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Combined Syngas and Hydrogen Production using Gas Switching Technology

[Image: see text] This paper focuses on the experimental demonstration of a three-stage GST (gas switching technology) process (fuel, steam/CO(2), and air stages) for syngas production from methane in the fuel stage and H(2)/CO production in the steam/CO(2) stage using a lanthanum-based oxygen carri...

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Autores principales: Ugwu, Ambrose, Zaabout, Abdelghafour, Donat, Felix, van Diest, Geert, Albertsen, Knuth, Müller, Christoph, Amini, Shahriar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8033639/
https://www.ncbi.nlm.nih.gov/pubmed/33840889
http://dx.doi.org/10.1021/acs.iecr.0c04335
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author Ugwu, Ambrose
Zaabout, Abdelghafour
Donat, Felix
van Diest, Geert
Albertsen, Knuth
Müller, Christoph
Amini, Shahriar
author_facet Ugwu, Ambrose
Zaabout, Abdelghafour
Donat, Felix
van Diest, Geert
Albertsen, Knuth
Müller, Christoph
Amini, Shahriar
author_sort Ugwu, Ambrose
collection PubMed
description [Image: see text] This paper focuses on the experimental demonstration of a three-stage GST (gas switching technology) process (fuel, steam/CO(2), and air stages) for syngas production from methane in the fuel stage and H(2)/CO production in the steam/CO(2) stage using a lanthanum-based oxygen carrier (La(0.85)Sr(0.15)Fe(0.95)Al(0.05)O(3)). Experiments were performed at temperatures between 750–950 °C and pressures up to 5 bar. The results show that the oxygen carrier exhibits high selectivity to oxidizing methane to syngas at the fuel stage with improved process performance with increasing temperature although carbon deposition could not be avoided. Co-feeding CO(2) with CH(4) at the fuel stage reduced carbon deposition significantly, thus reducing the syngas H(2)/CO molar ratio from 3.75 to 1 (at CO(2)/CH(4) ratio of 1 at 950 °C and 1 bar). The reduced carbon deposition has maximized the purity of the H(2) produced in the consecutive steam stage thus increasing the process attractiveness for the combined production of syngas and pure hydrogen. Interestingly, the cofeeding of CO(2) with CH(4) at the fuel stage showed a stable syngas production over 12 hours continuously and maintained the H(2)/CO ratio at almost unity, suggesting that the oxygen carrier was exposed to simultaneous partial oxidation of CH(4) with the lattice oxygen which was restored instantly by the incoming CO(2). Furthermore, the addition of steam to the fuel stage could tune up the H(2)/CO ratio beyond 3 without carbon deposition at H(2)O/CH(4) ratio of 1 at 950 °C and 1 bar; making the syngas from gas switching partial oxidation suitable for different downstream processes, for example, gas-to-liquid processes. The process was also demonstrated at higher pressures with over 70% fuel conversion achieved at 5 bar and 950 °C.
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spelling pubmed-80336392021-04-09 Combined Syngas and Hydrogen Production using Gas Switching Technology Ugwu, Ambrose Zaabout, Abdelghafour Donat, Felix van Diest, Geert Albertsen, Knuth Müller, Christoph Amini, Shahriar Ind Eng Chem Res [Image: see text] This paper focuses on the experimental demonstration of a three-stage GST (gas switching technology) process (fuel, steam/CO(2), and air stages) for syngas production from methane in the fuel stage and H(2)/CO production in the steam/CO(2) stage using a lanthanum-based oxygen carrier (La(0.85)Sr(0.15)Fe(0.95)Al(0.05)O(3)). Experiments were performed at temperatures between 750–950 °C and pressures up to 5 bar. The results show that the oxygen carrier exhibits high selectivity to oxidizing methane to syngas at the fuel stage with improved process performance with increasing temperature although carbon deposition could not be avoided. Co-feeding CO(2) with CH(4) at the fuel stage reduced carbon deposition significantly, thus reducing the syngas H(2)/CO molar ratio from 3.75 to 1 (at CO(2)/CH(4) ratio of 1 at 950 °C and 1 bar). The reduced carbon deposition has maximized the purity of the H(2) produced in the consecutive steam stage thus increasing the process attractiveness for the combined production of syngas and pure hydrogen. Interestingly, the cofeeding of CO(2) with CH(4) at the fuel stage showed a stable syngas production over 12 hours continuously and maintained the H(2)/CO ratio at almost unity, suggesting that the oxygen carrier was exposed to simultaneous partial oxidation of CH(4) with the lattice oxygen which was restored instantly by the incoming CO(2). Furthermore, the addition of steam to the fuel stage could tune up the H(2)/CO ratio beyond 3 without carbon deposition at H(2)O/CH(4) ratio of 1 at 950 °C and 1 bar; making the syngas from gas switching partial oxidation suitable for different downstream processes, for example, gas-to-liquid processes. The process was also demonstrated at higher pressures with over 70% fuel conversion achieved at 5 bar and 950 °C. American Chemical Society 2021-02-28 2021-03-10 /pmc/articles/PMC8033639/ /pubmed/33840889 http://dx.doi.org/10.1021/acs.iecr.0c04335 Text en © 2021 The Authors. Published by American Chemical Society Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Ugwu, Ambrose
Zaabout, Abdelghafour
Donat, Felix
van Diest, Geert
Albertsen, Knuth
Müller, Christoph
Amini, Shahriar
Combined Syngas and Hydrogen Production using Gas Switching Technology
title Combined Syngas and Hydrogen Production using Gas Switching Technology
title_full Combined Syngas and Hydrogen Production using Gas Switching Technology
title_fullStr Combined Syngas and Hydrogen Production using Gas Switching Technology
title_full_unstemmed Combined Syngas and Hydrogen Production using Gas Switching Technology
title_short Combined Syngas and Hydrogen Production using Gas Switching Technology
title_sort combined syngas and hydrogen production using gas switching technology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8033639/
https://www.ncbi.nlm.nih.gov/pubmed/33840889
http://dx.doi.org/10.1021/acs.iecr.0c04335
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