期刊文献+

侧链含萘可交联聚芳醚酮的合成及性能 被引量:5

Synthesis and Properties of a Novel Crosslinkable Poly(aryl ether ketone) Containing Naphthalene Group on a Side Chain
下载PDF
导出
摘要 以4,4'-二羟基苯基正戊酸和4,4'-二氟二苯酮为原料,二甲基亚砜(DMSO)为溶剂,采用亲核取代反应合成侧基含羧基的聚芳醚酮均聚物,进一步与1-萘酚和2-萘酚接枝制备新型含萘可交联聚芳醚酮.用核磁共振(NMR)、红外光谱(FTIR)、示差扫描量热(DSC)和热重分析(TGA)表征其结构和性能,含萘聚芳醚酮在常用有机溶剂如N,N-二甲基乙酰胺(DMAc)、DMSO,四氢呋喃(THF)中有良好的溶解性,并具有很好的成膜性.DSC测试结果显示,在170℃热处理2 h的交联聚合物的玻璃化转变温度(Tg)提高40℃.TGA数据显示接枝后的聚合物的5%热失重温度提高40~50℃,证明其发生交联反应.结果表明,新型含萘可交联聚芳醚酮具有热固性树脂的耐溶剂和耐高温特性,进一步拓宽了聚芳醚酮的应用前景. A novel crosslinkable poly(arylene ether ketone)s (PAEK) with naphthalene pendant was prepared from carboxyl-containing PAEK precursor and naphthalenol by graft reaction. The structures of the polymer before and after grafted were confirmed by FTIR and 1H NMR spectroscopy. These polymers exhibited good solubility in common organic solvents, such as dimethyl sulfoxide(DMSO), N,N-dimethylacetamide (DMAc), tetrahydrofuran (THF) and chloroform, and could be casted into flexible and transparent films. However, after thermally cross-linked at 170℃ for 2 h at air atmosphere, the resulting cross-linked polymer exhibited good chemical resistance, insoluble in above organic solvents. In addition, the cross-linked polymers displayed high thermal stability. The glass transition temperature(Tg) and thermal weight loss temperature were obviously increased respectively.
出处 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 2012年第11期2563-2566,共4页 Chemical Journal of Chinese Universities
基金 国家自然科学基金(批准号:51103056)资助
关键词 聚芳醚酮 羧基 萘酚 交联反应 Poly( aryl ether ketone)(PAEK) Carboxylic group Naphthalene Cross-linking reaction
  • 相关文献

参考文献17

  • 1Attwood T. E. , Dowson P. C. , Freeman J. L. , Hoy L. R. J. , Rose J. B. , Staniland P. A. . Polymer[J], 1981, 22: 1096-1103.
  • 2Moulinie P. , Paroli R. M. , Wang Z. Y. . J. Polymer Science, Part A: Polymer Chemistry[J], 1995, 33: 2741-2752.
  • 3Rose J. B. . Polymer[J], 1974, 15: 456-465.
  • 4Yoshihiro T. , Hiroshi U. , Shiro K. . J. Polym. Sci. , Part A: Polym. Chem. [J],1997, 35: 271-277.
  • 5Walker K. A. , Markoski L. J. , Moore J. S. . Macromolecules[J], 1993, 26: 3713-3716.
  • 6张云鹤,王冬,牛亚明,王贵宾,姜振华.新型含萘含氟聚芳醚酮的合成与表征[J].高等学校化学学报,2005,26(7):1378-1380. 被引量:5
  • 7Hergenrother P. M. , Jensen B. J. , Havens S. J. . Polymer[J], 1988, 29: 358-369.
  • 8Wang Z. Y. , Annele G. . Macromolecules[J], 1995, 28: 3728-3732.
  • 9Mami O. , Toshikazu T. , Takeshi E. . J. Polymer Sciene, Part A: Polymer Chemistry[J], 1995, 33: 2647-2655.
  • 10Thoms K. , Helmut R. . Macromolecules[J], 1995, 28: 4806-4809.

二级参考文献25

  • 1Rose J. B.. Polymer[J], 1974, 15: 456-465
  • 2Attwood T. E., Dowson P. C., Freeman J. L. et al.. Polymer[J], 1981, 22: 1096-1103
  • 3Moulinie P., Paroli R. M., Wang Zh. Y.. J. Polymer Science;Part A: Polymer Chemistry[J], 1996, 33: 2741-2752
  • 4Hergenrother P. M., Jensen B. J., Havens S. J.. Polymer[J], 1988, 29: 358-369
  • 5Wang Zhiyuan, Anne le Guen. Macromolecules[J], 1995, 28: 3728-3732
  • 6Mami Ohno, Toshikazu Takata, Takeshi Endo. J. Polymer Sciene, Part A: Polymer Chemistry[J], 1995, 33: 2647-2655
  • 7Mercer F. W., Fone M. M., Keddy V. N. et al.. Polymer[J], 1997, 38: 1989-1995
  • 8Goodwin A. A., Mercer F. W., Mckenzie M. T.. Macromolecules[J], 1997. 30: 2767-2774
  • 9Tohru M., Shigekuni S. et al.. Macromolecules[J], 1994, 27: 6665-6670
  • 10Liu Baijun, Hu Wei, Chen Chunhai et al.. Polymers For Advanced Technologies[J], 2003, 14: 221-225

共引文献19

同被引文献23

引证文献5

二级引证文献4

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