Preparation and Structural-Thermodynamical Investigation of Renewable Copolyesters Based on Poly (Ethylene Succinate) and Polyisosorbide

材料科学 异山梨酯 玻璃化转变 聚合物 共聚物 体积分数 热稳定性 表征(材料科学) 化学工程 热重分析 高分子化学 乙烯 复合材料 有机化学 化学 纳米技术 催化作用 工程类
作者
Chaima Bouyahya,Panagiotis Α. Klonos,Alexandra Zamboulis,Eleftheria Xanthopoulou,Nina Maria Ainali,Mustapha Majdoub,Apostolos Kyritsis,Dimitrios Ν. Bikiaris
出处
期刊:Polymers [Multidisciplinary Digital Publishing Institute]
卷期号:16 (15): 2173-2173 被引量:4
标识
DOI:10.3390/polym16152173
摘要

A series of novel renewable copolymers based on poly(ethylene succinate) (PESu) and poly(isosorbide succinate) (PISSu), with the Isosorbide (Is)/PESu molar ratio varying from 5/95 to 75/25, were synthesized in-situ and studied in this work. A sum of characterization techniques was employed here for the structural and thermo-dynamical characterization. The sophisticated technique of dielectric spectroscopy, along with proper analysis, enabled the molecular dynamics mapping of both the local and segmental types, which is presented for such materials for the first time. With increasing the Is fraction, shorter copolymeric entities were gradually formed. Based on the overall findings, the systems were found to be homogeneous, e.g., exhibiting single glass transitions, with the two polymer segments being found to be excellently distributed. The latter is indirect, although strong, evidence for the successful copolymerization. The thermal degradation mechanism for the copolymers was exhaustingly explored employing analytical pyrolysis. The systems exhibited, in general, good thermal stability, according to the thermogravimetric analysis. Confirming one of the initial scopes for the present systems, isosorbide plays here the role of hardener (PISSu) over the soft polymer (PESu), and this is reflected in the monotonic increase of the glass transition temperature, Tg, from -16 to ~56 °C. The introduction of Is results in an increase in constraints (hardening of the matrix), while there seems to be an overall densification of the polymer (decrease of the free volume).
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