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Dry synthesis of alumina-supported cobalt catalyst for highly enhanced catalytic oxidation

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Abstract
Alumina-supported cobalt oxide excels as an oxidation catalyst, however, strong metal-support interactions (SMSI) of cobalt and alumina can lead to inactive phases such as cobalt aluminate. To avoid the formation of the inactive phase, it was hypothesized that reducing the number of hydroxyl group anchoring sites on the alumina would enable a higher ratio of active cobalt oxide than inactive phases. We devised a dry synthesis method combined with alumina dehydroxylation and solid-state impregnation of cobalt. Characterization results including XRD, XPS, and Raman spectroscopy confirm the formation of the desired active phase on the dehydroxylated alumina. The resultant catalysts demonstrate a surprising decrease in the cobalt content (max. tenfold from 20 wt.% to 2 wt.% of cobalt loading) for oxidations of NH3 and CO, respectively, suggesting practically useful synthesis method for highly active supported catalysts. © 2023 Elsevier B.V.
Author(s)
Byun, Sang WooShin, HyeonwooBae, Woo BinHazlett, Melanie J.Kim, Young JinLee, Seong JunKim, MinkyuKang, Sung Bong
Issued Date
2024-02
Type
Article
DOI
10.1016/j.cej.2023.148316
URI
https://scholar.gist.ac.kr/handle/local/9744
Publisher
Elsevier BV
Citation
Chemical Engineering Journal, v.481
ISSN
1385-8947
Appears in Collections:
Department of Environment and Energy Engineering > 1. Journal Articles
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