Cu-Fe composite catalyst sulfonated by H2SO4 and application thereof
A catalyst and catalyst carrier technology, applied in physical/chemical process catalysts, chemical instruments and methods, chemical/physical processes, etc., can solve problems affecting ecological environment and life and health, achieve low cost, promote denitration efficiency, and broaden activity The effect of window temperature
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Embodiment 1
[0011] Example 1: Cu 3 -Fe 1 / Sn 0.33 Ti 0.67 o 2 Catalyst preparation.
[0012] 5.855g of SnCl 4 ·5H 2 O and 8.016g of Ti(SO 4 ) 2 Dissolve in 250mL of hydrochloric acid solution (0.1mol / L), record the above mixed solution as solution A, use 15.5wt.% ammonia water as precipitant, add solution A and ammonia water drop by drop under vigorous stirring until the pH is 8 In the phosphate buffer solution, control the drop rate of solution A to be less than 3mL / min, and maintain the pH at around 9. The suspension after the reaction was centrifuged and washed with deionized water and ethanol until it was washed with Ag(NO 3 ) 3 No white precipitate was detected. The resulting solid was dried at 100°C, calcined at 400°C, and ground to obtain Sn 0.33 Ti 0.67 o 2 Composite oxide powder. 3.986g of Cu(NO 3 ) 2 ·3H 2 O and 4.444g of Fe(NO 3 ) 3 9H 2 O was dissolved in 30 mL of deionized water, and 1 g of Sn was added to the above mixed solution 0.33 Ti 0.67 o 2 Comp...
Embodiment 2
[0013] Example 2: Cu 3 -Fe 1 / 0.2SO 4 2- -Sn 0.33 Ti 0.67 o 2 Catalyst preparation.
[0014] With the Sn prepared in embodiment 1 0.33 Ti 0.67 o 2 Composite oxides, impregnated with 0.2mol / L sulfuric acid, control 1.0g Sn 0.33 Ti 0.67 o 2 Composite oxide / 1.5mL impregnating solution, stand at room temperature for 12h, dry at 100°C for 1h, and finally roast at 300°C for 2h, and grind to obtain sulfonated 0.2SO 4 2- -Sn 0.33 Ti 0.67 o 2 Catalyst carrier. 3.986g of Cu(NO 3 ) 2 ·3H 2 O and 4.444g of Fe(NO 3 ) 3 9H 2 O was dissolved in 30 mL of deionized water, and 1 g of 0.2 SO was added to the above mixed solution 4 2- -Sn 0.33 Ti 0.67 o 2 Carrier, the total weight of the active component is controlled to be 10% of the carrier (with CuO, Fe 2 o 3 (meter), sonicated for 1h, dried at 100°C, then heated to 400°C at 3°C / min for calcination, kept for 2h, and ground to obtain Cu 3 -Fe 1 / 0.2SO 4 2- -Sn 0.33 Ti 0.67 o 2 catalyst.
Embodiment 3
[0015] Example 3: Cu 3 -Fe 1 / 0.4SO 4 2- -Sn 0.33 Ti 0.67 o 2 Catalyst preparation.
[0016] With the Sn prepared in embodiment 1 0.33 Ti 0.67 o 2 Composite oxides, impregnated with 0.4mol / L sulfuric acid, control 1.0g Sn 0.33 Ti 0.67 o 2 Composite oxide / 1.5mL impregnating solution, stand at room temperature for 12h, dry at 100°C for 1h, and finally roast at 300°C for 2h, and grind to obtain sulfonated 0.4SO 4 2- -Sn 0.33 Ti 0.67 o 2 Catalyst carrier. 3.986g of Cu(NO 3 ) 2 ·3H 2 O and 4.444g of Fe(NO 3 ) 39H 2 O was dissolved in 30 mL of deionized water, and 1 g of 0.4SO was added to the above mixed solution 4 2- -Sn 0.33 Ti 0.67 o 2 Carrier, the total weight of the active component is controlled to be 10% of the carrier (with CuO, Fe 2 o 3 (meter), sonicated for 1h, dried at 100°C, then heated to 400°C at 3°C / min for calcination, kept for 2h, and ground to obtain Cu 3 -Fe 1 / 0.4SO 4 2- -Sn 0.33 Ti 0.67 o 2 catalyst.
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