z-logo
Premium
Speciation of Selenium(IV) and Selenium(VI) using Coupled Ion Chromatography—Hydride Generation Atomic Absorption Spectrometry
Author(s) -
Goldberg Sabine,
Martens D. A.,
Forster H. S.,
Herbel M. J.
Publication year - 2006
Publication title -
soil science society of america journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.836
H-Index - 168
eISSN - 1435-0661
pISSN - 0361-5995
DOI - 10.2136/sssaj2005.0141
Subject(s) - selenium , chemistry , selenate , hydride , atomic absorption spectroscopy , ion chromatography , detection limit , genetic algorithm , ion exchange , adsorption , mass spectrometry , chromatography , ion , analytical chemistry (journal) , metal , physics , organic chemistry , quantum mechanics , evolutionary biology , biology
A simple method was developed to speciate inorganic Se in the μg L −1 range using coupled ion chromatography‐hydride generation atomic absorption spectrometry. Because of the differences in toxicity and adsorption behavior, determination of the redox states selenite, Se(IV), and selenate, Se(VI), is important. We used anion exchange chromatography to separate Se(IV) and Se(VI) based on differences in retention times. Samples were then mixed with concentrated HCl and passed through a 130°C sand bath to reduce Se(VI) to Se(IV) for Se determination as the hydride. Detection limits were 0.68 μg L −1 for Se(IV) and 0.55 μg L −1 for Se(VI). Spiking of actual sample solutions with Se(IV) and Se(VI) showed the procedure to be accurate for solutions with Se(IV)/Se(VI) ratios ranging from 1:4 to 4:1. Average recovery was 93.1% for Se(IV) and 108% for Se(VI). The technique was used to determine Se(IV) and Se(VI) in deionized water and actual and synthetic irrigation waters.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom