Composite material and its preparation method and catalyst as well as its preparation method and application and method for propane dehydrogenation to propylene
A composite material and catalyst technology, which is applied in the direction of molecular sieve catalysts, physical/chemical process catalysts, chemical instruments and methods, etc., can solve the problems of unstable mesopore structure, low propane conversion rate and low propylene selectivity, and achieve simple post-processing, Good dehydrogenation activity and selectivity, good product repeatability
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[0043] Preferably, in step (1), 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.
[0044] 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.
[0045] 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 a...
preparation example 1
[0076] Preparation Example 1: Preparation of composite material F1 containing spherical mesoporous molecular sieve C1 and ES955 silica gel A
[0077] (1) Add 1.5g (0.004mol) template agent CTAB (cetyltrimethylammonium bromide) and 1.5ml (0.002mol) polyethylene glycol octylphenyl ether (Triton-X100) Into the solution containing 37% by weight of hydrochloric acid (29.6g) and water (75g), stirred until CTAB was completely dissolved at 40°C; then 4.35g (0.02mol) ethyl orthosilicate was added to the above solution, in Stir at 40°C for 15 minutes, then transfer the resulting solution to a polytetrafluoroethylene-lined reactor, crystallize at 120°C for 24h, then filter and wash with deionized water 4 times, then suction filter and Drying to obtain the raw powder of mesoporous material; calcining the raw powder of mesoporous material at 600°C for 24 hours to remove the template agent to obtain spherical mesoporous molecular sieve C1;
[0078] (2) At 25° C., 20 g of spherical mesoporo...
preparation example 2
[0085] Preparation Example 2: Preparation of composite material F2 containing spherical mesoporous molecular sieve C2 and ES955 silica gel B
[0086] (1) Add 0.75g (0.002mol) template agent CTAB (cetyltrimethylammonium bromide) and 3ml (0.004mol) polyethylene glycol octylphenyl ether (Triton-X100) to In the solution that contains 37% by weight of hydrochloric acid (29.6g) and water (75g), stir until CTAB dissolves completely at 40 ℃; Then 4.35g (0.02mol) ethyl orthosilicate is added in the above-mentioned solution, at 40 After stirring for 15 minutes at ℃, the resulting solution was transferred to a polytetrafluoroethylene-lined reactor, crystallized at 100℃ for 24 h, then filtered and washed 4 times with deionized water, then suction filtered and dried , to obtain the raw powder of the mesoporous 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 C2;
[0087] (2) At...
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