Catalyst taking nitrogen-doped carbon material as carrier and preparation method of catalyst
A nitrogen-doped carbon and catalyst technology, applied in the direction of catalyst carrier, chemical instrument and method, hydrogen halide addition preparation, etc., can solve the problem of large distance between catalysts, achieve high stability, reduce the impact of mass transfer, The effect of promoting activation
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Embodiment 1
[0032] Nitrogen-doped activated carbon supported on 0.36 wt% Au and 14.7 wt% N-butylpyridine chloride catalyst. Weigh 10g of granular activated carbon, soak it with 200ml of deionized water at room temperature for 12 hours, then filter and wash it, and repeat this 3 times. Then place the activated carbon in the oven, 120 oC Let dry for 12 hours. at 650 o C Under oxygen-free conditions, 150ml / min of ammonia gas and 50ml / min of nitrogen gas were introduced for 5 hours, then the ammonia gas was turned off, and then gradually lowered to room temperature. At this time, the nitrogen doping amount in the bulk phase of activated carbon was 2.30%. Weigh 1.47g of N-butylpyridine chloride, and add 0.072g of chloroauric acid (HAuCl 4 ·3H 2 O), at a temperature of 130 o Mix evenly under C, and form the ionic liquid mixed solution after fully dissolving for 30 minutes. At room temperature, 10 g of nitrogen-doped activated carbon was added to the ionic liquid mixed solution, stirred fo...
Embodiment 2
[0035]Nitrogen-doped mesoporous carbon supported catalyst with 8.59 wt% Cu, 0.75 wt% Bi and 22.8 wt% N-hexylpyridine chloride. Weigh 10 g of granular mesoporous carbon, soak in 200 ml of deionized water at room temperature for 12 hours, then filter and wash, and repeat this 3 times. Then place the activated carbon in the oven, 120 oC Let dry for 12 hours. at 650 o C Under oxygen-free conditions, after passing through 100ml / min of ethylamine vapor and 50ml / min of nitrogen for 5 hours, turn off the ethylamine, and then gradually drop to room temperature. At this time, the nitrogen doping amount in the mesoporous carbon phase is 3.70 %. Weigh 2.28g of N-hexylpyridine chloride, and add 0.1201g of bismuth chloride (BiCl 3 ) and 2.3044g copper chloride (CuCl 2 2H 2 O), at a temperature of 120 o Mix evenly under C, and form the ionic liquid mixed solution after fully dissolving for 30 minutes. At room temperature, 10 g of nitrogen-doped mesoporous carbon was added to the ioni...
Embodiment 3
[0038] Nitrogen-doped activated carbon supported on 0.35 wt% Au and 15.0 wt% N-octylpyridine chloride catalyst. Weigh 10g of granular activated carbon, soak it with 200ml of deionized water at room temperature for 12 hours, then filter and wash it, and repeat this 3 times. Then place the activated carbon in the oven, 120 oC Let dry for 12 hours. at 650 o C Under anaerobic conditions, after passing through 110ml / min of nitrogen monoxide and 50ml / min of nitrogen for 6 hours, turn off the nitrogen monoxide, and then gradually lower to room temperature. At this time, the nitrogen doping amount in the bulk phase of activated carbon is 2.50%. . Weigh 1.5g of N-octylpyridine chloride, and add 0.035g of chloroauric acid (HAuCl 4 ·3H 2 O), at a temperature of 110 o Mix evenly under C, and form the ionic liquid mixed solution after fully dissolving for 30 minutes. At room temperature, 10 g of nitrogen-doped activated carbon was added to the ionic liquid mixed solution, stirred fo...
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