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Équation d'état de Peng-Robinson×Modèle de réacteur piston×Distillation Réactive×
DomainePhysique appliquéePhysique appliquéePhysique appliquée
FamilleProcess / pipelineProcess / pipelineProcess / pipeline
Année d'origine197619621995
Auteur d'origineDing-Yu Peng and David Bernard RobinsonOctave LevenspielKlaus Sundmacher
TypeEquation of state; thermodynamic property correlationMathematical model for plug-flow reactorIntegrated reaction-separation process model
Source fondatricePeng, D. Y., & Robinson, D. B. (1976). A new two-constant equation of state. Industrial & Engineering Chemistry Fundamentals, 15(1), 59-64. DOI ↗Levenspiel, O. (1999). Chemical Reaction Engineering (3rd ed.). John Wiley & Sons. ISBN: 978-0-471-25424-9Sundmacher, K., & Kienle, A. (2003). Reactive Distillation: Status and Future Directions. Wiley-VCH. ISBN: 978-3-527-30623-9
AliasPR-EOS, Peng-Robinson modelideal tubular reactor, plug-flow model, PFRintegrated distillation-reaction, reactive column, reaction with separation
Apparentées434
RésuméThe Peng-Robinson equation of state is a cubic model that describes the thermodynamic properties of pure fluids and mixtures. Introduced by Ding-Yu Peng and David Bernard Robinson in 1976, it improves upon earlier models (van der Waals, Redlich-Kwong) by better predicting compressibility factors and phase equilibria, especially near the critical point. It is widely used in petroleum engineering, chemical process design, and natural gas calculations.The PFR (Plug Flow Reactor) model describes the behavior of a tubular reactor in which fluid elements move through as distinct plugs with no axial mixing. Fluid at the inlet is freshly unreacted; as it travels downstream, reactions progress. This idealized model, formalized by Octave Levenspiel alongside CSTR theory, is the opposite extreme: while CSTRs are fully mixed, PFRs have no axial mixing. In practice, PFRs achieve higher conversion than CSTRs for the same residence time and are widely used in the chemical and petroleum industries.Reactive distillation couples reaction and separation in a single column, where reactants are separated from products continuously while simultaneously undergoing reaction on catalytic trays. Pioneered in the 1990s by Klaus Sundmacher and others, this process intensification technique dramatically reduces capital cost, energy consumption, and environmental impact for suitable reactions. It is now industrially proven for esterification, hydration, and transesterification processes.
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ScholarGateComparer des méthodes: Peng-Robinson Equation of State · PFR Model · Reactive Distillation. Consulté le 2026-06-20 sur https://scholargate.app/fr/compare