A new method for ¯ow injection analysis (FIA) of traces of uranium by catalytic amperometric detection in nitrate medium is described. Interfering oxygen was removed by in-line degassing. A simple adapter was designed to afford FIA with batch cells comprising a hanging mercury drop electrode. The ca
Flame atomic absorption determination of trace cobalt in steel samples using a flow-injection on-line separation system
✍ Scribed by M. C. Yebra-Biurrun
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 150 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0895-7533
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✦ Synopsis
A flow-injection on-line system was developed for the trace determination of cobalt by flame atomic absorption spectrometry (FAAS) with separation and preconcentration on a minicolumn packed with a poly(aminophosphonic acid) chelating resin (PAPhA). This resin allows the selective separation of cobalt at pH 2 because Co(II) and Fe(III) are the only metal ions retained quantitatively at this pH level, and Co(II) presents a greater selectivity coefficient than Fe(III); therefore, Co(II) is preferentially complexed over Fe(III) on the active groups of the chelating resin. Elution was performed by using a small volume of 0.2 M nitric acid. At a consumption of 7 mL sample volume, the procedure resulted in an enhancement factor of 83 and yielded a detection limit of 0.15 lg/L (3r) at a sampling frequency of 32 h 1מ . The precision (coefficient of variation, n ס 11) was in the range 0.5-1.0% at the 1-15 lg/L level. The procedure was applied to the determination of cobalt in steel samples with high tolerance to interferences, and results obtained for a standard reference material were in good agreement with the certified value.
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ment factor of 47 in comparison with direct injection of 45 lL aqueous solution was obtained at a sampling frequency of 31 h 1מ . The detection limit (3 r) was found to be 2.8 ng L 1מ . The precision was 3% relative standard deviation (RSD) at the 0.2 lg L 1מ level (n ס 11). The results obta
An automated robotic method for sample pretreatment was developed for copper determination in environmental and biological materials at the low microgram per gram level. The robotic station performing the preliminary operations as weighing of sample and acid digestion was coupled with the flowinject