Tetravalent uranium is commonly assumed to form insoluble species, resulting in the immobilization of uranium under reducing conditions. Here we present the first report of mobile U(IV)-bearing colloids in the environment, bringing into question this common assumption. We investigate the mobility of uranium in a mining-impacted wetland in France harbouring uranium concentrations of up to 14,000 p.p.m. As an apparent release of uranium into the stream passing through the wetland was observable, we examine soil and porewater composition as a function of depth to assess the geochemical conditions leading to this release. The analyses show the presence of U(IV) in soil as a non-crystalline species bound to amorphous Al-P-Fe-Si aggregates, and in porewater, as a distinct species associated with Fe and organic matter colloids. These results demonstrate the lability of U(IV) in these soils and its association with mobile porewater colloids that are ultimately released into surface water.
Uranium, a radioactive element used in the weapon and nuclear energy industries, is a source of contamination at numerous sites around the world owing to its mining, milling and processing at large scales. Moreover, naturally occurring high U concentrations in ground and surface water are common in alpine regions1,2 where the surrounding granitic bedrock contains trace amounts of uranium3. Wetlands often act as sinks for U and other trace metals and U has been shown to accumulate in wetland soils up to several thousand p.p.m.1,2. In natural settings, U occurs in the hexavalent [U(VI)] or tetravalent [U(IV)] oxidation states4. Because of the relatively high stability and low solubility of uraninite (UIVO2) under reducing conditions at near-neutral pH, its formation as a result of (bio)reduction is considered an efficient strategy for U immobilization in sediments5. A similar reductive immobilization process is sought in constructed wetland systems6. Thus, U(IV)—where it occurs in the environment—is generally expected to be a low mobility U species, in contrast to U(VI) species that are generally soluble and mobile. Recently, non-crystalline U(IV) species were discovered as the product of microbial U(VI) reduction in batch experiments7,8, flow-through columns with natural sediments9 and in field biostimulation10. It was also demonstrated that non-crystalline U(IV) was formed by the reduction of dissolved U(VI) by vivianite (Fe3(PO4)2) or phosphate-sorbed magnetite (Fe3O4)11. These non-crystalline species are being characterized in ongoing research but are commonly referred to as ‘monomeric U(IV)’ in reference to the lack of U–U pair correlations as observed in their X-ray absorption spectroscopy (XAS) spectra7.
A wetland in central France located adjacent to a former U mine was affected by mining activity for several decades. A recent study showed that there were hotspots within the wetland with soil U concentrations of up to 4,000 p.p.m.12. Here we show that the U concentration in a stream flowing through the wetland increases as a function of distance, suggesting U release into the stream. Major elements and U speciation analysis in porewater and soil as a function of depth allows linking of U(IV) mobilization in the porewater to its association with Fe and organic matter (OM) colloids. Furthermore, U in the soil occurs primarily as monomeric U(IV), more specifically, a U(IV) species bound to amorphous Al-P-Fe-Si aggregates through phosphate groups. The results imply that the non-crystalline form of U(IV) extant in the soil is labile and may complex with mobile Fe and OM colloids that are ultimately released into the stream. The environmental implication of these findings is that, currently, U(IV) mobility may be severely underestimated in high OM environments such as wetlands.
The studied wetland is located in the Limousin region of France, in the northwestern part of Massif Central, where igneous rocks such as granite dominate. A former open-pit and underground U mining site with adjacent waste rock piles and a high U clay deposit are located north of the wetland, which represents the lowest topographical point (Fig. 1). A stream flows through the wetland. Two locations harbouring high U concentrations, henceforth referred to as ‘spot A’ and ‘spot B’, were identified in the site after a gamma radiation survey. Spot A is located south of the eastern waste rock pile and the high U clay deposit; spot B is adjacent to the western waste rock pile (Fig. 1).
