Experimental Study of Contaminant Release from Reducing Grout
A column experiment was conducted to study the release behavior of technetium, uranium, and selenium initially sequestered in reducing grout similar in composition to Savannah River Site (SRS) saltstone, a cementitious waste form made by mixing salt solution from SRS liquid waste storage tanks with...
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2013-07-01
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Series: | EPJ Web of Conferences |
Online Access: | http://dx.doi.org/10.1051/epjconf/20135601010 |
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doaj-e363ed0bbc694dfabf4ab77a2dd613782021-08-02T11:58:14ZengEDP SciencesEPJ Web of Conferences2100-014X2013-07-01560101010.1051/epjconf/20135601010Experimental Study of Contaminant Release from Reducing GroutWaiting D.J.Alexander G.W.Pabalan R.T.Barr C.S.A column experiment was conducted to study the release behavior of technetium, uranium, and selenium initially sequestered in reducing grout similar in composition to Savannah River Site (SRS) saltstone, a cementitious waste form made by mixing salt solution from SRS liquid waste storage tanks with a dry mix containing blast furnace slag, fly ash, and Portland cement. The data suggest that uranium was retained in the grout possibly as a CaUO4 phase, whereas most of the selenium was released. Technetium release initially was relatively constant, and then increased significantly after 26 pore volumes. The increase in technetium release was slightly delayed relative to the observed Eh increase. The system Eh-pH started under conditions in which technetium solubility is low, constrained by Tc3O4 solubility, but eventually transitioned into the stability field of the pertechnetate ion. The delay in technetium release relative to the Eh increase was possibly due to slow oxidation of technetium at depth within the grout particles, which in turn was likely controlled by O2 diffusion into the particles. In contrast to technetium and uranium, selenium release was not solubility limited and selenium likely was present in the pore solution initially as a HSe− species. http://dx.doi.org/10.1051/epjconf/20135601010 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Waiting D.J. Alexander G.W. Pabalan R.T. Barr C.S. |
spellingShingle |
Waiting D.J. Alexander G.W. Pabalan R.T. Barr C.S. Experimental Study of Contaminant Release from Reducing Grout EPJ Web of Conferences |
author_facet |
Waiting D.J. Alexander G.W. Pabalan R.T. Barr C.S. |
author_sort |
Waiting D.J. |
title |
Experimental Study of Contaminant Release from Reducing Grout |
title_short |
Experimental Study of Contaminant Release from Reducing Grout |
title_full |
Experimental Study of Contaminant Release from Reducing Grout |
title_fullStr |
Experimental Study of Contaminant Release from Reducing Grout |
title_full_unstemmed |
Experimental Study of Contaminant Release from Reducing Grout |
title_sort |
experimental study of contaminant release from reducing grout |
publisher |
EDP Sciences |
series |
EPJ Web of Conferences |
issn |
2100-014X |
publishDate |
2013-07-01 |
description |
A column experiment was conducted to study the release behavior of technetium, uranium, and selenium initially sequestered in reducing grout similar in composition to Savannah River Site (SRS) saltstone, a cementitious waste form made by mixing salt solution from SRS liquid waste storage tanks with a dry mix containing blast furnace slag, fly ash, and Portland cement. The data suggest that uranium was retained in the grout possibly as a CaUO4 phase, whereas most of the selenium was released. Technetium release initially was relatively constant, and then increased significantly after 26 pore volumes. The increase in technetium release was slightly delayed relative to the observed Eh increase. The system Eh-pH started under conditions in which technetium solubility is low, constrained by Tc3O4 solubility, but eventually transitioned into the stability field of the pertechnetate ion. The delay in technetium release relative to the Eh increase was possibly due to slow oxidation of technetium at depth within the grout particles, which in turn was likely controlled by O2 diffusion into the particles. In contrast to technetium and uranium, selenium release was not solubility limited and selenium likely was present in the pore solution initially as a HSe− species. |
url |
http://dx.doi.org/10.1051/epjconf/20135601010 |
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