scholarly journals Structural and compositional characteristics of Fukushima release particulate material from Units 1 and 3 elucidates release mechanisms, accident chronology and future decommissioning strategy

2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Peter G. Martin ◽  
Christopher P. Jones ◽  
Stuart Bartlett ◽  
Konstantin Ignatyev ◽  
Dave Megson-Smith ◽  
...  

AbstractThe structural form and elemental distribution of material originating from different Fukushima Daiichi Nuclear Power Plant reactors (Units 1 and 3) is hereby examined to elucidate their contrasting release dynamics and the current in-reactor conditions to influence future decommissioning challenges. Complimentary computed X-ray absorption tomography and X-ray fluorescence data show that the two suites of Si-based material sourced from the different reactor Units have contrasting internal structure and compositional distribution. The known event and condition chronology correlate with the observed internal and external structures of the particulates examined, which suggest that Unit 1 ejecta material sustained a greater degree of melting than that likely derived from reactor Unit 3. In particular, we attribute the near-spherical shape of Unit 1 ejecta and their internal voids to there being sufficient time for surface tension to round these objects before the hot (and so relatively low viscosity) silicate melt cooled to form glass. In contrast, a more complex internal form associated with the sub-mm particulates invoked to originate from Unit 3 suggest a lower peak temperature, over a longer duration. Using volcanic analogues, we consider the structural form of this material and how it relates to its environmental particulate stability and the bulk removal of residual materials from the damaged reactors. We conclude that the brittle and angular Unit 3 particulate are more susceptible to further fragmentation and particulate generation hazard than the round, higher-strength, more homogenous Unit 1 material.

Author(s):  
R. L. Stears

Because of the nature of the bacterial endospore, little work has been done on analyzing their elemental distribution and composition in the intact, living, hydrated state. The majority of the qualitative analysis entailed intensive disruption and processing of the endospores, which effects their cellular integrity and composition.Absorption edge imaging permits elemental analysis of hydrated, unstained specimens at high resolution. By taking advantage of differential absorption of x-ray photons in regions of varying elemental composition, and using a high brightness, tuneable synchrotron source to obtain monochromatic x-rays, contact x-ray micrographs can be made of unfixed, intact endospores that reveal sites of elemental localization. This study presents new data demonstrating the application of x-ray absorption edge imaging to produce elemental information about nitrogen (N) and calcium (Ca) localization using Bacillus thuringiensis as the test specimen.


1999 ◽  
Vol 590 ◽  
Author(s):  
N. Mölders ◽  
P.J. Schilling ◽  
J.M. Schoonmaker

ABSTRACTAn x-ray microprobe beamline was recently developed and commissioned at the Center for Advanced Microstructures and Devices (CAMD), Louisiana State University. It achieves a moderate horizontal and vertical focal spot size of 18.8 µm × 7.0 µm (σ), respectively. The beamline and end-station are designed and optimized to perform (i) spatially-resolved x-ray fluorescence spectroscopy (spectro-microscopy) using the broad intense spectrum of the white synchrotron radiation, and (ii) spatially-resolved x-ray absorption spectroscopy (micro-spectroscopy) in the energy region of 2100eV to 12000 eV. These dual capabilities enable K-edge measurements and mapping, in non-vacuum conditions, of low-Z elements down to Cl, S, and P that are of both environmental interest and technological importance. In this paper, an application of this novel synchrotron tool to elucidate the elemental distribution (microstructure) and chemical state (speciation) of Mn, Cl, S, and P-containing particulates emitted from automobile engines burning methylcyclopentadienyl manganese tricarbonyl- (MMT-) added fuel will be discussed in detail. Future opportunities of this microbeam technique in materials science and materials characterization will also be outlined.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Hend M. H. Al-Kordy ◽  
Soraya A. Sabry ◽  
Mona E. M. Mabrouk

