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Investigating the Ionization of Dissolved Organic Matter by Electrospray
[Image: see text] Electrospray ionization (ESI) operating in the negative mode coupled to high-resolution mass spectrometry is the most popular technique for the characterization of dissolved organic matter (DOM). The vast molecular heterogeneity and the functional group diversity of this complex mi...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical
Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7584329/ https://www.ncbi.nlm.nih.gov/pubmed/32940031 http://dx.doi.org/10.1021/acs.analchem.0c03438 |
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author | Patriarca, Claudia Balderrama, Andrea Može, Martina Sjöberg, Per J. R. Bergquist, Jonas Tranvik, Lars J. Hawkes, Jeffrey A. |
author_facet | Patriarca, Claudia Balderrama, Andrea Može, Martina Sjöberg, Per J. R. Bergquist, Jonas Tranvik, Lars J. Hawkes, Jeffrey A. |
author_sort | Patriarca, Claudia |
collection | PubMed |
description | [Image: see text] Electrospray ionization (ESI) operating in the negative mode coupled to high-resolution mass spectrometry is the most popular technique for the characterization of dissolved organic matter (DOM). The vast molecular heterogeneity and the functional group diversity of this complex mixture prevents the efficient ionization of the organic material by a single ionization source, so the presence of uncharacterized material is unavoidable. The extent of this poorly ionizable pool of carbon is unknown, is presumably variable between samples, and can only be assessed by the combination of analysis with a uniform detection method. Charged aerosol detection (CAD), whose response is proportional to the amount of nonvolatile material and is independent from the physicochemical properties of the analytes, is a suitable candidate. In this study, a fulvic acid mixture was fractionated and analyzed by high-pressure liquid chromatography–mass spectrometry in order to investigate the polarity and size distributions of highly and poorly ionizable material in the sample. Additionally, DOM samples of terrestrial and marine origins were analyzed to evaluate the variability of these pools across the land–sea aquatic continuum. The relative response factor values indicated that highly ionizable components of aquatic DOM mixtures are more hydrophilic and have lower molecular weight than poorly ionizable components. Additionally, a discrepancy between the samples of terrestrial and marine origins was found, indicating that marine samples are better represented by ESI than terrestrial samples, which have an abundant portion of hydrophobic poorly ionizable material. |
format | Online Article Text |
id | pubmed-7584329 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American
Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-75843292020-10-26 Investigating the Ionization of Dissolved Organic Matter by Electrospray Patriarca, Claudia Balderrama, Andrea Može, Martina Sjöberg, Per J. R. Bergquist, Jonas Tranvik, Lars J. Hawkes, Jeffrey A. Anal Chem [Image: see text] Electrospray ionization (ESI) operating in the negative mode coupled to high-resolution mass spectrometry is the most popular technique for the characterization of dissolved organic matter (DOM). The vast molecular heterogeneity and the functional group diversity of this complex mixture prevents the efficient ionization of the organic material by a single ionization source, so the presence of uncharacterized material is unavoidable. The extent of this poorly ionizable pool of carbon is unknown, is presumably variable between samples, and can only be assessed by the combination of analysis with a uniform detection method. Charged aerosol detection (CAD), whose response is proportional to the amount of nonvolatile material and is independent from the physicochemical properties of the analytes, is a suitable candidate. In this study, a fulvic acid mixture was fractionated and analyzed by high-pressure liquid chromatography–mass spectrometry in order to investigate the polarity and size distributions of highly and poorly ionizable material in the sample. Additionally, DOM samples of terrestrial and marine origins were analyzed to evaluate the variability of these pools across the land–sea aquatic continuum. The relative response factor values indicated that highly ionizable components of aquatic DOM mixtures are more hydrophilic and have lower molecular weight than poorly ionizable components. Additionally, a discrepancy between the samples of terrestrial and marine origins was found, indicating that marine samples are better represented by ESI than terrestrial samples, which have an abundant portion of hydrophobic poorly ionizable material. American Chemical Society 2020-09-17 2020-10-20 /pmc/articles/PMC7584329/ /pubmed/32940031 http://dx.doi.org/10.1021/acs.analchem.0c03438 Text en This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Patriarca, Claudia Balderrama, Andrea Može, Martina Sjöberg, Per J. R. Bergquist, Jonas Tranvik, Lars J. Hawkes, Jeffrey A. Investigating the Ionization of Dissolved Organic Matter by Electrospray |
title | Investigating the Ionization of Dissolved Organic
Matter by Electrospray |
title_full | Investigating the Ionization of Dissolved Organic
Matter by Electrospray |
title_fullStr | Investigating the Ionization of Dissolved Organic
Matter by Electrospray |
title_full_unstemmed | Investigating the Ionization of Dissolved Organic
Matter by Electrospray |
title_short | Investigating the Ionization of Dissolved Organic
Matter by Electrospray |
title_sort | investigating the ionization of dissolved organic
matter by electrospray |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7584329/ https://www.ncbi.nlm.nih.gov/pubmed/32940031 http://dx.doi.org/10.1021/acs.analchem.0c03438 |
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