Method for synthesizing ZSM-5 zeolite with multilevel pore canals
A synthesis method, ZSM-5 technology, applied in chemical instruments and methods, crystalline aluminosilicate zeolite, borocarbane silicone crystalline aluminosilicate zeolite, etc., can solve the problems of unsuitable catalytic materials and achieve rich content The effects of specific surface area, reduced production cost, and simple operation process
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Embodiment 1
[0033] Stir 30ml of methyl orthosilicate, 6g of polyethylene glycol and 30ml of 0.01mol / L acetic acid solution evenly, seal it, and stir at 0°C for 50min. The obtained sol was poured into a polytetrafluoroethylene test tube or a glass tube, and aged in a water bath at 30°C for one day to obtain a wet silica gel column. Then soak the silica gel column with 0.01mol / L ammonia water to prepare mesopores. Then soak the column with 0.1mol / L nitric acid solution, distilled water, 30% ethanol / water ethanol solution and Tween 80 for 6 hours, finally dry and roast to obtain the silica gel monolithic column B 1 .
Embodiment 2
[0035] According to the mass ratio of 1.25 sucrose: 0.14H 2 SO 4 : 5 water to make a solution, put the silica gel monolithic column B1 into it and soak for 30 minutes, then dry at 100°C for 6 hours, 160°C for 6 hours, repeat the process of soaking, drying, and polymerization once, and then carbonize at 900°C for 4 hours to obtain carbon Silicon composite sample E1.
Embodiment 3
[0037] 0.038 gram of sodium aluminate, 0.08 gram of sodium hydroxide, 1 gram of tetraethylammonium hydroxide solution and 2 grams of water were mixed and stirred evenly, and then this solution was poured into a reaction kettle equipped with 1.3 gram of carbon-silicon complex E1, Stir to make it fully wet, seal the reactor and crystallize at 150°C for 48 hours. After crystallization, cool, filter and wash, then dry in an oven at 100-110°C for 3-4 hours, and then burn the resultant in a muffle furnace at 600°C for 5 hours to obtain the product multi-level channel ZSM-5 , denoted as A1.
[0038] The XRD spectrum of A1 is shown in Figure 1. It can be seen from Figure 1 that all the figures have diffraction peaks at 2θ angles of 7.9°, 8.9°, 23.1°, 23.9°, and 24.4°. The diffraction peaks at these five places are The characteristic peak of ZSM-5 shows that the crystal form of the product synthesized in this example is ZSM-5.
[0039] The SEM image of A1 is shown in Figure 3. It can...
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