesis and emulsion copolymerization of a block-type amphiphilic poly(2-oxazoline) macromonomer possessing a polymerizable vinyl ester group. The macromonomer was synthesized by one-pot two-stage block copolymerization of 2-oxazolines using vinyl iodoacetate as initiator. 2-Methyl- and 2-n-butyl-2-oxazolines were employed for the construction of hydrophilic and hydrophobic segments, respectively. The surface activities evaluated by the surface tension of the macromonomer in water were fairly good. Emulsion copolymerization of vinyl acetate with the macromonomer was carried out. The macromonomer acted as a polymeric surfactant, as well as a comonomer. The resulting copolymer latex particles were spherical and their diameter was in the sub-micron range. The effects of the composition of the macromonomer on the emulsion copolymerization and the resulting latex particles were examined. © 1993 John Wiley & Sons, Inc. 相似文献
135.
Gao Bo Bengt Wessln K. Bodil Wesslen 《Journal of polymer science. Part A, Polymer chemistry》1992,30(9):1799-1808
Comb-shaped amphiphilic graft copolymers composed of hydrophobic backbones and hydrophilic side chains were prepared by radical copolymerization of poly(ethylene glycol) monomethacrylate macromonomers, and methacrylate and acrylate comonomers in toluene. The copolymerizations were very sensitive to the reaction conditions, and insoluble cross-linked gels were easily formed. The yields of soluble copolymers were affected by the initiator concentration, the macromonomer concentration, and the choice of chain transfer agents and comonomers. Solubilities of the copolymers in water or methanol were found to depend on the sizes and the numbers of the PEG side chains. The copolymers showed surface activity with CMC:s in the order of 0.1–1.5 g/L and surface tensions of 36–56 dyn/cm. When tested as emulsifiers most of the copolymers gave oil-in-water type emulsions at room temperature. Polymers carrying MPEG 2000 side chains were crystalline with melting points of 38–44°C, while those based on PEG 400 and 1000 were mostly amorphous with glass transition temperatures between -55 and -60°C. © 1992 John Wiley & Sons, Inc. 相似文献