Please use this identifier to cite or link to this item: https://hdl.handle.net/11681/9031
Full metadata record
DC FieldValueLanguage
dc.contributorU.S. Army Toxic and Hazardous Materials Agency.-
dc.contributor.authorJenkins, Thomas F.-
dc.contributor.authorWalsh, Marianne E.-
dc.date.accessioned2016-06-20T13:39:57Z-
dc.date.available2016-06-20T13:39:57Z-
dc.date.issued1987-06-
dc.identifier.urihttp://hdl.handle.net/11681/9031-
dc.descriptionCRREL Report-
dc.descriptionAbstract: An analytical method was developed to determine the concentrations of HMX, RDX, TNB, DNB, Tetryl, TNT and 2,4-DNT in soil. The method involves extracting a 2-g sample with 50 mL of acetonitrile using an ultrasonic bath procedure for 18 hr. A 10-mL portion of the extract is diluted with 10 mL of water, filtered through a 0.45-~m Millex SR filter, and analyzed by RP-HPLC using a fixed 254-nm UV detector. Separations were obtained on an LC-18 column eluted with 50:50 water-methanol. Retention times were 2.55, 3.82, 5.16, 6.25, 7.04, 8.47 and 10.15 min for HMX, RDX, TNB, DNB, Tetryl, TNT and 2,4-DNT, respectively. Confirmation of analyte identities is recommended by RP-HPLC on an LC-CN column using 50:50 water-methanol. Kinetic studies using naturally contaminated soil indicated that equilibrium was achieved within 24 hr for the majority of soils and analytes studied. The method provides linear calibration curves over a wide range of concentrations. Reporting limits were conservatively estimated at 1.6, 1.8, 1.5, 0.5, 5.5, 0.8 and 0.8 ~g/g for HMX, RDX, TNB, DNB, Tetryl, TNT and 2,4-DNT. Analytical precision was estimated at ± 0.44, 0.51, 0.43, 0.13, 1.24, 0.27 and 0.20 ~g/g, respectively, in the range of homogeneous variance near the detection limits. At higher concentrations the relative standard deviation was constant at 2% for HMX, RDX, DNB and TNB, 3% for TNT and 2,4-DNT, and 6% for Tetryl. Recovery was found to be greater than 96% for all analytes from a spike-recovery study. The method was successfully tested using contaminated soil from the Iowa Army Ammunition Plant, which gave a range of analyte concentrations from near the detection limit to the percent levels. Several types of commercial 0.45-mm filters were tested. No loss of analytes was found when 50:50 acetonitrile-water solutions were filtered. Note: The presence of the symbol ~ indicates the absence of a scientific or mathematical symbol that could not be rendered by the character set of this system. The downloaded will contain the missing symbols.-
dc.publisherCold Regions Research and Engineering Laboratory (U.S.)-
dc.publisherEngineer Research and Development Center (U.S.)-
dc.relationhttp://acwc.sdp.sirsi.net/client/en_US/search/asset/1001168-
dc.relation.ispartofseriesCRREL report ; 87-7.-
dc.rightsApproved for public release; distribution is unlimited.-
dc.sourceThis Digital Resource was created from scans of the Print Resource-
dc.subjectAnalytical methods-
dc.subjectHigh-performance liquid chromatography-
dc.subjectContaminated soils-
dc.subjectSoils-
dc.subjectExplosives-
dc.titleDevelopment of an analytical method for explosive residues in soil-
dc.typeReporten_US
Appears in Collections:CRREL Report

Files in This Item:
File Description SizeFormat 
CRREL-87-7.pdf784.87 kBAdobe PDFThumbnail
View/Open