加氢脱氧
氢解
催化作用
双金属片
化学
溶剂
有机化学
无机化学
光化学
选择性
作者
Shiyou Xing,Yong Liu,Xiaochun Liu,Ming Li,Junying Fu,Pengfei Liu,Pengmei Lv,Zhongming Wang
标识
DOI:10.1016/j.apcatb.2020.118718
摘要
Abstract Solvent-free hydrodeoxygenation (HDO) of bio-lipids into renewable alkanes by non-precious Ni metal catalysts usually required harsh reaction conditions of, for example, over 360 °C. Herein, we reported a NiW bimetallic catalyst that reached a 100 % HDO efficiency over oleic acid under a mild condition of 320 °C. This was due to a catalytic synergy of Ni and oxygen vacancy (OV) site over the rate-determined step, C36 ester hydrogenolysis, in HDO. The OV site created by a partially H2 reduction of WO3 was confirmed by XPS and UV–vis characterizations. Primary density functional theory calculation demonstrated that OV had stronger adsorption over carbonyl oxygen atom in carboxyl group compared to Ni site. In this way, the activation and cleavage of Calkoxy O bond during C36 ester hydrogenolysis under mild conditions were realized. This developed NiW bimetallic catalyst highlighted a great promise for the solvent-free HDO of bio-lipids into renewable alkanes under mild conditions.
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