Diffusion-viscometric analysis and conformational characteristics of sodium polystyrenesulfonate molecules

Samples of sodium polystyrenesulfonate of molecular weights varying in a 20-fold range were synthesized. The hydrodynamic behavior of the samples was studied in a 0.2 M NaCl solution in which the initial polyelectrolyte effects are suppressed. Relationships between the molecular weight and the translational friction coefficient and intrinsic viscosity were obtained. The theory describing the hydrodynamic behavior of wormlike chains with taking into account both the percolation effects and the excluded-volume effects was applied to estimation of the length of the statistical segment and the cross section of the sodium polystyrenesulfonate molecules in 0.2 M NaCl solution.     

Synthesis and Polar and Electrooptical Properties of a Butylamine Derivative of Fullerene C<Subscript>60</Subscript>

A butylamine derivative of fullerene was prepared by the reaction of butylamine with fullerene C₆₀. The experimental electrooptical and dipole characteristics of the derivative were compared with the corresponding calculated PM3 data. The reaction product proved to be inhomogeneous in the number of the amine molecules added; it contains polar multiadducts of C₆₀ with noncentrosymmetric distribution of covalently bound amino groups over the fullerene core.__________Translated from Zhurnal Obshchei Khimii, Vol. 75, No. 5, 2005, pp. 795–802.Original Russian Text Copyright © 2005 by Evlampieva, Yakimanskii, Dobrodumov, Nazarova, Pashkov, Panarin, Ryumtsev.     

Relaxation properties and complex formation of copolymers of 2-deoxy-2-methacrylamido-D-glucose and unsaturated acids

With the use of polarized luminescence, relaxation times characterizing the intramolecular mobility of luminescent labeled copolymers of 2-deoxy-2-methacrylamido-D-glucose and unsaturated acids in solutions are determined in both nonionized and ionized states. Elements of the secondary structure typical for poly(methacrylic acid) are formed in copolymers with a high content of methacrylic acid (≥50 mol %) in their nonionized state. This structure is destroyed during ionization. Equilibrium stability constants for complexes of the copolymers with cationic surfactants are determined. Quantitative characteristics of the effects of the surfactant and copolymer structures and the ionic strength of solution on complex formation are estimated.     

Determining the energy balance in barrier-discharge Xe<Subscript>2</Subscript> excilamp by the pressure jump method

The energy redistribution in barrier-discharge Xe₂ excilamp in various excitation regimes is investigated using the pressure jump method. Analytic expressions are derived for calculating power W dissipated in the excilamp discharge plasma in the form of heat and for calculating total discharge heat power P_T spent on heating the excilamp. It is shown that the mechanism of the thermal energy dissipation gradually changes upon an increase in the xenon pressure in the excilamp. The conditions for generating the maximal radiation power of the excilamp are determined. It is shown that the maximum of the average radiation power is attained for an excitation pulse duration of 500 ns and the maximal pulse power is attained for a pulse duration of 100 ns. It is found that the optimal operation regime for the excilamp corresponds to the maximal values of the P_T–W difference.     

Properties of solutions of methyl cellulose blends with poly(N-methyl-N-vinylacetamide) in water and dimethylacetamide and of the related composite films

The rheological properties of dilute and moderately concentrated solutions of methyl cellulose blends with poly(N-methyl-N-vinylacetamide) in water and dimethylacetamide are studied, and the stressstrain characteristics of the composite films based on these blends are estimated. DSC, X-ray diffraction, and thermomechanical analysis are used to investigate the structural organization of composite films, to estimate the temperatures of relaxation transitions, and to determine the composition ranges in which the polymers are compatible and form mixed structures.     

Properties of the methyl cellulose-polyvinylpyrrolidone binary system in solution and in the solid state

Rheological properties of dilute and moderately concentrated aqueous solutions of methyl cellulose-polyvinylpyrrolidone blends, as well as the conditions of gelation in them, were studied. Films were obtained from solutions of the polymer blends, and their physicomechanical properties were examined. The range of the compositions corresponding to thermodynamic compatibility of methyl cellulose with polyvinylpyrrolidone was identified by the solvent vapor sorption method and by thermomechanical examinations of the films.     

Enzymatic polymerization of vinyl monomers

The possibility of using horse radish peroxidase as a catalyst for polymerization of monomers (vinylformamide and sodium vinylsulfonate) in the presence of hydrogen peroxide and 2,4-pentanedione in aqueous medium at room temperature was studied.     

Conformational and hydrodynamic properties of the homopolymer of 2-deoxy-2-methacrylamido-D-glucose and its copolymers with acrylic acid and methacrylic acid

Hydrodynamic properties of the homologous series of the homopolymer 2-deoxy-2-methacryla-mido-D-glucose and the copolymers of 2-deoxy-2-methacrylamido-D-glucose with unsaturated acids in 0.2 M NaCl are studied via static and dynamic light scattering, viscometry, refractometry, and translational diffusion. The copolymers synthesized via the free-radical copolymerization of 2-deoxy-2-methacrylamido-D-glucose with acrylic acid or methacrylic acid contain ～20 mol % acid units. At this amount of acid units, the equilibrium rigidity of copolymer chains corresponds to that of homopolymer chains. The copolymers are distinguished by the hydrodynamic characteristics of molecules. The copolymer with methacrylic acid is similar to the homopolymer, whereas the copolymer with acrylic acid features substantially different parameters of relationships relating the hydrodynamic characteristics of homologs to their molecular masses.