Page 168 - Illustrated Pocket Dictionary of Chromatography
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R f VALUE  169

        retention time window A predefined elution time range that is
        established for a unique analyte and specific operating conditions in
        order to assign peak identification. Instrument operational stability
        (e.g., pump, injector, column, detector, integrator) can also readily be
        assessed in this fashion.

        retention volume, V r  The retention time,  t r, multiplied by the
        flow rate F:

                                 V r = t r ¥  F
        reversed phase   Term derived from the fact that original LC sepa-
        rations were conducted on polar supports (e.g., silica) using nonpo-
        lar to slightly polar mobile phases (e.g., hexane or 99/1 v/v hexane/
        methylene chloride); these conditions were “normal.” Reversed
        phases have nonpolar supports (e.g., octadecyl) and polar hydroor-
        ganic mobile phases (e.g., 60/40 v/v water/methanol). Reversed-phase
        supports, in part because of the wide range available, are by far the
        most commonly used in LC separations. It should be noted that with
        the advent of polar bonded phases (e.g., diol) in conjunction with
        hydroorganic mobile phases the clear distinction between normal and
        reversed phase has blurred.

        Reynolds’ number, Re A dimensionless parameter that esti-
        mates the relative internal and viscous strengths in a flowing liquid:

                                Re =rvd  h

        where r is the fluid density,   is the fluid velocity, d is the tube diam-
        eter, and  h is the fluid viscosity. The Reynolds’ number is used to
        predict whether flow is laminar or turbulent. A low number signifies
        laminar flow.

        R f value  The thin-layer chromatography parameter that defines the
        position of the analyte band on the plate:
                    ( distance of the analyte band from initial spot)
              R f =
                  ( distance to the solvent front from the initial spot )

        Note that it is important that the solvent from never reach the top of
        the plate. If this happens, then an R f value cannot be calculated.
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