Catalytic cracking of organic compounds, using modified y zeolite
An organic compound, catalytic cracking technology, used in catalytic cracking, physical/chemical process catalysts, molecular sieve catalysts, etc., can solve problems such as dry gas increase
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Embodiment 1
[0035] Embodiment 1: the preparation of modified USY type zeolite
[0036] 30 g of CBV300 (Zeolyst International, silica:alumina ratio 5.1:1) was mixed with 14.4 g H 4 EDTA at 450cm 3 The solutions in distilled water were contacted and stirred vigorously at 100 °C for 24 h. The solids were then separated from the solution using standard procedures: the suspension was cooled, filtered, washed with distilled water and dried overnight at 65°C.
[0037] Make 20g of the obtained solid at 65°C, 2.4g NaOH at 600cm 3 The solution in distilled water was subjected to alkali treatment for 30 minutes under vigorous stirring, the resulting solid was separated from the solution according to the procedure described in the previous paragraph, and 15 g of this solid was treated with 9.2 g of NaH at 100 °C under vigorous stirring. 2 EDTA at 225cm 3 The solution in distilled water was treated for 6 hours. Finally, the solid was separated from the liquid, and in 0.1M NH 4 NO 3 The solution...
Embodiment 2
[0038] Example 2: Hydrothermal treatment of the modified zeolite.
[0039] The modified zeolite obtained according to the method described in Example 1 was calcined in a furnace at 750° C. for 5 hours in a neat powder form under a 100% steam atmosphere.
Embodiment 3
[0040] Example 3: Exchange of the modified zeolite with RE and hydrothermal treatment of the modified zeolite exchanged with RE.
[0041] The modified zeolite obtained according to the method described in Example 1 utilizes 0.1M RECl 3 The aqueous solution was subjected to an ion exchange process at 80°C for 2h under vigorous stirring and reflux conditions. The weight ratio of solution to zeolite used was 10. The solid was then isolated by filtration, washed with deionized water until the chloride was completely removed, and dried overnight at 100°C. The obtained solid was dried in an oven at 500° C. for 3 hours. This procedure was repeated a second time to obtain a final solid with an RE content of 3.5% by weight relative to REO. Finally, the resulting solid was calcined in a furnace at 800° C. for 5 hours in the form of a neat powder under a 100% steam atmosphere.
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