4.4 Article

In situ Fourier transform infrared and laser Raman spectroscopic study of the thermal decomposition of Co-Al and Ni-Al hydrotalcites

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VIBRATIONAL SPECTROSCOPY
卷 27, 期 1, 页码 75-88

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ELSEVIER SCIENCE BV
DOI: 10.1016/S0924-2031(01)00119-9

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Co; Ni; hydrotalcite; thermal decomposition; carbonate; infrared; Raman; in situ

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In situ infrared spectra and in situ laser Raman spectra of Co-Al and Ni-Al hydrotalcites (HTlcs) have revealed several novel aspects of the structure, and physico-chemical transformations upon thermal decomposition of these materials in air. The infrared spectra of the Co-Al-HTlc at room temperature show the presence of a fraction of the carbonate in a low symmetry, which was not observed for Ni-Al-HTlc. Furthermore, compared to Co-Al-HTlc, a relatively smaller ratio of carbonate over hydroxyls is present in the as-synthesized Ni-Al-HTlc, as revealed by the infrared and Raman spectra. This is in agreement with a mass spectrometric analysis of the as-synthesized materials upon thermal decomposition, and the relatively small c-parameter determined from the X-ray diffraction (XRD) pattern of the as-synthesized Ni-Al-HTlc. An extraordinary stability of interlayer water in Ni-Al-HTlc was found, which was only completely removed above 300 degreesC, a temperature of 100 degreesC higher than found for Co-Al-HTlc. Dehydroxylation of the octahedral layers and carbonate reorganization and decomposition also require higher temperatures for Ni-Al-HTlc (300-350 and >550 degreesC) than for Co-Al-HTlc (150-200 and 450-500 degreesC). Raman spectra indicate the presence of an intermediate cobalt oxide (CoOx) phase upon decomposition of Co-Al-HTlc in the temperature range of 175-250 degreesC, before formation of a solid solution of cobalt spinels (Co(Co, Al)(2)O-4) occurs. Highly dispersed NiO strongly interacting with the Al2O3 support was identified after decomposition of Ni-Al-HTlc at 550 degreesC. The spectroscopically determined transition temperatures are in excellent agreement with XRD, thermogravimetric, and mass spectrometric analyses. (C) 2001 Elsevier Science B.V. All rights reserved.

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