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在氧化钼钒催化剂上由5-羟甲基糠醛制备2,5-呋喃二甲酸生物单体

Production of the 2,5-Furandicarboxylic Acid Bio-Monomer From 5-Hydroxymethylfurfural Over a Molybdenum-Vanadium Oxide Catalyst.

作者信息

Liu Jian, Wen Sha, Wang Fei, Zhu Xiaoting, Zeng Zhijuan, Yin Dulin

机构信息

National and Local Joint Engineering Laboratory for New Petro-chemical Materials and Fine Utilization of Resources, Key Laboratory of the Assembly and Application of Organic Functional Molecules of Hunan Province, Hunan Normal University, Changsha, China.

出版信息

Front Chem. 2022 Mar 14;10:853112. doi: 10.3389/fchem.2022.853112. eCollection 2022.

Abstract

2, 5-Furandicarboxylic acid (FDCA) is an important bio-monomer that can potentially replace terephthalic acid to synthesize degradable polyesters. Efficient selective oxidation of biomass-based 5-hydroxymethylfurfural (HMF) to FDCA has been a significant but challenging work in the past decades. In this study, a novel molybdenum-vanadium oxide (Mo-V-O) catalyst was prepared by a simple method and showed excellent catalytic activity for converting HMF to FDCA. A high FDCA selectivity of 94.5 and 98.2% conversion of HMF were achieved under the optimal conditions with tert-butyl hydroperoxide as the oxidant. FT-IR, SEM, XRD and TG were applied to investigate the properties of Mo-V-O catalyst. After fitting experimental data with the first-order kinetics equation, the evaluated apparent activation energies of HMF oxidation were obtained. The experimental design and study were carried out by response surface methodology (RSM) to test the effects of reaction conditions on the catalytic process.

摘要

2,5-呋喃二甲酸(FDCA)是一种重要的生物单体,有望替代对苯二甲酸来合成可降解聚酯。在过去几十年中,将生物质基5-羟甲基糠醛(HMF)高效选择性氧化为FDCA一直是一项重要但具有挑战性的工作。在本研究中,通过一种简单的方法制备了一种新型钼钒氧化物(Mo-V-O)催化剂,该催化剂在将HMF转化为FDCA方面表现出优异的催化活性。以叔丁基过氧化氢为氧化剂,在最佳条件下实现了94.5%的高FDCA选择性和98.2%的HMF转化率。采用傅里叶变换红外光谱(FT-IR)、扫描电子显微镜(SEM)、X射线衍射(XRD)和热重分析(TG)对Mo-V-O催化剂的性能进行了研究。将实验数据与一级动力学方程拟合后,得到了HMF氧化的表观活化能。通过响应面法(RSM)进行实验设计和研究,以测试反应条件对催化过程的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d74c/8967152/3425d8422d6c/fchem-10-853112-g001.jpg

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