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  2. Distribution constant - Wikipedia

    en.wikipedia.org/wiki/Distribution_constant

    The distribution constant (or partition ratio) (K D) is the equilibrium constant for the distribution of an analyte in two immiscible solvents. [1] [2] [3]In chromatography, for a particular solvent, it is equal to the ratio of its molar concentration in the stationary phase to its molar concentration in the mobile phase, also approximating the ratio of the solubility of the solvent in each phase.

  3. Partition coefficient - Wikipedia

    en.wikipedia.org/wiki/Partition_coefficient

    The distribution coefficient, log D, is the ratio of the sum of the concentrations of all forms of the compound (ionized plus un-ionized) in each of the two phases, one essentially always aqueous; as such, it depends on the pH of the aqueous phase, and log D = log P for non-ionizable compounds at any pH.

  4. Partition equilibrium - Wikipedia

    en.wikipedia.org/wiki/Partition_equilibrium

    Partition equilibria are described by Nernst's distribution law. [3] Partition equilibrium are most commonly seen and used for Liquid–liquid extraction . The time until a partition equilibrium emerges is influenced by many factors, such as: temperature, relative concentrations, surface area of interface, degree of stirring, and the nature of ...

  5. Equilibrium chemistry - Wikipedia

    en.wikipedia.org/wiki/Equilibrium_chemistry

    In chromatography substances are separated by partition between a stationary phase and a mobile phase. The analyte is dissolved in the mobile phase, and passes over the stationary phase. Separation occurs because of differing affinities of the analytes for the stationary phase. A distribution constant, K d can be defined as

  6. Chromatography - Wikipedia

    en.wikipedia.org/wiki/Chromatography

    Chromatography, pronounced / ˌ k r oʊ m ə ˈ t ɒ ɡ r ə f i /, is derived from Greek χρῶμα chrōma, which means "color", and γράφειν gráphein, which means "to write".". The combination of these two terms was directly inherited from the invention of the technique first used to separate biological pigme

  7. Van Deemter equation - Wikipedia

    en.wikipedia.org/wiki/Van_Deemter_equation

    In liquid chromatography, the mobile phase velocity is taken as the exit velocity, that is, the ratio of the flow rate in ml/second to the cross-sectional area of the ‘column-exit flow path.’ For a packed column, the cross-sectional area of the column exit flow path is usually taken as 0.6 times the cross-sectional area of the column.

  8. Kovats retention index - Wikipedia

    en.wikipedia.org/wiki/Kovats_retention_index

    In gas chromatography, the Kovats retention index (shorter Kovats index, retention index; plural retention indices) is used to convert retention times into system-independent constants. The index is named after the Hungarian-born Swiss chemist Ervin Kováts , who outlined the concept in the 1950s while performing research into the composition ...

  9. Retardation factor - Wikipedia

    en.wikipedia.org/wiki/Retardation_factor

    In chromatography, the retardation factor (R) is the fraction of an analyte in the mobile phase of a chromatographic system. [1] In planar chromatography in particular, the retardation factor R F is defined as the ratio of the distance traveled by the center of a spot to the distance traveled by the solvent front. [2]