期刊文献+

聚左旋乳酸/聚丁二酸丁二醇酯共混物的结构与性能 被引量:4

Preparation and Characterization of Poly( L-Lactic Acid) / Poly( Butylene Succinate) Blends
下载PDF
导出
摘要 通过熔融共混制备出一系列不同组成比的聚左旋乳酸(PLLA)/聚丁二酸丁二醇酯(PBS)/醋酸锌(Zn(OAc)2)样品,通过扫描电子显微镜、动态力学性能分析仪、差示扫描量热仪及力学性能测试等,研究了不同PBS及Zn(OAc)2含量对PLLA/PBS共混物的形态结构、结晶性能和力学性能的影响。结果表明,PLLA和PBS属于非相容体系,Zn(OAc)2的加入能降低PBS相区的尺寸,提高PLLA/PBS体系的相容性,且质量分数为0.05%时增容效果最佳;PBS的加入可有效提高PLLA的结晶速率和结晶度;随着PBS含量的增加,共混物的断裂伸长率和冲击韧性与纯PLLA相比显著提高,共混物的断裂伸长率均在300%以上;当PLLA/PBS/Zn(OAc)2质量比为80/20/0.05时,共混物的综合性能最优。 Poly(L-lactide) (PLLA)/poly(butylene succinate) (PBS)/zinc acetate (Zn(OAc)2) blends with different compositions were prepared by melt blending. The morphology, crystallization behavior and mechanical properties of PLLA/PBS/Zn(OAc)2 blends were investigated by SEM, DMA, DSC and mechanical tests. The results show that PLLA/PBS blends are incompatible and exhibit phase-separated morphology. Addition of Zn(OAc)2 leads to a decrease of PBS domain size, thereby improving the compatibility between PLLA and PBS. The smallest domain size is found in PLLA/PBS blends containing 0.05% Zn(OAc)2. The addition of PBS can effectively improves the crystallization rate and crystaUinity of PLLA. Moreover, the impact strength and the fracture elongation of PLLA/PBS blends increase with increasing PBS content compared with pure PLLA. The elongation at break of PLLA containing PBS is above 300%. The blend with m (PLLA)/m (PBS)/rn (Zn(OAc)2) = 80/20/0.05 shows the best mechanical properties.
出处 《高分子材料科学与工程》 EI CAS CSCD 北大核心 2016年第3期48-53,共6页 Polymer Materials Science & Engineering
基金 新世纪优秀人才计划(NCET120601) 北京市教委重点基金(KZ201310012014) 科技北京百名领军人才(LJ201305)
关键词 聚左旋乳酸 聚丁二酸丁二醇酯 醋酸锌 共混 性能 poly (L-lactide) poly(butylene succinate) zinc acetate blend property
  • 相关文献

