Application of transition-edge sensors for micro-X-ray fluorescence measurements and micro-X-ray absorption near edge structure spectroscopy: a case study of uranium speciation in biotite obtained from a uranium mine.

In this study, we successfully applied a transition-edge sensor (TES) spectrometer as a detector for microbeam X-ray measurements from a synchrotron X-ray light source in the hard X-ray region to determine uranium (U) distribution at the micro-scale and its chemical species in biotite obtained from a U mine. It is difficult to separate the fluorescent X-ray of the U Lα1 line at 13.615 keV from that of the Rb Kα line at 13.395 keV in the X-ray fluorescence spectrum with an energy resolution of approximately 220 eV using a conventional silicon drift detector (SDD). Meanwhile, the fluorescent X-rays of U Lα1 and Rb Kα were fully separated by a TES with 50 eV energy resolution at an energy of around 13 keV. The successful peak separation by the TES led to an accurate mapping analysis of trace U in micro-X-ray fluorescence measurements and a decrease in the signal-to-background ratio in micro-X-ray absorption near edge structure spectroscopy. Thus, it could be a powerful tool for studying the U distribution and speciation in various environmental samples.

Application of High-Energy-Resolution X-ray Absorption Spectroscopy at the U L3-Edge to Assess the U(V) Electronic Structure in FeUO4.

FeUO4 was studied to clarify the electronic structure of U(V) in a metal monouranate compound. We obtained the peak splitting of spectra utilizing high-energy-resolution fluorescence detection-X-ray absorption near-edge structure (HERFD-XANES) spectroscopy at the U L3-edge, which is a novel technique in uranium(V) monouranate compounds. Theoretical calculations revealed that the peak splitting was caused by splitting of the 6d orbital of U(V) in FeUO4, which would be used to detect minor U(V) species. Such distinctive electronic states are of major interest to researchers and engineers working in various fields, from fundamental physics to the nuclear industry and environmental sciences for actinide elements.

Direct Quantitation of 135Cs in Spent Cs Adsorbent Used for the Decontamination of Radiocesium-Containing Water by Laser Ablation Inductively Coupled Plasma Mass Spectrometry.

The long-term safety assessment of spent Cs adsorbents produced during the decontamination of radiocesium-containing water at the Fukushima Daiichi nuclear power plant requires one to estimate their 135Cs content prior to final disposal. 135Cs is usually quantified by inductively coupled plasma mass spectrometry (ICP-MS), which necessitates the elution of Cs from Cs adsorbents. However, this approach suffers from the high radiation dose from 137Cs that is present in the contaminated water and Cs adsorption irreversibility. To address these challenges, we herein employed laser ablation ICP-MS for direct quantitation of 135Cs in Cs adsorbents and used a model Cs adsorbent prepared by immersion of a commercially available Cs adsorbent into radiocesium-containing liquid waste to verify the developed technique. Crushing and subsequent coating with a nitrocellulose-based curing agent provided a thin flat surface and thus allowed for stable solid sampling during laser ablation. The use of the 135Cs/137Cs ratio and 137Cs radioactivity obtained by gamma spectrometry achieved simple and precise quantitation of 135Cs. The obtained 135Cs/137Cs ratio of 0.41 ± 0.02 well agreed with that obtained for the original liquid waste sample by solution nebulization measurements, and the proposed method was concluded to be suitable for large-scale 135Cs quantitation, requiring only very small (<10 mg) samples with total 137Cs radioactivity.

Determination of 107Pd in Pd purified by selective precipitation from spent nuclear fuel by laser ablation ICP-MS.

Determination of radiopalladium 107Pd is required to ensure radiation safety of the Pd extracted from spent nuclear fuel for recycling or disposal. We employed nanosecond laser ablation inductively coupled plasma quadrupole mass spectrometry (ns-LA-ICP-QMS) to simplify the analytical procedure of 107Pd. Pd was separated through a selective Pd precipitation reaction induced by pulsed laser irradiation that reduces Pd(II) ions to metal Pd(0). Laser ablation facilitates direct measurement of the Pd precipitates, skipping the dissolution and dilution procedure with aqua regia and HCl, which causes serious corrosion damage to the introduction system of the ICP. In the present study, 102Pd in natural Pd standard solution was used as an internal standard owing to its absence in spent nuclear fuel. Pd precipitates with diameters ranging from 0.2 to 0.5 µm, obtained by pulsed laser irradiation, were embedded uniformly on the surface of the centrifugal filter to form a microscopically thin and flat Pd surface. The resulting homogeneous Pd layer is suitable for obtaining a stable signal ratio of 107Pd/102Pd (< 4%, 2RSD). The mass bias-corrected ratio of 107Pd/102Pd and the amount of 107Pd were 0.163 ± 0.004 and 17.8 ± 0.6 ng, respectively, which correspond to the values obtained by solution nebulization measurement after the dissolution of identical Pd precipitates. Graphical abstract ᅟ.

