A kind of supported bimetallic component catalyst and its preparation method and glycerol hydrogenolysis reaction method
A metal component and catalyst technology, which is applied in the field of supported bimetallic component catalyst and its preparation and glycerol hydrogenolysis reaction, achieves good glycerol hydrogenolysis activity, large increase in selectivity, high catalytic glycerol hydrogenolysis activity and selectivity sexual effect
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[0029]According to another aspect of the present invention, the present invention also provides a preparation method of a supported bimetallic component catalyst, the method comprising the steps of:
[0030] 1) impregnating the support with a solution containing a compound of the first metal component selected from Group VIII, and then drying, calcining and reducing activation of the impregnated support in sequence to obtain a catalyst precursor containing the first metal component;
[0031] 2) impregnating the catalyst precursor obtained in step 1) with a solution containing a compound of a second metal component selected from Group VIB and / or VIIB in a reducing atmosphere, and then drying to remove the solvent.
[0032] The compound of the first metal active component is nitrate, acetate, sulfate, basic carbonate, chloride containing one or more elements of Pt, Pd, Ru, Rh, Ir At least one, the compound of the second metal active component is at least one of soluble compounds...
Embodiment 1
[0054] This example is used to illustrate the catalyst provided by the present invention and its preparation method.
[0055] According to the required metal salt content of equal volume impregnation method, be prepared with the impregnation solution of 30.6 milliliters of dichlorotetraammine platinum containing 23.5 g / liter of platinum. Decant the impregnation solution to 36 g γ-Al 2 o 3 Carrier (product of Changling Catalyst Factory, particle size 20-40 mesh, the same below), stir well at 20°C, let stand for 4 hours, dry at 120°C, roast at 350°C for 4 hours, and reduce with hydrogen at 350°C for 4 hours , the hydrogen pressure is 0.1 MPa. After reduction, it was lowered to room temperature, and 55.1 ml of ammonium tungstate aqueous solution containing 7.84 g / L of tungsten was added under a hydrogen atmosphere, allowed to stand for 2 hours, and then dried with hydrogen. Then by O 2 / N 2 The mixed gas with a volume ratio of 0.5% is passivated for 0.5 hours, and stored in ...
Embodiment 2
[0062] This example is used to illustrate the catalyst provided by the present invention and its preparation method.
[0063]According to the required metal salt content of the equal volume impregnation method, 30.6 milliliters of dichloro tetraammine platinum and rhodium chloride impregnation solution containing 23.5 grams per liter of platinum and 23.5 grams per liter of rhodium are prepared. Decant the impregnation solution to 36 g SiO 2 Carrier (Qingdao Ocean Chemical Factory), stirred at 15°C, allowed to stand for 6 hours, dried at 100°C, calcined at 450°C for 2 hours, reduced with hydrogen at 450°C for 2 hours, and the hydrogen pressure was 1 MPa. After reduction, it was lowered to room temperature, and 55.1 ml of perrhenic acid aqueous solution containing 13.1 g / L of rhenium was added under a hydrogen atmosphere, allowed to stand for 2 hours, and then dried with hydrogen. Then by O 2 / N 2 The mixed gas with a volume ratio of 0.8% was passivated for 2 hours, and store...
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