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Determinations of N-Nitrosodimethylamine (NDMA) at part-per-trillion (ng/L) concentrations in contaminated groundwaters and drinking waters featuring carbon-based membrane extraction disks
Author(s) -
Bruce A. Tomkins,
W.H. Griest,
Gregory N. Connolly,
Hugh Hayes
Publication year - 1996
Language(s) - English
Resource type - Reports
DOI - 10.2172/261102
Subject(s) - detection limit , extraction (chemistry) , chemistry , n nitrosodimethylamine , aqueous solution , chromatography , analyte , gas chromatography , solid phase extraction , dichloromethane , analytical chemistry (journal) , carbon fibers , materials science , organic chemistry , carcinogen , composite material , solvent , composite number
A new solid phase extraction procedure extracts N- Nitrosodimethylamine (NDMA) at part-per-trillion (ng/L) concentrations from aqueous samples using a C{sub 18} (reversed-phase) membrane extraction disk layered over a carbon-based extraction disk. The reversed-phase disk removes nonpolar water-insoluble neutrals and is set aside; the carbon-based disk is extracted with a small volume of dichloromethane. NDMA is quantitated in the organic extract using a gas chromatograph equipped with both a short-path thermal desorber and a chemiluminescent nitrogen detector (CLND). The Method Detection Limit for the procedure is 2 ng of NDMA/L; the analyte recovery is approximately 57%. A related procedure substitutes a standard automatic sampler for the short-path thermal desorber, and is suitable for determining NDMA in heavily-contaminated aqueous samples. The Method Detection Limit for the `high-level` procedure, which employs an automatic sampler, is 180 ng of NDMA/L, with an analyte recovery of approximately 64%

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