Direct Conversion of n-Butane to Isobutene in a Membrane Reactor: Thermodynamic Analysis

被引:11
作者
Al-Megren, H. A. [3 ]
Barbieri, G. [1 ]
Mirabelli, I. [2 ]
Brunetti, A. [1 ]
Drioli, E. [1 ,2 ]
Al-Kinany, M. C. [3 ]
机构
[1] Univ Calabria, Natl Res Council, Inst Membrane Technol ITM CNR, I-87036 Rende Cs, Italy
[2] Univ Calabria, Chem Engn & Mat Dept, I-87036 Rende Cs, Italy
[3] King Abdulaziz City Sci & Technol, Riyadh 11442, Saudi Arabia
关键词
GAS SHIFT REACTION; PROCESS INTENSIFICATION; DEHYDROISOMERIZATION; DEHYDROGENATION; TEMPERATURE; STAGE;
D O I
10.1021/ie400006c
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Isobutene is an important intermediate compound in the petrochemical industry for the production of polymers (butyl rubber, polybutene, and isoprene) and methyl tert-butyl ether. In this work, the n-butane dehydroisomerization reaction in a membrane reactor (MR) was investigated by thermodynamic analysis in a wide range of temperatures, reaction pressures, and equilibrium hydrogen partial pressures, by means of a simplified reaction scheme. The shift of the equilibrium conversion in an MR was evaluated by taking into account the chemical reaction equilibrium and the permeative equilibrium through a 100% hydrogen-selective membrane. The evaluated limits imposed by thermodynamics on an MR are much wider than those of a traditional reactor so that a conversion of about 7 times higher could be obtained over that of the traditional process under a set of operating conditions. This gives a powerful indication on how the use of an MR can extend the thermodynamic limits of this reaction, in terms of conversion, even at thermodynamically unfavorable operating conditions.
引用
收藏
页码:10380 / 10386
页数:7
相关论文
共 31 条
[1]   Production of ethylene and cyclohexane in a catalytic membrane reactor [J].
Abashar, MEE ;
Al-Rabiah, AA .
CHEMICAL ENGINEERING AND PROCESSING-PROCESS INTENSIFICATION, 2005, 44 (11) :1188-1196
[2]  
Alireza S., 2008, J MEMBRANE SCI, V319, P279
[3]   Durability of PSS-supported Pd-membranes under mixed gas and water-gas shift conditions [J].
Augustine, Alexander S. ;
Mardilovich, Ivan P. ;
Kazantzis, Nikolaos K. ;
Ma, Yi Hua .
JOURNAL OF MEMBRANE SCIENCE, 2012, 415 :213-220
[4]   Theoretical study of hydrocarbon dehydrogenation at high temperatures [J].
Babak, V. N. ;
Babak, T. B. ;
Zakiev, S. E. ;
Kholpanov, L. P. .
THEORETICAL FOUNDATIONS OF CHEMICAL ENGINEERING, 2009, 43 (01) :74-87
[5]   A novel model equation for the permeation of hydrogen in mixture with carbon monoxide through Pd-Ag membranes [J].
Barbieri, G. ;
Scura, F. ;
Lentini, F. ;
De Luca, G. ;
Drioli, E. .
SEPARATION AND PURIFICATION TECHNOLOGY, 2008, 61 (02) :217-224
[6]   Pd-based membrane reactors for one-stage process of water gas shift [J].
Barbieri, G. ;
Brunetti, A. ;
Caravella, A. ;
Drioli, E. .
RSC ADVANCES, 2011, 1 (04) :651-661
[7]   Conversion-temperature diagram for a palladium membrane reactor. Analysis of an endothermic reaction: Methane steam reforming [J].
Barbieri, G ;
Marigliano, G ;
Perri, G ;
Drioli, E .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2001, 40 (09) :2017-2026
[8]   Simulation study of water gas shift reaction in a membrane reactor [J].
Brunetti, A. ;
Caravella, A. ;
Barbieri, G. ;
Drioli, E. .
JOURNAL OF MEMBRANE SCIENCE, 2007, 306 (1-2) :329-340
[9]   Process Intensification by Membrane Reactors: High-Temperature Water Gas Shift Reaction as Single Stage for Syngas Upgrading [J].
Brunetti, Adele ;
Caravella, Alessio ;
Drioli, Enrico ;
Barbieri, Giuseppe .
CHEMICAL ENGINEERING & TECHNOLOGY, 2012, 35 (07) :1238-1248
[10]  
Buonomo F., 1997, HDB HETEROGENEOUS CA, V5, P2140