Reversed-Phase High-Performance Liquid Chromatography for the Determination of 15 Rare Earth Elements in Surface Water Sample Collected in a Mining Area from Lavras do Sul/RS, Brazil

A methodology was developed to assay 15 rare earth elements (REE) (La to Lu and Y) in a surface water sample from a mining area. The samples were collected in the mining area of Lavras do Sul, RS, Brazil. Reversed phase high-performance liquid chromatography employing α-hydroxyisobutyric acid (HIBA)...

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Veröffentlicht in:Chromatographia 2019-05, Vol.82 (5), p.843-856
Hauptverfasser: Colim, Alexsandro Nunes, do Nascimento, Paulo Cícero, Wiethan, Bruna Avila, Adolfo, Franciéle Rovasi, Dresch, Lucielle Codeim, de Carvalho, Leandro Machado, Bohrer, Denise, da Rosa, Marcelo Barcellos
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container_issue 5
container_start_page 843
container_title Chromatographia
container_volume 82
creator Colim, Alexsandro Nunes
do Nascimento, Paulo Cícero
Wiethan, Bruna Avila
Adolfo, Franciéle Rovasi
Dresch, Lucielle Codeim
de Carvalho, Leandro Machado
Bohrer, Denise
da Rosa, Marcelo Barcellos
description A methodology was developed to assay 15 rare earth elements (REE) (La to Lu and Y) in a surface water sample from a mining area. The samples were collected in the mining area of Lavras do Sul, RS, Brazil. Reversed phase high-performance liquid chromatography employing α-hydroxyisobutyric acid (HIBA), sodium dodecyl sulfate as the ion interaction reagent, and acetonitrile as the organic modifier was used. Analytical detection was performed by spectrophotometry after post-column derivatization with 4-(2-pyridylazo)-resorcinol (PAR). Different chromatographic parameters such as ionic interaction reagent, HIBA concentration, pH, and PAR reagent concentration were studied to achieve the best conditions for the individual separation of REE. The method was validated in terms of the main analytical characteristics (linearity, limits of detection and quantification, precision, interferences, and accuracy). A method for sample cleanup was discussed. Under optimized conditions, it was possible to separate 15 REE (La to Lu and Y) in less than 15 min, with resolution of peaks Y and Dy. The cleanup procedure ensured the selectivity required to determine REE in natural water samples. The accuracy was assessed by regression analysis against measurements by ICP-MS. The calculated quantification limits ranged from 0.07 to 0.48 µg mL −1 , for the most sensitive (Dy) to least sensitive (La), respectively. Graphical Abstract
doi_str_mv 10.1007/s10337-019-03709-w
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The cleanup procedure ensured the selectivity required to determine REE in natural water samples. The accuracy was assessed by regression analysis against measurements by ICP-MS. The calculated quantification limits ranged from 0.07 to 0.48 µg mL −1 , for the most sensitive (Dy) to least sensitive (La), respectively. 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The samples were collected in the mining area of Lavras do Sul, RS, Brazil. Reversed phase high-performance liquid chromatography employing α-hydroxyisobutyric acid (HIBA), sodium dodecyl sulfate as the ion interaction reagent, and acetonitrile as the organic modifier was used. Analytical detection was performed by spectrophotometry after post-column derivatization with 4-(2-pyridylazo)-resorcinol (PAR). Different chromatographic parameters such as ionic interaction reagent, HIBA concentration, pH, and PAR reagent concentration were studied to achieve the best conditions for the individual separation of REE. The method was validated in terms of the main analytical characteristics (linearity, limits of detection and quantification, precision, interferences, and accuracy). A method for sample cleanup was discussed. Under optimized conditions, it was possible to separate 15 