Increase of U concentration in the stream
Stream water was sampled at various locations in three seasons and analysed for U content (Fig. 1). A steady increase of the stream concentration of soluble U from 0.012 to 0.13 μmol l−1 as a function of distance was observed, and this increase is proposed to correspond to the release of U into the stream. Hence, it was important to investigate the geochemical conditions leading to this release.
Profiles of porewater dissolved oxygen (DO), SO42−, Fe(II), FeT and U (Fig. 2) at spots A and B in November 2011 and July 2012 show a suboxic-anoxic environment where Fe(III) reduction—of possible microbial origin—as well as, to a lesser extent, sulphate reduction occur. At spots A and B, sulphate reduction proceeds as evidenced by the decreasing concentration of sulphate with depth and the presence of small concentrations of sulphide (1–4 μM) in the porewater (Supplementary Fig. S1). This process is more prevalent at spot B than at spot A, as X-ray diffraction (XRD) analysis shows the presence of pyrite in the soil at spot B at 30–40 cm but not at spot A (Supplementary Fig. S2). Sulphate reduction is unlikely to be a major process here because of the persistence of substantial porewater Fe(II) concentrations at both locations (Fig. 2). Fe(III) reduction is clearly ongoing due to the presence of high concentrations (up to ~400 μM) of Fe(II), which represents the entirety of Fe in the porewater. Hence, reducing conditions prevail throughout the depth profile with some seasonal excursions of the redox front in the top 40 cm. Most interestingly, despite reducing conditions, U content in the porewater is significant with a spot A average U concentration of 0.80±0.20 μM in November and 0.91±0.07 μM in July and up to 3 μM at spot B in November.
The reducing conditions that persist in this soil support the hypothesis that U is present in a reduced tetravalent form. Metal- and sulphate-reducing bacteria have been shown to enzymatically and indirectly reduce U(VI)13,14. To elucidate the valence state of porewater U, laser-induced fluorescence spectroscopic (LFS) analysis was conducted on selected spot A porewater samples (November, 15–20 cm and 35–40 cm; and July, 15–20 cm) and on the same samples oxidized by atmospheric oxygen as positive controls. The results (Supplementary Fig. S3) show a detectable U(VI) luminescence signal at ~493 and ~514 nm for the oxidized control samples. In contrast, the signal of the original samples was within the background noise. Thus, these results reveal that the predominant U redox state in porewater is tetravalent.
The relatively high U(IV) porewater concentrations are surprising because in this valence state, U is sparingly soluble at the porewater pH value (5.8). Dissolved OM may complex and stabilize U(IV) in aqueous phases15, which is consistent with high dissolved organic carbon values in the porewater (1.24±0.06 mM, Supplementary Fig. S1). In addition, U may be bound to colloidal phase(s) smaller than the filter pore size (0.22 μm).
Characterization of U-bound porewater colloids
To probe the potential for the presence of colloidal U in the porewater, freshly collected samples maintained under anoxic conditions were subjected to immediate on-site ultrafiltration. Porewater from selected depths at spot A was divided into subsamples that were filtered through membranes with pore sizes of 0.22 μm, 500 or 10 kDa (Fig. 3). At all depths investigated, 93–98% of U was present in the 500-kDa–0.22 μm size fraction along with >50% of Fe and 40–56% of organic carbon (OC). This finding supports the hypothesis that the high U concentration in the porewater is due to its association with Fe(II)-rich and OM-rich colloids.
Further characterization of U-bearing colloids using transmission electron microscopy (TEM) revealed a morphology reminiscent of beads on a string (Fig. 4 and Supplementary Fig. S4). Elemental mapping shows that these colloids are composed of Fe and C, suggesting OM threads extending for hundreds of nanometres with associated iron-rich nanoparticles. Point energy-dispersive X-ray spectroscopy (EDS) analyses show low but statistically relevant U concentrations in association with Fe and C (Supplementary Table S1). High-resolution transmission electron microscopic (HRTEM) observation reveals that string-associated crystalline nanoparticles of 2–3 nm and selected area electron diffraction (SAED) patterns are consistent with a mixture of trigonal FeII(OH)2 and cubic FeIIO nanoparticles (Fig. 4). FeIIO probably resulted from the sintering of Fe(OH)2 particles under the intense electron beam during SAED data collection. Altogether, these U-bearing colloids consist of FeII(OH)2 associated with OM as anisotropic threads that could pass through a 0.22-μm pore-size membrane but are retained by a 500-kDa pore-size filter. A previous study showed that OM-rich colloids with associated Fe and Ca precipitates were found in porewater of a wetland-karst system in Switzerland16, suggesting that this type of Fe- and OM-rich colloids may be common in mineral-rich wetland environments.
