Show simple item record

hal.structure.identifierCentre d'Etudes Nucléaires de Bordeaux Gradignan [CENBG]
dc.contributor.authorWILLIAMSON, Adam J.
dc.contributor.authorLLOYD, Jonathan R.
dc.contributor.authorBOOTHMAN, Christopher
dc.contributor.authorLAW, Gareth T.W.
dc.contributor.authorSHAW, Samuel
dc.contributor.authorSMALL, Joe S.
dc.contributor.authorVETTESE, Gianni F.
dc.contributor.authorWILLIAMS, Heather A.
dc.contributor.authorMORRIS, Katherine
dc.date.issued2021
dc.description.abstractEn99Tc will be present in significant quantities in radioactive wastes including intermediate-level waste (ILW). The internationally favored concept for disposing of higher activity radioactive wastes including ILW is via deep geological disposal in an underground engineered facility located ∼200–1000 m deep. Typically, in the deep geological disposal environment, the subsurface will be saturated, cement will be used extensively as an engineering material, and iron will be ubiquitous. This means that understanding Tc biogeochemistry in high pH, cementitious environments is important to underpin safety case development. Here, alkaline sediment microcosms (pH 10) were incubated under anoxic conditions under “no added Fe(III)” and “with added Fe(III)” conditions (added as ferrihydrite) at three Tc concentrations (10–11, 10–6, and 10–4 mol L–1). In the 10–6 mol L–1 Tc experiments with no added Fe(III), ∼35% Tc(VII) removal occurred during bioreduction. Solvent extraction of the residual solution phase indicated that ∼75% of Tc was present as Tc(IV), potentially as colloids. In both biologically active and sterile control experiments with added Fe(III), Fe(II) formed during bioreduction and >90% Tc was removed from the solution, most likely due to abiotic reduction mediated by Fe(II). X-ray absorption spectroscopy (XAS) showed that in bioreduced sediments, Tc was present as hydrous TcO2-like phases, with some evidence for an Fe association. When reduced sediments with added Fe(III) were air oxidized, there was a significant loss of Fe(II) over 1 month (∼50%), yet this was coupled to only modest Tc remobilization (∼25%). Here, XAS analysis suggested that with air oxidation, partial incorporation of Tc(IV) into newly forming Fe oxyhydr(oxide) minerals may be occurring. These data suggest that in Fe-rich, alkaline environments, biologically mediated processes may limit Tc mobility
dc.language.isoen
dc.title.enBiogeochemical Cycling of $^{99}$Tc in Alkaline Sediments
dc.typeArticle de revue
dc.identifier.doi10.1021/acs.est.1c04416
dc.subject.halPhysique [physics]
bordeaux.journalEnviron.Sci.Tech.
bordeaux.page15862-15872
bordeaux.volume55
bordeaux.issue23
bordeaux.peerReviewedoui
hal.identifierhal-03495653
hal.version1
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-03495653v1
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Environ.Sci.Tech.&rft.date=2021&rft.volume=55&rft.issue=23&rft.spage=15862-15872&rft.epage=15862-15872&rft.au=WILLIAMSON,%20Adam%20J.&LLOYD,%20Jonathan%20R.&BOOTHMAN,%20Christopher&LAW,%20Gareth%20T.W.&SHAW,%20Samuel&rft.genre=article


Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record