The new catalytic kinetic spectrophotometric method for Au（III） determination was developed and validated. It was based on the catalytic effect of gold on the oxidation of sudan red III by ammonium peroxodisulfate ...The new catalytic kinetic spectrophotometric method for Au（III） determination was developed and validated. It was based on the catalytic effect of gold on the oxidation of sudan red III by ammonium peroxodisulfate （（NH4）2S2O8） with nitrilo triacetic acid as an activator in microemulsion and H2SO4 medium. Under optimum conditions, there was the linearity of the calibration curve in the concentration range from 0 to 20 μg/L Au（Ⅲ） at 520 nm. The relative standard deviation was 3.0% with a correlation coefficient of 0.9986. The detection limit achieved was 9.75 × 10^-5 μg/mL. A new method using a column packed with sulfhydryl dextrose gel （SDG） as a solid-phase extractant has been developed for the preconcentration and separation of Au（Ⅲ） ions. The method has been applied to the determination of trace gold with satisfactory results.展开更多
Solid liquid extraction of copper ion (I) with 2, 9-dimethyl-1, 10-phenanthroline (neo-cuproine, DMP) into molten naphthalene followed by chloroform spectrophotometric determination has been studied experimentally. Th...Solid liquid extraction of copper ion (I) with 2, 9-dimethyl-1, 10-phenanthroline (neo-cuproine, DMP) into molten naphthalene followed by chloroform spectrophotometric determination has been studied experimentally. The ternary complex Cu(I)-DMP-ClO4 was extracted quantitatively into molten naphthalene in the range of pH from 5 to 6 at 85 C-. Absorbance was spectrophotometrically determined at 459 nm against the reagent blank after the solid naphthalene layer was anhydrously dissolved in chloroform. Beer's law is obeyed over a concentration range of 0.5-70 mug/mL. The molar absorptivity and Sandell's sensitivity are 1.0x10(4) L/(mol(.)cm) and 0.0099 mug(.)cm(2) respectively. In addition, the various conditions on determination and the interference of coexisted ions were discussed, and the method was applied to the determination of copper ion both in tea samples and cadmium sulfate reagents. The results are in good agreement with those obtained by ICP AES method.展开更多
Iron irrespective of its valency states forms bluish 1:1 cationic, bluish-violet 1:3 neutral and purple 1:3 anionic complexes with 2,3-dihydroxynaphthalene, at pH 2 - 3, 4 - 5 and 8 - 10, respectively. The cationic bl...Iron irrespective of its valency states forms bluish 1:1 cationic, bluish-violet 1:3 neutral and purple 1:3 anionic complexes with 2,3-dihydroxynaphthalene, at pH 2 - 3, 4 - 5 and 8 - 10, respectively. The cationic bluish complex is highly insensitive and not extractable in organic solvents. Similarly, the bluish violet 1:3 neutral complex is of moderate sensitivity, and it is extractable in organic solvents with reduced sensitivity. The purple 1:3 anionic complex is as such not extractable in any organic solvents. However, in the surfactant medium of the cationic surfactant, cetyltrimethylammonium bromide it is extractable in organic solvents with enhanced sensitivity. The 1:3 anionic complex which is extractable in organic solvents as an ion associate in the presence of cetyltrimethyl ammonium bromide is chosen for application to Silicate rocks, Minerals, Soils, Stream sediments, Concentrates, Tobacco leaves, Cigarettes and Waters, for accurate and sensitive determination of iron owing to facile extraction of iron, enhanced sensitivity high selectivity and better reproducibility of results. The present paper describes a systematic study on the development of an extraction spectrophotometric method for the determination of iron in samples of diverse matrices.展开更多
文摘The new catalytic kinetic spectrophotometric method for Au（III） determination was developed and validated. It was based on the catalytic effect of gold on the oxidation of sudan red III by ammonium peroxodisulfate （（NH4）2S2O8） with nitrilo triacetic acid as an activator in microemulsion and H2SO4 medium. Under optimum conditions, there was the linearity of the calibration curve in the concentration range from 0 to 20 μg/L Au（Ⅲ） at 520 nm. The relative standard deviation was 3.0% with a correlation coefficient of 0.9986. The detection limit achieved was 9.75 × 10^-5 μg/mL. A new method using a column packed with sulfhydryl dextrose gel （SDG） as a solid-phase extractant has been developed for the preconcentration and separation of Au（Ⅲ） ions. The method has been applied to the determination of trace gold with satisfactory results.
基金This research was financially supported by the project KJCXGC-01 of Northwest Normal University, China.
文摘Solid liquid extraction of copper ion (I) with 2, 9-dimethyl-1, 10-phenanthroline (neo-cuproine, DMP) into molten naphthalene followed by chloroform spectrophotometric determination has been studied experimentally. The ternary complex Cu(I)-DMP-ClO4 was extracted quantitatively into molten naphthalene in the range of pH from 5 to 6 at 85 C-. Absorbance was spectrophotometrically determined at 459 nm against the reagent blank after the solid naphthalene layer was anhydrously dissolved in chloroform. Beer's law is obeyed over a concentration range of 0.5-70 mug/mL. The molar absorptivity and Sandell's sensitivity are 1.0x10(4) L/(mol(.)cm) and 0.0099 mug(.)cm(2) respectively. In addition, the various conditions on determination and the interference of coexisted ions were discussed, and the method was applied to the determination of copper ion both in tea samples and cadmium sulfate reagents. The results are in good agreement with those obtained by ICP AES method.
文摘Iron irrespective of its valency states forms bluish 1:1 cationic, bluish-violet 1:3 neutral and purple 1:3 anionic complexes with 2,3-dihydroxynaphthalene, at pH 2 - 3, 4 - 5 and 8 - 10, respectively. The cationic bluish complex is highly insensitive and not extractable in organic solvents. Similarly, the bluish violet 1:3 neutral complex is of moderate sensitivity, and it is extractable in organic solvents with reduced sensitivity. The purple 1:3 anionic complex is as such not extractable in any organic solvents. However, in the surfactant medium of the cationic surfactant, cetyltrimethylammonium bromide it is extractable in organic solvents with enhanced sensitivity. The 1:3 anionic complex which is extractable in organic solvents as an ion associate in the presence of cetyltrimethyl ammonium bromide is chosen for application to Silicate rocks, Minerals, Soils, Stream sediments, Concentrates, Tobacco leaves, Cigarettes and Waters, for accurate and sensitive determination of iron owing to facile extraction of iron, enhanced sensitivity high selectivity and better reproducibility of results. The present paper describes a systematic study on the development of an extraction spectrophotometric method for the determination of iron in samples of diverse matrices.