Characterization of stream colloids
To elucidate the relationship between the steady increase in U concentration along the stream and the presence of mobile U-bearing colloids in the porewater, colloids in filtered stream water were analysed for their chemical composition and mineralogy. They were composed mainly of OC (26.6% w/w), Fe (22.3%), Si (1.9%), Ca (1.0%), Al (0.8%) and U (0.2%). Fe and OC, the main elemental components, are in an XRD amorphous phase(s) (Supplementary Fig. S2). These stream colloids thus bear an uncanny compositional resemblance to the U-bearing porewater colloids (that is, they are rich in Fe and OC and contain U).
Characterization of soil and U speciation
Soil samples from both spots A and B are rich in water (65–90% w/w in most cases). Chemical composition profiles in the soil show a U- and Fe-rich layer at 0–30 cm and 0–40 cm at spots A and B, respectively (Supplementary Fig. S5). Total organic carbon (TOC) content (w/w) in dried soil shows similar low average values at both spot A (16.3%±7.5%) and spot B (19.4%±7.4%), suggesting high mineral content. The Al and Si profiles, along with the XRD analysis (Supplementary Fig. S2), underscore the presence of aluminosilicates in the soil. Images of the cores (Supplementary Fig. S6) show the presence of a distinct clay-like layer at 10–25 cm for spot A and at 10–30 cm for spot B. XRD analysis confirmed the presence of muscovite (KAl3Si3O10(OH)2), smectite ((Ca0.5,Na)0.7(Al,Mg,Fe)4[(Si,Al)8O20]·nH2O), albite (NaAlSi3O8), orthoclase (KAlSi3O8) and kaolinite (Al2Si2O5(OH)4) as well as quartz (SiO2) (Supplementary Fig. S2). The origin of this clay layer, unexpected in a wetland, is discussed below in the Discussion section.
Fe concentrations (an average of 1.9±0.7% w/w) in the soil profile at spot A decrease from 0 to 30 cm (Supplementary Fig. S5), consistent with the increasing dissolved Fe(II) concentration in the porewater in the same depth range (Fig. 2). At spot B, the Fe situation is similar in the 0–30 cm range, but a spike in Fe concentration is visible at 30–40 cm (Supplementary Fig. S4), corresponding to pyrite precipitation at this depth (Supplementary Fig. S2). The soil U profile shows high U concentrations (2,400–4,400 p.p.m. for spot A and 1,000–14,000 p.p.m. for spot B) restricted to shallow depths (0–25 cm for spot A and 0–40 cm for spot B) comparing with low U concentrations (40–120 p.p.m.) beneath. Soil-associated rather than porewater-associated U represents >99% of U in the wetland. The high U zone corresponds to the abovementioned clay layer and immediately adjacent depths.
Scanning electron microscopic (SEM) observation of the 15–20 cm soil sample at spot A showed a majority of layered mineral particles, corresponding to the clay minerals detected by XRD. No detectable U was associated with these clay particles. However, a minor phase identified repeatedly by SEM as exhibiting a distinctive morphology and chemical composition (Fig. 5) was shown by HRTEM to be amorphous aggregates (Fig. 6). This phase contains Fe, P, Al, Si, O and U (Fig. 5, Supplementary Table S2). Similar aggregates were also observed at other depths (10–15 cm and 20–25 cm) corresponding to the clay layer at spot A (Supplementary Fig. S7). We conclude that this amorphous Al-P-Fe-Si phase binds U and controls U mobility in the soil.
