Preparation method for catalyst used in production of isobutene through cracking of methyl tert-butyl ether
A technology of methyl tert-butyl ether and catalyst, which is applied in the field of preparation of isobutylene catalysts from methyl tert-butyl ether cracking, can solve the problems affecting the improvement of catalyst reaction activity and selectivity, and the high content of MTBE cracking by-product dimethyl ether , small specific surface area, etc., to achieve strong hydrophobicity and lipophilicity, good catalytic performance, and increase the ratio of B acid/L acid
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preparation example Construction
[0033] 1. Sample preparation: Take 20 mg of the ground sample (particle size less than 200 mesh), press it into a thin slice with a diameter of 20 mm and place it in the infrared absorption cell, add 200 mg of the sample to the hanging cup at the lower end of the quartz spring, and pump the system to 1 ×10 -2 Pa, heated to 500°C for 1 hour to purify the sample, remove the adsorbate and water covering the surface of the sample;
[0034] 2. Decrease to room temperature under the above evacuation conditions, adsorb pyridine for 5 minutes, then raise the temperature to 160°C, equilibrate for 1 hour, desorb the physically adsorbed pyridine, use the pyridine gravimetric adsorption method to obtain the total acid content, and record the obtained infrared under the above conditions. Spectrum, where the band corresponding to B acid is 1545cm -1 , the band corresponding to L acid is 1455cm -1 , thus, the total acid content, B acid content and L acid content at 160°C are obtained;
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Embodiment 1
[0038] Silica sol, aluminum sol and Silicalite-1 molecular sieve crystallization liquid Si-1-A, and calculated on a dry basis (that is, silica sol is calculated as SiO 2 Al 2 o 3 Calculated, Silicalite-1 molecular sieve crystallization liquid is SiO 2 (the same below) was mixed at a weight ratio of 10:1:5, rolled into a ball, dried at 110°C for 3 hours, calcined at 500°C for 4 hours, then the material was treated with saturated water vapor at 300°C for 4 hours, and dried at 110°C for 3 hours to obtain catalyst C -1. The catalyst characterization data are listed in Table 1. Among them, the molecular sieve crystallization liquid Si-1-A is prepared by the following method: at room temperature, a tetrapropylammonium hydroxide solution with a concentration of 30wt% is added to tetrapropylammonium hydroxide solution, and the mixed slurry is stirred at 80° C. for 3 hours, and then Crystallized at 150°C for 48 hours and taken out to obtain Silicalite-1 molecular sieve crystallizat...
Embodiment 2
[0042] Same as Example 1, except that silica sol, aluminum sol and Silicalite-1 molecular sieve crystallization solution Si-1-A were mixed in a weight ratio of 15:2:4 on a dry basis. Catalyst C-2 was obtained, and the data are shown in Table 1.
[0043]
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