Preparation method of cooperating catalyst for demercuration and denitration
A catalyst, SCR catalyst technology, applied in chemical instruments and methods, physical/chemical process catalysts, separation methods, etc., can solve the problems of reducing the mechanical strength of the catalyst, high service temperature, secondary pollution, etc., and achieve good mercury and denitrification performance , good low-temperature performance, and the effect of prolonging the service life
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[0021] The invention provides a method for preparing a synergistic catalyst for demercuration and denitrification, comprising the following steps:
[0022] (1) First, wash or blow with water to remove the ash on the surface of the deactivated SCR catalyst; then soak the deactivated SCR catalyst in the divalent manganese salt solution, so that the deactivated SCR catalyst can fully absorb Valence manganese ion, wherein, the divalent manganese salt is manganese nitrate Mn(NO 3 ) 2 Or manganese acetate MnAc, etc., the concentration of divalent manganese ions in the divalent manganese salt solution is 0.5mol / L-2.5mol / L; the longer the soaking time, the more sufficient the adsorption, usually 12h-36h is required, and the higher the concentration of manganese salt If the concentration is high, the soaking time can be reduced. For example, when the concentration of manganese salt is 1mol / L, it needs to be soaked for 24h; , the impregnation time is too long will affect the mechanica...
Embodiment 1
[0025] Embodiment 1 contains 3.5% mass fraction MnO x The preparation method of the new catalyst
[0026] (1) First deactivate the commercial SCR catalyst V 2 o 5 -WO 3 (MoO 3 ) / TiO 2 Perform water washing and regeneration treatment to remove the ash on the surface of the catalyst; then immerse the de-ashed SCR catalyst module (150mm×150mm×1000mm) in 100L, 1mol / L manganese nitrate aqueous solution for 24 hours.
[0027] (2) The catalyst obtained in step (1) was dried at 105°C for 24 hours, and then calcined at 500°C for 5 hours in an air atmosphere to obtain MnO x The mass fraction is 3.5% (first calculate the quality of Mn by elemental analysis, and then use MnO 2 As the theoretical composition, converted to MnO x mass) of MnO x / DSCR, denoted as 3.5wt% MnO x / DSCR.
Embodiment 2
[0028] Embodiment 2 contains 6% mass fraction MnO x The preparation method of the new catalyst
[0029] Repeat embodiment 1 with described identical steps, difference is, after described step (2), then the 3.5wt%MnO that step (2) obtains x / DSCR, immersed in 100L, in the manganese nitrate aqueous solution of 1mol / L, leave standstill for 24 hours; And repeat step (2), obtain 6wt%MnO x / DSCR.
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