Storage reduction catalyst used for removing nitrogen oxide in lean burn engine tail gas and preparation method
A nitrogen oxide and engine technology, applied in the field of nitrogen oxide storage reduction catalyst and preparation, can solve the problems of poor hydrothermal aging ability, narrow active temperature window, anti-sulfur poisoning, etc., and achieves low cost, convenient operation, and preparation process. simple effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
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...
PUM
Property | Measurement | Unit |
---|---|---|
water absorption | aaaaa | aaaaa |
water absorption | aaaaa | aaaaa |
water absorption | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com