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XANES-Based Determination of Redox Potentials Imposed by Steel Corrosion Products in Cement-Based Media
Bin Ma,
Alejandro Fernandez-Martinez,
Benoît Madé,
Nathaniel Findling,
Ekaterina Markelova,
Eduardo Salas-Colera,
Thierry Maffeis
,
Aled R. Lewis,
Delphine Tisserand,
Sarah Bureau,
Laurent Charlet
Environmental Science & Technology
Swansea University Author:
Thierry Maffeis
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DOI (Published version): 10.1021/acs.est.8b03236
Abstract
The redox potential (Eh) in a cementitious nuclear waste repository is critical to the retardation behavior of redox-sensitive radionuclides (RNs), and largely controlled by embedded steel corrosion but hard to be determined experimentally. Here, we propose an innovative Eh determination method base...
Published in: | Environmental Science & Technology |
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ISSN: | 0013-936X 1520-5851 |
Published: |
2018
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URI: | https://cronfa.swan.ac.uk/Record/cronfa44923 |
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2020-06-17T12:08:02.8648380 v2 44923 2018-10-16 XANES-Based Determination of Redox Potentials Imposed by Steel Corrosion Products in Cement-Based Media 992eb4cb18b61c0cd3da6e0215ac787c 0000-0003-2357-0092 Thierry Maffeis Thierry Maffeis true false 2018-10-16 ACEM The redox potential (Eh) in a cementitious nuclear waste repository is critical to the retardation behavior of redox-sensitive radionuclides (RNs), and largely controlled by embedded steel corrosion but hard to be determined experimentally. Here, we propose an innovative Eh determination method based on chemical/spectroscopic measurements. Oxidized nuclides (UVI, SeIV, MoVI, and SbV) were employed as species probes to detect the Eh values imposed by steel (Fe0) and steel corrosion products (magnetite/hematite, and magnetite/goethite couples) in cement pore water. Nuclides showed good sorption affinity, especially toward Fe0, in decreasing Kd order for U > Sb > Se > Mo under both N2 and H2 atmospheres. The reduced nuclide species were identified as UO2, U4O9, FeSe, FeSe2, Se0, Sb0, and Sb2O3, but no redox transformation occurred for Mo. Eh values were obtained by using the Nernst equation. Remarkably, their values fell in a small range centered around −456 mV at pH ∼ 13.5 for both Fe0 and Fe-oxyhydroxides couples. This Eh value appears to be controlled by the nanocrystalline Fe(OH)2/Fe(OH)3 or (Fe1–x,Cax)(OH)2/Fe(OH)3 couple, whose presence was confirmed by pair distribution function analyses. This approach could pave the way for describing the Eh gradient in reinforced concrete where traditional Eh measurements are not feasible. Journal Article Environmental Science & Technology 0013-936X 1520-5851 31 12 2018 2018-12-31 10.1021/acs.est.8b03236 COLLEGE NANME Aerospace, Civil, Electrical, and Mechanical Engineering COLLEGE CODE ACEM Swansea University 2020-06-17T12:08:02.8648380 2018-10-16T16:20:16.1303975 Bin Ma 1 Alejandro Fernandez-Martinez 2 Benoît Madé 3 Nathaniel Findling 4 Ekaterina Markelova 5 Eduardo Salas-Colera 6 Thierry Maffeis 0000-0003-2357-0092 7 Aled R. Lewis 8 Delphine Tisserand 9 Sarah Bureau 10 Laurent Charlet 11 0044923-22102018140619.pdf fernandez-martinez2018.pdf 2018-10-22T14:06:19.6830000 Output 1608488 application/pdf Accepted Manuscript true 2019-09-13T00:00:00.0000000 true eng |
title |
XANES-Based Determination of Redox Potentials Imposed by Steel Corrosion Products in Cement-Based Media |
spellingShingle |
XANES-Based Determination of Redox Potentials Imposed by Steel Corrosion Products in Cement-Based Media Thierry Maffeis |
title_short |
XANES-Based Determination of Redox Potentials Imposed by Steel Corrosion Products in Cement-Based Media |
title_full |
XANES-Based Determination of Redox Potentials Imposed by Steel Corrosion Products in Cement-Based Media |
title_fullStr |
XANES-Based Determination of Redox Potentials Imposed by Steel Corrosion Products in Cement-Based Media |
title_full_unstemmed |
XANES-Based Determination of Redox Potentials Imposed by Steel Corrosion Products in Cement-Based Media |
title_sort |
XANES-Based Determination of Redox Potentials Imposed by Steel Corrosion Products in Cement-Based Media |
author_id_str_mv |
992eb4cb18b61c0cd3da6e0215ac787c |
author_id_fullname_str_mv |
992eb4cb18b61c0cd3da6e0215ac787c_***_Thierry Maffeis |
author |
Thierry Maffeis |
author2 |
Bin Ma Alejandro Fernandez-Martinez Benoît Madé Nathaniel Findling Ekaterina Markelova Eduardo Salas-Colera Thierry Maffeis Aled R. Lewis Delphine Tisserand Sarah Bureau Laurent Charlet |
format |
Journal article |
container_title |
Environmental Science & Technology |
publishDate |
2018 |
institution |
Swansea University |
issn |
0013-936X 1520-5851 |
doi_str_mv |
10.1021/acs.est.8b03236 |
document_store_str |
1 |
active_str |
0 |
description |
The redox potential (Eh) in a cementitious nuclear waste repository is critical to the retardation behavior of redox-sensitive radionuclides (RNs), and largely controlled by embedded steel corrosion but hard to be determined experimentally. Here, we propose an innovative Eh determination method based on chemical/spectroscopic measurements. Oxidized nuclides (UVI, SeIV, MoVI, and SbV) were employed as species probes to detect the Eh values imposed by steel (Fe0) and steel corrosion products (magnetite/hematite, and magnetite/goethite couples) in cement pore water. Nuclides showed good sorption affinity, especially toward Fe0, in decreasing Kd order for U > Sb > Se > Mo under both N2 and H2 atmospheres. The reduced nuclide species were identified as UO2, U4O9, FeSe, FeSe2, Se0, Sb0, and Sb2O3, but no redox transformation occurred for Mo. Eh values were obtained by using the Nernst equation. Remarkably, their values fell in a small range centered around −456 mV at pH ∼ 13.5 for both Fe0 and Fe-oxyhydroxides couples. This Eh value appears to be controlled by the nanocrystalline Fe(OH)2/Fe(OH)3 or (Fe1–x,Cax)(OH)2/Fe(OH)3 couple, whose presence was confirmed by pair distribution function analyses. This approach could pave the way for describing the Eh gradient in reinforced concrete where traditional Eh measurements are not feasible. |
published_date |
2018-12-31T07:36:58Z |
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1828452951370235904 |
score |
11.056938 |