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Preparation Of De-NOx Catalysts Containing V-W And Their Application In Selective Catalytic Reduction Of NO

Posted on:2012-01-13Degree:MasterType:Thesis
Country:ChinaCandidate:H Q LvFull Text:PDF
GTID:2131330338996887Subject:Chemistry
Abstract/Summary:PDF Full Text Request
Flue gas denitrification is one of effective ways to control NOx emissions from coal-fired power plants. Because of the high efficiency, selectivity, stability and reliability, selective catalytic reduction (SCR) technology has been widely used in the de-NOx processing. Catalyst is the key technology, currently, in China most of the SCR catalysts are imported and monolithic catalysts which used TiO2 as carrier, TiO2 account for about 80% of the total weight of catalysts, there are problems like high costs and insufficient use of highly active component in this method.In order to improve the shortcomings, vanadium-based catalysts are modified by WO3 to investigate the preparation methods and de-NOx applications of tungsten supported vanadium based catalysts. Meanwhile, there are preliminary studies about the performances of supported heteropoly compound catalysts. Respectively, a composite support TiO2/honeycomb cordierite modified by V2O5-WO3 has been prepared via static impregnation method and used for the preparation of V2O5-WO3 based monolith SCR catalyst, and particle catalysts were prepared by impregnated V2O5-WO3 on TiO2 powder and then mold it with Al2O3. The X-ray diffraction method, X-ray photoelectron spectroscopy and BET technology were applied for catalyst characterization, and the activity for NO catalytic removal by NH3 has been evaluated. During this process, the effect of preparation methods, temperature and a number of factors to flue gas conditions have been researched.The results showed that a lower NO conversion rate have been evaluated, because of surfaces of the particle catalysts do not have good diffusion conditions for the reaction gases. The influences of impregnation process on SCR activities indicated that the existence of oxalic acid in precursor solution decreased the SCR activity of the resulted catalyst, which is deduced as the major effect of the distribution and accumulation of V2O5 on the surface of catalyst. The effects of temperature, initial NO concentration, space velocity and NH3/NO ratio on the SCR reaction have been investigated. The prepared catalyst showed a good activity, the NO conversion can be more than 97% under the condition of 350℃400℃, NH3/NO of 0.81 and the space velocity of 10000 h-1. The V2O5-WO3/TiO2/CC catalyst was not obviously inhibited the oxidation of SO2, when CaO was deposited on catalyst, it will undermine the structure of the surface, resulting in lower activity. The Keggin structure is maintained when heteropoly compound is immobilized on TiO2/CC surface. When the HPC was loaded less than 20%, the main reason of the denitrification activity seems to be the amorphous phase which formed by the strong interaction between HPC and TiO2.The catalyst was evaluated higher activity when there were more vanadium atoms in heteropoly acid anions. The active center of catalyst was involved in vanadium species.
Keywords/Search Tags:Selective catalytic reduction (SCR), DeNOx catalysts, V2O5-WO3, Heteropoly compounds (HPC), Prepration
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