DSpace

King Saud University Repository >
King Saud University >
COLLEGES >
Science Colleges >
College of Engineering >
College of Engineering >

Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/12209

Title: Low temperature transalkylation of o-diethylbenzene with benzene to ethylbenzene using triflic acid as a catalyst
Authors: Al-Kinany M.C., Jibril, B.Y.,
Al-Khowaiter S.H. , Al-Dosari, M.A. ,
Al-Megren, Al-Zahrani, S.M., H.A.,
Alhumazi, K.
Keywords: Diethylbenzenes; Disproportionation; Ethylbenzene; Isomerization; Transalkylation; Trifilic acid
Issue Date: 2005
Publisher: Elsevier B.V.
Citation: Chemical Engineering and Processing: Process Intensification: Volume 44, Issue 8, Pages 841-846
Abstract: The catalytic performance of trifluoromethanesulphonic acid (triflic acid) has been investigated for synthesis of ethylbenzene (EB) by transalkylation of o-diethylbenzene (DEB) with benzene (B). Different mole ratios of benzene to the isomer (1:1, 3:1 and 6:1) were used at atmospheric pressure and low temperatures (15-35 °C). Ethylbenzene was the main product of the transalkylation. From isomerization reactions, the products were o-diethylbenzene isomers (meta- and para-), and from disproportionation reactions, 1,3,5-triethylbenzene was also obtained. In the case of 1:1 mole ratio of benzene to the isomer, yield of ethylbenzene of 49 mol% was obtained after 6 h of reaction at 35 °C. This decreased, at the same temperature, to 25 and 8 mol% for 3:1 and 6:1 mole ratios, respectively. A decrease in the temperature to 25 and 15 °C (with 1:1 mole ratio), caused the yield of ethylbenzene to decrease to 43 and 32 mol%, respectively. Similar trends were observed with 3:1 and 6:1 ratios. The conversion of o-diethylbenzene to ethylbenzene and ethylated benzenes appeared to depend strongly on mole ratio of benzene/diethylbenzene at a given temperature. The study has shown that the triflic acid is active as a catalyst for the reaction. It exhibited high yield of ethylbenzene from o-diethylbenzene at low temperatures and atmospheric pressure of the two systems. .
URI: http://hdl.handle.net/123456789/12209
ISSN: 02552701
Appears in Collections:College of Engineering

Files in This Item:

File Description SizeFormat
Eng-Che-Humaizi-12.docx36.2 kBMicrosoft Word XMLView/Open

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

 

DSpace Software Copyright © 2002-2007 MIT and Hewlett-Packard - Feedback