在温和条件下,在木质素裁剪钴单原子催化剂上通过提高钴负载量定向转化 HMF 为 FDCA

IF 11.3 1区 化学 Q1 CHEMISTRY, PHYSICAL ACS Catalysis Pub Date : 2024-10-16 DOI:10.1021/acscatal.4c0441910.1021/acscatal.4c04419
Junkai Li, Guanhua Wang*, Xiaoyi Wang, Yutong Zhao, Yuze Zhao, Wenjie Sui, Dingsheng Wang and Chuanling Si*, 
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引用次数: 0

摘要

单原子催化剂(SAC)具有原子利用率高、选择性/稳定性可靠等特点,因此在生物质衍生平台化学转化领域备受关注。本文采用分馏木质素衍生的 Co 单原子催化剂(Co-N/F1),在温和条件下将 5-hydroxymethylfurfural (HMF)(一种典型的葡萄糖衍生平台化学品)定向氧化为 2,5-呋喃二甲酸 (FDCA)。利用具有高官能团含量(如 Ph-OH 和 COOH)的低分子量木质素馏分(F1)获得了钴含量更高的 Co-N/F1,并证明制备的催化剂呈 Co-N4 构型。由于高温下 HMF 不会生成有色副产物,Co-N/F1 在温和条件下(65 °C,3 bar O2)实现了 HMF 向 FDCA 的高选择性转化(100% HMF 转化率,99.20% FDCA 收率),其性能优于大多数已报道的非贵金属支撑催化剂。密度泛函理论计算表明,Co-N/F1 中的 Co-N4 位点有助于 HMF 及其醛类中间体上 α-C 位点的脱氢反应,从而显著提高了催化效率。此外,由于 Co-N4 结构的耐碱性,Co-N/F1 表现出稳定的可重复使用性。我们的研究详细介绍了利用木质素分馏策略合成 Co-SACs 的方法,并进一步证明了其在温和条件下定向转化生物质衍生平台化学品的良好可行性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Oriented Conversion of HMF to FDCA under Mild Conditions over Lignin-Tailored Co Single-Atom Catalyst with Enhanced Co Loadings

Heterogeneous catalysis over single-atom catalysts (SACs) has garnered significant attention in biomass-derived platform chemical conversion owing to the high atomic utilization and reliable selectivity/stability. Herein, Co single-atom catalysts (Co–N/F1) derived from fractionated lignin were employed for the oriented oxidation of 5-hydroxymethylfurfural (HMF), a typical platform chemical derived from glucose, into 2,5-furandicarboxylicacid (FDCA) under mild conditions. The Co–N/F1 with enhanced Co content was obtained using the low-molecular-weight lignin fraction (F1) with high functional group contents (e.g., Ph–OH and COOH), and the as-prepared catalyst was demonstrated to present a Co–N4 configuration. Owing to the absence of colored byproduct formation from HMF at elevated temperatures, Co–N/F1 realized the highly selective conversion of HMF to FDCA (100% HMF conversion, 99.20% FDCA yield) under mild conditions (65 °C, 3 bar O2), which outperformed most reported non-noble metal-supported catalysts. Density functional theory calculations indicate that the Co–N4 site in Co–N/F1 facilitates the dehydrogenation of the α-C position on HMF and its aldehyde intermediates, resulting in a significantly enhanced catalytic efficiency. Furthermore, Co–N/F1 exhibited stable reusability due to the alkaline resistance of the Co–N4 structure. Our study details the insights into the synthesis of Co-SACs using a lignin fractionation strategy and further demonstrates its good feasibility for the oriented conversion of biomass-derived platform chemicals under mild conditions.

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来源期刊
ACS Catalysis
ACS Catalysis CHEMISTRY, PHYSICAL-
CiteScore
20.80
自引率
6.20%
发文量
1253
审稿时长
1.5 months
期刊介绍: ACS Catalysis is an esteemed journal that publishes original research in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. It offers broad coverage across diverse areas such as life sciences, organometallics and synthesis, photochemistry and electrochemistry, drug discovery and synthesis, materials science, environmental protection, polymer discovery and synthesis, and energy and fuels. The scope of the journal is to showcase innovative work in various aspects of catalysis. This includes new reactions and novel synthetic approaches utilizing known catalysts, the discovery or modification of new catalysts, elucidation of catalytic mechanisms through cutting-edge investigations, practical enhancements of existing processes, as well as conceptual advances in the field. Contributions to ACS Catalysis can encompass both experimental and theoretical research focused on catalytic molecules, macromolecules, and materials that exhibit catalytic turnover.
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