INTERFERENCE OF HUMIC SUBSTANCES ON THE SPECIATION ANALYSIS OF INORGANIC SELENIUM IN WATERS AND SOILS BY DPCSV

Citation
M. Potingautier et al., INTERFERENCE OF HUMIC SUBSTANCES ON THE SPECIATION ANALYSIS OF INORGANIC SELENIUM IN WATERS AND SOILS BY DPCSV, Fresenius' journal of analytical chemistry, 351(4-5), 1995, pp. 443-448
Citations number
32
Categorie Soggetti
Chemistry Analytical
ISSN journal
09370633
Volume
351
Issue
4-5
Year of publication
1995
Pages
443 - 448
Database
ISI
SICI code
0937-0633(1995)351:4-5<443:IOHSOT>2.0.ZU;2-T
Abstract
A speciation scheme allowing the study of selenium speciation in envir onmental samples has been developed in order to study the transfer mec hanism in the system water/soil/plant/animal. This scheme is based on a set of sample treatment procedures followed by Se(TV) determination by Differential Pulse Cathodic Stripping Voltammetry (DPCSV). Se(IV) m ay be determined with a detection limit close to 25 ng l(-1) and a lin ear response in the range 25-4000 ng l(-1). However, humic substances, present in some natural waters and soils, which are adsorbed at the m ercury drop electrode (HMDE) surface may alter the signal. This may be caused by a competition between adsorption of organic matter and merc ury(II) selenide formation at the electrode surface. As a consequence the detection limit has been increased to ca. 250 ng l(-1) in the pres ence of 1 mg l(-1) fulvic acids; the linear response range is then shi fted to 250-10000 ng l(-1). After an extensive study of these interfer ences and using standard additions procedures, the Se(TV) content of v arious waters and soil extracts has been determined by DPCSV with a go od reproducibility (RSD about 1%). Accuracy is satisfactory comparing the results obtained by DPCSV to those obtained by Hydride Generation/ Quartz Furnace Absorption Atomic Spectrometry (HG/QFAAS).