糠醛
催化作用
转移加氢
化学
氢
有机化学
无机化学
钌
作者
Debarun Banerjee,Sushant Yadav,Aloka Kumar Sahu,Jack K. Clegg,Sreedevi Upadhyayula
出处
期刊:Energy & Fuels
[American Chemical Society]
日期:2024-05-17
卷期号:38 (11): 9814-9826
被引量:1
标识
DOI:10.1021/acs.energyfuels.4c00915
摘要
Catalytic transfer hydrogenation of furfural is an environmentally friendly approach for the production of biofuels such as 2-methylfuran (2-MF). The presence of both metallic and Lewis acid sites in the catalyst is required to produce 2-MF by this process. However, the inherent unstable nature of these catalytic sites poses a significant challenge to controlling their stoichiometry. Herein, we report the preparation of a highly active and robust catalyst through the pyrolysis of a Cu-BTC metal–organic framework under controlled conditions. This catalyst exhibits outstanding performance in furfural transfer hydrogenation using isopropyl alcohol as the hydrogen donor. Under optimized conditions of 250 °C and 5 bar, we achieved 100% furfural conversion with a 77% selectivity toward 2-MF after 6 h reaction time by using Cu-BTC pyrolyzed at 310 °C as a catalyst. The observed superior activity could be attributed to the presence of both Cu(I) and Cu(0) sites in the catalyst, in combination with high acidic site concentrations. This work introduces a facile method for establishing a stable coexistence of metallic and acid sites in Cu-based catalysts, showcasing its potential for advancing sustainable biofuel production. Notably, this strategic catalyst design opens avenues for broader applications in sustainable catalysis.
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