Ceria-boosted Ni/Al2O3 catalysts for enhanced H2 production via acetic acid dry reforming
Acetic acid dry reforming (ADR) is a promising route for sustainable H2 generation. However, coke inhibition during ADR is the main challenge and not resolved by using suitable promoted catalysts. In this work, Ce promotion on 10%Ni/Al2O3 catalysts with 1-5 wt%Ce was evaluated for ADR at varied temp...
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my.utm.1089522024-12-16T00:45:28Z http://eprints.utm.my/108952/ Ceria-boosted Ni/Al2O3 catalysts for enhanced H2 production via acetic acid dry reforming Nguyen, Anh Tam Ng, Kim Hoong Kumar, Ponnusamy Senthil Pham, Thuy Phuong T. Setiabudi, Herma Dina Mohammad Yusuf, Mohammad Yusuf Pham, Le Kim Hoang Thao, Bui T. Thu Abdul Jalil, Aishah Bahari, Mahadi Al-Kahtany, Khaled Vo, Dai-Viet N. Q Science (General) Acetic acid dry reforming (ADR) is a promising route for sustainable H2 generation. However, coke inhibition during ADR is the main challenge and not resolved by using suitable promoted catalysts. In this work, Ce promotion on 10%Ni/Al2O3 catalysts with 1-5 wt%Ce was evaluated for ADR at varied temperatures of 923–998 K and stoichiometric feed in a fixed-bed rig. CeO2 addition of 1–3% enhanced metal dispersion, and surface area whilst basic CeO2 character significantly boosted the concentration and density of basic sites on catalysts. Particularly, the CO2 uptake of promoted catalysts was about 2.49–3.73 times greater than that of counterpart sample. CH3COOH and CO2 conversions were enhanced with rising Ce loading and the highest reactant conversions were observed at 3 wt%Ce. The improved adsorption of acidic CH3COOH and CO2 molecules due to increasing amount of basic sites as well as redox attributes of CeO2 promoter could be responsible for the enhancement in ADR activity and yield of H2 and CO. The mechanistic two-step pathway for coke suppression induced by CeO2 promotion was elaborated in this work. Generally, carbonaceous species formation on 3%Ce–10%Ni/Al2O3 was considerably reduced about 1.6–2.0 times. H2/CO ratio varied from 0.59 to 0.65 relying on ADR temperature over 3%Ce–10%Ni/Al2O3. These H2/CO values, two times higher than theoretical H2/CO ratio in ADR, are compatible for downstream gas-to-liquid processes to selectively yield high molecular weight olefins. Water formation rate increased from 8.67 × 10−6 to 4.71 × 10−5 molH gcat−1 s−1 with rising temperature within 923–998 K on 3%Ce–10%Ni/Al2O3. Elsevier Ltd 2024-12 Article PeerReviewed Nguyen, Anh Tam and Ng, Kim Hoong and Kumar, Ponnusamy Senthil and Pham, Thuy Phuong T. and Setiabudi, Herma Dina and Mohammad Yusuf, Mohammad Yusuf and Pham, Le Kim Hoang and Thao, Bui T. Thu and Abdul Jalil, Aishah and Bahari, Mahadi and Al-Kahtany, Khaled and Vo, Dai-Viet N. (2024) Ceria-boosted Ni/Al2O3 catalysts for enhanced H2 production via acetic acid dry reforming. Journal of the Energy Institute, 117 (NA). NA. ISSN 1743-9671 http://dx.doi.org/10.1016/j.joei.2024.101821 DOI:10.1016/j.joei.2024.101821 |
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Q Science (General) Nguyen, Anh Tam Ng, Kim Hoong Kumar, Ponnusamy Senthil Pham, Thuy Phuong T. Setiabudi, Herma Dina Mohammad Yusuf, Mohammad Yusuf Pham, Le Kim Hoang Thao, Bui T. Thu Abdul Jalil, Aishah Bahari, Mahadi Al-Kahtany, Khaled Vo, Dai-Viet N. Ceria-boosted Ni/Al2O3 catalysts for enhanced H2 production via acetic acid dry reforming |
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Acetic acid dry reforming (ADR) is a promising route for sustainable H2 generation. However, coke inhibition during ADR is the main challenge and not resolved by using suitable promoted catalysts. In this work, Ce promotion on 10%Ni/Al2O3 catalysts with 1-5 wt%Ce was evaluated for ADR at varied temperatures of 923–998 K and stoichiometric feed in a fixed-bed rig. CeO2 addition of 1–3% enhanced metal dispersion, and surface area whilst basic CeO2 character significantly boosted the concentration and density of basic sites on catalysts. Particularly, the CO2 uptake of promoted catalysts was about 2.49–3.73 times greater than that of counterpart sample. CH3COOH and CO2 conversions were enhanced with rising Ce loading and the highest reactant conversions were observed at 3 wt%Ce. The improved adsorption of acidic CH3COOH and CO2 molecules due to increasing amount of basic sites as well as redox attributes of CeO2 promoter could be responsible for the enhancement in ADR activity and yield of H2 and CO. The mechanistic two-step pathway for coke suppression induced by CeO2 promotion was elaborated in this work. Generally, carbonaceous species formation on 3%Ce–10%Ni/Al2O3 was considerably reduced about 1.6–2.0 times. H2/CO ratio varied from 0.59 to 0.65 relying on ADR temperature over 3%Ce–10%Ni/Al2O3. These H2/CO values, two times higher than theoretical H2/CO ratio in ADR, are compatible for downstream gas-to-liquid processes to selectively yield high molecular weight olefins. Water formation rate increased from 8.67 × 10−6 to 4.71 × 10−5 molH gcat−1 s−1 with rising temperature within 923–998 K on 3%Ce–10%Ni/Al2O3. |
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Article |
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Nguyen, Anh Tam Ng, Kim Hoong Kumar, Ponnusamy Senthil Pham, Thuy Phuong T. Setiabudi, Herma Dina Mohammad Yusuf, Mohammad Yusuf Pham, Le Kim Hoang Thao, Bui T. Thu Abdul Jalil, Aishah Bahari, Mahadi Al-Kahtany, Khaled Vo, Dai-Viet N. |
author_facet |
Nguyen, Anh Tam Ng, Kim Hoong Kumar, Ponnusamy Senthil Pham, Thuy Phuong T. Setiabudi, Herma Dina Mohammad Yusuf, Mohammad Yusuf Pham, Le Kim Hoang Thao, Bui T. Thu Abdul Jalil, Aishah Bahari, Mahadi Al-Kahtany, Khaled Vo, Dai-Viet N. |
author_sort |
Nguyen, Anh Tam |
title |
Ceria-boosted Ni/Al2O3 catalysts for enhanced H2 production via acetic acid dry reforming |
title_short |
Ceria-boosted Ni/Al2O3 catalysts for enhanced H2 production via acetic acid dry reforming |
title_full |
Ceria-boosted Ni/Al2O3 catalysts for enhanced H2 production via acetic acid dry reforming |
title_fullStr |
Ceria-boosted Ni/Al2O3 catalysts for enhanced H2 production via acetic acid dry reforming |
title_full_unstemmed |
Ceria-boosted Ni/Al2O3 catalysts for enhanced H2 production via acetic acid dry reforming |
title_sort |
ceria-boosted ni/al2o3 catalysts for enhanced h2 production via acetic acid dry reforming |
publisher |
Elsevier Ltd |
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2024 |
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http://eprints.utm.my/108952/ http://dx.doi.org/10.1016/j.joei.2024.101821 |
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1818834070807773184 |