Ozone-induced lean methane oxidation over cobalt ion-exchanged BEA catalyst under dry reaction conditions
- Authors
- Jin, So Min; Lee, Kwan-Young; Lee, Dae-Won
- Issue Date
- 25-8월-2022
- Publisher
- ELSEVIER SCIENCE INC
- Keywords
- Methane slip; Lean methane oxidation; Ozone; Co-BEA; Zeolite catalyst
- Citation
- JOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY, v.112, pp.296 - 306
- Indexed
- SCIE
SCOPUS
KCI
- Journal Title
- JOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY
- Volume
- 112
- Start Page
- 296
- End Page
- 306
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/143766
- DOI
- 10.1016/j.jiec.2022.05.025
- ISSN
- 1226-086X
- Abstract
- As the 'Global Methane Pledge' was launched at the UN COP26 climate conference in Glasgow, there is a growing need to develop efficient methods to remove lean methane emission or methane slip at low temperatures. In order to enhance the lean methane oxidation at temperatures lower than 200 degrees C, it can be effective to use ozone as an oxidant while applying an appropriate catalyst. In this study, we examined the activity of cobalt ion-exchanged BEA catalyst for ozone-induced lean methane oxidation under dry reaction conditions. The cobalt ion-exchanged BEA catalyst was more active than palladium and iron ion-exchanged BEA catalysts. It could initiate methane oxidation at-40 degrees C and reaches the highest methane conversion of 98% at 125 degrees C, maintaining the conversion higher than 50% in the temperatures from 55 to 185 degrees C. The most active cobalt species was the isolated mononuclear cobalt ions coordinated to BEA framework. Finally, we proposed the reaction mechanism based on the intermediate species identified by the Fourier transform infrared spectroscopy.(c) 2022 The Korean Society of Industrial and Engineering Chemistry. Published by Elsevier B.V. All rights reserved.
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