Catalyst used for preparing 2-alkylanthraquinone, and preparation method and application thereof
A technology of alkyl anthraquinone and catalyst is applied in the field of composite acid catalyst and preparation thereof, and can solve the problems of insufficient performance of molecular sieve, unsatisfactory reaction effect and low selectivity, etc.
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Embodiment 1
[0030] The preparation steps of a preparation method of the catalyst of the present invention are as follows:
[0031] (1) Weigh 30 grams of Beta zeolite, 40 grams of hexahydrate La(NO 3 ) 3 ·6H 2 O was mixed thoroughly with 150 ml of water, and dried at 120°C for 6 hours to obtain Beta zeolite containing rare earth metals.
[0032] (2) Add 105 grams of Zr(NO 3 ) 4 ·5H 2 O, 14 grams of ammonium sulfate, 150 grams of water and 35 grams of aluminum hydroxide are thoroughly mixed, and dried at 100°C for 12 hours to obtain aluminum oxide containing zirconium and sulfate radicals.
[0033] (3) The Beta zeolite containing rare earth metals obtained in step (1) and the alumina containing zirconium and sulfate groups obtained in step (2) are thoroughly mixed, and then an appropriate amount of water is added, fully kneaded into a plastic paste, and extruded into Four-leaf clover strips in cross section were dried at 180°C for 8 hours to obtain the catalyst of the present invention, numbered E...
Embodiment 2~7
[0037] The preparation method of the catalyst in each example is the same as that in Example 1, and the difference lies in the composition, evaluation conditions and evaluation results. The specific catalyst composition is shown in Table 1, the evaluation conditions are shown in Table 2, and the evaluation results are shown in Table 3.
Embodiment 8
[0039] A preparation method of the catalyst of the present invention is the same as that of Example 3. The difference is that the catalyst preparation step (1) and step (2) are combined together, that is, La(NO 3 ) 3 ·6H 2 O, Beta zeolite, ammonium sulfate, Zr(NO 3 ) 4 ·5H 2 O, alumina, nitric acid and water are fully kneaded into a plastic paste, extruded into a four-leaf clover strip, dried at 180°C for 8 hours to obtain the catalyst of the present invention, number E-8. The composition of the catalyst is shown in Table 1. The evaluation conditions are shown in Table 2, and the evaluation results are shown in Table 3.
[0040]
PUM
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