Chemical Stabilization of Hanford Tank Residual Waste
Chemical Stabilization of Hanford Tank Residual Waste
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汉福德罐残余废物的化学稳定
DOI:
10.1016/j.jnucmat.2013.10.060
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发表时间:
2014
影响因子:
3.1
通讯作者:
Edward J. Mausolf
中科院分区:
文献类型:
--
作者:
K. Cantrell;W. Um;B. Williams;M. Bowden;B. Gartman;W. Lukens;E. Buck;Edward J. Mausolf
Three different chemical treatment methods were tested for their ability to stabilize residual waste from Hanford tank C-202 for reducing contaminant release (Tc, Cr, and U in particular). The three treatment methods tested were lime addition [Ca(OH)2], an in situ Ceramicrete waste form based on chemically bonded phosphate ceramics, and a ferrous iron/goethite treatment. These approaches rely on formation of insoluble forms of the contaminants of concern (lime addition and Ceramicrete) and chemical reduction followed by co-precipitation (ferrous iron/goethite incorporation treatment). The results have demonstrated that release of uranium from tank residual wastes can be dramatically reduced after treatment compared to contact with simulated grout porewater without treatment. All three treatments methods reduced the leachable uranium concentrations by well over three orders of magnitude. In the case of uranium and technetium, released concentrations were well below their respective Maximum Contaminant Levels (MCLs) for the wastes tested. For tank C-202 residual waste, chromium release concentrations were above the MCL but were considerably reduced relative to untreated tank waste.This innovative approach has the potential to revolutionize Hanford’s tank retrieval process, by allowing larger volumes of residual waste to be left in tanks while providing an acceptably low level of risk with respect to contaminant release that is protective of the environment and human health. Such an approach could enable DOE to realize significant cost savings through streamlined retrieval and closure operations.