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Thermodynamic concepts describing interfacial free energy, surface excess and adsorption at phase boundaries.
Interfacial thermodynamics provides a framework for describing the energetic state and composition of a phase boundary. Surface and interfacial tension can be treated as thermodynamic quantities associated with the creation of additional interfacial area.
Gibbs introduced the concept of a dividing surface to separate the bulk phases mathematically while assigning excess quantities to the interface. This forms the basis for surface excess and the Gibbs adsorption equation.
Focused articles covering the thermodynamic quantities and models used to describe interfaces and adsorption.
For a reversible increase in interfacial area at constant temperature, pressure and component amounts, interfacial tension is the derivative of Gibbs free energy with respect to area.
Surface pressure expresses the reduction in tension of an adsorption-covered interface relative to a reference interface such as the clean solvent surface.
Gibbs replaces the finite interfacial region with an idealized mathematical dividing surface that separates bulk contributions from interfacial excess quantities.
Surface excess concentration describes the amount of a component assigned to the interface relative to the corresponding bulk phases.
The Gibbs adsorption equation relates changes in interfacial tension to surface excess and changes in the chemical potentials of components.