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Tracer Research Corporation <br /> I <br /> seconds An analysis of the headspace in the bottle determined the Response Factor <br /> 1 (RF) which was then used to calculate the sample concentrations <br /> ' 5.1 Chromatographic System <br /> A Varian 3300 gas chromatograph,equipped with a flame ionization detector <br /> (FID) and one computing integrator, was used for the soil gas and groundwater <br /> headspace analyses The compounds were separated in the GC on a 10 foot by 118 <br /> inch outer diameter (OD) packed analytical column (10% OV-101 stationary phase <br /> ' bonded to 801100 mesh Chromosorb W support) The column was in a temperature <br /> controlled oven Nitrogen was used as the carrier gas The following paragraphs <br /> ' explain the GC and FID processes. <br /> i <br /> GC Process <br /> The soil gas and groundwater headspace vapor is infected into the GC where <br /> it is swept through the analytical column by the carrier gas The detector senses the <br /> presence of a component different from the carrier gas and converts that information <br /> to an electrical signal The components of the sample pass through the column at <br /> different rates, according to their individual properties, and are detected by the <br /> detector Compounds are identified by the time it takes them to pass through the <br /> Lcolumn (retention time) <br /> ' FID Process <br /> The FID utilizes a flame produced by the combustion of hydrogen and air <br /> When a component, which has been separated on the GC analytical column, is <br /> introduced into the flame, a large increase in ions occurs A collector with a <br /> polarizing voltage is applied near the flame and the ions are attracted and produce a <br /> current, which is proportional to the amount of the sample compound m the flame <br /> The electrical current causes the computing integrator to record a peak on a <br /> chromatogram By measuring the area of the peak and companng that area to the <br /> integrator response of a known aqueous standard, the concentration of the analyte in <br /> the sample is determined <br /> I <br /> Iuty 19 1994 Page 5 1140291S <br />