Low-temperature water-resistant and sulfur-resistant denitration catalyst as well as preparation method and application thereof
A denitration catalyst and low temperature technology, applied in chemical instruments and methods, physical/chemical process catalysts, separation methods, etc., can solve the problems of low temperature sulfur poisoning, water poisoning inactivation, etc., to reduce the reduction of specific surface area and improve the denitration efficiency. , The effect of solving the sharp decline of low temperature poisoning activity
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Embodiment 1
[0019] 1. Catalyst preparation: Add 0.01mol ammonium metavanadate, 0.03mol oxalic acid and 0.03mol cerous nitrate hexahydrate to 200 mL deionized water in sequence, stir and disperse to form a mixed solution; then add 0.005mol ammonium heptamolybdate and 0.01mol of ammonium phosphate was stirred and dissolved evenly; then 10g of titanium dioxide carrier was added to the above mixture, stirred and evaporated to dryness at 80°C; the evaporated product was collected and calcined at 500°C for 3 hours to obtain a finished catalyst.
[0020] 2. Performance test of the catalyst: the specific surface area of the catalyst is 120 m 2 / g, measured by Tristar II 3020 automatic specific surface area and pore analyzer. Take 0.5 g of the prepared catalyst and put it into a fixed-bed quartz tube reactor, the inner diameter of the quartz tube is 0.8 cm, and the simulated flue gas is composed of NO, NH 3 , O 2 and N 2 Composition, of which NO 1000 ppm, NH 3 1000 ppm, O 2 3 %, airspeed 4...
Embodiment 2
[0023] 1. Preparation of catalyst: Add 0.01mol ammonium metavanadate and 0.04mol oxalic acid to 200 mL of deionized water in sequence, stir and disperse fully to form a mixed solution; then add 0.002mol ammonium metatungstate, 0.01mol nickel nitrate and 0.01mol phosphoric acid respectively , stirred and dissolved evenly; then 10g of titanium dioxide carrier was added to the above mixed solution, stirred and evaporated to dryness at 80°C; the evaporated product was collected and calcined at 350°C for 3 hours to obtain a finished catalyst.
[0024] 2. Performance test of the catalyst: the specific surface area of the catalyst is 145 m 2 / g, measured by Tristar II 3020 automatic specific surface area and pore analyzer. Take 0.5 g of the prepared catalyst and put it into a fixed-bed quartz tube reactor, the inner diameter of the quartz tube is 0.8 cm, and the simulated flue gas is composed of NO, NH 3 , O 2 and N 2 Composition, of which NO 500 ppm, NH 3 500 ppm, O 2 3 %, a...
Embodiment 3
[0027]1. Catalyst preparation: Add 0.01mol ammonium metavanadate, 0.03mol oxalic acid and 0.005mol cerous nitrate hexahydrate to 200 mL of deionized water in sequence, stir well and disperse to form a mixed solution; then add 0.002mol sodium tungstate, 0.01 1 mol of zirconium sulfate and 0.01 mol of ammonium dihydrogen phosphate were stirred and dissolved evenly; then 10 g of titanium dioxide carrier was added to the above mixture, stirred and evaporated to dryness at 80°C; the evaporated product was collected and calcined at 550°C for 3 hours to obtain a finished catalyst.
[0028] 2. Catalyst performance test: The specific surface area of the catalyst is 105 m 2 / g, measured by Tristar II 3020 automatic specific surface area and pore analyzer. Take 0.5 g of the prepared catalyst and put it into a fixed-bed quartz tube reactor, the inner diameter of the quartz tube is 0.8 cm, and the simulated flue gas is composed of NO, NH 3 , O 2 and N 2 Composition, of which NO 1500 p...
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