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Selective catalytic reduction

About: Selective catalytic reduction is a research topic. Over the lifetime, 10502 publications have been published within this topic receiving 226291 citations.


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Journal ArticleDOI
B. Q. Jiang1, Zhen Wu1, Yang Liu1, Shuncheng Lee1, Wingkei Ho1 
TL;DR: In this paper, the authors carried out an in situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFT) investigation for revealing the mechanism of the SO2 effect on the SCR reaction.
Abstract: SO2 would deactivate the low-temperature SCR (selective catalytic reduction) catalysts and reduce NO removal. In this study, Fe(0.1)−Mn(0.4)/TiO2 prepared by sol−gel method was selected to carry out the in situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFT) investigation for revealing the mechanism of the SO2 effect on the SCR reaction. The DRIFT spectroscopy showed that SO2 could be adsorbed on the surface of the catalyst as the bidentate mononuclear sulfate. This type of sulfate would retard the formation of NO complex on the surface of catalyst, resulting in the decrease of NO adsorption. For NH3 adsorption, the adsorption of SO2 had little effect on the coordinated NH3, but would increase the amount of NH4+ because of the formation of new Bronsted acid sites. Therefore, besides the deposition of ammonium sulfates, the competitive adsorption between SO2 and NO on the active sites of the catalysts also contributed to the poisoning effect of SO2 on the SCR reaction. When sulfate was ...

218 citations

Journal ArticleDOI
Xiaoyan Du1, Jiang He1, Jie Zhu1, Lijuan Sun1, Songsong An1 
TL;DR: In this article, a novel approach was successfully developed for advanced catalyst Ag-deposited silica-coated Fe 3 O 4 magnetic nanoparticles, which possess a silica coated magnetic core and growth active silver nanoparticles on the outer shell using n-butylamine as the reductant of AgNO 3 in ethanol.

218 citations

Journal ArticleDOI
TL;DR: In this article, a 25-wt% Mn 0.75 Fe 0.25 Ti-DP catalyst, prepared by deposition precipitation with ammonium carbamate (AC) as a precipitating agent, showed superior low-temperature SCR (selective catalytic reduction) of NO with NH 3.
Abstract: Mn/TiO 2 and Mn–Fe/TiO 2 catalysts have been prepared by impregnation (IMP) and deposition-precipitation (DP) techniques and characterized by N 2 physisorption, XRPD, NH 3 -TPD, H 2 -TPR, XPS and TGA. 25 wt% Mn 0.75 Fe 0.25 Ti-DP catalyst, prepared by deposition precipitation with ammonium carbamate (AC) as a precipitating agent, showed superior low-temperature SCR (selective catalytic reduction) of NO with NH 3 . The superior catalytic activity of the 25 wt% Mn 0.75 Fe 0.25 Ti-DP catalyst is probably due to the presence of amorphous phases of manganese oxide, iron oxide, high surface area, high total acidity, acid strength and ease of reduction of manganese oxide and iron oxide on TiO 2 in addition to formation of an SCR active MnO x phase with high content of chemisorbed oxygen (O α ). The optimum catalyst might be used as tail-end SCR catalysts in, e.g., biomass-fired power plants and waste incineration plants.

217 citations

Journal ArticleDOI
TL;DR: In this paper, a series of transition metals were added to the low-temperature SCR catalysts based on Mn/TiO 2, and the results of X-ray diffraction (XRD), transmission electron microscopy (TEM) and electron diffraction spectra (EDS) indicated that manganese oxides and titania could be better dispersed in the catalyst and higher catalytic activity was obtained.
Abstract: To retard the sintering, a series of transition metals were added to the low-temperature SCR catalysts based on Mn/TiO 2 , and activity of these catalysts was investigated. It was found that the transition metal had significant effects on the catalytic activity. With the addition of transition metals, more NO could be removed at lower temperature. The temperature of 90% NO conversion could decrease to 361 K by using Fe(0.1)–Mn(0.4)/TiO 2 . The results of X-ray diffraction (XRD), transmission electron microscopy (TEM) and electron diffraction spectra (EDS) indicated that manganese oxides and titania could be better dispersed in the catalyst, and higher catalytic activity was obtained. From X-ray photoelectron spectrum (XPS) it could be known that solid solution was formed among the transition metal, manganese oxides and titania. With the formation of this solid solution, the Brunauer–Emmett–Teller (BET) area and pore volume increased. Furthermore, the in situ diffuse reflectance infrared transform spectroscopy (DRIFT) results showed that by using these catalysts, more NO could be oxidized to NO 2 and nitrate, and then reacted with NH 3 . Therefore, the catalytic activity was greatly improved by the addition of transition metals.

217 citations

Journal ArticleDOI
TL;DR: In this article, the adsorption and coadsorption of NO, NO 2 and NH 3 on TiO 2 anatase has been studied by Fourier transform infrared (FT-IR) spectroscopy.

216 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
2023311
2022632
2021546
2020583
2019604
2018595