In situ synchrotron analysis of lattice rotations in individual grains during stress-induced martensitic transformations in a polycrystalline CuAlBe shape memory alloy

Two synchrotron diffraction techniques, three-dimensional X-ray diffraction and Laue microdiffraction, are applied to studying the deformation behaviour of individual grains embedded in a Cu74Al23Be3 superelastic shape memory alloy. The average lattice rotation and the intragranular heterogeneity of orientations are measured during in situ tensile tests at room temperature for four grains of mean size 1 mm. During mechanical loading, all four grains rotate and the mean rotation angle increases with austenite deformation. As the martensitic transformation occurs, the rotation becomes more pronounced, and the grain orientation splits into several sub-domains: the austenite orientation varies on both sides of the martensite variant. The mean disorientation is 1 . Upon unloading, the sub-domains collapse and reverse rotation is observed

Full elastic strain tensor determination at the phase scale in a powder metallurgy nickel-based superalloy using X-ray Laue microdiffraction

Laue microdiffraction is used to determine the full elastic strain tensor of the γ and γ′ phases in grains of a nickel-based superalloy with a coarse-grained microstructure. A `rainbow' filter and an energy dispersive point detector are employed to measure the energy of Bragg reflections. For the two techniques, an uncertainty of ±2.5 × 10−3 Å is obtained for the undetermined crystal lattice parameter. Our measurements show that the filter method provides better confidence, energy resolution, accuracy and acquisition time. The sensitivity of each method with respect to the γ–γ′ lattice mismatch is demonstrated with measurements in samples with average precipitate sizes of 200 and 2000 nm. For the 200 nm precipitate size, the lattice mismatch is less than 2 × 10−3 Å and the dilatational strains are close to ±1.5 × 10−3 depending on the considered phase. For the 2000 nm precipitate size, the lattice mismatch is close to 8 × 10−3 Å and almost no elastic strain occurs in the microstructure

Microstructural and Chemical Changes of a Ti-Stabilized Austenitic Stainless Steel After Exposure to Liquid Sodium at Temperatures Between 500 °C and 650 °C

Ti-stabilized austenitic stainless steel was carburized in sodium containing a high carbon activity at three different temperatures, 500 °C, 600 °C, and 650 °C during 1000 hours and 5000 hours. The carbon profile, the carbide volume fraction, and the lattice parameter evolution as function of depth were determined using high-energy X-ray diffraction and electron probe microanalysis. At 650 °C and 600 °C, the carbon precipitated as M23C6 and M7C3 carbides in the sample. The volume fraction of M7C3 carbides was lower than predicted by thermodynamic equilibrium using Thermo-Calc software®. At 500 °C, carbides almost did not form in the steel. Instead, high carbon supersaturation of the austenitic matrix occurred. Both results demonstrate that the carburization profile was strongly influenced by the kinetics of carbide formation at temperatures lower than 650 °C. High-energy X-ray diffraction measurements demonstrated that the austenite and carbide lattice parameters evolved along the carbon profile. Both measured lattice parameter profiles of austenite and M23C6 carbide were compared to the ones predicted from chemical changes of austenite and carbides

Determination of residual stress gradient in a Ti-stabilized austenitic stainless steel cladding candidate after carburization in liquid sodium at 500 °C and 600 °C

Non-destructive residual stress profile measurement with a micrometric depth resolution within the depth of carburized Ti-stabilized stainless steel cladding candidate was carried out by high-energy X-ray diffraction. The samples were carburized in carburizing nuclear liquid sodium at 500 °C and 600 °C for 1000 h. The full residual stress tensor profile was determined thanks to the estimation of the strain-free lattice parameter evolution using the carbon concentration profile measured by electron probe microanalysis and thermodynamic simulation. For the sample carburized at 500 °C, the residual stress genesis was governed by the carbon concentration within the steel and the formation of expanded austenite. For the sample carburized at 600 °C, the residual stress profile in the austenitic matrix depended on the precipitation of M23C6 carbide. Stress relaxation was observed in the intragranular carburization zone. For the two temperatures, compressive residual stresses developed in the carburized zone and tensile stresses developed in the rest of the sample

In situ synchrotron analysis of lattice rotations in individual grains during stress-induced martensitic transformations in a polycrystalline CuAlBe shape memory alloy

