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      Square Wave Voltammetric Determination of Residues of Carbendazim Using a Fullerene/Multiwalled Carbon Nanotubes/Nafion\(\circledR \)/Coated Glassy Carbon Electrode

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          Abstract

          A glassy carbon electrode (GCE) was modified with a fullerene/Multiwalled Carbon Nanotubes (MWCNTs)/Nafion composite and applied to the determination of carbendazim, a fungicide. The voltammetric behavior of the analyte was investigated using Cyclic Voltammetry (CV), on the bare GCE and on the same electrode coated by a thin film of the composite material. The electrode response was more than fourfold important on the modified electrode, due to electrical conductivity of fullerene and MWCNT and to favorable electrostatic interaction between the negatively charged Nafion and the protonated fungicide. A sensitive electroanalytical procedure based on Square Wave Voltammetry (SWV) was then developed to detect the analyte. Under the optimum conditions, a linear relationship was obtained between the peak current and the concentration of carbendazim, in the range from 2.0 × 10 −8 mol/L to 3.5 × 10 −7 mol/L, leading to a detection limit of 1.7 × 10 −8 mol/L and to a quantification limit of 5.57 × 10 −8 mol/L. The developed procedure was successfully applied to detect carbendazim upon adsorption by some ferritic soils.

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          Electrocatalytic Properties and Sensor Applications of Fullerenes and Carbon Nanotubes

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            Cyclodextrin-graphene hybrid nanosheets as enhanced sensing platform for ultrasensitive determination of carbendazim.

            In this paper, cyclodextrin-graphene hybrid nanosheets (CD-GNs) for the first time have been used as an enhanced material for ultrasensitive detection of carbendazim by electrochemistry method. The peak currents of carbendazim on the GNs modified glassy carbon electrode (GNs/GCE) and the CD-GNs/GCE are increased by 11.7 and 82.0 folds compared to the bare GCE, respectively. This indicates the nanocomposite film not only shows the excellent electrical properties of GNs but also exhibits high supramolecular recognition capability of CDs. At the CD-GNs/GCE, the peak currents increase linearly with the concentration of carbendazim in the range of 5 nM-0.45 μM. The detection limit of carbendazim reached to 2 nM on the basis of the signal-to-noise characteristics (S/N=3) and the recoveries were between 98.9% and 104.5%. The developed electrochemical sensor exhibited good stability and reproducibility for the detection of carbendazim. And the CD-GNs based electrochemical sensor was also successfully demonstrated for the detection of carbendazim in water sample with satisfactory results. Furthermore, this simple sensing platform can in principle be extended to the detection of other benzimidazole fungicide which can form host-guest complexes with cyclodextrin.
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              Multi-residue method for the analysis of 101 pesticides and their degradates in food and water samples by liquid chromatography/time-of-flight mass spectrometry.

              A comprehensive multi-residue method for the chromatographic separation and accurate mass identification of 101 pesticides and their degradation products using liquid chromatography/time-of-flight mass spectrometry (LC/TOF-MS) is reported here. Several classes of compounds belonging to different chemical families (triazines, organophosphorous, carbamates, phenylureas, neonicotinoids, etc.) were carefully chosen to cover a wide range of applications in the environmental field. Excellent chromatographic separation was achieved by the use of narrow accurate mass windows (0.05 Da) in a 30 min interval. Accurate mass measurements were always below 2 ppm error for all the pesticides studied. A table compiling the accurate masses for 101 compounds together with the accurate mass of several fragment ions is included. At least the accurate mass for one main fragment ion for each pesticide was obtained to achieve the minimum of identification points according to the 2002/657/EC European Decision, thus fulfilling the EU point system requirement for identification of contaminants in samples. The method was validated with vegetable samples. Calibration curves were linear and covered two orders of magnitude (from 5 to 500 microg/L) for most of the compounds studied. Instrument detection limits (LODs) ranged from 0.04 to 150 microg/kg in green-pepper samples. The methodology was successfully applied to the analysis of vegetable and water samples containing pesticides and their degradation products. This paper serves as a guide for those working in the analytical field of pesticides, as well as a powerful tool for finding non-targets and unknowns in environmental samples that have not been previously included in any of the routine target multi-residue methods.
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                Author and article information

                Journal
                International Journal of Electrochemistry
                International Journal of Electrochemistry
                Hindawi Limited
                2090-3529
                2090-3537
                2016
                2016
                : 2016
                :
                : 1-9
                Article
                10.1155/2016/7839708
                3c3a6a49-bfed-496a-aafc-61a86a65d6b0
                © 2016

                http://creativecommons.org/licenses/by/4.0/

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