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      Electrochemical Study of Iodide in the Presence of Phenol and o-Cresol: Application to the Catalytic Determination of Phenol and o-Cresol

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          Abstract

          The electrochemical oxidation of iodide in the presence of phenol and o-cresol was investigated at a glassy carbon electrode in buffered media by cyclic voltammetry, linear sweep voltammetry and controlled–potential coulometry. The experimental results indicate that the phenol and o-cresol convert to their derivatives after participating in a halogenation coupled reaction (quasi-catalytic reaction) following the oxidation of iodide to iodine. The concentrations of phenol and o-cresol have been determined in aqueous solutions according to the linear dependence of quasi-catalytic peak currents with the concentration. The calibration graphs show two linear sections of 0.0 to 1.0×10 -4 M and 2.0×10 -4 to 1.0 ×10 -3 M for phenol and 4.2×10 -5 to 1.0×10 -4 M and 2.0×10 -4 to 1.0×10 -3 M for o-cresol. The theoretical detection limits and the relative standard deviations for ten measurements of phenol and o-cresol are 1.125×10 -5 M, 1.06% and 4.201×10 -5 M, 1.44%, respectively.

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              Comparison of ASE and SFE with Soxhlet, Sonication, and Methanolic Saponification Extractions for the Determination of Organic Micropollutants in Marine Particulate Matter.

              The methods of accelerated solvent extraction (ASE) and supercritical fluid extraction (SFE) of polycyclic aromatic hydrocarbons (PAHs), aliphatic hydrocarbons, and chlorinated hydrocarbons from marine samples were investigated. The results of extractions of a certified sediment and four samples of suspended particulate matter (SPM) were compared to classical Soxhlet (SOX), ultrasonication (USE), and methanolic saponification extraction (MSE) methods. The recovery data, including precision and systematic deviations of each method, were evaluated statistically. It was found that recoveries and precision of ASE and SFE compared well with the other methods investigated. Using SFE, the average recoveries of PAHs in three different samples ranged from 96 to 105%, for ASE the recoveries were in the range of 97-108% compared to the reference methods. Compared to the certified values of sediment HS-6, the average recoveries of SFE and ASE were 87 and 88%, most compounds being within the limits of confidence. Also, for alkanes the average recoveries by SFE and ASE were equal to the results obtained by SOX, USE, and MSE. In the case of SFE, the recoveries were in the range 93-115%, and ASE achieved recoveries of 94-107% as compared to the other methods. For ASE and SFE, the influence of water on the extraction efficiency was examined. While the natural water content of the SPM sample (56 wt %) led to insufficient recoveries in ASE and SFE, quantitative extractions were achieved in SFE after addition of anhydrous sodium sulfate to the sample. Finally, ASE was applied to SPM-loaded filter candles whereby a mixture of n-hexane/acetone as extraction solvent allowed the simultaneous determination of PAHs, alkanes, and chlorinated hydrocarbons.
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                Author and article information

                Journal
                Sensors (Basel)
                Sensors (Basel)
                Sensors (Basel, Switzerland)
                Molecular Diversity Preservation International (MDPI)
                1424-8220
                November 2004
                30 November 2004
                : 4
                : 11
                : 170-180
                Affiliations
                [1 ] Department of Chemistry, Faculty of Science, Al-Zahra University, P.O. Box 1993891176, Tehran, Iran, Tel. (98)-21-8044051, Fax. (98)-21-8047861
                [2 ] Department of Chemistry, Faculty of Science, Bu-Ali-Sina University, Hamadan, Iran
                Author notes
                [* ] Author to whom correspondence should be addressed. Email: lfotouhi@ 123456alzahra.ac.ir
                Article
                sensors-04-00170
                10.3390/s041100170
                4008870
                f49a607a-19ca-4f89-a32c-ac27972463d5
                © 2004 by MDPI ( http://www.mdpi.net).

                Reproduction is permitted for non-commercial purposes.

                History
                : 10 May 2004
                : 25 October 2004
                Categories
                Article

                Biomedical engineering
                electrochemical study,determination,phenol,o-cresol
                Biomedical engineering
                electrochemical study, determination, phenol, o-cresol

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