Novel low-temperature SCR (selective catalytic reduction) catalyst based on cubic-phase zirconia carrier and preparation method of novel low-temperature SCR catalyst
A technology of SCR catalyst and phase zirconia, which is applied in the field of cubic phase zirconia-based low-temperature flue gas denitrification SCR catalyst and its preparation, which can solve the gaps in preparation technology that no one mentioned, affecting texture, catalytic activity and catalytic selectivity, and preparation technology and other problems, to achieve the effect of improving the uniformity, reducing the preparation cost, and controlling the problem of agglomeration
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Embodiment 1
[0033] (1) Take ZrOCl 2 ·8H 2 O(AR) is 15.388g, Y(NO 3 ) 3 ·6H 2 O(AR) is 0.862g, PEG-4000(CP) is 0.32g, and it is configured as a mixed solution. Under the condition of rapid stirring, slowly drop 0.5mol / L ammonia solution into the prepared solution at a rate of 1mL / min until the pH=9.5, after aging and precipitation for 24 hours, wash with water and alcohol (absolute ethanol, AR) Later until Cl - Removed, dried for 12 hours, and ground to obtain white precursor powder. The precursor powder was heated at a rate of 5°C / min without a protective atmosphere, kept at 650°C and calcined for 2 hours, and then naturally cooled to obtain cubic zirconia.
[0034] (2) Take the cubic phase zirconia powder obtained in (1) as 10g, 50% manganese nitrate solution (Sinopharm, AR) as 2.26mL, Ce(NO 3 ) 3 ·6H 2 O is 2.5g, according to the equal-volume impregnation method, dissolved in deionized water, ultrasonically treated for 30min, impregnated for 6h under rapid stirring conditions, ...
Embodiment 2
[0038] (1) Take ZrOCl 2 ·8H 2 O(AR) is 15.388g, Y(NO 3 ) 3 ·6H 2 O(AR) is 0.862g, PEG-4000(CP) is 0.32g, and it is configured as a mixed solution. Under the condition of rapid stirring, slowly drop 0.5mol / L ammonia solution into the prepared solution at a rate of 1mL / min until the pH=9.5, after aging and precipitation for 24 hours, wash with water and alcohol (absolute ethanol, AR) Later until Cl - Removed, dried for 12 hours, and ground to obtain white precursor powder. The precursor powder was heated at a rate of 5°C / min without a protective atmosphere, kept at 650°C and calcined for 2 hours, and then naturally cooled to obtain a cubic phase zirconia powder.
[0039] (2) Take 10g of cubic zirconia powder obtained in (1), 1.13mL of 50% manganese nitrate solution (Sinopharm, AR), Ce(NO 3 ) 3 ·6H 2 O is 1.25g, according to the equal-volume impregnation method, dissolved in deionized water, ultrasonically treated for 30min, impregnated for 6h under rapid stirring condit...
Embodiment 3
[0043] (1) Take ZrOCl 2 ·8H 2 O(AR) is 15.388g, Y(NO 3 ) 3 ·6H 2 O(AR) is 0.862g, PEG-4000(CP) is 0.32g, and it is configured as a mixed solution. Under the condition of rapid stirring, slowly drop 0.5mol / L ammonia solution into the prepared solution at a rate of 1mL / min until the pH=9.5, after aging and precipitation for 24 hours, wash with water and alcohol (absolute ethanol, AR) Later until Cl - Removed, dried for 12 hours, and ground to obtain white precursor powder. The precursor powder was heated at a rate of 5°C / min without a protective atmosphere, kept at 650°C and calcined for 2 hours, and then naturally cooled to obtain a cubic phase zirconia powder.
[0044] (2) Take 10g of cubic zirconia powder obtained in (1), 3.39mL of 50% manganese nitrate solution (Sinopharm, AR), Ce(NO 3 ) 3 ·6H 2 O is 3.75g, according to the equal-volume impregnation method, dissolved in deionized water, ultrasonically treated for 30min, impregnated for 6h under rapid stirring condit...
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