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The preparation of synthetic (Zr,U)SiO 4 solid solution is challenging, as the conventional high-temperature solid-state method limits the solubility of uranium (4 ± 1 mol%) in the orthosilicate phase due to its thermodynamic instability. However, these compounds are of great interest as a result of (Zr,U)SiO 4 solid solutions, with uranium contents exceeding this concentration, being observed as corium phases formed during nuclear accidents. It has been identified that hydrothermal synthesis pathways can be used for the formation of the metastable phase, such as USiO 4 . The investigation carried out in this study has indeed led to the confirmation of metastable (Zr,U)SiO 4 compounds with high uranium contents being formed. It was found that (Zr,U)SiO 4 forms a close-to-ideal solid solution with uranium loading of up to 60 mol% by means of hydrothermal treatment for 7 days at 250 °C, at pH = 3 and starting from an equimolar reactant concentration equal to 0.2 mol L -1 . A purification procedure was developed to obtain pure silicate compounds. After purification, these compounds were found to be stable up to 1000 °C under an inert atmosphere (argon). The characterisation methods used to explore the synthesis and thermal stability included powder X-ray diffraction (PXRD), Fourier transform infrared (FTIR) and Raman spectroscopies, scanning electron microscopy (SEM) and thermogravimetric analysis (TGA).

The FurnaSEM microfurnace was installed in the chamber of a scanning electron microscope to carry out in situ experiments at high temperatures and test its limits. The microfurnace was used in combination with different types of detectors (Everhart-Thornley for the collection of secondary electrons in a high vacuum, gas secondary electron detector for the specific collection of secondary electrons in the presence of gas, and Karmen© detector for the collection of backscattered electrons at high temperature). Experiments carried out on various samples (metal alloys and ceramics) show that the microfurnace operates in both high-vacuum and low-vacuum modes. Temperature ramp rates during temperature cycles applied to the sample range from 1 to 120 °C/min (temperature rise) and 1 to 480 °C/min (controlled and natural cooling). The maximum temperature at which images were recorded up to 25 k × magnification was 1340 °C, with a residual air atmosphere of 120 Pa. The choice of a flat furnace with the sample placed directly above it has enabled innovative experiments to be carried out, such as low-voltage imaging (using a shorter working distance-up to 10 mm-than is possible with conventional furnaces), 3D imaging (by tilting the stage by up to 10°), and high-temperature backscattered electron imaging (using a dedicated detector)., (© 2024 Author(s). Published under an exclusive license by AIP Publishing.)

When conducting in situ experiments at high temperatures in a scanning electron microscope using microfurnaces, controlling the temperature of a sample of a few mm3 placed in the hot zone of the furnace can be a complex task. In most cases, the temperature of the sample is estimated by means of a thermocouple placed in the hot body of the furnace, and the assumption made is that the temperature of the furnace is the temperature of the sample. In this work, a detailed understanding of the thermal response of the sample placed in the hot zone of the furnace is proposed. Temperature differences due to contact resistance between the furnace surface and the sample, the nature of the sample, and the sample geometry are calculated with a numerical model and measured experimentally on a dedicated test bench. Three technical solutions (bonding, sandwiching, and mini-crucible) for limiting temperature differences between the furnace surface and sample are proposed and validated by numerical calculations and experimental measurements., (© 2024 Author(s). Published under an exclusive license by AIP Publishing.)

The development of a new heating system dedicated to in situ scanning electron microscope (SEM) experimentation at high temperatures is reported. This system, called FurnaSEM, is a compact microfurnace, enabling heat treatments up to 1300 °C. The choice of materials for the microfurnace is explained. The design of the microfurnace is optimized by iterations of numerical simulations, and the thermal characteristics of the microfurnace are calculated numerically. The numerical results obtained are compared with the thermal characteristics of a manufactured microfurnace, measured on a specially developed dedicated test bench. This test bench includes a working chamber simulating a SEM chamber equipped with a thermal camera. The results obtained during various qualification tests enabled us to determine the main technical characteristics of the FurnaSEM microfurnace: temperature profiles on the sample support surface, energy consumption at high temperatures, and the range of achievable thermal cycles., (© 2024 Author(s). Published under an exclusive license by AIP Publishing.)

