Synthetic method and application for composite molecular sieve
A technology of composite molecular sieve and synthesis method, which is applied in the field of synthesis of composite molecular sieves, can solve the problems of poor stability and low catalytic activity of catalysts, and achieve the effects of stable structure, simple steps and good technical effects
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Embodiment 1
[0022] (1) 600 grams of 40% silica sol, 10.1 grams of sodium aluminate (alumina content 42%), 41.6 grams of 30wt% tetraethylammonium hydroxide (TEAOH), 168.0 grams of tetraethylammonium bromide (TEABr), 16.0 grams of sodium hydroxide and 925.1 grams of water were mixed, stirred evenly at room temperature, and left to stand for 6 hours. Then crystallization was carried out at 200° C. for 48 hours.
[0023] (2) Take the milky white slurry obtained in the previous step, wash it 5 times with deionized water, and then vacuum-dry it for 12 hours.
[0024] (3) Take the solid obtained in the previous step and bake it in a muffle furnace at 550° C. for 6 hours.
[0025] Mix 20 grams of the synthesized mixed crystal molecular sieve with 20 grams of alumina, knead the mixed powder and dilute nitric acid (0.5% by weight) according to the weight ratio of 80:20, shape and dry. After calcining at 550° C. in air for 6 hours, the catalyst precursor of the present invention is obtained.
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Embodiment 2
[0029] (1) Get 3.5g of aluminum tert-butoxide (wt97%), 160g of 30wt% tetraethylammonium hydroxide, 8g of sodium hydroxide mix, then add 160g TEOS (wt98%) and 140g deionized water therein, at room temperature Stir well and let stand for 4 hours. Then crystallization was carried out at 200° C. for 48 hours.
[0030] (2) Take the milky white slurry obtained in the previous step, wash it 5 times with deionized water, and then vacuum-dry it for 12 hours.
[0031] (3) Take the solid obtained in the previous step and bake it in a muffle furnace at 550° C. for 6 hours.
[0032] Mix 20 grams of the synthesized mixed crystal molecular sieve with 20 grams of alumina, knead the mixed powder and dilute nitric acid (0.5% by weight) according to the weight ratio of 80:20, shape and dry. After calcining at 550° C. in air for 6 hours, the catalyst precursor of the present invention is obtained.
[0033] The prepared catalyst precursor is ion-exchanged three times with 10 wt % ammonium nitra...
Embodiment 3
[0036] (1) Take silica sol (wt40%) 747.1g, sodium metaaluminate (alumina content 42%) 12.3g, 30wt% tetraethylammonium hydroxide 468.5g, deionized water 583.7g, mix, at room temperature Stir well. Adjust the pH to 13 with 10% aqueous sodium hydroxide solution and let stand for 6 hours. Then crystallization was carried out at 170° C. for 72 hours.
[0037] (2) Take the milky white slurry obtained in the previous step, wash it 5 times with deionized water, and then vacuum-dry it for 12 hours.
[0038] (3) Take the solid obtained in the previous step and bake it in a muffle furnace at 550° C. for 6 hours.
[0039] Mix 20 grams of the synthesized mixed crystal molecular sieve with 20 grams of alumina, knead the mixed powder and dilute nitric acid (0.5% by weight) according to the weight ratio of 80:20, shape and dry. After calcining at 550° C. in air for 6 hours, the catalyst precursor of the present invention is obtained.
[0040] The prepared catalyst precursor is ion-exchang...
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