Base-free aerobic oxidation of 5-hydroxymethylfurfural to 2,5-furandicarboxylic acid over a Fe single-atom catalyst†

IF 9.3 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Green Chemistry Pub Date : 2024-06-07 DOI:10.1039/D4GC01777C
Sohaib Hameed, Wengang Liu, Zhounan Yu, Jifeng Pang, Wenhao Luo and Aiqin Wang
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Abstract

2,5-Furandicarboxylic acid (FDCA) is one of the most promising biodegradable substitutes for fossil-derived terephthalic acid (PTA) and adipic acid. The production of FDCA from biomass-derived 5-hydroxymethylfurfural (HMF) is significant and has attracted great attention. However, the major challenge lies in the development of a non-precious metal-based catalyst system without employing a homogeneous base. Herein, we successfully prepared an atomically dispersed Fe–N–C/γ-Al2O3 catalyst, which affords superior catalytic performance in terms of activity and stability with a FDCA yield of 99.8% and reusability of five recycle times in the catalytic oxidation of HMF to FDCA under base-free mild conditions. Based on controlled experiments and complementary characterization studies, we found that the atomically dispersed medium-spin Fe–N5 active sites together with the surface acidic/basic sites of alumina synergistically enhanced the catalytic activity and selectivity towards FDCA under base-free conditions. Our process eliminates the employment of expensive oxidants and corrosive bases, leading to economic and green biomass transformations.

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在铁单原子催化剂上将 5-羟甲基糠醛无碱有氧氧化为 2,5-呋喃二羧酸†。
2,5-呋喃二甲酸(FDCA)是化石衍生的对苯二甲酸(PTA)和己二酸最有前途的可生物降解替代品之一。从生物质衍生的 5-hydroxymethylfurfural (HMF) 中生产 FDCA 意义重大,已引起人们的极大关注。然而,主要的挑战在于如何在不使用均相碱的情况下开发一种非贵金属基催化剂体系。在此,我们成功制备了一种原子分散的 Fe-N-C/γ-Al2O3 催化剂,在无碱温和条件下催化 HMF 氧化为 FDCA,该催化剂在活性和稳定性方面都具有优异的催化性能,FDCA 收率达 99.8%,可重复使用五次。基于对照实验和补充性表征研究,我们发现原子分散的中旋 Fe-N5 活性位点与氧化铝的表面酸碱位点协同增强了无碱条件下对 FDCA 的催化活性和选择性。我们的工艺无需使用昂贵的氧化剂和腐蚀性碱,从而实现了经济、绿色的生物质转化。
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来源期刊
Green Chemistry
Green Chemistry 化学-化学综合
CiteScore
16.10
自引率
7.10%
发文量
677
审稿时长
1.4 months
期刊介绍: Green Chemistry is a journal that provides a unique forum for the publication of innovative research on the development of alternative green and sustainable technologies. The scope of Green Chemistry is based on the definition proposed by Anastas and Warner (Green Chemistry: Theory and Practice, P T Anastas and J C Warner, Oxford University Press, Oxford, 1998), which defines green chemistry as the utilisation of a set of principles that reduces or eliminates the use or generation of hazardous substances in the design, manufacture and application of chemical products. Green Chemistry aims to reduce the environmental impact of the chemical enterprise by developing a technology base that is inherently non-toxic to living things and the environment. The journal welcomes submissions on all aspects of research relating to this endeavor and publishes original and significant cutting-edge research that is likely to be of wide general appeal. For a work to be published, it must present a significant advance in green chemistry, including a comparison with existing methods and a demonstration of advantages over those methods.
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