The states of gold species in CeO2 supported gold catalyst for formaldehyde oxidation

To develop HCHO oxidation catalysts which work at moderate temperatures, a series of Au/CeO2 catalysts with a gold content below 0.85wt.% were prepared by co-precipitation and subsequent calcinations at 300°C. Oxidation of formaldehyde on these catalysts at temperatures close to 100°C was conducted,...

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Published inApplied catalysis. B, Environmental Vol. 79; no. 2; pp. 142 - 148
Main Authors Shen, Yuenian, Yang, Xuzhuang, Wang, Yizheng, Zhang, Yanbing, Zhu, Huaiyong, Gao, Ling, Jia, Meilin
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier B.V 28.02.2008
Elsevier
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Summary:To develop HCHO oxidation catalysts which work at moderate temperatures, a series of Au/CeO2 catalysts with a gold content below 0.85wt.% were prepared by co-precipitation and subsequent calcinations at 300°C. Oxidation of formaldehyde on these catalysts at temperatures close to 100°C was conducted, and the structures of catalysts were characterized by X-ray diffraction (XRD) and transmission electronic microscopy (TEM) techniques. Gold exists in highly dispersed crystallite clusters in these catalysts, and we did not observe any gold crystals larger than 2–3nm. In contrast, the CeO2 support is well crystallized, the fringes from (111) lattice plane of the support CeO2 are very clear in the TEM image. Gold crystals with a mean size of about 10nm formed in a sample containing 0.78wt.% of gold (0.78Au) when it was calcinated at 400°C for 2h. However, the formation of larger gold crystals causes a decrease in the catalytic activity. It appears that the highly dispersed gold catalyst provides more active sites for the HCHO oxidation. When the sample 0.78Au was calcined at 700°C for 2h, large gold particles (≥50nm) appeared and the activity for HCHO oxidation decreased further but was still better than that of ceria. XRD and XPS results show an interesting fact that some of gold was incorporated into lattice of ceria.
Bibliography:ObjectType-Article-2
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content type line 23
ISSN:0926-3373
1873-3883
DOI:10.1016/j.apcatb.2007.09.042