U redox and coordination was investigated by U LIII-edge XAS on soil samples at 5–25 cm at spot A and at 5–40 cm at spot B, and the results are displayed in Fig. 7. X-ray absorption near-edge structure (XANES) spectra exhibit an absorption maximum at 17,175.0 eV for all samples, underscoring the predominantly tetravalent oxidation state of U in the soil, which is consistent with the metal-reducing conditions evidenced by high Fe(II) concentrations in the porewater. Unfiltered and k3-weighted extended X-ray absorption fine structure (EXAFS) spectra collected for soil samples show oscillations similar to those of a monomeric U(IV) model compound, suggesting a similar atomic environment. Fits of EXAFS data further confirm the absence of a U–U pair correlation typical of U(IV) minerals and the presence of U(IV) coordinated to phosphate, a monomeric-U(IV)-like species. There is no evidence for U association with clays. Hence, we conclude that U in the soil is predominantly tetravalent and bound to the amorphous Al-P-Fe-Si aggregates through phosphate groups.
Analytical results show that the mineralogical composition of the U-bearing clay layer at spots A and B is similar to that of the clay deposit identified as overflow from the former settling pond (Supplementary Figs S2 and S8), as is discussed in detail in Supplementary Note 1. This strongly suggests that the clay layer within the wetland and the clay deposit in the overflow area share the same origin.
The XAS results of the present field study evidence U(IV) binding to phosphate groups to form monomeric U(IV)-like species in the soil and are thus consistent with those of laboratory studies, which have previously demonstrated that U(VI) bioreduction could yield monomeric U(IV) characterized by U(IV) association to phosphate groups in batch and column systems7,8,9. In addition, abiotic U(VI) reduction via PO43−-sorbed magnetite (Fe3O4) and vivianite (Fe3(PO4)2)11 also produced a similar product. Interestingly, in another site also located in the same Massif Central region, Fe-rich particulate Si gels were observed in the surface water under oxic conditions with U(VI) in association with these phases17, underscoring the complex chemistry of U.
The high concentration of soluble U(IV) throughout the porewater profile while soil U(IV) is restricted to the top 30 cm is attributed to its mobility owing to its association with Fe(OH)2-OM colloids. The results in the present study demonstrate that U(IV) species in the porewater are distinct from those present in the soil in this wetland. This finding suggests that U(IV) bound to amorphous Al-P-Fe-Si aggregates in the soil is labile and complexes with mobile Fe and OM colloids. We propose that mobile OM-rich colloids form in the organic-rich layers and associate with Fe(II) originating from active Fe(III) reduction. The colloids are transported to the U-rich clay layer, where U(IV) may be transferred from the Al-P-Fe-Si aggregates in soil to the porewater colloids, because of the lability of the U-bearing soil aggregates. The presumed lability of this form of U(IV) is consistent with recent findings showing that monomeric U(IV), in contrast to UO2, appears to be mobile and reactive18. Moreover, the lability of U in a wetland soil reported by Schöner et al.19 was attributed to the presence of amorphous U(VI) rather than U(IV) phases despite the prevalence of reducing conditions because it was not conceivable at the time that U(IV) could be present in a non-crystalline form. However, the present study reveals a more likely interpretation of those data with the formation of labile non-crystalline U(IV) species in the soil. Finally, as the composition of the stream colloids remarkably resembles to that of the U-bearing porewater colloids, it is conceivable that the release of U from the wetland is due to the migration of mobile porewater colloids into the stream water. A scheme summarizing the entire process is presented in Fig. 8.
