期刊文献+

具有超支化结构的聚醚型脂肪族聚氨酯弹性体的合成与表征及力学性能研究 被引量:4

SYNTHESIS,CHARACTERIZATION AND MECHANICAL PROPERTIES OF POLYETHER-BASED ALIPHATIC POLYURETHANE ELASTOMERS COMPOSED OF HYPERBRANCHED POLYESTER SEGMENTS
原文传递
导出
摘要 用聚四氢呋喃醚二醇、端羟基超支化聚酯(HB-20)、异佛尔酮二异氰酸酯和1,4-丁二醇,合成了含有超支化结构的聚醚型脂肪族聚氨酯(PU)弹性体.通过Flory-Rehner公式计算了体系的交联密度;用FT-IR、WAXD和DSC表征了超支化PU的氢键化程度和形态.实验结果表明,在PU弹性体中引入少量的HB-20,能提高氨基甲酸酯羰基的氢键化程度和软硬段间的微相分离程度,从而显著提高材料的拉伸强度.由于氢键化程度和交联密度双重效应的影响,含6 wt%HB-20的聚醚型PU与不含HB-20的PU相比拉伸强度提高了2倍多,达到37.9 MPa,断裂伸长率仍高达414%. Aliphatic polyether-based polyurethane (PU) elastomers with hyperbranched polyester segments were synthesized by prepolymer process from polytetramethylene ether glycol, hydroxyl-terminated hyperbranched polyester (HB-20), IPDI and 1,4-butanediol. The crosslinking density of the PU elastomer was calculated by using the Flory- Rehner equation. The degree of hydrogen bonding, the microstrueture and the morphologies of these PU materials were characterized by means of FTIR, WAXD and DSC, respectively. The experimental results indicated that the PU elastomers containing small amount of HB-20 exhibited the enhanced hydrogen bonding and the micro-phase separated morphologies as well as the mechanical properties. As compared with the comparable PU specimen, the tensile strength of the polyether-based aliphatic PU containing 6 wt% HB-20 increased by 2.1 times, up to 37.9 MPa, and the elongation at break was still as high as 414%, resulting from the dual effects of the hydrogen bonding and the crosslinking density in the PU system.
作者 张杰 胡春圃
出处 《高分子学报》 SCIE CAS CSCD 北大核心 2009年第9期867-873,共7页 Acta Polymerica Sinica
基金 上海市重点学科建设项目(项目号B502)资助
关键词 超支化聚酯 聚醚型脂肪族聚氨酯 氢键 微相分离 交联密度 Hyperbranched polyester Polyether-based aliphatic polyurethane Hydrogen-bond Microphase separation Crosslinking density
  • 相关文献

参考文献21

  • 1Aulenta F, Hayes W, Rannard S. Eru Polym J, 2003,39 (9) : 1741 - 177.
  • 2Martin H, Kinns H, Mitchell N, Astier Y, Madathil R, Howorka S. J Am Chem Soc ,2007,129(31 ) :9640 - 9649.
  • 3Grundke K, Azizi M, Ziemer A, Michel S, Pleul D, Simon F, Voit B, Kreitschmann M, Kierkus P. Surface Coatings International Part B: Coatings Transactions, 2005,88 : 101 - 106.
  • 4Mikhaylova Y, Pigorsch E, Grundke K, Eichhorn K J, Voit B. Macromol Symp, 2004,210 : 271 - 280.
  • 5Xu G, Shi W F, Gong M, Yu F, Feng J P. Poly Adv Technol, 2004,15 : 639 - 644.
  • 6Lee D K,Tsai H B.J Appl Polym Sci,2000,75:167 - 174.
  • 7Jena K K, Chattopadhyay D K, Raju K V S N. Eur Polym J,2007,43:1825 - 1837.
  • 8Sheth J P, U nal S, Yilgor E, Yilgor I, Beyer F L, Long T E, Wilkes G L. Polymer, 2005,46:10180- 10190.
  • 9Nasar A S, Jikei M, Kakimoto M-a. Eur Polym J, 2003,39 : 1201 - 1208.
  • 10Okrasa L, Zigon M, Zagar E, Czech P, Boiteux G. J Non-Cryst Solids, 2005,351 : 2753 - 2758.

二级参考文献1

共引文献18

同被引文献56

  • 1Feng X, Taton D, Borsali R, Chaikof E L, Gnanou Y. J Amer Chem Soe,2006,128 ( 35 ) : 11551 - 11562 Chem,2009,20 (5) : 1054 - 1057.
  • 2Chen W, Meng F, Li F, Ji S, Zhong Z. Biomaeromoleeules,2009,10 ( 7 ) : 1727 - 1735.
  • 3Jones M, Ranger M, Leroux J. Bioeonj Chem,2003,14 (4) :774 - 781.
  • 4Kojima C, Yoshimura K, Harada A, Sakanishi Y, Kono K. Bioeonj.
  • 5Gillies E R,Jonsson T B,Fr6chet J M J. J American Chem Soc,2004,126(38) :11936 - 11943.
  • 6Guo Z, Zhang Y, Huang W, Zhou Y, Yan D. Macromole Rapid Comm,2008,29 (21 ) : 1746 - 1751.
  • 7Lee S, Saito K, Lee H, Lee M J, Shibasaki Y, Oishi Y, Kim B. Biomacromolecules,2012,13 (4) : 1190 - 1196.
  • 8B0hm I, Ritter H. Maeromole Chem and Phys,2011,212 (10) : 1080 - 1085.
  • 9Liu Y,Liu X,Liu H,Cheng F,Chen Y. Macromole Res,2012,20(6) :578 -584.
  • 10Zhou Y,Yan D. Chem Comm,2009, (10):1172 -1188.

引证文献4

二级引证文献35

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