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Author:

Ye, Q. (Ye, Q..) (Scholars:叶青) | Yan, L.-N. (Yan, L.-N..) | Luo, C.-W. (Luo, C.-W..) | Huo, F.-F. (Huo, F.-F..) | Cheng, S.-Y. (Cheng, S.-Y..) (Scholars:程水源) | Kang, T.-F. (Kang, T.-F..) (Scholars:康天放)

Indexed by:

Scopus PKU CSCD

Abstract:

Au/OMS-2 catalysts were prepared by pre-incorporation (QI), typical wet impregnation (IM) and deposition-precipitation (DP) methods. The influences of prepared methods and conditions on the catalytic activity of CO oxidation were studied. The samples were characterized by X-ray diffraction (XRD) and Brunaner-Emmett-Teller (BET). As compared with pre-incorporation and typical wet impregnation methods, Au/OMS-2-DP prepared from deposition-precipitation (DP) method revealed the highest activity, due to the largest surface area and the smallest Au particle size. A study was conducted on the effects of different preparation conditions (i.e., precipitating agents, pH of solution, Au loading and calcinations temperature) on the catalytic oxidation of CO over Au/OMS-2-DP. Effects of precipitating agents on catalytic activity were obvious. The best catalytic activity was shown by the Au/OMS-2-DP catalyst prepared with KOH as a precipitating agent, which could be explained in terms of the smallest Au particle size. A pH of 9 generated greater amounts of Au loading and smaller Au particles on OMS-2 than other pH value. The sample calcined at 300°C showed the highest activity, which may be due to the sample's calcined at 200°C inability to decompose completely to metallic gold while the sample calcined at 400°C had larger particles of gold deposited on the support. Au/OMS-2-DP prepared from a gold solution with KOH as a precipitating agent, pH of 9, Au loading at 5 wt%, and a calcination temperature of 300°C provides the optimum catalytic activity for CO oxidation, i.e. 100% CO conversion at 67°C.

Keyword:

Au/OMS-2; Low temperature catalytic oxidation; Preparation condition; Preparation methods

Author Community:

  • [ 1 ] [Ye, Q.]Department of Environmental Science, College of Environmental and Energy Engineering, Beijing University of Technology, Beijing 100124, China
  • [ 2 ] [Yan, L.-N.]Department of Environmental Science, College of Environmental and Energy Engineering, Beijing University of Technology, Beijing 100124, China
  • [ 3 ] [Luo, C.-W.]Department of Environmental Science, College of Environmental and Energy Engineering, Beijing University of Technology, Beijing 100124, China
  • [ 4 ] [Huo, F.-F.]Department of Environmental Science, College of Environmental and Energy Engineering, Beijing University of Technology, Beijing 100124, China
  • [ 5 ] [Cheng, S.-Y.]Department of Environmental Science, College of Environmental and Energy Engineering, Beijing University of Technology, Beijing 100124, China
  • [ 6 ] [Kang, T.-F.]Department of Environmental Science, College of Environmental and Energy Engineering, Beijing University of Technology, Beijing 100124, China

Reprint Author's Address:

  • 叶青

    [Ye, Q.]Department of Environmental Science, College of Environmental and Energy Engineering, Beijing University of Technology, Beijing 100124, China

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Source :

China Environmental Science

ISSN: 1000-6923

Year: 2012

Issue: 4

Volume: 32

Page: 609-616

Cited Count:

WoS CC Cited Count: 0

SCOPUS Cited Count:

ESI Highly Cited Papers on the List: 0 Unfold All

WanFang Cited Count:

Chinese Cited Count:

30 Days PV: 1

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