In situ XAFS-XRD study of the Zr-Y2O3 interaction at extra-high temperatures.

The in situ measurement technique for a metal/metal-oxide mixture at extra-high temperature above 2000 K has been desired in the field of nuclear safety engineering. In the present study, we succeeded in simultaneous XAFS-XRD measurements of the Zr oxidation [Zr + O → Zr(O) + ZrO2] up to 1952 K and ZrO2-Y2O3 reaction from 1952 to 2519 K. The chemical shift during Zr oxidation was observed in the absorption spectra around the Zr K-edge, and the interatomic cation-cation and cation-oxygen distances obtained by the fitting analysis of EXAFS during the Y2O3-ZrO2 reaction are explained. Also, the temperature dependency of the anharmonic effect was investigated by comparing the fitted second- and third-order cumulants with the theoretical ones in which the Morse potential was applied as an interatomic potential, giving a good explanation about the local structure dynamics. Finally, the applicability of the developed system to investigation of nuclear fuel materials, such as UO2-Zr, is discussed.

Study on Phenanthroline Carboxamide for Lanthanide Separation: Influence of Amide Substituents.

Phenanthroline carboxamide compounds are promising for lanthanide intra-series separation. This paper presents a study on the effect of structure modification of phenanthroline carboxamides on the extraction of the whole lanthanide series. The study consists of theoretical calculations, extraction experiments of the 14 stable lanthanides, and extended X-ray absorption fine structure (EXAFS) analyses of Nd and Dy complexes. Tridentate monocarboxamides and tetradentate dicarboxamides show different trends in series extraction, although both preferentially extract the light lanthanides. The amide substituents, although not directly coordinating the metal ions, were also found to impact the distribution ratio, most probably due to a modification in the internal polarity of the molecules. This latter effect, if extrapolated to other nitrogen-based ligands such as pyridines or triazines, can be used to further fine-tune extractants for a process improvement.

Proton Chelating Ligands Drive Improved Chemical Separations for Rhodium.

Current methods for the extraction of rhodium carry the highest carbon footprint and worst pollution metrics of all of the elements used in modern technological applications. Improving upon existing methods is made difficult by the limited understanding of the molecular-level chemistry occurring in extraction processes, particularly in the hydrometallurgical separation step. While many of the precious metals can be separated by solvent extraction, there currently exist no commercial extractants for Rh. This is due to its complicated mixed speciation upon leaching into hydrochloric acid, which gives rise to difficulties in designing effective reagents for solvent extraction. Herein we show that the diamidoamine reagent N- n-hexylbis( N-methyl- N- n-octylethylamide)amine transports Rh(III) from aqueous HCl into an organic phase as the monoaquated dianion [RhCl5(H2O)]2- through the formation of an outer-sphere assembly; this assembly has been characterized by experimentation (slope analysis, FT-IR and NMR spectroscopy, EXAFS, SANS, and ESI-MS) and computational modeling. The paper demonstrates the importance of applying a broad range of techniques to obtain a convincing mode of action for the complex processes involved in anion recognition in the solution phase. A consistent and comprehensive understanding of how the ligand operates to achieve Rh(III) selectivity over the competitor anion Cl- has emerged. This knowledge will guide the design of extractants and thus offers promise for improving the sustainability of metal extraction from both traditional mining sources and the recycling of secondary source materials.

Nosyl (2-Nitrobenzenesulfonyl) Annulation Strategy toward Winding Vine-Shaped Bithiophenes.

Winding vine-shaped bithiophene was synthesized through the nosyl (2-nitrobenzenesulfonyl) cyclization protocol. The reaction of bithiophene bearing bromomethyl groups at the 3,3'-positions with nosylated 1,2-ethylenediamine in the presence of potassium carbonate afforded the annulated product in excellent yield. The obtained bithiophene was found to contain a 10-membered ring, which was confirmed by X-ray analysis. The related nosyldiamine bearing a tri- or tetramethylene group also reacted in a similar manner, affording an 11- or 12-membered macrocycle, respectively.

