Isobutane dehydrogenation catalyst and preparation method thereof and method for preparing isobutene from isobutane dehydrogenation
A dehydrogenation catalyst, isobutane technology, applied in catalyst activation/preparation, catalyst, molecular sieve catalyst and other directions, can solve the problems of uneven dispersion of precious metal active components, poor catalytic activity and stability, complex preparation process, etc. The effect of carbon deposition risk, high membrane surface flow rate, and simple preparation process
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[0048] According to the present invention, in step (b), the preparation method of the silica gel preferably comprises: contacting water glass, inorganic acid solution, n-butanol and glycerol.
[0049] Preferably, the conditions for contacting the water glass with the inorganic acid include: the temperature can be 10-60°C, preferably 20-40°C; the time can be 1-5h, preferably 1.5-3h, and the pH value is 2-4 . In order to increase the pore size of the prepared silica gel, preferably, the weight ratio of the amount of water glass, inorganic acid solution, n-butanol and glycerol is 3-6:1:0.8-2.5:0.8-2.5, more preferably Preferably, the water glass, inorganic acid solution, n-butanol and glycerol are used in a weight ratio of 3-6:1:1:1. In order to be more conducive to the uniform mixing between the various substances, the contact of the water glass, the inorganic acid solution, n-butanol and glycerol is preferably carried out under stirring conditions.
[0050] According to the p...
Embodiment 1
[0084] This example is used to illustrate the isobutane dehydrogenation catalyst and its preparation method.
[0085] (1) Preparation of spherical double mesoporous composite support
[0086] Dissolve 6g (0.001mol) of triblock copolymer surfactant P123 in 10ml of hydrochloric acid aqueous solution with a pH value of 4 and 220ml of deionized aqueous solution, stir for 4h until P123 dissolves to form a transparent solution, and then add it to the transparent solution Add 6g (0.08mol) of n-butanol and stir for 1h, then place it in a water bath at 40°C, slowly add 12.9g (0.062mol) of tetraethyl orthosilicate into the solution, and keep the temperature at about 40°C. Stirring for 24 hours at a pH value of 4.5, and then hydrothermally treating at 100°C for 24 hours, and then obtaining mesoporous molecular sieve material A1 with three-dimensional cubic channels;
[0087] Water glass with a concentration of 15% by weight, sulfuric acid solution with a concentration of 12% by weight, ...
Embodiment 2
[0109] This example is used to illustrate the isobutane dehydrogenation catalyst and its preparation method.
[0110] (1) Preparation of spherical double mesoporous composite carrier
[0111] Dissolve 6g (0.001mol) of triblock copolymer surfactant P123 in 10ml of hydrochloric acid aqueous solution with a pH value of 4 and 220ml of deionized aqueous solution, stir for 4h until P123 dissolves to form a transparent solution, and then add it to the transparent solution Add 6.7g (0.09mol) n-butanol and stir for 1h, then place it in a water bath at 40°C, slowly add 10.4g (0.05mol) ethyl tetrasilicate to the solution dropwise, and keep the temperature at about 40°C Stirring for 24 hours at a pH value of 5, and then hydrothermally treating at 90°C for 36 hours, and then obtaining mesoporous molecular sieve material A2 with three-dimensional cubic channels;
[0112] Water glass with a concentration of 15% by weight, sulfuric acid solution with a concentration of 12% by weight, n-butan...
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