聚酯纤维
缩聚物
聚合物
二醇
玻璃化转变
材料科学
木质素
纤维素
分解
有机化学
化学工程
加氢脱氧
动态力学分析
化学
高分子化学
催化作用
工程类
选择性
作者
Xianyuan Wu,Mario De bruyn,Gregor Trimmel,Klaus Zangger,Katalin Barta
出处
期刊:ACS Sustainable Chemistry & Engineering
[American Chemical Society]
日期:2023-02-06
卷期号:11 (7): 2819-2829
被引量:10
标识
DOI:10.1021/acssuschemeng.2c05998
摘要
Polyesters are an important class of thermoplastic polymers, and there is a clear demand to find high-performing, recyclable, and renewable alternatives. In this contribution, we describe a range of fully bio-based polyesters obtained upon the polycondensation of the lignin-derived bicyclic diol 4,4'-methylenebiscyclohexanol (MBC) with various cellulose-derived diesters. Interestingly, the use of MBC in combination with either dimethyl terephthalate (DMTA) or dimethyl furan-2,5-dicarboxylate (DMFD) resulted in polymers with industrially relevant glass transition temperatures in the 103-142 °C range and high decomposition temperatures (261-365 °C range). Since MBC is obtained as a mixture of three distinct isomers, in-depth NMR-based structural characterization of the MBC isomers and thereof derived polymers is provided. Moreover, a practical method for the separation of all MBC isomers is presented. Interestingly, clear effects on the glass transition, melting, and decomposition temperatures, as well as polymer solubility, were evidenced with the use of isomerically pure MBC. Importantly, the polyesters can be efficiently depolymerized by methanolysis with an MBC diol recovery yield of up to 90%. The catalytic hydrodeoxygenation of the recovered MBC into two high-performance specific jet fuel additives was demonstrated as an attractive end-of-life option.
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