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Effect of the preparation method on the catalytic activity and stability of Au/Fe2O3 catalysts in the low-temperature water–gas shift reaction
•Three different synthesis methods of nanosized Au-based catalysts are reported.•Gold promotes the reducibility of the Fe2O3 support.•Activity strongly depends on both Au dispersion and reducibility of the support.•The Au/Fe2O3 catalysts prepared by deposition–precipitation method are more active. T...
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Published in: | Applied catalysis. A, General General, 2014, Vol.470, p.45-55 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | •Three different synthesis methods of nanosized Au-based catalysts are reported.•Gold promotes the reducibility of the Fe2O3 support.•Activity strongly depends on both Au dispersion and reducibility of the support.•The Au/Fe2O3 catalysts prepared by deposition–precipitation method are more active.
The low temperature water–gas-shift reaction has been studied over a series of nanosized Au/Fe2O3 catalysts. The effect of the synthesis method on the catalytic activity has been analysed. A series of catalysts with different Au loadings has been prepared by different methods: deposition–precipitation (DP), liquid phase reductive deposition (LPRD) and double impregnation method (DIM). The Au/Fe2O3 catalysts prepared by DP showed the highest CO conversion. The catalysts were characterised by hydrogen temperature programmed reduction (TPR-H2), high-resolution transmission electron microscopy (HRTEM), X-ray powder diffraction and X-ray photoelectron spectroscopy. TPR-H2 analysis revealed that gold promotes the reducibility of the Fe2O3 support, which is crucial in this redox reaction. HRTEM evidences a very good dispersion of gold over the iron support, with nanoparticles in the range 2.2–3.1nm for the DP and LPRD series, and a negligible increase in the average particle size of the used samples. For the DIM series, much larger Au particles (∼6.6nm) were obtained. |
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ISSN: | 0926-860X 1873-3875 |
DOI: | 10.1016/j.apcata.2013.10.034 |