Dry reforming of methane at high temperature and elevated pressure over nickel spinellized powder catalyst and pellets prepared from a metallurgical residue

颗粒 甲烷 残留物(化学) 冶金 材料科学 催化作用 二氧化碳重整 弹丸 高压 废物管理 化学 合成气 复合材料 工程类 有机化学 工程物理
作者
Muhammad Irfan Malik,Maroua Rouabah,Nicolas Abatzoglou,Inès Esma Achouri
出处
期刊:Biofuels, Bioproducts and Biorefining [Wiley]
标识
DOI:10.1002/bbb.2659
摘要

Abstract The coke deposition on catalysts is a significant problem in the dry reforming of methane at elevated pressures. Understanding and controlling the mechanisms of such deposition is essential in developing a techno‐economically viable industrial application for the production of synthesis gas and/or hydrogen. The patent‐pending nickel‐supported upgraded slag oxide (Ni‐UGSO) catalysts, in powder form, have demonstrated excellent performance and achieved equilibrium in dry reforming, steam reforming and mixed methane reforming in a gram‐scale laboratory packed bed reactor under barometric pressure. In this extended study, Ni‐UGSO pellets were prepared using the wet impregnation method. The pelletized form of said catalyst was studied under elevated pressure to imitate the industrial operating conditions in a kilogram‐scale laboratory packed bed reactor. The characterization of the fresh and used catalytic formulation produced data allowing the investigation of the physicochemical properties of catalysts and the effects of metal dispersion, reaction pressure and crystallite size, as well as the role of side reactions on the nature of the coke. The metal support nature favored the interaction between the Ni metal and spinels (UGSO), and the presence of the clay binder (kaolinite, quartz) improved the pellet morphology, provided higher Ni dispersion, maintained the crystallite size, reduced the coke formation and achieved similar or higher performance with respect to Ni‐UGSO powder despite having 85% less surface area. The Ni‐UGSO pellet showed negligible coke deposits from 1 to 6.5 atm and operated successfully for 24 h at 5.5 atm, 800°C and gas hourly space velocity 810 L/(h kg cat). This study provides new insight into the design of a more efficient and robust catalyst for methane dry reforming at elevated pressures, which is critical for potential future transfer at the industrial level.
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