加氢脱硫
四氢噻吩
化学
催化作用
傅里叶变换红外光谱
噻吩
磷化物
镍
X射线吸收精细结构
无机化学
X射线吸收光谱法
反应机理
光谱学
红外光谱学
化学工程
核化学
吸收光谱法
有机化学
工程类
物理
量子力学
作者
Kyoko Kitamura Bando,Takahiro Wada,Takeshi Miyamoto,Kotaro Miyazaki,Satoru Takakusagi,Yuichiro Koike,Yasuhiro Inada,Masaharu Nomura,Aritomo Yamaguchi,Travis Gott,Shigeo Ted Oyama,Kiyotaka Asakura
标识
DOI:10.1016/j.jcat.2011.10.025
摘要
Abstract Supported Ni2P catalysts are active for hydrodesulfurization (HDS) of petroleum feedstocks and have attracted considerable attention. In order to find out the structure of the active catalyst and to obtain insight into the reaction mechanism of thiophene HDS over Ni2P/MCM-41, we conducted a simultaneous time-resolved (STR) study with in situ X-ray absorption fine structure (XAFS) spectroscopy and Fourier transform infrared (FTIR) spectroscopy together with time-resolved product analysis. At 513 K, adsorbed tetrahydrothiophene (THT) was observed by FTIR, following the formation of a nickel phosphosulfide phase (NiPS). Detection of the HDS products coincided with the THT formation. All these experimental data indicated that NiPS worked as the active phase and identified THT as a reaction intermediate for the HDS reaction. The STR study proved to be a powerful tool for the precise study of reaction intermediates and the catalytic reaction path.
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