scholarly journals Thermally Induced Anomaly in the Shear Behavior of Magnetite at High Pressure

2018 ◽  
Vol 10 (2) ◽  
Author(s):  
Yongtao Zou ◽  
Wei Zhang ◽  
Ting Chen ◽  
Xing-ao Li ◽  
Chun-Hai Wang ◽  
...  
1996 ◽  
Vol 7 (1) ◽  
pp. 127-138 ◽  
Author(s):  
Rosa M. Ortuño ◽  
Javier Ibarzo ◽  
Jean d'Angelo ◽  
Françoise Dumas ◽  
Angel Alvarez-Larena ◽  
...  

1995 ◽  
Vol 398 ◽  
Author(s):  
L.M. Wang ◽  
W.L. Gong ◽  
R.C. Ewing ◽  
W.J. Webert

ABSTRACTThe roles of irradiation temperature and interfaces (free surfaces and grain boundaries) in irradiation- and thermally- induced amorphization of ceramics (coesite, apatite, olivines and spinels) have been studied by transmission electron microscopy (TEM). The irradiations were performed with 1.5 MeV Kr+, 200 keV and 1 MeV electrons over a wide temperature range (20-700 K). The critical amorphization dose at which amorphization is complete, Dc, increased with increasing irradiation temperature for most materials except coesite (a high pressure polymorph of Si02) which showed a decreasing Dc with increasing temperature under 1 MeV electron irradiation. Although amorphization may occur directly within a displacement cascade or by cascade overlap, this study shows that free surfaces and grain boundaries are favorable sites for nucleation of amorphous volumes. Once the amorphous volume is formed at interfaces, it may grow rapidly under continued irradiation. Coesite which has a glass transition temperature higher than its melting temperature underwent spontaneous amorphization during thermal annealing at 1200 K. This thermally-induced amorphization also started at free surface and grain boundaries and propagated into the interior of the crystal. The interface-mediated amorphization is analogous to the process of thermodynamic melting.


Author(s):  
Marek Malecki ◽  
James Pawley ◽  
Hans Ris

The ultrastructure of cells suspended in physiological fluids or cell culture media can only be studied if the living processes are stopped while the cells remain in suspension. Attachment of living cells to carrier surfaces to facilitate further processing for electron microscopy produces a rapid reorganization of cell structure eradicating most traces of the structures present when the cells were in suspension. The structure of cells in suspension can be immobilized by either chemical fixation or, much faster, by rapid freezing (cryo-immobilization). The fixation speed is particularly important in studies of cell surface reorganization over time. High pressure freezing provides conditions where specimens up to 500μm thick can be frozen in milliseconds without ice crystal damage. This volume is sufficient for cells to remain in suspension until frozen. However, special procedures are needed to assure that the unattached cells are not lost during subsequent processing for LVSEM or HVEM using freeze-substitution or freeze drying. We recently developed such a procedure.


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