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Low-temperature thermocatalytic removal of formaldehyde in air using copper manganite spinels

Authors
Hua, YongbiaoVikrant, KumarKim, Ki-HyunHeynderickx, Philippe M.Boukhvalov, Danil W.
Issue Date
Aug-2024
Publisher
Academic Press
Keywords
Formalde; hydeVolatile organic compounds; Catalytic oxidation; Copper manganite spinel
Citation
Environmental Research, v.255, pp 1 - 13
Pages
13
Indexed
SCIE
SCOPUS
Journal Title
Environmental Research
Volume
255
Start Page
1
End Page
13
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/209589
DOI
10.1016/j.envres.2024.119186
ISSN
0013-9351
1096-0953
Abstract
The removal of formaldehyde (FA) is vital for indoor air quality management in light of its carcinogenic propensity and adverse environmental impact. A series of copper manganite spinel structures (e.g., CuMn2O4) are prepared using the sol-gel combustion method and treated with reduction or oxidation pretreatment at 300 °C condition. Accordingly, CuMn2O4–O (“O” suffix for oxidation pre-treatment in air) is identified as the best performer to achieve 100% conversion (XFA) of FA (50 ppm) at 90 °C; its performance, if assessed in terms of reaction kinetic rate (r) at XFA = 10%, is 5.02E-03 mmol g−1 h−1. The FA removal performance increases systematically with decreases in flow rate, FA concentration, and relative humidity (RH) or with increases in bed mass. The reaction pathways and intermediates of FA catalytic oxidation on CuMn2O4-A are studied with density functional theory simulations, temperature-programmed characterization experiments, and in-situ diffuse reflectance infrared Fourier transform spectroscopy. The synergistic combination of large quantities of adsorbed oxygen (OA) species and oxidized metal species (e.g., Cu2+) contribute to the enhanced catalytic performance of CuMn2O4–O to oxidize FA into CO2 with the reaction intermediates of H2CO2 (DOM), HCOO−, and CO. The present study is expected to provide valuable insights into the thermocatalytic oxidation of FA over spinel CuMn2O4 materials and their catalytic performances in relation to the key process variables.
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