High Active Co/Mg1-xCex3+O Catalyst: Effects of Metal-Support Promoter Interactions on CO2 Reforming of CH4 Reaction

Co/Mg1−XCe3+XO (x = 0, 0.03, 0.07, 0.15; 1 wt% cobalt each) catalysts for the dry reforming of methane (DRM) reaction were prepared using the co-precipitation method with K2CO3 as precipitant. Characterization of the catalysts was achieved by X-ray diffraction (XRD), X-ray fluorescence spectroscopy...

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Main Authors: Al-Doghachi, Faris A. Jassim (Author), Murad, Diyar M. A. (Author), Al-Niaeem, Huda S. (Author), Al-Jaberi, Salam H. H. (Author), Mohamad, Surahim (Author), Taufiq-Yap, Yun Hin (Author)
Format: EJournal Article
Published: Department of Chemical Engineering - Diponegoro University, 2021-03-31.
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LEADER 03269 am a22003013u 4500
001 BCREC_UNDIP_9969_5244
042 |a dc 
100 1 0 |a Al-Doghachi, Faris A. Jassim  |e author 
700 1 0 |a Murad, Diyar M. A.  |e author 
700 1 0 |a Al-Niaeem, Huda S.  |e author 
700 1 0 |a Al-Jaberi, Salam H. H.  |e author 
700 1 0 |a Mohamad, Surahim  |e author 
700 1 0 |a Taufiq-Yap, Yun Hin  |e author 
245 0 0 |a High Active Co/Mg1-xCex3+O Catalyst: Effects of Metal-Support Promoter Interactions on CO2 Reforming of CH4 Reaction 
260 |b Department of Chemical Engineering - Diponegoro University,   |c 2021-03-31. 
500 |a https://ejournal2.undip.ac.id/index.php/bcrec/article/view/9969 
520 |a Co/Mg1−XCe3+XO (x = 0, 0.03, 0.07, 0.15; 1 wt% cobalt each) catalysts for the dry reforming of methane (DRM) reaction were prepared using the co-precipitation method with K2CO3 as precipitant. Characterization of the catalysts was achieved by X-ray diffraction (XRD), X-ray fluorescence spectroscopy (XRF), X-ray photoelectron spectroscopy (XPS), temperature programmed reduction (H2-TPR), Brunauer-Emmett-Teller (BET), transmission electron microscopy (TEM), and thermal gravimetric analysis (TGA). The role of several reactant and catalyst concentrations, and reaction temperatures (700-900 °C) on the catalytic performance of the DRM reaction was measured in a tubular fixed-bed reactor under atmospheric pressure at various CH4/CO2 concentration ratios (1:1 to 2:1). Using X-ray diffraction, a surface area of 19.2 m2.g−1 was exhibited by the Co/Mg0.85Ce3+0.15O catalyst and MgO phase (average crystallite size of 61.4 nm) was detected on the surface of the catalyst. H2 temperature programmed reaction revealed a reduction of CoO particles to metallic Co0 phase. The catalytic stability of the Co/Mg0.85Ce3+0.15O catalyst was achieved for 200 h on-stream at 900 °C for the 1:1 CH4:CO2 ratio with an H2/CO ratio of 1.0 and a CH4, CO2 conversions of 75% and 86%, respectively. In the present study, the conversion of CH4 was improved (75%-84%) when conducting the experiment at a lower flow of oxygen (1.25%). Finally, the deposition of carbon on the spent catalysts was analyzed using TEM and Temperature programmed oxidation-mass spectroscopy (TPO-MS) following 200 h under an oxygen stream. Better anti-coking activity of the reduced catalyst was observed by both, TEM, and TPO-MS analysis. Copyright © 2021 by Authors, Published by BCREC Group. This is an open access article under the CC BY-SA   License (https://creativecommons.org/licenses/by-sa/4.0).  
540 |a Copyright (c) 2021 by Authors, Published by BCREC Group 
540 |a https://creativecommons.org/licenses/by-sa/4.0 
546 |a eng 
690 |a Dry reforming of methane; MgO-Ce2O3 catalyst; Synthesis gas; H2 production 
655 7 |a info:eu-repo/semantics/article  |2 local 
655 7 |a info:eu-repo/semantics/publishedVersion  |2 local 
655 7 |2 local 
786 0 |n Bulletin of Chemical Reaction Engineering & Catalysis; 2021: BCREC Volume 16 Issue 1 Year 2021 (March 2021); 97-110 
786 0 |n 1978-2993 
787 0 |n https://ejournal2.undip.ac.id/index.php/bcrec/article/view/9969/5244 
856 4 1 |u https://ejournal2.undip.ac.id/index.php/bcrec/article/view/9969/5244  |z Get Fulltext