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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Published in: | EPJ Web of conferences Vol. 56; p. 1010 |
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Main Authors: | , , , |
Format: | Journal Article |
Language: | English |
Published: |
EDP Sciences
01-01-2013
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Subjects: | |
Online Access: | Get full text |
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Summary: | 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 CaUO sub(4) 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 Tc sub(3)O sub(4) 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 O sub(2) 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. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISBN: | 2759810461 9782759810468 |
ISSN: | 2100-014X 2100-014X |
DOI: | 10.1051/epjconf/20135601010 |