ISSN: 0256-1115 (print version) ISSN: 1975-7220 (electronic version)
Copyright © 2024 KICHE. All rights reserved

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 20, 2014
Accepted April 23, 2015
articles 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

Copper-based nanocatalysts for 2-butanol dehydrogenation: Screening and optimization of preparation parameters by response surface methodology

Department of Chemistry, Amirkabir University of Technology, P. O. Box 15875-4413, Tehran, Iran 1Catalysis Research Group, Petrochemical Research & Technology Company, P. O. Box 1493, Tehran, Iran
shariati@aut.ac.ir
Korean Journal of Chemical Engineering, December 2015, 32(12), 2418-2428(11), 10.1007/s11814-015-0087-x
downloadDownload PDF

Abstract

Two types of copper-based dehydrogenation nanocatalysts (Cu/ZnO/Al2O3 and Cu/SiO2) were prepared from various precursors by impregnation (IM), sol-gel (SG) and co precipitation (COPRE) methods. The structures of samples were characterized by N2 adsorption-desorption, XRD, XRF, TPR, N2O-Titration, FT-IR, FE-SEM and TEM techniques. The catalytic performance tests in vapor-phase dehydrogenation of 2-butanol to methyl ethyl ketone (MEK) were carried out in a fixed-bed reactor at a temperature of 260 oC under atmospheric pressure and LHSV of 4mL/(h·g cat). The experimental results indicated that (i) the copper oxide over the COPRE nanocatalyst was reduced at a lower temperature (222 oC) in comparison with the CuO reduced on the SG and IM samples (243 and 327 oC, respectively). Also, the percentage of reduction of CuO species on COPRE catalyst was the highest (98.8%) in comparison with the two other samples, (ii) the COPRE nanocatalyst exhibited the highest activity for the dehydrogenation of 2-butanol to MEK, and (iii) co-precipitation method was selected as an optimum method for preparation of nanocatalyst. The central composite experimental design method was applied for investigation of the effects of four critical preparation factors on the MEK selectivity of Cu/ZnO/Al2O3 nanocatalyst. The results showed that Cu/Zn molar ratio and precipitation pH are the most effective factors on the response and the optimum conditions for synthesis of Cu/ZnO/Al2O3 nanocatalyst with maximum selectivity of MEK were T(pre)=67.5 oC, T(aging)=68.8 oC, pH(pre)=7.27 and Cu/Zn molar ratio=1.38. The performance of the prepared nanocatalyst at the optimum conditions was comparable to the commercially available nanocatalyst.

References

Bolder FHA, Ind. Eng. Chem. Res., 47(19), 7496 (2008)
Liu ZH, Huo WZ, Ma H, Qiao K, Chin. J. Chem. Eng., 14(5), 676 (2006)
Keuler JN, Lorenzen L, Miachon S, Appl. Catal. A: Gen., 218(1-2), 171 (2001)
Fang D, Ren W, Liu Z, Xu XF, Xu L, Lu H, Liao W, Zhang H, J. Nat. Gas Chem., 18, 179 (2009)
Perez-Lopez OW, Farias AC, Marcilio NR, Bueno JMC, Mater. Res. Bull., 40(12), 2089 (2005)
Grover GS, Chaudhari RV, J. Mol. Catal. A-Chem., 49, 143 (1989)
Cheikhi N, Kacimi M, Rouimi M, Ziyad D, Liotta LF, Pantaleo G, Deganello G, J. Catal., 232(2), 257 (2005)
Driver P, Glowa G, Wren JC, Radiat. Phys. Chem., 57, 37 (2000)
Smetana JF, Falconer JL, Noble RD, J. Membr. Sci., 114(1), 127 (1996)
Zhu WC, Wang LX, Liu SY, Wang ZL, React. Kinet. Catal. Lett., 93(1), 93 (2008)
Jeon GS, Chung JS, Korean J. Chem. Eng., 14(1), 49 (1997)
Wang ZL, Ma HC, Zhu WC, Wang GJ, React. Kinet. Catal. Lett., 76(2), 271 (2002)
Wang ZL, Liu QS, Yu HF, Wu TH, Wang GJ, Appl. Catal. A: Gen., 239(1-2), 87 (2003)
Lambert S, Cellier C, Ferauche F, Gaigneaux EM, Heinrichs B, Catal. Commun., 8, 2032 (2007)
Han YW, Shen JY, Chen Y, Appl. Catal. A: Gen., 205(1-2), 79 (2001)
Chang HF, Yang CF, Ind. Eng. Chem. Res., 36(6), 2080 (1997)
Mapa M, Sivaranjani K, Bhange DS, Saha B, Chakraborty P, Viswanath AK, Gopinath CS, Chem. Mater., 22, 565 (2010)
Gaigneaux EM, Carrazan SRG, Ruiz P, Delmon B, Thermochim. Acta, 388(1-2), 27 (2002)
Khachani M, Kacimi M, Ensuque A, Piquemal JY, Connan C, Bozon-Verduraz F, Ziyad M, Appl. Catal. A: Gen., 388(1-2), 113 (2010)
Moradi GR, Nosrati S, Yaripour F, Catal. Commun., 8, 598 (2007)
Jensen JR, Johannessen T, Livbjerg H, Appl. Catal. A: Gen., 266(1), 117 (2004)
Raoufi D, Renew. Energy, 50, 932 (2013)
Spencer MS, Catal. Lett., 50(1-2), 37 (1998)

The Korean Institute of Chemical Engineers. F5, 119, Anam-ro, Seongbuk-gu, 233 Spring Street Seoul 02856, South Korea.
TEL. No. +82-2-458-3078FAX No. +82-507-804-0669E-mail : kiche@kiche.or.kr

Copyright (C) KICHE.all rights reserved.

- Korean Journal of Chemical Engineering 상단으로