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Combined in situ QXAFS and FTIR analysis of a Ni phosphide catalyst under hydrodesulfurization conditions

机译:加氢脱硫条件下磷化镍催化剂的原位QXAFS和FTIR组合分析

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Supported Ni _2P 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 Ni _2P/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.
机译:负载的Ni _2P催化剂对石油原料的加氢脱硫(HDS)具有活性,并引起了广泛的关注。为了找出活性催化剂的结构并深入了解噻吩HDS在Ni _2P / MCM-41上的反应机理,我们进行了原位X射线吸收精细结构的同时时间分辨(STR)研究(XAFS)光谱和傅里叶变换红外(FTIR)光谱以及时间分辨的产物分析。在513 K处,在形成磷硫镍相(NiPS)之后,通过FTIR观察到了吸附的四氢噻吩(THT)。 HDS产物的检测与THT形成相吻合。所有这些实验数据表明,NiPS充当活性相,并确定THT是HDS反应的反应中间体。 STR研究证明是精确研究反应中间体和催化反应路径的有力工具。

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