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Strontium‐promoted Ni/ZrO<sub>2</sub>–Al<sub>2</sub>O<sub>3</sub> catalysts for dry reforming of methane

Ahmed S. Al‐Fatesh, Ahmed A. Ibrahim, Ahmed I. Osman, Ahmed E. Abasaeed, Mohammed F. Alotibi, Sadeq A. Alfatesh, David W. Rooney, Anis H. Fakeeha, Chun‐Yang Yin

2023Energy Science & Engineering11 citationsDOIOpen Access PDF

Abstract

Abstract Dry reforming of methane (DRM) is an established process that utilizes CH 4 and CO 2 to produce syngas, which is subsequently used to produce liquid fuel. Developing an optimized catalyst with favorable physicochemical properties is essential to enhance the effectiveness of the DRM process. In this study, we report novel findings on Ni/ZrO 2 + Al 2 O 3 catalyst performance promoted with strontium (Sr) for DRM reaction. The characteristics of fresh and spent catalysts were evaluated via a suite of analytical characterization techniques, including physisorption analysis, temperature‐programmed reduction, transmission electron microscopy, X‐ray diffractometry, Raman spectroscopy, temperature‐programmed desorption, temperature‐programmed oxidation, and thermogravimetric analysis before actual DRM performance analysis. The integration of Sr essentially enhanced the basicity, imparted CO 2 adsorption stability, and improved the reducibility of the catalyst. An optimal concentration of 3.0 wt% Sr promoted on the catalyst afforded the highest CH 4 and CO 2 conversions. The work presented in this contribution affords an understanding of optimum Sr loading and provides insights into the synergistic role of Sr on catalytic performances as applied to the DRM process.

Topics & Concepts

PhysisorptionCatalysisSyngasThermogravimetric analysisMethaneDesorptionCarbon dioxide reformingStrontiumTemperature-programmed reductionChemical engineeringRaman spectroscopyMaterials scienceAdsorptionChemistryInorganic chemistryAnalytical Chemistry (journal)Physical chemistryOrganic chemistryOpticsEngineeringPhysicsCatalytic Processes in Materials ScienceCatalysts for Methane ReformingCatalysis and Oxidation Reactions