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Study On The Performance Of Sn-Ce-PO Catalysts For The Selective Reduction Of Nitrogen Oxides With Ammonia

Posted on:2022-08-28Degree:MasterType:Thesis
Country:ChinaCandidate:C ZhaoFull Text:PDF
GTID:2511306605988659Subject:Inorganic Chemistry
Abstract/Summary:PDF Full Text Request
With the development of industrial society,all kinds of factories have appeared rapidly.Excessive emission of nitrogen oxides has caused serious harm to human and environment.Selective catalytic reduction of NOx by Ammonia(NH3-SCR)has become an efficient denitration method in many flue gas desolation technologies.In the industry,the earliest V2O5-WO3/TiO2 catalyst has the disadvantages of narrow operating temperature window,poor sulfur resistance ability and V has the biological toxicity.Therefore,the research and development of V-free NH3-SCR catalyst has very important practical significance.In this paper,CePO4 catalysts with different crystal phases,SnxCe-P-Oy(x=0.1,0.2,0.3,0.4)and Sn0.2-Ce-Px-Oy(x=0.8,0.6,0.4,0.2)were prepared by co-precipitation method and hydrothermal method,respectively.Their catalytic performance in the denitration of NH3-SCR was tested.XRD,N2 adsorptio-desorption test,NH3-TPD,H2-TPR,XPS,in situ DRIFTS and other characterization methods were used to investigate the relationship between the physical and chemical properties of the catalysts and catalytic denitration performance.The NO conversion and N2 selectivity of hexagonal CePO4-H catalysts at 300-500? are greater than 95%and 100%.It also exhibits excellent stability and H2O+SO2 resistance.Mainly because it has more Br?nsted acid sites.Sn0.2-Ce-P-Oy catalyst can achieve more than 90%conversion at 240-450? and maintain 100%N2 selectivity throughout the operating temperature window.Catalytic performance is almost unaffected by 100 ppm SO2 at 270 ?.The excellent performance is attributed to the increased variety of acid sites and appropriate oxidation capacity.Sn0.2-Ce-P0.4-Oy catalyst achieved 100%conversion at 210-450? and maintained more than 90%N2 selectivity throughout the activity temperature window.Catalytic activity was barely affected by 100 ppm SO2 and 5%H2O at 240?.These are due to the interaction between Sn and Ce(2Ce4++Sn2+(?)2Ce3++Sn4+),promoted the catalyst with more acid,surface adsorption oxygen and appropriate oxidation capacity.The surface acid sites and the adsorbed species of nitrogen oxides on the catalysts were studied in detail by in situ DRIFTS,the changes of the adsorbed species on the surface during the reaction process were analyzed,and the corresponding reaction mechanism was proposed.
Keywords/Search Tags:Selective catalytic reduction with NH3, Nitrogen oxides, Acid sites, Oxidation ability, cerium phosphate, Sn
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