N-alkane isomerization catalyst and preparation method thereof
A technology of n-alkane and catalyst, which is applied in the field of n-alkane isomerization catalyst and its preparation, can solve the problems of selectivity and catalytic activity that cannot meet the requirements of n-alkane isomerization, and achieve high catalytic activity and multi-branched The effect of isomerization selectivity
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[0014] The present invention provides a kind of preparation method of n-alkane isomerization catalyst, this method comprises: (1) active metal component platinum is supported on the alumina carrier, obtains the first intermediate after drying; (2) step (1) performing a reduction treatment on the obtained first intermediate to obtain a second intermediate; (3) loading the heteropolyacid on the second intermediate obtained in step (2) and drying to obtain a catalyst.
[0015] In the method of the present invention, the impregnation method can be used to support the metal platinum component on the alumina. The impregnation method can be a saturated impregnation method or a supersaturated impregnation method. The saturated impregnation method is preferred in the present invention. For example, with respect to 100 parts by weight of an alumina carrier, 70-150 mL of platinum containing 0.14-20 mg / mL can be used. The aqueous solution of the platinum compound impregnates the alumina s...
Embodiment 1
[0030] 10g γ-Al 2 o 3Put it into a rotary evaporator, add 15 mL of chloroplatinic acid solution with a platinum content of 6.67 mg / mL, soak at 60° C. for 4 hours, and then evaporate to dryness to obtain the first intermediate.
[0031] The above-mentioned first intermediate is loaded into the reactor, and the reduction treatment is carried out to obtain the second intermediate, wherein the conditions of the reduction treatment include: the hydrogen volume space velocity is 1200 hours -1 , the reduction temperature is 480°C, and the reduction time is 4 hours.
[0032] Then use 15mL of 0.33g / mL aqueous solution of phosphotungstic acid to impregnate the above-mentioned second intermediate at 60°C for 2 hours, and then rotate to dryness to obtain the catalyst, whose composition is shown in Table 1.
Embodiment 2
[0034] 10gη-Al 2 o 3 Put it into a rotary evaporator, add 8 mL of chloroplatinic acid solution with a platinum content of 5.63 mg / mL, soak at 60° C. for 4 hours, and dry by rotary evaporation to obtain the first intermediate.
[0035] The above-mentioned first intermediate is loaded into the reactor, and the reduction treatment is carried out to obtain the second intermediate, wherein the conditions of the reduction treatment include: the hydrogen volume space velocity is 30 hours -1 , the reduction temperature was 200° C., and the reduction time was 8 hours to obtain the second intermediate.
[0036] Then, 8 mL of 0.38 g / mL silicotungstic acid aqueous solution was used to impregnate the above-mentioned second intermediate at 60°C for 2 hours, and then evaporated to dryness to obtain the catalyst, whose composition is shown in Table 1.
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