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首页> 外文期刊>European Polymer Journal >Kinetic studies of biocatalyzed copolyesters of poly(butylene succinate) (PBS) containing fully bio-based dilinoleic diol
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Kinetic studies of biocatalyzed copolyesters of poly(butylene succinate) (PBS) containing fully bio-based dilinoleic diol

机译:含有全生物基稀释二醇的聚(丁烯琥珀酸酯)(PBS)生物催化剂共聚酯的动力学研究

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摘要

A series of segmented bio-copolyesters based on crystallizable hard segments of poly(butylene succinate) (PBS) and fully bio-based dilinoleic diol (DLAOH), creating dilinoleic succinate (DLS) soft segments, were prepared by enzymatically catalyzed polycondensation. The kinetic studies performed with H-1 NMR and SEC have proved incorporation of highly hydrophobic DLAOH into the polymer backbone. We found that the efficacy of DLAOH incorporation was limited by the catalytic pocket size of the enzyme and its hydrophobic nature favouring the formation of long PBS sequences, especially at the early synthesis stages and having an effect on final content of soft segments compared to feed ratio. Based on quantitative C-13 NMR analysis we found that copolymers had R-values lower than 1, that is low degree of randomness. Differential scanning calorimetry (DSC) revealed changes in degree of crystallinity and the presence of a phase mixed system.
机译:通过酶促催化缩聚制备基于聚(丁烯琥珀酸盐)(PBS)(PBS)和完全生物基稀释二醇(DLaOH)的结晶硬区段的一系列分段生物共聚酯,并通过酶促致缩聚来制备产生稀释琥珀酸盐(DLAOH)的软链段。 用H-1 NMR和SEC进行的动力学研究证明了高度疏水的DLaOH掺入聚合物主链中。 我们发现,与进料比相比,酶的催化口袋尺寸及其疏水性质的催化口袋尺寸有限地受到酶的催化口袋尺寸的限制,特别是在早期合成阶段和对软链段的最终含量的影响 。 基于定量C-13 NMR分析,我们发现共聚物具有低于1的R值,即低随机性。 差分扫描量热法(DSC)显示结晶度的变化和相混合体系的存在。

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