期刊文献+

以水作相分离造孔剂制备P(VDF-HFP)/PMMA聚合物电解质膜 被引量:8

Preparation of P(VDF-HFP)/PMMA Blend Polymer Electrolyte Membrane with Water as Material for Phase Separation and Pore Producer
下载PDF
导出
摘要 介绍了一种以水代替常用的有机物质作为相分离造孔剂制备混合型聚合物电解质的新方法 .所研究的混合型聚合物为聚 (偏二氟乙烯 -六氟丙烯 )和聚甲基丙烯酸甲酯的混合物 .扫描电镜 SEM图表明这种混合型聚合物膜具有蜂窝状结构 ,有利于膜电导率的增加 .利用 FTIR,XRD和 DSC等方法研究了混合型聚合物电解质中两种聚合物间的相互作用 .用电化学交流阻抗方法测得在 3 0℃下 P( VDF-HFP) /PMMA摩尔比为 1 :1的混合型聚合物电解质的离子电导率为 0 .80 4× 1 0 - 3S/cm.对照其它方法 ,本方法具有制备容易。 A new method is proposed to prepare blend polymer electrolyte by using water as the material for phase separation and pore producer instead of traditional organic material. The blend polymer electrolyte consisting of polyvinylidene fluoride-co-hexafluoropropylene P(VDF-HFP) and poly(methyl methacrylate) (PMMA) was prepared by this method. The SEM images show that the blend polymer electrolyte films have alveolate network structures, which benefit the increase of ionic conductivity. The interaction between two kinds of polymers within the blend polymer was confirmed by FTIR, XRD and DSC studies. The ionic conductivity for the blend polymer electrolyte film with m(VDF-HFP)∶ m(PMMA)=1∶1 was measured as 0.804×10 -3 S/cm at 30 ℃ by using electrochemical impedance method. Compared with other approaches the method introduced here is a very easy, cost-saving, and more environmental friendly method.
机构地区 复旦大学化学系
出处 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 2004年第5期922-925,共4页 Chemical Journal of Chinese Universities
基金 国家自然科学基金 (批准号 :2 0 3 3 3 0 40 )资助
  • 相关文献

参考文献13

  • 1Dias F. B., Plomp L., Veldhuis J. B. J.. J. Power Sources[J], 2000, 88: 169-191
  • 2Song J. Y., Wang Y. Y., Wan C. C.. J. Power Sources[J], 1999, 77: 183-197
  • 3Tarascon J. M., Gozdz A. S., Schmutz C. et al.. Solid State Ionics[J], 1996, 86-88: 49-54
  • 4Bookeun O., Young R. K.. Solid State Ionics[J], 1999, 124: 83-89
  • 5Lee Y. G., Park J. K.. J. Power Sources[J], 2001, 97-98: 616-620
  • 6Gozdz A. S., Tarascon J. M.. U. S. Patent 5 418 091[P], 1995
  • 7Gozdz A. S., Tarascon J. M., Warren P. C.. U. S. Patent 5 460 904[P], 1995
  • 8Rajendran S., Mahendran O., Mahalingam T.. European Polymer Journal[J], 2002, 38: 49-55
  • 9Rajendran S., Mahendran O., Kannan R.. Materials Chemistry and Physics[J], 2002, 74: 52-57
  • 10Rajendran S., Mahendran O., Kannan R.. Fuel[J], 2002, 81: 1 077-1 081

二级参考文献7

  • 1[1]Feuillade G., Perche P.. J. Appl. Electrochem.[J], 1975, 5: 63-67
  • 2[2]Abraham K. M., Alamgir M.. J. Electrochem. Soc.[J], 1990, 137: 1 657-1 659
  • 3[3]Apetecchi G. B., Croce F., Scrosati B.. Electrochim. Acta[J], 1995, 40: 991-998
  • 4[4]Gozdz A. S., Tarascon J. M.. U. S. Patent, 5 418 091[P], 1995
  • 5[5]Gozdz A. S., Tarascon J. M., Warren P. C.. U.S. Patent, 5 460 904[P], 1995
  • 6[6]GU Hui(顾辉), HUANG Xue-Jie(黄学杰), CHEN Li-Quan(陈立泉) et al.. Chinese Patent, 0 0107 243.9[P], 2000
  • 7[7]Fong R., Sacken U., Dahn J. R.. J. Electrochem. Soc.[J], 1990, 137: 2 009-2 013

共引文献22

同被引文献256

引证文献8

二级引证文献23

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