A novel route to produce 4-t-butyltoluene by t-butylation of toluene with t-butylalcohol over mesoporous Al-MCM-41 molecular sieves

Authors
Selvaraj, MJeon, SHHan, JSinha, PKLee, TG
Issue Date
2005-05-26
Publisher
ELSEVIER SCIENCE BV
Citation
APPLIED CATALYSIS A-GENERAL, v.286, no.1, pp.44 - 51
Abstract
t-Butylation of toluene with t-butylalcohol (t-BuOH) as alkylating agent was conducted under liquid phase reaction conditions over Al-MCM-41 with different Si/Al ratios for highly selective synthesis of 4-t-butyltoluene. For the reactions, the influences of various reaction parameters such as reaction temperature, time and t-BuOH to toluene ratio are discussed. With increasing the Si/Al ratios of Al-MCM-41 catalysts from 21 to 104, the conversion of toluene, and the yield and selectivity of 4-t-butyltoluene decreased because the number of Bronsted acid sites in Al-MCM-41 catalysts is found to decrease almost linearly with increasing ratios of Si/Al. The conversion and selectivity is increased in Al-MCM-41(21) with each cycling of reaction. The Si/Al ratio of 21 is found to be more suitable for the t-butylation of toluene to highly selective synthesis of 4-t-butyltoluene. Thus the selectivity of 4-t-butyltoluene is higher in Al-MCM-41(21) than that in other Al-MCM-41 samples. (c) 2005 Elsevier B.V. All rights reserved.
Keywords
SOLID ACID CATALYSTS; NAPHTHYL ETHER NEROLINE; AROMATIC-HYDROCARBONS; TERT-BUTYL; ALKYLATION; ISOPROPYLATION; CYCLIZATION; ZEOLITES; BENZENE; OLEFINS; SOLID ACID CATALYSTS; NAPHTHYL ETHER NEROLINE; AROMATIC-HYDROCARBONS; TERT-BUTYL; ALKYLATION; ISOPROPYLATION; CYCLIZATION; ZEOLITES; BENZENE; OLEFINS; Al-MCM-41; catalytic activity; bronsted acidity; conversion of toluene; selectivity of 4-t-butyltoluene
ISSN
0926-860X
URI
https://pubs.kist.re.kr/handle/201004/136456
DOI
10.1016/j.apcata.2005.02.027
Appears in Collections:
KIST Article > 2005
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