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  2. Resolution (chromatography) - Wikipedia

    en.wikipedia.org/wiki/Resolution_(chromatography)

    Example chromatogram showing signal as a function of retention time. In chromatography, resolution is a measure of the separation of two peaks of different retention time t in a chromatogram. [1] [2] [3] [4]

  3. 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 ]

  4. Kovats retention index - Wikipedia

    en.wikipedia.org/wiki/Kovats_retention_index

    The Kovats index of n-alkanes is 100 times their carbon number, e.g. the Kovats index of n-butane is 400. The Kovats index is dimensionless, unlike retention time or retention volume. For isothermal gas chromatography, the Kovats index is given by the equation:

  5. Chromatography - Wikipedia

    en.wikipedia.org/wiki/Chromatography

    Retention time – the characteristic time it takes for a particular analyte to pass through the system (from the column inlet to the detector) under set conditions. See also: Kovats' retention index; Sample – the matter analyzed in chromatography. It may consist of a single component or it may be a mixture of components.

  6. Binding selectivity - Wikipedia

    en.wikipedia.org/wiki/Binding_selectivity

    where α is selectivity factor, N is the number of theoretical plates k A and k B are the retention factors of the two analytes. Retention factors are proportional to distribution coefficients. In practice substances with a selectivity factor very close to 1 can be separated. This is particularly true in gas-liquid chromatography where column ...

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  8. Gel permeation chromatography - Wikipedia

    en.wikipedia.org/wiki/Gel_permeation_chromatography

    Schematic of pore vs analyte size. The smaller analytes relative to the pore sizes can permeate these pores and spend more time inside the gel particles, increasing their retention time. Conversely, larger analytes relative to the pores sizes spend little if any time inside the column, hence they elute sooner.

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