AbstractGreen synthesis of zinc oxide nanoparticles (ZnO NPs) through simple, rapid, eco-friendly and an economical method with a new haloalkaliphilic bacterial strain (Alkalibacillus sp. W7) was investigated. Response surface methodology (RSM) based on Box-Behnken design (BP) was used to optimize the process parameters (ZnSO4.7H2O concentration, temperature, and pH) affecting the size of Alkalibacillus-ZnO NPs (Alk-ZnO NPs). The synthesized nanoparticles were characterized using UV–visible spectrum, X-ray diffraction (XRD), Scanning electron microscope-energy dispersive X-ray spectroscopy (SEM–EDX), Transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FTIR) and Zeta potential. The UV–Vis spectrum of ZnO NPs revealed a characteristic surface plasmon resonance (SPR) peak at 310 nm. XRD pattern confirmed the hexagonal wurtzite structure of highly pure with a crystallite size 19.5 nm. TEM proved the quasi-spherical shape nanoparticles of size ranging from 1 to 30 nm. SEM–EDX showed spherical shaped and displayed a maximum elemental distribution of zinc and oxygen. FTIR provided an evidence that the biofunctional groups of metabolites in Alkalibacillus sp.W7 supernatant acted as viable reducing, capping and stabilizing agents.


1998 ◽  
Vol 5 (3) ◽  
pp. 1099-1101 ◽  
Author(s):  
Atsushi Ito ◽  
Kunio Shinohara ◽  
Yutaka Mizukami ◽  
Hisako Nakano ◽  
Keiji Yada ◽  
...  

An X-ray contact microscopy system has been developed for the study of molecular and elemental distributions in biological specimens based on X-ray absorption characteristics. The system consists of a chamber for measuring XANES (X-ray absorption near-edge structure) of biomolecules, and a contact microscopy system for dried specimens with an electronic zooming tube. With this system the elemental distribution of carbon, nitrogen, oxygen, Ca and Fe in an HeLa cell has been studied, and the DNA-related image using a peak from the XANES profile of the DNA at the K-absorption edge of phosphorus has been obtained.


2014 ◽  
Vol 90 ◽  
pp. 111-120 ◽  
Author(s):  
Araceli de Pablos-Martín ◽  
Maria J. Pascual ◽  
Alicia Durán

Rare-earth (RE) ions-doped oxyfluoride transparent glass-ceramics containing nano-crystalline phases with very low phonon energies like LaF3, NaLaF4 and KLaF4 combine the superior optical performance of low phonon energy phases with the high mechanical, chemical and thermal stability of oxide silicates. The insertion of the doping RE ions in the fluoride nanocrystals enhances the radiative optical emission processes currently focused on up- and down-conversion emissions. Thus, a key point is to identify and quantify the RE ions in the fluoride nano-crystals. In this contribution an oxyfluoride glass and the corresponding glass-ceramics of composition 55 SiO2. 20 Al2O3.15 Na2O.10 LaF3 mol % doped with 1 mol % Tm2O3 is presented. The Tm3+ incorporation in the precipitated LaF3 nano-crystals has been analysed by two different techniques. Firstly, TEM and Energy Dispersive X-Ray Spectroscopy (EDXS) were used to perform elemental distribution mappings of RE elements that allow to directly localising RE ions in the glass and glass-ceramics. Additionally, X-ray absorption spectroscopy (XAS) measurements were performed to analyse the distribution and first coordination sphere of Tm3+ ions in the glass and glass–ceramics by using X-ray absorption near edge structure spectroscopy (XANES) and extended absorption X-ray fine structure spectroscopy (EXAFS), which have allow to quantify the Tm3+ incorporation in the LaF3 nano-crystals.


