Denitration catalyst with high sulfur resistance and high alkali metal resistance, and preparation method thereof
A denitration catalyst, alkali metal technology, applied in metal/metal oxide/metal hydroxide catalysts, chemical instruments and methods, physical/chemical process catalysts, etc. It can make up for the problems of poor temperature and good denitrification efficiency and stability.
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Embodiment 1
[0022] 362.12g of tetrabutyl titanate and 52.05g of tetraethyl silicate were added to 300g of absolute ethanol and stirred evenly to obtain mixed solution A; 1.07g of vanadyl sulfate and 0.96g of neodymium nitrate were dissolved in 60g of Stir uniformly in water ethanol to obtain solution B; dissolve 0.88g cerium nitrate and 0.2g ammonium molybdate in 5g oxalic acid solution (mass concentration 5%) and mix uniformly to obtain solution C; slowly pour B solution into A solution, Stir evenly and let it stand for no less than 30 minutes; slowly add solution C to the mixed solution of A and B, stir evenly, age for 2 hours at a temperature of 50°C to obtain a gel;
[0023] (2) Dry and grind the obtained gel under a nitrogen atmosphere to obtain a precursor;
[0024] (3) Weigh 90g of the precursor, mix it with 20% concentrated ammonia solution, and stir it magnetically for 6h.
[0025] (4) Transfer the suspension in (3) into a high-temperature and high-pressure reaction kettle, and ...
Embodiment 2
[0030] A certain amount of 404.63g tetrabutyl titanate and 17.34g tetraethyl silicate were respectively added to 320g of absolute ethanol and stirred evenly to obtain a mixed solution A; 7.16g of vanadyl sulfate and 2.40g of neodymium nitrate were dissolved in Stir in 80g of absolute ethanol to prepare solution B; dissolve 22.7g of cerium nitrate and 1.36g of ammonium molybdate in 55g of oxalic acid solution (mass concentration 8%) and mix evenly to obtain solution C; slowly pour B solution into A In the solution, stir evenly, and let stand for no less than 30 minutes; slowly add solution C to the mixed solution of A and B, stir evenly, and age for 12 hours at a temperature of 90°C to obtain a gel;
[0031] (2) Dry and grind the obtained gel under a nitrogen atmosphere to obtain a precursor;
[0032] (3) Weigh 100 g of the precursor, mix it with 25% concentrated ammonia solution, and stir it magnetically for 8 hours.
[0033] (4) Transfer the suspension in (3) into a high-tem...
Embodiment 3
[0038] 383.34g of tetrabutyl titanate and 34.68g of tetraethyl silicate were added to 450g of absolute ethanol and stirred uniformly to obtain mixed solution A; 3.76g of vanadyl sulfate and 2.15g of neodymium nitrate were dissolved in 65g of Stir uniformly in water ethanol to obtain solution B; dissolve 16.14g cerium nitrate and 2.18g ammonium molybdate in 80g oxalic acid solution (mass concentration 10%) and mix uniformly to obtain solution C; slowly pour B solution into A solution, Stir evenly, and let stand for no less than 30 minutes; slowly add solution C to the mixed solution of A and B, stir evenly, and age for 12 hours at a temperature of 90°C to obtain a gel;
[0039] (2) Dry and grind the obtained gel under a nitrogen atmosphere to obtain a precursor;
[0040] (3) Weigh 90g of the precursor, mix it with 22% concentrated ammonia solution, and stir it magnetically for 8h.
[0041](4) Transfer the suspension in (3) into a high-temperature and high-pressure reaction ket...
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