期刊文献+

Stannous oxalate as a novel catalyst for the synthesis of polytrimethylene terephthalate 被引量:3

Stannous oxalate as a novel catalyst for the synthesis of polytrimethylene terephthalate
下载PDF
导出
摘要 Stannous oxalate was prepared efficiently and characterized by XRD and FT-IR. It exhibited higher catalytic activity and had profitable effect than tetrabutyl titanate and stannous octoate for the synthesis of polytrimethylene terephthalate (PTT) via esterification-route. Over this catalyst, the degree of esterification of pure terephthalic acid was up to 94.4% at 260 ℃ after 1.5 h,while the intrinsic viscosity and content of terminal carboxyl groups of the corresponding PTT polyester, polymerized at 260 ℃,60 Pa for 2 h, was 0.8950 dL/g and 15 mol/t, respectively. Stannous oxalate was a promising catalyst for the synthesis of PTT polyester. Stannous oxalate was prepared efficiently and characterized by XRD and FT-IR. It exhibited higher catalytic activity and had profitable effect than tetrabutyl titanate and stannous octoate for the synthesis of polytrimethylene terephthalate (PTT) via esterification-route. Over this catalyst, the degree of esterification of pure terephthalic acid was up to 94.4% at 260 ℃ after 1.5 h,while the intrinsic viscosity and content of terminal carboxyl groups of the corresponding PTT polyester, polymerized at 260 ℃,60 Pa for 2 h, was 0.8950 dL/g and 15 mol/t, respectively. Stannous oxalate was a promising catalyst for the synthesis of PTT polyester.
出处 《Chinese Chemical Letters》 SCIE CAS CSCD 2007年第7期872-874,共3页 中国化学快报(英文版)
关键词 Polytrimethylene terephthalate POLYESTER Stannous oxalate Esterification-route Intrinsic viscosity Polytrimethylene terephthalate Polyester Stannous oxalate Esterification-route Intrinsic viscosity
  • 相关文献

参考文献11

  • 1[1]I.J.Desborough,I.H.Hall,J.Z.Neisser,Polymer 20 (5) (1979) 545.
  • 2[2]F.Simon,M.I.Richard,D.Bruce Chase,et al.Macromolecules 37 (16) (2004) 6027.
  • 3[3]B.J.Wang,C.Y.Li,J.Hanzlicek,et al.Polymer 42 (16) (2001) 7171.
  • 4[4]D.R.Kelsey,K.S.Kiibler,P.N.Tutunjian,Polymer 46 (21) (2005) 8937.
  • 5[5]K.Fujimoto,J.Kato.US Patent 6,284,370 (2001).
  • 6[6]K.Q.Chen,X.Z.Tang,J.Appl.Polym.Sci.91 (3) (2004) 1967.
  • 7[7]Y.Mitsuyuki,JP2000282342 (2000).
  • 8[8]E.M.Woo,L.T.Lee,Polym.Bull.50 (1-2) (2003) 33.
  • 9[9]J.L.Zhang,J.Appl.Polym.Sci.91 (3) (2004) 1657.
  • 10[10]W.Fritz,S.Eckhard,R.Hans,et al.,EP1046662 (2000).

同被引文献31

引证文献3

二级引证文献11

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