加氢脱硫
二苯并噻吩
磷化物
催化作用
化学
三元运算
化学吸附
加氢脱氮
无机化学
噻吩
氮化物
碳化物
化学工程
图层(电子)
有机化学
工程类
程序设计语言
计算机科学
作者
Feng Sun,Weicheng Wu,Zili Wu,Jun Guo,Zhaobin Wei,Yongxing Yang,Zongxuan Jiang,Fuping Tian,Can Li
标识
DOI:10.1016/j.jcat.2004.09.002
摘要
Silica-supported binary and ternary phosphides, MoP/SiO2, Ni2P/SiO2, and NiMoP/SiO2 have been prepared and characterized by X-ray diffraction (XRD), BET surface area, CO chemisorption, transmission electron microscopy (TEM), and infrared spectroscopy (IR). The hydrodesulfurization (HDS) activities of dibenzothiophene (DBT) were measured and compared at 593 K and 3.0 MPa for MoP/SiO2, Ni2P/SiO2, and NiMoP/SiO2 catalysts with different Mo and Ni loadings. The activities of the phosphides follow the order Ni2P/SiO2 > NiMoP/SiO2 > MoP/SiO2. The Ni sites in the NiMoP/SiO2 catalysts play a major role in the conversion of DBT, and the activity of the catalysts increases with increasing Ni content. This is different from sulfides, nitrides, and carbides, as no synergetic effect is observed between the phosphided Ni and the Mo atoms. The surface of these phosphide catalysts is partially sulfided forming a surface phosphosulfide phase, while the bulk structure of the phosphides is maintained in the HDS reactions.
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