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Electrodialytic Enrichment and Matrix Conversion for the Determination of Trace Metals in Ultra-Pure Water
[Image: see text] The presence of trace contaminants in ultra-pure water (UPW) used in fabrication process can greatly affect the yield and quality of industrial products. In the present study, the electrodialytic enrichment of metal cations as a means of continuously monitoring the UPW quality was...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9089387/ https://www.ncbi.nlm.nih.gov/pubmed/35559174 http://dx.doi.org/10.1021/acsomega.2c00648 |
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author | Okazaki, Yusuke Hoshi, Shigeyuki Kato, Toshimasa Fukui, Takeo Toda, Kei Ohira, Shin-Ichi |
author_facet | Okazaki, Yusuke Hoshi, Shigeyuki Kato, Toshimasa Fukui, Takeo Toda, Kei Ohira, Shin-Ichi |
author_sort | Okazaki, Yusuke |
collection | PubMed |
description | [Image: see text] The presence of trace contaminants in ultra-pure water (UPW) used in fabrication process can greatly affect the yield and quality of industrial products. In the present study, the electrodialytic enrichment of metal cations as a means of continuously monitoring the UPW quality was studied. A newly designed electrodialytic enrichment device (EED) was used to quantitatively transfer metal ions from samples to dilute nitric acid, which was then directly introduced into an inductively coupled plasma—mass spectrometry (ICP–MS) instrument. This process could be performed without contamination of the sample, and the enrichment factor was solely dependent on the flow rate ratio of the sample and acceptor solutions. The transference of analytes into the acidic solution improved the responsivity of the ICP–MS analysis, especially at low concentrations of less than 1 μg/L. Blank solutions to support the analysis of UPW could be produced using the EED effluent, from which metal ions were quantitatively removed. In addition, calibration curves with concentration ranges of several nanograms per liter were obtained by preparing standards using a dynamic gravimetric method while employing a single bottle and continuous mass monitoring to avoid any contamination from the volumetric flasks. The sensitivities associated with the ICP–MS analysis of a number of trace metal ions were improved by one or two orders of magnitude. The data show that the present EED is able to continuously produce enriched analyte solutions to allow the ongoing monitoring of UPW quality. |
format | Online Article Text |
id | pubmed-9089387 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-90893872022-05-11 Electrodialytic Enrichment and Matrix Conversion for the Determination of Trace Metals in Ultra-Pure Water Okazaki, Yusuke Hoshi, Shigeyuki Kato, Toshimasa Fukui, Takeo Toda, Kei Ohira, Shin-Ichi ACS Omega [Image: see text] The presence of trace contaminants in ultra-pure water (UPW) used in fabrication process can greatly affect the yield and quality of industrial products. In the present study, the electrodialytic enrichment of metal cations as a means of continuously monitoring the UPW quality was studied. A newly designed electrodialytic enrichment device (EED) was used to quantitatively transfer metal ions from samples to dilute nitric acid, which was then directly introduced into an inductively coupled plasma—mass spectrometry (ICP–MS) instrument. This process could be performed without contamination of the sample, and the enrichment factor was solely dependent on the flow rate ratio of the sample and acceptor solutions. The transference of analytes into the acidic solution improved the responsivity of the ICP–MS analysis, especially at low concentrations of less than 1 μg/L. Blank solutions to support the analysis of UPW could be produced using the EED effluent, from which metal ions were quantitatively removed. In addition, calibration curves with concentration ranges of several nanograms per liter were obtained by preparing standards using a dynamic gravimetric method while employing a single bottle and continuous mass monitoring to avoid any contamination from the volumetric flasks. The sensitivities associated with the ICP–MS analysis of a number of trace metal ions were improved by one or two orders of magnitude. The data show that the present EED is able to continuously produce enriched analyte solutions to allow the ongoing monitoring of UPW quality. American Chemical Society 2022-04-14 /pmc/articles/PMC9089387/ /pubmed/35559174 http://dx.doi.org/10.1021/acsomega.2c00648 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Okazaki, Yusuke Hoshi, Shigeyuki Kato, Toshimasa Fukui, Takeo Toda, Kei Ohira, Shin-Ichi Electrodialytic Enrichment and Matrix Conversion for the Determination of Trace Metals in Ultra-Pure Water |
title | Electrodialytic Enrichment and Matrix Conversion for
the Determination of Trace Metals in Ultra-Pure Water |
title_full | Electrodialytic Enrichment and Matrix Conversion for
the Determination of Trace Metals in Ultra-Pure Water |
title_fullStr | Electrodialytic Enrichment and Matrix Conversion for
the Determination of Trace Metals in Ultra-Pure Water |
title_full_unstemmed | Electrodialytic Enrichment and Matrix Conversion for
the Determination of Trace Metals in Ultra-Pure Water |
title_short | Electrodialytic Enrichment and Matrix Conversion for
the Determination of Trace Metals in Ultra-Pure Water |
title_sort | electrodialytic enrichment and matrix conversion for
the determination of trace metals in ultra-pure water |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9089387/ https://www.ncbi.nlm.nih.gov/pubmed/35559174 http://dx.doi.org/10.1021/acsomega.2c00648 |
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