scholarly journals Technology of thermally stimulated diagnostics of anisotropy and optical axes in crystals

2020 ◽  
Vol 6 (4) ◽  
pp. 125-132
Author(s):  
Viktor M. Timokhin ◽  
Vladimir M. Garmash ◽  
Valentin A. Tedzhetov

For implementing the technology of thermally stimulated diagnostics of anisotropy and optical axes in crystals, the sample is thermostated at a temperature not exceeding the melting point, an electric field not exceeding the breakdown field is applied to the sample and polarization is produced for a time greater than the relaxation time at this temperature. After that, without switching off the electric field, the sample is cooled to the liquid nitrogen temperature, following which the field is switched off, the sample is linearly heated to a temperature above the polarization temperature and the resultant thermally stimulated depolarization (TSD) spectra taken along and perpendicular to the optical axis of the crystal are examined. When comparing the spectra the presence of anisotropy is detected and the direction of the optical axes is determined from the magnitude and presence of the TSD maxima.

Author(s):  
V. M. Timokhin ◽  
V. M. Garmash ◽  
V. A. Tedzhetov

To implement the technology of thermally stimulated diagnostics of anisotropy and optical axes of crystals, the sample is thermostated at a temperature not exceeding the melting point, an electric field not exceeding the breakdown field is applied to the sample, polarization is produced for a time greater than the relaxation time at this temperature. After that, without disconnecting the electric field, cooling to the temperature of liquid nitrogen is performed, then the field is switched off, the sample is linearly heated to a temperature above the polarization temperature and the obtained thermally stimulated depolarization (TSD) spectra taken along and perpendicular to the optical axis of the sixth order C6 crystal are examined. When comparing the obtained spectra, the presence of anisotropy is determined, and the exact direction of the optical axes is determined by the magnitude and presence of the TSD maxima.


2003 ◽  
Vol 386 ◽  
pp. 206-210 ◽  
Author(s):  
X.F. Sun ◽  
X. Chen ◽  
L. Zhang ◽  
A. Narlikar ◽  
H. Zhang

2001 ◽  
Vol 44 (2) ◽  
Author(s):  
C. Anastasiadis ◽  
D. Triantis ◽  
F. Vallianatos ◽  
G. Nover ◽  
C. Nomicos

The technique of thermally stimulated depolarization currents (TSDC) was applied to fine grained amphibolite rock samples extracted from KTB drilling. Each sample was cooled down to liquid nitrogen temperature and consequently heated at a constant rate b = 4 K/min while at the same time it was shorted by a sensitive electrometer. Thermocurrent glow curves were detected in the range from 180 to 360 K. By applying the TSDC method, an effort was made to carry out a preliminary analysis of the TSDC spectrum.


Author(s):  
Claude Lechene

Electron probe microanalysis of frozen hydrated kidneysThe goal of the method is to measure on the same preparation the chemical elemental content of the renal luminal tubular fluid and of the surrounding renal tubular cells. The following method has been developed. Rat kidneys are quenched in solid nitrogen. They are trimmed under liquid nitrogen and mounted in a copper holder using a conductive medium. Under liquid nitrogen, a flat surface is exposed by sawing with a diamond saw blade at constant speed and constant pressure using a custom-built cryosaw. Transfer into the electron probe column (Cameca, MBX) is made using a simple transfer device maintaining the sample under liquid nitrogen in an interlock chamber mounted on the electron probe column. After the liquid nitrogen is evaporated by creating a vacuum, the sample is pushed into the special stage of the instrument. The sample is maintained at close to liquid nitrogen temperature by circulation of liquid nitrogen in the special stage.


Author(s):  
O. T. Inal ◽  
L. E. Murr

When sharp metal filaments of W, Fe, Nb or Ta are observed in the field-ion microscope (FIM), their appearance is differentiated primarily by variations in regional brightness. This regional brightness, particularly prominent at liquid nitrogen temperature has been attributed in the main to chemical specificity which manifests itself in a paricular array of surface-atom electron-orbital configurations.Recently, anomalous image brightness and streaks in both fcc and bee materials observed in the FIM have been shown to be the result of surface asperities and related topographic features which arise by the unsystematic etching of the emission-tip end forms.


Author(s):  
T. G. Naymik

Three techniques were incorporated for drying clay-rich specimens: air-drying, freeze-drying and critical point drying. In air-drying, the specimens were set out for several days to dry or were placed in an oven (80°F) for several hours. The freeze-dried specimens were frozen by immersion in liquid nitrogen or in isopentane at near liquid nitrogen temperature and then were immediately placed in the freeze-dry vacuum chamber. The critical point specimens were molded in agar immediately after sampling. When the agar had set up the dehydration series, water-alcohol-amyl acetate-CO2 was carried out. The objectives were to compare the fabric plasmas (clays and precipitates), fabricskeletons (quartz grains) and the relationship between them for each drying technique. The three drying methods are not only applicable to the study of treated soils, but can be incorporated into all SEM clay soil studies.


Author(s):  
M.K. Lamvik ◽  
D.A. Kopf ◽  
S.D. Davilla ◽  
J.D. Robertson

Last year we reported1 that there is a striking reduction in the rate of mass loss when a specimen is observed at liquid helium temperature. It is important to determine whether liquid helium temperature is significantly better than liquid nitrogen temperature. This requires a good understanding of mass loss effects in cold stages around 100K.


1997 ◽  
Vol 117 (11) ◽  
pp. 1109-1114
Author(s):  
Yoshiyuki Suda ◽  
Kenji Mutoh ◽  
Yosuke Sakai ◽  
Kiyotaka Matsuura ◽  
Norio Homma

Sign in / Sign up

Export Citation Format

Share Document