Sodium doping effect on physicochemical properties of K1−xNaxCaPb3(PO4)3 (0 ≤ x ≤ 1) for the determination of mercury(II): Application in seawater samples

Abstract

A new chemically modified electrode was synthesized for the determination of mercury(II) using differential pulse anodic stripping voltammetry (DPASV). The electrode was modified by lacunar apatite K1−xNaxCaPb3(PO4)3 (0≤x≤1) synthesized using solid reaction. These powders were crystallized in the hexagonal system, space group P63/m. The effect of sodium content on structural, thermodynamic and electrochemical properties of prepared apatite has been studied. Therefore, the best results was obtained using NaCaPb3(PO4)3 (x=1) as modifier of carbon paste electrode for the electrochemical detection of mercury(II). The later ions were preconcentrated on the surface of the modified electrode and oxidized at 0.06V vs. Ag/AgCl. The electroanalytical procedure comprises of two steps: the chemical accumulation of the analyte under open-circuit conditions followed by the electrochemical detection of the preconcentrated species using differential pulse voltammetry. The different parameters that govern the two steps were optimized. A linear response was obtained in the concentration range from 1.0molL−1×10−4molL−1 to 2.0molL−1×10−7molL−1 Hg(II) after activation of the electrode surface under the optimized conditions. The standard deviation was evaluated in a high and low concentration of mercury(II). The values ​​obtained for seven consecutive measurements were 1.24% and 5.07% of 1.0molL−1×10−4molL−1 and 5.0molL−1×10−6molL−1 mercury(II) solutions respectively. The detection limit and quantification limit for mercury(II), calculated from nine times standard deviation of blank/slope of the calibration graph, were 1.086molL−1×10−8molL−1 and 3.62molL−1×10−8molL−1, respectively. The proposed chemically modified electrode was applied to determine mercury(II) in seawater samples.