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of naphthalene,then performance testing for naphthalene recovery and carryover from where soil permeability is not an issue,a vacuum of less than 100-inches of water <br /> each laboratory should be conducted. Acceptable recovery of naphthalene should be should be applied in conjunction with a Bow rate of less than or equal to 100 mUmin <br /> demonstrated by EPA Method TO-15 from a gas standard at a concentration of 32 (e.g.,50 mUmin for 30 min to collect a 1.5 L sample). Since naphthalene contamination <br /> ug/m or less prepared in a passivated canister of the same make and approximate age from industrial activities,such as those from manufactured gas plants,is frequently <br /> as those used for sampling. A blank sample should be processed and analyzed to encountered at shallow depths(e.g.5 it bgs or less),quantitative tracer testing using <br /> check for any carry over after the naphthalene gas standard is analyzed and after the helium is recommended to monitor potential ambient air breakthrough.An example <br /> highest naphthalene standard analyzed for the calibration curve is processed. Any sampling setup using Tenax GR for naphthalene can be found in the reference provided <br /> subsequent carryover concentration of naphthalene from the blank sample,which is below by Hayes at al.,2008. A field duplicate should be collected and a trip blank <br /> greater than the method detection limit(MDL),should be substantially lower than the should be used. When sample collection is complete,the sorbent tube is sealed with <br /> reporting limit(RL)to assure that the following analyses are not compromised. dedicated fittings or non-sorbing,non-reactive caps,and the tubes are shipped to the <br /> laboratory in a cooler chilled to<4'C. Standard chain-of-custody protocols should be . <br /> Naphthalene may also condense onto the surface of canisters;therefore,storage followed. Holding times for most EPA Method TO-17 samples is 30 days. <br /> stability tests for the prepared naphthalene vapor standards should be performed for the - <br /> duration of expected holding time. A calibration curve,which takes into account any Items to consider when soil gas sampling and analyses pursuant to Sorbent/Method <br /> expected carry over or condensation,should be used for quantification. Furthermore, TO-17 areas follows: <br /> naphthalene readily sorbs onto traditional soil gas sampling tubing such as polyethylene <br /> and nylaflow(Hayes et al.,2006;Ouellette,2004). Thus,the entire sampling system • Practitioner's Unfamiliarity,.The practitioner's unfamiliarity with sampling using a <br /> should be composed of Teflon,Polyetheretherketones.(PEEK).or other tubing types vacuum pump due to the recommendation of many guidance documents for use of <br /> with demonstrated inertness for naphthalene and with acceptable background criteria. fixed flow rate(generally 100 or 200 mUmin)rather than the applied vacuum for <br /> Using proper materials in the sampling system will ensure that soil gas samples are - collection of soil gas samples. The applied vacuum,which is the more important <br /> representative of subsurface conditions. component of soil gas permeability,is frequently overlooked in collecting soil gas <br /> Future recommendation for the naphthalene sample collection method may ultimately samples. <br /> depend on the capability of the stationary laboratory performing the analyses. As an Perceived Limitations with Sorb nt Tubes.Other concerns and perceived limitations <br /> example,some laboratories are now equipped with updated Thermal Desorption(TD) with use of the sorbent tube include:.(1)lack of repeat analysis for samples collected <br /> units capable of sample reruns as well as dilutions for EPA Method TO-17. The in sorbent;(2)breakthroughof target analytes during sampling;and(3)potential <br /> improved TO unit overcomes the perceived limitation of sorbent method being a"one- mass spectrometer overload from high VOCs concentrations. By practice,the <br /> shot deal"without repeat analysis and reduces concern for the potential mass trapped VOCs/SVOCs constituents are desorbed completely from the sorbent into <br /> spectrometer overload(Hayes, H.et al,2007). A new innovation for EPA Method TO- the mass spectrometer;therefore.the potential for instrument overload is still <br /> 15 analysis includes design to allow recovery of C2 to C25 compounds with extremely possible even with use of the updated TD instrumentation. Unlike the ambient air <br /> low carryover(<0.1%);therefore,extending EPA Method TO-15 analysis to include a and indoor air samples where the concentrations of VOCs and SVOCs are in the <br /> similar compound range as the Tenax/TO-17. The low carryover within the system lower,more predictable range,soil gas concentrations can be variable and are <br /> alleviates the potential for reported naphthalene concentrations to be biased low due to potentially much greater than 1000-fold above the ambient air concentration. <br /> losses within the internal hardware. Therefore;if the soil gas constituent concentrations from probes are not pre- <br /> screened using another active(or passive)method prior to sorbent sampling,there <br /> Sample Collection Method for Naphthalene is a potential for analytical instrumentation overload. In this regard,sorbent/EPA <br /> Method TO-17 as a"stand alone"method for naphthalene deserves caution. The <br /> Soil gas samples for analysis by EPA Method TO-17 should be collected with sampling reporting limit of handheld photo-ionization detectors(PID)are in the range of parts <br /> tubes packed with an appropriate sorbent material. For naphthalene,the sorbent per million(ppmv)and is too elevated for screening chemical constituents for vapor <br /> material is usually Tenax(e.g.,Tenax TA or GR). The analytical laboratory conducting intrusion purposes(except if a more sensitive PID such as ppbRAET"is used). <br /> the analysis typically supplies the sorbent tubes used for sampling. As an example,two <br /> 3.5-inch Tenax GR traps in series(i.e..front to back)with 200 mg sorbent in each Breakthrough Volumes The sampling volume should be calculated by taking two- <br /> column can be used to monitor breakthrough.Sampling should be based on both flow thirds of the estimated breakthrough volume. If breakthrough volumes cannot be <br /> rate and applied vacuum to address the gas permeability of the soil. Nested semi- determined,sorbent tubes should be arranged in series(as described above)and all <br /> permanent or permanent probes should be used for soil gas sampling,with hydrated tubes should be submitted to the laboratory for analysis. <br /> bentonite seals throughout the annulus with compression fittings. For a probe location <br /> 12/10/2009 -65- <br /> 12/10/2009 -66- <br />