Non-toxic medium-high temperature alkali-resistant metal denitration catalyst and preparation method and application thereof
A denitration catalyst, medium and high temperature technology, applied in catalyst activation/preparation, chemical instruments and methods, physical/chemical process catalysts, etc., can solve the problems of biological toxicity, susceptibility to alkali metal poisoning, etc.
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Embodiment 1
[0018] 1 preparation of catalyst:
[0019] (1) Add 0.01 mol of cerous nitrate hexahydrate and 0.04 mol of ferric nitrate nonahydrate to 100 mL of deionized water in sequence, stir well to dissolve, and then add 10 g of TiO 2 , stir evenly, then add 10mL 25% ammonia water, fully stir the precipitate, filter, wash and dry;
[0020] (2) Add 0.001 mol of niobium oxalate and 0.001 mol of ammonium metatungstate to 200 mL of deionized water in sequence, stir and dissolve to form a mixed solution;
[0021] (3) Add the precipitate in step (1) to the solution in step (2), stir and evaporate to dryness at 100°C;
[0022] (4) The evaporated product was collected and calcined at 500°C for 3 hours to obtain the finished catalyst.
[0023] 2. Catalyst performance test: 0.5 g of the prepared catalyst was put into a fixed-bed quartz tube reactor, the inner diameter of the quartz tube was 0.8 cm, and the simulated flue gas was composed of NO, NH 3 , O 2 and N 2 Composition, of which NO 500...
Embodiment 2
[0027] 1. Preparation of catalyst:
[0028] (1) Add 0.001mol of nickel nitrate hexahydrate and 0.04mol of iron nitrate nonahydrate to 100 mL of deionized water in turn, stir and dissolve, then add 10g of TiO 2 , stir evenly, then add 10mL 25% ammonia water, fully stir the precipitate, filter, wash and dry;
[0029] (2) Add 0.001mol of niobium oxalate and 0.004mol of ammonium heptamolybdate to 200 mL of deionized water in sequence, stir and dissolve to form a mixed solution;
[0030](3) Add the precipitate in step (1) to the solution in step (2), stir and evaporate to dryness at 100°C;
[0031] (4) The evaporated product was collected and calcined at 550°C for 3 hours to obtain the finished catalyst.
[0032] 2. Catalyst performance test: 0.5 g of the prepared catalyst was put into a fixed-bed quartz tube reactor, the inner diameter of the quartz tube was 0.8 cm, and the simulated flue gas was composed of NO, NH 3 , O 2 and N 2 Composition, of which NO 500 ppm, NH 3 500 ...
Embodiment 3
[0036] 1. Preparation of catalyst:
[0037] (1) Add 0.001mol nickel nitrate hexahydrate, 0.04mol ferric nitrate nonahydrate, and 0.005mol cerium chloride to 100 mL deionized water in sequence, stir and dissolve, then add 10g TiO 2 , stir evenly, then add 12mL 25% ammonia water, fully stir the precipitate, filter, wash and dry;
[0038] (2) Add 0.001mol of ammonium heptamolybdate and 0.004mol of ammonium metatungstate to 200 mL of deionized water in turn, stir and dissolve to form a mixed solution;
[0039] (3) Add the precipitate in step (1) to the solution in step (2), stir and evaporate to dryness at 100°C;
[0040] (4) The evaporated product was collected and calcined at 600°C for 3 hours to obtain the finished catalyst.
[0041] 2. Catalyst performance test: 0.5 g of the prepared catalyst was put into a fixed-bed quartz tube reactor, the inner diameter of the quartz tube was 0.8 cm, and the simulated flue gas was composed of NO, NH 3 , O 2 and N 2 Composition, of whic...
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