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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

In situ determination of V(V) by diffusive gradients in thin films and inductively coupled plasma mass spectrometry techniques using amberlite IRA-410 resin as a binding layer

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Autor(es):
Luko, Karen Silva ; Menegario, Amauri Antonio ; Suarez, Carlos Alfredo ; Tafurt-Cardona, Makenly ; Pedrobom, Jorge Henrique ; Cavinato Marchini Rolisola, Ana Marta ; Sulato, Everton Tiago ; Kiang, Chang Hung
Número total de Autores: 8
Tipo de documento: Artigo Científico
Fonte: Analytica Chimica Acta; v. 950, p. 32-40, JAN 15 2017.
Citações Web of Science: 3
Resumo

Amberlite IRA-410 anionic exchange resin was evaluated as the binding layer for sampling V(V) by using Diffusive Gradients in Thin Films (DGT). V(V) was determined by inductively coupled plasma mass spectrometry (ICP-MS). Mass vs. time DGT deployments (ionic strength = 0.03 mol L-1 NaNO3, pH = 5.6 and T = 23.5 +/- 0.5 degrees C) was characterized by excellent linear relationship (R-2 = 0.9993) and a significant retention of V(V) by the binding layer. An exchange capacity of at least 4014 V g(-1) resin was achieved for the proposed binding layer. The diffusion coefficient obtained (7.13 +/- 0.6 10(-6) cm(2) s(-1)) agrees with the literature. The accumulation rate of V(V) was not significantly affected by ionic strength of solutions up to 0.03 mol L-1 and for the entire studied pH range (from 3 to 9). Furthermore, when comparing the concentrations obtained using IRA-410-DGT and those obtained by direct measurement of the solution concentrations, the proposed approach provided a reduction of the (CIO)-C-35-O-16 interference on V(V),determination by ICP-MS. Determination of V in normal mode (without collision cell) in solutions containing (CIO+)-C-35-O-16 analyte:Cl- concentration ratio up to 1:500,000 was not affected by interference of polyatomic ion even when normal mode ICP-MS was used. Potential interfering ions on sampling V(V) by DGT (PO43- and SO42-) showed no significant effects on the accumulation rate of V(V). Laboratory tests performed using synthetic samples, natural freshwater and acid drainage water showed an excellent performance (recoveries from 93% to 110%). For in situ deployment, measurements of V(V) by the proposed approach was not significantly different (95.5%) from the value of dissolved V concentration. (C) 2016 Elsevier B.V. All rights reserved. (AU)

Processo FAPESP: 15/03397-4 - Especiação e fracionamento de metais (e alguns semi-metais) em água e solo
Beneficiário:Amauri Antonio Menegário
Modalidade de apoio: Auxílio à Pesquisa - Regular