Mechanisms of Se(IV) Co-precipitation with Ferrihydrite at Acidic and Alkaline Conditions and Its Behavior during Aging.

Understanding the form of Se(IV) co-precipitated with ferrihydrite and its subsequent behavior during phase transformation is critical to predicting its long-term fate in a range of natural and engineered settings. In this work, Se(IV)-ferrihydrite co-precipitates formed at different pH were characterized with chemical extraction, transmission electron microscopy (TEM), and X-ray absorption spectroscopy (XAS) to determine how Se(IV) is associated with ferrihydrite. Results show that despite efficient removal, the mode and stability of Se(IV) retention in the co-precipitates varied with pH. At pH 5, Se(IV) was removed dominantly as a ferric selenite-like phase intimately associated with ferrihydrite, while at pH 10, it was mostly present as a surface species on ferrihydrite. Similarly, the behavior of Se(IV) and the extent of its retention during phase transformation varied with pH. At pH 5, Se(IV) remained completely associated with the solid phase despite the phase change, whereas it was partially released back into solution at pH 10. Regardless of this difference in behavior, TEM and XAS results show that Se(IV) was retained within the crystalline post-aging products and possibly occluded in nanopore and defect structures. These results demonstrate a potential long-term immobilization pathway for Se(IV) even after phase transformation. This work presents one of the first direct insights on Se(IV) co-precipitation and its behavior in response to iron phase transformations.

Characterization of Adsorbed Alkali Metal Ions in 2:1 Type Clay Minerals from First-Principles Metadynamics.

Adsorption states of alkali metal ions in three kinds of 2:1 type clay minerals are systematically investigated via first-principles-based metadynamics. Our reconstructed free energy surfaces in a two-dimensional space of coordination numbers specifically employed as collective variables for describing the interlayer cations show that an inner-sphere (IS) complex is preferentially formed for Cs(+) in the 2:1 type trioctahedral clay minerals with saponite-like compositions, where lighter alkali metal ions show a tendency to form an outer-sphere one instead. The strong preference for an IS complex observed for Cs(+) is found to result partially from the capability of recognizing selectively Cs(+) ions at the basal O atoms with the Lewis basicity significantly enhanced by the isomorphic substitution in tetrahedral sheets.

Mesoscopic structures of vermiculite and weathered biotite clays in suspension with and without cesium ions.

The effect of cesium (Cs) adsorption on the mesoscopic structure of the clay minerals vermiculite and weathered biotite (WB) in suspensions was elucidated by small-angle X-ray scattering (SAXS). The clay minerals form multilayered structures, and the Cs cations (Cs(+)) are strongly adsorbed in the interlayer space of the soil clays, in particular vermiculite and WB. SAXS was used to monitor the relationship between Cs(+) adsorption at the clay interlayers and the structural changes at length scales from 1 to 1000 Å. The variation in the distance between the neighboring clay sheets and the spatial arrangement of the clay sheets with and without Cs(+) were clarified. Our quantitative analyses revealed that the number of stacked layers of pure vermiculite was decreased by Cs(+) addition, whereas that of WB increased. Moreover, the average distance between the neighboring layers of vermiculite in suspension was larger than that of WB, which reflects the different conditions of Cs(+) intercalation. These findings provide fundamental insights that are important for predicting the environmental fate of radioactive Cs in contaminated regions and for developing methods for extracting Cs from soil.

Speciation of radioactive soil particles in the Fukushima contaminated area by IP autoradiography and microanalyses.

Radioactive soil particles several tens of micrometers in size were collected from litter soil in the radiation contaminated area by the Fukushima nuclear plant accident and characterized using electron and X-ray microanalyses. The radioactive particles were discriminated by autoradiography using imaging plates (IP) on which microgrids were formed by laser ablation in order to find the particles under microscopy. Fifty radioactive particles were identified and classified into three types from their morphology and chemical composition, namely: (1) aggregates of clay minerals, (2) organic matter containing clay mineral particulates, and (3) weathered biotite originating from local granite. With respect to the second type, dissolution of the organic matter did not reduce the radiation, suggesting that the radionuclides were also fixed by the clay minerals. The weathered biotite grains have a plate-like shape with well-developed cleavages inside the grains, and kaolin group minerals and goethite filling the cleavage spaces. The reduction of the radiation intensity was measured before and after the trimming of the plate edges using a focused ion beam (FIB), to examine whether radioactive cesium primarily sorbed at frayed edges. The radiation was attenuated in proportion to the volume decrease by the edge trimming, implying that radioactive cesium was sorbed uniformly in the porous weathered biotite.

