Diffusion bonding in the solid state between the zirconium alloy (Zircaloy-4) and AISI 304L stainless steel (304L SS) was studied at a temperature of 1,050 C under a dynamic pressure in a controlled atmosphere. We discussed the morphology of the interface formed by determining the distribution of the various chemical constituents as well as the location and the identification of the different phases nature formed through due to chemical exchange reactions that occurred by diffusion through the interface. Observations and chemical analysis were performed by environmental scanning electron microscope (ESEM), energy dispersive X-ray spectroscopy (EDS), and X-ray diffraction (XRD). The junction is composed of three distinct zones formed of a solid solution (FeCr)a rich in Cr as a homogeneous edging from steel side. The type phase Zr(Fe,Cr) 2 occupies the Zone II and phase Zr 2 (Fe,Ni) Zone III between them settled the eutectic Zr a -Zr(Fe,Cr) 2 . . The observations and analysis of the fracture surfaces obtained by impact testing showed a morphology of a brittle fracture by cleavage which is located at the interface. The microhardness filiation at the interface of both materials diffusion bonded is very heterogeneous.
New nuclear glass-ceramics are extensively studied for the radioactive waste
confinement, due to the double confinement conferred by the glass-ceramics.
In this study, a glass-ceramic constituted by an aluminosilicate glass in the
system: SiO2-Al2O3-CaO-MgOZrO2-TiO2, containing 2wt.% of
Ca0.83Ce0.17ZrTi1.66Al0.34O7 zirconolite, has been synthesized by the
discontinuous method. Cerium, an actinide surrogate is introduced both in the
glass and ceramic phases. The synthesis is performed by a double melting at
1350?C, followed by a nucleation at 564?C, during 2 h, and a crystal growth
at 1010?C during 3 h. Then effect of Ca/Mg ratio on the distribution of the
crystalline network in the material was studied for Ca / Mg ratios ranging
from 0.4 to 5.5. For the whole of the materials, Archimedes density is about
2.80 g/cm3. X-ray diffraction (XRD) analysis shows that the increase of Ca/Mg
ratio leads to the increase of aluminosilicated crystalline phases with high
Ca contents; the materials molar volumes remaining constant. The zirconolite
phase is not affected by these additive aluminosilicated phases. The scanning
electron microscopy analysis (SEM) coupled with energy dispersive X-ray (EDX)
analysis confirmed these results; and shows the uniformity of distribution of
the ceramics in the bulk of the materials.
This study focused on the effect of TiO 2 addition on the crystallines phases’ formation, structure and chemical durability of a nuclear glass ceramic constituted by an aluminosilicate glass in the system: SiO2-Al2O3-CaO-MgO-ZrO2-TiO2 . The materials with four contents of TiO2 , ranging from 4.11 to 7.11 wt.%, are synthesized by a discontinuous method,. For the whole of materials, X-ray diffraction analysis allow identifying an aluminosilicate belonging to pyroxenes silicates family as a main phase, powelite and calzirtite. Both SEM and DTAanalyses confirmed these results. The materials FTIR analysis reveals the glass ceramics complex chemical composition. MCC1 and MCC2 tests, performed on selected glass ceramic materials, indicate that the materials with 4.11 and 5.11 wt.% TiO2 are the most durable against Si, Al, Mg and Ce elements release, in MCC2 test; The results make conclusions valuable on the selection of such glass ceramics as candidate for the disposal of high-level waste.
AbstractPerovskite is able to sequester simultaneously, in its structure, both actinides and alkaline-earth elements. This study is an attempt to synthesize a complex perovskite Ca0.91-xCe0.09Rb0.04Csx[(Zr0.50Ti0.45)Al0.05]O3 (0.2≤x≤0.4), doped in the same time, with Ce, Cs and Rb. The synthesis is conducted by sintering at 1150°C during 16h. XRX analysis confirms the perovskite formation. SEM observations show a less porous microstructure. FTIR analysis reveals TiO6, Ti-O-Ti, Ti-O and Zr-O vibrations. Raman spectroscopy indicates many orthorhombic perovskite active modes, as: Ti-O6 and Ti-O3 torsions, ZrO7, CaO8 vibrations, the totally symmetric oxygen, and the O-octahedron cage rotation.
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