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Indexed by:期刊论文

Date of Publication:2014-08-01

Journal:MATERIALS RESEARCH BULLETIN

Included Journals:SCIE、EI

Volume:56

Page Number:54-64

ISSN No.:0025-5408

Key Words:Thiosalts; Spectroscopic investigation; Sulfide catalysts; Thermal decomposition

Abstract:The thermal decomposition of ammonium thiomolybdate (ATM), ammonium thiotungstate (ATT), tetramethylammonium thiomolybdate (TMATM) and tetramethylammonium thiotungstate (TMATT) are investigated as a function of temperature by using thermogravimetric analysis (TGA), temperature-programmed decomposition with mass spectroscopy (TPS-MS), in-situ Fourier transform infrared (FTIR) and Raman spectroscopies, and X-ray photoelectron spectroscopy (XPS). The results allow for correlations to be made between the changes in the bulk and surface structures of the materials, and the evolution of gas-phase decomposition products. The major difference between the ammonium and tetramethylammonium precursors is the complexity of the thermal decomposition profile, which is found to follow two steps over a wide temperature range for the former, but one step over a relatively narrow range for the latter materials. Raman and FTIR spectra reveal the decomposition of the ammonium and tetramethylammonium groups, along with the decomposition of the initial sulfide structures to metal disulfides. For both sets of precursors, XPS results show that the surface of the resulting materials at various temperatures of treatment does not track directly with the state of the bulk material. While the ATM, TMATM, and TMATT-derived material surfaces are reduced to the 4(+) state at the highest temperature, indicating disulfides, the ATT-derived materials still retained a significant amount of W6+ state consistent with the starting precursor. (C) 2014 Elsevier Ltd. All rights reserved.