Determination of 107Pd in Pd Recovered by Laser-Induced Photoreduction with Inductively Coupled Plasma Mass Spectrometry.

Safety evaluation of a radioactive waste repository requires credible activity estimates confirmed by actual measurements. A long-lived radionuclide, 107Pd, which can be found in radioactive wastes, is one of the difficult-to-measure nuclides and results in a deficit in experimentally determined contents. In this study, a precipitation-based separation method has been developed for the determination of 107Pd with inductively coupled plasma mass spectrometry. The photoreduction induced by pulsed laser irradiation at 355 nm provides short-time and one-step recovery of Pd. The proposed method was verified by applying it to a spent nuclear fuel sample. To recover Pd efficiently, a natural Pd standard was employed as the Pd carrier. Taking advantage of the absence of 102Pd in spent nuclear fuel, 102Pd in the Pd carrier was utilized as the internal standard. The chemical yield of Pd was about 90% with virtually no impurities, allowing accurate quantification of 107Pd. The amount of 107Pd in the Pd precipitate was 17.3 ± 0.7 ng, equivalent to 239 ± 9 ng per mg of 238U in the sample.

Analysis of particles containing alpha emitters in stagnant water in Fukushima Daiichi Nuclear Power Station's Unit 3 reactor building.

Particles containing alpha (α) nuclides were identified from sediment in stagnant water in the Unit 3 reactor building of the Fukushima Daiichi Nuclear Power Station (FDiNPS). We analyzed different concentrations of α-nuclide samples collected at two sampling sites, the torus room and the main steam isolation valve (MSIV) room. The solids in the stagnant water samples were classified, and the uranium (U) and total alpha concentrations of each fraction were measured by dissolution followed by inductively coupled plasma mass spectrometry and α-spectrometry. Most of the α-nuclides in the stagnant water samples from the torus and MSIV rooms were in particle fractions larger than 10 µm. We detected uranium-bearing particles ranging from sub-µm to 10 µm in size by scanning electron microscopy-energy-dispersive X-ray (SEM-EDX) observations. The chemical forms of U particles were determined in U-Zr oxides, oxidized UO2, and U3O8 with micro-Raman spectroscopy. Other short-lived α-nuclides (plutonium [Pu], americium [Am], and curium [Cm]) were detected by alpha track detection, and the particles with α-nuclides was characterized by SEM-EDX analysis. α-nuclide-containing particles with several tens to several 100 µm in size mainly comprised iron (Fe) oxyhydroxides. In addition, we detected adsorbed U onto Fe oxyhydroxide particles in the MSIV room sample, which indicated nuclear fuel dissolution and secondary U accumulation. This study clarifies the major characteristics of U and other α-nuclides in sediment in stagnant water in the FDiNPS Unit 3 reactor building, which significantly contribute to the consideration of removal methods for particles containing α-nuclides in the stagnant water.

Globular pattern formation of hierarchical ceria nanoarchitectures.

Dissipative structures often appear as an unstable counterpart of ordered structures owing to fluctuations that do not form a homogeneous phase. Even a multiphase mixture may simultaneously undergo one chemical reaction near equilibrium and another one that is far from equilibrium. Here, we observed in real time crystal seed formation and simultaneous nanocrystal aggregation proceeding from CeIV complexes to CeO2 nanoparticles in an acidic aqueous solution, and investigated the resultant hierarchical nanoarchitecture. The formed particles exhibited two very different size ranges, resulting in further pattern formation with opalescence. The hierarchically assembled structures in solutions were CeO2 colloids, viz. primary core clusters (1-3 nm) of crystalline ceria and secondary clusters (20-30 nm) assembled through surface ions. Such self-assembly is widespread in multi-component complex fluids, paradoxically moderating hierarchical reactions. Stability and instability are not only critical but also complementary for co-optimisation around the nearby free energy landscape prior to bifurcation.

High-sensitive XANES analysis at Ce L2-edge for Ce in bauxites using transition-edge sensors: Implications for Ti-rich geological samples.