Molecular geochemistry of radium: A key to understanding cation adsorption reaction on clay minerals.

Adsorption reactions of various cations on clay minerals have different effects on their environmental behaviors depending on the molecular-scale adsorption structure. Some cations form outer-sphere complexes via hydration, while others create inner-sphere complexes through dehydration. This preference dictates their environmental impact. However, the factors controlling these complex formations remain unclear. Furthermore, research on the adsorption preferences of radium (Ra) is lacking. Thus, this study conducted the first EXAFS study of Ra2+ adsorbed on clay minerals and showed that Ra2+ forms inner-sphere complexes on vermiculite, which can be surprising because Ra2+ is a divalent cation and prefers to be hydrated. In order to investigate the factors controlling the complex formations, this study conducted systematic EXAFS measurements and DFT calculations for alkali and alkaline earth metal cations. The results showed the importance of the size-matching effect between the adsorbed cation and the cavity of the tetrahedral sheets and that the complex formation can be estimated by the combination of the ionic radius and hydration enthalpy of the adsorbed cation. Furthermore, this study also analyzed environmental core samples. Their results showed the fixation of Ra2+ by clay minerals and the controlling factors can effectively predict cation environmental behavior.

Hydrolysis of tetravalent cerium for a simple route to nanocrystalline cerium dioxide: an in situ spectroscopic study of nanocrystal evolution.

Despite the rapid developments in recent nanocrystal research and their expanding applications, the evolution mechanism of nanocrystals remains veiled for the most part due to the lack of appropriate analytical techniques. Here we demonstrate one promising multi-spectroscopic approach for the in situ investigation of nanocrystal evolution. That is, the formation of nanocrystalline cerium dioxide (NC-CeO2) has been probed by dynamic light scattering (DLS), X-ray absorption spectroscopy (XAS) and high-energy X-ray scattering (HEXS). The obtained results indicate that the fine colloidal particles of NC-CeO2 are formed in an acidic aqueous solution simply through the hydrolysis of the initial precursor of small oligomer Ce(IV) species. This information on how NC-CeO2 evolves is fundamental to simplifying and alleviating the synthetic strategy for NC-CeO2 production.

Extraction of Se(iv) and Se(vi) from aqueous HCl solution by using a diamide-containing tertiary amine.

Here, we investigated the mechanism underlying the extraction of Se(iv) and Se(vi) from aqueous HCl solutions by N-2-ethylhexyl-bis(N-di-2-ethylhexyl-ethylamide)amine (EHBAA). In addition to examining extraction behavior, we also elucidated structural properties of the dominant Se species in solution. Two types of aqueous HCl solutions were prepared by dissolving a SeIV oxide or a SeVI salt. X-ray absorption near edge structure analyses revealed that Se(vi) was reduced to Se(iv) in 8 M HCl. Using 0.5 M EHBAA, ∼50% of Se(vi) was extracted from 0.5 M HCl. In contrast, Se(iv) was hardly extracted from 0.5 to 5 M HCl; however, at molar concentrations above 5 M, the extraction efficiency of Se(iv) increased drastically, reaching ∼85%. Slope analyses for the distribution ratios of Se(iv) in 8 M HCl and Se(vi) in 0.5 M HCl showed that apparent stoichiometries of Se(iv) or Se(vi) to EHBAA were 1 : 1 and 1 : 2, respectively. Extended X-ray absorption fine structure measurements revealed that the inner-sphere of the Se(iv) and Se(vi) complexes extracted with EHBAA was [SeOCl2] and [SeO4]2-, respectively. Together, these results indicate that Se(iv) is extracted from 8 M HCl with EHBAA via a solvation-type reaction, whereas Se(vi) is extracted from 0.5 M HCl via an anion-exchange-type reaction.