Bauxite residues (BRs) are highly alkaline wastes generated during alumina production from bauxite ore. Billions of tons have been accumulating worldwide for more than 100 years, they are stored in various forms, and pose environmental and societal issues. At the same time, BRs are promising secondary sources for the production of critical metals including rare earth elements (REEs). However, knowledge on REE speciation is lacking, and is consequently an obstacle to the development of large-scale extraction process. This study analyses the influence of origin of the bauxite ore (lateritic or karstic), the storage conditions and storage time on the properties of ten BR samples, with a particular focus on the speciation of yttrium, which is used as a proxy to identify the behaviour of heavy REE. A multi-scale approach linked yttrium speciation and the origin of the bauxite ore whereas no major variation was observed as a function of storage conditions or ageing of the BRs. Yttrium is mainly found in the form of xenotime phosphate particles in BRs of lateritic origin, while in karstic BRs, the majority of yttrium is probably adsorbed or incorporated into other minerals including iron oxyhydroxide and hydroxyapatite minerals., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier B.V. All rights reserved.)

Sintering is a very important process in materials science and technological applications. Despite breakthroughs in achieving optimized piezoelectric properties, fundamentals of K 0.5 Na 0.5 NbO 3 (KNN) sintering are not yet fully understood, facing densification versus grain growth competition. At present, microscale events during KNN sintering under reducing atmospheres are real-time monitored using a High Temperature-Environmental Scanning Electron Microscope. A two contacting KNN particles model satisfying the Kingery and Berg's bulk diffusion model is reported. Dynamic events like individual grain growth and grain elimination process are explored through a postanalysis of recorded image series. The diffusion coefficient for oxygen vacancies of 10 -8 cm 2 s -1 and average boundary mobility of 10 -9 cm 4 J -1 s -1 are reported for the KNN ceramics. Moreover, the local pore shrinkage is consistent with the Kingery and François's concept of pore stability except that pore curvatures are not all concave, convex or flat due to anisotropic grain-boundary energies. The global grain growth kinetics are described using parabolic and/or cubic laws. The effect of atmospheres and microstructure evolution on the intrinsic and extrinsic contributions to the dielectric response using Rayleigh's law is also explored. These results bring a new breath for KNN sintering studies in order to adapt the sintering process., (© 2022 Wiley-VCH GmbH.)

Understanding the kinetic selectivity of carbon nanotube growth at the scale of individual nanotubes is essential for the development of high chiral selectivity growth methods. Here we demonstrate that homodyne polarization microscopy can be used for high-throughput imaging of long individual carbon nanotubes under real growth conditions (at ambient pressure, on a substrate) and with subsecond time resolution. Our in situ observations on hundreds of individual nanotubes reveal that about half of them grow at a constant rate all along their lifetime while the other half exhibits stochastic changes in growth rates and/or switches between growth, pause, and shrinkage. Statistical analysis shows that the growth rate of a given nanotube essentially varies between two values, with a similar average ratio (∼1.7) regardless of whether the rate change is accompanied by a change in chirality. These switches indicate that the nanotube edge or the catalyst nanoparticle fluctuates between different configurations during growth.

Two-grain model systems formed by ThO 2 nanospheres have been used to experimentally study for the first time the initial stage of sintering from room temperature to 1050 °C using high temperature high resolution transmission electron microscopy. In each grain, oriented attachment drove the reorganization and growth of the crystallites up to 300 °C to form a pseudo single crystal. Crystallite size kept growing up to 950 °C. At this temperature, a fast transformation probably corresponding to the elimination of stacking faults or dislocation walls led to the formation of single-crystals. The contact formed at room temperature between the two grains was stabilized during heat treatment by a slight reorientation of the crystallographic planes (T≈ 400 °C), leading the neck to be formed by numerous boundaries between the crystallites. At higher temperatures, the neck evolved and stabilized in the form of a plane of crystallographic orientation mismatch between the grains, which corresponds to the usual definition of the grain boundary. The growth of the neck by the addition of atomic columns was further observed in real time and quantified. At T = 950 °C, the evolution of the microscopic sintering parameter λ was obtained from HT-HRTEM images and indicated that the neck formation mostly proceeded through volume diffusion.

