ABSTRACT
A novel electrochemical sensor was developed for the detection of lead (Pb) and copper (Cu) ions using spent coffee grounds decorated with iron oxide particles (FeO/SCG). The FeO-decorated SCG was used to modify a glassy carbon electrode (GCE). FeO, SCG, and FeO/SCG were characterized by scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR). The electrochemical properties of the modified electrode were characterized by electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV). The electrode modifications increased the active surface area and electron transfer and enhanced the accumulation of the target analyte. In the optimal condition, the developed sensor showed linear ranges of 1.0 µg L-1-0.05 mg L-1 and 0.05 mg L-1-0.8 mg L-1 for Pb2+ and 5.0 µg L-1-0.1 mg L-1 and 0.1 mg L-1-0.8 mg L-1 for Cu2+. The limit of detection (LOD) was 1.0 µg L-1 for Pb2+ and 2.4 µg L-1 for Cu2+. The developed sensor was successfully applied to determine Pb2+ and Cu2+ in bullet holes. The results were in good agreement with those obtained by inductively coupled plasma optical emission spectrometry (ICP/OES).
ABSTRACT
An electrochemical free chlorine sensor was developed by modifying a lab-made screen-printed carbon electrode (SPCE) with gold nanoparticles synthesized with polyvinylpyrrolidone (AuNPs-PVP). The electrode was made by screen printing carbon ink on a waste digital versatile disc (SPC-wDVD). PVP was used to stabilize AuNPs. Scanning electron microscopy showed that AuNPs aggregated without the stabilizer. The electrochemical behavior of the SPC-wDVD was evaluated by comparison with commercial SPCEs from two companies. Electrochemical characterization involved cyclic voltammetry and electrochemical impedance spectroscopy. The detection of free chlorine in water samples was continuous, facilitated by a flow-injection system. In the best condition, the developed sensor exhibited linearity from 0.25 to 3.0 and 3.0 to 500 mg L-1. The limit of detection was 0.1 mg L-1. The stability of the sensor enabled the detection of free chlorine at least 475 times with an RSD of 3.2 %. The AuNPs-PVP/SPC-wDVD was able to detect free chlorine in drinking water, tap water and swimming pool water. The agreement between the results obtained with the proposed method and the standard spectrophotometric method confirmed the precision of the developed sensor.
ABSTRACT
Formalin is illegally used as an antibacterial and a preservative in seafood products. It is extremely important for public health reasons to be able to simply, rapidly, and accurately detect formalin in fresh seafood. In this work, we developed a flow injection amperometric (FI-Amp) formalin sensor based on a glassy carbon electrode modified with a composite of palladium particles and carbon microspheres (PdPs-CMs/GCE). The CMs were decorated with PdPs via an electroless deposition method. The surface morphology of the CMs and the PdPs-CMs composite was characterized by scanning electron microscopy/energy dispersive X-ray spectroscopy (SEM/EDX). The electrochemical behavior and measurement of formalin at the PdPs-CMs/GCE was evaluated by cyclic voltammetry and amperometry. The modified electrode demonstrated good electrocatalytic performance for the oxidation of formalin. The synthesis method and FI-Amp operating conditions were optimized. Under the optimal conditions, the developed sensor showed a linear range of 0.025 to 15.00 mmol L-1 and a detection limit of 8 µmol L-1. Repeatability (RSD < 4.1%, n = 30), reproducibility (RSD = 0.25%, n = 5), stability (RSD = 3.2%, n = 80), and selectivity were good. The fabricated sensor achieved recoveries of formalin in seafood between 96 ± 1 to 105 ± 3 (n = 3).
