Macroporous Ce-Zr based composite metal oxide catalyst, preparation method, and application thereof
A composite oxide and composite metal technology, applied in the field of environmental purification, can solve the problems of high specific surface area, high porosity, and unsatisfactory purification effect of PM and NOx, and achieve low catalyst cost, uniform pore wall thickness, and favorable catalyst active effect
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Embodiment 1
[0057] Example 1: Ce 0.8 Fe 0.1 Zr 0.1 o 2 Catalyst preparation
[0058] At a stirring rate of 200r / min, 0.176g of cerium ammonium nitrate, 0.061g of ferric sulfate and 0.129 g of zirconium oxychloride (wherein the molar ratio of cerium ammonium nitrate, ferric sulfate and zirconium oxychloride is 8:1:1) Dissolve in a mixed solution of absolute ethanol and methanol, then stir evenly at 25°C to form a precursor solution; weigh 6g of the template polymethyl methacrylate (PMMA) and add it to the precursor solution at room temperature (15-25°C ) impregnated for 12 hours, and then suction filtered, and the obtained solid was dried at 40°C for 8 hours; the dried obtained solid was heated from room temperature (15-25°C) to 310°C in a tubular heating furnace and kept for 4 hours, and then heated at the same heating rate to 450°C and keep it warm for 4h, the composition is Ce 0.8 Fe 0.1 Zr 0.1 o 2 three-dimensional composite oxide catalysts.
[0059] Utilize the Ce that embodi...
Embodiment 2
[0066] Example 2: Ce 0.8 mn 0.1 Zr 0.1 o 2 Catalyst preparation
[0067] At a stirring rate of 200r / min, 0.176g cerium ammonium nitrate, 0.072g manganese nitrate and 0.129g zirconium oxychloride (wherein the molar ratio of cerium ammonium nitrate, manganese nitrate and zirconium oxychloride is 8:1:1 ) was dissolved in a mixed solution of polyethylene glycol and methanol, and then stirred evenly at 25°C to form a precursor solution; 6g of the template polymethyl methacrylate (PMMA) was weighed and added to the precursor solution at room temperature (15~ 25°C) for 12 hours, then suction filtered, and the obtained solid was dried at 40°C for 6 hours; the dried solid was raised from room temperature (15-25°C) to 310°C in a tubular heating furnace and kept for 4 hours, and then heated at the same temperature Raise the temperature to 500°C and hold it for 4 hours, and then the composition becomes Ce 0.8 mn 0.1 Zr 0.1 o 2 three-dimensional composite oxide catalysts.
[0068]...
Embodiment 3
[0075] Example 3: Ce 0.8 co 0.1 Zr 0.1 o 2 Catalyst preparation
[0076] At a stirring rate of 200r / min, dissolve 0.139g of cerium nitrate, 0.116g of cobalt nitrate and 0.129g of zirconium oxychloride (wherein the molar ratio of cerium nitrate, cobalt nitrate and zirconium oxychloride is 8:1:1) In a mixed solution of absolute ethanol and methanol, then stir evenly at 25°C to form a precursor solution; weigh 6g of the template polymethyl methacrylate (PMMA) and add it to the precursor solution at room temperature (15-25°C) Immerse for 12 hours, then filter with suction, and dry the obtained solid at 40°C for 10 hours; heat the dried obtained solid from room temperature (20-30°C) to 310°C in a tubular heating furnace and keep it warm for 4 hours, and then heat up to 450°C and keep it warm for 4h, the composition is Ce 0.8 co 0.1 Zr 0.1 o 2 three-dimensional composite oxide catalysts.
[0077] Utilize the Ce that embodiment 3 makes 0.8 co 0.1 Zr 0.1 o 2 Catalyst elim...
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