U(IV) association to colloids in natural environments was suspected but never proven in numerous U solubility or mobility studies. For instance, Ollila et al.20, Noseck et al.21 and Delecaut et al.22 observed that the solubility of U under reducing conditions exceeded the solubility limit of the U(IV) phase. To explain their results, they speculated that U(IV) colloids enhanced the observed U(IV) solubility in experiments with groundwater from granitic bedrock, a uranium ore deposit or porewater from Boom Clay, respectively. While U(VI) mobility in association with colloids has been documented in the field23,24,25, and recent laboratory studies evidenced the formation of U(IV) silicate colloids 20 nm in size26 and that of UIVO2 colloids27, this study is the first to demonstrate the association of U(IV) with colloids in natural environments and its resulting increased mobility.
Reductive precipitation of uranium minerals is regarded as a major and sustainable mechanism to control U mobility. This mechanism is targeted by constructed wetland systems6 that aim at stimulating microbial-mediated reduction of uranyl ions as described by Lovley et al.13 Recent work has shown that the dominant species formed in the field by microbially mediated U(VI) reduction is monomeric U(IV)10. The present study further shows that the lability of non-crystalline U(IV) species may lead to the release of highly mobile U(IV)-bearing colloids. Both the formation of labile U(IV) and the potential release of U(IV)-bearing colloids should be considered carefully when designing wetland-based U remediation strategies.
Stream water sampling and analysis
The stream flowing through the wetland is shallow, with a maximum depth of ~20 cm. Stream water was sampled from a depth of ~10 cm. The sampling took place at various locations in April and November 2011 and July 2012, and each sample was divided into two parts, one of which was measured for pH (using WTW Multi 350i or HORIBA W20 multiparameter instruments) and alkalinity (using HACH titration cartridge with sulphuric acid and bromocresol green/methyl red colour indicators) and the other was filtered using 0.22 μm pore-size polyethersulfone (PES) membranes and analysed for U content using inductively coupled plasma mass spectrometry on a Thermo X7 analyser (detection limit for U: 4.2 nM). The pH and alkalinity values are reported in Supplementary Table S4, and the U concentrations are shown in Fig. 1. Stream water was also sampled near location 3 in Fig. 1, filtered using 0.22 μm pore-size PES membranes and dried at 100 °C to obtain a powder. A part of the powder was dissolved completely using a three-step HNO3/HF microwave digestion procedure with a high-performance microwave and then analysed using inductively coupled plasma optical emission spectroscopy (ICP-OES) for main elements and U content, and another part was analysed using XRD for mineralogy. The results are shown in the main text and in Supplementary Fig. S2.
Porewater and soil sampling
Soil and porewater sampling campaigns were carried out in November 2011 and July 2012. Soil core samples were only collected in November 2011, and porewater was sampled both in November and July to capture seasonal variations. The core was sampled under a high-flow Ar stream, sealed in airtight sterile bags and then conditioned in an anoxic chamber (N2 atmosphere) 5 min away from the sampling spots. The vertical soil core was collected using a Russian corer, cut into 5 cm slices and each slice divided into two fractions, one of which was sealed in 0.127-mm-thick (0.005 inches) MYLAR bags and was stored at 4 °C for XAS analysis, and the other was dried by heating at 80 °C in an anoxic chamber for 24 h and then ground and homogenized to a fine powder for the remainder of the analyses. The porewater was sampled with a vertical resolution of 5 cm using multi-chambered piezometers designed and manufactured at EPFL. The concept of the piezometers is illustrated in Supplementary Fig. S9. The piezometers were installed at spot A and spot B in April and June 2011, respectively, with the help of a peat soil corer28. The porewater in each chamber was pumped to the surface using a LAMBDA HIFLOW peristaltic pump and Tygon R-3603 tubing, and the pH and DO of the porewater was measured using airtight flow-through cells custom made for the probes at EPFL. The porewater was then sampled under a high-flow Ar stream, sealed in serum bottles with blue butyl rubber stoppers and then handled in an anoxic chamber (N2 atmosphere) 5 min away from the sampling spots. In the anoxic chamber, the samples were filtered using 0.22 μm pore-size PES membranes, and divided into three fractions: one amended with anoxic 2 M HCl (1:1 volume ratio) for Fe(II) analysis, one amended with 5 M HNO3 (1:5 volume ratio) for metal ion analysis and the rest stored in a serum bottle sealed with a butyl rubber stopper for the remainder of the analyses.
