Publication detail

Trace Determination of Carbendazim Fungicide Using Adsorptive Stripping Voltammetry with a Carbon Paste Electrode Containing Tricresyl Phosphate

Year: 2012

Type of publication: článek v odborném periodiku

Name of source: International Journal of Electrochemical Science

Publisher name: Electrochemical Science Group

Place: Belgrade

Page from-to: 9717-9731

Titles:

Language	Name	Abstract	Keywords
cze	Stanovení stopového množství carbendazimu pomocí adsorptivní rozpouštěcí voltametrie na uhlíkové pastové elektrodě s trikresyl-fosfátem..	V této studie byla použita uhlíková pastová elektroda s obsahem trikresyl-fosfátu pro stavení stopového množství fungicidu Carbendazimu za využití adsorptivní rozpouštěcí voltammetrie.	carbendazim; adsorptivní rozpouštěcí voltametrie; uhlíková pastová elektroda; trikresyl-fosfát..
eng	Trace Determination of Carbendazim Fungicide Using Adsorptive Stripping Voltammetry with a Carbon Paste Electrode Containing Tricresyl Phosphate	In this study, a carbon paste electrode based on tricresyl phosphate (TCP-CPE) as a binder has been applied to the voltammetric characterization and determination of Carbendazim fungicide (methyl-1H-benzimidazol-2-yl-carbamate, MBC). The pH effect (in Britton-Robinson buffers, pH 2.0-8.0), as well as the presence of 2-hydroxypropyl--cyclodextrin (HPCD) on the electrochemical behavior of MBC were investigated. In the potential range of interest, the oxidation signal was observed with the overall shape strongly dependent upon pH and exhibiting the most favorable signal-to-noise ratio in mild acidic solutions (pH 4.0). This has indicated that also protons are involved in the electrode transformation of MBC. Furthermore, it was confirmed that addition of 3.6•10-5 mol L-1 HPCD significantly enhanced the sensitivity towards the target analyte. The experimental conditions optimised for the determination of MBC in the differential pulse adsorptive stripping voltammetric mode (DPAdSV) were as follows: initial potential, -0.10 V vs. Ag/AgCl; final potential, +1.30 V; accumulation potential, -0.35 V; accumulation time, 120 s, and the scan rate, 100 mV s-1. The method developed offers linearity in the concentration range of 5.0 •10-7 – 1.0•10-5 mol L-1 MBC, with r = 0.995 and the limit of detection of about 3.0•10-7 mol L-1. In a model sample of spiked river water, the recovery rate achieved was 101.9 % (at the concentrations from 1.0•10-6 to 3.0•10-6 mol L-1 MBC), suggesting one that the procedure can be applied in analysis of real samples	Carbendazim; Adsorptive stripping voltammetry; Carbon paste electrode

Search

Login for students

Login for employees

Publication detail

Departments

Other Parts

Map

Services

Popular Links