A new high-temperature detector dedicated to the collection of backscattered electrons is used in combination with heating stages up to 1050°C, in high-vacuum and low-vacuum modes in order to evaluate its possibilities through signal-to-noise ration measurements and different applications. Four examples of material transformations occurring at high temperature are herein reported: grain growth during annealing of a rolled platinum foil, recrystallisation of a multiphased alloy, oxidation of a Ni-based alloy and complex phase transformations occurring during the annealing of an Al-Si coated boron steel. The detector could be potentially adapted to any type of SEM and it offers good opportunities to perform high-temperature experiments in various atmospheres., (© 2020 Royal Microscopical Society.)

Electron energy-loss spectroscopy was used to characterize the boron profile and its coordination (B III and B IV ), along the complex alteration layer of glass samples altered for 511 days at 50 °C in solution containing FeCl 2 , MgCl 2 and/or CaCl 2 . To reach this goal, the impact of both TEM operating conditions and sample preparation on the determination of the boron coordination was first studied using mineralogical and pristine glasses reference samples. Then, the boron concentration profiles were characterized in the glass alteration layer. These profiles were found to be S-shaped with a thickness around forty nanometers. The proportion of B III was found to decrease with the boron total concentration (from the pristine glass to the gel layer), which suggests a higher bonding strength for B IV bonds than that of B III bonds under the alteration conditions. These findings are of tremendous interest to advance further in the understanding of glass alteration mechanisms., (Copyright © 2020 Elsevier Ltd. All rights reserved.)

Most of the highly radioactive spent nuclear fuel (SNF) around the world is destined for final disposal in deep-mined geological repositories. At the end of the fuel's useful life in a reactor, about 96% of the SNF is still UO 2 . Thus, the behaviour of UO 2 in SNF must be understood and evaluated under the weathering conditions of geologic disposal, which extend to periods of hundreds of thousands of years. There is ample evidence from nature that many uranium deposits have experienced conditions for which the formation of coffinite, USiO 4 , has been favoured over uraninite, UO 2+x , during subsequent alteration events. Thus, coffinite is an important alteration product of the UO 2 in SNF. Here, we present the first evidence of the formation of coffinite on the surface of UO 2 at the time scale of laboratory experiments in a solution saturated with respect to amorphous silica at pH = 9, room temperature and under anoxic conditions.

The thermal decomposition of actinide oxalates is greatly dependent on the oxidation state of the cation, the gas involved, and the physical characteristics of the precursor. In the actinides series, uranium(IV) oxalate U(C 2 O 4 ) 2 ·6H 2 O can be viewed as a peculiar case, as its sensibility toward oxidation leads to a specific series of reactions when heating under an oxygen atmosphere. In order to clarify the disagreements existing in the literature, particularly concerning potential carbonate intermediates and the possible transitory existence of UO 3 , we show here an extended characterization of the different intermediates through a combination of X-ray diffraction, vibrational spectroscopies and X-ray absorption near-edge spectroscopy. In this frame, uranium oxidation was found to occur at low temperature (200 °C) concomitantly to the onset of oxalate groups decomposition, leading to an amorphous oxo-oxalato compound. Pursuing the thermal conversion up to 350 °C led to complete oxidation of U(IV) into U(VI), then to the formation of amorphous UO 3 still bearing adsorbed carbonates. The first pure oxide formed during the thermal conversion was further identified to substoichiometric UO 3-δ after heating at 550 °C. Finally, U 3 O 8 was obtained as the final stable phase after heating above 660 °C. The mechanism of thermal conversion of uranium(IV) oxalate into oxide under oxygen is then driven by a complex interplay between redox reactions and decomposition of the organic fractions. Such chemical reactions were also found to significantly modify the morphology of the powder through high-temperature environmental scanning electron microscopy observations: decomposition led to a 20% reduction in the size of the aggregates, while uranium oxidation clearly promoted growth within the agglomerates.

High-temperature scanning electron microscopy allows the direct study of the temperature behavior of materials. Using a newly developed heating stage, tilted images series were recorded at high temperature and 3D images of the sample surface were reconstructed. By combining 3D images recorded at different temperatures, the variations of material roughness can be accurately described and associated with local changes in the topography of the sample surface.

