Direct Electrodeposition of Carbon Dots Modifying Bismuth Film Electrode for Sensitive Detection of Cd2+ and Pb2+

A sensitive, selective, and stable sensor for the simultaneous determination of Cd2+ and Pb2+ in aqueous solution has been developed based on the carbon dots (CDs) and Nafion-modified bismuth film glassy carbon electrode (GCE). High graphitized CDs prepared by the sulfuric acid-assisted hydrothermal synthesis were directly electrodeposited on the GCE surface by cyclic voltammetry. Compared with the conventional bismuth film electrodes, CDs greatly improved the electrochemical activity of the bismuth film electrode for the detection of Cd2+ and Pb2+. After decorating CDs, the surface impedance of the GCE was decreased from 10.9 kΩ to 4.84 kΩ. Meanwhile, the corresponding response currents of the Bi/GCE were increased over 7.4 and 2.4 times for Cd2+ and Pb2+ with a wide linear range of 0.05-0.50 mg/L, respectively. High sensitivity was obtained with the detection limits of 3.1 μg L-1 (Cd2+) and 2.3 μg L-1 (Pb2+). Moreover, good stability was obtained for the simultaneous determination of Cd2+ and Pb2+ in the practical underground water with the relative standard deviations less than 10%. The results indicated that the CDs-modified bismuth film electrode could potentially be applied to detect the heavy metal ion concentrations in practical environment.

New Strategies for the Simple and Sensitive Voltammetric Direct Quantification of Se(IV) in Environmental Waters Employing Bismuth Film Modified Glassy Carbon Electrode and Amberlite Resin

An analytical procedure regarding the determination of selenium(IV) by anodic stripping voltammetry exploiting the in situ plated bismuth film electrode is described. Since organics are commonly present in untreated natural water samples, the use of Amberlite XAD-7 resin turns out to be quite important to avoid problems such as the adsorption of these compounds on the working electrode. The optimum circumstances for the detection of selenium in water using differential pulse voltammetry techniques were found to be as follows: 0.1 mol L−1 acetic acid, 1.9 × 10−5 mol L−1 Bi(III), 0.1 g Amberlite XAD-7 resin, and successive potentials of −1.6 V for 5 s and −0.4 V for 60 s, during which the in situ formation of the bismuth film on glassy carbon and the accumulation of selenium took place. The current of the anodic peak varies linearly with the selenium concentration ranging from 3 × 10−9 mol L−1 to 3 × 10−6 mol L−1 (r = 0.9995), with a detection limit of 8 × 10−10 mol L−1. The proposed procedure was used for Se(IV) determination in certified reference materials and natural water samples, and acceptable results and recoveries were obtained.

Implementation of Metallic Film Electrodes for Catalytic Adsorptive Stripping Voltammetric Determination of Germanium(IV)

In the present work, it has been shown that bismuth film electrodes deposited on screen-printed carbon supports could be successfully used to provide well-shaped, sensitive and reproducible catalytic adsorptive stripping signals of Ge(IV) in the presence of catechol and V(IV)-HEDTA (HEDTA-N-hydroxyethyl-ethylene diamine-triacetic acid) complex.