Isobutane dehydrogenation catalyst with spherical small-pore mesoporous silica gel composite material as supporter as well as preparation method and application of isobutane dehydrogenation catalyst
A dehydrogenation catalyst and isobutane technology, applied in the direction of carbon compound catalysts, catalysts, catalyst carriers, etc., can solve the problems of uneven dispersion of precious metal active components, poor catalytic activity and stability, and reduce the risk of carbon deposition and conditions Ease of control, enhanced selectivity effects
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[0037] Preferably, in step (a), the mixing and contacting conditions include: a temperature of 25-60°C, and a time of 0.1-48h. 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.
[0038] In the present invention, the amount of the templating agent, the nonionic surfactant and the silicon source can vary within a wide range, such as the molar ratio of the template agent, the nonionic surfactant and the silicon source. Be (0.1-0.6): (0.1-0.5): 1; More preferably, the molar ratio of template agent, described nonionic surfactant and described silicon source consumption is (0.1-0.3): (0.1-0.3 ):1.
[0039] In the present invention, the silicon source can be various silicon sources conventionally used in the art, preferably the silicon source is ethyl orthosilicate, methyl orthosilicate, propyl orthosilicate, sodium orthosilicate ...
Embodiment 1
[0088] This example is used to illustrate the isobutane dehydrogenation catalyst and its preparation method.
[0089] (1) Preparation of carrier
[0090] Add 1.5g (0.004mol) of template agent CTAB (cetyltrimethylammonium bromide) and 1.5ml (0.002mol) of polyethylene glycol octylphenyl ether (Triton-X100) to 37 In a solution of weight % hydrochloric acid (29.6g) and water (75g), stir at 40°C until CTAB is completely dissolved; then add 4.35g (0.02mol) ethyl orthosilicate to the above solution, at 40°C After stirring for 15 minutes, the obtained solution was transferred to a polytetrafluoroethylene-lined reactor, crystallized at 120° C. for 24 h, then filtered and washed 4 times with deionized water, then suction filtered and dried to obtain Raw powder of mesoporous material; calcining the raw powder of mesoporous material at 600°C for 24 hours to remove template agent to obtain spherical mesoporous molecular sieve A1;
[0091] The water glass with a concentration of 15% by we...
Embodiment 2
[0110] This example is used to illustrate the isobutane dehydrogenation catalyst and its preparation method.
[0111] (1) Preparation of carrier
[0112] Add 0.75g (0.002mol) of template agent CTAB (cetyltrimethylammonium bromide) and 3ml (0.004mol) of polyethylene glycol octylphenyl ether (Triton-X100) to 37 wt. % hydrochloric acid (29.6g) and water (75g) solution, stirred at 40°C until CTAB was completely dissolved; then added 4.35g (0.02mol) ethyl orthosilicate to the above solution, stirred at 40°C 15 minutes, then the resulting solution was transferred to a polytetrafluoroethylene-lined reactor, crystallized at 100 ° C for 24 h, then filtered and washed with deionized water for 4 times, then suction filtered and dried to obtain a medium The raw powder of the pore material; calcining the raw powder of the mesoporous material at 600° C. for 24 hours to remove the template agent to obtain spherical mesoporous molecular sieve A2;
[0113] The water glass with a concentratio...
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