Process for the alkylation of aromatic hydrocarbons with C1-C8 alcohols
A technology for alkylation and aromatic hydrocarbons, used in chemical instruments and methods, carbon-based compound preparation, hydroxyl compound preparation, etc.
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example 1
[0069] 135 g of catalyst comprising ZSM-12, prepared as described in Example 2 of US2003 / 0069459, were charged into a tubular, jacketed reactor with a diameter of 2.2 cm heated by diathermic oil. After removal of water by stratification / decantation, according to the recirculation ratio 4:1, the IPA content equal to 20% by weight relative to the mixture of benzene / IPA (isopropanol), mixed with the distillate from the same reaction , 540 g / hour of a benzene / IPA mixture was fed to the reactor from above. The reaction conditions are as follows:
[0070] temperature = 190°C,
[0071]Pressure=1.3MPa
[0072] These conditions correspond to operation in the "trickle" state, the reagents, benzene and isopropanol are fed from above and are present in the reactor in the gas phase and the alkylation product is present in the reactor in the liquid phase. Assignment of the physical states of reagents and products is performed by comparison with existing phase diagrams for the components ...
example 2
[0075] 135 g of the same catalyst comprising ZSM-12 as used in Example 1 was charged to a 2.2 cm diameter tubular, jacketed reactor heated by diathermic oil. After removal of the water, a mixture of 718 g / hour of benzene / IPA with an IPA content equal to 15% by weight mixed with the reaction distillate was fed to the reactor from above according to a recycle ratio of 4:1. The amount of IPA fed to the reactor per hour was the same as Example 1. The reaction conditions are as follows:
[0076] temperature = 190°C,
[0077] Pressure=1.3MPa
[0078] These conditions correspond to operation in the "trickle" state, the reagents, benzene and isopropanol are fed from above and are present in the reactor in the gas phase and the alkylation product is present in the reactor in the liquid phase. The assignment of the physical states of reagents and products was performed as described in Example 1.
[0079] Under these conditions, a quantitative conversion of IPA was obtained with a se...
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