Nanostructure Evolution of Oxide Dispersion Strengthened Steels under Fe Ion Irradiation at 350°C

Physics of Atomic Nuclei - Improved mechanical properties of oxide dispersion strengthened (ODS) steels, the advanced materials for the reactor core, are due to the high density of uniformly...     

Pairwise Correlations in a Multicomponent Anisotropic Liquid

We investigate a multicomponent anisotropic liquid system. The first spatial moment of the direct correlation function is taken into account to obtain asymptotic expressions for the pairwise correlation functions. In this approximation, we obtain the pairwise correlation functions that describe the system behavior not only in the critical-state neighborhood but also in the noncritical domain. We show that the critical parameters for the anisotropic system differ from those for the isotropic system.     

Basic principles of technological shaping of optical properties and radiation hardness of PWO crystals

Technological conditions ensuring growth of optically homogeneous lead tungstate (PWO) crystals are reported. It is shown that the basic scintillator characteristics of PWO grown from highly purified raw material and properly doped with lanthanides are mainly determined by inclusions of oxides W_1−yL_yO_3−x (L=Y, La, Gd; 0<x<0.3). Moreover, surface-located inclusions with structure close to tungstenite may also be of importance. It is demonstrated that the scintillation properties can be intentionally designed by varying the oxygen content in the inclusions x and the surface structure. The optimal value for x and the most favorable surface structure are achieved by proper thermal regimes and environment content during the crystal annealing. The results enabled low-cost fabrication of PWO scintillators with steady and reproducible characteristics acceptable for the CERN project ALICE and ensured production of PWO on an industrial scale by “North Crystals” company at a rate of 125–135 crystals per year from every growth apparatus.     

Searches for single-spin asymmetry in the inclusive production of neutral pions in the central region at a proton beam energy of 70 GeV

Results are presented that were obtained by measuring single-spin asymmetry in the inclusive production of neutral pions in the reaction p+p ↑→ π ⁰+X at x _F≈0. A beam of 70-GeV protons was extracted directly from the vacuum chamber of the accelerator by means of a bent single crystal. For transverse momenta in the range 1.0<p _T<3.0 GeV/c, the single-spin asymmetry independently measured by two detectors is zero within the errors. This result is in agreement with Fermilab data obtained at 200 GeV, but it is at odds with CERN data measured at 24 GeV.     

General features of single-spin asymmetry in inclusive pion production in fixed-target experiments

Physics of Atomic Nuclei - The results of various experiments that measured a single-spin asymmetry in inclusive pion production are analyzed in the energy range between 13 and 200 GeV. The...     

Resonant Phenomena in Slowly Irregular Rectangular Waveguides

A waveguide with a rectangular cross section of size and orientation slowly changing along the length of the waveguide is considered. Methods of the canonical perturbation theory are used to describe the ray dynamics in the waveguide. As the size and orientation of the cross section slowly change along the ray trajectory, certain resonance conditions may be satisfied. The phenomena of scattering on resonance and capture into resonance is studied. These phenomena lead to destruction of the adiabatic invariance in the system. Bibliography: 12 titles.__________Published in Zapiski Nauchnykh Seminarov POMI, Vol. 300, 2003, pp. 173–179     

Mechanism of phase transitions in the (NH4)2WO2F4 ferroelastic

Precision studies of the thermophysical properties and structure of an (NH₄)₂WO₂F₄ crystal have been performed. It was established reliably that there is a sequence of two phase transitions at T ₁ = 201 K and T ₂ = 160 K characterized by wedging out of an intermediate phase with an increase in pressure. The role of tetrahedral and octahedral ionic groups in the mechanism of the structural transitions was determined.     

Magnetic and transport properties of double distorted perovskites CaCuMn6O12 and CaCu2Mn5O12

Magnetic and transport properties of double distorted perovskites CaCuMn₆O₁₂ and CaCu₂Mn₅O₁₂ are studied in a range 2–300 K. The leading role in magnetism of these compounds belongs to antiferromagnetic exchange interaction of Cu²⁺ in square coordination with Mn³⁺/Mn⁴⁺ in octahedral coordination. The values of saturation magnetization indicate that Mn³⁺ ions in square coordination are coupled ferromagnetically with Mn³⁺/Mn⁴⁺ in octahedral coordination. The colossal magnetoresistance in the pellet samples is due assumingly to intergranular spin-polarized tunneling of current carriers.     

Crystal structure of the synthetic analog of radtkeite Hg<Subscript>3</Subscript>S<Subscript>2</Subscript>Cl<Subscript>1.00</Subscript>I<Subscript>1.00</Subscript>

The results of structural studies of the synthetic analog of the radtkeite mineral Hg₃S₂Cl_1.00I_1.00 are analyzed. The crystal structure of the compound has been refined; the unit cell parameters are a _m = 16.827(4) , b _m = 9.117(1) , c _m = 13.165(5) , = 130.17(2)°, V = 1543.3(8) ³, space group C2/m, Z = 8, R = 0.0527. A possible transition a ₀ = a _m; b ₀ = a _m + 2c _m; c ₀ = –b _m to the pseudo-orthorhombic F cell previously determined for radtkeite, where one of the angles ( ₀ ) is slightly different from 90° (89.55°), has been found. Each sulfur atom in the structure is bonded to three mercury atoms, forming SHg₃ umbrellas with distances 2.240(6) –2.474(8) and angles HgSHg 94.7(2)°–102.9(2)°. The SHg₃ fragments are linked through Hg vertices to form corrugated [Hg₁₂S₈] layers. The halogen atoms lie inside and between the [Hg₁₂S₈] layers; the distances are Hg-Cl and Hg-I 2.783(7) , 2.961(7) , and 3.083(4) –3.311(3) , respectively.Original Russian Text Copyright © 2004 by N. V. Pervukhina, S. V. Borisov, S. A. Magarill, D. Yu. Naumov, V. I. Vasiliev, and B. G. NenashevTranslated from Zhurnal Strukturnoi Khimii, Vol. 45, No. 4, pp. 755–758, July–August, 2004.This revised version was published online in April 2005 with a corrected cover date.     

Crystal and Molecular Structure of the Nitramino Derivatives of Tetrazole and 1,2,4-Triazole. III. 5-Nitraminotetrazole Lithium Salt Monohydrate

The structure of 5-nitraminotetrazole lithium salt monohydrate was determined by X-ray diffraction analysis. Crystals are monoclinic, space group P2₁/c; a = 8.3789(5), b = 10.1872(6), c = 6.6709(5) ; = 106.63(1)°; V = 545.60(98) ³; Z = 4; _calc = 1.875 g/cm³. The anion has a planar nitrimine structure with a delocalized negative charge. Each lithium cation (c.n. 5) is bound to three anions and two hydration water molecules. Both oxygen atoms of the nitro groups and the N(3) atom of the tetrazole ring are involved in cation coordination. The geometrical characteristics of the anion are similar to those found for other monosalts of 5-nitraminotetrazole.