A highly selective voltammetric sensor for nanomolar detection of mercury ions using a carbon ionic liquid paste electrode impregnated with novel ion imprinted polymeric nanobeads

• Synthesis and characterization of Hg2 + imprinted polymeric nanobeads via precipitation polymerization.
• Use of dithizone as a suitable host for quantitative and selective enrichment of Hg2 + ions.
• Construction of a highly selective IIP-based voltammetric sensor for nanomolar detection of Hg2 +.
• Linear responses of 0.5 nM–10 nM and 0.08 μM–2 μM with a limit of detection of 0.1 nM.
• Application to separation and detection of mercury content of different waste water samples

This work reports the preparation of a voltammetric sensor for selective recognition and sensitive determination of mercury ions using a carbon ionic liquid paste electrode (CILE) impregnated with novel Hg2 +-ion imprinted polymeric nanobeads (IIP) based on dithizone, as a suitable ligand for complex formation with Hg2 + ions. The differential pulse anodic stripping voltammetric technique was employed to investigate the performance of the prepared IIP-CILE for determination of hazardous mercury ions. The designed modified electrode revealed linear responses in the ranges of 0.5 nM–10 nM and 0.08 μM–2 μM with a limit of detection of 0.1 nM (S / N = 3). It was found that the peak currents of the modified electrode for Hg2 + ions were at a maximum value in phosphate buffer of pH 4.5. The optimized preconcentration potential and accumulation time were to be − 0.9 V and 35 s, respectively. The applicability of the proposed sensor to mercury determination in waste water samples is reported.

Figure optionsDownload as PowerPoint slide