Propane dehydrogenation catalyst, preparation method thereof and method for preparing propylene through propane dehydrogenation
A propane dehydrogenation and catalyst technology, applied in the direction of catalyst activation/preparation, catalyst, metal/metal oxide/metal hydroxide catalyst, etc., can solve complex preparation process, environmental pollution, low propane conversion rate and propylene selectivity, etc. problem, to achieve the effect of simple preparation process, high conversion rate of propane and good catalytic performance
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[0023] The present invention also provides a method for preparing a propane dehydrogenation catalyst, wherein the preparation method comprises: immersing the carrier in a mixed solution containing Pt salt, Sn salt and Na salt, and then removing the solvent from the impregnated solution Drying and firing, wherein the carrier is a three-hole spherical mesoporous composite material, the average particle diameter of the three-hole spherical mesoporous composite material is 20-50 microns, the specific surface area is 150-600 square meters per gram, and the pores The volume is 0.5-1.5 ml / g, the pore size distribution is a three-peak distribution, and the most probable pore sizes corresponding to the three peaks are respectively 2-4 nm, 5-15 nm and 10-40 nm.
[0024] In the present invention, the amount of the carrier, Pt salt, Sn salt and Na salt is such that in the prepared propane dehydrogenation catalyst, based on the total weight of the propane dehydrogenation catalyst, the conte...
Embodiment 1
[0060] This example is used to illustrate the propane dehydrogenation catalyst and its preparation method.
[0061] (1) Preparation of three-porous spherical mesoporous composites
[0062] Add 1.0 g (0.0001 mol) of triblock copolymer polyethylene glycol-polyglycerol-polyethylene glycol (P123) and 1.69 g (0.037 mol) of ethanol to 28 mL of acetic acid and sodium acetate at pH 4.4 In the buffer solution, stir at 15°C until P123 is completely dissolved, then add 6g (0.053mol) of trimethylpentane to the above solution, and stir at 15°C for 8 hours, then add 2.13g (0.014mol) ) tetramethoxysilane, then stirred at 15°C and pH 5 for 20 hours, and transferred the resulting solution to a polytetrafluoroethylene-lined reactor for oven crystallization at 60°C for 24 hours, The obtained crystallized product was suction filtered and washed four times with distilled water to obtain No. 1 mesoporous material filter cake;
[0063] At 80°C, cetyltrimethylammonium bromide and tetraethyl orthosili...
Embodiment 2
[0075] This example is used to illustrate the propane dehydrogenation catalyst and its preparation method.
[0076] (1) Preparation of three-porous spherical mesoporous composites
[0077] Add 1.0 g of triblock copolymer P123 and 1 g of ethanol (0.022 mol) to 28 mL of a buffer solution of acetic acid and sodium acetate with a pH value of 5, stir at 20°C until P123 is completely dissolved, and then add 2.86 g (0.025mol) of trimethylpentane was added to the above solution, and after stirring for 1 hour at 20°C, 1.07g (0.007mol) of tetramethoxysilane was added, and then at 20°C, the pH was 6 Stirred under the conditions for 30 hours, and the resulting solution was transferred to a polytetrafluoroethylene-lined reaction kettle, oven crystallized at 40 ° C for 40 hours, and the obtained crystallized product was suction filtered and washed four times with distilled water to obtain No. 1 mesoporous material filter cake;
[0078] At 100°C, cetyltrimethylammonium bromide and tetraeth...
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Abstract
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