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首页> 外文期刊>Journal of the Taiwan Institute of Chemical Engineers >Thermal degradation behaviors and biodegradability of novel nanocomposites based on various poly[(butylene succinate)-co-adipate] and modified layered double hydroxides
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Thermal degradation behaviors and biodegradability of novel nanocomposites based on various poly[(butylene succinate)-co-adipate] and modified layered double hydroxides

机译:基于各种聚[(丁烯琥珀酸)-CO-己二酸酯的新型纳米复合材料的热降解行为及生物降解性,并改性层状双氢氧化物

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摘要

Synthesized via a polycondensation reaction, three biodegradable poly[(butylene succinate)-co-adipate] (PBSA) containing various succinic acid (SA) and adipic acid (AA) ratios were combined with an organically modified layered double hydroxide (m-LDH) to manufacture PBSA/m-LDH nanocomposites. The structures of these PBSA/m-LDH nanocomposites were studied via wide-angle X-ray diffraction (WAXD) and transmission electron microscopy (TEM). The WAXD and TEM analyses demonstrated that the various nanocomposites formed with exfoliated LDHs were effectively dispensed in the PBSA matrix. The effects of m-LDH on the biodegradation of PBSA/m-LDH nanocomposites were explored using lipase from Pseudomonas fluorescens. The degradation rates of the neat PBSA copolymers decrease in the order PBSA-25 > PBSA-50 > PBSA-75. The faster degradation rate of PBSA-25 is a consequence of the lower melting temperature and flexibility of its chain backbone. Moreover, weight loss decreases with increasing loading of m-LDH, suggesting that the presence of m-LDH hinders the degradation of the PBSA copolymers. On the basis of the molecular weight and polydispersity index of the remaining PBSA-based specimens, we propose that the degradation behavior of PBSA using P. fluorescens lipase is controlled by exo-type hydrolysis activity wherein PBSA copolymer degradation arises from both ends of the polymer chains. (C) 2017 Taiwan institute of Chemical Engineers. Published by Elsevier B.V. All rights reserved.
机译:通过缩聚反应合成,将含有各种琥珀酸(SA)和己二酸(AA)比的三种可生物降解的聚苯酸(丁二酸酯)-CO-己二酸酯(PBSA)与有机改性的层双氢氧化物(M-LDH)合并制造PBSA / M-LDH纳米复合材料。通过宽角X射线衍射(WAXD)和透射电子显微镜(TEM)研究了这些PBSA / M-LDH纳米复合材料的结构。 WAXD和TEM分析证明,在PBSA基质中有效地分配了用剥离的LDH组形成的各种纳米复合材料。利用来自假单胞菌荧光的脂肪酶探讨了M-LDH对PBSA / M-LDH纳米复合材料的生物降解的影响。纯PBSA共聚物的降解速率在阶PBSA-25> PBSA-50> PBSA-75中降低。 PBSA-25的更快降解速率是其链骨架较低的熔融温度和柔韧性的结果。此外,随着M-LDH的增加而减少减肥,表明M-LDH的存在阻碍了PBSA共聚物的降解。在剩余的PBSA标本的分子量和多分散指数的基础上,我们提出使用P.荧光脂肪酶PBSA的降解行为由外型水解活性控制,其中PBSA共聚物降解来自聚合物的两端链条。 (c)2017台湾化工工程师研究所。 elsevier b.v出版。保留所有权利。

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