Radiotracer study of deposition caused by suspended sediments of river seman

The deposition caused by suspended sediments in three points at the Seman river mouth was determined by means of¹³⁷Cs. The soil pollution with this radionuclide, caused by the Chernobyl accident is given, too.     

Spectral distributions in nuclei: General principles and applications

The subject of spectral distribution methods where one derives and applies the locally smoothed forms of observables in nuclei is briefly reviewed. It is well understood that the local forms (with respect to energy) of the level density function, expectation values and strength densities are Gaussian, linear (or ratio of Gaussians) and a bivariate Gaussian respectively. To accomodate symmetries in the above forms, one has to deal with multivariate distributions in general; for example the angular-momentum (J) decomposition leads to a bivariate Gaussian form for the level density. These results extend to indefinitely large spaces by method of partitioning and they generate convolution forms. The origin of these remarkable spectral properties is discussed and shell model examples are given to substantiate their applicability to nuclear systems. Spectral distribution theory is a practical, usable theory because the smoothed forms are defined in terms of traces of low particle-rank operators, and the trace information propagates. Finally we discuss the application of the spectral methods for a wide range of nuclear problems; these include binding energies, orbit occupancies, electromagnetic andβ-decay sum rule quantities, analysis of operators, symmetry breaking, numerical level densities, and determination of bounds on time-reversal non-invariant part of nucleon-nucleon interaction.     

A comparison of spin relaxation and local motion between symmetrically and asymmetrically ring-substituted bisphenol units in dissolved polycarbonates

Carbon-13 and proton spin-lattice relaxation times were measured at two field strengths on solutions 10% by weight of two polycarbonates in C₂D₂Cl₄ from ?20 to +120°C. The first polycarbonate is an asymmetrically substituted form with one chlorine on one of the two phenylene aromatic rings of the bisphenol unit, whereas the second polycarbonate is symmetrically substituted with two chlorines on each of the two rings. The nuclear spin relaxation data are interpreted in terms of several local motions likely in these polymers. Segmental motion was described by the Hall–Helfand correlation function. Segmental motion in the monosubstituted polycarbonate is somewhat slower than in unsubstituted polycarbonate, whereas segmental motion in the tetrasubstituted polycarbonate is considerably slower. Phenylene ring rotation is observed in unsubstituted polycarbonate and in the monosubstituted polycarbonate above 40°C. Below 40°C in the monosubstituted species, and at all temperatures in the tetrasubstituted species, ring rotation is replaced by ring libration as the predominant motion contributing to spin lattice relaxation. In addition, the rotational motion of the two types of rings in the asymmetric monosubstituted form are very similar although not identical. The substituted ring is slightly less mobile than the rings of unsubstituted polycarbonate. This indicates a strong coupling of ring motion, although the coupling leads to less than synchronous motion. Methyl group rotation is present in both polymers and is little affected by the various structural modifications.     

Number albedo measurements from stratified layers of iron,concrete and aluminium

A layer of stratified combination composed of selected radiation shielding materials acquires better shielding property. Albedo is used in such measurements as an integral measure ofγ-ray scattering. The stratified slabs of alternating heterogeneous layers have been found to have a virtual homogeneous property with a definite effective atomic number. The angular distribution of back-scattered photons as well as the total number albedo values for iron, aluminium and concrete in stratified combination for 662 keV and 1250 keV photons are reported.     

Nonlinear Theory of the Plasma Wave Excitation in a Bounded Beam-Plasma System

The excitation of symmetric and antisymmetric plasma waves by a beam layer that moves within a homogeneous plasma enclosed by a metallic wall was dealt with theoretically. Investigations were carried out for the magnetic field free case and for a magnetized electron beam. In the latter case, the beam electrons are assumed to be unable to move in the perpendicular direction. The theoretical model bases upon an extension of the well known single wave theory to a two-dimensional beam-plasma system. Special emphasis should be paid to the fact that the perpendicular wave profile of the excited waves was determined self-consistently. Energy and momentum balance equations are derived for this system. The theoretical method outlined in this paper which is based on a Green's-function technique can be extended easily to three-dimensional systems or to beam-plasma systems with other boundary conditions. The main features of the saturation process of the basic unstable wave types are discussed. Several interesting effects were found in the magnetic field free case: (i) numerical solutions describe an increasing steepening of the wave amplitudes in perpendicular direction near the center of the system for the symmetric potential wave; (ii) for the antisymmetric wave, a smoothing tendency was found in the development of the perpendicular wave potential profile; (iii) spatial separation of the slow and fast beam electrons was observed; (iv) it is shown for the antisymmetric potential wave type that, under certain conditions, a very efficient beam particle retardation mechanism occurs which is connected with a strong reduction of the formation of a fast particle group; (v) generally it was shown that the conversion of the kinetic energy of the beam electrons into the plasma wave energy may be more effective as compared with the case of the magnetized beam.     

Quantification of midodrine and its active metabolite in plasma using a high performance liquid chromatography column switching technique

An automated column-switching HPLC system is described for the simultaneous determination of midodrine, an alpha-adrenergic stimulating drug, and its active metabolite, ST-1059. Serum or plasma (850 microliters) is directly injected onto a RP18 (30 micrograms particle size) pre-column (9 x 4 mm ID) which acts as an on-line liquid-solid extractor and analyte enrichment system. The injection is followed by washing steps. The fraction containing the analytes is transferred onto an analytical RP18 column via step gradient elution where the final analysis is performed. Fluorescence detection is used (lambda ex 290 nm and lambda em 322 nm), and method detection limits of 0.8 ng/mL plasma were reached. These were sufficiently low to determine the plasma concentration-time profiles for both compounds following oral administration of 2.5 mg and 5 mg midodrine hydrochloride. The assay in serum or plasma was linear in the range of 1 to 15 ng analyte/mL, the recovery was greater than 95%, and the reproducibility was sufficient. The assay was rugged and was maintained by routinely changing the home-made, dry packed pre-column every 20th serum injection.     

Transmission of XeCl excimer laser pulses through optical fibers: Dependence on fiber and laser parameters

Measurements of the transmission of XeCl excimer laser pulses (308 nm) through optical all-silica fibers are reported. The observed photodegradation effects during long time irradiation are dependent on the laser energy density and the laser repetition rate. Also the influence of the fiber drawing parameters and fiber geometry have been investigated. Absorption spectra of the fibers in the wavelength range from 200nm to 400nm before and after the irradiation with the excimer laser give some insight in the physical reasons for the changes in transmission properties. A spectral analysis of the fiber fluorescence has been performed.Presented at LASERION '91, June 12–14, 1991, München (Germany)     

Coercivity analysis in R17Fe83−χBχ magnets

We studied the coercivity in magnets of composition R₁₇Fe_83−χB_χ (R = Nd, Pr and χ = 8, 30), using measurements of the coercive field H_c, its angular dependence, and the magnetic viscosity coefficient S_v, for temperatures between 4.2 and 500 K. The results are discussed in relation to a model which does not specifically consider the detailed mechanisms involved in magnetization reversal, but which provides information about the magnetic properties in the activation volume v where magnetization reversal is initiated. It is concluded that the ordering temperature in v tends to be slightly smaller than in the bulk and that the room temperature anisotropy in v is not strongly reduced with respect to the bulk value. Finally, a direct evaluation of the dipolar interactions is in good agreement with results obtained from H_c(T).