Abstract
In solution antimony exists either in the pentavalent or trivalent oxidation state. As Sb(III) is more toxic
than Sb(V), it is important to be able to perform a quantitative speciation analysis of Sb’s oxidation
state. The most commonly applied chromatographic methods used for this redox speciation analysis
do, however, often show a low chromatographic Sb recovery when samples of environmental or
biological origin are analysed. In this study we explored basal chemistry of antimony and found that
formation of macromolecules, presumably oligomeric and polymeric Sb(V) species, is the primary cause
of low chromatographic recoveries. A combination of HPLC-ICP-MS, AFFF-ICP-MS and spinfiltration
was applied for analysis of model compounds and biological samples. Quantitative
chromatographic Sb redox speciation analysis was possible by acidic hydrolysis of the antimony
polymers prior to analysis. Sample treatment procedures were studied and the optimum solution was
acidic hydrolysis by 1 M HCl in the presence of chelating ligands (EDTA, citrate), which stabilise the
trivalent oxidation state of Sb.
| Original language | English |
|---|---|
| Journal | Analyst |
| Volume | 136 |
| Issue number | 5 |
| Pages (from-to) | 996-1002 |
| ISSN | 0003-2654 |
| DOIs | |
| Publication status | Published - 2011 |
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