Catalyst for ethylbenzene and ethanol synthesis to realize shape-selectivity alkylation for diethylbenzene
A technology for p-diethylbenzene and shape-selective alkane, which is applied in the field of shape-selective alkylation catalysts, can solve problems such as serious disproportionation side reactions, shortage of petrochemical raw materials, etc., and achieves high selectivity, less side reactions, and good actual process effects. Effect
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Embodiment 1
[0026] Using SiO 2 / Al 2 o 3 42 grams of hydrogen-type HZSM-5 molecular sieve with a molar ratio of 140 and 12 grams of r-Al 2 o 3 Mix, then add 1.8 grams of Tianqing powder and mix evenly, then add a certain amount of 3% dilute nitric acid as a binder, knead well, carry out extrusion molding, dry at 120°C for 2 hours, and then roast at 540°C for 1 hour . The shaped zeolite is impregnated with a n-hexane solution of 15% active hydrogen siloxane modifier, dried at 120°C for 2 hours, and then calcined at 500°C for 3 hours, and the surface is modified by liquid-phase silicon deposition. Catalyst I was processed and the deposition amount of silicon dioxide was 6.7wt%.
Embodiment 2
[0028] The HZSM-5 molecular sieve prepared by the method described in Example 1 was impregnated with the obtained molecular sieve in 7.0% concentration of magnesium nitrate and 2.3% concentration of barium nitrate aqueous solution. After the impregnation, the remaining impregnation solution was filtered off. It was dried at 120°C for 3 hours, and then calcined at 540°C for 4 hours. The temperature was programmed to rise at a rate of 3°C / min. It was designated as catalyst II, with a loading of magnesia of 3.2% and a loading of barium oxide of 1.5%.
Embodiment 3
[0030] The HZSM-5 molecular sieve prepared by the method described in Example 1 was impregnated with the obtained molecular sieve in 6.5% concentration of cerium nitrate and 5.1% concentration of lanthanum nitrate aqueous solution. After the impregnation, the remaining impregnation solution was filtered off. It was dried at 120°C for 3 hours, and then calcined at 540°C for 4 hours. The temperature was programmed at a rate of 3°C / min. It was designated as Catalyst III, with a loading of cerium oxide of 3.5% and a loading of lanthanum oxide of 2.4%.
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