Catalyst for preparing dimethyl ether from methanol
A technology for the preparation of methanol and dimethyl ether, applied in the direction of catalyst carrier, physical/chemical process catalyst, ether preparation, etc., to achieve high anti-sintering properties, high selectivity, and good stability
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Embodiment 1
[0023] The niobium amine complex was dissolved in water to make a solution with a concentration of 0.12 g / ml, and 0.6% polyacrylamide (calculated as tetra-n-butoxy zirconium) was added at the same time. Add the above solution into tetra-n-butoxyzirconium, stir vigorously at 40°C for 30 minutes, then add the calculated amount of concentrated sulfuric acid into the above solution, continue vigorously stirring for 10 minutes, and then stand still at 60°C until a gel is formed. It was left at room temperature for 48 hours, aged at 80°C for 16 hours, dried at 120°C for 4 hours, and calcined at 600°C for 4 hours in an ammonia atmosphere to obtain catalyst B. The composition of the catalyst is shown in Table 1.
Embodiment 2
[0025] Mix 40% (weight concentration) silica sol and titanium sol, and stir evenly. Then quickly add niobium ethoxide liquid to the above solution, stir vigorously at 40°C for 30 minutes, then add the calculated amount of concentrated sulfuric acid into the above solution, continue vigorously stirring for 10 minutes, and then stand still at 60°C until a gel is formed . It was left at room temperature for 48 hours, aged at 80°C for 16 hours, dried at 120°C for 4 hours, and calcined in a carbon dioxide atmosphere at 500°C for 4 hours to obtain catalyst C. The composition of the catalyst is shown in Table 1.
Embodiment 3
[0027] The niobium oxalate solution was vacuum impregnated on HZSM-5 molecular sieve, and dried at 150°C for 2 hours. Then, the calculated amount of phosphoric acid solution was impregnated on the catalyst precursor, vacuum-dried at 120°C for 2 hours, and vacuum-calcined at 500°C for 4 hours to obtain catalyst E. The catalyst composition is shown in Table 1.
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