High Tg copolyesters of lactide, isosorbide and isophthalic acid

被引:24
|
作者
Kricheldorf, Hans R. [1 ]
Weidner, Steffen M. [2 ]
机构
[1] Univ Hamburg, Inst Tech & Makromol Chem, D-20146 Hamburg, Germany
[2] Fed Inst Mat Res & Testing, BAM, D-12498 Berlin, Germany
关键词
Lactide; Isosorbide; Ring-opening polymerization; Polycondensation; Cyclization; ALIPHATIC POLYESTERS; DICARBOXYLIC-ACID; RENEWABLE RESOURCES; POLYMERS; MACROCYCLES; POLYCONDENSATIONS; POLYCARBONATES;
D O I
10.1016/j.eurpolymj.2013.05.007
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Using SnCl2, ZnCl2, Zn-lactate or Zr-acetylacetonate as catalysts L-lactide was oligomerized in bulk with isosorbide as initiator. The ratio isosorbide/lactide was varied from 8/2 to 2/8. The resulting oligomers were in situ polycondensed with isophthaloyl chloride in various aromatic solvents. In chlorobenzene homogeneous reaction mixtures were obtained, whereas molten copolyesters precipitated from toluene and xylene. The obtained average molecular weights indicated high polydispersities. According to MALDI-TOF MS the low molar mass reaction products (<4 kDa) almost exclusively consisted of cyclics with a composition depending on the feed ratio. The glass-transition temperatures (T-g) varied between the values of poly(L-lactide (64 degrees C) and poly(isosorbide isophthalate) (180 degrees C). Four polyesters prepared from 5-tert-butyl isophthalic acid displayed higher T-g values. Differential thermoanalysis evidenced that the thermostability decreases with higher fractions of lactide, but processing from the melt seems to be feasible up to temperatures of 260 degrees C without risking degradation. (c) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2293 / 2302
页数:10
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