4.7 Article

Catalytically efficient Co-CoOx-Al2O3 interface for mild temperature fatty alcohol production via fatty acid transfer hydrogenation

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FUEL
卷 345, 期 -, 页码 -

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ELSEVIER SCI LTD
DOI: 10.1016/j.fuel.2023.128136

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Fatty alcohols; Transfer hydrogenation; Co-Al hydrotalcite; Synergy catalysis

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In this study, two-dimensional Co-Al hydrotalcite catalysts were successfully fabricated for the conversion of biomass to value-added chemicals under mild conditions. The optimized CoAl-LDO600 catalyst achieved a high yield (94.2%) of octadecanol from oleic acid using iso-propanol as hydrogen donor at 200 degrees C. This catalyst exhibited excellent magnetic separability, stability, and versatility for various fatty acids with alcohol yields ranging from 89.1% to 96.7%.
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 iso-propanol (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 degrees 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 cat-alytic system for biomass-related hydrogenation reactions without any external hydrogen supply.

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