Analysis of porewater chemistry
The Fe(II) concentration in porewater samples was determined using the ferrozine colorimetric method described by Stookey29. A solution of ferrozine [3-(2-pyridyl)-5,6-bis(4-phenylsulfonic acid)-1,2,4-triazine] was prepared at 1 g l−1 in 50 mM HEPES at pH 7.0. Acidified porewater samples were analysed by mixing 15 μl of sample with 1,485 μl of ferrozine solution. The absorbance at 562 nm was measured with a Shimadzu UV-2501 PC spectrophotometer. Metal ion concentrations in porewater samples were obtained using ICP-OES on a Shimadzu ICPE-9000 analyser (respective detection limit for Fe and U: 1.8 and 21 nM). Anion concentrations were measured using a Dionex ICS 3000 ion chromatograph. Dissolved organic carbon and dissolved inorganic carbon (bicarbonate) in porewater were analysed using a Shimadzu TOC-Analyzer 5000 (detection limit: 16.7 μM).
Laser-induced fluorescence spectroscopy
The samples for LFS analysis were prepared at EPFL in an H2/N2 (3–4% H2) anoxic chamber. Two spot A porewater samples from November (15–20 and 35–40 cm) and one from July (15–20 cm) were selected for LFS analysis. LFS is only able to detect dissolved U(VI). Each sample was divided into two 4 ml subsamples acidified using 1 ml of N2-purged anoxic 1 M HCl to release U from the Fe-rich colloids. Previous tests showed that no U(VI) could be detected if it was bound to Fe-rich colloids. One subsample was sealed in a serum bottle with a butyl rubber stopper until the analysis, and the other was exposed to air for at least 24 h to oxidize U(IV) to U(VI). The samples were then sent to HZDR for analysis. On arrival, the serum bottles containing anoxic subsamples were opened in a glove box (Braun, Germany) with an N2 atmosphere (<6 p.p.m. O2), and the oxidized ones were opened to the air. The subsamples were transferred into a plastic cuvette and sealed with a teflon plug. The closed cuvette was then stored for 24 h in a freezer at 253 K. The formed ice block was extracted from the cuvette and immediately transferred to the cold gas system sample holder. This cold gas system allows cooling the sample to 120 K by use of N2 gas from a liquid nitrogen source (Isotherm, Germany). Acquiring spectra at this temperature minimizes the quenching effect of chloride in the samples. The thermostat housing has three windows, where two opposing windows allow the laser beam through while the third, at a right angle, is used for collecting the emitted luminescence. The luminescence light is focused onto an optical fibre and transmitted into a spectrograph (Acton Research, USA). The resolved spectrum is measured by an intensified charge-coupled device camera system (Roper Scientific, USA). A laser source (Inlite, Continuum, USA) is used for U excitation. The fourth harmonic of a Nd:YAG laser (wavelength=266 nm) was used to excite the uranium(VI) species in the frozen sample. The duration of the laser pulses was 10 ns. The repetition rate of the laser was 20 Hz and the energy of the laser pulses was adjusted to about 5 mJ. The measurement by the camera system started immediately after application of the laser pulse (30 ns). The gate width of the camera was set to 500 μs. Three hundred laser shots were collected for each spectrum and repeated three times. Because of the low luminescence intensities detected, no time-resolved spectra were collected.
Ultrafiltration of the porewater samples was performed in July 2012. The system consisted of a 0.45-μm pre-filtration through a cellulose acetate in-line filter, followed by parallel filtration through a 0.22-μm pore-size Millipore PES membrane and ultrafiltration through 500 and 10 kDa pore-size Millipore Biomax PES membranes. These membranes were secured in stainless steel mounts, with polytetrafluoroethylene (PTFE)-coated inner walls to prevent metal contamination. The whole procedure was performed in an anoxic glove bag purged and filled with N2 gas. Blank samples were obtained for each filtration threshold by running ultrapure water through the system. Between each sample, the cleaning procedure consisted of rinsing the entire system with 2% HNO3 followed by ultrapure water until the pH was back to neutral.
