加氢脱氧
愈创木酚
水滑石
磷化物
木质素
催化作用
镍
化学
密度泛函理论
加氢脱氮
材料科学
选择性
化学工程
有机化学
无机化学
加氢脱硫
计算化学
工程类
作者
Zhichao Jia,Na Ji,Xinyong Diao,Xinxin Li,Yujun Zhao,Xuebin Lu,Qingling Liu,Caixia Liu,Guanyi Chen,Longlong Ma,Shurong Wang,Chunfeng Song,Changzhi Li
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2022-01-07
卷期号:12 (2): 1338-1356
被引量:123
标识
DOI:10.1021/acscatal.1c05495
摘要
A strategy for low-temperature synthesis of hydrotalcite-based nickel phosphide catalysts (Ni2P-Al2O3) with flower-like porous structures was proposed. The in situ reduction of red phosphorus at 500 degrees C enables Ni2P catalysts with small particle size and abundant active and acidic sites, which facilitate the activation of substrates and H-2. In the hydrodeoxygenation of guaiacol, a 100% conversion and 94.5% yield of cyclohexane were obtained over the Ni2P-Al2O3 catalyst under 5 MPa H2 at 250 degrees C for 3 h. Other lignin-derived phenolic compounds could also afford the corresponding alkanes with yields higher than 85%. Moreover, Ni2P-Al2O3 exhibited high hydrodeoxygenation activity in the deconstruction of more complex wood structures, including lignin oil and real lignin. Among the two different types of Ni sites of Ni(1) and Ni(2) in Ni2P, density functional theory (DFT) calculations showed that the Ni(2) site, highly exposed on the Ni2P-Al2O3 surface, possesses a stronger ability to break C-OH bonds during the hydrodeoxygenation of guaiacol in comparison with the Ni(1) site.
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