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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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TL;DR: In this article, the combined effect of H 2 O and SO 2 on V 2 O 5 /AC was studied for selective catalytic reduction (SCR) of NO with NH 3 at lower temperatures.
Abstract: Combined effect of H 2 O and SO 2 on V 2 O 5 /AC the activity of catalyst for selective catalytic reduction (SCR) of NO with NH 3 at lower temperatures was studied. In the absence of SO 2 , H 2 O inhibits the catalytic activity, which may be attributed to competitive adsorption of H 2 O and reactants (NO and/or NH 3 ). Although SO 2 promotes the SCR activity of the V 2 O 5 /AC catalyst in the absence of H 2 O, it speeds the deactivation of the catalyst in the presence of H 2 O. The dual effect of SO 2 is attributed to the SO 4 2− formed on the catalyst surface, which stays as ammonium-sulfate salts on the catalyst surface. In the absence of H 2 O, a small amount of ammonium-sulfate salts deposits on the surface of the catalyst, which promote the SCR activity; in the presence of H 2 O, however, the deposition rate of ammonium-sulfate salts is much greater, which results in blocking of the catalyst pores and deactivates the catalyst. Decreasing V 2 O 5 loading decreases the deactivation rate of the catalyst. The catalyst can be used stably at a space velocity of 9000 h −1 and temperature of 250 °C.

148 citations

Journal ArticleDOI
TL;DR: A comparison of impacts of halogen species on the elemental mercury (Hg(0) oxidation in a real coal-derived flue gas atmosphere is presented and the effectiveness of conversion of hydrogen halogens to halogen molecules or interhalogens seemed to be attributed to their impacts on Hg( 0) oxidation.
Abstract: This paper presents a comparison of impacts of halogen species on the elemental mercury (Hg(0)) oxidation in a real coal-derived flue gas atmosphere. It is reported there is a higher percentage of Hg(0) in the flue gas when burning sub-bituminous coal (herein Powder River Basin (PRB) coal) and lignite, even with the use of selective catalytic reduction (SCR). The higher Hg(0)concentration in the flue gas makes it difficult to use the wet-FGD process for the mercury emission control in coal-fired utility boilers. Investigation of enhanced Hg(0) oxidation by addition of hydrogen halogens (HF, HCl, HBr, and HI) was conducted in a slipstream reactor with and without SCR catalysts when burning PRB coal. Two commercial SCR catalysts were evaluated. SCR catalyst no. 1 showed higher efficiencies of both NO reduction and Hg(0) oxidation than those of SCR catalyst no. 2. NH3 addition seemed to inhibit the Hg(0) oxidation, which indicated competitive processes between NH3 reduction and Hg(0) oxidation on the surface of SCR catalysts. The hydrogen halogens, in the order of impact on Hg(0) oxidation, were HBr, HI, and HCl or HF. Addition of HBr at approximately 3 ppm could achieve 80% Hg(0) oxidation. Addition of HI at approximately 5 ppm could achieve 40% Hg(0) oxidation. In comparison to the empty reactor, 40% Hg(0) oxidation could be achieved when HCl addition was up to 300 ppm. The enhanced Hg(0) oxidation by addition of HBr and HI seemed not to be correlated to the catalytic effects by both evaluated SCR catalysts. The effectiveness of conversion of hydrogen halogens to halogen molecules or interhalogens seemed to be attributed to their impacts on Hg(0) oxidation.

148 citations

Journal ArticleDOI
TL;DR: It is revealed that oxidized mercury can transform into Hg(0) under SCR atmosphere, which is of fundamental importance in developing efficient and economical mercury control technologies for coal-fired power plants.
Abstract: CuO−CeO2/TiO2 (CuCeTi) catalyst synthesized by a sol–gel method was employed to investigate mercury conversion under a selective catalytic reduction (SCR) atmosphere (NO, NH3 plus O2). Neither NO nor NH3 individually exhibited an inhibitive effect on elemental mercury (Hg0) conversion in the presence of O2. However, Hg0 conversion over the CuCeTi catalyst was greatly inhibited under SCR atmosphere. Systematic experiments were designed to investigate the inconsistency and explore the in-depth mechanisms. The results show that the copresence of NO and NH3 induced reduction of oxidized mercury (Hg2+, HgO in this study), which offset the effect of catalytic Hg0 oxidation, and hence resulted in deactivation of Hg0 conversion. High NO and NH3 concentrations with a NO/NH3 ratio of 1.0 facilitated Hg2+ reduction and therefore lowered Hg0 conversion. Hg2+ reduction over the CuCeTi catalyst was proposed to follow two possible mechanisms: (1) direct reaction, in which NO and NH3 react directly with HgO to form N2 an...

148 citations

Journal ArticleDOI
TL;DR: In this paper, an alumina-supported manganese oxide catalysts (2-8.4 wt% Mn) were characterized by in situ infrared (IR) spectroscopy and temperature-programmed reaction and desorption (TPRD) in relation to the selective catalytic reduction (SCR) of NO with NH 3.

147 citations

Journal ArticleDOI
TL;DR: In this article, a complete mechanism for describing the low-temperature (125°C) selective catalytic reduction of NO with NH 3 over carbon-supported Mn 3 O 4 is discussed.

147 citations


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