Synthesis and rheology of biodegradable poly(glycolic acid) prepared by melt ring‐opening polymerization of glycolide

摩尔质量 聚合 材料科学 高分子化学 乙醇酸 玻璃化转变 流变学 开环聚合 本体聚合 流变仪 聚合物 化学工程 复合材料 自由基聚合 乳酸 生物 细菌 工程类 遗传学
作者
Estelle Gautier,Patrick Fuertès,Philippe Cassagnau,Jean‐Pierre Pascault,Étienne Fleury
出处
期刊:Journal of Polymer Science Part A [Wiley]
卷期号:47 (5): 1440-1449 被引量:43
标识
DOI:10.1002/pola.23253
摘要

Abstract Ring‐opening polymerization (ROP) of glycolide was studied in melt conditions and in the presence of two different initiators: 1‐dodecanol and 1,4‐butanediol and tin(II) 2‐ethylhexanoate as catalyst. Its subsequent polymerization provided poly(glycolic acid) with controlled molar masses ranging from 2000 to 42,000 g/mol with well‐defined structures characterized by NMR. Their thermal properties were evaluated by DSC analysis, and a glass transition temperature at infinite molar mass ( T g∞ ) of 44.8 °C was thus calculated. From rheological data, the critical molar mass for entanglement, M c , was estimated to be near 11,000 g/mol. Furthermore, in situ polymerizations were also performed between the plates of the rheometer within a same temperature range from 210 to 235 °C. The variation of the storage and loss moduli during the polymerization step have been monitored by time sweep oscillatory experiments under an angular frequency ω = 10 rad/s. Finally, the development of an inverse rheological method allowed to calculate the bulk polymerization kinetics in the temperature range 200–230 °C. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 1440–1449, 2009

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