The microstructure of poly(butylene terephthalate) copolymers via 13C NMR sequence distribution analysis:: Solid-state copolymerization versus melt copolymerization

被引:20
作者
Jansen, MAG
Goossens, JGP
de Wit, G
Bailly, C
Koning, CE
机构
[1] Eindhoven Univ Technol, Fac Chem Engn & Chem, Lab Polymer Technol, NL-5600 MB Eindhoven, Netherlands
[2] Eindhoven Univ Technol, Fac Chem Engn & Chem, Polymer Chem Lab, NL-5600 MB Eindhoven, Netherlands
[3] Univ Catholique Louvain, Lab Chim & Phys Hauts Polymeres, B-1348 Louvain, Belgium
[4] Dutch Polymer Inst, NL-5600 AX Eindhoven, Netherlands
关键词
C-13 NMR sequence distribution analysis; polycondensation; PBT; microstructure;
D O I
10.1016/j.aca.2005.05.063
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Two diols, 2,2-bis(4-[hydroxyethoxy]phenyl)propane (Dianol 220 (R)) and bis(2-hydroxyethyl)terephthalate (BHET), were incorporated into poly(butylene terephthalate) (PBT) by solid-state polymerization (SSP) and melt polymerization (MP). Different PBT/diol ratios were used to obtain copolymers with different compositions. C-13 NMR spectroscopy was used to analyze the sequence distribution and the data analysis was discussed in detail. Both Dianol and BHET were randomly incorporated in the MP copolymers. For both PBT-Dianol and PBT-BHET copolymers obtained via SSP, a non-random, blocky microstructure was obtained. For the PBT-Dianol copolymers, the randomness increased for increased fractions of incorporated Dianol. For the PBT-BHET copolymers, the randomness continuously decreased with increased fractions of incorporated BHET. (c) 2005 Elsevier B.V. All rights reserved.
引用
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页码:19 / 30
页数:12
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