On decoupling rate processes in chemical reaction systems - Methods and applications

被引:5
|
作者
Billeter, Julien [1 ]
Rodrigues, Diogo [1 ]
Srinivasan, Sriniketh [1 ]
Amrhein, Michael [1 ]
Bonvin, Dominique [1 ]
机构
[1] Ecole Polytech Fed Lausanne, Lab Automat, CH-1015 Lausanne, Switzerland
关键词
Chemical reaction systems; Reaction variants; Vessel extents; Data reconciliation; State and rate estimation; Modeling and identification; Control and optimization; TARGET FACTOR-ANALYSIS; INCREMENTAL IDENTIFICATION; STATE ESTIMATION; EXTENTS; OPTIMIZATION; CALIBRATION; STABILITY; VARIANTS; REACTORS;
D O I
10.1016/j.compchemeng.2017.09.021
中图分类号
TP39 [计算机的应用];
学科分类号
081203 ; 0835 ;
摘要
Models of chemical reaction systems can be complex as they need to include information regarding the reactions and the mass and heat transfers. The commonly used state variables, namely, concentrations and temperatures, express the interplay between many phenomena. As a consequence, each state variable is affected by several rate processes. On the other hand, it is well known that it is possible to partition the state space into a reaction invariant subspace and its orthogonal complement using a linear transformation involving the reaction stoichiometry. This paper uses a more sophisticated linear transformation to partition the state space into various subspaces, each one linked to a single rate process such as a particular reaction, mass transfer or heat transfer. The implications of this partitioning are discussed with respect to several applications related to data reconciliation, state and rate estimation, modeling, identification, control and optimization of reaction systems. (C) 2017 Elsevier Ltd. All rights reserved.
引用
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页码:296 / 305
页数:10
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