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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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Bibliographic Details
Published in:Analytica chimica acta 1998-07, Vol.367 (1), p.55-61
Main Authors: Ali Taher, Mohammad, Mostafavi Dehzoei, Ali, Krishan Puri, Bal, Puri, Swati
Format: Article
Language:English
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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.
ISSN:0003-2670
1873-4324
DOI:10.1016/S0003-2670(98)00063-4