催化作用
脱氢
酒
转移加氢
化学
油酸
产量(工程)
氢
脂肪酸
甲醇
化学工程
脂肪醇
制氢
生物量(生态学)
有机化学
材料科学
钌
生物化学
工程类
冶金
海洋学
地质学
作者
Yi Chen,Yongsheng Zhang,Wei Lin,Xianglin Cheng,Jianshe Wang,Xiaolong Liu,Chunbao Xu,Renfeng Nie
出处
期刊:Fuel
[Elsevier]
日期:2023-03-29
卷期号:345: 128136-128136
被引量:4
标识
DOI:10.1016/j.fuel.2023.128136
摘要
The cost-effective and environmentally friendly conversion of biomass to value-added chemicals under mild conditions is highly desirable but challenging. Herein, two-dimensional Co-Al hydrotalcite catalysts (CoAl-LDOx) were fabricated for selective catalytic transfer hydrogenation (CTH) of fatty acids to fatty alcohols with isopropanol (2-PrOH) as hydrogen donor. The structure and morphology of surface Co species can be regulated via reduction temperature. The optimal CoAl-LDO600 with high Co dispersion, modest reducibility, and rich Co-CoOx-Al2O3 interface achieved the highest octadecanol yield (94.2%) at full oleic acid conversion under 200 °C for 3 h. This catalyst was magnetically separable, highly stable and versatile for various fatty acids to achieve 89.1–96.7% alcohol yields. Controlled experiments suggest that 2-PrOH dehydrogenation was not highly dependent on Co structure, while the interfacial synergy of metallic Co and oxidized Co boosted the active hydrogen transfer, thus accelerating the overall reaction. The present work provided a boosted and stable catalytic system for biomass-related hydrogenation reactions without any external hydrogen supply.
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