Growth, characterization and estimation of lattice strain and size in CdS nanoparticles: X-ray peak profile analysis

2017 ◽  
Vol 92 (5) ◽  
pp. 595-603 ◽  
Author(s):  
Rekha Garg Solanki ◽  
Poolla Rajaram ◽  
P K Bajpai
1992 ◽  
Vol 36 ◽  
pp. 595-601
Author(s):  
P. Newcomer ◽  
B. Morosin ◽  
R. A. Graham

AbstractX-ray diffraction line-profile analysis on tetragonal forms of SnO2 (cassiterite), MnO2 (pyrolusite), and previously studied TiO2 (rutile), which were subjected to high pressure shock loading, show that residual lattice strain and coherent “crystal” size are a function of shock parameters. An interesting observation on a sample of MnO2 concerns the recovery of cubic Mn2O3 (bixbyite) in the material subjected to 22 GPa, indicating a shock-induced chemical synthesis.


1993 ◽  
Vol 37 ◽  
pp. 351-358
Author(s):  
Zenjxo Yajima ◽  
Ken-ichi Ishikawa ◽  
Toshihiko Sasaki ◽  
Yukio Hirose

X-ray line broadening is caused by variations in lattice strain and small particle size. When hydrogen is introduced into the steel by the electrolytica! method, structural changes are observed. X-ray line broadening is a suitable measurement in such cases. The Warren and Averbach Fourier analysis is a good method for line broadening studies. In this method, strain and particle size effects can be separated because broadening due to particle size is independent of order of the diffraction peaks, while broadening due to strain is not.


1970 ◽  
Vol 14 ◽  
pp. 408-432
Author(s):  
M. A. Clegg ◽  
J. A. Lund

AbstractA refined x-ray line profile analysis was used to determine the lattice strain distribution and crystallite domain size in nickel and a series of alloys, Ni-Cr, Ni-ThO2 and Ni-Cr-ThO2 in a wide range of thermo-mechanical conditions. Corrections were made for instrumental broadening and doublet broadening according to Stokes and Rachinger respectively, for errors due to the “hook effect”, for terminal errors in the series arising from Instability of the components, and for the presence of stacking faults and twins on the basis of peak shift and asymmetry. The internal consistency of the x-ray data was reviewed critically and good agreement was found. The values of lattice strain and domain size were used to evaluate the presence of a dislocation substructure and the degree of polygonization of the subgraln boundaries.It was concluded that the thoria-free materials developed much higher lattice strains during cold rolling than did the Ni-ThO2, due it is thought to the operation of multiple slip in the latter. The Ni-Cr-ThO2 also developed high lattice strains during cold rolling, similar to those of the thoria-free lattices, and this was explained by the influence of chromium on cross-slip. It was postulated that the regions of high lattice strain act as driving forces in the process of recrystallization and promote grain growth during heat treatment following cold rolling.The x-ray results were correlated with transmission electron microscopy and tensile data in a parallel study in which models for room temperature and high temperature strengthening were proposed.


2017 ◽  
Vol 4 (8) ◽  
pp. 9237-9245 ◽  
Author(s):  
M. Vishnu Chittan ◽  
C. Mani Kumar ◽  
K. Sowjanya ◽  
B. Rajesh Kumar

2004 ◽  
Vol 837 ◽  
Author(s):  
Yumiko Nakamura ◽  
Robert C. Bowman ◽  
Etsuo Akiba

ABSTRACTWe have studied structural change and lattice strain formation during absorption and desorption of hydrogen (deuterium) by high purity LaNi5-x Snx alloys (x = 0.22, 0.25) using in situ X-ray and neutron diffraction along with simultaneously measuring the P-C isotherms. From profile analysis of the X-ray diffraction data, lattice parameter and lattice strain in each hydriding state are evaluated. In situ neutron diffraction data provided hydrogen occupation changing with hydrogen content. Significant lattice contract and strain formation were observed in the hydride phase in desorption. This behavior was related with decrease in hydrogen occupation in the hydride phase revealed from the neutron diffraction data.


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