Influence of solute mobility on dislocation motion I. Basic model

Dislocation motion in the real lattice of alloys is highly complex. In a certain temperature range the dynamic strain ageing phenomena have been reported. In this paper the influence of mobile solute atoms (as obstacles) on the motion of dislocation is analysed. Both processes are assumed to be thermally activated. A new model based on this assumption is proposed. The dislocation velocity and the friction stress (due to solute-dislocation interactions) are calculated. A change in the friction stress caused by solute mobility is discussed.     

Thickness dependence of exciton absorption in pure GaAs crystals at the “prequantum” limit

The optical absorption of GaAs crystals with thicknesses d=0.4−4.4 μm is measured in the exciton-polariton resonance region at a temperature of 1.7 K. As the thickness is reduced, both a broadening of the exciton line and increased absorption with a negligible Stark shift are observed. The way the absorption spectra vary with crystal thickness is examined in terms of a competition between two regions for light-exciton interactions in the crystal: in the field of surface charges and electric-field free. Fiz. Tverd. Tela (St. Petersburg) 40, 869–871 (May 1998)     

Conductivity and field and current distributions in a two-component system composed of regular triangles

The problem of the effective conductivity and the distributions of a field and currents is analyzed in a regular two-component system composed of regular triangles. An efficient solution method is developed that admits a generalization to multicomponent systems.     

Galvanomagnetic and thermoelectric properties of multicomponent n-type solid solutions based on Bi and Sb chalcogenides

The galvanomagnetic and thermoelectric properties of n-Bi_2-x Sb_xTe_3-y-z Se_yS_z multicomponent solid solutions with atomic substitutions (Sb → Bi; Se, S → Te) are studied. The principal components of the effective mass tensor (m ₁, m ₂, m ₃) for the isotropic mechanism of charge carrier scattering are determined within a many-valley model of the energy spectrum for compositions 0.08 ≤ x ≤ 0.4 and 0.06 ≤ y = z ≤ 0.15. The effect of a variation in the parameters of the constant-energy surface on the thermoelectric efficiency is analyzed for different compositions and carrier concentrations in solid solutions.     

The influence of temperature on superplasticity of Zn-Al-Cd alloy

Experimental results of the study of superplastic behaviour in Zn-0·35 wt. % Al-0·25 wt. % Cd alloy are presented. The attention has been paid to the influence of temperature on stress-strain curves, ductility, strain rate sensitivy parameterm and activation energy of superplastic flow. The best superplastic properties have been established at temperatures T370 K (0·53 T_m): ductilityA=600% and parameterm=0·56. A fast grain growth observed at temperaturesT 380 K has been suggested to be responsible both for the decrease in ductility and parameterm values and for the origin of an anomaly in the decreasing temperature dependence of flow stress. The measurements of activation energy have shown an expected decrease in activation energy at the transition from the non-superplastic region at lower temperatures to the superplastic region at higher temperatures. Significant transient effects after strain rate changes have been observed. The experimental results obtained in the Zn-Al-Cd alloy have been compared with those obtained in binary Zn-1·1 wt. % Al alloy and discussed from the point of view of possible models of structural superplasticity.     

Softening during and after the hot deformation of the AISI 321 steel with respect to practical applications

The softening processes during and after the hot deformation (850–1180 C) in AISI 321 stainless steel were studied with respect to true strains _D and true strain rates . The analysis of deformation curves indicates the occurrence of dynamic recrystallization for values of Zener-Hollomon parameterZ10¹⁵ s^–1. The retardation of static recrystallization by fine Ti(N, C) precipitates is documented by microstructure studies and by variations of annealing conditions.     

Structure of the asparagine-linked sugar chains of porcine kidney and human urine cerebroside sulfate activator protein

The specific sugar residues and their linkages in the oligosaccharides from pig kidney and human urine cerebroside sulfate activator proteins (saposin B), although previously hypothesized, have been unambiguously characterized. Exhaustive sequential exoglycosidase digestion of the trimethyl-p-aminophenyl derivatives, followed by either matrix-assisted laser desorption/ionization and/or mass spectrometry, was used to define the residues and their linkages. The oligosaccharides were enzymatically released from the proteins by treatment with peptidyl-N-glycosidase F and separated from the proteins by reversed-phase high-performance liquid chromatography (HPLC). Reducing termini were converted to the trimethyl-p-aminophenyl derivative and the samples were further purified by normal-phase HPLC. The derivatized carbohydrates were then treated sequentially with a series of exoglycosidases of defined specificity, and the products of each digestion were examined by mass spectrometry. The pentasaccharides from pig kidney and human urine protein were shown to be of the asparagine-linked complex type composed of mannose-alpha 1-6-mannose-beta 1-4-N-acetylglucosamine-N-acetylglucosamine(alpha 1-6-fucose). This highly degraded structure probably represents the final product of intra-lysosomal exoglycosidase digestion. Oligosaccharide sequencing by specific exoglycosidase degradation coupled with mass spectrometry is more rapid than conventional oligosaccharide sequencing. The procedures developed will be useful for sequencing other oligosaccharides including those from other members of the lipid-binding protein class to which cerebroside sulfate activator belongs. (c) 2000 John Wiley & Sons, Ltd.     

Pyranoxanthones from Calophyllum Inophyllum

Phytochemical investigation of the stem bark of Calophyllum inophyllum resulted in the isolation of a new dipyrenoxanthone, calophinone ( 1 ), together with four related xanthones ( 2–5 ). Identification of the isolated compounds was achieved through intensive studies of their spectral data, especially 2D NMR.