{"title":"Boosting the catalytic performance of MnOx in acetone oxidation by weakening the MnO bond strength","authors":"Rui Han, Mingke Peng, Xueqian Wu, Caihong Pang, Yanfei Zheng, Caixia Liu, Qingling Liu","doi":"10.1016/j.seppur.2024.130540","DOIUrl":null,"url":null,"abstract":"Manganese oxides (MnO<sub>x</sub>) exhibit considerable potential in the catalytic degradation of volatile organic compounds (VOCs) due to their excellent catalytic activity, superior stability and economic cost. In this work, a two-step calcination strategy was developed to prepare MnO<sub>x</sub>/CeO<sub>2</sub> catalysts with low Mn<img alt=\"single bond\" src=\"https://sdfestaticassets-us-east-1.sciencedirectassets.com/shared-assets/55/entities/sbnd.gif\" style=\"vertical-align:middle\"/>O bond strengths and highly active lattice oxygens. The obtained Mn<sub>4</sub>Ce<sub>1</sub>-NA after the optimization has a smaller grain size, enhanced specific surface area and weakened Mn<img alt=\"single bond\" src=\"https://sdfestaticassets-us-east-1.sciencedirectassets.com/shared-assets/55/entities/sbnd.gif\" style=\"vertical-align:middle\"/>O bonds, which is attributed to the in situ restriction of the manganese oxides by the two-step calcination. Moreover, the entrance of Ce into the MnO<sub>x</sub> lattice further weakened the Mn<img alt=\"single bond\" src=\"https://sdfestaticassets-us-east-1.sciencedirectassets.com/shared-assets/55/entities/sbnd.gif\" style=\"vertical-align:middle\"/>O bonds, leading to superior low-temperature reducibility and lattice oxygen activity, which effectively promoted the catalytic activity of the catalysts. The optimal samples displayed outstanding acetone degradation performance, capable of completing 90 % acetone conversion at 172 °C. The catalyst also exhibits excellent stability, with the conversion of acetone maintained at around 95 % for 64 h. This work contributes to a deeper understanding of reactive oxygen species in the catalytic oxidation of VOCs, while providing a new strategy for the rational design of efficient catalysts for the oxidation of VOCs.","PeriodicalId":427,"journal":{"name":"Separation and Purification Technology","volume":"163 1","pages":""},"PeriodicalIF":8.1000,"publicationDate":"2024-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Separation and Purification Technology","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1016/j.seppur.2024.130540","RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Manganese oxides (MnOx) exhibit considerable potential in the catalytic degradation of volatile organic compounds (VOCs) due to their excellent catalytic activity, superior stability and economic cost. In this work, a two-step calcination strategy was developed to prepare MnOx/CeO2 catalysts with low MnO bond strengths and highly active lattice oxygens. The obtained Mn4Ce1-NA after the optimization has a smaller grain size, enhanced specific surface area and weakened MnO bonds, which is attributed to the in situ restriction of the manganese oxides by the two-step calcination. Moreover, the entrance of Ce into the MnOx lattice further weakened the MnO bonds, leading to superior low-temperature reducibility and lattice oxygen activity, which effectively promoted the catalytic activity of the catalysts. The optimal samples displayed outstanding acetone degradation performance, capable of completing 90 % acetone conversion at 172 °C. The catalyst also exhibits excellent stability, with the conversion of acetone maintained at around 95 % for 64 h. This work contributes to a deeper understanding of reactive oxygen species in the catalytic oxidation of VOCs, while providing a new strategy for the rational design of efficient catalysts for the oxidation of VOCs.
期刊介绍:
Separation and Purification Technology is a premier journal committed to sharing innovative methods for separation and purification in chemical and environmental engineering, encompassing both homogeneous solutions and heterogeneous mixtures. Our scope includes the separation and/or purification of liquids, vapors, and gases, as well as carbon capture and separation techniques. However, it's important to note that methods solely intended for analytical purposes are not within the scope of the journal. Additionally, disciplines such as soil science, polymer science, and metallurgy fall outside the purview of Separation and Purification Technology. Join us in advancing the field of separation and purification methods for sustainable solutions in chemical and environmental engineering.