Abhängigkeit des Torsionsmoduls von stahl von der Torsionsvorspannung

Ohne Zusammenfassung

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160Tb nuclear orientation in yttrium single crystal

First experimental results of¹⁶⁰Tb nuclear orientation in yttrium single crystal matrix are described. The influence of external magnetic field in combination with the crystal field interaction is discussed.     

Møller was right

Direct calculation proves that the total energy-momentum vector derived from the Møller energy-momentum complex from 1958 does not transform like a free 4-vector with respect to the Lorentz transformation. This conforms with the conclusion formulated by Møller himself, but it contradicts the result of the critical analysis of Kovacs. Defects in Kovacs argumentation are found.     

Magneto-optical effects in crystals at the normal incidence

We consider the interaction of a polarized electromagnetic wave in a magnetically ordered crystal plate surrounded by an isotropic ambient at the normal incidence. The crystalline medium of the plate is specified by the general non-symmetric permittivity tensor. The results are expressed in terms of the transmission and reflection matrices which relate the electric fields of the incident wave to those of transmitted and reflected waves. Their applications are illustrated by examples of an isotropic plate magnetized normal to the interface, a cubic crystal magnetized parallel to the interface and an orthorhombic crystal magnetized along the axis normal to the interface. The effect of the reflection from the interfaces and the interference effect are included. The paper treats the reflection at an interface between an isotropic ambient and an absorbing magnetic crystal at small non-zero angles of incidence. The general reflection matrix is applied to the determination of the magneto-optical effects quadratic in magnetization.     

Internal friction in cd+zn alloy single crystals

Internal friction measurements were used for the examination of Cd + Zn alloy single crystals. It was established that the interaction energy between solute Zn atoms and dislocations in basal planes is 0·12 eV.The authors thank Dr. P.Luká, CSc., for valuable discussions.     

The temperature vibrations of urea molecules

The structural and dynamic parameters of urea at 112°K and 295°K were determined by the least squares method. The characteristic temperature of the torsional optical vibrations of a molecule about a C-O bond was determined and is in good agreement with the value determined by Raman scattering. The fractional X-coordinate of the nitrogen atom corrected for torsional vibrations was determined and it was found that the magnitude of the projection of the C-N bond in the given temperature range changes only within the limits of observational errors. A new method, called temperature difference synthesis, is described and it is shown that it is suitable for rapid qualitative determination of the thermal anisotropy of the vibrations of atoms in a crystal lattice.

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112°K 295°K. C-O , , . X- , C-N . , , , .

     

Theory of tamm surface states in approximation higher than tight-binding approximation

The influence of the non-zero value of exchange integrals between Wannier functions, localized in non-neighbouring elementary cells (higher approximation than tight-binding), on the conditions of existence of Tamm surface states and the position of the energy level corresponding to the surface state is shown.

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This paper is part of M. Tomáek's candidate's thesis.     

Dislocations in plastically deformed Fe-3% Si alloy single crystals

The plastic deformation of Fe-3%Si alloy single crystals made from the melt is studied by the method of etching of dislocations. At a room-temperature and at static stress deformation by slip occurs in the 1/2〈111〉 directions along planes of maximum resolved shear stress. The plastic properties are determined by the motion of screw dislocations which cause the broadening of slip bands.     

Analysis of R. P. Smith's and D. C. Parris-R. B. Mclellan's carbon diffusivity data

A phenomenological model is proposed to account for the variation of carbon diffusivityD(N₁) with composition in austenite. This model is based on Parris-McLellan's statement that the increase ofD(N₁) with carbon concentrationN ₁ is due to the increase in chemical driving force. The gradient of the carbon activity in Wagner's and in Zupp-Stevenson's interpretation is presumed to be the intrinsic driving force. The predictions of the model are compared with carbonD(N₁) values both with [1] and without [5] a chemical concentration gradient. TheD(0) values and the carbon-carbon interaction coefficients ₁ are calculated by the use of the least squares method from the experimental data. The application of Zupp-Stevenson's definition of the activity coefficient ₁ results in a better fit of the theory to the experimental data.