Abstract
Formaldehyde, after in situ conversion to an ionic derivative with Girard's reagent T, was first accumulated on a Nafion-coated mercury film electrode. The adsorbed derivative was then determined in aqueous solution using differential-pulse voltammetry. A single peak centred at -1.24 V (versus Ag-AgCl) was observed at pH 9.7 when using 0.4 mol l-1 NH4Cl-NH3 as the supporting electrolyte. The calibration graphs were rectilinear over the range from 2.0 × 10-7 to 1.0 × 10-5 mol l-1 formaldehyde. By incorporating a preconcentration step via the Nafion-modified electrode, the detection limit of the method for formaldehyde was calculated to be 3.4 × 10-8 mol l-1. The reproducibility and lifetime studies of the electrodes indicated that a newly prepared electrode could be repeatedly used for more than ten measurements with satisfactory precision. In addition, the method can be extended, without any modification, to the determination of acetaldehyde.
| Original language | English |
|---|---|
| Pages (from-to) | 1727-1730 |
| Number of pages | 4 |
| Journal | Analyst |
| Volume | 121 |
| Issue number | 11 |
| DOIs | |
| Publication status | Published - Nov 1996 |
User-Defined Keywords
- Differential-pulse voltammetry
- Formaldehyde determination
- Girard's reagent T
- Nafion-modified electrode
- Organic analysis
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