No Arabic abstract
The microstructural parameters like the average domain size, effective domain size at a particular crystallographic direction and microstrain within the domains of titanium and Ti-5%Ta-2%Nb, irradiated with 116 MeV O5+ ion, have been characterized as a function of dose by X-Ray Diffraction Line Profile Analysis using different model based approaches. Dislocation Density and stacking fault probabilities have also been estimated from the analysis. The analysis revealed that there was a significant decrease of the average domain size with dose as compared to the unirradiated sample. The estimated values of dislocation density increased significantly for the irradiated samples and was found to be an order of magnitude more as compared to the unirradiated one. However, the dislocation density saturated with increase in dose. The deformation (stacking) fault probabilities were found to be negligible even with the increase in dose of irradiation.
Zirconium based alloys have been irradiated with 11 and 15 MeV proton and 116 MeV oxygen ions at different doses. The changes in the microstructure have been studied for the ion irradiated alloys as a function of dose using X-Ray Diffraction Line Profile Analysis (XRDLPA) based on the whole powder pattern fitting technique. It was observed that the microstructural parameters like domain size, microstrain within the domain, dislocation density did not change significantly with the increase in dose for proton irradiated samples. A clear change was noticed in these microstructural parameters as a function of dose for oxygen irradiated samples. There was a drastic decrease in domain size at a dose of 1x10^17 O5+/m2 but these values reached a plateau with increasing dose. The values of microstrain and dislocation density increased significantly with the dose of irradiation.
Two sets of amorphous carbon materials prepared at different routes are irradiated with swift (145 MeV) heavy ion (Ne6+). The structural parameters like the size of ordered grains along c and a axis i.e. Lc & La, the average spacing of the crystallographic planes (002) i.e. d002 and the fraction of the amorphous phase of the unirradiated and the irradiated samples are estimated by X-ray diffraction technique. The fraction of the amorphous phase is generally found to increase with the irradiation dose for both sets of the samples. The estimated and values are found to be almost unaffected by irradiation. The estimated values of corroborate with the increase of disorder in both sets of the samples with the increasing dose of irradiation. Keywords: X-ray Diffraction, Amorphous Carbon, Irradiation
In the quest of understanding significant variations in the physical, chemical and electronic properties of the novel functional materials, low temperature Synchrotron X-ray Diffraction (LT-SXRD) measurements on CTO (a type-II) and CMTO (a type-I) multiferroics are presented. Magnetic phase diagram of CTO shows multiple magnetic transitions at zero fields, whereas, in CMTO, 20 K enhancement in the antiferromagnetic transition temperature is observed followed by near room temperature Griffiths phase. Rietveld analysis on LT-SXRD data of both the samples indicates important observations. For both CTO and CMTO, the magnetic anomalies are followed by structural anomalies, which is a clear signature of spin lattice coupling and the positive shift of spin lattice coupling from CTO to CMTO.
We have investigated the plastic deformation properties of non-equiatomic single phase Zr-Nb-Ti-Ta-Hf high-entropy alloys from room temperature up to 300 {deg}C. Uniaxial deformation tests at a constant strain rate of 10$^{-4}$ s$^{-1}$ were performed including incremental tests such as stress-relaxations, strain-rate- and temperature changes in order to determine the thermodynamic activation parameters of the deformation process. The microstructure of deformed samples was characterized by transmission electron microscopy. The strength of the investigated Zr-Nb-Ti-Ta-Hf phase is not as high as the values frequently reported for high-entropy alloys in other systems. We find an activation enthalpy of about 1 eV and a stress dependent activation volume between 0.5 and 2 nm$^3$. The measurement of the activation parameters at higher temperatures is affected by structural changes evolving in the material during plastic deformation.
The mechanism of the evolution of the deformed microstructure at the earliest stage of annealing where the existence of the lowest length scale substructure paves the way to the formation of the so-called subgrains, has been studied for the first time. The study has been performed at high temperature on heavily deformed Ti-modified austenitic stainless steel using X-ray diffraction technique. Significant changes were observed in the values of the domain size, both with time and temperature. Two different types of mechanism have been proposed to be involved during the microstructural evolution at the earliest stages of annealing. The nature of the growth of domains with time at different temperatures has been modelled using these mechanisms. High-resolution transmission electron microscopy has been used to view the microstructure of the deformed and annealed sample and the results have been corroborated successfully with those found from the X-ray diffraction techniques.