Catalytic reforming of biomass pyrolysis gas over Ni catalysts: alumina, spent fluid catalytic cracking catalyst and char as supports

Abstract

The potential replaceability of a Ni catalyst supported on commercial α-Al2O3 (Ni/Al2O3) by Ni on biomass-derived char (Ni/Char), and Ni on spent fluid catalytic cracking catalyst (Ni/FCC) for steam reforming of biomass pyrolysis gas was investigated (14 h at 850°C, steam/carbon ratio = 5). The catalysts reformed 60–80 % of C2-C5 hydrocarbons, producing 2.7–4.1 mg min−1 of H2. The reforming activity of Ni/Al2O3 and Ni/FCC was higher compared to Ni/Char, indicating the beneficial role of metal oxide supports. The use of Al2O3 and FCC resulted in a lower thermo-oxidative stability of coke formed on Ni/Al2O3 and Ni/FCC compared to Ni/Char. Furthermore, the deposited Ni showed higher stability towards oxidation by steam into NiO in case of Al2O3 and FCC compared to char. According to reforming activity, H2 production rate, coking, and Ni oxidation of the catalysts, FCC has better prospects as an alternative support in a reforming catalyst than char.Agency for Science, Technology and Research (A*STAR)National Research Foundation (NRF)Public Utilities Board (PUB)This research is supported by A*STAR under its RIE2025 Industry Alignment Fund- Industry Collaboration Projects (IAF-ICP) Programme (Award I2101E0006). This research is also supported by the National Research Foundation, Singapore, and PUB, Singapore’s National Water Agency under its RIE2025 Urban Solutions and Sustainability (USS) (Water) Centre of Excellence (CoE) Programme which provides funding to the Nanyang Environment & Water Research Institute (NEWRI) of the Nanyang Technological University, Singapore (NTU). Any opinions, findings and conclusions or recommendations expressed in this material are those of the author(s) and do not reflect the views of National Research Foundation, Singapore and PUB, Singapore’s National Water Agency

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Last time updated on 31/01/2025

This paper was published in DR-NTU (Digital Repository of NTU).

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