Alkylation of benzene with propylene catalyzed by FeCl3-chloropyridine ionic liquid

2007, Volume 1, Issue 3

Abstract

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Frontiers of Chemical Science and Engineering >> 2007, Volume 1, Issue 3 doi: 10.1007/s11705-007-0053-1

State Key Laboratory of Heavy Oil Processing, China Petroleum University (Beijing), Beijing 102249, China;

Available online: 2007-09-05

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Abstract

Alkylation of benzene with propylene was carried out with FeCl3-chloro-butyl-pyridine (FeCl-[bpc]) ionic liquid as catalyst to obtain cumene. Significant improvements in propylene conversion and cumene selectivity under mild reaction conditions were attained by modification of the catalyst with HCl. Under 20ºC, 0.1 MPa, reaction time 5 min, mole ratio of benzene to propylene 10:1 and mass ratio of FeCl-[bpc] to benzene 1:100, conversion of propylene can increase from 83.60% to 100.00% and selectivity of cumene can increase from 90.86% to 98.47%. If reaction is carried out in following two stages, the result will be very good. At the initial stage of the reaction, alkylation is the main reaction and a higher conversion of propylene is obtained at a lower temperature. At the later stage of the reaction, transalkylation is the main reaction and selectivity to cumene can be increased by appropriately raising the reaction temperature.

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