On Site Method For Measuring Nitroaromatic And Nitramine Explosives In Soil And Groundwater Using Gc Npd
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On-site Method for Measuring Nitroaromatic and Nitramine Explosives in Soil and Groundwater Using GC-NPD
An on-site method has been developed for estimating concentrations of TNT, RDX, 2,4-DNT, and the two most commonly encountered environmental transformation products of TNT, 2-amino-4,6-dinitrotoluene and 4-amino-2,6-dinitrotoluene, in soil and groundwater using gas chromatography and the nitrogen-phosphorus detector (NPD). Soil samples (20 g) are extracted by shaking with 20 mL of acetone, and extracts are filtered through a Millex SR (0.5-micrometers) filter. Groundwater samples (1 L) were passed through SDB-RPS extraction disks that were subsequently extracted with 5 mL of acetone. A 1-micro-L volume of a soil or water extract is manually injected into a field-transportable gas chromatograph equipped with a NPD and a heated injection port. Separations are conducted on a Restek Crossbond 100% dimethyl polysiloxane column, 6 m x 0.53-mm i.d., 1.5 mm, using nitrogen carrier gas at 9.5 mL/min. Retention times range from 3.0 min. for 2,4-dinitrotoluene (2,4-DNT) to 5.6 min. for 2-amino-4,6-dinitrotoluene. Method detection limits were less than 0.16 mg/kg for soil and less than 1.0 microgram/L for groundwater. One of the major advantages of this method, over currently available colorimetric and enzyme immunoassay on-site methods, is the ability to quantify individual target analytes that often coexist in soils and groundwater contaminated with explosive residues. This method will be particularly useful at military antitank firing ranges where it is necessary to quantify residual concentrations of RDX in the presence of high concentrations of HMX, and when the transformation products of TNT need to be identified.
Field Gas Chromatography/thermionic Detector System for On-site Determination of Explosives in Soils
On-site determination of nitroaromatic, nitramine, and nitrate ester explosives compounds in soils was performed using a field-portable gas chromatograph (GC)equipped with a thermionic ionization detector (TID)selective for compounds with nitro functional groups. Soil samples were extracted with acetone. A 1 microliter volume of the filtered soil extract was manually injected into the GC, allowing for the rapid qualification and quantification of the suite of explosives that often coexist in soils at military training facilities and other defense-related sites. Good agreement was established for the concentrations of several explosives analytes when this method of analysis was compared to either high-performance liquid chromatography (Method 8330)or GC electron capture (Method 8095)analysis. Comparisons were performed for sample extracts and for soil subsample replicates distributed for on-site preparation and analysis during a field verification test performed under the auspices of the U.S. Environmental Protection Agency's Environmental Technology Verification (ETV)Program.
On-Site Method for Measuring Nitroaromatic and Nitramine Explosives in Soil and Groundwater Using GC-NPD: Feasibility Study
An on-site method has been developed for estimating concentrations of TNT, RDX, 2,4-DNT, and the two most commonly encountered environmental transformation products of TNT, 2-amino-4,6-dinitrotoluene and 4-amino-2,6-dinitrotoluene, in soil and groundwater using gas chromatography and the nitrogen-phosphorus detector (NPD). Soil samples (20 g) are extracted by shaking with 20 mL of acetone, and extracts are filtered through a Millex SR (0.5-micrometers) filter. Groundwater samples (1 L) were passed through SDB-RPS extraction disks that were subsequently extracted with 5 mL of acetone. A 1-micro-L volume of a soil or water extract is manually injected into a field-transportable gas chromatograph equipped with a NPD and a heated injection port. Separations are conducted on a Restek Crossbond 100% dimethyl polysiloxane column, 6 m x 0.53-mm i.d., 1.5 mm, using nitrogen carrier gas at 9.5 mL/min. Retention times range from 3.0 min. for 2,4-dinitrotoluene (2,4-DNT) to 5.6 min. for 2-amino-4,6-dinitrotoluene. Method detection limits were less than 0.16 mg/kg for soil and less than 1.0 microgram/L for groundwater. One of the major advantages of this method, over currently available colorimetric and enzyme immunoassay on-site methods, is the ability to quantify individual target analytes that often coexist in soils and groundwater contaminated with explosive residues. This method will be particularly useful at military antitank firing ranges where it is necessary to quantify residual concentrations of RDX in the presence of high concentrations of HMX, and when the transformation products of TNT need to be identified.