Tailoring strontium-promoted alumina-zirconia supported Ni-catalysts for enhanced CO2 utilization via dry reforming of methane: Sr loading effects and process optimization

Ahmed S. Al-Fatesh*, Maher M. Alrashed, Radwa A. El-Salamony, Mai H. Roushdy, Saba M. Alwan, Ahmed I. Osman *, Mohammed Bayazed, Anis H . Fakeeha, Ahmed A. Ibrahim, Rawesh Kumar*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

6 Citations (Scopus)
44 Downloads (Pure)

Abstract

An urgent need exists in the dry reforming of methane (DRM) community for a cost-effective and high-performance catalyst system to facilitate the industrial production of H2-rich syngas. In this study, we propose a catalyst composed of a 10 wt% ZrO2-90 wt% Al2O3 support, Ni as active sites, and a strontium promoter, which offers a promising solution. Characterization of the 5NixSr/10Zr+Al catalyst series (x = 0–4 wt%) was conducted using XRD, surface area and porosity analysis, and TPR, TPO, TPD techniques, revealing the stability of metallic Ni derived from the reduction of "moderately interacted NiO-species" under oxidizing-reducing conditions. Incorporating 3 wt% Sr in the 5Ni/10Zr+Al catalyst enhanced reducibility and promoted efficient oxidation of carbon deposits by CO2. The resulting 5Ni3Sr/10Zr+Al catalyst exhibited additional strong basic sites, leading to ∼82% H2 yield and effective inhibition of parallel H2-consuming reactions. Remarkably, the H2 yield remained stable at ∼79% over a 51-hour time on stream, while process optimization using response surface methodology yielded an optimized H2 yield of 89% under specific conditions. Experimental validation demonstrated an H2 yield of 87.4% with excellent stability for a 10-hour time on stream. Overall, the proposed catalyst system demonstrates cost-effectiveness, high performance, and stability, making it a promising candidate for DRM applications.


Original languageEnglish
Article number102578
Number of pages14
JournalJournal of CO2 Utilization
Volume75
Early online date26 Aug 2023
DOIs
Publication statusPublished - Sept 2023

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