what is the relative retention time in G.C&H.P.L.C how it is find out?

7 Answers

  • Anonymous
    1 decade ago
    Favourite answer

    Don't know.

  • 4 years ago

    Relative Retention Time

  • 4 years ago

    Retention Time Definition

  • 1 decade ago

    The relative retention time is the ratio of the retention times of two chromatographic peaks. One is the reference peak and all other peaks are measured relative to it. This is done because retention times shift depending on chromatographic conditions, but relative retention time remains the same. Often the peak chosen as the reference is the internal standard, a compound added to the sample for QC purposes. Pure internal standard is analyzed first. The retention time is recorded, and then a mix of internal standard and sample is analyzed. The relative retention time is then used to help identify the other peaks.

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  • Anonymous
    5 years ago

    For the best answers, search on this site https://shorturl.im/axt56

    I have (some) experience with HPLC in the lab. A simple answer is that when you run HPLC on 1 ion, you will get a retention time of a specific number, but when you do it on a multitude of ions all in one solution, the retention times can shift (upwards or downwards) so you calculate the concentrations of ions based on the relative retention times and not the single ion retention times.

  • sb
    Lv 7
    1 decade ago

    GC :

    In a GC analysis, a known volume of gaseous or liquid analyte is injected into the "entrance" (head) of the column, usually using a microsyringe (or, solid phase microextraction fibers, or a gas source switching system). As the carrier gas sweeps the analyte molecules through the column, this motion is inhibited by the adsorption of the analyte molecules either onto the column walls or onto packing materials in the column. The rate at which the molecules progress along the column depends on the strength of adsorption, which in turn depends on the type of molecule and on the stationary phase materials. Since each type of molecule has a different rate of progression, the various components of the analyte mixture are separated as they progress along the column and reach the end of the column at different times (retention time). A detector is used to monitor the outlet stream from the column; thus, the time at which each component reaches the outlet and the amount of that component can be determined. Generally, substances are identified by the order in which they emerge (elute) from the column and by the retention time of the analyte in the column.


    In isocratic HPLC the analyte is forced through a column of the stationary phase (usually a tube packed with small round particles with a certain surface chemistry) by pumping a liquid (mobile phase) at high pressure through the column. The sample to be analyzed is introduced in a small volume to the stream of mobile phase and is retarded by specific chemical or physical interactions with the stationary phase as it traverses the length of the column. The amount of retardation depends on the nature of the analyte, stationary phase and mobile phase composition. The time at which a specific analyte elutes (comes out of the end of the column) is called the retention time and is considered a reasonably unique identifying characteristic of a given analyte. The use of pressure increases the linear velocity (speed) giving the components less time to diffuse within the column, leading to improved resolution in the resulting chromatogram. Common solvents used include any miscible combinations of water or various organic liquids (the most common are methanol and acetonitrile). Water may contain buffers or salts to assist in the separation of the analyte components, or compounds such as Trifluoroacetic acid which acts as an ion pairing agent.

    A further refinement to HPLC has been to vary the mobile phase composition during the analysis, this is known as gradient elution. A normal gradient for reverse phase chromatography might start at 5% methanol and progress linearly to 50% methanol over 25 minutes, depending on how hydrophobic the analyte is. The gradient separates the analyte mixtures as a function of the affinity of the analyte for the current mobile phase composition relative to the stationary phase. This partitioning process is similar to that which occurs during a liquid-liquid extraction but is continuous, not step-wise. In this example, using a water/methanol gradient, the more hydrophobic components will elute (come off the column) under conditions of relatively high methanol; whereas the more hydrophilic compounds will elute under conditions of relatively low methanol. The choice of solvents, additives and gradient depend on the nature of the stationary phase and the analyte. Often a series of tests are performed on the analyte and a number of generic runs may be processed in order to find the optimum HPLC method for the analyte - the method which gives the best separation of peaks.

  • Anonymous
    5 years ago

    Relative must mean relative to some other peak,or to a standard.

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