Hydrogen type ZSM-35/EU-1 eutectic zeolite, aromatic isomerization catalyst, preparation method and application
A ZSM-35, eutectic zeolite technology, applied in catalyst activation/preparation, physical/chemical process catalysts, molecular sieve catalysts, etc., can solve the problem of high non-aromatic hydrocarbon content, affecting the yield and energy consumption of aromatic hydrocarbon complexes, and reducing the purity of benzene And other issues
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Embodiment 1
[0073] Add the EU-1 zeolite into the NaOH solution, stir evenly, then add ethylenediammonium, silica sol, silica-alumina microspheres and water, and stir evenly. Transfer the solution to a stainless steel kettle, take it out after crystallization at 200°C for 20 hours, wash it with water until neutral after cooling to room temperature, and dry it at 100°C after suction filtration to obtain different SiO 2 / Al 2 o 3 The ZSM-35 / EU-1 eutectic zeolite.
Embodiment 2
[0075] Add the EU-1 zeolite into the NaOH solution, stir evenly, then add pyrrolidine, butanediammonium, silica sol and water, and stir evenly. Transfer the solution to a stainless steel kettle, take it out after crystallization at 220°C for 18 hours, cool to room temperature, wash with water until neutral, and dry at 100°C after suction filtration to obtain different SiO 2 / Al 2 o 3 The ZSM-35 / EU-1 eutectic zeolite.
[0076] Catalyst preparation
Embodiment 3
[0078] Containing 80.0w% ZSM-35 / EU-1 eutectic zeolite (SiO 2 / Al 2 o 3 =15), 3.0w% Re, 17.0w% alumina, catalyst C3.
[0079] SiO synthesized in embodiment 1 2 / Al 2 o 3 100 ZSM-35 / EU-1 eutectic zeolite, fully mixed with pseudo-boehmite powder, added 3.0w% nitric acid solution and mixed evenly, extruded into strips using cylindrical orifice; cylindrical strips at room temperature After standing for 4 hours, dry at 120°C for 2 hours, and bake at 500°C in the air for 4 hours to make a catalyst support; -1 In the ammonium chloride solution, exchange at 60-90°C for 2 hours, wash with deionized water, and filter; the exchanged support is immersed in a solution containing ammonium perrhenate for 12 hours at room temperature, and then dried at 120°C Calcined at 500°C for 2 hours for 4 hours, and reduced in hydrogen at 500°C for 4 hours to prepare catalyst C3.
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