Catalyst for simultaneous catalytic reduction of both NO and SO2 through CO and preparation method and application of catalyst
A catalyst and oxide technology, applied in chemical instruments and methods, physical/chemical process catalysts, metal/metal oxide/metal hydroxide catalysts, etc., to achieve the effects of good adsorption performance, easy access, and high catalytic activity
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Embodiment 1
[0026] Example 1 10%Cu / γ-Al 2 O 3
[0027] According to the loading capacity of the active components of the catalyst, weigh 1.8875g of Cu(NO 3 ) 2 ·3H 2 O and 5g γ-Al 2 O 3 powder, add 100ml deionized water to prepare a mixed solution, stir in a constant temperature water bath at 40°C for 2 hours to mix the carrier and nitrate evenly, leave it in the air for 24 hours, put it in a rotary evaporator at 80°C and evaporate in vacuum until the water evaporates dry, the obtained catalyst precursor was dried in an electric blast drying oven at 110°C for 12h, and then placed in a muffle furnace for roasting at 450°C for 3h to decompose copper nitrate to form copper oxide active components, and obtained 10% (Metal mass as a percentage of carrier mass) Cu / γ-Al 2 O 3 catalyst.
[0028] After taking it out, cool it and press it into tablets. The pressure is generally 20MP, and the catalyst of 20-40 meshes is sieved out.
[0029] Take 0.4g of catalyst and place it in...
Embodiment 2
[0030] Example 2 4%Cu-6%Ni / γ-Al 2 O 3
[0031]According to the loading capacity of the active components of the catalyst, weigh 0.755g of Cu(NO 3 ) 2 ·3H 2 O and 1.47g of Ni(NO 3 ) 2 ·6H 2 O and 5g γ-Al 2 O 3 powder, add 100ml deionized water to prepare a mixed solution, stir in a constant temperature water bath at 40°C for 2 hours to mix the carrier and nitrate evenly, leave it in the air for 24 hours, put it in a rotary evaporator at 80°C and evaporate in vacuum until the water evaporates dry, the obtained catalyst precursor was dried in an electric blast drying oven at 110°C for 12h, and then placed in a muffle furnace for roasting at 450°C for 3h to decompose copper nitrate and nickel nitrate to form oxide active components, and obtained 4%Cu-6%Ni (Metal mass as a percentage of carrier mass) / γ-Al 2 O 3 catalyst.
[0032] After taking it out, cool it and press it into tablets. The pressure is generally 20Mp, and the catalyst of 20-40 meshes is sc...
Embodiment 3
[0034] Example 3 8%Ni- 2%Fe / γ-Al 2 O 3
[0035] According to the loading capacity of the active components of the catalyst, weigh 1.96g of Ni(NO 3 ) 2 ·6H 2 O, 0.72g of Fe(NO 3 ) 3 9H 2 O and 5g γ-Al 2 O 3 powder, add 100ml of deionized water to prepare a mixed solution, stir in a constant temperature water bath at 40°C for 2 hours to mix the carrier and nitrate evenly, leave it in the air for 24 hours, put it in a rotary evaporator at 80°C and evaporate in a vacuum until the water evaporates dry, the obtained catalyst precursor was dried in an electric blast drying oven at 110°C for 12h, and then placed in a muffle furnace for 3h roasting at 450°C to decompose nitrates to generate oxide active components, and obtained 8%Ni- 2%Fe (Metal mass as a percentage of carrier mass) / γ-Al 2 O 3 catalyst.
[0036] After taking it out, cool it and press it into tablets. The pressure is generally 20Mp, and the catalyst of 20-40 meshes is screened out.
[0037] T...
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