Catalyst for methanol oxidation and reforming for hydrogen making, manufacture method and uses
A technology for reforming hydrogen production and methanol oxidation, which is applied in chemical instruments and methods, hydrogen, inorganic chemistry, etc., can solve the complex process of methanol hydrogen production in the conversion reaction process, the stability problem is not solved, and it is not conducive to mobile hydrogen production. and other problems, to achieve the effect of high methanol utilization rate, control of CO generation, and simplified control
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Embodiment 1
[0033] Weigh 0.0607 g of copper nitrate, 44 g of zinc nitrate, and 13.2 g of ammonium dichromate, and dissolve all three components in 500 ml of distilled water as solution A; prepare 0.5 M sodium carbonate solution as solution B. Add 100ml of distilled water into the precipitation tank first, heat it to 40°C, then use two dropping funnels for solution A and solution B respectively, under rapid stirring (stirring speed is 400 rpm), and flow into the tank at the same speed middle. During the precipitation process, the pH is kept at about 7.5, the temperature is 40-45°C, and the sodium carbonate solution dropped in is 1.1 times the theoretically calculated value. After the precipitation is complete, age for 1 hour, wash until neutral, filter, and the product is oven-dried overnight , roasted at 500°C for 3 hours, the powder was ground and sieved with 100 meshes, and pressed into tablets. The catalyst weight composition obtained is: 0.1% CuO-60% ZnO-39.9% Cr 2 o 3 .
Embodiment 2
[0035]Weigh 6.0734 grams of copper nitrate, 43.8 grams of zinc nitrate, 9.9 grams of ammonium dichromate, and 3 grams of urea, mix and grind them evenly in a mortar, put them into a muffle furnace at 500 ° C for rapid decomposition, and then cool to 20 ° C, powder After the material is sieved with 100 meshes, it is rolled into a ball. The weight composition of the obtained catalyst is 10%CuO-60%ZnO-30%Cr 2 o 3 .
Embodiment 3
[0037] After dissolving 1.5 grams of copper nitrate, 21.2 grams of zinc nitrate, and 6.1 grams of ammonium dichromate into 40ml of aqueous solution, impregnate to 100 grams of Al 2 o 3 On the ball, dry at 110°C for 12 hours, then bake at 500°C for 3 hours to get the finished catalyst
[0038] (0.45%CuO-5%ZnO-3.6%Cr 2 o 3 ) / 90.95%Al 2 o 3 (wt%).
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