Effects of Synthesis Conditions on Rare Earth Doped Iron Oxide Catalyst for Selective Catalytic Reduction of NOx with NH3

Abstract A series of rare earth-doped Fe-based oxide catalysts were prepared by co-precipitation method as Selective Catalytic Reduction (SCR) catalysts. The effects of the various rare earth species, doping amount of Sm, calcination temperature and the kind of precipitant on the deNOx activity of t...

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Main Authors: Ying Wei, Bingquan Wang, Ruiyi Ren, Rui Wang
Format: Article
Language:English
Published: Springer 2023-03-01
Series:Aerosol and Air Quality Research
Subjects:
Online Access:https://doi.org/10.4209/aaqr.220438
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author Ying Wei
Bingquan Wang
Ruiyi Ren
Rui Wang
author_facet Ying Wei
Bingquan Wang
Ruiyi Ren
Rui Wang
author_sort Ying Wei
collection DOAJ
description Abstract A series of rare earth-doped Fe-based oxide catalysts were prepared by co-precipitation method as Selective Catalytic Reduction (SCR) catalysts. The effects of the various rare earth species, doping amount of Sm, calcination temperature and the kind of precipitant on the deNOx activity of the catalysts were systematically investigated. The SO2 resistance performance was tested on the optimal catalyst. The catalysts have been characterized by X-ray diffraction (XRD), The X-ray photoelectron spectra (XPS), scanning electron microscopy (SEM) and Brunner Emmet Teller (BET). The results showed that the doping of Sm significantly improves the removal efficiency of Fe-based oxides. Sm0.075Fe0.925 catalyst showed the optimal deNOx performance and excellent resistance to SO2. At the optimal doping rate (0.075), the denitrification rate was close to 100% between 200 and 250°C. The calcination temperature has a significant effect on the catalyst. The order of catalytic activity for different calcination temperatures was 350°C ≈ 400°C > 450°C > 500°C. The Sm0.075Fe0.925 achieved 100% the de-NOx efficiencies at calcination temperatures of 350–400°C. It was also found that the deNOx performance of the catalyst prepared by using NH3·H2O as the precipitating agent was better than the catalyst prepared by using (NH3)2CO3 or NaOH as the precipitating agent. Normally a small amount of SO2 would render the catalyst inactive, but the Sm0.075Fe0.925 catalyst was basically regenerated after 0.05% SO2 removal in this resistance test.
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spelling doaj-art-438fdbdd0e374f1497fbc944e4ab93eb2025-02-09T12:21:53ZengSpringerAerosol and Air Quality Research1680-85842071-14092023-03-0123411310.4209/aaqr.220438Effects of Synthesis Conditions on Rare Earth Doped Iron Oxide Catalyst for Selective Catalytic Reduction of NOx with NH3Ying Wei0Bingquan Wang1Ruiyi Ren2Rui Wang3School of Environmental Science and Engineering, Shandong UniversitySchool of Chemistry and Molecular Engineering, Qingdao University of Science and TechnologySchool of Environmental Science and Engineering, Shandong UniversitySchool of Environmental Science and Engineering, Shandong UniversityAbstract A series of rare earth-doped Fe-based oxide catalysts were prepared by co-precipitation method as Selective Catalytic Reduction (SCR) catalysts. The effects of the various rare earth species, doping amount of Sm, calcination temperature and the kind of precipitant on the deNOx activity of the catalysts were systematically investigated. The SO2 resistance performance was tested on the optimal catalyst. The catalysts have been characterized by X-ray diffraction (XRD), The X-ray photoelectron spectra (XPS), scanning electron microscopy (SEM) and Brunner Emmet Teller (BET). The results showed that the doping of Sm significantly improves the removal efficiency of Fe-based oxides. Sm0.075Fe0.925 catalyst showed the optimal deNOx performance and excellent resistance to SO2. At the optimal doping rate (0.075), the denitrification rate was close to 100% between 200 and 250°C. The calcination temperature has a significant effect on the catalyst. The order of catalytic activity for different calcination temperatures was 350°C ≈ 400°C > 450°C > 500°C. The Sm0.075Fe0.925 achieved 100% the de-NOx efficiencies at calcination temperatures of 350–400°C. It was also found that the deNOx performance of the catalyst prepared by using NH3·H2O as the precipitating agent was better than the catalyst prepared by using (NH3)2CO3 or NaOH as the precipitating agent. Normally a small amount of SO2 would render the catalyst inactive, but the Sm0.075Fe0.925 catalyst was basically regenerated after 0.05% SO2 removal in this resistance test.https://doi.org/10.4209/aaqr.220438SCRRare earthFe oxideMesoporous structureSO2 resistance
spellingShingle Ying Wei
Bingquan Wang
Ruiyi Ren
Rui Wang
Effects of Synthesis Conditions on Rare Earth Doped Iron Oxide Catalyst for Selective Catalytic Reduction of NOx with NH3
Aerosol and Air Quality Research
SCR
Rare earth
Fe oxide
Mesoporous structure
SO2 resistance
title Effects of Synthesis Conditions on Rare Earth Doped Iron Oxide Catalyst for Selective Catalytic Reduction of NOx with NH3
title_full Effects of Synthesis Conditions on Rare Earth Doped Iron Oxide Catalyst for Selective Catalytic Reduction of NOx with NH3
title_fullStr Effects of Synthesis Conditions on Rare Earth Doped Iron Oxide Catalyst for Selective Catalytic Reduction of NOx with NH3
title_full_unstemmed Effects of Synthesis Conditions on Rare Earth Doped Iron Oxide Catalyst for Selective Catalytic Reduction of NOx with NH3
title_short Effects of Synthesis Conditions on Rare Earth Doped Iron Oxide Catalyst for Selective Catalytic Reduction of NOx with NH3
title_sort effects of synthesis conditions on rare earth doped iron oxide catalyst for selective catalytic reduction of nox with nh3
topic SCR
Rare earth
Fe oxide
Mesoporous structure
SO2 resistance
url https://doi.org/10.4209/aaqr.220438
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AT bingquanwang effectsofsynthesisconditionsonrareearthdopedironoxidecatalystforselectivecatalyticreductionofnoxwithnh3
AT ruiyiren effectsofsynthesisconditionsonrareearthdopedironoxidecatalystforselectivecatalyticreductionofnoxwithnh3
AT ruiwang effectsofsynthesisconditionsonrareearthdopedironoxidecatalystforselectivecatalyticreductionofnoxwithnh3