SEM observation on selected soil samples was conducted without C coating using a Carl Zeiss Merlin microscope with GEMINI II column at 1 kV and 100 pA at EPFL. TEM observation was conducted on selected porewater and soil samples at EPFL. The TEM grids and windows were prepared in an H2/N2 (3–4% H2) anoxic chamber. For the porewater sample, several microlitres were extracted by a needle and a syringe and dropped onto the TEM SiN window. The liquid was left on the window for about 10 s and then wicked away using a paper towel. This procedure was repeated three to five times. TEM observation showed that porewater colloids were loaded onto the grid. For soil samples, finely ground dry soil powder was loaded onto C-coated TEM grids by spraying powder onto the grid. The grids and the windows were transferred to the microscope in an anoxic jar. The chemical composition of porewater colloids and soil U-rich aggregates was studied by scanning TEM and X-ray energy-dispersive spectroscopy (EDS) in an FEI Tecnai Osiris microscope at 200 kV (FEI, Eindhoven, The Netherlands) equipped with four windowless Super-X silicon drift detector (SDD) EDX detectors. Quantitative EDS results were obtained with Bruker Esprit software (Bruker Corporation). The morphology and phase composition were studied by conventional and HRTEM (TEM and HRTEM) and electron diffraction in an FEI CM300UT/FEG microscope at 300 kV (FEI). Images and SAED patterns were recorded on a Gatan 797 slow scan charge-coupled device camera and processed with the Gatan Digital Micrograph software (Gatan, Inc., Pleasanton, CA, USA). Phase identification was performed by analysing SAED patterns using a software known as JEMS ( http://www.cimewww.epfl.ch/people/stadelmann/jemsWebSite/jems.html) for the electron-optical parameters of the microscope and the structural data of Fe oxides (27856) and hydroxides (53992) taken from the Inorganic Crystal Structure Database, FIZ Karlsruhe, Germany and NIST, US Department of Commerce, 2013.
Analysis of soil chemistry
Water content of the soil samples was obtained by weighing the samples before and after drying. Soil TOC content was measured in dried homogenized samples with a Shimadzu TOC-V CPH/CPN analyser. To study the soil chemical composition and U content, soil samples were dissolved completely using a three-step microwave digestion procedure with a high-performance microwave (Microwave Laboratory Systems). Hundred milligrams of dried and homogenized sample was mixed first with 4 ml of HNO3 (65%) and 4 ml of H2O2, and the first microwave digestion step (all steps were carried out at 100 °C) was started followed by the second, which involved the addition of 2 ml of HF (48%), and finally the third with the addition of 20 ml of H3BO3 (4.5%). The final extract was diluted with MilliQ water to 100 ml and analysed using ICP-OES for main elements and U content. The main elements’ composition is shown in Supplementary Fig. S5.
To avoid oxidation by air during analysis, XRD analysis was conducted under anoxic conditions at the Institut de Minéralogie et de Physique de Milieux Condensés (IMPMC) in Paris. Finely ground dry soil samples were sealed in serum bottles with butyl rubber stoppers before analysis. Powder samples were loaded onto a Si single crystal ‘zero diffraction plate’ under a N2 atmosphere in a Jacomex glove box (O220 p.p.m.) at IMPMC. XRD measurements were performed with CoKa (6.93 keV, wavelength=1.79 Å) radiation on a Panalytical X’Pert Pro MPD diffractometer mounted in Debye–Scherrer configuration using an X'Celerator detector to collect the diffracted beam. Data were recorded in the continuous-scan mode in the 3–80° 2θ range with a step of 0.0330°.
