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Organic Copper Speciation by Anodic Stripping Voltammetry in Estuarine Waters With High Dissolved Organic Matter

The determination of copper (Cu) speciation and its bioavailability in natural waters is an important issue due to its specific role as an essential micronutrient but also a toxic element at elevated concentrations. Here, we report an improved anodic stripping voltammetry (ASV) method for organic Cu...

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Autores principales: Pađan, Jasmin, Marcinek, Saša, Cindrić, Ana-Marija, Santinelli, Chiara, Retelletti Brogi, Simona, Radakovitch, Olivier, Garnier, Cédric, Omanović, Dario
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7901884/
https://www.ncbi.nlm.nih.gov/pubmed/33634075
http://dx.doi.org/10.3389/fchem.2020.628749
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author Pađan, Jasmin
Marcinek, Saša
Cindrić, Ana-Marija
Santinelli, Chiara
Retelletti Brogi, Simona
Radakovitch, Olivier
Garnier, Cédric
Omanović, Dario
author_facet Pađan, Jasmin
Marcinek, Saša
Cindrić, Ana-Marija
Santinelli, Chiara
Retelletti Brogi, Simona
Radakovitch, Olivier
Garnier, Cédric
Omanović, Dario
author_sort Pađan, Jasmin
collection PubMed
description The determination of copper (Cu) speciation and its bioavailability in natural waters is an important issue due to its specific role as an essential micronutrient but also a toxic element at elevated concentrations. Here, we report an improved anodic stripping voltammetry (ASV) method for organic Cu speciation, intended to eliminate the important problem of surface-active substances (SAS) interference on the voltammetric signal, hindering measurements in samples with high organic matter concentration. The method relies on the addition of nonionic surfactant Triton-X-100 (T-X-100) at a concentration of 1 mg L(−1). T-X-100 competitively inhibits the adsorption of SAS on the Hg electrode, consequently 1) diminishing SAS influence during the deposition step and 2) strongly improving the shape of the stripping Cu peak by eliminating the high background current due to the adsorbed SAS, making the extraction of Cu peak intensities much more convenient. Performed tests revealed that the addition of T-X-100, in the concentration used here, does not have any influence on the determination of Cu complexation parameters and thus is considered "interference-free." The method was tested using fulvic acid as a model of natural organic matter and applied for the determination of Cu speciation in samples collected in the Arno River estuary (Italy) (in spring and summer), characterized by a high dissolved organic carbon (DOC) concentration (up to 5.2 mgC L(−1)) and anthropogenic Cu input during the tourist season (up to 48 nM of total dissolved Cu). In all the samples, two classes of ligands (denoted as L(1) and L(2)) were determined in concentrations ranging from 3.5 ± 2.9 to 63 ± 4 nM eq Cu for L(1) and 17 ± 4 to 104 ± 7 nM eq Cu for L(2), with stability constants logK (Cu,1) = 9.6 ± 0.2–10.8 ± 0.6 and logK (Cu,2) = 8.2 ± 0.3–9.0 ± 0.3. Different linear relationships between DOC and total ligand concentrations between the two seasons suggest a higher abundance of organic ligands in the DOM pool in spring, which is linked to a higher input of terrestrial humic substances into the estuary. This implies that terrestrial humic substances represent a significant pool of Cu-binding ligands in the Arno River estuary.
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spelling pubmed-79018842021-02-24 Organic Copper Speciation by Anodic Stripping Voltammetry in Estuarine Waters With High Dissolved Organic Matter Pađan, Jasmin Marcinek, Saša Cindrić, Ana-Marija Santinelli, Chiara Retelletti Brogi, Simona Radakovitch, Olivier Garnier, Cédric Omanović, Dario Front Chem Chemistry The determination of copper (Cu) speciation and its bioavailability in natural waters is an important issue due to its specific role as an essential micronutrient but also a toxic element at elevated concentrations. Here, we report an improved anodic stripping voltammetry (ASV) method for organic Cu speciation, intended to eliminate the important problem of surface-active substances (SAS) interference on the voltammetric signal, hindering measurements in samples with high organic matter concentration. The method relies on the addition of nonionic surfactant Triton-X-100 (T-X-100) at a concentration of 1 mg L(−1). T-X-100 competitively inhibits the adsorption of SAS on the Hg electrode, consequently 1) diminishing SAS influence during the deposition step and 2) strongly improving the shape of the stripping Cu peak by eliminating the high background current due to the adsorbed SAS, making the extraction of Cu peak intensities much more convenient. Performed tests revealed that the addition of T-X-100, in the concentration used here, does not have any influence on the determination of Cu complexation parameters and thus is considered "interference-free." The method was tested using fulvic acid as a model of natural organic matter and applied for the determination of Cu speciation in samples collected in the Arno River estuary (Italy) (in spring and summer), characterized by a high dissolved organic carbon (DOC) concentration (up to 5.2 mgC L(−1)) and anthropogenic Cu input during the tourist season (up to 48 nM of total dissolved Cu). In all the samples, two classes of ligands (denoted as L(1) and L(2)) were determined in concentrations ranging from 3.5 ± 2.9 to 63 ± 4 nM eq Cu for L(1) and 17 ± 4 to 104 ± 7 nM eq Cu for L(2), with stability constants logK (Cu,1) = 9.6 ± 0.2–10.8 ± 0.6 and logK (Cu,2) = 8.2 ± 0.3–9.0 ± 0.3. Different linear relationships between DOC and total ligand concentrations between the two seasons suggest a higher abundance of organic ligands in the DOM pool in spring, which is linked to a higher input of terrestrial humic substances into the estuary. This implies that terrestrial humic substances represent a significant pool of Cu-binding ligands in the Arno River estuary. Frontiers Media S.A. 2021-02-02 /pmc/articles/PMC7901884/ /pubmed/33634075 http://dx.doi.org/10.3389/fchem.2020.628749 Text en Copyright © 2021 Pad−an, Marcinek, Cindrić, Santinelli, Retelletti Brogi, Radakovitch, Garnier and Omanović. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Chemistry
Pađan, Jasmin
Marcinek, Saša
Cindrić, Ana-Marija
Santinelli, Chiara
Retelletti Brogi, Simona
Radakovitch, Olivier
Garnier, Cédric
Omanović, Dario
Organic Copper Speciation by Anodic Stripping Voltammetry in Estuarine Waters With High Dissolved Organic Matter
title Organic Copper Speciation by Anodic Stripping Voltammetry in Estuarine Waters With High Dissolved Organic Matter
title_full Organic Copper Speciation by Anodic Stripping Voltammetry in Estuarine Waters With High Dissolved Organic Matter
title_fullStr Organic Copper Speciation by Anodic Stripping Voltammetry in Estuarine Waters With High Dissolved Organic Matter
title_full_unstemmed Organic Copper Speciation by Anodic Stripping Voltammetry in Estuarine Waters With High Dissolved Organic Matter
title_short Organic Copper Speciation by Anodic Stripping Voltammetry in Estuarine Waters With High Dissolved Organic Matter
title_sort organic copper speciation by anodic stripping voltammetry in estuarine waters with high dissolved organic matter
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7901884/
https://www.ncbi.nlm.nih.gov/pubmed/33634075
http://dx.doi.org/10.3389/fchem.2020.628749
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