Determination of the pesticide naptalam and its degradation products by positive and negative ion mass spectrometry

Citation
A. Ghassempour et al., Determination of the pesticide naptalam and its degradation products by positive and negative ion mass spectrometry, FRESEN J AN, 369(2), 2001, pp. 176-183
Citations number
22
Categorie Soggetti
Spectroscopy /Instrumentation/Analytical Sciences
Journal title
FRESENIUS JOURNAL OF ANALYTICAL CHEMISTRY
ISSN journal
09370633 → ACNP
Volume
369
Issue
2
Year of publication
2001
Pages
176 - 183
Database
ISI
SICI code
0937-0633(200101)369:2<176:DOTPNA>2.0.ZU;2-Z
Abstract
N-1-Naphthylphtalamic acid (naptalam) and its degradation products, 1-napht hylamine and N-(1-naphthyl) phthalimide were simultaneously determined in r iver water by two independent mass spectrometric (MS) methods. These were n egative ion MS (NIMS) and programmable temperature vaporizer gas chromatogr aphy mass spectrometry (PTV-GC MS) with electron impact ionization (positiv e ions). Prior to the NIMS analysis, the samples were preconcentrated by so lid phase extraction (SPE) of C-18 membrane discs. The PTV-GC MS studies we re performed without any preconcentration procedure. Selected ion monitorin g (SIM) and internal standardization with naphthalene were applied in both methods. The limits of determination (LOD) of NIMS studies were 230, 270 an d 260 ng L-1 for naptalam, 1-naphthylamine and N(1-naphthyl) phthalimide, r espectively, with relative standard deviation (RSD) < 1% (n = 5) and of PTV -GC MS 17, 11 and 15 ng L-1 (RSD < 0.7%, n = 5). The LOD, linearity, RSD an d time required for these methods are far better than for HPLC analyses.