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Temperature-programmed desorption/pulse surface reaction (tpd/tpsr) studies of CH4, C2H6, C2H4, and CO over a cobalt/MWNTs catalyst
Authors:Shengfu Ji  Jian Yang  Cigang Xu  Jiaxin Wang and Jinzhen Xue
Institution:(1) State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, 15 Beisanhuan Dong Road, P.O. Box 35, Beijing 100029, China.;(2) State Key Laboratory for Oxo Synthesis and Selective Oxidation, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, 342 Tianshui Road, Lanzhou 730000, China;(3) Department of Electronics and Electrical Engineering, University of Glasgow, Glasgow G12 8LT, UK;(4) State Key Laboratory for Oxo Synthesis and Selective Oxidation, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, 342 Tianshui Road, Lanzhou 730000, China;(5) State Key Laboratory for Oxo Synthesis and Selective Oxidation, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, 342 Tianshui Road, Lanzhou 730000, China
Abstract:Summary Temperature-programmed desorption (TPD) of CH4, C2H6, C2H4, and CO and temperature-programmed pulse surface reactions (TPSR) of CH4, C2H6, C2H4, CO, and CO/H2 over a Co/MWNTs catalyst have been investigated. The TPD results indicated that CH4 and C2H6 mainly exist as physisorbed species on the Co/MWNTs catalyst surface, whilst C2H4 and CO exist as both physisorbed and chemisorbed species. The TPSR results indicated that CH4 and C2H6 do not undergo reaction between room temperature and 450oC. Pulsed C2H4 can be transformed into CH4 at 400 oC whilst pulsed CO can be transformed into CO2 at 100 or 150oC. In gaseous mixtures of CO and H2 containing excess CO, the products of pulsed reaction were CH3CHO and CH3OH. When the ratio of CO and H2 was 1:2, pulsed CO and H2 were transformed into CH3CHO, CH3OH and CH4. In H2 gas flow, pulsed CO was transformed into a mixture of CH3CHO and CH4 between 200 and 250oC and was transformed into CH4 only above 250oC.
Keywords:Co/MWNTs catalyst  hydrocarbon  TPSR  TPD
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