State of and prospects for XeF(C−A) optically pumped lasers

Experimental and theoretical results are presented on an XeF(C?A) blue-green laser driven by 5-kJ energy. The laser was pumped by a ferrite-induced discharge of 90 cm in length. The output energy of 0.22 J was obtained with a plane-parallel resonator. A program to simulate laser operation has been developed. Numerical results for a wide range of conditions are compared with experiments performed by us and by other authors. It is found that intracavity refractive losses limit laser operation for XeF pressures above 3 torr. The laser efficiency strongly depends on the discharge-to-cavity length ratio. Possible ways to increase the laser power and efficiency are discussed.     

Redox kinetic measurements of glutathione at the mercury electrode by means of square-wave voltammetry. The role of copper, cadmium and zinc ions

The electrode reaction of glutathione (GSH) at the hanging mercury drop electrode is studied by means of square-wave voltammetry (SWV). At potentials more positive than -0.350 V (vs. Ag/AgCl (3 mol/l KCl)) the oxidation of the mercury electrode in the presence of GSH leads to creation of a sparingly soluble mercury-GSH complex that deposits onto the electrode surface. Under cathodic potential scan, the deposited complex acts as a reducible reactant, giving raise to a well-defined cathodic stripping reversible SW voltammetric response. The electrode reaction can be described by the scheme: Hg(SG)(2(s))+e(-)+2H((aq))(+) = Hg((l))+2GSH((aq)). Thus, the electrode reaction provides information on both thermodynamics and kinetics of the chemical interactions of GSH with mercury. An experimental methodology for measuring the kinetics of the electrode reactions, based on the property known as "quasireversible maximum", is developed. The standard redox rate constant is 5.09, 5.75 and 5.22 cm s(-1) in a phosphate buffer at pH 5.6, 7.0 and 8.5, respectively, with a precision of +/-10%. The high rate of the electrode reaction reflects the strong affinity of GSH towards chemical interaction with mercury. The electrode reaction is particularly sensitive to the presence of heavy metal ions such as Cu(2+), Cd(2+), and Zn(2+.) The rate of the electrode reaction decreases significantly in the presence of these ions due to simultaneous interactions of GSH with the respective ion and mercury.     

Raman and IR Spectroscopy of a Mixed CH3CN-H2O Solvent in the Cn Stretching Region

Raman and IR spectroscopy have been used to elucidate the solvation process in a mixed water-acetonitrile solvent in the CN stretching region. The number and positions of the components forming the spectral contour are established by Fourier deconvolution and Factor analysis and their areas are determined by fitting. The forms of existence of acetonitrile in the mixed solvent are discussed.     

An intracloud discharge caused by extensive atmospheric shower

The observational evidence of RB-EAS discharge in a thunderstorm atmosphere is presented. After RB-EAS discharge we name a discharge of a special type developing due to the runaway breakdown (RB) mechanism while an extensive atmosphere shower (EAS) passes through a thundercloud electric field. The observations were fulfilled at the Tien-Shan Mountain Cosmic Ray Station. The widely spread system of oscillation detectors, the special EAS trigger array and the HF radio interferometer were used for measurements.     

The effective growth of gamma-ray background during a thunderstorm

We present here the results of gamma-ray emission intensity measurements made during thunderstorm. The gamma-ray intensity background (GRB) grows up in an order of magnitude in the active phase of a storm. This growth is shown to be directly connected with the growth of the thundercloud electric field. Besides, the fast changes of GRB (GRB-jumps) are revealed. GRB-jumps are shown to be determined by atmospheric discharges exactly, what mean the strong direct influence of the electric field in atmosphere on gamma-ray emission.     

Dry-Ashing Preconcentration for Micro-Reactor-Based Neutron Activation Analysis of Food and Plant Samples

The application of preconcentration by dry-ashing to the neutron activation analysis of biological samples using a SLOWPOKE-2 low-power reactor is reported. Samples of selected food crops (banana, callaloo, carrot, mango, and yam) and bioindicator plants (lichen, moss, Tillandsia sp., and tree bark) were analysed both as plant tissue, and as ashed sample. The results are presented for 21 elements. Good agreement between both procedures (<10% relative standard error) was obtained for 13 elements: Al, Ca, Cd, Cr, Fe, K, La, Mg, Mn, Na, Sm, Ti, and V. For Dy, Rb, and Zn the agreement was 10-15%. Relatively poorer agreement (>15-30%) was obtained for As, Br, Cl, and Sb. Dry ashing produced improved analytical results for those samples that were of low ash content. However, the increased background counts observed in ashed samples can sometimes negate the concentration gain, particularly in plants with high ash contents but low levels of certain elements.     

Scaling of the coercive field in ferroelectrics at the nanoscale

The scaling of the coercive field in ferroelectric films at the nanoscale is investigated experimentally. The scaling in the films of copolymer vinylidene fluoride and BaTiO₃ with thickness equal by the order of value to the critical domain nucleus size 1–10 nm reveals deviation from the well-known Kay-Dunn law. At this thickness region coercive field does not depend on thickness and coincides with Landau-Ginzburg-Devonshire value.     

Comparative study of the thermodynamics and kinetics of the ion transfer across the liquid/liquid interface by means of three-phase electrodes

A comparative study of the behavior of different sorts of three-phase electrodes applied for assessing the thermodynamics and kinetics of the ion transfer across the liquid/liquid (L/L) interface is presented. Two types of three-phase electrodes are compared, that is, a paraffin-impregnated graphite electrode at the surface of which a macroscopic droplet of an organic solvent is attached and an edge pyrolytic graphite electrode partly covered with a very thin film of the organic solvent. The organic solvent contains either decamethylferrocene or lutetium bis(tetra-tert-butylphthalocyaninato) as a redox probe. The role of the redox probe, the type of the electrode material, the mass transfer regime, and the effect of the uncompensated resistance are discussed. The overall electrochemical process at both three-phase electrodes proceeds as a coupled electron-ion transfer reaction. The ion transfer across the L/L interface, driven by the electrode reaction of the redox compound at the electrode/organic solvent interface, is independent of the type of redox probe. The ion transfer proceeds without involving any chemical coupling between the transferring ion and the redox probe. Both types of three-phase electrodes provide consistent results when applied for measuring the energy of the ion transfer. Under conditions of square-wave voltammetry, the coupled electron-ion transfer at the three-phase electrode is a quasireversible process, exhibiting the property known as "quasireversible maximum". The overall electron-ion transfer process at the three-phase electrode is controlled by the rate of the ion transfer. It is demonstrated for the first time that the three-phase electrode in combination with the quasireversible maximum is a new tool for assessing the kinetics of the ion transfer across the L/L interface.     

On the surface topography of ultrashort laser pulse treated steel surfaces

This paper concentrates on observations of the surface topography by scanning electron microscopy (SEM) on alloyed and stainless steels samples treated by ultrashort laser pulses with duration of 210 fs and 6.7 ps. Globular-like and jet-like objects were found depending on the various levels of the fluence applied. It is shown that these features appear due to solid-liquid and liquid-gas transitions within surface layer irradiated by intense laser light. The observations are confronted to the theory of short-pulsed laser light-matter interactions, including interference, excitation of electrons, electron-phonon coupling as well as subsequent ablation. It is shown that the orientation of small ripples does not always depend on the direction of the polarization of laser light.