{"title":"Effects of Synthesis Conditions on Rare Earth Doped Iron Oxide Catalyst for Selective Catalytic Reduction of NOx with NH3","authors":"Ying Wei, Bingquan Wang, Ruiyi Ren, Rui Wang","doi":"10.4209/aaqr.220438","DOIUrl":null,"url":null,"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 deNO x activity of the catalysts were systematically investigated. The SO 2 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. Sm 0.075 Fe 0.925 catalyst showed the optimal deNO x performance and excellent resistance to SO 2 . 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 Sm 0.075 Fe 0.925 achieved 100% the de-NOx efficiencies at calcination temperatures of 350–400 ° C. It was also found that the deNO x performance of the catalyst prepared by using NH 3 ·H 2 O as the precipitating agent was better than the catalyst prepared by using (NH 3 ) 2 CO 3 or NaOH as the precipitating agent. Normally a small amount of SO 2 would render the catalyst inactive, but the Sm 0.075 Fe 0.925 catalyst was basically regenerated after 0.05% SO 2 removal in this resistance test.","PeriodicalId":7402,"journal":{"name":"Aerosol and Air Quality Research","volume":null,"pages":null},"PeriodicalIF":2.5000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Aerosol and Air Quality Research","FirstCategoryId":"93","ListUrlMain":"https://doi.org/10.4209/aaqr.220438","RegionNum":4,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ENVIRONMENTAL SCIENCES","Score":null,"Total":0}
引用次数: 0
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 deNO x activity of the catalysts were systematically investigated. The SO 2 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. Sm 0.075 Fe 0.925 catalyst showed the optimal deNO x performance and excellent resistance to SO 2 . 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 Sm 0.075 Fe 0.925 achieved 100% the de-NOx efficiencies at calcination temperatures of 350–400 ° C. It was also found that the deNO x performance of the catalyst prepared by using NH 3 ·H 2 O as the precipitating agent was better than the catalyst prepared by using (NH 3 ) 2 CO 3 or NaOH as the precipitating agent. Normally a small amount of SO 2 would render the catalyst inactive, but the Sm 0.075 Fe 0.925 catalyst was basically regenerated after 0.05% SO 2 removal in this resistance test.
期刊介绍:
The international journal of Aerosol and Air Quality Research (AAQR) covers all aspects of aerosol science and technology, atmospheric science and air quality related issues. It encompasses a multi-disciplinary field, including:
- Aerosol, air quality, atmospheric chemistry and global change;
- Air toxics (hazardous air pollutants (HAPs), persistent organic pollutants (POPs)) - Sources, control, transport and fate, human exposure;
- Nanoparticle and nanotechnology;
- Sources, combustion, thermal decomposition, emission, properties, behavior, formation, transport, deposition, measurement and analysis;
- Effects on the environments;
- Air quality and human health;
- Bioaerosols;
- Indoor air quality;
- Energy and air pollution;
- Pollution control technologies;
- Invention and improvement of sampling instruments and technologies;
- Optical/radiative properties and remote sensing;
- Carbon dioxide emission, capture, storage and utilization; novel methods for the reduction of carbon dioxide emission;
- Other topics related to aerosol and air quality.