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Derivative UV-visible spectrophotometric determination of nickel in alloys and biological samples after preconcentration with the ion pair of 2-nitroso-1-naphthol-4-sulfonic acid and tetradecyldimethylbenzylammonium chloride onto microcrystalline naphthalene or by a column method
Nickel is quantitatively retained by tetradecyldimethylbenzylammonium 2-nitroso-1-naphthol-4-sulfonate in microcrystalline naphthalene in the pH range 7.2–11.8 from a large volume of aqueous solutions of various alloys and biological samples. After filtration, the solid mass consisting of the nickel...
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Published in: | Analytica chimica acta 1998-07, Vol.367 (1), p.55-61 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Nickel is quantitatively retained by tetradecyldimethylbenzylammonium 2-nitroso-1-naphthol-4-sulfonate in microcrystalline naphthalene in the pH range 7.2–11.8 from a large volume of aqueous solutions of various alloys and biological samples. After filtration, the solid mass consisting of the nickel complex of 2-nitroso-1-naphthol-4-sulfonate and naphthalene was dissolved in 5
ml of dimethylformamide and the nickel as determined by first derivative UV-visible spectrophotometry. Nickel can alternatively be quantitatively adsorbed on a 2-nitroso-1-naphthol-4-sulfonic acid-tetradecyldimethylbenzylammonium-naphthalene adsorbent packed in a column and determined similarly. The detection limit is 0.3
μg
ml
−1 (signal to noise ratio=2) and the calibration graph is linear over the concentration range 0.9–120
μg
ml
−1 in dimethylformamide solution with a correlation coefficient of 0.9995 (
n=6) and relative standard deviation for 8
μg
ml
−1 nickel of 1.4% (
n=6). Various parameters such as the effect of pH, volume of aqueous phase and interference of a number of metal ions on the determination of nickel have been studied in detail to optimize the conditions for determination in standard alloys and biological samples. |
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ISSN: | 0003-2670 1873-4324 |
DOI: | 10.1016/S0003-2670(98)00063-4 |