Dong, L, Wu, C, Ling, H et al. (3 more authors) (2017) Development of Fe-Promoted Ni–Al Catalysts for Hydrogen Production from Gasification of Wood Sawdust. Energy & Fuels, 31 (3). pp. 2118-2127. ISSN 0887-0624
Abstract
The production of renewable hydrogen-enriched gas from biomass waste is a promising technology for the development of a sustainable economy and society. Until now, there are still challenges of the technology in terms of the efficiency of hydrogen production. A catalyst is known and has been tested to enhance hydrogen production from biomass gasification, in particular, using Ni-based catalysts, which have high reactivity for hydrogen production and are cost-effective. However, developing a Ni-based catalyst with high thermal stability and resistance of coke deposition on the surface of the catalyst is still a challenging topic. In this work, Ni–Al catalysts doped with low-cost Fe metal were investigated for hydrogen-enriched syngas production from gasification of biomass using a two-stage fixed bed reactor. NiO–Fe2O3–Al2O3 catalysts with various Ni/Fe molar ratios (9:1, 8:2, 6:4, 5:5, 4:6, 2:8, and 1:9) were studied, aiming to understand the influence of Fe addition on the production of hydrogen and the catalyst stability in terms of coke deposition on the surface. X-ray diffraction, temperature-programmed reduction, and transmission electron microscopy (TEM) analysis of the fresh catalysts showed that nanoparticles (mainly NiAl2O4 spinel phase and Al2O3, ∼5 nm) were identified in the catalysts. High dispersion of metal particles was obtained using a co-precipitation method of catalyst preparation. With the increase of Fe addition, hydrogen production was reduced from around 11 to 8 mmol of H2 g–1 of biomass. However, the addition of Fe to the Ni-based catalyst significantly reduced the amount of coke deposited on the surface of the catalyst. The H2/CO molar ratio was maximized to 1.28 when the Ni/Fe molar ratio was 1:1. In addition, sintering of metal particles was not observed through the TEM analysis of the fresh and reacted catalysts.
Metadata
Item Type: | Article |
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Authors/Creators: |
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Copyright, Publisher and Additional Information: | © 2016 American Chemical Society. This document is the Accepted Manuscript version of a Published Work that appeared in final form in Energy & Fuels, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acs.energyfuels.6b02050. Uploaded in accordance with the publisher's self-archiving policy. |
Dates: |
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Institution: | The University of Leeds |
Academic Units: | The University of Leeds > Faculty of Engineering & Physical Sciences (Leeds) > School of Chemical & Process Engineering (Leeds) |
Depositing User: | Symplectic Publications |
Date Deposited: | 02 May 2017 11:18 |
Last Modified: | 25 Oct 2017 14:05 |
Published Version: | https://doi.org/10.1021/acs.energyfuels.6b02050 |
Status: | Published |
Publisher: | American Chemical Society |
Identification Number: | 10.1021/acs.energyfuels.6b02050 |
Related URLs: | |
Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:115760 |