Catalytic deoxygenation of triolein to green fuel over mesoporous TiO2 aided by in situ hydrogen production

The greenhouse gases contributed by combustion of fossil fuel has urged the need for sustainable green fuel production. Deoxygenation is the most reliable process to convert bio-oil into green fuel. In this study, the deoxygenation of triolein was investigated via mesoporous TiO2 calcined at differe...

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Main Authors: Oi, L. E., Choo, Min-Yee, Lee, Hwei Voon, Taufiq-Yap, Y. H., Cheng, C. K., Juan, Joon Ching
Format: Article
Language:English
English
Published: Elsevier 2020
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Online Access:http://umpir.ump.edu.my/id/eprint/28617/1/Catalytic%20deoxygenation%20of%20triolein%20to%20green%20fuel%20over%20mesoporous_FULL.pdf
http://umpir.ump.edu.my/id/eprint/28617/2/Catalytic%20deoxygenation%20of%20triolein%20to%20green%20fuel%20over%20mesoporous%20.pdf
http://umpir.ump.edu.my/id/eprint/28617/
https://doi.org/10.1016/j.ijhydene.2019.07.172
https://doi.org/10.1016/j.ijhydene.2019.07.172
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spelling my.ump.umpir.286172022-11-03T06:20:51Z http://umpir.ump.edu.my/id/eprint/28617/ Catalytic deoxygenation of triolein to green fuel over mesoporous TiO2 aided by in situ hydrogen production Oi, L. E. Choo, Min-Yee Lee, Hwei Voon Taufiq-Yap, Y. H. Cheng, C. K. Juan, Joon Ching QD Chemistry TP Chemical technology The greenhouse gases contributed by combustion of fossil fuel has urged the need for sustainable green fuel production. Deoxygenation is the most reliable process to convert bio-oil into green fuel. In this study, the deoxygenation of triolein was investigated via mesoporous TiO2 calcined at different temperature in the absence of external H2. The high conversion of fuel-liked hydrocarbons showed the in situ H2 produced from the reaction. The mesoporous TiO2 calcined at 500 °C (M500) demonstrated the highest activity, around 76.9% conversion was achieved with 78.9% selectivity to hydrocarbon. The reaction proceed through second order kinetic with a rate constant of 0.0557 g−1trioleinh−1. The major product of the reaction were diesel range saturated and unsaturated hydrocarbon (60%) further the formation of in situ H2. It is interesting to observe that higher calcination temperature improve crystallinity and remove surface hydroxyls, meanwhile increase the acid density and medium strength acid site. The conversion of triolein increased linearly with the amount of medium strength acid sites. This result suggests that medium-strength acidity of catalyst is a critical factor in determining deoxygenation activities. In addition, the presence of mesopores allow the diffusion of triolein molecules and improve the selectivity. Hence, mesoporous TiO2 with Lewis acidity is a fascinating catalyst and hydrogen donor in high-value green fuel. Elsevier 2020-04-14 Article PeerReviewed pdf en http://umpir.ump.edu.my/id/eprint/28617/1/Catalytic%20deoxygenation%20of%20triolein%20to%20green%20fuel%20over%20mesoporous_FULL.pdf pdf en http://umpir.ump.edu.my/id/eprint/28617/2/Catalytic%20deoxygenation%20of%20triolein%20to%20green%20fuel%20over%20mesoporous%20.pdf Oi, L. E. and Choo, Min-Yee and Lee, Hwei Voon and Taufiq-Yap, Y. H. and Cheng, C. K. and Juan, Joon Ching (2020) Catalytic deoxygenation of triolein to green fuel over mesoporous TiO2 aided by in situ hydrogen production. International Journal of Hydrogen Energy, 45 (20). pp. 11605-11614. ISSN 0360-3199 https://doi.org/10.1016/j.ijhydene.2019.07.172 https://doi.org/10.1016/j.ijhydene.2019.07.172
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
English
topic QD Chemistry
TP Chemical technology
spellingShingle QD Chemistry
TP Chemical technology
Oi, L. E.
Choo, Min-Yee
Lee, Hwei Voon
Taufiq-Yap, Y. H.
Cheng, C. K.
Juan, Joon Ching
Catalytic deoxygenation of triolein to green fuel over mesoporous TiO2 aided by in situ hydrogen production
description The greenhouse gases contributed by combustion of fossil fuel has urged the need for sustainable green fuel production. Deoxygenation is the most reliable process to convert bio-oil into green fuel. In this study, the deoxygenation of triolein was investigated via mesoporous TiO2 calcined at different temperature in the absence of external H2. The high conversion of fuel-liked hydrocarbons showed the in situ H2 produced from the reaction. The mesoporous TiO2 calcined at 500 °C (M500) demonstrated the highest activity, around 76.9% conversion was achieved with 78.9% selectivity to hydrocarbon. The reaction proceed through second order kinetic with a rate constant of 0.0557 g−1trioleinh−1. The major product of the reaction were diesel range saturated and unsaturated hydrocarbon (60%) further the formation of in situ H2. It is interesting to observe that higher calcination temperature improve crystallinity and remove surface hydroxyls, meanwhile increase the acid density and medium strength acid site. The conversion of triolein increased linearly with the amount of medium strength acid sites. This result suggests that medium-strength acidity of catalyst is a critical factor in determining deoxygenation activities. In addition, the presence of mesopores allow the diffusion of triolein molecules and improve the selectivity. Hence, mesoporous TiO2 with Lewis acidity is a fascinating catalyst and hydrogen donor in high-value green fuel.
format Article
author Oi, L. E.
Choo, Min-Yee
Lee, Hwei Voon
Taufiq-Yap, Y. H.
Cheng, C. K.
Juan, Joon Ching
author_facet Oi, L. E.
Choo, Min-Yee
Lee, Hwei Voon
Taufiq-Yap, Y. H.
Cheng, C. K.
Juan, Joon Ching
author_sort Oi, L. E.
title Catalytic deoxygenation of triolein to green fuel over mesoporous TiO2 aided by in situ hydrogen production
title_short Catalytic deoxygenation of triolein to green fuel over mesoporous TiO2 aided by in situ hydrogen production
title_full Catalytic deoxygenation of triolein to green fuel over mesoporous TiO2 aided by in situ hydrogen production
title_fullStr Catalytic deoxygenation of triolein to green fuel over mesoporous TiO2 aided by in situ hydrogen production
title_full_unstemmed Catalytic deoxygenation of triolein to green fuel over mesoporous TiO2 aided by in situ hydrogen production
title_sort catalytic deoxygenation of triolein to green fuel over mesoporous tio2 aided by in situ hydrogen production
publisher Elsevier
publishDate 2020
url http://umpir.ump.edu.my/id/eprint/28617/1/Catalytic%20deoxygenation%20of%20triolein%20to%20green%20fuel%20over%20mesoporous_FULL.pdf
http://umpir.ump.edu.my/id/eprint/28617/2/Catalytic%20deoxygenation%20of%20triolein%20to%20green%20fuel%20over%20mesoporous%20.pdf
http://umpir.ump.edu.my/id/eprint/28617/
https://doi.org/10.1016/j.ijhydene.2019.07.172
https://doi.org/10.1016/j.ijhydene.2019.07.172
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