Analysis and Model-Based Description of the Total Process of Periodic Deactivation and Regeneration of a VOx Catalyst for Selective Dehydrogenation of Propane

被引:8
作者
Brune, Andreas [1 ,2 ]
Seidel-Morgenstern, Andreas [1 ]
Hamel, Christof [1 ,2 ]
机构
[1] Otto von Guericke Univ, Inst Proc Engn, Univ Pl 2, D-39106 Magdeburg, Germany
[2] Anhalt Univ Appl Sci, Proc Engn, Bernburger Str 55, D-06354 Kothen, Germany
关键词
deactivation; coking; regeneration; propane dehydrogenation; VOx catalyst; periodic operation; kinetic modeling; reaction kinetics; ISOBUTANE DEHYDROGENATION; COKE; KINETICS; COMBUSTION; SIMULATION; OXIDATION; REACTORS; SINGLE;
D O I
10.3390/catal10121374
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
This study intends to provide insights into various aspects related to the reaction kinetics of the VOx catalyzed propane dehydrogenation including main and side reactions and, in particular, catalyst deactivation and regeneration, which can be hardly found in combination in current literature. To kinetically describe the complex reaction network, a reduced model was fitted to lab scale experiments performed in a fixed bed reactor. Additionally, thermogravimetric analysis (TGA) was applied to investigate the coking behavior of the catalyst under defined conditions considering propane and propene as precursors for coke formation. Propene was identified to be the main coke precursor, which agrees with results of experiments using a segmented fixed bed reactor (FBR). A mechanistic multilayer-monolayer coke growth model was developed to mathematically describe the catalyst coking. Samples from long-term deactivation experiments in an FBR were used for regeneration experiments with oxygen to gasify the coke deposits in a TGA. A power law approach was able to describe the regeneration behavior well. Finally, the results of periodic experiments consisting of several deactivation and regeneration cycles verified the long-term stability of the catalyst and confirmed the validity of the derived and parametrized kinetic models for deactivation and regeneration, which will allow model-based process development and optimization.
引用
收藏
页码:1 / 28
页数:28
相关论文
共 46 条
[11]  
Chernick MR., 2008, BOOTSTRAP METHODS GU
[12]   Experimental Investigation of the Oxidative Coupling of Methane in a Porous Membrane Reactor: Relevance of Back-Permeation [J].
Cruellas, Aitor ;
Ververs, Wout ;
Annaland, Martin van Sint ;
Gallucci, Fausto .
MEMBRANES, 2020, 10 (07) :1-24
[13]   Oxidative Coupling of Methane in Membrane Reactors; A Techno-Economic Assessment [J].
Cruellas, Aitor ;
Heezius, Jelle ;
Spallina, Vincenzo ;
Annaland, Martin van Sint ;
Medrano, Jose Antonio ;
Gallucci, Fausto .
PROCESSES, 2020, 8 (03)
[14]   DEHYDROGENATION OF 1-BUTENE INTO BUTADIENE - KINETICS, CATALYST COKING, AND REACTOR DESIGN [J].
DUMEZ, FJ ;
FROMENT, GF .
INDUSTRIAL & ENGINEERING CHEMISTRY PROCESS DESIGN AND DEVELOPMENT, 1976, 15 (02) :291-301
[15]  
Eisele P., 2010, ULLMANNS ENCY IND CH, P101
[16]   Steady state modeling and simulation of the Oleflex process for isobutane dehydrogenation considering reaction network [J].
Farsi, M. ;
Jahanmiri, A. ;
Rahimpour, M. R. .
ASIA-PACIFIC JOURNAL OF CHEMICAL ENGINEERING, 2013, 8 (06) :862-869
[17]   Modeling and Design Optimization of Multifunctional Membrane Reactors for Direct Methane Aromatization [J].
Fouty, Nicholas J. ;
Carrasco, Juan C. ;
Lima, Fernando V. .
MEMBRANES, 2017, 7 (03)
[18]   Process Intensification via Membrane Reactors, the DEMCAMER Project [J].
Gallucci, Fausto ;
Medrano, Jose Antonio ;
Roses, Leonardo ;
Brunetti, Adele ;
Barbieri, Giuseppe ;
Luis Viviente, Jose .
PROCESSES, 2016, 4 (02)
[19]   Propane dehydrogenation over a Cr2O3/Al2O3 catalyst:: transient kinetic modeling of propene and coke formation [J].
Gascón, J ;
Téllez, C ;
Herguido, J ;
Menéndez, M .
APPLIED CATALYSIS A-GENERAL, 2003, 248 (1-2) :105-116
[20]  
Gentle JE, 2009, STAT COMPUT SER, P3