Isobutane dehydrogenation catalyst and 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, molecular sieve catalysts, chemical instruments and methods, etc., can solve the problems of uneven dispersion of noble metal active components, poor catalytic activity and stability, etc. The effect of carbon risk, good stability and good catalytic performance
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Embodiment 1
[0063] This example is used to illustrate the isobutane dehydrogenation catalyst and its preparation method.
[0064] The artificial zeolite A1 was calcined at 400° C. for 10 hours under the protection of nitrogen to perform heat activation treatment to remove the hydroxyl group and residual moisture of the artificial zeolite A1 to obtain the heat-activated zeolite carrier B1.
[0065] 0.080g H 2 PtCl 6 ·6H 2 O and 0.457g Zn(NO 3 ) 2 ·6H 2 O was dissolved in 100ml of deionized water to obtain a mixture solution, and 10 g of the thermally activated zeolite carrier B1 obtained after the aforementioned heat activation treatment was immersed in the mixture solution, and after immersion at 25°C for 5 hours, evaporated with a rotary evaporator The solvent water in the system was used to obtain a solid product, which was placed in a drying oven at a temperature of 120° C. and dried for 3 hours. Then in the muffle furnace, the temperature is 600 ℃ roasting 6h to obtain the isobu...
Embodiment 2
[0078] This example is used to illustrate the isobutane dehydrogenation catalyst and its preparation method.
[0079] The artificial zeolite A2 was calcined at 400° C. for 10 hours under the protection of nitrogen to carry out thermal activation treatment to remove the hydroxyl group and residual moisture of the artificial zeolite A2 to obtain the thermally activated zeolite carrier B2.
[0080] 0.080g H 2 PtCl 6 ·6H 2 O and 0.457g Zn(NO 3 ) 2 ·6H 2 O was dissolved in 100ml of deionized water to obtain a mixture solution, and 10 g of the heat-activated zeolite carrier B2 obtained after the aforementioned heat-activation treatment was immersed in the mixture solution, and after soaking at 25°C for 5 hours, evaporated with a rotary evaporator The solvent water in the system was used to obtain a solid product, which was placed in a drying oven at a temperature of 120° C. and dried for 3 hours. Then in the muffle furnace, the temperature is 600 ℃ roasting 6h to obtain the is...
Embodiment 3
[0086] The artificial zeolite A3 was calcined at 400° C. for 10 hours under the protection of nitrogen to perform thermal activation treatment to remove the hydroxyl group and residual moisture of the artificial zeolite A3 to obtain the thermally activated zeolite carrier B3.
[0087] 0.080g H 2 PtCl 6 ·6H 2 O and 0.457g Zn(NO 3 ) 2 ·6H 2 O was dissolved in 100ml of deionized water to obtain a mixture solution, and 10 g of the thermally activated zeolite carrier B3 obtained after the aforementioned heat activation treatment was immersed in the mixture solution, and after immersion at 25°C for 5 hours, evaporated with a rotary evaporator The solvent water in the system was used to obtain a solid product, which was placed in a drying oven at a temperature of 120° C. and dried for 3 hours. Then in the muffle furnace, the temperature is 600 ℃ roasting 6h to obtain the isobutane dehydrogenation catalyst Cat-3 (based on the total weight of the isobutane dehydrogenation catalyst...
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