Differential Pulse Polarographic Determination of Cadmium After Solid Liquid Extraction and Preconcentration Using PAN

A highly selective, sensitive, rapid and economical differential pulse polarographic method has been developed for the determination of trace amounts of cadmium in various samples after the adsorption of its 1-(2-pyridylazo)-2-naphthol (PAN) complex on microcrystalline naphthalene in the pH range of 8.2-11.0. After filtration, the solid mass is shaken with 9.0 mL of 1 M hydrochloric acid and cadmium is determined by differential pulse polarography. Cadmium can alternatively be quantitatively adsorbed on [1-(2-pyridylazo)-2-naphthol]-naphthalene adsorbent packed in a column and determined similarly. The detection limit is 0.07 m g/mL (signal-to noise ratio = 2) and the linearity is maintained in the concentration range 0.1-150 m g/mL with a correlation coefficient of 0.9995 and relative standard deviation of \pm 0.98%. Characterization of the electroactive process included an examination of the degree of reversibility. Various parameters such as the effect of pH, volume of aqueous phase and interference of a number of metal ions on the determination of cadmium have been studied in detail to optimize the conditions for determination in various samples.

Differential Pulse Polarographic Determination of Cadmium After Solid Liquid Extraction and Preconcentration Using PAN

A highly selective, sensitive, rapid and economical differential pulse polarographic method has been developed for the determination of trace amounts of cadmium in various samples after the adsorption of its 1-(2-pyridylazo)-2-naphthol (PAN) complex on microcrystalline naphthalene in the pH range of 8.2-11.0. After filtration, the solid mass is shaken with 9.0 mL of 1 M hydrochloric acid and cadmium is determined by differential pulse polarography. Cadmium can alternatively be quantitatively adsorbed on [1-(2-pyridylazo)-2-naphthol]-naphthalene adsorbent packed in a column and determined similarly. The detection limit is 0.07 m g/mL (signal-to noise ratio = 2) and the linearity is maintained in the concentration range 0.1-150 m g/mL with a correlation coefficient of 0.9995 and relative standard deviation of \pm 0.98%. Characterization of the electroactive process included an examination of the degree of reversibility. Various parameters such as the effect of pH, volume of aqueous phase and interference of a number of metal ions on the determination of cadmium have been studied in detail to optimize the conditions for determination in various samples.