Development of highly stable Ni-doped zeolitic imidazole framework (ZIF-67) based catalyst for CO2 methanation reaction

The conversion of CO2 into synthetic natural gas via methanation reaction has been gaining more attention. The development of active and stable catalysts at relatively low reaction temperatures is a critical issue to be addressed. Highly porous metal-organic framework (MOF) material, ZIF-67 doped wi...

Full description

Saved in:
Bibliographic Details
Main Authors: Aldoghachi, Ali, Yun Hin, Taufiq-Yap, Saiman, Mohd Izham, Lee, Hwei Voon, Zheng, Alvin Lim Teik, Seenivasagam, Sivasangar
Format: Article
Published: Elsevier Ltd 2024
Subjects:
Online Access:http://eprints.um.edu.my/44844/
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Universiti Malaya
id my.um.eprints.44844
record_format eprints
spelling my.um.eprints.448442024-07-01T04:47:20Z http://eprints.um.edu.my/44844/ Development of highly stable Ni-doped zeolitic imidazole framework (ZIF-67) based catalyst for CO2 methanation reaction Aldoghachi, Ali Yun Hin, Taufiq-Yap Saiman, Mohd Izham Lee, Hwei Voon Zheng, Alvin Lim Teik Seenivasagam, Sivasangar QD Chemistry The conversion of CO2 into synthetic natural gas via methanation reaction has been gaining more attention. The development of active and stable catalysts at relatively low reaction temperatures is a critical issue to be addressed. Highly porous metal-organic framework (MOF) material, ZIF-67 doped with 1–12 wt of nickel, was prepared via the wet-impregnation method. The catalytic test was started with in situ reductions of 0.05 g of catalyst. The reaction was performed at the temperature range of 200–400 °C, with a flow rate of 108,000 mL g−1 h−1 using a feed gas mixture (CO2:H2:N2) in a 1:4:5 ratio. Physicochemical characterisation showed that a highly porous and uniformly dispersed Ni-added ZIF-67-based catalyst was obtained and exhibited excellent catalytic activity in CO2 conversion. Preliminary catalytic testing showed that the 8 wt ZIF-67 catalyst was very active in methanation reactions, with CO2 conversion of ∼56 and CH4 selectivity of ∼96 at 300 °C. Furthermore, the catalyst was very stable and maintained high catalytic activity (conversion ∼53 , selectivity ∼94 ) without any sign of deactivation for 500 h of methanation reaction. Hence, the MOF-based Ni/ZIF-67 catalyst showed excellent potential to be explored as an effective methanation catalyst, and further investigation of the reaction parameters could lead to exceptional catalytic performance. © 2024 Hydrogen Energy Publications LLC Elsevier Ltd 2024 Article PeerReviewed Aldoghachi, Ali and Yun Hin, Taufiq-Yap and Saiman, Mohd Izham and Lee, Hwei Voon and Zheng, Alvin Lim Teik and Seenivasagam, Sivasangar (2024) Development of highly stable Ni-doped zeolitic imidazole framework (ZIF-67) based catalyst for CO2 methanation reaction. International Journal of Hydrogen Energy, 57. 1474 – 1485. ISSN 0360-3199, DOI https://doi.org/10.1016/j.ijhydene.2024.01.104 <https://doi.org/10.1016/j.ijhydene.2024.01.104>. 10.1016/j.ijhydene.2024.01.104
institution Universiti Malaya
building UM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaya
content_source UM Research Repository
url_provider http://eprints.um.edu.my/
topic QD Chemistry
spellingShingle QD Chemistry
Aldoghachi, Ali
Yun Hin, Taufiq-Yap
Saiman, Mohd Izham
Lee, Hwei Voon
Zheng, Alvin Lim Teik
Seenivasagam, Sivasangar
Development of highly stable Ni-doped zeolitic imidazole framework (ZIF-67) based catalyst for CO2 methanation reaction
description The conversion of CO2 into synthetic natural gas via methanation reaction has been gaining more attention. The development of active and stable catalysts at relatively low reaction temperatures is a critical issue to be addressed. Highly porous metal-organic framework (MOF) material, ZIF-67 doped with 1–12 wt of nickel, was prepared via the wet-impregnation method. The catalytic test was started with in situ reductions of 0.05 g of catalyst. The reaction was performed at the temperature range of 200–400 °C, with a flow rate of 108,000 mL g−1 h−1 using a feed gas mixture (CO2:H2:N2) in a 1:4:5 ratio. Physicochemical characterisation showed that a highly porous and uniformly dispersed Ni-added ZIF-67-based catalyst was obtained and exhibited excellent catalytic activity in CO2 conversion. Preliminary catalytic testing showed that the 8 wt ZIF-67 catalyst was very active in methanation reactions, with CO2 conversion of ∼56 and CH4 selectivity of ∼96 at 300 °C. Furthermore, the catalyst was very stable and maintained high catalytic activity (conversion ∼53 , selectivity ∼94 ) without any sign of deactivation for 500 h of methanation reaction. Hence, the MOF-based Ni/ZIF-67 catalyst showed excellent potential to be explored as an effective methanation catalyst, and further investigation of the reaction parameters could lead to exceptional catalytic performance. © 2024 Hydrogen Energy Publications LLC
format Article
author Aldoghachi, Ali
Yun Hin, Taufiq-Yap
Saiman, Mohd Izham
Lee, Hwei Voon
Zheng, Alvin Lim Teik
Seenivasagam, Sivasangar
author_facet Aldoghachi, Ali
Yun Hin, Taufiq-Yap
Saiman, Mohd Izham
Lee, Hwei Voon
Zheng, Alvin Lim Teik
Seenivasagam, Sivasangar
author_sort Aldoghachi, Ali
title Development of highly stable Ni-doped zeolitic imidazole framework (ZIF-67) based catalyst for CO2 methanation reaction
title_short Development of highly stable Ni-doped zeolitic imidazole framework (ZIF-67) based catalyst for CO2 methanation reaction
title_full Development of highly stable Ni-doped zeolitic imidazole framework (ZIF-67) based catalyst for CO2 methanation reaction
title_fullStr Development of highly stable Ni-doped zeolitic imidazole framework (ZIF-67) based catalyst for CO2 methanation reaction
title_full_unstemmed Development of highly stable Ni-doped zeolitic imidazole framework (ZIF-67) based catalyst for CO2 methanation reaction
title_sort development of highly stable ni-doped zeolitic imidazole framework (zif-67) based catalyst for co2 methanation reaction
publisher Elsevier Ltd
publishDate 2024
url http://eprints.um.edu.my/44844/
_version_ 1805881176343183360