Citation: XUE Wen-Juan, ZHANG Xin-Yan, LI Peng, LIU Zhao-Tie, HAO Zheng-Ping, MA Chun-Yan. Catalytic Activities for the Complete Oxidation of Ethylene over Au-Cu/Co3O4 Catalysts[J]. Acta Physico-Chimica Sinica, ;2011, 27(07): 1730-1736. doi: 10.3866/PKU.WHXB20110719 shu

Catalytic Activities for the Complete Oxidation of Ethylene over Au-Cu/Co3O4 Catalysts

  • Received Date: 7 April 2011
    Available Online: 25 May 2011

  • A series of Au-Cu/Co3O4 catalysts with different mass fractions of Cu were synthesized by a two-step method that consists of depositing ld and copper onto a Co3O4 support, which was synthesized by coprecipitation. The effect of copper on the catalytic activity of Au-Cu/Co3O4 was evaluated for the complete oxidation of ethylene at different temperatures and the prepared catalysts were characterized by X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM), H2 temperature- programmed reduction (H2-TPR), and O2 temperature-programmed desorption (O2-TPD). The results show that Au-Cu/Co3O4 bimetal catalysts exhibit higher catalytic activities than the Au/Co3O4 catalyst. At a ld loading amount of 4% (w, mass fraction) the AuCu3/Co3O4 catalyst gives higher catalytic activity compared to catalysts AuCu/Co3O4 and Au3Cu/Co3O4. Ethylene conversion was 15.3% for AuCu3/Co3O4 even at 0 ℃ whereas at 120 ℃ the full conversion of ethylene was obtained. The results of XRD and HRTEM indicate the formation of an Au-Cu alloy in AuCu3/Co3O4. However, we have found that the majority of Cu is present in the form of Cu2O in Au3Cu/Co3O4. The interaction between Au and Cu on the surface of the catalysts decreases the particle size of the ld and, therefore, it is much easier to activate ethylene. H2-TPR and O2-TPD results show that the high reduction ability and the high intensity of surface oxygen active species contribute to the excellent catalytic activity of the AuCu3/Co3O4 catalyst.

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