Method for synthesizing cyclohexylbenzene by using fixed bed
A technology of cyclohexylbenzene and fixed bed, which is applied in the chemical industry and can solve the problem of low selectivity of cyclohexylbenzene
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Embodiment 1
[0033] (1) Preparation of hydroalkylation catalyst
[0034] At room temperature, weigh a certain amount of RuCl 3 ·3H 2 Dissolve O in deionized water, add molecular sieves, stir for 10 minutes, heat up to 60°C, add 10% ammonium carbonate solution dropwise, stop dropping when pH>8, stir for 30 minutes, measure pH value, if pH 8, then stirred for 30 min, and measured the pH value, and so on until pH > 8, and then continued to stir for 2 h. Filtration, washing, drying, roasting, tablet forming, sieving, and standby.
[0035] (2) Preparation of transalkylation catalyst
[0036] Weigh 30g of USY molecular sieve with a silicon-aluminum ratio of 12, add 120g of citric acid aqueous solution with a mass concentration of 2%, treat at 80°C for 4h, filter, wash, dry, roast at 580°C for 4h, press into tablets, sieve, and set aside.
[0037] (3) Reaction process
[0038] Firstly, the hydroalkylation catalyst and the transalkylation catalyst were loaded respectively, and the two ends of ...
Embodiment 2
[0044] Catalyst preparation is the same as in Example 1.
[0045] reaction process
[0046] Firstly, the hydroalkylation catalyst and the transalkylation catalyst were loaded respectively, and the two ends of the hydroalkylation reaction tube and the transalkylation reaction tube were respectively filled with quartz sand, and the loading amount of the catalyst was 4 g. The hydroalkylation catalyst is reduced, and the reduction temperature is 250°C. Hydroalkylation reaction conditions: benzene space velocity is 2.0h -1 , the reaction temperature is 180°C, the reaction pressure is 2.0MPa, and the molar ratio of hydrogen to benzene is 0.6. Transalkylation reaction conditions: reaction temperature 240°C, reaction pressure 2.0MPa. After 24 hours of reaction, samples were taken and analyzed. The mass percentages of cyclohexane, benzene, cyclohexylbenzene and dicyclohexylbenzene in the second stream and the third stream are shown in Table 1.
[0047] Table 1
[0048]
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