沸石咪唑盐骨架
催化作用
纳米孔
选择性
咪唑酯
杂原子
化学
热解
化学稳定性
羟甲基糠醛
化学工程
乙酰丙酸
碳纤维
无机化学
金属有机骨架
材料科学
糠醛
有机化学
吸附
复合材料
戒指(化学)
工程类
复合数
作者
Mihai Bordeiasu,Joanna Gościańska,Rafał Panek,Adela Nicolaev,Bogdan Jurcă,Vasile I. Pârvulescu,Simona M. Coman
标识
DOI:10.1002/cssc.202500678
摘要
Zeolitic imidazolate frameworks (ZIFs) have recently emerged as promising precursors for the synthesis of heteroatom‐doped nanocarbon materials. The chemical and structural features of these frameworks are influenced by the synthesis methodology, which directly affects their catalytic efficiency and stability. This study aims to investigate such frameworks by exploring a Co‐ZIF structure doped with iron. Part of the Fe x Co y ‐ZIF ( x = 0.05–0.15; y = 0.95–0.85) precursors is directly pyrolyzed to form Fe x Co y ‐NPC (NPC—nanoporous carbon), while another part is coated with a silica shell, followed by the pyrolysis of the Fe x Co y ‐ZIF@SiO 2 intermediates to produce Fe x Co y ‐NCF (NCF—nanocarbon framework). To elucidate their chemical, structural, and catalytic properties, the synthesized materials are comprehensively characterized and finally investigate in the base‐free oxidation of 5‐hydroxymethylfurfural (HMF) to 2,5‐furandicarboxylic acid (FDCA). The optimal catalyst (Fe 0.15 Co 0.85 ‐NCF) demonstrates complete conversion of HMF (>99.9%) to FDCA with a pretty high selectivity (82.4%) after 6 h reaction at 80 °C. The correlation of the catalytic features with the efficiency of the catalysts provides insight into the catalytic characteristics responsible for the highest HMF conversion and selectivity to FDCA. The stability and recyclability of the catalysts are also examined.
科研通智能强力驱动
Strongly Powered by AbleSci AI