A kind of simultaneous denitrification, demercury and dedioxin rare earth-based catalyst, its preparation method and application
A technology for removing dioxins and catalysts, which is applied in the field of flue gas purification in chemical plants and coal-fired power plants, and achieves the effects of simple preparation process, excellent resistance to sulfur poisoning, and environmental friendliness
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0029] (1) Preparation of active component precursor solution
[0030] Weigh 2.498g cerium nitrate hexahydrate, 0.024g erbium nitrate hexahydrate and 0.504g ascorbic acid, add 12.610g deionized water and place in a 50°C constant temperature water bath and stir for 30min until the solution is clear and transparent and the viscosity reaches 500cP to obtain the active component Precursor solution;
[0031] (2) Co-catalyst precursor ion solution configuration
[0032] Weigh 13.076g of zirconium oxychloride octahydrate and 2.615g of ascorbic acid, add 13.076g of deionized water and place in a constant temperature water bath at 60°C and stir for 60min until the solution is clear and transparent and the viscosity reaches 1000cP to obtain the co-catalyst precursor ion solution;
[0033] (3) Preparation of catalyst carrier
[0034] Measure 5mL of tetrabutyl titanate, 10mL of 2.5M hydrochloric acid and 50mL of deionized water, put them in a hydrothermal reaction kettle, heat at 180°C ...
Embodiment 2
[0042] (1) Preparation of active component precursor solution
[0043] Weigh 11.015g of anhydrous cerium chloride, 4.679g of erbium chloride hexahydrate and 3.139g of ascorbic acid, add 15.694g of deionized water and place in a 60°C constant temperature water bath and stir for 60min until the solution is clear and transparent and the viscosity reaches 1000cP, and the active Component precursor solution;
[0044] (2) Co-catalyst precursor ion solution configuration
[0045] Weigh 2.058g of manganese nitrate (50wt.%) solution and 0.412g of ascorbic acid, add 2.058g of deionized water and place in a 50°C constant temperature water bath and stir for 30min until the solution is clear and transparent and the viscosity reaches 500cP to obtain the co-catalyst precursor ion solution ;
[0046] (3) Preparation of catalyst carrier
[0047] Measure 5mL of tetrabutyl titanate, 10mL of 2.5M hydrochloric acid and 50mL of deionized water, put them in a hydrothermal reaction kettle, heat at...
Embodiment 3
[0055] (1) Preparation of active component precursor solution
[0056] Weigh 11.015g of anhydrous cerium chloride, 4.679g of erbium chloride hexahydrate and 3.139g of ascorbic acid, add 15.694g of deionized water and place in a 60°C constant temperature water bath and stir for 60min until the solution is clear and transparent and the viscosity reaches 1000cP, and the active Component precursor solution;
[0057] (2) Co-catalyst precursor ion solution configuration
[0058] Weigh 16.964g of yttrium nitrate hexahydrate and 3.393g of ascorbic acid, add 16.964g of deionized water and place in a 60°C constant temperature water bath and stir for 60min until the solution is clear and transparent and the viscosity reaches 1000cP to obtain the ion solution of the co-catalyst precursor;
[0059] (3) Preparation of catalyst carrier
[0060] Measure 5mL of tetrabutyl titanate, 10mL of 2.5M hydrochloric acid and 50mL of deionized water, put them in a hydrothermal reaction kettle, heat at...
PUM
Property | Measurement | Unit |
---|---|---|
denitrification rate | aaaaa | aaaaa |
denitrification rate | 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