Isobutane dehydrogenation catalyst and preparation method thereof and method for preparing isobutene from isobutane dehydrogenation
A dehydrogenation catalyst and isobutane technology, which is applied in the field of isobutane dehydrogenation catalyst and isobutane dehydrogenation to isobutene, can solve the problems of poor catalytic activity and stability, uneven dispersion of precious metal active components, etc., and achieve stability Good performance, reduce the risk of carbon deposition, and inhibit the deactivation effect
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[0040] The present invention has no special limitation on the conditions of the mixing and contacting, for example, the conditions of the mixing and contacting may include: a temperature of 25-60° C., a time of 10-72 hours, and a pH value of 1-7. 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.
[0041] According to a preferred embodiment of the present invention, the process of mixing and contacting the templating agent, potassium sulfate, acid agent and orthosilicate comprises: making the templating agent triblock copolymer polyoxyethylene-polyoxyisobutylene-polyoxyethylene F108 Added to the aqueous solution of hydrochloric acid, according to the molar feed ratio, triblock copolymer polyoxyethylene-polyoxyisobutylene-polyoxyethylene F108: potassium sulfate: water: hydrogen chloride = 1: 200-400: 10000-30000: 100-900 , sti...
Embodiment 1
[0076] This example is used to illustrate the isobutane dehydrogenation catalyst and its preparation method.
[0077] (1) Preparation of hexagonal mesoporous material carrier
[0078] 2g (1.4×10 -4 mol) template agent F108, 5.24g (0.03mol) of K 2 SO 4 Add it to 60g of hydrochloric acid solution with an equivalent concentration of 2 (2N), stir at 38°C until F108 is completely dissolved; add 4.2g (0.02mol) of tetraethyl orthosilicate to the above solution, stir at 38°C for 15min, Stand at 38°C for 24h; then transfer it to an agate-lined reactor, crystallize at 100°C for 24h, then filter and wash 4 times with deionized water, and then suction filter to obtain the raw material with a cubic center Im3m structure. powder; the raw powder having a cubic center of 1m3m structure was calcined in a muffle furnace at 400°C for 10 hours to remove the template agent to obtain the hexagonal mesoporous material carrier A1.
[0079] (2) Preparation of isobutane dehydrogenation catalyst
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Embodiment 2
[0098] This example is used to illustrate the isobutane dehydrogenation catalyst and its preparation method.
[0099] (1) Preparation of hexagonal mesoporous material carrier
[0100] 1.46g (1×10 -4 mol) template agent F108, 6.96g (0.04mol) of K 2 SO 4Add it to 60g of hydrochloric acid solution with an equivalent concentration of 2 (2N), stir at 38°C until F108 is completely dissolved; add 3.1g (0.015mol) of tetraethyl orthosilicate to the above solution, stir at 38°C for 15min, Stand still at 38°C for 24h; then transfer it to an agate-lined reactor, crystallize at 120°C for 30h, then filter and wash 4 times with deionized water, and then suction filter to obtain the raw material with a cubic center Im3m structure powder; the raw powder having a cubic center of 1m3m structure was calcined in a muffle furnace at 500°C for 15 hours to remove the template agent to obtain a hexagonal mesoporous material carrier A2.
[0101] (2) Preparation of isobutane dehydrogenation catalyst...
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