2020 ◽  
Vol 53 (1A) ◽  
pp. 117-127
Author(s):  
Tayel El-Hasa

The current work investigates the Cambrian Manganese ore deposits from Wadi Dana at central Wadi Araba region. This investigation aims to unravel the chemistry and micro-textures of the mineral paragenetic sequence for these manganese ore deposits. Particularly the Fe–Mn intimate intergrowth micro texture and the epigenetic Mn mineralization associated with Cu minerals. The combination of the synchrotron-based X-ray fluorescence (syn-XRF) micro-mapping and X-ray absorption fine structure (XAFS) techniques were used. They provide a clear picture of the elemental distribution of Mn, Fe, Cu, and Pb and other elements presented within the ore micro textures. Besides, it determines the exact elemental speciation. The results obtained gave a better understanding of the elemental atomic structures and eventually the depositional environment. Particularly, the syn-XRF micro-mapping reveals the existing of many successive evolution stages in the Mn ores. Besides, the X-ray Absorption Near Edge Structure (XANES) results showed that the micro-rhythmic texture is changing from Mn+4 (Pyrolusite) into Fe+3 (Hematite). This is evidence for the role of Eh as the main controlling factor during the ore formation. Eventually, indicating tentatively the paleoceanography setting of the Mn deposits. This is related to the continuous transgression-regression on the sea level in a semi-closed sea.


2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Carlo Marini ◽  
Anna Maria Diaz Rovira ◽  
Nitya Ramanan ◽  
Wojciech Olszewski ◽  
Boby Joseph ◽  
...  

AbstractCombining micro-X-ray absorption spectroscopy (μXAS) and micro-X-ray fluorescence spectroscopy (μXRF) is a promising approach for the investigation of complex multi-phase systems. In this work, we have employed this approach to investigate natural sphalerite, the most common form of Zinc Sulfide. Spatially resolved elemental distribution maps of common 3d metal atoms (Zn, Cu, Ni, Co, and Fe) are superimposed with chemical speciation and structural parameter maps in order to understand the sphaleriteore-formation process and metamorphosis. Chemical speciation and structural parameters have been obtained by analyzing the μXAS spectra collected in several representative points of the sample, after μXRF mapping. In the present case, this X-ray based approach has permitted to determine the spatial distribution of the Zn species in sphalerite. The presence of two main zincite and smithsonite inclusions has been established, with the latter located close to copper impurity center. Since copper is known to remarkably reduce the corrosion resistance of zinc, resulting in the formation of carbonate as the corrosion product, this implies a possible role of Cu in the growth of the carbonate inclusions. The results obtained highlight the efficiency of this method in univocally identifying the spatial distribution of phases in complex systems, thanks to the simultaneous access to complementary information.


Minerals ◽  
2021 ◽  
Vol 11 (12) ◽  
pp. 1386
Author(s):  
Arjen van Veelen ◽  
Paul C. M. Francisco ◽  
Nicholas P. Edwards ◽  
Julian Frederick W. Mosselmans ◽  
Tsutomu Sato ◽  
...  

In order to provide important details concerning the adsorption reactions of Sr, batch reactions and a set of both ex situ and in situ Grazing Incidence X-ray Absorption Fine Structure (GIXAFS) adsorption experiments were completed on powdered TiO2 and on rutile(110), both reacted with either SrCl2 or SrCO3 solutions. TiO2 sorption capacity for strontium (Sr) ranges from 550 ppm (SrCl2 solutions, second order kinetics) to 1400 ppm (SrCO3 solutions, first order kinetics), respectively, and is rapid. Sr adsorption decreased as a function of chloride concentration but significantly increased as carbonate concentrations increased. In the presence of carbonate, the ability of TiO2 to remove Sr from the solution increases by a factor of ~4 due to rapid epitaxial surface precipitation of an SrCO3 thin film, which registers itself on the rutile(110) surface as a strontianite-like phase (d-spacing 2.8 Å). Extended X-ray Absorption Fine Structure (EXAFS) results suggest the initial attachment is via tetradental inner-sphere Sr adsorption. Moreover, adsorbates from concentrated SrCl2 solutions contain carbonate and hydroxyl species, which results in both inner- and outer-sphere adsorbates and explains the reduced Sr adsorption in these systems. These results not only provide new insights into Sr kinetics and adsorption on TiO2 but also provide valuable information concerning potential improvements in effluent water treatment models and are pertinent in developing treatment methods for rutile-coated structural materials within nuclear power plants.


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