Storage reduction catalyst used for removing nitrogen oxide in lean burn engine tail gas and preparation method
A nitrogen oxide and engine technology, which is applied in the field of nitrogen oxide storage and reduction catalyst and preparation, can solve the problems of anti-sulfur poisoning, narrow active temperature window, poor hydrothermal aging ability, etc., and achieves convenient operation, low cost, and easy preparation process simple effect
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Embodiment 1
[0031] Take 30.38g of cerous nitrate and 9.63g of zirconium nitrate and dissolve them in 100mL of deionized water, the molar ratio Ce:Zr=7:3, the molar concentration is [Ce+Zr]=1mol / L, use 3mol / LNH under rapid stirring 3 ·H 2 O for precipitation, adjust the pH value to 7, add 0.5 g of polyethylene glycol, fully stir for 30 min, let stand at room temperature for 1 h, and age at 80 ° C for 3 h; vacuum filter to obtain the precipitate, and use deionized water to wash the precipitate until The filtrate is neutral, and then the resulting filter cake is dried at 120°C for 12 hours, pre-calcined at 300°C for 1 hour, and roasted at 500°C for 3 hours to obtain cerium-zirconium powder Ce 0.7 Zr 0.3 o 2 .
[0032] Measured cerium zirconium powder Ce 0.7 Zr 0.3 o 2 The water absorption rate is 0.5mL / g.
[0033] Weigh 6.6776g Ba(CH 3 COO) 2 Dissolve in 10ml of water, load on the cerium-zirconium carrier by equal volume impregnation method, dry in the shade at room temperature, dry...
Embodiment 2
[0038] Take 12.12g of cerium sulfate and 6.42g of zirconium oxynitrate and dissolve them in 50mL of deionized water, the molar ratio Ce:Zr=6:4, the molar concentration is [Ce+Zr]=1mol / L, use 4mol / LNH under rapid stirring 3 ·H 2 O for precipitation, adjust the pH value to 9, add 0.15 g of polyethylene glycol, fully stir for 30 min, let stand at room temperature for 1 h, and age at 80 ° C for 3 h; vacuum filter to obtain the precipitate, and use deionized water to wash the precipitate until The filtrate is neutral, and then the resulting filter cake is dried at 120°C for 12 hours, pre-calcined at 300°C for 1 hour, and roasted at 500°C for 3 hours to obtain cerium-zirconium powder Ce 0.6 Zr 0.4 o 2 .
[0039] Measured cerium zirconium powder Ce 0.6 Zr 0.4 o 2 The water absorption rate is 1.2mL / g. Weigh 10.44g Ba(NO 3 ) 2 Dissolve in 10ml of water, load on the cerium-zirconium carrier by equal volume impregnation method, dry in the shade at room temperature, dry at 120°C ...
Embodiment 3
[0044] Take 14.92g of cerous chloride and 3.22g of zirconium chloride and dissolve them in 50mL of deionized water, the molar ratio Ce:Zr=8:2, the molar concentration is [Ce+Zr]=1mol / L, use 4mol / LNH under rapid stirring 4 HCO 3 Precipitate, adjust the pH value to 11, add 0.3g of polyethylene glycol, stir thoroughly for 30min, let stand at room temperature for 1h, and age at 80°C for 3h; vacuum filter to obtain the precipitate, and use deionized water to wash the precipitate to the filtrate It is neutral, and then the obtained filter cake is dried at 120°C for 12 hours, pre-calcined at 300°C for 1 hour, and fired at 500°C for 3 hours to obtain cerium-zirconium powder Ce 0.8 Zr 0.2 o 2 .
[0045] Measured cerium zirconium powder Ce 0.8 Zr 0.2 o 2 The water absorption rate is 1.0mL / g. Weigh 13.36g Ba(CH 3 COO) 2 Dissolve in 10ml of water, load on the cerium-zirconium carrier by equal volume impregnation method, dry in the shade at room temperature, dry at 120°C for 0.5-3...
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