Study on Denitrification Performance and Mechanism of NH 3 - SCR Catalyst for Modification of Rare Earth Tailings by Ce Combined with Mn

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The paper studied Ce–Mn modified rare earth tailings catalysts, prepared by hydrothermal synthesis, for NH3–SCR denitrification performance and mechanistic behavior across temperatures, reporting that an optimal Ce/Mn ratio of 1:1 achieved about 90% NOx conversion at 100–300°C. It found that adding Mn improved the dispersion of CeCO3F on the catalyst surface, increasing active adsorption sites, and that MnO_x interactions with Ce and Fe promoted redox processes that supported oxidation of NO to NO2. The authors report that Mn increased the abundance and stability of NO-adsorption species and Lewis acid sites, generating intermediates including Mn4+–ONO2, NH4NO3, and NH2NO. A key limitation noted in the abstract is that Mn’s strong oxidizing ability and nitrate–NH3 reaction pathways cause a rapid decrease in N2 selectivity, and the study concludes the reaction follows both Eley–Rideal and Langmuir–Hinshelwood mechanisms. This paper does not explicitly discuss endometriosis or adenomyosis; it was included in the corpus via a keyword match in the upstream search index.

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Abstract

Abstract CeMn-rare earth tailings catalysts with wide temperature window and high denitrification were prepared by hydrothermal method. The results show that the optimum ratio of Ce/Mn is 1:1, and the NOx conversion can reach 90% at the range of 100–300℃. The introduction of Mn improves the dispersion of CeCO3F on the catalyst surface, exposing more active adsorption sites. In addition, the interaction of MnOx with Ce and Fe in the rare earth tailings promotes redox, which facilitates the oxidation of NO to NO2. Meanwhile Mn also increases the abundance and stability of NO adsorption species and Lewis acid sites, forming important intermediates such as Mn4+-ONO2, NH4NO3 and NH2NO. But the strong oxidizing ability of Mn and the reaction between monodentate nitrate and adsorbed NH3 results in N2 selectivity decrease rapidly. Catalysts follow both E-R and L-H mechanism in the NH3-SCR reaction. Moreover, the excellent redox performance and Lewis acid sites improve the NH3-SCR catalytic activity together.
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Study on Denitrification Performance and Mechanism of NH 3 - SCR Catalyst for Modification of Rare Earth Tailings by Ce Combined with Mn | Research Square window.SnipcartSettings = { analytics: { enabled: false } }; (function() { var accessVector = localStorage.getItem('access_vector') || ''; window.dataLayer = window.dataLayer || []; if (accessVector) { window.dataLayer.push({ user: { profile: { profileInfo: { snid: accessVector } } } }); } })(); (function(w,d,s,l,i){w[l]=w[l]||[];w[l].push({'gtm.start':new Date().getTime(),event:'gtm.js'});var f=d.getElementsByTagName(s)[0],j=d.createElement(s),dl=l!='dataLayer'?'&l='+l:'';j.async=true;j.src='https://www.googletagmanager.com/gtm.js?id='+i+dl;f.parentNode.insertBefore(j,f);})(window,document,'script','dataLayer','GTM-K279D39R'); Browse Preprints In Review Journals COVID-19 Preprints AJE Video Bytes Research Tools Research Promotion AJE Professional Editing AJE Rubriq About Preprint Platform In Review Editorial Policies Our Team Advisory Board Help Center Sign In Submit a Preprint Cite Share Download PDF Research Article Study on Denitrification Performance and Mechanism of NH 3 - SCR Catalyst for Modification of Rare Earth Tailings by Ce Combined with Mn Xiankang Sun, Jiaming Li, Linbo Lu, Tiantian Wang, Wenfei Wu, and 1 more This is a preprint; it has not been peer reviewed by a journal. https://doi.org/ 10.21203/rs.3.rs-5163376/v1 This work is licensed under a CC BY 4.0 License Status: Published Journal Publication published 08 Jan, 2025 Read the published version in Research on Chemical Intermediates → Version 1 posted 9 You are reading this latest preprint version Abstract CeMn-rare earth tailings catalysts with wide temperature window and high denitrification were prepared by hydrothermal method. The results show that the optimum ratio of Ce/Mn is 1:1, and the NO x conversion can reach 90% at the range of 100–300℃. The introduction of Mn improves the dispersion of CeCO 3 F on the catalyst surface, exposing more active adsorption sites. In addition, the interaction of MnO x with Ce and Fe in the rare earth tailings promotes redox, which facilitates the oxidation of NO to NO 2 . Meanwhile Mn also increases the abundance and stability of NO adsorption species and Lewis acid sites, forming important intermediates such as Mn 4+ -ONO 2 , NH 4 NO 3 and NH 2 NO. But the strong oxidizing ability of Mn and the reaction between monodentate nitrate and adsorbed NH 3 results in N 2 selectivity decrease rapidly. Catalysts follow both E-R and L-H mechanism in the NH 3 -SCR reaction. Moreover, the excellent redox performance and Lewis acid sites improve the NH 3 -SCR catalytic activity together. CeO2 MnOx rare earth tailings NH3-SCR denitrification mechanism Full Text Additional Declarations No competing interests reported. Cite Share Download PDF Status: Published Journal Publication published 08 Jan, 2025 Read the published version in Research on Chemical Intermediates → Version 1 posted Editorial decision: Revision requested 23 Nov, 2024 Reviews received at journal 23 Nov, 2024 Reviewers agreed at journal 23 Nov, 2024 Reviews received at journal 29 Oct, 2024 Reviewers agreed at journal 16 Oct, 2024 Reviewers invited by journal 15 Oct, 2024 Editor assigned by journal 29 Sep, 2024 Submission checks completed at journal 29 Sep, 2024 First submitted to journal 27 Sep, 2024 You are reading this latest preprint version Research Square lets you share your work early, gain feedback from the community, and start making changes to your manuscript prior to peer review in a journal. As a division of Research Square Company, we’re committed to making research communication faster, fairer, and more useful. We do this by developing innovative software and high quality services for the global research community. Our growing team is made up of researchers and industry professionals working together to solve the most critical problems facing scientific publishing. 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