Compara mètodes

	Isotermes d'adsorció (Langmuir-Freundlich)	Model PFR	Destil·lació reactiva
Camp	Física aplicada	Física aplicada	Física aplicada
Família	Process / pipeline	Process / pipeline	Process / pipeline
Any d'origen	1918	1962	1995
Autor original	Irving Langmuir	Octave Levenspiel	Klaus Sundmacher
Tipus	Empirical and theoretical adsorption equilibrium model	Mathematical model for plug-flow reactor	Integrated reaction-separation process model
Font seminal	Langmuir, I. (1918). The adsorption of gases on plane surfaces of glass, mica, and platinum. Journal of the American Chemical Society, 40(9), 1361-1403.	Levenspiel, O. (1999). Chemical Reaction Engineering (3rd ed.). John Wiley & Sons. ISBN: 978-0-471-25424-9	Sundmacher, K., & Kienle, A. (2003). Reactive Distillation: Status and Future Directions. Wiley-VCH. ISBN: 978-3-527-30623-9
Àlies	Langmuir isotherm, Freundlich isotherm, sorption equilibrium	ideal tubular reactor, plug-flow model, PFR	integrated distillation-reaction, reactive column, reaction with separation
Relacionats	3	3	4
Resum	Adsorption isotherms describe the equilibrium uptake of a substance on a solid surface as a function of gas or solution phase concentration at constant temperature. The Langmuir isotherm (1918) and Freundlich isotherm (1906) are classical empirical models. The Langmuir model assumes monolayer coverage and is mechanistic; the Freundlich model is empirical and describes multilayer or heterogeneous adsorption. These isotherms are essential for designing separation processes (activated carbon filters, molecular sieves) and understanding pollutant sorption.	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.