Skip to contentScholarGate
LibraryBookshelfDeskReview StudioAssistant
Sign in
On this page
IntuitionHow it worksWhen to use itStrengths & limitationsCommon pitfallsApplicationsFrequently asked🔒 Read the full methodSourcesRelated methods
Cite this pageSpotted an issue on this page? Report or suggest a fix →
Home›Applied Physics›Adsorption Isotherm (Langmuir-Freundlich)
Process / pipelineSurface Chemistry

Adsorption Isotherm (Langmuir-Freundlich)

Adsorption Isotherm Models (Langmuir, Freundlich, and Combined) · Also known as: Langmuir isotherm, Freundlich isotherm, sorption equilibrium

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.

ScholarGate
  1. Process / pipeline
  2. v1
  3. 3 Sources
  4. PUBLISHED
Cite this page →
Tools & resources
Download slides
Learn & explore

Read the full method

Members only

Sign in with a free account to read this section.

Sign in

Method map

The neighbourhood of related methods — select a node to explore.

Adsorption Isotherm (Langmuir-Freundlich)
CSTR ModelPFR ModelReactive Distillation

When to use it

Use adsorption isotherms to design fixed-bed adsorbers for gas or liquid separation. They are essential for predicting breakthrough curves and sizing carbon filters, zeolite beds, and ion exchangers. Apply when the system is at or near equilibrium. Avoid when kinetics (adsorption rate) is rate-limiting or when temperature changes significantly during the process.

Strengths & limitations

Strengths
  • Simple models (Langmuir, Freundlich) are easy to fit and interpret
  • Mechanistic basis (Langmuir) provides physical insight
  • Widely applicable across gas and liquid phase systems
  • Enables quick estimation of column performance without detailed kinetics
Limitations
  • Assumes equilibrium; does not account for mass transfer kinetics or breakthrough transients
  • Langmuir assumes monolayer coverage, which is violated at high loadings (especially in liquids)
  • Freundlich is purely empirical; parameters lack physical meaning
  • Does not capture site heterogeneity well; multilayer or competitive adsorption requires more sophisticated models

Frequently asked

What is the difference between Langmuir and Freundlich isotherms?

Langmuir assumes a fixed number of adsorption sites (monolayer saturation); uptake plateaus. Freundlich is empirical; uptake increases indefinitely (at decreasing rate). Langmuir works well for homogeneous surfaces and single-layer coverage; Freundlich fits heterogeneous surfaces and multilayer systems.

How do you choose between isotherm models?

Fit several models (Langmuir, Freundlich, Sips) to your data and compare R² values. Sips (combines both) often fits best. Consider the surface chemistry: homogeneous → Langmuir; heterogeneous → Freundlich or Sips.

What is the relationship between isotherm and breakthrough curve?

The isotherm defines equilibrium, but the breakthrough curve shows the dynamic column performance. Isotherms alone do not predict when breakthrough occurs; you need kinetics and column mass transfer data.

Sources

  1. 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. DOI: 10.1021/ja02242a004 ↗
  2. Freundlich, H. M. F. (1906). Über die Adsorption in Lösungen. Zeitschrift für Physikalische Chemie, 57(1), 385-470. link ↗
  3. Yang, R. T. (1997). Gas Separation by Adsorption Processes. Butterworth-Heinemann. ISBN: 978-0-7506-3897-0

How to cite this page

ScholarGate. (2026, June 3). Adsorption Isotherm Models (Langmuir, Freundlich, and Combined). ScholarGate. https://scholargate.app/en/applied-physics/adsorption-isotherm

Related methods

CSTR ModelPFR ModelReactive Distillation

Which method?

Set this method beside its closest kin and read them side by side — the library lays the books on the table; the choice is yours.

  • CSTR ModelApplied Physics↔ compare
  • PFR ModelApplied Physics↔ compare
  • Reactive DistillationApplied Physics↔ compare
Compare side by side →

Referenced by

PFR Model

Similar methods

BET Surface AreaFick's LawsStefan-Maxwell DiffusionCSTR ModelUNIFACPFR ModelPeng-Robinson Equation of StateHeavy Metal Speciation

Related reference concepts

Adsorption and Surface ThermodynamicsSurface and Colloid ChemistrySorption and Ion ExchangeContaminant Transport in GroundwaterHeterogeneous Catalytic MaterialsElectrochemical Impedance Spectroscopy

Spotted an issue on this page? Report or suggest a fix →

ScholarGate — Adsorption Isotherm (Langmuir-Freundlich) (Adsorption Isotherm Models (Langmuir, Freundlich, and Combined)). Retrieved 2026-07-21 from https://scholargate.app/en/applied-physics/adsorption-isotherm · Dataset: https://doi.org/10.5281/zenodo.20539026
Quick facts
Originator
Irving Langmuir
Subfamily
Surface Chemistry
Year
1918
Type
Empirical and theoretical adsorption equilibrium model
Related methods
CSTR ModelPFR ModelReactive Distillation
ScholarGate

A content-first reference library for research methods — what each one is, how it works, and where it comes from.

Open data (CC-BY)

Explore

  • Library
  • Search the library…
  • Browse by field
  • Fields
  • Journey
  • Compare
  • Which method?

Reference

  • Subjects
  • Atlas
  • Glossary
  • Methodology
  • Philosophy

Your tools

  • Bookshelf
  • Desk
  • Chat

Company

  • About
  • Pricing
  • Contact
  • Suggest a method

Entries are compiled from published sources for reference. Verifying the accuracy and suitability of any information for your own use remains your responsibility.

© 2026 ScholarGate · A research-method reference library
  • Privacy
  • Cookies
  • Terms
  • Delete account