Non-noble metal catalyst used for catalytic combustion of PTA exhaust gas and preparation method thereof
A catalytic combustion, non-precious metal technology, applied in the direction of catalyst activation/preparation, combustion methods, metal/metal oxide/metal hydroxide catalysts, etc., can solve the problems of poor toxicity resistance and high cost, and achieve good toxicity resistance and low price The effect of low cost and wide source of raw materials
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0027] Measure 2 L of 0.25mol / L cerium nitrate solution, add dropwise 0.25mol / L sodium carbonate solution to the solution while stirring until the pH value is 8, continue stirring for 0.5h, age for 12h, and then suction filter, Wash with deionized water until the pH of the filtrate becomes neutral, then dry at 100 °C for 8 h, and bake at 500 °C for 5 h to obtain the coated CeO 2 . Measure 30mL of 0.5mol / L copper nitrate solution, 150mL of 0.5mol / L manganese nitrate solution and 420mL of deionized water to make a mixed solution. 96.615gCeO 2 Add it to the soaking solution, stir and soak for 2 h. Then transferred to an oven to dry at 100 °C for 10 h, and finally calcined at 500 °C for 5 h to prepare CuMn / CeO with a loading capacity of 5%. 2 catalyst. Weigh 100g of catalyst powder and put it into a ball mill tank, add 400g of water ball mill for 2 h to make a coating solution, the solid content in the coating solution is 20%. The solution is an aqueous solution or a suspensi...
Embodiment 2
[0032] Measure 1 L of 0.5 mol / L cerium nitrate solution, add dropwise 0.5 mol / L ammonium carbonate solution to the solution while stirring, add dropwise until the pH value is 10, continue stirring for 3 hours, age for 48 hours, then suction filter, use Wash with deionized water until the pH of the filtrate becomes neutral, then dry at 120 °C for 20 h, and bake at 700 °C for 2 h to obtain the coated CeO 2 . Measure 500mL of 0.5mol / L copper sulfate solution, 500mL of 0.5mol / L manganese sulfate solution and 1L of deionized water to make a mixed solution. 89.25gCeO 2 Add to the soaking liquid, stirring and soaking for 12h. Then transferred to an oven to dry at 120 °C for 20 h, and finally calcined at 700 °C for 2 h to prepare CuMn / CeO with a loading capacity of 25%. 2 catalyst. Weigh 200g of catalyst powder and put it into a ball mill tank, add 300g of water ball mill for 2 h to make a coating solution, the solid content of the coating solution is 40%.
[0033] Honeycomb cera...
Embodiment 3
[0036] Measure 1L of 0.5mol / L cerium nitrate solution, add dropwise 0.5mol / L ammonium bicarbonate solution to the solution while stirring, dropwise add to pH value of 9, continue stirring for 2h, age for 24h, then suction filter, use Wash with deionized water until the pH of the filtrate becomes neutral, then dry at 110 °C for 12 h, and bake at 600 °C for 3 h to obtain the coated CeO 2 . Measure 100mL of 0.5mol / L copper acetate solution, 700mL of 0.5mol / L manganese acetate solution and 1.2L of deionized water to make a mixed solution. 127.217gCeO 2 Add to the impregnating solution, stirring and impregnating for 10h. Then transferred to an oven to dry at 110 °C for 12 h, and finally calcined at 600 °C for 3 h to prepare CuMn / CeO with a loading capacity of 15%. 2 catalyst. Weigh 150g of catalyst powder and put it into a ball mill tank, add 350g of water ball mill for 2 h to make a coating solution, the solid content in the coating solution is 30%. 300~600mL of 0.5mol / L mang...
PUM
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