Effects of Ce/Zr ratio on the structure and performances of Co-Ce_(1-x)Zr_xO_2 catalysts for carbon

来源 :Journal of Natural Gas Chemistry | 被引量 : 0次 | 上传用户:tedloo
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The Co-incorporated Ce1-xZrxO2 catalysts were prepared by co-precipitation for carbon dioxide reforming of methane.The ratio of Ce to Zr was varied to optimize the performances of co-precipitated Co-Ce-Zr-Ox catalysts.The prepared catalysts were characterized by various physico-chemical characterization techniques including TPR,X-ray diffraction,N2 adsorption at low temperature,XPS and CO2-TPSR.The co-precipitated Co-Ce0.8Zr0.2O2 sample containing 16% CoO exhibited a higher catalytic activity among the five catalysts,and the activity was maintained without significant loss during the reaction for 60 h.Under the conditions of 750 ℃,0.1 MPa,36000 ml/(h gcat),and CO2/CH4 molar ratio of 1:1,the CO2 conversion over this catalyst was 75% while the CH4 conversion was 67%.The cubic Ce0.8Zr0.2O2 facilitated a higher dispersion and a higher reducibility of the cobalt component,and the apparent activation energy for Co-Ce0.8Zr0.2O2 sample was 49.1 kJ/mol in the CO2/CH4 reforming reaction.As a result,the Co-Ce0.8Zr0.2O2 sample exhibited a higher activity and stability for the reforming of CH4 with CO2. The Co-incorporated Ce1-xZrxO2 catalysts were prepared by co-precipitation for carbon dioxide reforming of methane. The ratio of Ce to Zr was varied to optimize the performances of co-precipitated Co-Ce-Zr-Ox catalysts. The prepared catalysts were characterized by various physico-chemical characterization techniques including TPR, X-ray diffraction, N2 adsorption at low temperature, XPS and CO2-TPSR. The co-precipitated Co-Ce0.8Zr0.2O2 sample containing 16% CoO exhibited a higher catalytic activity among the five catalysts, and the activity was maintained without significant loss during the reaction for 60 h. Bundes the conditions of 750 ° C, 0.1 MPa, 36000 ml / (h gcat), and CO2 / CH4 molar ratio of 1: 1, the CO2 conversion over this catalyst was 75% while the CH4 conversion was 67%. The cubic Ce0.8Zr0.2O2 facilitated a higher dispersion and a higher reducibility of the cobalt component, and the apparent activation energy for Co-Ce0.8Zr0.2O2 sample was 49.1 kJ / mol in the CO2 / CH4 reforming reaction. As ar esult, the Co-Ce0.8Zr0.2O2 sample showing a higher activity and stability for the reforming of CH4 with CO2.
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