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Open Chemistry
|
2011
|
vol. 9
|
issue 3
432-436
EN
A combined method involving electrochemical oxidation of iodide to iodate at a platinum electrode followed by extraction in CCl4 of ionic associates of iodine-iodide complexes with brilliant green, formed in excess of iodide, was developed for the spectrophotometric quantification of iodide. The slope of the calibration curve yields a molar extinction coefficient of ɛ = 3·105 L mol−1cm−1. This method can be used for the quantification of iodide in the concentration range of 3·10−7 − 3·10−6 mol L−1 with a detection limit of 5·10−8 mol L−1. The interfering effect of other ions on the determination of the iodide concentration was also investigated. The method was successfully applied for the determination of iodide in real samples of NaCl and spring water. Relative standard deviation is 1–2%.
EN
This study examined the direct spectrometric method for determining non-ionic surfactants in highly-polluted samples (i.e., soil leachates) containing high concentrations of humic acids. Meso-tetra-(3,5-dibromo-4-hydrooxyphenyl)-porphyrin served as a coloration agent. The method was tested by use of two polyethoxylate/polypropoxylate - based non-ionic surfactants: Triton CF-21 containing aromatic groups in the structure and Novanik 1047A containing only linear hydrocarbon chains. The main goal was to quantify the influence of interfering species to the results. A test for coincidence of regression lines was employed for objective evaluation of the humic acid influence on the determination. It was observed that for linear surfactant Novanik 1047 A the method provides reliable result and thus, can serve for routine analyses. Regarding Triton CF-21, an interfering effect of humic acids was observed; however, after sufficient dilution of the samples, the method can be used as well. Finally, the method can be used for simple analyses of problematic samples without complicated sample-pretreatment. [...]
Open Chemistry
|
2009
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vol. 7
|
issue 4
870-875
EN
Two simple, rapid, accurate and sensitive spectrophotometric methods are described for the determination of sulpiride. They are based on charge transfer complexation between the drug as n-electron donor and p-chloranilic acid as π acceptor or iodine as σ-acceptor. These give highly coloured complexes with absorption maxima at 518 and 363, 294 nm, respectively. Beer’s law linear ranges were 13.7–341.4 and 1.7–20.5 µg mL−1 for the p-chloranilic acid and iodine methods. The methods were successfully applied to the determination of the drug in Dogmatil® Fort tablets and the results compared with the official method. The complex association constants and standard free energy changes were calculated using Benesi-Hildebrand plots. [...]
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