4.8 Article

In situ FTIR and XANES studies of thiophene hydrodesulfurization on Ni2P/MCM-41

期刊

JOURNAL OF CATALYSIS
卷 268, 期 2, 页码 209-222

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcat.2009.09.018

关键词

FTIR; XANES; Hydrodesulfurization; Thiophene; Nickel phosphide; Ni2P; ACT; In situ

资金

  1. US Department of Energy, Office of Basic Energy Sciences [DE-FG02-963414669]
  2. JST [16106010]
  3. [2008G129]
  4. Grants-in-Aid for Scientific Research [16106010] Funding Source: KAKEN

向作者/读者索取更多资源

The hydrodesulfurization (HDS) of thiophene was studied over Ni2P/MCM-41 by in situ Fourier transform infrared (FTIR) spectroscopy and X-ray absorption near-edge structure (XANES) measurements at atmospheric pressure and 393-723 K (120-450 degrees C). FTIR showed the presence of adsorbed molecular thiophene principally on the MCM-41 support. In the presence of hydrogen new bands in the aliphatic CH stretching region (2953, 2918, and 2876 cm(-1)) and the CH2 scissoring region (1464 cm(-1)) appeared and grew with temperature up to 553 K (280 degrees C). These were assigned to a tetrahydrothiophene surface intermediate, whose presence is consistent with the high hydrogenation activity of nickel phosphide. XANES measurements between 353 and 573 K (180-300 degrees C) also showed growth of a signal (8330.9 eV) attributed to Ni-S interactions of either the adsorbed tetrahydrothiophene or a surface phosphosulfide. Transient XANES measurements showed that the sulfur species responded dynamically at the same rate as the steady-state rate, indicating that it was associated with an intermediate in the reaction. (c) 2009 Elsevier Inc. All rights reserved.

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