期刊文献+

两亲性聚乳酸嵌段共聚物的制备及性能研究 被引量:11

Synthesis and properties of amphiphilic block polylactide copolymers
下载PDF
导出
摘要 以端羟基聚乳酸和α-溴代丙酰溴为原料,制备了溴端基的聚乳酸;再以其为大分子引发剂,以溴化亚铜/2,2’-联吡啶为催化体系进行N-乙烯基吡咯烷酮的原子转移自由基聚合,制得了两亲性聚乳酸嵌段共聚物。用IR、GPC对聚合物进行了表征,用接触角测定仪测定了聚合物薄膜的水接触角,并考察了不同反应时间对共聚物的特性黏度和吸水率的影响。结果表明,该聚乳酸共聚物的亲水性较聚乳酸均聚物明显增大,TEM证实共聚物在水相中可形成一壳多核球状胶束,进一步佐证了该共聚物具有明显的两亲性。 Novel amphiphilic block copolymers of poly-N-vinylpyrrolidone and poly (D, L-tactide) were synthesized by atom transfer radical polymerization using N-vinylpyrrolidone as the monomer and a polylactideterminated with bromine, which was prepared by reaction of a hydroxy-terminated polylactide oligomer with α-bromopropanoyl bromide in the presence of a CuBr/2, 2'-bipyridine catalyst, as a functional macromolecular initiator. The products were characterized by IR and GPC. The properties and morphology of the copolymers were determined by contact angle and water take-up measurements and by TEM. The results showed that introduction of the PVP chain markedly enhances the surface hydrophilicity of the copolymers and the amphiphilic polymer can self-assemble into a core-shell structure (polymer micelle).
出处 《北京化工大学学报(自然科学版)》 EI CAS CSCD 北大核心 2006年第3期52-55,共4页 Journal of Beijing University of Chemical Technology(Natural Science Edition)
关键词 两亲共聚物 原子转移自由基聚合 聚乳酸 N-乙烯基吡咯烷酮 amphiphilic copolymer atom transfer radical polymerization polylactide N-vinylpyrrolidone
  • 相关文献

参考文献10

  • 1Chen D P,Sun B Q.New tissue engineering material copolymers of derivatives of cellulose and lactide:their synthesis and characterization [J].Materials Science and Engineering C,2000,11:57-60.
  • 2Schnabelrauch M,Vogt S,Larcher Y,et al.Biodegradable polymer networks based on oligolactide macromers:synthesis,properties and biomedical applications [J].Biomolecular Engineering,2002,19:295-298.
  • 3Cai Q,Bei J Z,Wang S G.Synthesis and properties of ABA-type triblock copolymers of poly (glycolide-cocaprolactone) (A) and poly (ethylene glycol) (B) [J].Polymer,2002,43:3585-3591.
  • 4Korhonen H,Helminen A,Seppala J V.Synthesis of polylactides in the presence of co-initiators with different numbers of hydroxyl groups [J].Polymer,2001,42:7541-7549.
  • 5Janata M,Masar B,Toman L,et al.Synthesis of novel types of graft copolymers by a "grafting-from" method using ring-opening polymerization of lactones and lactides[J].Reactive & Functional Polymers,2003,57:137-146.
  • 6罗丙红,全大萍,廖凯荣,卢泽俭.聚乳酸接枝乙烯基吡咯烷酮的初步研究[J].中山大学学报(自然科学版),2001,40(5):62-64. 被引量:19
  • 7汪朝阳,赵耀明,麦杭珍,严冰.熔融聚合法直接合成聚乳酸的研究[J].合成纤维,2002,31(2):11-13. 被引量:45
  • 8周桢,张勇,周正发,袁茂全.端羟基乳酸预聚物的合成[J].塑料,2004,33(5):87-90. 被引量:9
  • 9马晓妍,石淑先,夏宇正,焦书科,李效玉.聚乳酸及其共聚物的制备和降解性能[J].北京化工大学学报(自然科学版),2004,31(1):51-56. 被引量:45
  • 10杨淑丽,刘晓亚,杨成,陈明清.聚合物溶液自组装胶束的研究进展[J].日用化学工业,2003,33(3):163-166. 被引量:4

二级参考文献57

  • 1吴素坤,赵炯心.聚乳酸直接缩聚反应的研究[J].国际纺织导报,2001,29(4):30-33. 被引量:13
  • 2王勤,张娟.乳酸缩聚反应动力学[J].应用化学,1994,11(1):76-79. 被引量:16
  • 3申有青,张富尧,张一峰,沈之荃.稀土化合物催化内酯开环聚合 Ⅱ.异丙氧基稀土催化D.L-丙交酯开环聚合[J].高分子学报,1995,5(2):222-227. 被引量:25
  • 4严瑞Xuan.水溶性高分子[M].北京:化学工业出版社,1998..
  • 5刘国军 王国昌.嵌段共聚物纳米结构材料[M].北京:化学工业出版社,1997.39—50.
  • 6[2]Tsuji H.Properties and morphologies of poly(L-lactide):1 Anealing condition effects on properties and morphologiesof poly(L-lactide)[J].Polymer.1994,36(14):2709-2716.
  • 7[6]Fukuzaki H,Yoshida M,Asano M,et al.Synthesis of low-molecular-weight copoly(L-lactic acid/ε-caprolactone)by direct copolycondensation in the absence of catalysts,and enzymatic degradation of the polymers[J].Polymer.1990,31(10):2006-2014.
  • 8[7]Hiltunen K,Jukka V S,Mika H.Lactic acid based poly(ester-urethanes):use of hydroxyl terminated prepolymerin urethane synthesis[J].Journal of AppliedPolymer Science.1997,63:1091-1100.
  • 9[8]Hiltunen K,Jukka V S,Mika H.Lactic acid based poly(ester-urethanes):the effects of different polymerizationconditions on the polymer structure and properties[J].Journal of Applied Polymer Science.1997,64:865-873.
  • 10[9]Hiltunen K,Jukka V S,Mika H.The synthesis of lactic-acid-based telechelic prepolymers[J].Journal of AppliedPolymer Science.1998,67:1011-1016.

共引文献113

同被引文献160

引证文献11

二级引证文献61

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部