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Relative retention time entries

Chemical Analysis of Extracts. The extracts were analyzed by capillary column GC-MS for OCs, TAAPs, and PAHs (see the list on page 313). The GC-MS parameters used at the two laboratories are shown in Table II. The identification and quantitation were all done by using automatic routines based on a mass spectra library created from authentic standards of the selected compounds. Compounds were located by searching the reconstructed ion chromatogram for each library entry within a narrow retention time window relative to the internal standard (anthracene-dio or phenanthrene-dio). Quantitation was achieved by comparison of characteristic ion areas in the field samples with ion areas of the internal standard. These ion areas were normalized by response factors established by comparison of ion ratios of a standard mixture of all 66 analytes at a concentration of 2.5 ng//zL. [Pg.310]

The opportunity to measure the dilute polymer solution viscosity in GPC came with the continuous capillary-type viscometers (single capillary or differential multicapillary detectors) coupled to the traditional chromatographic system before or after a concentration detector in series (see the entry Viscometric Detection in GPC-SEC). Because liquid continuously flows through the capillary tube, the detected pressure drop across the capillary provides the measure for the fluid viscosity according to the Poiseuille s equation for laminar flow of incompressible liquids [1], Most commercial on-line viscometers provide either relative or specific viscosities measured continuously across the entire polymer peak. These measurements produce a viscometry elution profile (chromatogram). Combined with a concentration-detector chromatogram (the concentration versus retention volume elution curve), this profile allows one to calculate the instantaneous intrinsic viscosity [17] of a polymer solution at each data point i (time slice) of a polymer distribution. Thus, if the differential refractometer is used as a concentration detector, then for each sample slice i. [Pg.855]


See other pages where Relative retention time entries is mentioned: [Pg.56]    [Pg.248]    [Pg.283]    [Pg.1109]    [Pg.243]    [Pg.1710]    [Pg.1037]    [Pg.134]    [Pg.134]    [Pg.288]    [Pg.288]    [Pg.11]    [Pg.539]   


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