期刊文献+

阳离子烷基钪配合物催化体系催化乙烯与丙烯共聚合的研究

COPOLYMERIZATION OF ETHYLENE AND PROPYLENE BY CATIONIC SCANDIUM ALKYL CATALYST SYSTEM
原文传递
导出
摘要 双烷基钪配合物LSc(CH2SiMe3)2(L=(2,6-iPr2C6H3)NC(Me)CHPPh2N(2,6-Me2C6H3))在助催化剂[Ph3C][B(C6F5)4]的作用下能够高活性地催化乙烯和丙烯共聚.在反应温度30℃和乙烯与丙烯常压(1.0×105Pa)下聚合,共聚活性能够达到7.5×105g(PE)mol-1h-1(105Pa)-1.单体的竞聚率分别为rE=29.75和rP=0.015.13C-NMR和DSC分析表明所得到的乙丙共聚物是弹性体,且丙烯单体无规分布在共聚物链中. The scandium dialkyl complex LSc(CH2SiMea)2(L = (2,6-iPr2C6H3)NC(Me)CHPPh2N-(2,6- Me2C6H3 ) ) activated with [ Ph3C] [ B( C6F5 ), ] could initiate ethylene and propylene copolymerization with high activity (7.5×105g(PE)mo1-1 h-1(10SPa) -1) under the conditions of room temperature (30 ℃ ) and atomphere pressure ( 1.0 × 105 Pa). The influence of comonomer feed content and polymerization temperature on activity and the composition of the copolymers using LSc ( CH2 SiMe3 ) 2/[ Ph3 C ] [ B ( C6 F5 ) 4 3 catalytic system were investigated. An increase in the initial propylene feed content leads to the increase in the incorporated propylene content of the resulting copolymer. At 30 ℃ , the highest activity and incorporation of propylene were achieved. Determination of the reactivity ratios shows a much high reactivity for ethylene (rE = 29.75 and rp = 0. 015 ). The resultant copolymers are elastomers having random sequence distibution of the two monomeric units evidenced by 13C-NMR spectroscopy and DSC analyses.
出处 《高分子学报》 SCIE CAS CSCD 北大核心 2013年第5期649-653,共5页 Acta Polymerica Sinica
基金 国家自然科学基金青年基金(基金号21104072)资助项目
关键词 稀土配合物 乙烯 丙烯 共聚合 Rare earth metal complex, Ethylene, Propylene, Copolymerization
  • 相关文献

参考文献55

  • 1Natta G,Pasquon I,Zambelli A. J Am Chem Soc, 1962,84:1488 -1490.
  • 2Cozewith C, Ver Strate G. Maeromolecules, 1971,4:482 -489.
  • 3Kakugo M, Naito Y, Miyatake T, Mizunuma K. Macromolecules, 1980,13 : 1150 - 1152.
  • 4Soga K,Shiono T,Doi Y,Polym Bu11,1983,10:168 -174.
  • 5Doi Y, Ohnishi R, Soga K. Makromol Chem Rapid Commun, 1983,4 : 169 - 174.
  • 6Cheng H N. Macromoleeules,1984,17:1950 - 1955.
  • 7Kashiwa N ,Tsutsui T,Toyota A. Polym Bull, 1985,13:511 - 517.
  • 8Jin J, Uozumi T, Sano T, Teranishi T, Soga K, Shiono T. Maeromol Rapid Commun, 1998,19:337 - 339.
  • 9Leelere M K, Waymouth R M,Angew Chem Int Ed, 1998,37:922 - 925.
  • 10Galimberti M, Mascellani N, Piemontesi F, Camurati I. Maeromol Rapid Commun, 1999,20:214 - 218.

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