Determination of zinc in water samples by flame atomic absorption spectrometry after homogeneous liquid-liquid extraction
In this study, a new and simple homogeneous liquid-liquid extraction ( HLLE ) method based on a pH-independent phase-separation process was developed using a ternary solvent system [water-tetrabutylammonium ion ( TBA + )-chloroform] for the preconcentration of Zn 2+ ions. A Schiff’s base ligand was...
Gespeichert in:
Veröffentlicht in: | Journal of analytical chemistry (New York, N.Y.) N.Y.), 2011-06, Vol.66 (6), p.612-617 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | In this study, a new and simple homogeneous liquid-liquid extraction (
HLLE
) method based on a pH-independent phase-separation process was developed using a ternary solvent system [water-tetrabutylammonium ion (
TBA
+
)-chloroform] for the preconcentration of Zn
2+
ions. A Schiff’s base ligand was used as the chelating agent prior to Zn
2+
ions extraction. Flame atomic absorption spectrophotometry using acetylene-air flame was used for the quantification of analyte after preconcentration. The phase separation occurred due to ion-pair formation of TBA and perchlorate ion. The sedimented phase was then separated using a 100 μL micro-syringe and diluted to 1.0 mL with ethanol. The sample was introduced into the flame by conventional aspiration. After the optimization of complexation and extraction conditions such as pH 9.0, [ligand] = 1.0 × 10
−5
M, [TBA
+
] = 2.0 × 10
−2
M, 100.0 μL of [CHCl
3
] and [CLO
4
−
] = 2.0 × 10
−2
M, a preconcentration factor of 100 was achieved for only 10 mL of the sample. The relative standard deviation was 2.3% (
n
= 10). The limit of detection was sufficiently low and at ppb level. The proposed method was applied to the extraction and determination of Zn
2+
in natural water samples with satisfactory results. |
---|---|
ISSN: | 1061-9348 1608-3199 |
DOI: | 10.1134/S1061934811060062 |