RESUMO
A facile supported liquid membrane (SLM) system for the selective and efficient transport of silver ion is introduced. The SLM used is a thin porous polyvinyldifluoride membrane impregnated with hexathia-18-crown-6 (HT18C6) dissolved in nitrophenyloctyl ether. HT18C6 acts as a specific carrier for the uphill transport of Ag+ ion as its picrate ion paired complex through the SLM. In the presence of thiosulfate ion as a suitable stripping agent in the strip solution, transport of silver occurs almost quantitatively after 4 h. The selectivity and efficiency of silver transport from aqueous solutions containing other Mn+ cations such as Mg2+, Ca2+, Co2+, Ni2+, Cu2+, Zn2+, Pb2+, Cd2+, Hg2+, Fe3+ and Cr3+ ions were investigated.
Assuntos
Éteres de Coroa , Compostos Heterocíclicos com 1 Anel/química , Íons/metabolismo , Membranas Artificiais , Polivinil/metabolismo , Prata/química , Fenômenos Químicos , Físico-Química , Poluentes Ambientais/metabolismo , Indicadores e Reagentes/metabolismo , Picratos/química , Soluções/metabolismo , Compostos de Enxofre , Tiossulfatos/químicaRESUMO
A new polyvinylchloride membrane sensor for Cd(2+) ions based on tetrathia-12-crown-4 as an ionophore was prepared. The sensor exhibits a Nernstian response for cadmium ions over a wide concentration range (4.0 x 10(-7) to 1.0 x 10(-1) M) with a slope of 29+/-1 mV decade(-1). The limit of detection is 1.0 x 10(-7) M (0.01 ppm). It has a fast response time of <10 s and can be used for at least 6 weeks without any divergence in potential. The electrode can be used in the pH range from 2.5 to 8.5. The proposed sensor shows fairly good discriminating ability towards Cd(2+) ion in comparison with some alkali, alkaline earth, transition and heavy metal ions. It was successfully applied for the direct determination of Cd(2+) in solution and, as an indicator electrode, in potentiometric titration of cadmium ions.
RESUMO
A simple and reliable method has been developed to selectively separate and concentrate trace amounts of silver ion from aqueous samples for the subsequent measurement by atomic absorption spectrometry. Ag+ ions are absorbed quantitatively during passage of aqueous samples through an octadecyl-bonded silica membrane disk modified by hexathia-18-crown-6. Almost all matrix elements will pass through the disk to drain. The retained Ag+ ions are then stripped from the disk with a minimal amount of thiosulfate solution as eluent. The proposed method permitted large enrichment factors of about 200 and higher. The limit of detection of the proposed method is 50 ng Ag+ per 1,000 mL. The effects of various cationic interferences on the recovery of silver in binary mixtures were studied. The method was applied to the recovery of Ag+ ions from different synthetic and water samples.