Catalyst for preparing 2-alkylanthraquinone, preparation method and application thereof
A technology of alkyl anthraquinone and catalyst, which is applied in the field of composite acid catalyst and its preparation, can solve the problems of unsatisfactory reaction effect, low selectivity, insufficient performance of molecular sieve and the like
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Embodiment 1
[0030] The preparation steps of a kind of preparation method of the catalyst of the present invention are as follows:
[0031] (1) Weigh 30 grams of Beta zeolite, 40 grams of La (NO) hexahydrate 3 ) 3 ·6H 2 Mix O thoroughly with 150 ml of water, mix well, and dry at 120° C. for 6 hours to obtain Beta zeolite containing rare earth metals.
[0032] (2) 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 alumina containing zirconium and sulfate radicals.
[0033] (3) The rare earth metal-containing Beta zeolite obtained in step (1) and the zirconium- and sulfate-containing alumina obtained in step (2) are fully mixed, and then an appropriate amount of water is added, fully kneaded into a plastic paste, and extruded into a The cross-section is a strip of four-leaf clover, and dried at 180° C. for 8 hours to obtain the catalyst of the present in...
Embodiment 2~7
[0036] The preparation method of the catalyst of each embodiment is the same as that of Example 1, except that the composition, evaluation conditions and evaluation results are different. 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
[0038] A preparation method of the catalyst of the present invention is the same as that of Example 3, except that the catalyst preparation step (1) and step (2) are combined together, namely 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 strip with a four-leaf clover section, and dried at 180 ° C for 8 hours to obtain the catalyst of the present invention, number E-8, and 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.
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