Abstract
The simultaneous determination of three isomers of phenylenediamines (o, m, and p-phenylenediamine) and two isomers of dihydroxybenzenes (catechol and resorcinol) in hair dyes was performed by capillary zone electrophoresis coupled with amperometric detection (CZE-AD). The effects of working electrode potential, pH and concentration of running buffer, separation voltage, and injection time on CZE-AD were investigated. Under the optimum conditions the five analytes could be perfectly separated in 0.30 mol L-1 borate-0.40 mol L-1 phosphate buffer (pH 5.8) within 15 min. A 300 μm diameter platinum electrode had good responses at +0.85 V (versus SCE) for the five analytes. Their linear ranges were from 1.0∈×∈10 -6 to 1.0∈×∈10-4 mol L-1 and the detection limits were as low as 10-7 mol L-1 (S/N∈=∈3). This working electrode was successfully used to analyze eight kinds of hair dye sample with recoveries in the range 91.0-108.0% and RSDs less than 5.0%. These results demonstrated that capillary zone electrophoresis coupled with electrochemical detection using a platinum working electrode as detector was convenient, highly sensitive, highly repeatable and could be used in the rapid determination of practical samples. [Figure not available: see fulltext.]
| Original language | English |
|---|---|
| Pages (from-to) | 653-659 |
| Number of pages | 7 |
| Journal | Analytical and Bioanalytical Chemistry |
| Volume | 391 |
| Issue number | 2 |
| DOIs | |
| State | Published - May 2008 |
Keywords
- Amperometric detection
- Capillary zone electrophoresis
- Hair dyes
- Isomers
- Platinum working electrode
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