Phytotoxic effect of the insecticide imidacloprid in Phaseolus vulgaris L. plant and evaluation of its bioaccumulation and translocation by electrochemical methods.

The objective of this work is to study the toxicological effect of the imidacloprid (IMD) on common bean plants (Phaseolus vulgaris L) when used at high doses and its quantification by electrochemical method. Common bean plants were exposed to increasing concentrations of IMD and the different plant tissues were subjected to various analyses. The IMD detection in different tissues of the bean plant was performed after extraction on the metallic silver electrode using square wave voltammetry. The analytical and calibration parameters (Slope, correlation coefficient, linear range, detection limit and relative standard deviation) were calculated for the different plant tissues. The effect of different doses (5.0 × 10-3 to 5.0 × 10-2 mol L-1) of IMD was evaluated on germination, seedling (vigour, growth) and photosynthetic pigments in the bean plant. The results indicate that germination rate and seed vigour index reduced significantly (p ≤ 0.05) only in the applied concentrations above the recommended dose. A similar effect of IMD was observed on seedling development in term of roots length, plant length, number of leaves and number of nods. Concerning pigments content, chlorophyll a, b and total chlorophyll maximally decreased by 95.26%, 80.44% and 82.15% respectively at high applied dose. The bioaccumulation and translocation behaviour of IMD in bean plant was investigated, revealing that the IMD can be bioaccumulated in roots and can easily be translocated into stems and leaves.

Electrodeposition of silver onto carbon graphite and their catalysis properties toward thiamethoxam reduction: application in food and beverage samples.

The purpose of this paper is the electrodeposition of silver particles on graphite electrode (Ag@GrCE) using chronoamperometry and the use of this electrode for the determination of thiamethoxam. The electrode was prepared by chronoamperometry and characterized by X-Ray diffraction (XRD), fourier transform infrared spectroscopy (FT-IR), EDX analysis and electrochemical impedance spectroscopy. The obtained electrode exhibits excellent electrocatalytic activity toward thiamethoxam reduction. The voltammetric response was linear as function of TXM concentration with a limit of detection around to 1.92 × 10-6 mol L-1. The proposed electrode was successfully used to analyze thiamethoxam residue in some food samples including orange and tomato juices.

Recent progress in controlling the synthesis and assembly of nanostructures: Application for electrochemical determination of p-nitroaniline in water.

The development of nanoparticle research has grown considerably in recent years. One of the reasons for the considerable current interest in nanoparticles is because such materials frequently display unusual physical (structural, electronic, magnetic, and optical) and chemical (catalytic) properties. The development of nanomaterials is of interest to the scientific community and industrial companies. Different methods (physical, chemical, and biological) allow their manufacture. In particular, a major effort has been devoted to the development and improvement of synthesis methods in order to obtain nano-objects of controlled size and shape, a necessary pre-requisite to their organization, and to the study of their intrinsic and collective properties. Reviews play an important role in keeping interested parties up to date on the current state of the research in any academic field. This review aims to focus on the development of nanoparticles and stabilization with adsorbed/covalently attached ligands in solution phase since these factors are deeply related to the origins of the particles' stability, the media to which they are exposed, and the involved applications. This study also examines the factors that influence the synthesis of nanoparticles. It aims to provide an overview of existing electrochemical sensors, particularly those that operate with nanomaterial-based electrode modifications for p-nitroaniline (PNA) determination and to propose guidelines for related research and development activities. Emphasis was placed on the procedure for the analysis of PNA in water samples using nanosilver-based electrodes.

Synthesis of silver nanoparticles assisted by chitosan and its application to catalyze the reduction of 4-nitroaniline.

This paper reports on the fabrication of material comprised of chitosan stabilized silver nanoparticles on the carbon paste and its electro-catalytic reduction toward 4-nitroaniline. The synthesized material was obtained when AgNO3 was mixed with chitosan as a stabilizing agent and NaBH4 as a reducing agent. The developed Chitosan-AgNPs has been confirmed using UV-Vis spectroscopy, X-Ray diffraction analysis, scanning electron microscopy (SEM) and infrared spectroscopy. The synthesized chitosan-Ag NPs exhibit particle size around 51 nm. To build a voltammetric sensor (Chitosan-Ag NPs/CPE), a carbon paste electrode has immersed in the liquid suspension of chitosan-Ag NPs, thus, it could be employed for electro-catalytic reduction of 4-NA in 0.1 M Britton-Robinson buffer solution (B-R, pH 2). Therefore, the reduction over-potential of 4-NA shifted from -752.26 mV at CPE to -304 mV at chitosan-Ag NPs/CPE, and then showing a surface controlled process with the catalytic rate constant (Kcat) of 0.125 × 10-3 M-1 s-1 and a coefficient of diffusion (D) of 2.20 × 10-6 cm2 s-1 with an enhanced current response. Under optimized conditions, the electro-catalytic reduction peak current of 4-NA increased linearly with increasing of 4-NA concentration over the range of 1 µM to 0.5 mM (R2 = 0.9866) with a detection limit of 0.86 µM (3 × Sb/P).