期刊文献+

端羟基聚(乳酸-己内酯)共聚物的合成及表征 被引量:1

Synthesis and Characterization of Hydroxyl-terminated Poly(lacticacid-co-ε-caprolactone)
下载PDF
导出
摘要 以乳酸(D,L-LA)和ε-己内酯(-εCL)为原料,采用梯度升温法,通过直接熔融缩聚合成了系列端羟基聚(乳酸-己内酯)共聚物(PLCA)。最佳工艺条件为:压力0.098MPa,催化剂Sn(Oct)2用量0.8%(质量分数),n(D,L-LA)∶n(-εCL)=8∶2,聚合温度170℃,反应7h。用特性粘度、FT-IR1、H-NMR、XRD、DSC等对其进行表征,结果表明,系列PLCA中的粘均分子量最大可达20785,Tg均比PLA的小,且随-εCL含量的增加,Tg越小,有效改善了PLA的脆性。结晶度比PLA有所降低,说明-εCL的加入使柔韧性增强。 The hydroxyl-terminated modified poly(lactic acid-co-ε-caprolactone) copolymers(PLCA) were syn thesized via directly melt polycondensation with lactic acid(D, L-LA) and ε-caprolactone(ε-CL) as raw material using linear heating method. The best synthesis conditions were pressure 0. 098 MPa, catalyst dosage 0. 8% (mass frac tion), n(D, L-LA) : n(ε-CL)=8 : 2, polymerization temperature of 170℃ and polymerization time 7h. The copoly- mers were characterized by viscosity-average molecular weight, FT-IR, ^1H-NMR, DSC, TGA and XRD. The results demonstrate that the biggest viscosity average molecular weight of PLCA is 20785, Tg of PLCA is lower than PLA, and with the ε-CL content increased, the Tg is smaller, which improved the brittleness of PLA effectively, the crystallinity of PLCA is lower than PLA, it indicates that the flexibility increases because of the addition of ε-CL.
出处 《材料导报》 EI CAS CSCD 北大核心 2011年第8期38-41,共4页 Materials Reports
基金 陕西省科技攻关项目(2008K07-32) 陕西省教育厅重点实验室重点科研计划项目(09JS061) 陕西科技大学研究生创新基金
关键词 聚乳酸ε-己内酯直接熔融缩聚梯度升温法增韧 polylactic acid, ε-caprolactone, direct melt polycondensation, gradient temperature method, toughening
  • 相关文献

参考文献11

  • 1Gan Zhihua(甘志华).1 lactide copolymers(生物降解ε-己内酯/d,Synthesis and characterization of biodegradable ε-cap-rolactone/d,Zhang Jie(张杰),Jing Xiabin(景遐斌),1-丙交酯共聚物的合成与表征).应用化学,1997,14(2).
  • 2Ramiro D, Gabriel G, Giovanni M, et al. Immiscible poly- mer blends of semicrystalline bioeompatible components: Thermal properties and phase morphology analysis of PL- LA/PCL blends[J]. Polymer, 2001,42(18) : 831.
  • 3唐文珺,蔡伟.PLLA-PCL无规共聚物的冷变形形状记忆效应[J].功能材料,2007,38(12):2011-2014. 被引量:5
  • 4Hideto T, Tamami Y, Masakzn S. Effects of poly(L-lac- tide-eo-ε-caprolaetone) on morphology, structure, crystalli- zation, and physical properties of blends of poly(L-lactide) and poly(ε-caprolaetone) [J]. Polymer, 2003,52(2): 269.
  • 5WooS I, Kim B O, Jun H S,et al. Polymerization of aqueo- us lactic acid to prepare high molecular weight poly (lactic acid) by chain-extending with hexamethylene diisocyanate [J]. Polym Bull, 1995,35(4) : 415.
  • 6Inata H, Matsumura S. Recommended practice for determi- ning the biodegradation of plastic materials in different envi- ronments[J]. J Appl Polym Sci, 1986,32:4581.
  • 7Harkonen M, Hiltunen K, Malin M, et al. Synthesis of high-molecule-weight poly(L-Lactid) initiated with 2-ethyl- hexanoate[J]. J Macromol Sci Pure Appl Chem, 1995, 32 (4) : 857.
  • 8张建安,吴明元,吴庆云,杨建军,程杰.生物降解材料聚乳酸的合成与表征[J].安徽大学学报(自然科学版),2008,32(6):78-81. 被引量:6
  • 9DongC M, Qiu K Y, Gu Z W, et al. Synthesis of star- shaped poly ( ε-caprolactone)-b-poly ( DL-Lactic acid-alt-gly- colic acid) with multifunctional initiator and stannous oc- toate catalyst [J]. Macromolecules, 2001,34 : 4691.
  • 10Stolt M, Viljanmaa M, Sodergard A, et al. Blends of poly (ε-caprolactone-b-lactic acid) and poly(lactic acid) for hot- melt applications[J]. J Appl Polym Sci, 2004,91 : 96.