Accurate determination of cerium (Ce) valence state is important for interpreting the Ce anomaly in geological archives for (paleo)redox reconstruction. However, the routine application of Ce L3-edge X-ray absorption near-edge structure (XANES) spectroscopy for detecting trace Ce in geological samples can often be restricted by coexisting titanium (Ti) due to the proximity of their fluorescence emission lines. Therefore, the signal-to-noise ratio of Ce L3-edge XANES spectra may not be sufficiently high for high-quality spectroscopic analysis. This study introduces a semi-quantitative approach appropriate for Ti-rich, Ce-dilute geological materials by synchrotron-based X-ray measurement at the Ce L2-edge. First, the results confirm that Ce L2-edge XANES spectra are able to avoid overlapping Ti Kß emissions and provide more reliable information on the Ce valence state in Ti-rich materials relative to L3-edge XANES. Moreover, the application of transition-edge sensor (TES) could reach the higher sensitivity with better energy resolution than conventional silicon drift detector (SDD) to detect fluorescence X-ray (Ce Lß1). The investigation on bauxites developed from the Columbia River Basalts shows that combining Ce L2-edge XANES and TES allows for resolving weak Ce fluorescence lines at the L2-edge from Ti-rich, Ce-dilute samples (Ti/Ce mass ratio up to ∼6000, tens of ppm Ce). The outcome emphasizes the practical possibility of investigating Ce redox state in Ti-rich geological samples.

Analysis of particles containing alpha-emitters in stagnant water at torus room of Fukushima Dai-ichi Nuclear Power Station's Unit 2 reactor.

Particles containing alpha (α) nuclides were identified from sediment in stagnant water in the torus room of the Fukushima Dai-ichi Nuclear Power Station(FDiNPS)'s Unit 2 reactor. We analyzed uranium (U), which is the main component of nuclear fuel, using scanning electron microscopy (SEM). Other α-nuclides (plutonium [Pu], americium [Am], and curium [Cm]) were detected by alpha track detection and the morphology of particles with α-nuclides were analyzed by SEM-energy dispersive X-Ray (EDX) analysis. Several uranium-bearing particles ranging from sub-µm to several µm in size were identified by SEM observation. These particles contained zirconium (Zr) and other elements which constituted fuel cladding and structural materials. The 235U/238U isotope ratio in the solid fractions that included U particles was consistent with what was found for the nuclear fuel in the Unit 2 reactor. This indicated that the U of similar fuel composition had made finer. The α-nuclide-containing particles identified by alpha track analysis were several tens to several hundred µm in size. The EDX spectra showed that these particles mainly comprised iron (Fe). Since the amount of α-nuclide material was very small, Pu, Am, and Cm were adsorbed on the Fe particles. This study clarifies that the major morphologies of U and other α-nuclides in the sediment of stagnant water in the torus room of FDiNPS's Unit 2 reactor differed.

Selective Pd Separation from Simulated Radioactive Liquid Waste by Precipitation Using Xenon Lamp Irradiation for a Simplified Procedure.

In this study, we developed a simple and one-step Pd separation technique based on photoreduction with Xe lamp irradiation for the determination of 107Pd in highly radioactive samples. A simulated high-level radioactive liquid wastes (HLLW) solution, consisting of 14 major elements in a 3 mol L-1 HNO3 solution, was used to evaluate the separation performance. The Pd precipitate was formed by Xe lamp irradiation, and recovered by centrifugation. The Pd recovery from the simulated HLLW solution reached up to 50%, while 99.5% of the other 13 elements was separated. These results indicate that the applicability of the proposed separation technique to HLLW samples.

Application of an Augmentation Method to MCR-ALS Analysis for XAFS and Raman Data Matrices in the Structural Change of Isopolymolybdates.

We measured X-ray absorption fine structure (XAFS) and Raman spectra of isopolymolybdates(VI) in highly concentrated HNO3 solution (0.15 - 4.0 M), which change their geometries depending on the acid concentration, and performed the simultaneous resolution of the XAFS and Raman data using a multivariate curve resolution by alternating least-squares (MCR-ALS) analysis. In iterative ALS optimization, initial data matrices were prepared by two different methods. For low sensitivity of the XAFS spectra to the geometrical change of the isopolymolybdates, the MCR-ALS result of single XAFS data matrix shows a large dependence on the preparation method of the initial data matrices. This problem is improved by the simultaneous resolution of the XAFS and Raman data: the MCR-ALS result of an augmented matrix of these data has little dependence on the initial data matrices. This indicates that the augmentation method effectively improves the rotation ambiguities in the MCR-ALS analysis of the XAFS data.

In situ observation of carrier transfer in the Mn-oxide/Nb:SrTiO3 photoelectrode by X-ray absorption spectroscopy.

The Mn-oxide/Nb:SrTiO3 photoelectrode for oxygen evolution reaction was investigated by in situ Mn K-edge XAFS spectroscopy under UV irradiation. The oxidization of the Mn oxide was observed via photoexcited carrier transfer, which results in the positive potential shift of the Mn oxide cocatalyst toward oxygen evolution reaction.