Steam reforming of gasified biomass tar for hydrogen production over nickel–dolomite based catalyst

Catalytic steam reforming is a promising approach to address tar formation and improve hydrogen (H2) production from biomass gasification. In this research, multi-compound tar model (phenol, toluene, naphthalene, and pyrene) was steam reformed for H2 production over various types of 10 wt.% dolomite...

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Main Author: Tan, Ru Shien
Format: Thesis
Language:English
Published: 2019
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Online Access:http://eprints.utm.my/id/eprint/87148/1/TanRuShienMSChE2019.pdf
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spelling my-utm-ep.871482020-11-30T08:56:52Z Steam reforming of gasified biomass tar for hydrogen production over nickel–dolomite based catalyst 2019 Tan, Ru Shien TP Chemical technology Catalytic steam reforming is a promising approach to address tar formation and improve hydrogen (H2) production from biomass gasification. In this research, multi-compound tar model (phenol, toluene, naphthalene, and pyrene) was steam reformed for H2 production over various types of 10 wt.% dolomite promoted 10 wt.% nickel based catalysts supported on alumina, lanthana, ceria, and zirconia. The research aims to synthesize nickel-dolomite catalyst for steam reforming of gasified biomass tar for optimum H2 production. The catalysts were characterized by thermogravimetric analysis, temperature programmed reduction, temperature programmed desorption, nitrogen physisorption, and X-ray diffraction. The results showed that the addition of dolomite promoter to the catalysts strengthened the metal-support interaction and basicity of the catalyst. Steam reforming for catalyst screening was carried out at 700 oC with steam to carbon (S/C) molar ratio of 1 and gas hourly space velocity (GHSV) of 20,453 mL/h·gcat. The Ni/dolomite/La2O3 (NiDLa) catalyst displayed mesoporous structure, high reducibility, and basicity, which lead to superior carbon conversion to gas (77.66 mol%) and H2 yield (66.20 mol%). In addition, spent NiDLa exhibited the lowest amount of filamentous coke (110 mg/gcat) formation after 5 hours of reaction compared to the other catalysts investigated. Findings on effect of reaction condition revealed that higher temperature (> 750 oC), S/C ratio that is close to the stoichiometric value (1), and moderate GHSV (12,000 – 18,000 h-1) can improve carbon conversion to gas and H2 yield. The optimum conditions were found to be 775 oC of temperature, 1.02 of S/C molar ratio, and 14,648 h-1 of GHSV which resulted in 99.94 mol% of carbon conversion to gas and 82.84 mol% of H2 yield. This finding is close to the predicted 98.96 mol% of carbon conversion to gas and 82.00 mol% of H2 yield by response surface method. 2019 Thesis http://eprints.utm.my/id/eprint/87148/ http://eprints.utm.my/id/eprint/87148/1/TanRuShienMSChE2019.pdf application/pdf en public http://dms.library.utm.my:8080/vital/access/manager/Repository/vital:131863 masters Universiti Teknologi Malaysia, Faculty of Chemical and Energy Engineering Faculty of Chemical and Energy Engineering
institution Universiti Teknologi Malaysia
collection UTM Institutional Repository
language English
topic TP Chemical technology
spellingShingle TP Chemical technology
Tan, Ru Shien
Steam reforming of gasified biomass tar for hydrogen production over nickel–dolomite based catalyst
description Catalytic steam reforming is a promising approach to address tar formation and improve hydrogen (H2) production from biomass gasification. In this research, multi-compound tar model (phenol, toluene, naphthalene, and pyrene) was steam reformed for H2 production over various types of 10 wt.% dolomite promoted 10 wt.% nickel based catalysts supported on alumina, lanthana, ceria, and zirconia. The research aims to synthesize nickel-dolomite catalyst for steam reforming of gasified biomass tar for optimum H2 production. The catalysts were characterized by thermogravimetric analysis, temperature programmed reduction, temperature programmed desorption, nitrogen physisorption, and X-ray diffraction. The results showed that the addition of dolomite promoter to the catalysts strengthened the metal-support interaction and basicity of the catalyst. Steam reforming for catalyst screening was carried out at 700 oC with steam to carbon (S/C) molar ratio of 1 and gas hourly space velocity (GHSV) of 20,453 mL/h·gcat. The Ni/dolomite/La2O3 (NiDLa) catalyst displayed mesoporous structure, high reducibility, and basicity, which lead to superior carbon conversion to gas (77.66 mol%) and H2 yield (66.20 mol%). In addition, spent NiDLa exhibited the lowest amount of filamentous coke (110 mg/gcat) formation after 5 hours of reaction compared to the other catalysts investigated. Findings on effect of reaction condition revealed that higher temperature (> 750 oC), S/C ratio that is close to the stoichiometric value (1), and moderate GHSV (12,000 – 18,000 h-1) can improve carbon conversion to gas and H2 yield. The optimum conditions were found to be 775 oC of temperature, 1.02 of S/C molar ratio, and 14,648 h-1 of GHSV which resulted in 99.94 mol% of carbon conversion to gas and 82.84 mol% of H2 yield. This finding is close to the predicted 98.96 mol% of carbon conversion to gas and 82.00 mol% of H2 yield by response surface method.
format Thesis
qualification_level Master's degree
author Tan, Ru Shien
author_facet Tan, Ru Shien
author_sort Tan, Ru Shien
title Steam reforming of gasified biomass tar for hydrogen production over nickel–dolomite based catalyst
title_short Steam reforming of gasified biomass tar for hydrogen production over nickel–dolomite based catalyst
title_full Steam reforming of gasified biomass tar for hydrogen production over nickel–dolomite based catalyst
title_fullStr Steam reforming of gasified biomass tar for hydrogen production over nickel–dolomite based catalyst
title_full_unstemmed Steam reforming of gasified biomass tar for hydrogen production over nickel–dolomite based catalyst
title_sort steam reforming of gasified biomass tar for hydrogen production over nickel–dolomite based catalyst
granting_institution Universiti Teknologi Malaysia, Faculty of Chemical and Energy Engineering
granting_department Faculty of Chemical and Energy Engineering
publishDate 2019
url http://eprints.utm.my/id/eprint/87148/1/TanRuShienMSChE2019.pdf
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