Nanoparticles are defined as elementary particles with a size between 1 and 100 nm for at least 50% (in number). They can be made from natural materials, or manufactured. Due to their small sizes, novel toxicological issues are raised and thus determining the accurate size of these nanoparticles is a major challenge. In this study, we performed an intercomparison experiment with the goal to measure sizes of several nanoparticles, in a first step, calibrated beads and monodispersed SiO₂ Ludox®, and, in a second step, nanoparticles (NPs) of toxicological interest, such as Silver NM-300 K and PVP-coated Ag NPs, Titanium dioxide A12, P25(Degussa), and E171(A), using commonly available laboratory techniques such as transmission electron microscopy, scanning electron microscopy, small-angle X-ray scattering, dynamic light scattering, wet scanning transmission electron microscopy (and its dry state, STEM) and atomic force microscopy. With monomodal distributed NPs (polystyrene beads and SiO₂ Ludox®), all tested techniques provide a global size value amplitude within 25% from each other, whereas on multimodal distributed NPs (Ag and TiO₂) the inter-technique variation in size values reaches 300%. Our results highlight several pitfalls of NP size measurements such as operational aspects, which are unexpected consequences in the choice of experimental protocols. It reinforces the idea that averaging the NP size from different biophysical techniques (and experimental protocols) is more robust than focusing on repetitions of a single technique. Besides, when characterizing a heterogeneous NP in size, a size distribution is more informative than a simple average value. This work emphasizes the need for nanotoxicologists (and regulatory agencies) to test a large panel of different techniques before making a choice for the most appropriate technique(s)/protocol(s) to characterize a peculiar NP.

This manuscript describes the original structuring of Mg materials under ultrasound irradiation in mild conditions. Golf ball like extended structures can be prepared in dilute oxalic solutions at 20°C under high frequency ultrasound (200kHz). An original approach carried out through iterative 3D reconstruction of sonicated surfaces is used to describe surface evolutions and characterize the formed microstructures. A combination of SEM, ICP-AES, contact-angle measurements, and 3D image analyses allows to characterize the roughness and mass loss evolutions, and investigate the mechanism of formation for such architectures. A screening of the sonication experiments clearly points out an ultrasound frequency dependency for the effects generated at the surface. 200kHz sonication in 0.01M oxalic acid provides an unprecedented manufacturing of Mg samples which result from a controlled and localized dissolution of the material and characterized by a strong wetting surface with a roughness of 170nm. The additional formation of newly formed secondary phases appearing with surface dissolution progress is also deciphered. More generally, the ultrasonic procedure used to prepare these engineered surfaces opens new alternatives for the nano- and micro-structuring of metallic materials which may exhibit advanced physical and chemical properties of potential interest for a large community., (Copyright © 2017 Elsevier B.V. All rights reserved.)

Monitoring individual single-walled carbon nanotubes (SWCNTs) during their growth is a highly sought-after goal in view of understanding the processes involved in the nucleation, elongation and termination which ultimately control the diameter and chiral selectivity. Here, we report on the first truly in situ observations of SWCNT growth in an environmental scanning electron microscope (ESEM). The CNT growth from lithographically patterned catalysts was investigated as a function of the catalyst type (Fe, Co or Ni), temperature, type of precursor (ethanol or acetylene), gas phase composition and pressure, and pretreatment conditions, and we report on the most appropriate conditions for SWCNT growth in ESEM conditions. We show that this approach allows the observation at the submicron scale of the different steps of the nanotube synthesis including the catalyst reduction, the growth and percolation of the nanotube network, and the deposition of individual nanotubes grown in the gas phase on the substrate. Despite these obvious advantages, we identified a few limitations which will need to be tackled for fully taking advantage of the approach, for instance for monitoring the growth of individual SWCNTs by ESEM, including the short lifetime of the catalyst nanoparticles, the preference for kite growth (by opposition to surface growth) and the influence of the electron beam on the nanotube growth.

Glass thin films (with nanometer to micrometer thicknesses) are promising in numerous applications, both as passive coatings and as active components. Self-healing is a feature of many current technological developments as a means of increasing the lifetime of materials. In the context of these developments, we report on the elaboration of the first self-healing glassy thin-film coating developed specifically for high-temperature applications. This coating is obtained by pulsed laser deposition of alternating layers of vanadium boride (VB) and a multicomponent oxide glass. Self-healing is obtained through the oxidation of VB at the operating temperature. The investigation of the effect of elaboration parameters on the coating composition and morphology made it possible to obtain up to seven-layer coatings, with good homogeneity and perfect interfaces, and with a total thickness of less than 1 μm. The autonomic self-healing capacity of the coating has been demonstrated by an in situ experiment, which shows that a crack of nanometric dimension can be healed within a few minutes at 700 °C.

