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A solid-phase extraction method using Transcarpathian clinoptilolite for preconcentration of trace amounts of terbium in water samples

BACKGROUND: In spite of the fact that terbium is one of the rarest elements in the Earth’s crust, it is frequently used for the production of high technological materials. At the result, an effective combination of sample preparation procedure and detection method for terbium ions in different matri...

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Autores principales: Vasylechko, Volodymyr O., Gryshchouk, Galyna V., Zakordonskiy, Victor P., Vyviurska, Olga, Pashuk, Andriy V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4550638/
https://www.ncbi.nlm.nih.gov/pubmed/26322121
http://dx.doi.org/10.1186/s13065-015-0118-z
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author Vasylechko, Volodymyr O.
Gryshchouk, Galyna V.
Zakordonskiy, Victor P.
Vyviurska, Olga
Pashuk, Andriy V.
author_facet Vasylechko, Volodymyr O.
Gryshchouk, Galyna V.
Zakordonskiy, Victor P.
Vyviurska, Olga
Pashuk, Andriy V.
author_sort Vasylechko, Volodymyr O.
collection PubMed
description BACKGROUND: In spite of the fact that terbium is one of the rarest elements in the Earth’s crust, it is frequently used for the production of high technological materials. At the result, an effective combination of sample preparation procedure and detection method for terbium ions in different matrices is highly required. The solid-phase extraction procedure with natural Transcarpathian clinoptilolite thermally activated at 350 °C was used to preconcentrate trace amounts of terbium ions in aqueous solutions for a final spectrophotometric determination with arsenazo III. RESULTS: Thermogravimetric investigations confirmed the existence of relations between changes that appeared during dehydratation of calcined zeolite and its sorption affinity. Since the maximum of sorption capacity towards terbium was observed at pH 8.25, a borate buffer medium (2.5 · 10(−4) М) was used to maintain ionic force and solution acidity. Terbium was quantitatively removed from the solid-phase extraction column with a 1.0 M solution of sodium chloride (pH 2.5). The linearity of the proposed method was evaluated in the range of 2.5-200 ng · mL(−1) with detection limit 0.75 ng · mL(−1). CONCLUSIONS: Due to acceptable recoveries (93.3–102.0 %) and RSD values (6–7.1) from spiked tap water, the developed method can be successfully applied for the determination of trace amounts of terbium ions in the presence of major components of water. [Figure: see text]
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spelling pubmed-45506382015-08-28 A solid-phase extraction method using Transcarpathian clinoptilolite for preconcentration of trace amounts of terbium in water samples Vasylechko, Volodymyr O. Gryshchouk, Galyna V. Zakordonskiy, Victor P. Vyviurska, Olga Pashuk, Andriy V. Chem Cent J Research Article BACKGROUND: In spite of the fact that terbium is one of the rarest elements in the Earth’s crust, it is frequently used for the production of high technological materials. At the result, an effective combination of sample preparation procedure and detection method for terbium ions in different matrices is highly required. The solid-phase extraction procedure with natural Transcarpathian clinoptilolite thermally activated at 350 °C was used to preconcentrate trace amounts of terbium ions in aqueous solutions for a final spectrophotometric determination with arsenazo III. RESULTS: Thermogravimetric investigations confirmed the existence of relations between changes that appeared during dehydratation of calcined zeolite and its sorption affinity. Since the maximum of sorption capacity towards terbium was observed at pH 8.25, a borate buffer medium (2.5 · 10(−4) М) was used to maintain ionic force and solution acidity. Terbium was quantitatively removed from the solid-phase extraction column with a 1.0 M solution of sodium chloride (pH 2.5). The linearity of the proposed method was evaluated in the range of 2.5-200 ng · mL(−1) with detection limit 0.75 ng · mL(−1). CONCLUSIONS: Due to acceptable recoveries (93.3–102.0 %) and RSD values (6–7.1) from spiked tap water, the developed method can be successfully applied for the determination of trace amounts of terbium ions in the presence of major components of water. [Figure: see text] Springer International Publishing 2015-08-27 /pmc/articles/PMC4550638/ /pubmed/26322121 http://dx.doi.org/10.1186/s13065-015-0118-z Text en © Vasylechko et al. 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Research Article
Vasylechko, Volodymyr O.
Gryshchouk, Galyna V.
Zakordonskiy, Victor P.
Vyviurska, Olga
Pashuk, Andriy V.
A solid-phase extraction method using Transcarpathian clinoptilolite for preconcentration of trace amounts of terbium in water samples
title A solid-phase extraction method using Transcarpathian clinoptilolite for preconcentration of trace amounts of terbium in water samples
title_full A solid-phase extraction method using Transcarpathian clinoptilolite for preconcentration of trace amounts of terbium in water samples
title_fullStr A solid-phase extraction method using Transcarpathian clinoptilolite for preconcentration of trace amounts of terbium in water samples
title_full_unstemmed A solid-phase extraction method using Transcarpathian clinoptilolite for preconcentration of trace amounts of terbium in water samples
title_short A solid-phase extraction method using Transcarpathian clinoptilolite for preconcentration of trace amounts of terbium in water samples
title_sort solid-phase extraction method using transcarpathian clinoptilolite for preconcentration of trace amounts of terbium in water samples
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4550638/
https://www.ncbi.nlm.nih.gov/pubmed/26322121
http://dx.doi.org/10.1186/s13065-015-0118-z
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