Hydrogen production from CO2 reforming of methane over cobalt-based catalysts

Increased concerns on anthropogenic greenhouse gas emissions have renewed interest in the CO2 (dry) reforming process as an alternative to steam reforming for synthesis gas production from natural gas. For hydrocarbon dry reforming, where the product stream H2:CO ratio is less than 3, synfuel produc...

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Main Author: Ji Siang, Tan
Format: Undergraduates Project Papers
Language:English
Published: 2015
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Online Access:http://umpir.ump.edu.my/id/eprint/11049/1/FKKSA%20-%20TAN%20JI%20SIANG%20%28CD8976%29.pdf
http://umpir.ump.edu.my/id/eprint/11049/
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spelling my.ump.umpir.110492022-01-17T08:36:19Z http://umpir.ump.edu.my/id/eprint/11049/ Hydrogen production from CO2 reforming of methane over cobalt-based catalysts Ji Siang, Tan TP Chemical technology Increased concerns on anthropogenic greenhouse gas emissions have renewed interest in the CO2 (dry) reforming process as an alternative to steam reforming for synthesis gas production from natural gas. For hydrocarbon dry reforming, where the product stream H2:CO ratio is less than 3, synfuel production is more amenable and acceptable for downstream methanol and other oxygenated synthesis. However, dry reforming is highly endothermic, and suffers from carbon-induced catalyst deactivation. This thesis therefore investigates and evaluates the performance of methane dry reforming process at different operation conditions such as reaction temperature and feed composition, and the effects of loaded metals (Mo and Ni) on alumina-supported Co-based catalyst. Runs of the methane dry reforming experiment were conducted in a computer-controlled fixebed reactor at different feed compositions and reaction temperature. Both MoO3 and NiO phases were formed during wetness co-impregnation with a mixture of deionized water and alumina support as measured in X-ray diffraction. Temperature-programmed calcination showed that the transformations from MoO3 to CoMoO4 phase and NiO to NiAl2O4 phase were a 2 step process involving the formation of an oxidation intermediate form. Calcination of co-impregnated catalysts at 500 0C for 5 h appeared to be optimal preparation condition for H2 selectivity. Al2O3 support was the best support to give the highest H2 to CO ratio. Second metal promotion did not alter reaction rate significantly. However the interaction of loaded metal oxides with the surface carbonaceous species resulted in substantially reduced carbon deposition on Co-based catalyst, with Ni providing the greatest coking resistance compared to Mo. A quantitative relationship between activation energy and feed composition of CO2:CH4 ( 1:1, 2:1 and 3:1 ) as well as reaction temperatures (923 K, 953 K and 973 K) was obtained over bimetallic 5%Ni-10%Co/Al2O3 catalyst which gave the highest value of H2/CO ratio in the methane dry reforming process. Methane dry reforming activity was stable with time-on-stream for 4 h. 2015 Undergraduates Project Papers NonPeerReviewed pdf en http://umpir.ump.edu.my/id/eprint/11049/1/FKKSA%20-%20TAN%20JI%20SIANG%20%28CD8976%29.pdf Ji Siang, Tan (2015) Hydrogen production from CO2 reforming of methane over cobalt-based catalysts. Faculty of Chemical & Natural Resources Engineering, Universiti Malaysia Pahang.
institution Universiti Malaysia Pahang
building UMP Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaysia Pahang
content_source UMP Institutional Repository
url_provider http://umpir.ump.edu.my/
language English
topic TP Chemical technology
spellingShingle TP Chemical technology
Ji Siang, Tan
Hydrogen production from CO2 reforming of methane over cobalt-based catalysts
description Increased concerns on anthropogenic greenhouse gas emissions have renewed interest in the CO2 (dry) reforming process as an alternative to steam reforming for synthesis gas production from natural gas. For hydrocarbon dry reforming, where the product stream H2:CO ratio is less than 3, synfuel production is more amenable and acceptable for downstream methanol and other oxygenated synthesis. However, dry reforming is highly endothermic, and suffers from carbon-induced catalyst deactivation. This thesis therefore investigates and evaluates the performance of methane dry reforming process at different operation conditions such as reaction temperature and feed composition, and the effects of loaded metals (Mo and Ni) on alumina-supported Co-based catalyst. Runs of the methane dry reforming experiment were conducted in a computer-controlled fixebed reactor at different feed compositions and reaction temperature. Both MoO3 and NiO phases were formed during wetness co-impregnation with a mixture of deionized water and alumina support as measured in X-ray diffraction. Temperature-programmed calcination showed that the transformations from MoO3 to CoMoO4 phase and NiO to NiAl2O4 phase were a 2 step process involving the formation of an oxidation intermediate form. Calcination of co-impregnated catalysts at 500 0C for 5 h appeared to be optimal preparation condition for H2 selectivity. Al2O3 support was the best support to give the highest H2 to CO ratio. Second metal promotion did not alter reaction rate significantly. However the interaction of loaded metal oxides with the surface carbonaceous species resulted in substantially reduced carbon deposition on Co-based catalyst, with Ni providing the greatest coking resistance compared to Mo. A quantitative relationship between activation energy and feed composition of CO2:CH4 ( 1:1, 2:1 and 3:1 ) as well as reaction temperatures (923 K, 953 K and 973 K) was obtained over bimetallic 5%Ni-10%Co/Al2O3 catalyst which gave the highest value of H2/CO ratio in the methane dry reforming process. Methane dry reforming activity was stable with time-on-stream for 4 h.
format Undergraduates Project Papers
author Ji Siang, Tan
author_facet Ji Siang, Tan
author_sort Ji Siang, Tan
title Hydrogen production from CO2 reforming of methane over cobalt-based catalysts
title_short Hydrogen production from CO2 reforming of methane over cobalt-based catalysts
title_full Hydrogen production from CO2 reforming of methane over cobalt-based catalysts
title_fullStr Hydrogen production from CO2 reforming of methane over cobalt-based catalysts
title_full_unstemmed Hydrogen production from CO2 reforming of methane over cobalt-based catalysts
title_sort hydrogen production from co2 reforming of methane over cobalt-based catalysts
publishDate 2015
url http://umpir.ump.edu.my/id/eprint/11049/1/FKKSA%20-%20TAN%20JI%20SIANG%20%28CD8976%29.pdf
http://umpir.ump.edu.my/id/eprint/11049/
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