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.     

Emission properties of apokamp discharge at atmospheric pressure in air,argon, and helium

Emission spectra of the plasma jet of apokamp discharge in air, helium, and argon are studied. Apokamp at atmospheric pressure is formed in the areas of strengthening of the electric field near the bends in the channel of the pulse-periodic discharge and is directed perpendicularly to the discharge channel. Apokamp consists of a bright narrow “appendage” connected with the discharge channel and with the diffuse jet emerging from the channel. It is shown that, in helium, the emission of the diffuse part of apokamp is dominated by N₂ and N₂ ⁺, while emission of the “appendage” display lines and bands of He, N₂, N₂ ⁺, O, and OH. In argon, emission spectra of the diffuse part of the plasma jets contain not only N₂ and N₂ ⁺, but also Ar lines. It is assumed that the surrounding air plays an important role in the formation of the diffuse part of apokamp in helium and argon.     

Water-soluble polymer derivatives of cholesterol

New cholesterol-containing water-soluble polymers based on N-methacryloyl aminoglucose and N-vinylpyrrolidone are synthesized by free-radical copolymerization and polymer-analogous transformations. Binary and ternary copolymers of various composition containing N-allylamine and N,N,N-trimethylaminoethyl methacrylate methyl sulfate units and cholesterol residues are prepared. Luminescently labeled copolymers of the same composition are obtained. Effects of the nature of polymers and the amount of cholesterol in them on the intramolecular mobility of macromolecules in solution are studied with polarized luminescence. When 2–4 mol % of cholesterol residues are incorporated into the copolymer, the intramolecular mobility of macromolecules decreases, thus indicating formation of intramolecular compact structures via interaction of nonpolar cholesterol groups. In copolymers containing charged groups, these structures are looser than those in neutral copolymers. It is shown that macromolecules of cholesterol-containing polymers of various types can interact with each other. 1 This work was supported by the Russian Foundation for Basic Research (project no. 08-03-00324) and the Council for Grants of the President of the Russian Federation for Support of Leading Institutes of Higher Education (NSh-4391.2008.3).     

Dynamic birefringence of poly(styrene-4-sulfonate sodium) macromolecules in aqueous solutions at high ionic strengths

For samples of various molecular masses, the flow birefringence of poly(styrene-4-sulfonate sodium) macromolecules in aqueous solutions at various ionic strengths is studied in relation to the concentration of NaCl. It is shown that the sign of birefringence changes from negative to positive with an increase in the ionic strength of a solution. Application of the macroform theory to the Maxwell effect makes it possible to estimate the intrinsic optical anisotropy of the repeating unit of poly(styrene-4-sulfonate sodium) (a||- a⊥) = −17 × 10^-25 cm³), which nearly coincides with similar values known for atactic polystyrene and poly(κ-methylstyrene).     

Sequence of four orthogonal smectic phases in an achiral bent-core liquid crystal: evidence for the SmAP(α) phase

The mesomorphic properties of an achiral bent-core liquid crystal derived from 4-cyanoresorcinol are studied by polarizing optical microscopy, x-ray diffraction, and second harmonic electro-optic response. It shows a novel sequence of four nontilted or orthogonal smectic phases on cooling: SmA-SmAP(R)-SmAP(X)-SmAP(A). Here SmAP(X) is the new orthogonal polar uniaxial smectic phase. The electric-field-induced transformations in the SmAP(X) phase give rise to two biaxial states separated by a uniaxial one. The second harmonic electro-optic response in this phase is interpreted in terms of the polar interaction with the electric field. A comparison of the experimental results with the next-nearest-neighbor model for the structure of the SmAP(X) phase shows it to be an SmAP(α) phase.     

The effect of chiral doping in achiral smectic liquid crystals on the de Vries characteristics: smectic layer thickness,electro-optics and birefringence

An addition of chiral dopant to two achiral smectic liquid crystals from a homologous series, by varying weight percentages with known low values of layer shrinkage, leads to chiral smectic-C* phase with a finite value of the spontaneous polarisation. The electro-optical response arising from changes in the induced apparent tilt angle brought about by a weak electric field in the SmA* phase gives rise to power law dependency on the reduced temperature. The critical exponent γ of the power law depends on the dopant concentration but its value is found to be greater than the typical value of 1.32. This implies that the short-range correlation extends from two dimensions to three dimensions in these materials in the SmA phase. The layer thickness of smectic layers in the guest–host system remains unaltered up to the 15 wt % addition of the chiral dopant to two achiral smectics. The system thus retains the low layer shrinkage of the achiral smectic as evidenced by measurements of the layer thickness from X-ray scattering and thickness measurements from optical interferometry. Results on the optical birefringence and the apparent tilt angle lead us to the conclusion of having successfully obtained chiral smectic materials for devices with de Vries characteristics by chiral doping.     

The mutual effect of absorption of biologically active substances and microstructure of native cellulose matrix on the properties of resulting compounds

In order to obtain multicomponent polymer systems exhibiting biological activity microcrystalline cellulose was used as a matrix for biologically active compounds, such as dimethylbenzylalkylammonium chloride, poly-N-vinylpyrrolidone, copolymer of N-vinylpyrrolidone and crotonic acid, and complex of dimethylbenzylalkylammonium chloride with copolymer of N-vinylpyrrolidone and crotonic acid. Adsorption interaction of microcrystalline cellulose with these was studied under various conditions. Adsorption isotherms of compounds of polymer nature are of similar character and are described by the Freundlich equation. The isotherms of dimethylbenzylalkylammonium chloride are described by the Langmuir equation. Characteristics of the resulting compounds were obtained using XPS and IR Fourier spectroscopy, WAXS, and SEM. Chemical interaction between microcrystalline cellulose and dimethylbenzylalkylammonium chloride takes place. This interaction leads to a new labile morphological cellulose structure accessible to penetration, which is confirmed at a morphological level by SEM.