Kinetic features of ethylene polymerization over supported catalysts [2,6‐bis(imino)pyridyl iron dichloride/magnesium dichloride] with AlR3 as an activator

The effects of polymerization temperature, polymerization time, ethylene and hydrogen concentration, and effect of comonomers (hexene‐1, propylene) on the activity of supported catalyst of composition LFeCl₂/MgCl₂‐Al(i‐Bu)₃ (L = 2,6‐bis[1‐(2,6‐dimethylphenylimino)ethyl] pyridyl) and polymer characteristics (molecular weight (MW), molecular‐weight distribution (MWD), molecular structure) have been studied. Effective activation energy of ethylene polymerization over LFeCl₂/MgCl₂‐Al(i‐Bu)₃ has a value typical of supported Ziegler–Natta catalysts (11.9 kcal/mol). The polymerization reaction is of the first order with respect to monomer at the ethylene concentration >0.2 mol/L. Addition of small amounts of hydrogen (9–17%) significantly increases the activity; however, further increase in hydrogen concentration decreases the activity. The IRS and DSC analysis of PE indicates that catalyst LFeCl₂/MgCl₂‐Al(i‐Bu)₃ has a very low copolymerizing ability toward propylene and hexene‐1. MW and MWD of PE produced over these catalysts depend on the polymerization time, ethylene and hexene‐1 concentration. The activation effect of hydrogen and other kinetic features of ethylene polymerization over supported catalysts based on the Fe (II) complexes are discussed. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 5057–5066, 2007     

Control of the temperature hysteresis and diffuse dielectric anomaly in the temperature range of the ferroelectric-antiferroelectric phase transition in PbZr1 − x TixO3 (0.03 ≤ x ≤ 0.05) ceramics

The magnitudes of the temperature hysteresis and diffuse dielectric anomaly corresponding to the transition from the antiferroelectric phase to the ferroelectric phase in PbZr_{1 ? x} Ti_xO₃ (0.03 ≤ x ≤ 0.05) ceramics can be reversibly changed by varying the temperatures of heating and cooling in the course of thermocycling. The results obtained indicate that the antiferroelectric-ferroelectric transition in the PbZr_{1 ? x} Ti_xO₃ ceramics materials is a smeared first-order phase transition.     

Axisymmetric excitation of a dielectric torus: Numerical solution

The article considers the mathematical model of a lens antenna in the shape of a homogeneous dielectric torus excited by an axial magnetic dipole. The boundary-value problem for an elliptical differential equation is posed and reduced by the fundamental solution method to an integral equation of 2nd kind over the torus section. A numerical algorithm is proposed, and the numerical results are compared with experimental findings. Translated from Obratnye Zadachi Estestvoznaniya, Published by Moscow University, Moscow, 1997, pp. 109–115.     

The role of finite kinematic bounds in the induced gluon emission from fast quarks in a finite size quark-gluon plasma

We study the influence of finite kinematic boundaries on the induced gluon radiation from a fast quark in a finite size quark-gluon plasma. The calculations are carried out for fixed and running coupling constant. We find that, for running coupling constant, the kinematic correction to the radiative energy loss is small for quark energy ?5 GeV. Our results differ both analytically and numerically from that obtained by the GLV group [6]. The effect of the kinematic cutoffs is considerably smaller than reported in [6].     

Lysine-containing calcium hydroxylapatite: Synthesis and physicochemical characterization

The CaCl₂-(NH₄)₂HPO₄-NH₂(CH₂)₄NH₂CHCOOH-NH₃-H₂O system at 25°C is studied using Tananaev’s solubility (residual concentrations) method and pH measurements. Lysine-containing calcium hydroxylapatite Ca₁₀(PO₄)₆(OH)_1.9[NH₂(CH₂)₄NH₂CHCOO]_0.1 · 6H₂O is identified using chemical analysis, thermogravimetry, powder X-ray diffraction, and IR spectroscopy.     

Influence of the surface on the elastic properties of liquid crystals

A statistical approach including direct correlation functions is applied to study the influence of the surface confining the nematic liquid phase on the Franck elastic coefficients. Specific calculations are made for a model system composed of ellipsoidal molecules interacting by means of the Gay-Berne potential near the interacting surface. Fiz. Tverd. Tela (St. Petersburg) 40, 1356–1359 (July 1998)