Isobutane dehydrogenation catalyst, preparation method thereof, and method for producing isobutene from isobutane dehydrogenation
A technology of dehydrogenation catalyst and isobutane, which is applied in the direction of catalyst activation/preparation, catalyst, molecular sieve catalyst, etc., can solve the problems of poor catalytic activity and stability, uneven dispersion of noble metal active components, etc., and achieve high selectivity and low The risk of carbon deposition and the effect of low carbon deposition
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[0038] Preferably, in step (a), the conditions of the mixed contact include: a temperature of 25-60° C. and a time of 0.1-48 h. In order to be more conducive to the uniform mixing of various substances, according to a preferred embodiment of the present invention, the mixing and contacting is carried out under stirring conditions.
[0039] In the present invention, the consumption of described templating agent, nonionic surfactant and industrial sodium silicate can change in a wide range, for example described template agent, described nonionic surfactant and described industrial sodium silicate The molar ratio of the amount used is 0.1-0.6:0.1-0.5:1; more preferably, the molar ratio of the template agent, the nonionic surfactant and the industrial sodium silicate is 0.1-0.3:0.1-0.3: 1.
[0040] In the present invention, the industrial sodium silicate refers to the industrial sodium silicate having the parameters specified in GB / T 4209-2008.
[0041] Preferably, in the step (b...
Embodiment 1
[0073] This example is used to illustrate the isobutane dehydrogenation catalyst and its preparation method.
[0074] (1) Preparation of the carrier
[0075] 1.5 g (0.004 mol) of templating agent CTAB (hexadecyl trimethyl ammonium bromide) and 1.5 ml (0.002 mol) of polyethylene glycol octyl phenyl ether (Triton-X100) were added to the solution containing 37 In the solution of wt% hydrochloric acid (29.6g) and water (75g), stir at 40°C until CTAB is completely dissolved; then add 4.6g of industrial sodium silicate to the above solution, stir at 40°C for 15 minutes, and then The obtained solution was transferred to a polytetrafluoroethylene-lined reaction kettle, crystallized at 120°C for 24 hours, then filtered and washed with deionized water for 4 times, then suction filtered and dried to obtain the raw mesoporous material powder ; The mesoporous material raw powder was calcined at 600° C. for 24 h, the template agent was removed, and the spherical mesoporous molecular sieve ...
Embodiment 2
[0097] This example is used to illustrate the isobutane dehydrogenation catalyst and its preparation method.
[0098] (1) Preparation of the carrier
[0099] 0.75 g (0.002 mol) of templating agent CTAB (hexadecyl trimethyl ammonium bromide) and 3 ml (0.004 mol) of polyethylene glycol octyl phenyl ether (Triton-X100) were added to a solution containing 37 wt. % hydrochloric acid (29.6g) and water (75g), stir at 40°C until CTAB is completely dissolved; then add 4.35g of industrial sodium silicate to the above solution, stir at 40°C for 15 minutes, and then The obtained solution was transferred to a polytetrafluoroethylene-lined reaction kettle, crystallized at 100° C. for 24 hours, then filtered and washed with deionized water for 4 times, then suction filtered and dried to obtain the raw mesoporous material powder; The mesoporous material raw powder was calcined at 600° C. for 24 hours to remove the template agent to obtain spherical mesoporous molecular sieve material C2.
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Abstract
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