Temperature Dependence of Lattice Distortion in Strongly Creep-Deformed Single Crystal Superalloy SC16

2007 ◽  
Vol 539-543 ◽  
pp. 3048-3052 ◽  
Author(s):  
G. Schumacher ◽  
N. Darowski ◽  
I. Zizak ◽  
Hellmuth Klingelhöffer ◽  
W. Chen ◽  
...  

Specimens of single crystal superalloy SC16 have been pre-deformed at 1223 K to strain of 15 % under tensile load of 150 MPa. The profiles of the 001 superlattice reflection of the γ’ precipitate phase as well as the profiles of the 002 reflections of the fcc matrix phase and of γ’-precipitate phase have been measured between RT and 1073 K by means of X-ray diffraction (XRD). From these measurements the lattice distortion of the γ’ precipitates and the lattice misfit between γ and γ’ phase have been determined as a function of temperature. The width of the 001 reflection as well as the lattice misfit decreased as a function of temperature. The results are ascribed to the anisotropic arrangement of dislocations at the γ/γ’ interfaces and to the different thermal expansion coefficients of the γ- and γ’-phase. A comparison of lattice misfit with previous measurements on moderately strained specimens suggests that the measured changes in lattice structure are predominantly created in stage I of creep-deformation.

2007 ◽  
Vol 539-543 ◽  
pp. 3059-3063 ◽  
Author(s):  
G. Schumacher ◽  
N. Darowski ◽  
I. Zizak ◽  
Hellmuth Klingelhöffer ◽  
W. Chen ◽  
...  

The profiles of 001 and 002 reflections have been measured at 1173 K as a function of time by means of X-ray diffraction (XRD) on tensile-creep deformed specimens of single crystal superalloy SC16. Decrease in line width (full width at half maximum: FWHM) by about 7 % and increase in peak position by about 3x10-4 degrees was detected after 8.5x104 s. Broadening of the 002 peak profile indicated a more negative value of the lattice misfit after the same time period. The results are discussed in the context of the anisotropic arrangement of dislocations at the γ/γ’ interfaces during creep and their rearrangement during the thermal treatment at 1173 K.


2007 ◽  
Vol 310 (2) ◽  
pp. e446-e447 ◽  
Author(s):  
S. Michimura ◽  
A. Shigekawa ◽  
F. Iga ◽  
M. Sera ◽  
T. Takabatake ◽  
...  

2012 ◽  
Vol 152-154 ◽  
pp. 634-637 ◽  
Author(s):  
Yi Ze Sun ◽  
Zi Na Zhu ◽  
Zhuo Meng ◽  
Xiao Ping Gao

In order to test whether the crystallinity and orientation of ramie fibers have changed after they are treated by the lattice distortion modification processing technology, this paper does some experiments on it. Firstly, process ramie fibers by the lattice distortion modification processing equipment. Then use X-ray diffraction method to determine the crystallinity and orientation of pristine and modified ramie fibers. Finally analyse the effect of lattice distortion modification processing on the lattice structure of ramie fiber. The experimental results show that the lattice structure of ramie fiber has changed after modification processing, with crystallinity, grain size decreasing obviously and orientation slight descent, which make ramie fibers appear softer and more puffy from macrocosmic perspective.


2014 ◽  
Vol 592 ◽  
pp. 164-169 ◽  
Author(s):  
Cheng Ai ◽  
Shusuo Li ◽  
Heng Zhang ◽  
Lei Liu ◽  
Yue Ma ◽  
...  

2000 ◽  
Vol 64 (6) ◽  
pp. 983-993 ◽  
Author(s):  
A. Pavese ◽  
R. Bocchio ◽  
G. Ivaldi

AbstractIn situ high temperature single crystal X-ray diffraction (XRD) experiments have been performed on a chemically quasi-ideal omphacite sample up to 1000°C. The lattice parameters were studied as a function of temperature, and their thermal expansion coefficients determined. The b and c cell edges show discontinuities as a function of temperature which are interpreted here in terms of intracrystalline cation diffusion processes. Structure refinements have been carried out using data collected at room temperature, at 800°C and at ambient conditions after cooling. The structural behaviour as a function of temperature of chemically quasi-ideal omphacites is compared with those of jadeite and diopside.


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