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MnOx-based materials have attracted significant attention for ozone decomposition due to their excellent catalytic activity. However, improving their stability and water resistance under humid conditions remains a major challenge. In this work, a K-doped ε-MnO catalyst was synthesized in situ using ozone as an oxidant. The resulting catalyst exhibited outstanding ozone decomposition performance under both low temperature (0 °C) and high humidity conditions. Ozone treatment contributed to the formation of a more complete crystal structure and a higher concentration of oxygen vacancies. K doping further increased the specific surface area (174.1 m/g), reduced the grain size, and enhanced the catalyst's redox properties and surface reactive oxygen species content. Post-reaction XPS, FTIR, and Raman analyses revealed that no accumulation of O species was detected on the surface under these conditions. This absence of peroxide intermediates is believed to contribute to the catalyst's excellent stability and water resistance. This study provides new insights into the design of highly efficient and durable ozone decomposition catalysts for environmental applications.
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http://dx.doi.org/10.1016/j.envres.2025.122719 | DOI Listing |
Environ Res
August 2025
School of Resources and Environmental Engineering, Jiangsu University of Technology, Changzhou, Jiangsu, 213001, PR China.
MnOx-based materials have attracted significant attention for ozone decomposition due to their excellent catalytic activity. However, improving their stability and water resistance under humid conditions remains a major challenge. In this work, a K-doped ε-MnO catalyst was synthesized in situ using ozone as an oxidant.
View Article and Find Full Text PDFEnviron Sci Technol
September 2025
Particle Engineering Laboratory, School of Chemical and Environmental Engineering, and State Key Laboratory of Bioinspired Interfacial Materials Science, College of Chemistry Chemical Engineering and Materials Science, Soochow University, Suzhou City, Jiangsu 2151213, P. R. China.
Metal oxides are promising for catalytic ozone (O) decomposition to tackle the O pollution problem. However, reported metal oxides for O decomposition are predominantly crystalline and often suffer from low active site exposure and easy deactivation. Here, fully amorphous Ce/C-doped MnO materials with tailor-made macro-mesopores and electronic properties are developed.
View Article and Find Full Text PDFJ Hazard Mater
September 2025
Department of Chemical and Biological Engineering, Institute of Chemical Process (ICP), Institute of Engineering Research, Seoul National University, Seoul 08826, Republic of Korea. Electronic address:
The transformation of ozone (O) into hydroxyl radical (OH) during the ozonation was evaluated in the presence of granular activated carbon (GAC) and biofilm-covered granular activated carbon (BGAC). While both GAC and BGAC accelerated O decomposition, the manner in which they generated OH was different. GAC catalyzed the conversion of O into OH, with increasing hydroxyl radical exposure (∫[OH]dt) by 24 -72 % depending on the GAC dose.
View Article and Find Full Text PDFEnviron Health
August 2025
Chinese PLA Center for Disease Control and Prevention, 20 Dongda Street, Beijing, 100071, China.
Background And Objective: To provide guidance on management strategies for chronic obstructive pulmonary disease (COPD), this study systematically analyzed the burden of the disease due to ozone (O) exposure in adults aged ≥ 65 years.
Methods: Data from the Global Burden of Disease Study 2021 were used to analyse trends in the age-standardized mortality rate (ASMR) for O-related COPD in the elderly (≥ 65 years). Age-period-cohort (APC) model was used to analyse independent age, period and cohort effects.
J Hazard Mater
September 2025
School of Ecology and Environment, Anhui Normal University, Wuhu, China; Center of Cooperative Innovation for Recovery and Reconstruction of Degraded Ecosystem in Wanjiang City Belt, Wuhu, China. Electronic address:
Aromatic hydrocarbons have emerged as critical precursors in tropospheric ozone formation and secondary organic aerosol production, drawing significant scientific interest. While anthropogenic emissions and biomass burning remain well-characterized sources, biogenic origins, particularly cyanobacterial blooms, have been increasingly recognized. However, uncertainties persist regarding emission dynamics and formation pathways during algal decomposition.
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