X-ray absorption spectroscopy
The monomeric U(IV) model compound was obtained by following the procedure described by Bernier-Latmani et al.,7 whereas the U(VI)-acetate model compound was prepared by diluting U(VI)-acetate powder (Fluka) into cellulose. Soil samples for XAS analysis were mounted onto sample holders, sealed in individual MYLAR bags (0.127 mm thick) and sealed in a metallic jar at EPFL in an H2/N2 (3–4% H2) anoxic chamber. The jar was then shipped to XAS beamlines and was kept sealed until analysis. Uranium LIII-edge (17.166 keV) XANES and EXAFS data of selected spot A and spot B samples were obtained at the Core EXAFS beamline (B18) of Diamond Light Source and Rossendorf Beamline (BM20) of the European Synchrotron Radiation Facility, respectively. On analysis, the sample was mounted quickly onto the cryostat rod and inserted into the cryostat. XANES data showed no evidence of air-induced oxidation with this approach. We collected XANES and EXAFS data in fluorescence mode under N2-liquid temperature (~77 K) at B18 of Diamond Light Source or He-liquid temperature (~10 K) at BM20 of European Synchrotron Radiation Facility. The Si(111) double-crystal monochromator was used in channel-cut mode. The spectra were collected in fluorescence mode using multielement solid-state Ge detector, together with I0, I1 and I2 signals using ionization chambers. Energy was calibrated by using double-transmission set-up in which a uranium LIII-edge spectrum of the sample and that of Y metal (first inflection point at 17,038 eV) foil reference sample placed between I1 and I2 were simultaneously recorded. Several EXAFS scans were summed for each sample to obtain an adequate signal-to-noise ratio at k=10 Å−1. Athena of IFEFFIT program package30 was used for normalization and background removal. The EXAFS oscillations were extracted from raw spectra by standard methods including a spline approximation for the atomic background. Artemis of IFEFFIT program package was used for shell-by-shell fitting of EXAFS data. Theoretical backscattering phase and amplitude functions were calculated with the FEFF 8.4 code31 using Artemis. The Fourier transform peaks are shifted to lower values, R+ΔR, relative to the true near-neighbor distances, R, due to the phase shift of the electron wave in the adjacent atomic potentials. This ΔR shift is considered as a variable during the shell fits. The data-fitting ranges were k=3–11 Å−1 and R+ΔR=1–3.5 Å for the EXAFS and Fourier back transform, respectively. The amplitude reduction factor, S02, was defined as 0.9 in the data fits. Numerical constraints were applied to keep the values of the fits within a physically reasonable range, and the number of free parameters was kept maximally at four for most cases.
How to cite this article: Wang, Y. et al. Mobile uranium(IV)-bearing colloids in a mining-impacted wetland. Nat. Commun. 4:2942 doi: 10.1038/ncomms3942 (2013).
We thank A. Bagnoud, L. Falquet, L. Chesaux, J. Gay-des-Combes and E. McGivney from EPFL and J. Nos and E. de Boissezon from AREVA for help with fieldwork, F. Comino from EPFL for help in designing and manufacturing the porewater samplers, Professor A. Buttler from EPFL for lending us a peat soil corer, E. Rossel from EPFL for help with IC, dissolved organic carbon and TOC analyses, CEAL of EPFL for analytical support, CIME of EPFL for electron microscopy. The anoxic XRD experiments were carried out at IMPMC, Paris, France. We are grateful to Dr G. Morin and L. Delbes for their assistance in planning XRD experiments. The XAS experiments were performed on the BM20 beamline at the European Synchrotron Radiation Facility (ESRF), Grenoble, France and B18 beamline at Diamond Light Source, Oxfordshire, UK. We are indebted to A. Scheinost and A. Rossberg from ESRF and A. Dent and S. Parry from Diamond for their assistance in XAS data acquisition. Financial support of this research from AREVA is gratefully acknowledged.
Supplementary Figures S1-S9, Supplementary Tables S1-S4 and Supplementary Note 1
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