4.8 Article

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

Journal

JOURNAL OF CATALYSIS
Volume 286, Issue -, Pages 165-171

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcat.2011.10.025

Keywords

Ni2P; HDS; QXAFS; FTIR; Thiophene; MCM-41; In situ; Simultaneous time-resolved study

Funding

  1. US Department of Energy, Office of Basic Energy Sciences [DE-FG02-963414669]
  2. JST [16106010, 16360405]
  3. Catalysis Research Center, Hokkaido University [10B1001, 10B2009]
  4. PF-PAC [2010G127, 2008G129, 2006G109]
  5. Grants-in-Aid for Scientific Research [16360405, 23550001] Funding Source: KAKEN

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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 RIR, 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. (C) 2011 Elsevier Inc. All rights reserved.

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