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  2. Resolution (chromatography) - Wikipedia

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

    Chromatographic peak resolution is given by = + where t R is the retention time and w b is the peak width at baseline. The bigger the time-difference and/or the smaller the bandwidths, the better the resolution of the compounds.

  3. 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.

  4. Purnell equation - Wikipedia

    en.wikipedia.org/wiki/Purnell_equation

    The Purnell equation is an equation used in analytical chemistry to calculate the resolution R s between two peaks in a chromatogram. [1] [2]= (′ + ′) where R s is the resolution between the two peaks

  5. Resolution (mass spectrometry) - Wikipedia

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

    The valley definition defines ΔM as the closest spacing of two peaks of equal intensity with the valley (lowest value of signal) between them less than a specified fraction of the peak height. Typical values are 10% or 50%. The value obtained from a 5% peak width is roughly equivalent to a 10% valley. [1]

  6. Theoretical plate - Wikipedia

    en.wikipedia.org/wiki/Theoretical_plate

    It is simply a hypothetical equilibrium stage. However, the theoretical plate in packed beds, chromatography and other applications is defined as having a height. The empirical formula known as Van Winkle's Correlation can be used to predict the Murphree plate efficiency for distillation columns separating binary systems. [4]

  7. Standard addition - Wikipedia

    en.wikipedia.org/wiki/Standard_addition

    The Standard addition method, often used in analytical chemistry, quantifies the analyte present in an unknown.This method is useful for analyzing complex samples where a matrix effect interferes with the analyte signal.

  8. Isothermal titration calorimetry - Wikipedia

    en.wikipedia.org/wiki/Isothermal_Titration...

    By integrating each peak from the baseline, the total heat associated with each injection is obtained, including both reaction-specific and non-reaction-related contributions. [3] The pattern of these heat effects as a function of the molar ratio [ligand]/[macromolecule] can then be analyzed to give the thermodynamic parameters of the ...

  9. Chromatography software - Wikipedia

    en.wikipedia.org/wiki/Chromatography_software

    Chromatography software is called also Chromatography Data System. [1] It is located in the data station of the modern liquid, gas or supercritical fluid chromatographic systems. This is a dedicated software connected to an hardware interface within the chromatographic system, which serves as a central hub for collecting, analyzing, and ...