Options
Optimal design of extraction-distillation hybrid processes by combining equilibrium and rate-based modeling
Citation Link: https://doi.org/10.15480/882.16127
Publikationstyp
Journal Article
Date Issued
2025-07-27
Sprache
English
TORE-DOI
Journal
Volume
4
Start Page
1005
End Page
1010
Citation
Systems & Control Transactions 4: 1005-1010 (2025)
Contribution to Conference
Publisher DOI
Publisher
PSE Press
Liquid-liquid extraction (LLX) is an essential technique for separating heat-sensitive, highly diluted, or azeotropic mixtures. However, the design and optimization of LLX processes can be challenging due to mass transfer limitations and complex fluid dynamics. While distillation can often be modeled using equilibrium-based (EQ-based) approaches with (constant) height equivalent to theoretical stage (HETS) values, these kinetic effects can limit the applicability of EQ-based LLX models for conceptual design. Non-equilibrium (NEQ) or rate-based modeling can account for detailed mass transfer and fluid dynamics but further increases the nonlinearity and complexity of the respective optimization problems, which should account for closed-loop solvent recovery. To successfully address these complexities, we propose an integrated methodology combining NEQ-based simulation with EQ-based superstructure optimization to design a hybrid extraction-distillation process. An NEQ model is first used to derive operation-dependent HETS correlations, which are then incorporated into an EQ-based superstructure model for techno-economic optimization targeting total annualized cost. This approach balances model fidelity and computational efficiency, providing more reliable solutions by capturing the solvent-specific mass transfer behavior. We illustrate the methodology for a dilute acetone-water system with different solvents.
Subjects
Hybrid Processes
Process Design
Superstructure Optimization
DDC Class
660: Chemistry; Chemical Engineering
004: Computer Sciences
Publication version
publishedVersion
Loading...
Name
LAPSE-2025.0313-1v1.pdf
Type
Main Article
Size
437.95 KB
Format
Adobe PDF