ABSTRACT
The copper electrode modified by bacteria immobilised by a polycaprolactone film was successfully developed by electropolymerisation for the purpose of determining the presence of phenol. Electrochemical techniques such as square-wave voltammetry (SWV), cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) were used to characterize the electrochemical properties of the Cu-polymer/bacteria electrode. The results show that the intensity of the phenol oxidation peak increases with concentration, allowing us to obtain good analytical results with DL of 2.156 × 10-7 M and QL which is 7.2 × 10-7 M , confirming that the biosensor has excellent electroanalytical activity for phenol oxidation, with good stability and a wide linear range. Our electrode is based on a easily available and inexpensive material, as well as on its simple preparation, which has demonstrated high performance for phenol.
ABSTRACT
Various applications of electrochemical sensors and biosensors have been reported in many fields. These include pharmaceuticals, drug detection, cancer detection, and analysis of toxic elements in tap water. Electrochemical sensors are characterised by their low cost, ease of manufacture, rapid analysis, small size and ability to detect multiple elements simultaneously. They also allow the reaction mechanisms of analytes, such as drugs, to be taken into account, giving a first indication of their fate in the body or their pharmaceutical preparation. Several materials are used in the construction of sensors, such as graphene, fullerene, carbon nanotubes, carbon graphite, glassy carbon, carbon clay, graphene oxide, reduced graphene oxide, and metals. This review covers the most recent progress in electrochemical sensors used to analyze drugs and metabolites in pharmaceutical and biological samples. We have highlighted carbon paste electrodes (CPE), glassy carbon electrodes (GCE), screen-printed carbon electrodes (SPCE) and reduced graphene oxide electrodes (rGOE). The sensitivity and analysis speed of electrochemical sensors can be improved by modifying them with conductive materials. Different materials used for modification have been reported and demonstrated, such as molecularly imprinted polymers, multiwalled carbon nanotubes, fullerene (C60), iron(III) nanoparticles (Fe3O4NP), and CuO micro-fragments (CuO MF). Manufacturing strategies and the detection limit of each sensor have been reported.
ABSTRACT
During the present study, biopolymer lignin was extracted, in particular, from sugar beet pulp (molasses) from the Tadla region (224 km from Marrakech, Morocco). The lignin was characterized by infrared spectroscopy (FTIR) and thermogravimetric TG/DTA analysis and then used as a modifier to enhance the electroanalytical detection of heavy metal ion traces. The performance of the lignin/CPE sensor to detect lead (II) was studied by cyclic voltammetry (CV) and square-wave voltammetry in 0.3 mol L-1 NaCl. With optimized experimental parameters, the lignin/CPE sensor developed has a minimum detection limit of 2.252.10-11 M for Pb (II). The proposed working electrode has been successfully applied for the coanalysis of Pb (II) in tap water with good results.
ABSTRACT
Calcinated and acidified clay modified carbon graphite electrode was deployed in the simultaneous evaluation of traces of Pb2+ and Cd2+ in solution. After 5 minutes of accumulation in the circuit, the sensitivity of the electrode was evaluated in a solution of Na2SO4 (0.1 M) by square wave voltammetry on the one hand with Pb (II) and on the other hand with Cd (II). Several experimental conditions such as the composition of the carbon clay paste, the effect of preconcentration time, the sweeping speed, concentration effect, media pH, and interference ionic response to the electrochemical response of the working electrode were examined. It was observed that, after 5 minutes of preconcentration, detection limits of 0.15513 µmol·L-1 and 0.24227 µmol·L-1 were obtained for Pb2+ and Cd2+ in the electrolyte solution and 0.08438 µmol·L-1 and 0.46522 µmol·L-1, respectively, when tap water was used. The detection was effective by square wave voltammetry with a more intense current density with respect to lead.
