Zeolite imidazole framework structure composite material for removing NOx, preparation method and application
A technology of zeolite imidazolate and composite materials, applied in chemical instruments and methods, separation methods, catalyst activation/preparation, etc., can solve the problem that the nitrogen oxides to be treated have high temperature requirements, it is difficult to obtain catalytic purification effects, and the active component vanadium Biotoxicity and other problems, to achieve the effect of easy promotion, strong practicability and simple preparation method
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example 1
[0028] Example 1: The preparation method of the zeolite imidazolate framework structure composite material modified by manganese oxide
[0029] (1) Accurately weigh 3.528g zinc nitrate hexahydrate, 1.944g dimethylimidazole, 0.807g sodium formate, mix with 78.5ml anhydrous methanol, stir magnetically, and add 1.5mL 50% manganese nitrate solution dropwise, keep magnetic stirring 5min.
[0030] (2) The resulting mixed solution was treated under 30 kHz ultrasonic for 5 min.
[0031] (3) The obtained ultrasonically pretreated mixture was put into a 100 mL polytetrafluoroethylene-lined reaction kettle, placed in an oven, and slowly heated to 140° C. for 24 hours.
[0032] (4) The resulting suspension was washed three times with anhydrous methanol, and then dried in an oven at 60°C for 8 hours.
[0033] (5) The obtained solid powder is put into the tube furnace, and after being sealed, 50mL / min of high-purity nitrogen is introduced; the tube furnace is heated to 250°C at a rate of ...
example 2
[0034] Example 2: The preparation method of the manganese oxide modified zeolite imidazolate framework structure composite material
[0035] (1) Accurately weigh 3.528g of zinc nitrate hexahydrate, 1.944g of dimethylimidazole, and 0.807g of sodium formate, mix them with 74ml of anhydrous methanol, stir magnetically, and add 6mL of 50% manganese nitrate solution dropwise, and keep stirring magnetically for 5min.
[0036] (2) The resulting mixed solution was ultrasonically treated at 30 kHz for 10 min.
[0037] (3) The obtained ultrasonically pretreated mixture was put into a 100 mL polytetrafluoroethylene-lined reaction kettle, placed in an oven, and slowly heated to 140° C. for 24 hours.
[0038] (4) The resulting suspension was washed three times with anhydrous methanol, and then dried at 60° C. for 12 h.
[0039] (5) The obtained solid powder is put into the tube furnace, and after being sealed well, 50mL / min of high-purity nitrogen is introduced; the tube furnace is heated...
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