Articles & Issues
- Language
- English
- Conflict of Interest
- In relation to this article, we declare that there is no conflict of interest.
- Publication history
-
Received December 9, 2002
Accepted January 14, 2003
- This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright © KIChE. All rights reserved.
All issues
Deactivation Control through Accelerated Precoking for the CoMo/γ-Al2O3 Catalysts in Thiophene Hydrodesulfurization
National Research Laboratory for Environmental Catalysis, Department of Chemical and Biomolecular Engineering, Korea Advanced Institute of Science and Technology, 373-1 Gusung-dong, Yusung-gu, Daejeon 305-701, Korea
skihm@mail.kaist.ac.kr
Korean Journal of Chemical Engineering, March 2003, 20(2), 284-287(4), 10.1007/BF02697242
Download PDF
Abstract
Information on the degree of deactivation is very important for predicting catalyst life, from which the catalyst design could be further improved. The CoMo/Al2O3 catalysts, used for the hydrodesulfurization of light oil, are known to have a commercial operation time of around two years. Our goal was to establish the accelerated precoking conditions for obtaining a desired degree of deactivation for CoMo/Al2O3 catalysts. The effect of coking temperature on the catalytic activity for thiophene hydrodesulfurization was investigated for three coke precursors. Precoking_x000D_
with heavier precursors resulted in higher coke content and higher aromaticity as expected, i.e., in order of anthracene>naphthalene>cyclohexene. It is suggested that the established conditions of precoking for the commercial catalysts could provide a quantitive reference for evaluating the lifetime of any commercial catalysts.
References
Brito A, Gonzalez AR, Borges ME, Garcia MT, Appl. Catal. A: Gen., 205(1-2), 173 (2001)
Callejas MA, Martinez MT, Blasco T, Sastre E, Appl. Catal. A: Gen., 218(1-2), 181 (2001)
Choi JG, J. Ind. Eng. Chem., 8(1), 1 (2002)
Kim DW, Lee DK, Ihm SK, Korean J. Chem. Eng., 19(4), 587 (2002)
Li D, Xu HF, Guthrie GD, J. Catal., 189(2), 281 (2000)
Makishima H, Tanaka Y, Kato Y, Kure S, Shimada H, Matsubayashi N, Nishijima A, Nomura M, Catal. Today, 29(1-4), 267 (1996)
Tanaka Y, Shimada H, Matsubayashi N, Nishijima A, Nomura M, Catal. Today, 45(1-4), 319 (1998)
Yokoyama Y, Ishikawa N, Nakanishi K, Satoh K, Nishijima A, Shimada H, Matsubayashi N, Nomura M, Catal. Today, 29(1-4), 261 (1996)
Callejas MA, Martinez MT, Blasco T, Sastre E, Appl. Catal. A: Gen., 218(1-2), 181 (2001)
Choi JG, J. Ind. Eng. Chem., 8(1), 1 (2002)
Kim DW, Lee DK, Ihm SK, Korean J. Chem. Eng., 19(4), 587 (2002)
Li D, Xu HF, Guthrie GD, J. Catal., 189(2), 281 (2000)
Makishima H, Tanaka Y, Kato Y, Kure S, Shimada H, Matsubayashi N, Nishijima A, Nomura M, Catal. Today, 29(1-4), 267 (1996)
Tanaka Y, Shimada H, Matsubayashi N, Nishijima A, Nomura M, Catal. Today, 45(1-4), 319 (1998)
Yokoyama Y, Ishikawa N, Nakanishi K, Satoh K, Nishijima A, Shimada H, Matsubayashi N, Nomura M, Catal. Today, 29(1-4), 261 (1996)