Two synchrotron diffraction techniques, three-dimensional X-ray diffraction and Laue microdiffraction, are applied to studying the deformation behaviour of individual grains embedded in a Cu74Al23Be3 superelastic shape memory alloy. The average lattice rotation and the intragranular heterogeneity of orientations are measured during in situ tensile tests at room temperature for four grains of mean size 1 mm. During mechanical loading, all four grains rotate and the mean rotation angle increases with austenite deformation. As the martensitic transformation occurs, the rotation becomes more pronounced, and the grain orientation splits into several sub-domains: the austenite orientation varies on both sides of the martensite variant. The mean disorientation is 1 . Upon unloading, the sub-domains collapse and reverse rotation is observed

Elastic-strain distribution in metallic film-polymer substrate composites

Synchrotron x-ray radiation was used for in situ strain measurements during uniaxial tests on polymer substrates coated by a metallic gold film 400 nm thick deposited without interlayer or surface treatment. X-ray diffraction allowed capturing both components elastic strains and determining how these were partitioned between the metallic film and the polymeric substrate. For strains below 0.8%, deformation is continuous through the metal-polymer interface while above, the onset of plasticity in the metallic film induces a shift between film and substrate elastic strains

Suivi de la cinétique associée à la phase gamma' dans le superalliage N18 en utilisant des mesures de résisitivité électrique in situ

International audienceIn nickel-based superalloys, temperatures related to the formation or the dissolution of the different types of γ' precipitates are important parameters for optimizing the mechanical properties of components but also for developing models which can reproduce the kinetics of their phase transformation. We showed that the electrical resistivity variations during heat treatment of the N18 superalloy was sufficient to monitor the kinetics related to secondary and tertiary γ' precipitates. In particular, the effects of the heating rate and the initial microstructure on the dissolution kinetics of the γ' phase were investigated. Experimental results were also compared to outputs of a precipitation model developed for the N18 alloy showing that in situ electrical resistivity measurements can be used for calibration and validation purposes

X-Light: an open-source software written in Python to determine the residual stress by X-ray diffraction

X-Light is an open-source software that is written in Python with a graphical user interface. X-Light was developed to determine residual stress by X-ray diffraction. This software can process the 0D, 1D and 2D diffraction data obtained with laboratory diffractometers or synchrotron radiation. X-Light provides several options for stress analysis and five functions to fit a peak: Gauss, Lorentz, Pearson VII, pseudo-Voigt and Voigt. The residual stress is determined by the conventional sin2 method and the fundamental method

Carbon content evolution in austenite during austenitization studied by in situ synchrotron X-ray diffraction of a hypoeutectoid steel

Using in situ high energy X-ray diffraction study of austenite formation in hypoeutectoid steel with three differ- ent initial microstructures (ferrite-pearlite, tempered martensite and bainite), the lattice parameters of ferrite, cementite and austenite are examined on heating at 0.25, 10 and 100 °C/s. The lattice parameters of ferrite, cementite and austenite do not vary linearly with the temperature, especially, in the temperature range where the austenitization takes place. For the austenite, it is suggested that the deviation from the linearity is mainly associated to the carbon content variation. Using Dyson and Holmes equation, the carbon content in austenite is evaluated for any moment of the austenite formation for each initial microstructure and all heating rates. For the ferrite-pearlite microstructure heated at 0.25 °C/s, the carbon content in austenite after complete cementite dissolution corresponds to that of pearlite. Moreover, a rapid decrease in carbon content in the austenite is observed during the first stage of the austenitization (simultaneous dissolution of ferrite and cementite) followed by a slow further decrease during the transformation of the remaining ferrite. The obtained results are discussed using thermodynamic calculations

Controlled biaxial deformation of nanostructured W/Cu thin films studied by X-ray diffraction

The deformation behaviour of 150. nm thick W/Cu nanocomposite deposited on polyimide substrates has been analysed under equi-biaxial tensile testing coupled to X-ray diffraction technique. The experiments were carried out using a biaxial device that has been developed for the DiffAbs beamline of SOLEIL synchrotron source. Finite element analysis has been performed to study the strain distribution into the cruciform shape substrate and define the homogeneous deformed volume. X-ray measured elastic strains in tungsten sub-layers could be carried out for both principal directions. The strain field was determined to be almost equi-biaxial as expected and compared to finite element calculations