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Hydrolytic degradation of ROMP thermosetting materials catalysed by bio-derived acids and enzymes : from networks to linear materials.

机译:生物衍生的酸和酶催化的ROMP热固性材料的水解降解:从网络到线性材料。

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摘要

This paper reports the first example of degradable ROMP thermosetting materials catalysed by bio-derived acids and cutinase from Thermobifida cellulosilytica (Thc_Cut1). The ROMP thermosetting materials are based on norbornene dicarboximides containing acetal ester groups only in the crosslinking moiety. The insoluble cross-linked materials were subjected to acid-catalysed hydrolysis using bio-derived acetic and citric acids as well as enzymatic degradation using Thc_Cut1, resulting in the materials becoming completely soluble in dichloromethane. 1H NMR and rheological analysis performed on materials after acid-catalysed hydrolysis showed characteristics indistinguishable to those of the linear polymer analogues. These analyses confirmed the cleavage of the crosslinking moiety upon degradation with the main backbone chains remaining intact. The glass transition temperatures of the polymer materials after acid-catalysed hydrolysis were the same as those observed for the linear polymer analogues. TGA showed that the cross-linked polymers were thermally stable to 150 °C, beyond which they showed weight losses due to the thermal cleavage of the acetal ester linkages.
机译:本文报道了可分解的ROMP热固性材料的第一个实例,该材料是由来自Thermobifida cellulosilytica(Thc_Cut1)的生物衍生酸和角质酶催化的。 ROMP热固性材料基于仅在交联部分中含有缩醛酯基的降冰片烯二甲酰亚胺。使用生物来源的乙酸和柠檬酸对不溶性交联材料进行酸催化水解,并使用Thc_Cut1进行酶促降解,从而使材料完全溶于二氯甲烷。酸催化水解后对材料进行的1 H NMR和流变分析表明,该特性与线性聚合物类似物没有区别。这些分析证实了降解时交联部分的裂解,而主要主链保持完整。酸催化水解后聚合物材料的玻璃化转变温度与线性聚合物类似物所观察到的相同。 TGA表明,交联的聚合物在150℃下是热稳定的,超过此温度,由于缩醛酯键的热裂解,它们显示出重量损失。

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