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  2. Vacancy defect - Wikipedia

    en.wikipedia.org/wiki/Vacancy_defect

    Vacancies occur naturally in all crystalline materials. At any given temperature, up to the melting point of the material, there is an equilibrium concentration (ratio of vacant lattice sites to those containing atoms). [2] At the melting point of some metals the ratio can be approximately 1:1000. [3] This temperature dependence can be modelled by

  3. Lattice diffusion coefficient - Wikipedia

    en.wikipedia.org/wiki/Lattice_diffusion_coefficient

    Since the prevalence of point vacancies increases in accordance with the Arrhenius equation, the rate of crystal solid state diffusion increases with temperature. For a single atom in a defect-free crystal , the movement can be described by the " random walk " model.

  4. Van 't Hoff equation - Wikipedia

    en.wikipedia.org/wiki/Van_'t_Hoff_equation

    The Van 't Hoff equation relates the change in the equilibrium constant, K eq, of a chemical reaction to the change in temperature, T, given the standard enthalpy change, Δ r H ⊖, for the process. The subscript r {\displaystyle r} means "reaction" and the superscript ⊖ {\displaystyle \ominus } means "standard".

  5. Beveridge curve - Wikipedia

    en.wikipedia.org/wiki/Beveridge_curve

    The Beveridge curve, or UV curve, was developed in 1958 by Christopher Dow and Leslie Arthur Dicks-Mireaux. [2] [3] They were interested in measuring excess demand in the goods market for the guidance of Keynesian fiscal policies and took British data on vacancies and unemployment in the labour market as a proxy, since excess demand is unobservable.

  6. Kröger–Vink notation - Wikipedia

    en.wikipedia.org/wiki/Kröger–Vink_Notation

    Using equation 5, the formula can be simplified into the following form where the enthalpy of formation can be directly calculated: [v ⁠ ′ ′ {\displaystyle \prime \prime } ⁠ Mg ] = exp ( − ⁠ Δ f H / 2 k B T ⁠ + ⁠ Δ f S / 2 k B ⁠ ) = A exp ( − ⁠ Δ f H / 2 k B T ⁠ ) , where A is a constant containing the entropic term.

  7. Phase rule - Wikipedia

    en.wikipedia.org/wiki/Phase_rule

    In thermodynamics, the phase rule is a general principle governing multi-component, multi-phase systems in thermodynamic equilibrium.For a system without chemical reactions, it relates the number of freely varying intensive properties (F) to the number of components (C), the number of phases (P), and number of ways of performing work on the system (N): [1] [2] [3]: 123–125

  8. Job plot - Wikipedia

    en.wikipedia.org/wiki/Job_plot

    In solutions where two species are present (i.e. species A and species B), one species (A) may bind to the other species (B). In some cases, more than one A will bind with a single B. One way to determine the amount of A binding to B is by using a Job plot.

  9. Langmuir adsorption model - Wikipedia

    en.wikipedia.org/wiki/Langmuir_adsorption_model

    This equation implies that if one makes a log–log plot of adsorption data, the data will fit a straight line. The Freundlich isotherm has two parameters, while Langmuir's equations has only one: as a result, it often fits the data on rough surfaces better than the Langmuir isotherm.