4.6 Article

Oxidative coupling of methane to C2 hydrocarbons on the Mg-Ti mixed oxide-supported catalysts at the lower reaction temperature: Role of surface oxygen atoms

Journal

APPLIED CATALYSIS A-GENERAL
Volume 464, Issue -, Pages 68-77

Publisher

ELSEVIER
DOI: 10.1016/j.apcata.2013.05.020

Keywords

Oxidative coupling of methane; Mg-Ti mixed oxide; Catalyst; Surface lattice oxygen

Funding

  1. Korea Institute of Science and Technology (KIST)
  2. Advanced Track of Green Production Processing for Reducing Greenhouse Gas Emission of the KETEP
  3. Ministry of Knowledge Economy [20114010203140]
  4. Korea Evaluation Institute of Industrial Technology (KEIT) [20114010203140] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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The oxidative coupling of methane (OCM) couples methane molecules, which are the major components of natural gas, to form ethane and ethylene in order to produce fuels and chemicals. Because of the high reaction temperature (700-900 degrees C) to obtain high yields of desirable products, the OCM process has been difficult to commercialize. We have developed a less energy-intensive OCM process that exhibits higher activity at a lower reaction temperature using Mg-Ti mixed oxide-supported Na/W/Mn catalysts. The catalyst consisting of Mg/(Mg + Ti) = 0.5 (mol/mol) exhibited the highest C-2 hydrocarbons yields (i.e., 18.1% at 825 degrees C and 16.5% at 775 degrees C) among the mixed oxide-supported catalysts, which were higher than those of the conventional SiO2-supported catalyst particularly at a low temperature of 775 degrees C (12.8%). Based on catalyst characterization by transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), UV-vis spectroscopy (UV-vis), O-2-temperature programmed desorption (O-2-TPD), and CO2-temperature programmed desorption (CO2-TPD), the improved catalytic activity of the mixed oxide-supported catalysts was attributed to more active surface lattice O atoms. (C) 2013 Elsevier B.V. All rights reserved.

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