酶催化4-甲基儿茶酚低聚物的合成及其作为聚丙烯稳定剂的初步评价

IF 3.2 3区 化学 Q2 POLYMER SCIENCE e-Polymers Pub Date : 2023-01-01 DOI:10.1515/epoly-2023-0008
Yanpeng Wang, Fan Jiang, Lei Zhang
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引用次数: 1

摘要

摘要采用酶催化水溶液聚合的方法制备了4-甲基邻苯二酚低聚物,并对其作为聚丙烯(PP)稳定剂的性能进行了初步评价。与本征PP相比,4-甲基邻苯二酚低聚物/PP复合材料的氧化起始温度增加了66°C,氧化诱导时间增加了40 min。此外,4-甲基邻苯二酚低聚物与PP的混合(即,在形成4-甲基邻苯二苯酚低聚物/PP复合物中)确实显著增强了PP在热氧化环境中的长期稳定性。此外,该复合材料的拉伸强度在老化800小时后没有显著降低 h。这些结果表明,即使在极端条件下,加入4-甲基邻苯二酚低聚物也会显著延缓PP材料的老化和降解。因此,酚类化合物的酶催化聚合可以为制备新型抗氧化剂提供新的途径。
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Enzyme-catalyzed synthesis of 4-methylcatechol oligomer and preliminary evaluations as stabilizing agent in polypropylene
Abstract In the present work, 4-methylcatechol oligomer has been prepared by using enzyme-catalyzed polymerization in water and preliminary evaluations as stabilizing agent in polypropylene (PP) was performed. In comparison with intrinsic PP, the oxidation onset temperature of the 4-methylcatechol oligomer/PP composite increased by 66°C, and the oxidation induction time increased by 40 min. In addition, the mixing of a 4-methylcatechol oligomer with PP (i.e., in the formation of a 4-methylcatechol oligomer/PP composite) did significantly enhance the long-term stability of PP in a thermal oxidative environment. Moreover, the tensile strength of this composite did not significantly decrease after aging for 800 h in an air atmosphere at 120°C. These results show that the addition of a 4-methylcatechol oligomer will markedly delay the aging and degradation of PP materials, even under extreme conditions. Thus, an enzyme-catalyzed polymerization of phenol compounds may provide a new avenue toward the preparation of novel antioxidants.
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来源期刊
e-Polymers
e-Polymers 化学-高分子科学
CiteScore
5.90
自引率
10.80%
发文量
64
审稿时长
6.4 months
期刊介绍: e-Polymers is a strictly peer-reviewed scientific journal. The aim of e-Polymers is to publish pure and applied polymer-science-related original research articles, reviews, and feature articles. It includes synthetic methodologies, characterization, and processing techniques for polymer materials. Reports on interdisciplinary polymer science and on applications of polymers in all areas are welcome. The present Editors-in-Chief would like to thank the authors, the reviewers, the editorial staff, the advisory board, and the supporting organization that made e-Polymers a successful and sustainable scientific journal of the polymer community. The Editors of e-Polymers feel very much engaged to provide best publishing services at the highest possible level.
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