Is the olivine–spinel phase transformation martensitic?

Nature ◽  
1982 ◽  
Vol 298 (5872) ◽  
pp. 357-358 ◽  
Author(s):  
P. J. Vaughan ◽  
H. W. Green ◽  
R. S. Coe
RSC Advances ◽  
2016 ◽  
Vol 6 (28) ◽  
pp. 23677-23685 ◽  
Author(s):  
Wuwei Yan ◽  
Yongning Liu ◽  
Shaokun Chong ◽  
Yi-Fang Wu

The initial stepwise charging suppresses oxygen release and restrains the layered to spinel phase transformation.


2014 ◽  
Vol 733 ◽  
pp. 6-19 ◽  
Author(s):  
Prasant Kumar Nayak ◽  
Judith Grinblat ◽  
Mikhael Levi ◽  
Yan Wu ◽  
Bob Powell ◽  
...  

1987 ◽  
Vol 94 ◽  
Author(s):  
Y. Kouh Simpson ◽  
C. B. Carter

ABSTRACTThe initial stage of topotactic growth of Ni-Al spinel into Al2O3 has been examined using transmission electron microscopy. A new experimental approach to the study of solid-state reactions, which may be adapted for in-situ experiments for low-temperature systems, has been used in this study. In its present form, the technique involves heating a thin film of one oxide in the presence of a vapor of the second oxide. In the study of the growth characteristics of Ni-Al spinel phase, the orientation of the Al2O3 substrate has been found to influence greatly both the structural and morphological aspects of the spinel growth. In particular, the topotactic relationship between the spinel and the alumina are very different for (0001) and {1120} substrate orientations. The very early stage of the kinetics of the spinel growth, in which the length and the width of the spinel particles are only a few hundred angstroms, is illustrated with the results obtained from the re-heating experiments. The structure of the spinel-alumina interface has also been studied using high-resolution electron microscopy. These results are discussed in relation to the different models proposed for the spinel-alumina phase transformation.


2017 ◽  
Vol 121 (3) ◽  
pp. 1421-1430 ◽  
Author(s):  
Hanlei Zhang ◽  
Khim Karki ◽  
Yiqing Huang ◽  
M. Stanley Whittingham ◽  
Eric A. Stach ◽  
...  

1987 ◽  
Vol 92 (B7) ◽  
pp. 6207 ◽  
Author(s):  
Takehiko Yagi ◽  
Masaki Akaogi ◽  
Osamu Shimomura ◽  
Toshihiro Suzuki ◽  
Syun-Iti Akimoto

1994 ◽  
Vol 9 (10) ◽  
pp. 2627-2633 ◽  
Author(s):  
Hyun M. Jang ◽  
Byung C. Lim

Effects of the scale of precursor mixing on densification behaviors and phase-transformation kinetics of multicomponent aluminosilicate gels were examined using cordierite gels prepared by two different processing routes: a monophasic (single phase) gel having molecular homogeneity, and a triphasic gel in which constitutive precursor phases are uniformly mixed in a nanometer scale (∼50 nm). In the case of the monophasic cordierite gel, homogeneous molecular-scale mixing of precursors induces a direction formation of μ-cordierite without a preceding crystallization, and the densification stops at the onset of crystallization to μ-cordierite at 960 °C. On the other hand, the densification of triphasic cordierite gel was not affected by the crystallization of intermediate spinel phase at 700 °C. The triphasic gel continues to densify until amorphous silica matrix crystallizes to quartz at 1180 °C. The enhanced densification observed in the triphasic gel was attributed to the retarded crystallization of amorphous silica component caused by the increase in diffusion distances.


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