Low-temperature methanation of fermentation gas with Ni-based catalysts in a multicomponent system

A large amount of greenhouse gases, such as carbon dioxide and methane, are released during the production process of bioethanol and biogas. Converting CO into methane is a promising way of capturing CO and generating high-value gas. At present, CO methanation technology is still in the early stage....

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Veröffentlicht in:Biotechnology for biofuels 2024-01, Vol.17 (1), p.12-12, Article 12
Hauptverfasser: Yin, Jie, Yao, Zihui, Zhao, Qizhi, Cheng, Shikun, Wang, Xuemei, Li, Zifu
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Sprache:eng
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Zusammenfassung:A large amount of greenhouse gases, such as carbon dioxide and methane, are released during the production process of bioethanol and biogas. Converting CO into methane is a promising way of capturing CO and generating high-value gas. At present, CO methanation technology is still in the early stage. It requires high temperature (300-400 ℃) and pressure (> 1 MPa), leading to high cost and energy consumption. In this study, a new catalyst, Ni-Fe/Al-Ti, was developed. Compared with the activity of the common Ni/Al O catalyst, that of the new catalyst was increased by 1/3, and its activation temperature was reduced by 100℃. The selectivity of methane was increased to 99%. In the experiment using simulated fermentation gas, the catalyst showed good catalytic activity and durability at a low temperature and atmospheric pressure. Based on the characterization of catalysts and the study of reaction mechanisms, this article innovatively proposed a Ni-Fe/Al-Ti quaternary catalytic system. Catalytic process was realized through the synergism of Al-Ti composite support and Ni-Fe promotion. The oxygen vacancies on the surface of the composite carrier and the higher activity metals and alloys promoted by Fe accelerate the capture and reduction of CO . Compared with the existing catalysts, the new Ni-Fe/Al-Ti catalyst can significantly improve the methanation efficiency and has great practical application potential.
ISSN:2731-3654
2731-3654
1754-6834
DOI:10.1186/s13068-023-02455-4