Quantification of iron in seawater at the low picomolar range based on optimization of bromate/ammonia/dihydroxynaphtalene system by catalytic adsorptive cathodic stripping voltammetry

7 páginas, 4 figuras, 2 tablas A new analytical protocol for the challenging analysis of total dissolved iron at the low picomolar level in oceanic waters suitable for onboard analysis is presented. The method is based on the revision of the adsorptive properties of the iron/2,3-dihydroxynaphthalene...

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Published in:Analytical Chemistry
Main Authors: Laglera, Luis M., Santos-Echeandía, Juan, Caprara, Salvatore, Montecelli, Damiano
Format: Article in Journal/Newspaper
Language:English
Published: American Chemical Society 2013
Subjects:
Online Access:http://hdl.handle.net/10261/71863
https://doi.org/10.1021/ac303621q
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spelling ftcsic:oai:digital.csic.es:10261/71863 2024-02-11T10:08:53+01:00 Quantification of iron in seawater at the low picomolar range based on optimization of bromate/ammonia/dihydroxynaphtalene system by catalytic adsorptive cathodic stripping voltammetry Laglera, Luis M. Santos-Echeandía, Juan Caprara, Salvatore Montecelli, Damiano 2013 http://hdl.handle.net/10261/71863 https://doi.org/10.1021/ac303621q en eng American Chemical Society http://dx.doi.org/10.1021/ac303621q Analitycal Chemistry 85(4): 2486-2492 (2013) 0003-2700 http://hdl.handle.net/10261/71863 doi:10.1021/ac303621q 1520-6882 open artículo http://purl.org/coar/resource_type/c_6501 2013 ftcsic https://doi.org/10.1021/ac303621q 2024-01-16T09:47:29Z 7 páginas, 4 figuras, 2 tablas A new analytical protocol for the challenging analysis of total dissolved iron at the low picomolar level in oceanic waters suitable for onboard analysis is presented. The method is based on the revision of the adsorptive properties of the iron/2,3-dihydroxynaphthalene (Fe/DHN) complexes on the hanging mercury drop electrode with catalytic enhancement by bromate ions. Although it was based on a previously proposed reagent combination, we show here that the addition of an acidification/alkalinization step is essential in order to cancel any organic complexation, and that an extra increment of the pH to 8.6–8.8 leads to the definition of a preconcentration-free procedure with the lowest detection limit described up to now. For total dissolved iron analysis, samples were acidified to pH 2.0 in the presence of 30 μM DHN and left to equilibrate overnight. A 10 mL sample was subsequently buffered to a pH of 8.7 in the presence of 20 mM bromate: a 60 s deposition at 0 V led to a sensitivity of 34 nA nM–1 min–1, a 4-fold improvement over previous methods, that translated in a limit of detection of 5 pM (2–20 fold improvement). Several tests proved that a nonreversible reaction in the time scale of the analysis, triggered by the acidification/alkalinization step, was behind the signal magnification. The new method was validated onboard via the analysis of reference material and via intercalibration against flow injection analysis-chemiluminescence on Southern Ocean surface samples. This work was funded by the MINECO of Spain (Grant CGL2010-11846-E) and the Government of the Balearic Islands (Grant AAEE083/09). L.M.L. was supported by a Ramon y Cajal (MINECO) fellowship. J.S.E. was supported by the JAEDoc program of the CSIC Peer reviewed Article in Journal/Newspaper Southern Ocean Digital.CSIC (Spanish National Research Council) Southern Ocean Analytical Chemistry 85 4 2486 2492
institution Open Polar
collection Digital.CSIC (Spanish National Research Council)
op_collection_id ftcsic
language English
description 7 páginas, 4 figuras, 2 tablas A new analytical protocol for the challenging analysis of total dissolved iron at the low picomolar level in oceanic waters suitable for onboard analysis is presented. The method is based on the revision of the adsorptive properties of the iron/2,3-dihydroxynaphthalene (Fe/DHN) complexes on the hanging mercury drop electrode with catalytic enhancement by bromate ions. Although it was based on a previously proposed reagent combination, we show here that the addition of an acidification/alkalinization step is essential in order to cancel any organic complexation, and that an extra increment of the pH to 8.6–8.8 leads to the definition of a preconcentration-free procedure with the lowest detection limit described up to now. For total dissolved iron analysis, samples were acidified to pH 2.0 in the presence of 30 μM DHN and left to equilibrate overnight. A 10 mL sample was subsequently buffered to a pH of 8.7 in the presence of 20 mM bromate: a 60 s deposition at 0 V led to a sensitivity of 34 nA nM–1 min–1, a 4-fold improvement over previous methods, that translated in a limit of detection of 5 pM (2–20 fold improvement). Several tests proved that a nonreversible reaction in the time scale of the analysis, triggered by the acidification/alkalinization step, was behind the signal magnification. The new method was validated onboard via the analysis of reference material and via intercalibration against flow injection analysis-chemiluminescence on Southern Ocean surface samples. This work was funded by the MINECO of Spain (Grant CGL2010-11846-E) and the Government of the Balearic Islands (Grant AAEE083/09). L.M.L. was supported by a Ramon y Cajal (MINECO) fellowship. J.S.E. was supported by the JAEDoc program of the CSIC Peer reviewed
format Article in Journal/Newspaper
author Laglera, Luis M.
Santos-Echeandía, Juan
Caprara, Salvatore
Montecelli, Damiano
spellingShingle Laglera, Luis M.
Santos-Echeandía, Juan
Caprara, Salvatore
Montecelli, Damiano
Quantification of iron in seawater at the low picomolar range based on optimization of bromate/ammonia/dihydroxynaphtalene system by catalytic adsorptive cathodic stripping voltammetry
author_facet Laglera, Luis M.
Santos-Echeandía, Juan
Caprara, Salvatore
Montecelli, Damiano
author_sort Laglera, Luis M.
title Quantification of iron in seawater at the low picomolar range based on optimization of bromate/ammonia/dihydroxynaphtalene system by catalytic adsorptive cathodic stripping voltammetry
title_short Quantification of iron in seawater at the low picomolar range based on optimization of bromate/ammonia/dihydroxynaphtalene system by catalytic adsorptive cathodic stripping voltammetry
title_full Quantification of iron in seawater at the low picomolar range based on optimization of bromate/ammonia/dihydroxynaphtalene system by catalytic adsorptive cathodic stripping voltammetry
title_fullStr Quantification of iron in seawater at the low picomolar range based on optimization of bromate/ammonia/dihydroxynaphtalene system by catalytic adsorptive cathodic stripping voltammetry
title_full_unstemmed Quantification of iron in seawater at the low picomolar range based on optimization of bromate/ammonia/dihydroxynaphtalene system by catalytic adsorptive cathodic stripping voltammetry
title_sort quantification of iron in seawater at the low picomolar range based on optimization of bromate/ammonia/dihydroxynaphtalene system by catalytic adsorptive cathodic stripping voltammetry
publisher American Chemical Society
publishDate 2013
url http://hdl.handle.net/10261/71863
https://doi.org/10.1021/ac303621q
geographic Southern Ocean
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genre_facet Southern Ocean
op_relation http://dx.doi.org/10.1021/ac303621q
Analitycal Chemistry 85(4): 2486-2492 (2013)
0003-2700
http://hdl.handle.net/10261/71863
doi:10.1021/ac303621q
1520-6882
op_rights open
op_doi https://doi.org/10.1021/ac303621q
container_title Analytical Chemistry
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container_issue 4
container_start_page 2486
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