REE (La to Lu and Y) in less than 15 min, with resolution of peaks Y and Dy. The cleanup procedure ensured the selectivity required to determine REE in natural water samples. The accuracy was assessed by regression analysis against measurements by ICP-MS. The calculated quantification limits ranged from 0.07 to 0.48 µg mL −1 , for the most sensitive (Dy) to least sensitive (La), respectively. Graphical Abstract</description><subject>Acetonitrile</subject><subject>Analytical Chemistry</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Chromatography</subject><subject>Dysprosium</subject><subject>Earth surface</subject><subject>High performance liquid chromatography</subject><subject>Hydroxyisobutyric acid</subject><subject>Interaction parameters</subject><subject>Ionic interactions</subject><subject>Ions</subject><subject>Laboratory Medicine</subject><subject>Linearity</subject><subject>Mining</subject><subject>Original</subject><subject>Pharmacy</subject><subject>Proteomics</subject><subject>Rare earth elements</subject><subject>Reagents</subject><subject>Regression analysis</subject><subject>Selectivity</subject><subject>Sodium dodecyl sulfate</subject><subject>Spectrophotometry</subject><subject>Surface water</subject><subject>Trace elements</subject><subject>Yttrium</subject><issn>0009-5893</issn><issn>1612-1112</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp9kcFu00AQhi0EEqHwApxG4srS2XXstY8lhLZSEFVSxNGa2ON4K9ubzjqt2gfr83VLkLgxl9HM_N8_hz9JPmr8ohHtadCYplahLhWmFkt1_yqZ6VwbpbU2r5MZYlxmRZm-Td6FcBNHU-b5LHla8x1L4EZddRQYLtyuU1csrZeBxpph5W4ProFFJ36gye-E9t0DxDNMHcM3nlgGN9Lk_Ai-BZ3BmoRhSTJ1sOx54HEK4EbYHKSlaPibIgIbGvY9w8L3PdcTNy8Kgh9udOMOzoQJ2vgQVnQnFKDxEe9P15vP8FXo0fXvkzct9YE__O0nya_vy-vFhVr9PL9cnK1UnepyUvMGbVO0emu3RdZs2Ziac0tk5wU2lnPEbMu1adBkXBTIRtdFiTbnOaUZW5ueJJ-OvnvxtwcOU3XjDzLGl5WJZdGgMVFljqpafAjCbbUXN5A8VBqrl3yqYz5VzKf6k091H6H0CIUoHncs_6z_Qz0D1d-U1Q</recordid><startdate>20190503</startdate><enddate>20190503</enddate><creator>Colim, Alexsandro Nunes</creator><creator>do Nascimento, Paulo Cícero</creator><creator>Wiethan, Bruna Avila</creator><creator>Adolfo, Franciéle Rovasi</creator><creator>Dresch, Lucielle Codeim</creator><creator>de Carvalho, Leandro Machado</creator><creator>Bohrer, Denise</creator><creator>da Rosa, Marcelo Barcellos</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0002-2110-8358</orcidid></search><sort><creationdate>20190503</creationdate><title>Reversed-Phase High-Performance Liquid Chromatography for the Determination of 15 Rare Earth Elements in Surface Water Sample Collected in a Mining Area from Lavras do Sul/RS, Brazil</title><author>Colim, Alexsandro Nunes ; 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The cleanup procedure ensured the selectivity required to determine REE in natural water samples. The accuracy was assessed by regression analysis against measurements by ICP-MS. The calculated quantification limits ranged from 0.07 to 0.48 µg mL −1 , for the most sensitive (Dy) to least sensitive (La), respectively. Graphical Abstract</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><doi>10.1007/s10337-019-03709-w</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0002-2110-8358</orcidid></addata></record>
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subjects Acetonitrile
Analytical Chemistry
Chemistry
Chemistry and Materials Science
Chromatography
Dysprosium
Earth surface
High performance liquid chromatography
Hydroxyisobutyric acid
Interaction parameters
Ionic interactions
Ions
Laboratory Medicine
Linearity
Mining
Original
Pharmacy
Proteomics
Rare earth elements
Reagents
Regression analysis
Selectivity
Sodium dodecyl sulfate
Spectrophotometry
Surface water
Trace elements
Yttrium
title Reversed-Phase High-Performance Liquid Chromatography for the Determination of 15 Rare Earth Elements in Surface Water Sample Collected in a Mining Area from Lavras do Sul/RS, Brazil
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