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Abstract: Np(V) behaviour in alkaline, calcite containing systems was studied over a range of neptunium concentrations (1.62 × 10−3 μM–1.62 μM) in two synthetic, high pH, cement leachates under a CO2 controlled atmosphere. The cement leachates were representative of conditions expected in an older (pH 10.5, Ca2+) and younger (pH 13.3, Na+, K+, Ca2+) cementitious geological disposal facility. These systems were studied using a combination of batch sorption and solubility experiments, X-ray absorption spectroscopy, and geochemical modelling to describe Np behaviour. Np(V) solubility in calcite equilibrated old and young cement leachates (OCL and YCL) was 9.7 and 0.084 μM, respectively. In the OCL system, this was consistent with a Np(V)O2OH(am) phase controlling solubility. However, this phase did not explain the very low Np(V) solubility observed in the YCL system. This inconsistency was explored further with a range of pH 13.3 solubility experiments with and variable Ca2+(aq) concentrations. These experiments showed that at pH 13.3, Np(V) solubility decreased with increasing Ca2+ concentration confirming that Ca2+ was a critical control on Np solubility in the YCL systems. X-ray absorption near-edge structure spectroscopy on the precipitate from the 42.2 μM Np(V) experiment confirmed that a Np(V) dioxygenyl species was dominant. This was supported by both geochemical and extended X-ray absorption fine structure data, which suggested a calcium containing Np(V) hydroxide phase was controlling solubility. In YCL systems, sorption of Np(V) to calcite was observed across a range of Np concentrations and solid to solution ratios. A combination of both surface complexation and/or precipitation was likely responsible for the observed Np(V) reaction with calcite in these systems. In the OCL sorption experiments, Np(V) sorption to calcite across a range of Np concentrations was dependent on the solid to solution ratio which is consistent with the formation of a mono-nuclear surface complex. All systems demonstrated slow sorption kinetics, with reaction times of weeks needed to reach apparent equilibrium. This could be explained by slow recrystallisation of the calcite surface and/or the presence of Np(V) colloidal species. Overall, these data provide valuable new insights into Np(V) and actinide(V) behaviour in alkaline conditions of relevance to the disposal of intermediate level radioactive wastes.

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Abstract: Background: Orthopaedic implants made of cobalt-chromium alloy undergo wear and corrosion that can lead to deposition of cobalt and chromium in vital organs. Elevated cardiac tissue cobalt levels are associated with myocardial injury while chromium is a well-established genotoxin. Though metal composition of tissues surrounding hip implants has been established, few investigators attempted to characterize the metal deposits in systemic tissues of total joint arthroplasty patients. Methods: We report the first use of micro-X-ray fluorescence coupled with micro-X-ray absorption spectroscopy to probe distribution and chemical form of cobalt, chromium and titanium in postmortem samples of splenic, hepatic and cardiac tissue of patients with metal-on-polyethylene hip implants (n = 5). Results: Majority of the cobalt was in the 2+ oxidation state, while titanium was present exclusively as titanium dioxide, in either rutile or anatase crystal structure. Chromium was found in a range of forms including a highly oxidised, carcinogenic species (CrV/VI), which has never been identified in human tissue before. Conclusions: Carcinogenic forms of chromium might arise in vital organs of total joint arthroplasty patients. Further studies are warranted with patients with metal-on-metal implants, which tend to have an increased release of cobalt and chromium compared to metal-on-polyethylene hips.

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Abstract: Stainless steel coupons have been exposed to uranium-containing nitric acid solutions, in conditions similar to those found in various uranium handling nuclear facilities across the nuclear fuel cycle. Solid state analysis of the stainless steel samples and solution composition analysis were undertaken to gain a better understanding of the contamination process mechanisms. Stainless steel coupons were immersed in 12 M HNO3 containing uranium (1 g/L), in the form of uranyl, for periods of up to 255 days. Uranium contamination was observed across all time lengths of exposure. Solution analysis indicated that the levels of contamination reached an equilibrium state after ~14 days. Investigations using Raman microscopy, synchrotron microfocus X-ray fluorescence and X-ray absorption spectroscopy showed inhomogeneous localization of uranyl species within the passive layer of the stainless steel surface. Over longer time lengths of exposure these contaminant species were predominantly found to locate within intergranular regions of the stainless steel. This finding should be taken into consideration when developing decontamination protocols for corroded stainless steel that has been exposed to uranium, to facilitate metal reuse/recycle and minimize hazardous waste volumes.

Open Access

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Abstract: The imaging of catalysts and other functional materials under reaction conditions has advanced significantly in recent years. The combination of the computed tomography (CT) approach with methods such as X-ray diffraction (XRD), X-ray fluorescence (XRF) and X-ray absorption near-edge spectroscopy (XANES) now enables local chemical and physical state information to be extracted from within the interiors of intact materials which are, by accident or design, inhomogeneous. In this work, we follow the phase evolution during the initial reduction step(s) to form Co metal, for Co-containing particles employed as Fischer–Tropsch synthesis (FTS) catalysts; firstly, working at small length scales (approx. micrometre spatial resolution), a combination of sample size and density allows for transmission of comparatively low energy signals enabling the recording of ‘multimodal’ tomography, i.e. simultaneous XRF–CT, XANES–CT and XRD–CT. Subsequently, we show high-energy XRD–CT can be employed to reveal extent of reduction and uniformity of crystallite size on millimetre-sized TiO2 trilobes. In both studies, the CoO phase is seen to persist or else evolve under particular operating conditions and we speculate as to why this is observed.

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Abstract: Osmium nanocrystals can be fabricated by electron (3–50 nm, formed by atom migration), 785–815 nm laser (20–50 nm, in micelle islands), and microwave (ca. 1 nm in arrays, >100 mg scale) irradiation of a polymer-encapsulated OsII carborane; microfocus X-ray absorption studies at the Os LIII-edge show differences between the three preparation methods, suggesting that the electron-beam irradiated materials have a significant support interaction and/or surface oxidation, while the laser and microwave samples are more like metallic osmium.