参考文献10

  • 1Zhang X Q, Schneider K, Liu G M, et cd, Structure variation oftensile-deformed amorphous poly ( 1-lactic acid ) : effects ofdeformation rate and strain[j]. Polymer, 2011, 52: 4141-4149.
  • 2熊祖江,张秀芹,刘国明,赵莹,王锐,王笃金.聚左旋乳酸/聚氧化乙烯共混物的拉伸行为及结构转变[J].高等学校化学学报,2013,34(5):1288-1294. 被引量:7
  • 3Yokohara T, Yamaguchi M. Structure and properties for biomass*based polyester blends of PL A and PBS[J]. Eur. Polym. J.,2008,44: 677-685.
  • 4招启强,肖敏,王拴紧,阮镜棠,孟跃中.以二异氰酸酯为增容剂的聚甲基乙撑碳酸酯/聚乳酸共混材料的制备与性能[J].高分子材料科学与工程,2011,27(5):152-155. 被引量:8
  • 5Harada M, Ohya T, Iida K, et al. Increased impact strength ofbiodegradable poly (lactic acid)/poly ( butylene succinate ) blendccanposites by using isocyanate as a reactive processing agent「J] . J.Appl. Polym. Sci. , 2007, 106: 1813-1820.
  • 6Capelot M, Wontamal D, Toumilhac F, et al. Metal-catalyzedtransesterification for healing and assembling of thermosets [J]. J.Am. Chan. Soc., 2012,134: 7664-7667.
  • 7Ji Df Liu Z Y, Lan X R, et al. Morphology, rKeology,crystallization behavior, and mechanical properties of poly (lacticacid)/poly(butylene succinate)/dicumyl peroxide reactive blends[J].J. Appl. Polym. Sci., 2014, 131 : 1082-1090.
  • 8Wang R Y,Wang S F, Zhang Y, et al. Toughening modificationof PLLA/PBS blends via in situ cx>mpatibilization[J]. Polym. Eng.Sci.,2009, 49: 26-33.
  • 9王燕燕,陈思翀,王玉忠,李洪超,华尔德.PC/PLA共混物的酯交换反应与相容性[J].高分子材料科学与工程,2009,25(11):45-48. 被引量:8
  • 10Kawai T, Rahman Nt Matsuba G, et al. Crystallization andmelting behavior of poly (L-lactic acid) [ J]. Macromolecules,2007,40: 9463-9469.

二级参考文献40

  • 1FIORINI M, PILATI F, BERTI C, et al. Reactive blending of poly(ethylene terephthalate) and bisphenoI-A polycarbonate: effect of various catalysts and mixing time on the extent of exchange reactions[J]. Polymer, 1997, 38(2): 413-419.
  • 2IGNATOV N V, CARRARO C, TARTARI V, et al. PET/PC blends and copolyrners by one-step extrusion: 1. chemical structure and physical properties of 50/50 blends[J]. Polymer, 1997, 38(1) : 195-200.
  • 3LEE L T, WOO E M. Reaction-induced miscibility in blends comprised of bisphenol-A polycarbonate and poly (trimethylene terephthalate) [J]. Colloid Polymer Science, 2004, 282: 1308- 1315.
  • 4PILATI F, MARIANUCCI E, BERTI C. Study of the reaction occurring during melt mixing of poly (ethylene terephthalate) and polycarhonate[J]. Journal of Applied Polymer Science, 1985, 30 (3) : 1267-1275.
  • 5GODARD P, DEKONINCK J M, DEVLESAVER V, et al. Molten bisphenol-A 10olycarbonate-poly (ethylene terephthalate ) blends. II. kinetics of the exchange reaction[J]. Journal of Polymer Science Part A: Polymer Chemistry, 1986, 24(12): 3315-3324.
  • 6Darrembourg D J, Holtcamp M W. Catalytic activity of Zine(II) phenoxides which possess readily accessible coordination sites. oopolymerization and terpolymerization of epoxides and carbon dioxide[J]. Macromolecules, 1995, 28: 7577-7579.
  • 7Jiao J, Wang S J, Xiao M, et al. Process,ability, property, and morphology of biodegradable blends of poly(propylene carbonate) and poly(ethylene-co-vinyl alcohol)[J]. Polym. Eng. Sci., 2007,47 (2) :174-180.
  • 8Pang M Z, O.iao J J, Jiao J, et al. Miscibility and properties of completely biodegradable blends of poly ( propylene carbonate) and poly(butylenes sueeinate)[J]. J. Appl. Polym. Sei., 2008, 107 (5) : 2854-2860.
  • 9孟跃中,李秀华,诸泉,等.天然植物纤维增强的可完全降解的聚合物复合材料及其制备方法:中国,02149613.7[P].2003-06-11.
  • 10XuJ, Li R K Y, Meng Y Z, et al. Biodegradable Poly(propylene carbonate)/montmorillonite nanocomposites prepared by direct melt intercalation[J]. Mater. Res. Bull., 2006, 41: 244-252.

共引文献20

同被引文献23

引证文献4

二级引证文献8

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