Lanthanide extraction using a thiodiglycolamic acid extractant: effect of S-donor on lanthanide separation.

Liquid-liquid extraction of lanthanide (Ln) ions was investigated using N,N-dioctylthiodiglycolamic acid (DOTDGAA), which is a sulfur donor ligand with an amide group and a carboxyl group connected by a thioether chain. The extraction performance and selectivity of DOTDGAA for Ln ions were compared with those of N,N-dioctyldiglycolamic acid (DODGAA), which is also an oxygen donor ligand with a similar chemical structure, to assess the effect of the soft/hard donor atom on Ln separation. DOTDGAA quantitatively extracted all Ln ions while being selective toward the light and middle Ln ions, in contrast to the selectivity of DODGAA for heavier Ln ions. Slope analysis demonstrated that the Ln3+ transfer using DOTDGAA proceeded through a proton-exchange reaction, forming a 1:3 complex, Ln(DOTDGAA)3. The back-extraction of Ln ions from the extracting phase was successfully achieved under acidic conditions.

Sr(ii) extraction by crown ether in HFC: entropy driven mechanism through H2PFTOUD.

The solvent extraction of Sr(ii) was carried out using dicyclohexano-18-crown-6 (DCH18C6) and two HFC mixed solvents MS1 and MS2, where MS1 was composed of 30/60 (w/w)% trans-1,2-dichloroethylene/HFC-43 (HFC-43: 1,1,1,2,2,3,4,5,5,5-decafluoropentane) and MS2 was 5/95 (w/w)% heptane/HFC-43. Nitric acid and perfuruoro-3-6-9-trioxaundecane-1,11-dioic acid (H2PFTOUD) were used to study the effect of acid on the extraction. The maximum distribution ratio of Sr(ii) (D Sr) observed for H2PFTOUD conditions was ∼180, and >10 times larger than aqueous nitric acid conditions. The D Sr value was influenced by concentrations of the DCH18C6, Sr(ii), and acid, and by temperature. The composition of extracted complexes was estimated using slope analysis as an Sr(ii)-anion-DCH18C6 ratio of ∼1 : 2 : 1. From the extended X-ray absorption fine structure (EXAFS) measurements of Sr(ii) in the aqueous and organic phases, it is inferred that regardless of the acid used, DCH18C6 coordinates to the first coordination sphere of the Sr(ii) extracted complexes and Sr(ii) is hydrated (complexation with H2PFTOUD cannot be distinguished) in the aqueous phase. Thermodynamic data were significantly changed by choice of acid, i.e., both enthalpy and entropy values were negative for nitric acid conditions, on the other hand, entropy values were large and positive for H2PFTOUD conditions. These results have demonstrated that the combination of HFC solvent and crown ether is applicable for metal extraction.

Marking actinides for separation: Resonance-enhanced multiphoton charge transfer in actinide complexes.

Precise separation and purification of f-block elements are important and challenging especially for the reduction of nuclear waste and the recycling of rare metals but are practically difficult mainly because of their chemical similarity. A promising way to overcome this difficulty is controlling their oxidation state by nonchemical processes. Here, we show resonance-enhanced multiphoton charge transfer in actinide complexes, which leads to element-specific control of their oxidation states owing to the distinct electronic spectra arising from resonant transitions between f orbitals. We observed oxidation of trivalent americium in nitric acid. In addition, we found that the coordination of nitrates is essential for promoting the oxidation reaction, which is the first finding ever relevant to the primary process of photoexcitation via resonant transitions of f-block elements. The resonance-enhanced photochemical process could be used in the nuclear waste management, as it would facilitate the mutual separation of actinides, such as americium and curium.

Extended X-ray absorption fine structure spectroscopy measurements and ab initio molecular dynamics simulations reveal the hydration structure of the radium(II) ion.

