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Mechanistic Study of Ni/ CeO 2 ‐catalyzed CO 2 / CH 4 Reaction Using Flow and Static Methods
Author(s) -
Kang JinGyu,
Roh JoongSeok,
Kim JiYeong,
Lee SungHan,
Choi JoongGill
Publication year - 2016
Publication title -
bulletin of the korean chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.237
H-Index - 59
ISSN - 1229-5949
DOI - 10.1002/bkcs.10838
Subject(s) - catalysis , analytical chemistry (journal) , chemistry , atmospheric temperature range , methane , activation energy , torr , volumetric flow rate , photoacoustic imaging in biomedicine , reaction rate , nuclear chemistry , thermodynamics , chromatography , organic chemistry , physics , optics
Ni/ CeO 2 catalysts with different Ni loadings (5, 7, 10, 12, and 14 wt% Ni) were prepared by an impregnation method and examined for the CO 2 reforming of methane using flow and static reactors. Their catalytic activities and selectivities were measured under CO 2 / CH 4 /Ar (=5/5/40 cm 3 /min) flow at 450–800°C using a flow reactor system with an on‐line gas chromatography. At fixed temperature, the CO 2 and CH 4 conversions varied only slightly with the Ni wt%, whereas the H 2 / CO ratio increased with increasing Ni wt%. The conversions increased with temperature, reaching 98% at 800°C. The H 2 / CO ratio varied with temperature in the range of 450–800°C, from less than 1 below 550°C to close to 1 at 550–600°C and then back to less than 1 above 600°C. The apparent activation energies were determined to be 43.1 kJ /mol for the CO 2 consumption and 50.2 kJ /mol for the CH 4 consumption based on the rates measured for the reforming reaction over 5 wt% Ni/ CeO 2 catalyst at 550–750°C. Additionally, the catalytic reforming reaction at low pressure (40 Torr) was investigated by a static reactor system by using a differential photoacoustic cell, in which the rates were measured from the CO 2 photoacoustic signal data at early reaction times over the temperature range of 460–610°C. Apparent activation energies of 25.5–30.1 kJ /mol were calculated from the CO 2 disappearance rates. The CO 2 adsorption on the Ni/ CeO 2 catalyst was investigated by the CO 2 photoacoustic spectroscopy and Fourier transform infrared spectroscopy. Feasible side reactions during the catalytic CO 2 / CH 4 reaction were suggested on the basis of the kinetic and spectroscopic results.