期刊
TALANTA
卷 222, 期 -, 页码 -出版社
ELSEVIER
DOI: 10.1016/j.talanta.2020.121460
关键词
Ionic liquid; In-situ solvent formation; Tellurium; Selenium; Speciation; Preconcentration
资金
- Consejo Nacional de Investigaciones Cientificas y Tecnicas (CONICET) (Argentina)
- Agencia Nacional de Promocion Cientifica y Tecnologica (FONCYT) (Argentina) [PICT-2016-2506-BID]
- Universidad Nacional de Cuyo (Argentina) [06/M129]
A novel online preconcentration and speciation analysis method for inorganic Se and Te species was developed in this study. By forming a hydrophobic ionic liquid directly in the liquid sample stream, efficient extraction of analytes complexed with ammonium pyrrolidine dithiocarbamate was achieved. The method showed high sensitivity and was successfully applied to environmental sample analysis.
A novel on-line preconcentration and speciation analysis method for the simultaneous determination of inorganic Se and Te species is presented in this work. The methodology is based on the on-line formation of a hydrophobic ionic liquid (IL) directly in the liquid sample stream of a flow injection system, thus achieving an efficient and rapid extraction of the analytes complexed with ammonium pyrrolidine dithiocarbamate into the finely dispersed extractant droplets, that were then retained in a column filled with cotton. A full study of the chemical and hydrodynamical parameters was developed, including the right selection of the IL used as extractant and its concentration, pH, complexing reagent, sample and ion-exchange reagent volumes and column design. Addi-tionally, a miniaturized external hydride generator was adapted to the spectrometer in order to increase the sensitivity of the atomic fluorescence measurements using only 250 mu L of 5 mol L-1 HNO3 in methanol as eluent. The analytical figures of merit obtained for 15 mL of sample included sensitivity enhancement factors of 71, 70, 49 and 40 for Te(IV), Te(VI), Se(IV) and Se(VI), respectively, and limits of detection of 1.8 ng L-1 for both Te species, 2.6 ng L-1 for Se(IV) and 3.2 ng L-1 for Se(VI). After optimization, the method was successfully applied for the analysis of environmental samples: soils and sediments, as well as sea, river, underground and tap water.
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