Radium is refocused from the viewpoint of an environmental pollutant and cancer therapy using alpha particles, where it mainly exists as a hydrated ion. We investigated the radium hydration structure and the dynamics of water molecules by extended X-ray absorption fine structure (EXAFS) spectroscopy and ab initio molecular dynamics (AIMD) simulation. The EXAFS experiment showed that the coordination number and average distance between radium ion and the oxygen atoms in the first hydration shell are 9.2 ± 1.9 and 2.87 ± 0.06 Å, respectively. They are consistent with those obtained from the AIMD simulations, 8.4 and 2.88 Å. The AIMD simulations also revealed that the water molecules in the first hydration shell of radium are less structured and more mobile than those of barium, which is an analogous element of radium. Our results indicate that radium can be more labile than barium in terms of interactions with water.

Speciation and separation of platinum(iv) polynuclear complexes in concentrated nitric acid solutions.

Understanding the solution chemistry of Pt(iv) is crucial for the hydrometallurgy of precious metals. To gain such an understanding, the speciation and separation of Pt(iv) complexes in concentrated HNO3 solutions were investigated via Pt LIII edge X-ray absorption fine structure (XAFS) spectroscopy. The XAFS results for concentrated HNO3 solutions of Na2Pt(OH)6 revealed the dominant presence of Pt polynuclear complexes, wherein the formation of Pt(iv) polynuclear complexes depended on the metal concentration and the Na2Pt(OH)6 dissolution temperature. The dominant species present in a heated nitrate solution of 0.90 g-Pt L-1 and a non-heated nitrate solution of 3.2 g-Pt L-1 were dinuclear Pt(iv) complexes, whereas those in a heated solution of 3.0 g-Pt L-1 were predominantly larger polynuclear complexes, such as, tetra- and hexa-nuclear complexes. The presence of larger Pt(iv) complexes was confirmed via XAFS spectroscopy, wherein the adsorption of Pt(iv) ions from a 10 M HNO3 solution by a chelating resin functionalised with iminodiacetic acid and a strongly basic anion-exchange resin bearing trimethyl ammonium nitrate was examined. The adsorption of 50 mg L-1 of Pt(iv) by the two resins was tested using aqueous solutions diluted from heated HNO3 solutions with varying metal concentrations, and also from a non-heated solution. We found that Pt(iv) complexes from heating solutions containing high Pt(iv) concentrations displayed high adsorption percentages. In addition, the selective adsorption of Pt(iv) over Pd(ii), Ag(i), Cu(ii), Ni(ii), and Fe(iii) from a 10 M HNO3 solution was achieved using a strongly basic anion-exchange resin.

Local coordination about La(3+) in molten LaCl3 and its mixtures with alkali chlorides.

The local structure around the La(3+) ions in molten LaCl(3) and its mixtures with alkali and alkaline earth chlorides has been investigated by using extended X-ray absorption fine structure (XAFS) and molecular dynamics (MD) techniques. Such mixtures, which are of current technological interest, are known to be thermodynamically nonideal, and there has been a good deal of work to understand the structural effects factors that contribute to the nonideality. New experimental methods allow observations at the La K-absorption edge at the high temperatures of interest, and the ability of the technique to obtain reliable information even at very low La(3+) concentrations in multicomponent mixtures is demonstrated. Both the mean La(3+)-Cl(-) interionic separation and the mean La(3+) coordination number are found to decrease as the concentration of La(3+) in the mixture decreases. The rate of decrease depends on the identity of the alkali and alkaline earth cations present in the mixtures in a way that parallels the degree of nonideality of the different systems; it is greatest for those alkali cations that coordinate Cl(-) weakly. In dilute mixtures with such cations La(3+) is able to adopt a very stable octahedral coordination geometry but this is inhibited by the presence of more strongly coordinating cations like Li(+) and Mg(2+).

Solvent Extraction of Technetium(VII) and Rhenium(VII) Using a Hexaoctylnitrilotriacetamide Extractant.