We have developed two integrated thermocouple (TC) crucible systems that allow precise measurement of sample temperature when using a furnace associated with an environmental scanning electron microscope (ESEM). Sample temperatures measured with these systems are precise (±5°C) and reliable. The TC crucible systems allow working with solids and liquids (silicate melts or ionic liquids), independent of the gas composition and pressure. These sample holder designs will allow end users to perform experiments at high temperature in the ESEM chamber with high precision control of the sample temperature.

We report the design of new catanionic vesicles decorated with iron oxide nanoparticles, which could be used as a model system to illustrate controlled delivery of small solutes under mild hyperthermia. Efficient release of fluorescent dye rhodamine 6G was observed when samples were exposed to an oscillating magnetic field. Our system provides direct evidence for reversible permeability upon magnetic stimulation.

Self-assembly of neodymium nitrate and 2,5-dihydroxyl-1,4-benzoquinone (DHBQ) leads to the formation of a metal organic framework (MOF) of formula [Nd2(DHBQ)3(H2O)6]·18H2O. X-ray diffraction studies show that its crystalline structure is that of a two-dimensional coordination polymer packed in parallel sheets, with organised clusters of water molecules lying between the sheets and bridging them via a dense H-bond network. However, instead of forming faceted crystals, this MOF assembles into unusually shaped cylindrical particles of micrometre size. Scanning electron microscopy revealed that the particles are indeed mesoparticles from aggregated MOF crystalline nano-grains. The mesoparticles are stimuli-responsive and shrink in size upon exposure to reduced water vapour pressure. The shrinkage is isotropic and depends on temperature, which allows measuring the coexistence curve of water inside the particles and in the gas phase. Owing to an elaborated environmental scanning-electron microscopy (ESEM) study, it was possible to determine the association energy of water in the mesoparticles. We found a value of 16 ± 6.5 kJ mol(-1). Since the only water present in the particles is the lattice water in the nano-grains, this association energy is the lattice energy of water in the nano-sized MOF crystals. This value allowed us to draw a model for the building process of these originally shaped cylindrical mesoparticles. This is the first example of determination of a thermodynamic value by ESEM.

Ruthenium, a fission product arising from the reprocessing of spent uranium oxide (UOX) fuel, crystallizes in the form of acicular RuO(2) particles in high-level waste containment glass matrices. These particles are responsible for significant modifications in the physicochemical behavior of the glass in the liquid state, and their formation mechanisms are a subject of investigation. The chemical reactions responsible for the crystallization of RuO(2) particles with acicular or polyhedral shape in simplified radioactive waste containment glass are described. In situ high-temperature environmental scanning electron microscopy (ESEM) is used to follow changes in morphology and composition of the ruthenium compounds formed by reactions at high temperature between a simplified RuO(2)-NaNO(3) precursor and a sodium borosilicate glass (SiO(2)-B(2)O(3)-Na(2)O). The key parameter in the formation of acicular or polyhedral RuO(2) crystals is the chemistry of the ruthenium compound under oxidized conditions (Ru(IV), Ru(V)). The precipitation of needle-shaped RuO(2) crystals in the melt might be associated with the formation of an intermediate Ru compound (Na(3)Ru(V)O(4)) before dissolution in the melt, allowing Ru concentration gradients. The formation of polyhedral crystals is the result of the direct incorporation of RuO(2) crystals in the melt followed by an Ostwald ripening mechanism., (© 2012 American Chemical Society)

