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The surface energy of a liquid may be measured by stretching a liquid membrane (which increases the surface area and hence the surface energy). In that case, in order to increase the surface area of a mass of liquid by an amount, δA, a quantity of work, γ δA, is needed (where γ is the surface energy density of the liquid).
Gibbs emphasized that for solids, the surface free energy may be completely different from surface stress (what he called surface tension): [13]: 315 the surface free energy is the work required to form the surface, while surface stress is the work required to stretch the surface. In the case of a two-fluid interface, there is no distinction ...
(σ: surface tension, ΔP max: maximum pressure drop, R cap: radius of capillary) Later, after the maximum pressure, the pressure of the bubble decreases and the radius of the bubble increases until the bubble is detached from the end of a capillary and a new cycle begins. This is not relevant to determine the surface tension. [3]
Here σ is the surface tension, n, t and s are unit vectors in a local orthogonal coordinate system (n,t,s) at the free surface (n is outward normal to the free surface while the other two lie in the tangential plane and are mutually orthogonal). The indices 'l' and 'g' denote liquid and gas, respectively and K is the curvature of the free surface.
This may be written in the following form, known as the Ostwald–Freundlich equation: =, where is the actual vapour pressure, is the saturated vapour pressure when the surface is flat, is the liquid/vapor surface tension, is the molar volume of the liquid, is the universal gas constant, is the radius of the droplet, and is temperature.
Cloth, treated to be hydrophobic, shows a high contact angle. The theoretical description of contact angle arises from the consideration of a thermodynamic equilibrium between the three phases: the liquid phase (L), the solid phase (S), and the gas or vapor phase (G) (which could be a mixture of ambient atmosphere and an equilibrium concentration of the liquid vapor).
Here () denotes the surface tension (or (excess) surface free energy) of a liquid drop with radius , whereas denotes its value in the planar limit. In both definitions (1) and (2) the Tolman length is defined as a coefficient in an expansion in 1 / R {\displaystyle 1/R} and therefore does not depend on R {\displaystyle R} .
In physics, the Young–Laplace equation (/ l ə ˈ p l ɑː s /) is an algebraic equation that describes the capillary pressure difference sustained across the interface between two static fluids, such as water and air, due to the phenomenon of surface tension or wall tension, although use of the latter is only applicable if assuming that the wall is very thin.