Catalyst for ammonia selective reduction of nitrogen oxide and preparation method of catalyst
A technology of nitrogen oxides and catalysts, applied in the field of environmental pollution control, can solve the problems of lower operating temperature, poor low-temperature activity, etc., and achieve the effects of lower operating temperature, high low-temperature activity, and simple preparation process
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Embodiment 1
[0020] A preparation method of the described low-temperature ammonia selective catalytic reduction nitrogen oxide catalyst for denitrification of flue gas or removal of nitrogen oxides in motor vehicle exhaust gas, comprising the following steps:
[0021] Weigh 6.66 g of Sm(NO 3 ) 3 ·6H 2 O and 17.9 g of 50% by weight Mn(NO 3 ) 2 The solution was dissolved in deionized water to make a mixed solution, i.e. Sm / Mn=0.03 (molar ratio).
[0022] Preset 100 mL of deionized water in a beaker, and slowly add 0.2 M Na 2 CO 3 solution until the pH value of the aqueous solution is 11, then drop the mixed metal salt solution and 0.2 M Na into the beaker at the same time 2 CO 3 Solution, control the rate of addition of the two, so that the pH value of the solution remains at 11. After the dropwise addition, the resulting mixture was stirred at room temperature for 24 h, then suction filtered and washed until the filtrate was neutral, and the obtained filter cake was placed in an ove...
Embodiment 2
[0025] Weigh 6.66 g of Sm(NO 3 ) 3 ·6H 2 O and 7.35 g of Mn(Ac) 2 4H 2 O was dissolved in deionized water to make a mixed solution, that is, Sm / Mn = 0.5 (molar ratio).
[0026] Preset 100 mL of deionized water in a beaker, and slowly add 0.2 M Na 2 CO 3 solution until the pH value of the aqueous solution is 8, then drop the mixed metal salt solution and 0.2 M Na into the beaker at the same time 2 CO 3 Solution, control the rate of addition of the two, so that the pH value of the solution remains at 8. After the dropwise addition, the resulting mixture was stirred at room temperature for 24 h, then suction filtered and washed until the filtrate was neutral, and the obtained filter cake was placed in an oven at 120 °C for 12 h, and finally placed in a Calcined in static air at 350°C for 6 h in a muffle furnace to obtain catalyst 2#.
[0027]The method of Example 1 was used to test the activity of catalyst 2# on ammonia selective catalytic reduction of nitrogen oxides. T...
Embodiment 3
[0029] Weigh 6.66 g of Sm(NO 3 ) 3 ·6H 2 O, 3.906 g of Ce(NO 3 ) 3 ·6H 2 O and 22.65 g of anhydrous MnSO 4 Dissolved in deionized water to make a mixed solution, namely Sm / Mn=0.1 (molar ratio), Ce / Mn=0.06 (molar ratio).
[0030] Preset 100 mL of deionized water in a beaker, and slowly add 0.2 M Na 2 CO 3 solution until the pH value of the aqueous solution is 11, then drop the mixed metal salt solution and 0.2 M Na into the beaker at the same time 2 CO 3 Solution, control the rate of addition of the two, so that the pH value of the solution remains at 11. After the dropwise addition, the resulting mixture was continuously stirred at room temperature for 2 h, then suction filtered and washed until the filtrate was neutral, and the obtained filter cake was placed in an oven at 120 ° C for 12 h, and finally placed in Calcined in static air at 450°C for 2 h in a muffle furnace to obtain catalyst 3#.
[0031] The catalyst obtained after calcining is pressed into tablets a...
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