scholarly journals Microbially mediated reduction of Np(V) by a consortium of alkaline tolerant Fe(III)-reducing bacteria

2015 ◽  
Vol 79 (6) ◽  
pp. 1287-1295 ◽  
Author(s):  
Adam J. Williamson ◽  
Katherine Morris ◽  
Christopher Boothman ◽  
Kathy Dardenne ◽  
Gareth T.W. Law ◽  
...  

AbstractNeptunium-237 will be present in radioactive wastes over extended time periods due to its long half-life (2.13 × 106years). Understanding its behaviour under conditions relevant to radioactive waste disposal is therefore of particular importance. Here, microcosm experiments were established using sediments from a legacy lime workings with high-pH conditions as an analogue of cementitious intermediate-level radioactive waste disposal. To probe the influence of Fe biogeochemistry on Np(V) in these systems, additional Fe(III) (as ferrihydrite) was added to select experiments. Biogeochemical changes were tracked in experiments with low levels of Np(V) (20 Bq ml–1; 3.3 μM), whilst parallel higher concentration systems (2.5 KBq ml–1;414 μM) allowed X-ray absorption spectroscopy. As expected, microbial reduction processes developed in microbially-active systems with an initial pH of 10; however, during microbial incubations the pH dropped from 10 to ∼7, reflecting the high levels of microbial metabolism occurring in these systems. In microbially-active systems without added Fe(III), 90% sorption of Np(V) occurred within one hour with essentially complete removal by one day. In the ferrihydrite-amended systems, complete sorption of Np(V) to ferrihydrite occurred within one hour. For higher-activity sediments, X-ray absorption spectroscopy (XAS) at end points where Fe(II) ingrowth was observed confirmed that complete reductive precipitation of Np(V) to Np(IV) had occurred under similar conditions to low-level Np experiments. Finally, pre-reduced, Fe(III)-reducing sediments, with and without added Fe(III) and held at pH 10, were spiked with Np(V). These alkaline pre-reduced sediments showed significant removal of Np to sediments, and XAS confirmed partial reduction to Np(IV) with the no Fe system, and essentially complete reduction to Np(IV) in the Fe(III)-enriched systems. This suggested an indirect, Fe(II)-mediated pathway for Np(V) reduction under alkaline conditions. Microbial analyses using 16S rRNA gene pyrosequencing suggested a role for alkali-tolerant, Gram-positive Firmicutes in coupled Fe(III) reduction and Np immobilization in these experiments.

2015 ◽  
Vol 17 (10) ◽  
pp. 1760-1768 ◽  
Author(s):  
E. Curti ◽  
A. Puranen ◽  
D. Grolimund ◽  
D. Jädernas ◽  
D. Sheptyakov ◽  
...  

The long-lived fission product79Se is tightly bound to the UO2lattice in spent nuclear fuel; it will thus be released only very slowly from a geological repository for radioactive waste.


1991 ◽  
Vol 257 ◽  
Author(s):  
R. Gauglitz ◽  
M. Holterdorf ◽  
W. Franke ◽  
G. Marx

ABSTRACTIn cooperation with the Ministry of Research and Technology we investigated the influence of hydroxylapatite (HAP) added to the backfill material of a radioactive waste disposal located in a salt dome. The time dependence of the sorption and precipitation of radionuclides has been studied in three different praxisrelevant salt brines under variation of temperature and pH-value.Performing batch experiments uranium and thorium phosphates were precipitated from UO2(NO3)2 and Th(NO3)4 solutions at 75°C, the amounts of the relevant actinide compounds also exceeding that of HAP. The isolated precipitates were investigated by use of X-ray-powder-diffractometry and SEM. For the various uranium systems two mineral phases were obtained. From solution II and also from Q-brine the mineral saléeite Mg(UO2)2 (PO4)2 · 9H2O was formed. From solution III meta-autunite Ca(UO2)2(PO4)2 · 6H2O, a dehydration product of autunite, was precipitated.


1986 ◽  
Vol 47 (C8) ◽  
pp. C8-237-C8-242 ◽  
Author(s):  
B. S. CLAUSEN ◽  
B. LENGELER ◽  
B. S. RASMUSSEN ◽  
W. NIEMANN ◽  
H. TOPSØE

1986 ◽  
Vol 47 (C8) ◽  
pp. C8-149-C8-151
Author(s):  
F. W. LYTLE ◽  
R. B. GREEGOR ◽  
G. H. VIA ◽  
J. M. BROWN ◽  
G. MEITZNER

1986 ◽  
Vol 47 (C8) ◽  
pp. C8-1155-C8-1157
Author(s):  
E. C. THEIL ◽  
D. E. SAYERS ◽  
C. Y. YANG ◽  
A. FONTAINE ◽  
E. DARTYGE

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