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KIRTLAND AIR FORCE BASE ALBUQUERQUE, NEW MEXICO ...

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APPENDIX B<br />

Field Analysis with a Portable Gas Chromatograph<br />

This method entails analyzing the soil gas samples with a portable gas chromatograph set up in the field.<br />

Portable units, such as a Photovac Model 10S PLUS, can be used. This analysis method has the inherent<br />

advantage of giving the user immediate results, so the survey can be directed based on the incoming data.<br />

This is the most common method for analysis of soil gas samples.<br />

With the portable gas chromatograph, a gas sample is injected directly into the machine using a gas-tight<br />

syringe. The GC then chromatographically separates and detects the organics present. The results are<br />

recorded in the form of a chromatograph. Each peak on the chromatograph is indicative of a single<br />

compound. The area under the peak is indicative of the concentration of that compound.<br />

In most cases, the portable GCs use flame ionization detectors (FIDs) or PIDs for detection. FIDs detect<br />

all hydrocarbons, but for that reason can suffer from interference. Photoionization detectors detect most<br />

compounds except methane and halogenated alkanes. For sites where low levels of chlorinated<br />

compounds are expected, electron-capture detectors are used. electron capture detectors are selective<br />

detector allowing considerable lower detection limits for halogenated compounds than do the PID or FID.<br />

Using a portable GC, the soil gas samples are analyzed anywhere from a few minutes to several hours<br />

after collection. The results are then available to direct additional soil gas identification and<br />

quantification of each compound present in the sample is possible. To be quantified, standards of the<br />

compounds present in a sample must be included in the instrument calibration.<br />

Calibration<br />

Standards should be prepared each day and can consist of one or several of the compounds suspected to<br />

be present at the site. An alternative to preparing standards on site is having gas standards prepared by a<br />

specialty gas vendor. The instrument should be calibrated at the beginning of each day and the<br />

calibration should be checked at the end of each day and at least every ten samples.<br />

Standards can be prepared by several procedures, each of which is acceptable if performed properly.<br />

Preferably, the standards should be prepared in glass bottles fitted with Teflon ® septa, but inert gas<br />

sampling bags are also acceptable. The preferred standard preparation method is to inject calculated<br />

volumes of spectroscopic-grade liquid reagents into an amber glass bottle that has been filled with<br />

hydrocarbon-free air. The vapor from that bottle is used to produce serial dilutions in other bottles.<br />

Another method is to collect headspace vapor above a liquid solvent of interest and inject it into a bottle<br />

and again make serial dilutions. If the vapor is collected above a liquid solvent, the solvent must be kept<br />

in a temperature-controlled bath. If a laboratory-type GC is used, standards can be prepared in methanol.<br />

Methanol-based standards are prepared by serial dilution from spectroscopic-grade liquid reagents and<br />

may be used for up to one week.<br />

Calibration consists of injecting the standard into the gas chromatograph and setting the integrator to<br />

recognize and quantify the peaks in the standard. Standards are run throughout the soil gas program to<br />

check the calibration and the GC. Following the initial calibration, calibration should not be changed<br />

unless the integrator is not recognizing or quantifying the compounds in the standard.<br />

Analysis<br />

Sample analysis consists of injecting the sample into the calibrated gas chromatograph. A chromatogram<br />

is produced, and the integrator will identify the peaks in the standard. If the field chemist determines that<br />

Kirtland AFB<br />

SOPs for Field Investigations B-104 April 2004

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