Advances in X-Ray Analysis 1991
DOI: 10.1007/978-1-4615-3744-1_53
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The Substructure of Austenite and Martensite through a Carburized Surface

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Cited by 11 publications
(12 citation statements)
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“…Generally the X-ray diffraction peak broadening is due to the instrumental broadening, increase in crystallite size and lattice strain due to dislocation [23]. To decouple these contributions, it is necessary to collect a diffraction pattern of a standard material such as silicon to determine the instrumental broadening [24].…”
Section: Determination Of Crystallite Size By Scherrer Analysismentioning
confidence: 99%
“…Generally the X-ray diffraction peak broadening is due to the instrumental broadening, increase in crystallite size and lattice strain due to dislocation [23]. To decouple these contributions, it is necessary to collect a diffraction pattern of a standard material such as silicon to determine the instrumental broadening [24].…”
Section: Determination Of Crystallite Size By Scherrer Analysismentioning
confidence: 99%
“…Also X-ray peak intensities decreased while background increased, with increasing ion fluence. We believe this is due to an accumulation of lattice defects produced during irradiation as suggested by Makinson et al [30] in their study of defects in nanocrystalline materials. tion.…”
Section: Resultsmentioning
confidence: 86%
“…It shows a shift in the peak position toward the higher angle side and this may be due to because of the following reasons: the internal stress/strain of the material, doping of lower ionic radii into the host lattice, and stacking fault of doping in the host lattice [23]. in that region.…”
Section: Resultsmentioning
confidence: 93%