Preparation method of methanol synthesis catalyst
A technology for synthesizing methanol and catalysts, applied in the preparation of organic compounds, chemical instruments and methods, preparation of hydroxyl compounds, etc., can solve the problems of easy deactivation of auxiliary components and uneven distribution of auxiliary agents on the surface of catalysts, and increase the effective surface area. , Improve the overall activity and thermal stability, the effect of saving dosage
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Embodiment 1
[0017] 1) Add the co-solution containing 30g of copper nitrate and 11.8g of zinc nitrate into the sodium bicarbonate solution for mixing, and the mixed solution is neutralized at 50°C until the final pH is 6.5, and the copper-zinc suspension is obtained after aging solution; the ammonium bicarbonate solution is added to the solution containing 16.2g of aluminum nitrate, and after neutralization, it is mixed with the copper-zinc solution in parallel to obtain the parent body, which is washed with deionized water and filtered to NaNO 3 Disappeared, after repeating the filter press process for 3 times, dried at 100°C for 12 hours, and then roasted at 250°C for 5 hours to prepare a mixture containing copper, zinc and aluminum, which was tabletted, crushed, and sieved into 20-40 The mesh granules are obtained to obtain the parent granules.
[0018] 2) Prepare a potassium carbonate solution with a concentration of 1%, then impregnate the matrix particles with the same volume of the ...
Embodiment 2
[0020] Use the parent particle prepared in Example 1, then prepare the potassium carbonate solution with a concentration of 5.7%, impregnate the parent particle with the equal volume of the solution under vacuum conditions, the impregnated material is dried at 130° C., and the dried material is dried at 300 After calcination at ℃ for 4 hours, the finished catalyst C2 was obtained. The physical and chemical properties of C2 are shown in Table 1.
Embodiment 3
[0022] Use the parent particle prepared in Example 1, then prepare a potassium permanganate solution with a concentration of 12%, impregnate the parent particle with the same volume of the solution under vacuum conditions, and dry the impregnated material at 120 ° C. The dried material The finished catalyst C3 was obtained after calcination at 250° C. for 5 h. The physical and chemical properties of C3 are shown in Table 1.
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