Catalyst for methanol oxidation and reforming for hydrogen making, manufacture method and uses
A technology of reforming hydrogen production and methanol oxidation, which is applied to the application of the above catalyst in the partial oxidation of methanol to hydrogen production. The preparation of the above catalyst, high stability, high selectivity and low copper catalyst field can solve the problem of methanol production in the shift reaction process. The hydrogen process is complicated, the stability problem has not been solved, and it is not conducive to the mobile hydrogen source of hydrogen production, etc., to achieve high methanol utilization, simplified control, and good temperature resistance
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Embodiment 1
[0032] 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 to 100 mesh and sieved, and pressed into tablets. The catalyst weight composition obtained is: 0.1% CuO-60% ZnO-39.9% Cr 2 o 3 .
Embodiment 2
[0034] 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
[0036] 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, and then bake at 500°C for 3 hours to obtain the finished catalyst (0.45%CuO-5%ZnO-3.6%Cr2 o 3 ) / 90.95%Al 2 o 3 (wt%).
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