二级参考文献16

  • 1罗丙红,周长忍,梁敏,缪婧,杨媛.功能化聚乳酸大分子单体的合成与表征[J].中山大学学报(自然科学版),2005,44(3):67-70. 被引量:6
  • 2杜杰,郑玉斌,李冬梅,段久芳,徐亮.生物降解性脂肪族聚酯改性的研究进展[J].合成树脂及塑料,2006,23(1):70-73. 被引量:6
  • 3Krieheldorf H R. Syntheses and application of polylaetides[J].Chemosphere, 2001,43 : 49 -54.
  • 4Erba R D, Groeninckx G, Maglio G, et al. hnmiscible polymer blends of semicrystalline biocompatible components : thermal properties and phase morphology analysis of PLLA/PCL blends [ J]. Polymer, 2001,42:7831 -7840.
  • 5Vandijk J A P P, Smit J A M, Kohn F E, et al. Characterization of poly ( D, L - lactic acid) by gel permeation chromatography[J]. J Polym Sci: Polym Chem Ed, 1983, 21:197 -208.
  • 6Moon S I, Lee C W, Taniguchi I, et al. Melt/solid polycondensation of L - lactic acid : An ahemative route to poly ( L - lactic) with high molecular weight[ J]. Polymer, 2001,42 : 5059 - 5062.
  • 7Lendlein A, Langer R.[J]. Science, 2002, 296..1673.
  • 8Shikinami Y.[P]. US: 6281262, 2001.
  • 9Min C C, Cui W J, Wang S G. [J]. Polymers for Advanced Technologyes, 2005, 16:608.
  • 10Hashimoto T. [J]. Intell Mater Syst Struct, 1998, 9 : 127.

共引文献8

同被引文献34

  • 1Liu Q Y,Jiang L,Shi R,Zhang L Q. Synthesis,preparation,in vitro degradation,and application of novel degradable bioelastomers:A review[J].Progress in Polymer Science,2012,(05):715-765.
  • 2Tian H Y,Tang Zh H,Zhuang X L. Biodegradable synthetic polymers:Preparation,functionalization and biomedical application[J].Progress in Polymer Science,2012.237-280.
  • 3Seyednejad H,Ghassemi A H,Nostrum C F. Functional aliphatic polyesters for biomedical and pharmaceutical applications[J].Journal of Controlled Release,2011.168-176.
  • 4Jér?me C,Lecomte P. Recent advances in the synthesis of aliphatic polyesters by ring-opening polymerization[J].Advanced Drug Delivery Reviews,2008.1056-1076.
  • 5Coulembier O,Degee P,Hedrick J L. From controlled ringopening polymerization to biodegradable aliphatic polyester:Especially poly(b-malicacid) derivatives[J].Progress in Polymer Science,2006.723-747.
  • 6Nottelet B,Coudane J,Vert M. Synthesis of an X-ray opaque biodegradable copolyester by chemical modification of poly (ε-caprolactone)[J].BIOMATERIALS,2006.4948-4954.
  • 7Hvilsted S. Facile design of biomaterials by ' click' chemistry[J].Polymer International,2012.485-494.
  • 8Yu Y,Wu D,Liu C B. Lipase/esterase-catalyzed synthesis of aliphatic polyesters via polycondensation:A review[J].Process Biochemistry,2012.1027-1036.
  • 9Albertsson A C,Srivastava R K. Recent developments in enzymecatalyzed ring-opening polymerization[J].Advanced Drug Delivery Reviews,2008.1077-1093.
  • 10You Z W,Cao H P,Gao J. A functionalizable polyester with free hydroxyl groups and tunable Physiochemical and biological properties[J].BIOMATERIALS,2010.3129-3138.

引证文献1

二级引证文献6

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