Various matrix modifiers were investigated for the determination of molybdenum in human urine samples by electrothermal atomization atomic absorption spectrometry. Methods with nitric acid, barium difluoride, magnesium nitrate, palladium-magnesium nitrate and palladium-hydroxylamine hydrochloride we
Automated direct determination of chromium in blood and urine by electrothermal atomic absorption spectrometry
β Scribed by J.J. McAughey; N.J. Smith
- Publisher
- Elsevier Science
- Year
- 1987
- Tongue
- English
- Weight
- 707 KB
- Volume
- 193
- Category
- Article
- ISSN
- 0003-2670
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β¦ Synopsis
A simple direct procedure for the determination of chromium in whole blood and urine by graphite-furnace atomic absorption spectrometry is described. Whole blood samples are diluted with 0.1% Triton-X solution before injection, whereas urine samples are injected directly. Calibration is done by direct comparison against matrix-matched standards. Between-run precision is 6.4% at 154 nmol 1-l for urine and 3.6% at 142 nmol 1-l for blood. The detection limits are 3.8 nmol 1-l for urine and 11.5 nmol 1-l for blood, each for a 20+1 sample. The calibration range extends up to 770 nmol 1-l for both blood and urine. This allows the determination of chromium in both occupationally exposed and unexposed groups. The graphite-furnace conditions for each matrix are similar. Elimination of sample pretreatment minimizes the risk of contamination and allows a rapid sample throughput of 50-60 samples per day. The methods described are particularly suited for the screening and surveying of populations occupationally exposed to chromium.
π SIMILAR VOLUMES
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