To underline the potential links between the crystallization state and the microstructure of powdered cerium-neodymium oxides and their chemical durability, several Ce(IV)(1-x)Nd(III)(x)O(2-x/2) mixed dioxides were prepared in various operating conditions from oxalate precursors and then leached. The powdered samples were first examined through several physicochemical properties (crystallization state and associated crystallite size, reactive surface area, porosity...). The dependence of the normalized dissolution rates on various parameters (including temperature, nitric acid concentration, crystallization state) was examined for pure CeO(2) and Ce(1-x)Nd(x)O(2-x/2) solid solutions (with x = 0.09 and 0.16). For CeO(2), either the partial order related to the proton activity (n = 0.63) or the activation energy (E(A) = 37 kJ·mol(-1)) suggested that the dissolution was mainly driven by surface reactions occurring at the solid-liquid interface. The chemical durability of the cerium-neodymium oxides was also strongly affected by chemical composition. The initial normalized dissolution rates were also found to slightly depend on the crystallization state of the powders, suggesting the role played by the crystal defects in the dissolution mechanisms. On the contrary, the crystallite size had no important effect on the chemical durability. Finally, the normalized dissolution rates measured near the establishment of saturation conditions were less affected, which may be due to the formation of a gelatinous protective layer at the solid/liquid interface.

Several CeO(2)-based mixed oxides with general composition Ce(1-x)Ln(x)O(2-x/2) (for 0 ≤ x ≤ 1 and Ln = La, Nd, Sm, Eu, Gd, Dy, Er, or Yb) were prepared using an initial oxalic precipitation leading to a homogeneous distribution of cations in the oxides. After characterization of the Ce/Nd oxalate precursors and then thermal conversion to oxides at T = 1000 °C, investigation of the crystalline structure of these oxides was carried out by XRD and μ-Raman spectroscopy. Typical fluorite Fm ̅3m structure was obtained for relatively low Ln(III) contents, while a cubic Ia ̅3̅ superstructure was evidenced above x ≈ 0.4. Moreover, since Nd(2)O(3) does not crystallize with the Ia ̅3̅-type structure, two-phase systems composed with additional hexagonal Nd(2)O(3) were obtained for x(Nd) ≥ 0.73 in the Ce(1-x)Nd(x)O(2-x/2) series. The effect of heat treatment temperature on these limits was explored through μ-Raman spectroscopy, which allowed determining the presence of small amounts of the different crystal structures observed. In addition, the variation of the Ce(1-x)Ln(x)O(2-x/2) unit cell parameter was found to follow a quadratic relation as a result of the combination between increasing cationic radius, modifications of cation coordination, and decreasing O-O repulsion caused by oxygen vacancies., (© 2011 American Chemical Society)

It is shown that coupling nuclear magnetic resonance (NMR) 1D-imaging with the measure of NMR relaxation times and self-diffusion coefficients can be a very powerful approach to investigate fluid infiltration into porous media. Such an experimental design was used to study the very slow seeping of pure water into hydrophobic materials. We consider here three model samples of nuclear waste conditioning matrices which consist in a dispersion of NaNO(3) (highly soluble) and/or BaSO(4) (poorly soluble) salt grains embedded in a bitumen matrix. Beyond studying the moisture progression according to the sample depth, we analyze the water NMR relaxation times and self-diffusion coefficients along its 1D-concentration profile to obtain spatially resolved information on the solution properties and on the porous structure at different scales. It is also shown that, when the relaxation or self-diffusion properties are multimodal, the 1D-profile of each water population is recovered. Three main levels of information were disclosed along the depth-profiles. They concern (i) the water uptake kinetics, (ii) the salinity and the molecular dynamics of the infiltrated solutions and (iii) the microstructure of the water-filled porosities: open networks coexisting with closed pores. All these findings were fully validated and enriched by NMR cryoporometry experiments and by performing environmental scanning electronic microscopy observations. Surprisingly, results clearly show that insoluble salts enhance the water progression and thereby increase the capability of the material to uptake water., (Copyright © 2011 Elsevier Inc. All rights reserved.)

In situ high-temperature healing of cracks in composites made of glass and vanadium boride (VB) particles was observed using an environmental scanning electron microscope equipped with a high-temperature chamber (HT-ESEM). HT-ESEM is an adequate tool for studying the self-healing property of these materials. The change in crack length as a function of redox atmospheric conditions is reported. No self-healing behaviour was observed under reducing conditions, while a complete and rapid healing of the cracks was measured under oxidizing conditions. HT-ESEM image analyses enabled the monitoring of the healing effect. The self-healing mechanism was identified as a consequence of the VB active particles oxidation and subsequent pouring of fluid oxides into the cracks. These innovative composites offer an interesting potential in the domain of solid oxide fuel cell sealants.