Liquid-liquid extraction for the removal of pertechnetate (99TcO4-) and perrhenate (ReO4-) is reported based on using the tripodal extractant N,N,N',N',N″,N″-hexa-n-octylnitrilotriacetamide (HONTA) composed of three amide groups and a tertiary amine. The extraction behaviors were compared with those using alkyldiamideamines (ADAAM(Oct) and ADAAM(EH)), and the commercial amine-type extractant, trioctylamine (TOA). HONTA quantitatively extracted 99TcO4- and ReO4- in the pH range from 1.0 to 2.5 by the co-extraction of protons. The extraction performance of the extractants was improved in the order of HONTA > ADAAM(Oct) > ADAAM(EH) > TOA. 99TcO4- and ReO4- in the extracting phase were successfully stripped using neutral aqueous solutions as the receiving phase, and the extraction ability of HONTA was maintained after five repeated uses.

Speciation and structural study of U(IV) and -(VI) in perchloric and nitric acid solutions.

In order to elucidate the uranium solution chemistry at the high HNO(3) concentrations typically employed for the reprocessing of spent nuclear fuels, speciation and complex structures of U(IV) and U(VI) are studied in aqueous HNO(3) solutions, as well as in HClO(4) solutions, by means of UV-visible-near-infrared and X-ray absorption spectroscopies and density functional theory calculations. In 1.0 M HClO(4), U(IV) exists as a spherical cation of U(4+), which is surrounded by 9-10 water molecules in the primary coordination sphere, while it forms a colloidal hydrous oxide, U(IV)O(2) x nH(2)O, at a lower acidic concentration of 0.1 M HClO(4). U(VI) exists as a transdioxo uranyl cation, UO(2)(2+), and forms a 5-fold pure hydrate complex of [U(VI)O(2)(H(2)O)(5)](2+) in 1.0 M HClO(4). With increasing HNO(3) concentration, the water molecules of the U(IV) and U(VI) hydrate complexes are successively replaced by planar bidentate coordinating nitrate ions (NO(3)(-)), forming dominant species of [U(IV)(H(2)O)(x)(NO(3))(5)](-) in 9.0 M HNO(3) and [U(VI)O(2)(NO(3))(3)](-) in 14.5 M HNO(3), respectively. The present multitechnique approach also suggests the formation of two intermediate U(VI) species, a 5-fold mononitrato complex ([U(VI)O(2)(H(2)O)(3)(eta(2)-NO(3))](+)) and a 6-fold dinitrato complex ([U(VI)O(2)(H(2)O)(2)(eta(2)-NO(3))(2)](0)), involving an increase in the total coordination number on the uranyl(VI) equatorial plane from 5 to 6 with increasing HNO(3) concentration. The presence of unidentate coordinate nitrato complexes or tetranitrato U(VI) complexes is less probable in the present HNO(3) system.

Neptunium carbonato complexes in aqueous solution: an electrochemical, spectroscopic, and quantum chemical study.

The electrochemical behavior and complex structure of Np carbonato complexes, which are of major concern for the geological disposal of radioactive wastes, have been investigated in aqueous Na(2)CO(3) and Na(2)CO(3)/NaOH solutions at different oxidation states by using cyclic voltammetry, X-ray absorption spectroscopy, and density functional theory calculations. The end-member complexes of penta- and hexavalent Np in 1.5 M Na(2)CO(3) with pH = 11.7 have been determined as a transdioxo neptunyl tricarbonato complex, [NpO(2)(CO(3))(3)](n-) (n = 5 for Np(V), and 4 for Np(VI)). Hence, the electrochemical reaction of the Np(V/VI) redox couple merely results in the shortening/lengthening of bond distances mainly because of the change of the cationic charge of Np, without any structural rearrangement. This explains the observed reversible-like feature on their cyclic voltammograms. In contrast, the electrochemical oxidation of Np(V) in a highly basic carbonate solution of 2.0 M Na(2)CO(3)/1.0 M NaOH (pH > 13) yielded a stable heptavalent Np complex of [Np(VII)O(4)(OH)(2)](3-), indicating that the oxidation reaction from Np(V) to Np(VII) in the carbonate solution involves a drastic structural rearrangement from the transdioxo configuration to a square-planar-tetraoxo configuration, as well as exchanging the coordinating anions from carbonate ions (CO(3)(2-)) to hydroxide ions (OH(-)).