We present an electroanalytical method using square-wave anodic stripping voltammetry on electrochemically-treated screen-printed gold electrodes to the simultaneous determination of lead(II), copper(II) and mercury(II) in struvite (natural fertilizer produced from urine). Electrochemical treatment via cyclic voltammetry of the working electrodes increased surface rugosity that improved the electroanalytical responses for the three metals. Under optimized conditions and using a deposition time of 90 s, the proposed method presented the following limit of detection values: 1.3 µg L-1 for lead(II), 2.0 µg L-1 for copper(II) and 0.9 µg L-1 for mercury(II). Struvite samples were easily dissolved in supporting electrolyte solution (0.05 mol L-1 HCl). Satisfactory recovery values between 91 and 111% were obtained for the analysis of spiked samples. Hence, we can infer that the proposed electroanalytical method is an effective alternative for the determination of trace metals, since it provides precise and accurate direct analyses, with rapid responses without interference from sample matrix and enabling in field analysis.

This work presents the development and characterization of a new chemically modified electrode exploiting recordable Au-rewritable compact discs (AuCDs) as substrate for drop casting of a chemically-reduced graphene-oxide slurry focusing on simple and low-cost electrochemical sensors. Increase in electrochemical responses in cyclic voltammetric and amperometric measurements were achieved using the proposed sensor. Both scanning electron microscopy and atomic force microscopy data showed increase in rugosity (about 46% higher) for the chemically reduced graphene oxide (CRGO) AuCD surface while Raman spectroscopy confirmed the presence of structural defects of graphene. The calculated charge transfer resistances (Rct) and heterogeneous electron transfer rate constants (k0) were 1638 Ω and 0.0022 cm s-1 for the bare substrate, and 91 Ω and 0.0027 cm s-1 for the modified electrode, evidencing the facilitated electron transfer of the CRGO-AuCD surface. The dopamine (DP) amperometric detection using CRGO-AuCD provided low detection limit (0.12 µg L-1) compared with other modified electrodes already reported, high precision (relative standard deviation (RSD) < 5%) and analytical frequency (370 h-1). As a proof-of-concept, DP determination in synthetic saliva samples was performed and a satisfactory recovery value (98.6 ± 0.9%) was obtained.

This work presents a simple electrochemical method for 2-naphthylamine (2NAP) determination in perfume by differential-pulse voltammetry (DPV) employing a boron-doped diamond (BDD) electrode cathodically treated. Simple dilution of sample in supporting electrolyte was performed before electrochemical analysis. A borate buffer solution of pH 10.0 containing 20% (v/ (LOD) of 0.0046 µmol L-1 with a linear range between 0.5 and 90 µmol L-1, and RSD < 2.9%, respectively. Recovery values for spiked samples with 2NAP were between 102 and 104%. The proposed method is feasible to be applied for 2NAP detection and quantification on perfume samples with simple sample preparation.