TY - JOUR Y1 - 2022/// AV - none A1 - Farooqi, A.S. A1 - Yusuf, M. A1 - Zabidi, N.A.M. A1 - Saidur, R. A1 - Shahid, M.U. A1 - Ayodele, B.V. A1 - Abdullah, B. SP - 2529 PB - John Wiley and Sons Ltd KW - Amorphous carbon; Carbon dioxide; Catalyst supports; Greenhouse gases; Hydrogenation; Magnesia; Nickel compounds; Physicochemical properties; Zirconia KW - Bi-reforming of methane; CH 4; Co-precipitation; Greenhouses gas; Methane reaction; Ni/MgO catalyst; Performance; Reforming of methane; Syngas production; ]+ catalyst KW - Coprecipitation VL - 46 TI - Hydrogen-rich syngas production from bi-reforming of greenhouse gases over zirconia modified Ni/MgO catalyst N1 - cited By 15 IS - 3 JF - International Journal of Energy Research SN - 0363907X UR - https://www.scopus.com/inward/record.uri?eid=2-s2.0-85116027489&doi=10.1002%2fer.7325&partnerID=40&md5=31b3d96480bc535d8ac4cc830b416cce EP - 2545 ID - scholars16982 N2 - Bi-reforming of methane (BRM) is gaining an increase interest due to the critical requirements to mitigate global warming and provide alternative energy resources. However, there has been a serious challenge to the scale-up of the process to commercial production due to the catalyst deactivation. In the present study, the influence of ZrO2 modifications on the activity and stability of MgO-supported Ni catalyst in the BRM reaction was investigated. The ZrO2-MgO mixed oxide support was prepared by co-precipitation method with variation in the ZrO2 composition and subsequently impregnated with Ni. The characterization of the freshly prepared Ni/MgO and Ni/MgO-ZrO2 catalysts using N2 physisorption analysis, X-Ray Diffraction (XRD), FESEM, XPS, H2-TPR, and CO2-TPD techniques revealed suitable physicochemical properties for the BRM reaction. The Ni/MgO-ZrO2 catalysts showed an improved performance in the BRM reaction in terms of activity and stability compared to the Ni/MgO at 800°C and CH4, H2O, CO2 ratio of 3:2:1, respectively. The best performance was obtained using the Ni/15ZrO2-MgO for the BRM with CO2 and CH4 conversion of 81.5 and 82.5, respectively. The characterization of the spent Ni/MgO catalyst using Raman spectroscopy, FESEM, and High Resolution Transmission Electron Microscopy (HRTEM) analysis revealed the formation of amorphous carbon that could be responsible for its fast deactivation. © 2021 John Wiley & Sons Ltd. ER -