On the basis of optimized grinding/heating cycles developed for several phosphate-based ceramics, the preparation of brabantite and then monazite/brabantite solid solutions loaded with tetravalent thorium, uranium, and cerium (as a plutonium surrogate) was examined versus the heating temperature. The chemical reactions and transformations occurring when heating the initial mixtures of AnO2/CeO2, CaHPO(4).2H2O (or CaO), and NH4H2PO4 were identified through X-ray diffraction (XRD) and thermogravimetric/differential thermal analysis experiments. The incorporation of thorium, which presents only one stabilized oxidation state, occurs at 1100 degrees C. At this temperature, all the thorium-brabantite samples appear to be pure and single phase as suggested by XRD, electron probe microanalyses, and micro-Raman spectroscopy. By the same method, tetravalent uranium can be also stabilized in uranium-brabantite, i.e., Ca0.5U0.5PO4, after heating at 1200 degrees C. Both brabantites, Ca0.5Th0.5PO4 and Ca0.5U0.5PO4, begin to decompose when increasing the temperature to 1400 and 1300 degrees C, respectively, leading to a mixture of CaO and AnO2 by the volatilization of P4O10. In contrast to the cases of thorium and uranium, cerium(IV) is not stabilized during the heating treatment at high temperature. Indeed, the formation of Ca0.5Ce0.5PO4 appears impossible, due to the partial reduction of cerium(IV) into cerium(III) above 840 degrees C. Consequently, the systems always appear polyphase, with compositions of CeIII1-2xCeIVxCaxPO4 and Ca2P2O7. The same conclusion can be also given when discussing the incorporation of cerium(IV) into La1-2xCeIIIx-yCeIVyCay(PO4)1-x+y. This incomplete incorporation of cerium(IV) confirms the results obtained when trying to stabilize tetravalent plutonium in Ca0.5PuIV0.5PO4 samples.

To study the simultaneous incorporation of both tri- and tetravalent actinides in phosphate ceramics, we prepared several beta-TUPD/monazite-based radwaste matrices through two different chemical routes (called dry and wet routes) involving the initial precipitation of crystallized precursors of each phase, i.e., TUPHPH solid solutions on the one hand, and rhabdophane (LnPO(4).xH(2)O) on the other. The final material was obtained after heating above 1000 degrees C, and no additional phase was detected from elementary analyses and XRD. Moreover, the complete segregation of tri- and tetravalent cations was evidenced when using dry chemical processes. This method also allows for the preparation of dense pellets (90% < d(exp)/d(calc) < 95%) after only 10-20 h of heat treatment at 1250 degrees C. Finally, the chemical durability of the pellets was examined through several leaching experiments in acidic media. The normalized dissolution rate determined from the uranium release in the leachate varies from (8.2 +/- 0.7) x 10(-6) to (2.7 +/- 0.4) x 10(-2) g m(-2) day(-1) between 25 and 120 degrees C in 10(-1) M HNO(3). Near equilibrium, thorium and lanthanide ions were found to quickly precipitate as phosphate-based neoformed phases in the back end of the initial dissolution process. These phases were identified as uranium-depleted T(U)PHPH and as rhabdophane or monazite.

Apatite appears a useful compound for removing lead from water, due to its ability to immobilize the metal by precipitation. In dilute solution, dissolved hydroxyapatite [HA, Ca1O(P04)6(OH)2] provided phosphates that were reactive with aqueous lead (molar ratio HA/Pb= 1/10) forming precipitates at around pH 6. These dissolved at a more acidic pH (3). Solid HA in contact with Pb2+ions, led to the formation of pyromorphite [Pblo(P04)6(OH)2], identified by X-ray diffraction and insoluble at pH tested (3-8). The amount of pyromorphite increased with the weight ratio of HA/Pb. When this one increased from 1 to 1000, lead precipitated as pyromorphite rose from 19 to 99%. In vivo experiments on rats confirmed the in vitro results. In fact, lead bioavailability assessed by intestinal perfusion was unchanged in the presence of dissolved HA, whereas it was significantly lower in the presence of solid HA, evaluated by gastric intubation, at a weight ratio equal to 10 (amount of lead absorbed decreased by 60%). Apatite could bean effective means of immobilizing lead in drinking or sewage, since accidental pyromorphite ingestion does not yield bioavailable lead.