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  2. Gibbs–Thomson equation - Wikipedia

    en.wikipedia.org/wiki/Gibbs–Thomson_equation

    The technique is closely related to using gas adsorption to measure pore sizes, but uses the Gibbs–Thomson equation rather than the Kelvin equation.They are both particular cases of the Gibbs Equations of Josiah Willard Gibbs: the Kelvin equation is the constant temperature case, and the Gibbs–Thomson equation is the constant pressure case. [1]

  3. Gibbs isotherm - Wikipedia

    en.wikipedia.org/wiki/Gibbs_isotherm

    The Gibbs adsorption isotherm for multicomponent systems is an equation used to relate the changes in concentration of a component in contact with a surface with changes in the surface tension, which results in a corresponding change in surface energy. For a binary system, the Gibbs adsorption equation in terms of surface excess is

  4. TEOS-10 - Wikipedia

    en.wikipedia.org/wiki/TEOS-10

    For the calculation of the thermodynamic properties of seawater and ice, TEOS-10 uses the specific Gibbs potential g(T,P)=G/m, G=F+pV, because the pressure is a more easily measurable property than density in a geophysical context. Gibbs energies are multivalued around phase boundaries and need to be defined for each phase separately. [6]

  5. Gibbs free energy - Wikipedia

    en.wikipedia.org/wiki/Gibbs_free_energy

    In thermodynamics, the Gibbs free energy (or Gibbs energy as the recommended name; symbol ) is a thermodynamic potential that can be used to calculate the maximum amount of work, other than pressure–volume work, that may be performed by a thermodynamically closed system at constant temperature and pressure.

  6. Gibbs–Duhem equation - Wikipedia

    en.wikipedia.org/wiki/Gibbs–Duhem_equation

    When pressure and temperature are variable, only of components have independent values for chemical potential and Gibbs' phase rule follows. The Gibbs−Duhem equation cannot be used for small thermodynamic systems due to the influence of surface effects and other microscopic phenomena. [2]

  7. Gibbs–Helmholtz equation - Wikipedia

    en.wikipedia.org/wiki/Gibbs–Helmholtz_equation

    The definition of the Gibbs function is = + where H is the enthalpy defined by: = +. Taking differentials of each definition to find dH and dG, then using the fundamental thermodynamic relation (always true for reversible or irreversible processes): = where S is the entropy, V is volume, (minus sign due to reversibility, in which dU = 0: work other than pressure-volume may be done and is equal ...

  8. Surface energy - Wikipedia

    en.wikipedia.org/wiki/Surface_energy

    As such the Gibbs free energy of the system is minimized when the surface is curved. Vapor pressure of flat and curved surfaces. The vapor pressure of a curved surface is higher than the vapor pressure of a flat surface due to the Laplace pressure that increases the chemical potential of the droplet causing it to vaporize more than it normally ...

  9. Helmholtz free energy - Wikipedia

    en.wikipedia.org/wiki/Helmholtz_free_energy

    In contrast, the Gibbs free energy or free enthalpy is most commonly used as a measure of thermodynamic potential (especially in chemistry) when it is convenient for applications that occur at constant pressure. For example, in explosives research Helmholtz free energy is often used, since explosive reactions by their nature induce pressure ...