Study of the peak effect phenomenon in single crystals of 2H-NbSe2

The weakly pinned single crystals of the hexagonal 2H-NbSe₂ compound have emerged as prototypes for determining and characterizing the phase boundaries of the possible order-disorder transformations in the vortex matter. We present here a status report based on the ac and dc magnetization measurements of the peak effect phenomenon in three crystals of 2H-NbSe₂, in which the critical current densities vary over two orders of magnitude. We sketch the generic vortex phase diagram of a weakly pinned superconductor, which also utilizes theoretical proposals. We also establish the connection between the metastability effects and pinning.     

Adsorption of the Cu<Superscript>2+</Superscript> ions from aqueous solutions on the active carbon oxidized with hydrogen peroxide and impregnated with nitrogen-containing compounds

Adsorption of the copper ions from aqueous solutions, benzene, and water on the active carbon obtained by chemical activation from walnut shells was studied. The active carbon was additionally oxidized with hydrogen peroxide and then impregnated with nitrogen-containing compounds. As a result of impregnation with melamine, a secondary porosity is formed within the oxidized active carbon, leading to an increase in the specific surface of the sorbent. A modified carbon surface is heterogeneous, and the carbons themselves exhibit catalytic activity in the oxidation of luminol and decomposition of hydrogen peroxide.     

Thermal behaviour of polyacrylamidoxime-copper chelates

The purpose of this work was to investigate the effect of several factors (anion type in the copper salt, pH and concentration of the salt solution) on the structure and thermo-oxidative degradation of the polyacrylamidoxime-copper chelates, by using elemental analysis, IR spectroscopy and dynamic thermogravimetry. The chelates containing copper ions as sulphate exhibit a better initial thermal stability than the polyacrylamidoxime fibre presumably due to the crosslinking generated by the intermolecular complexation of the ions; the removal of the sulphate anions takes place concomitantly with the second step of polymeric chain decomposition. The initial thermal decomposition of the chelates formed by copper ions as nitrate begins at lower temperatures as compared to the polyacrylamidoxime fibre, probably by the nitrate anion release, which partly overlaps the initial decomposition of the copper ion-crosslinked polymeric chains. Copper ions as either sulphate or nitrate catalyse the reactions involved in the main step of polyacrylamidoxime fibre decomposition; the higher the copper amount, the stronger the catalytic effect.     

On the efficiency of exchange in parallel tempering monte carlo simulations

We introduce the concept of effective fraction, defined as the expected probability that a configuration from the lowest index replica successfully reaches the highest index replica during a replica exchange Monte Carlo simulation. We then argue that the effective fraction represents an adequate measure of the quality of the sampling technique, as far as swapping is concerned. Under the hypothesis that the correlation between successive exchanges is negligible, we propose a technique for the computation of the effective fraction, a technique that relies solely on the values of the acceptance probabilities obtained at the end of the simulation. The effective fraction is then utilized for the study of the efficiency of a popular swapping scheme in the context of parallel tempering in the canonical ensemble. For large dimensional oscillators, we show that the swapping probability that minimizes the computational effort is 38.74%. By studying the parallel tempering swapping efficiency for a 13-atom Lennard-Jones cluster, we argue that the value of 38.74% remains roughly the optimal probability for most systems with continuous distributions that are likely to be encountered in practice.     

Investigation of the cellulose ethers effect on the Portland cement hydration by thermal analysis

Cellulose ethers (CE) are introduced in almost all cement-based dry mortars in order to retain water in mortar mass avoiding losing it too quickly by substrate absorption or water evaporation. In this way the workability of the fresh material, the adherence to the substrate and internal-strength characteristics of mortar, render or tile adhesive are improved. One of the side effects of cellulose ethers is the Portland cement hydration delaying. The influence of six commercial cellulose ethers, hydroxyethylmethyl cellulose (HEMC) type, on the hydration of Portland cement CEM I 42.5 R, was followed by thermal analysis (TG and DTA curves). Three of these cellulose ethers are unmodified, and have different viscosities, while three of them have the same viscosity but differ in the degree of modification (unmodified, one with medium modification and one with high modification). The interest of dry mortars producers for the effects of these cellulose ethers, is generated by the wide offer available on the market and by the absence of systematic data on the effect of different viscosities and degrees of modification on dry mortars properties. In order to quantify the effect of the CE on the cement hydration, the surface area of the endothermic effect corresponding to the dehydration of portlandite (Ca(OH)₂), formed after 1, 3, and 7 days of hydration, was defined. It was noted that the proportion of Ca(OH)₂ in samples containing CE after 1 day was 30–40 % lower than in reference sample. After 3 and 7 days of hydration the proportion of Ca(OH)₂ in samples containing CE approaches that of reference sample (10–20 % less). For the same period of hydration, the different viscosity, and different degree of modification of cellulose ethers cause variations in narrow limits of the proportion of Ca(OH)₂, and the degree of cement hydration, respectively.     

About collapse and revivals of two quantum oscillators in off-resonance interaction

The off-resonance effect and its influence on the reversibility between two quantum subsystems in interaction (single mode cavity field and a three-level atom in cascade configuration) are studied. The partial restoration condition is found at which these radiators can restore their diagonal moments, while the non-diagonal ones remain correlated after the interaction process.     

3D MR microscopy with resolution 3.7 microm by 3.3 microm by 3.3 microm

The technique of magnetic resonance imaging microscopy holds promise of bringing the full capabilities of NMR to arbitrarily specified positions within spatially inhomogeneous systems, including biological cells, yet the possibilities are limited by the need for adequate sensitivity and spatial resolution. We report proton magnetic resonance images obtained by combining advances in receiver coil sensitivity, gradient strength, and pulse/gradient sequence design. We achieve resolution of 3.7 +/- 0.4 microm by 3.3 +/- 0.3 microm by 3.3 +/- 0.3 microm for a volume resolution approximately 40 femtoliters (corresponding to approximately 3 x 10(12) proton spins).     

Reduced data acquisition time in multi-dimensional NMR spectroscopy using multiple-coil probes

A new hardware-based approach is presented to reduce data acquisition times in multi-dimensional NMR spectroscopy using a multiple-coil probe. Using a four-coil setup, two-dimensional COSY and TOCSY spectra were acquired in one-quarter the time of conventional spectra by simultaneous acquisition of different effective t1 evolution times for each coil. Data processing consists of simple phase-shifting and intensity normalization of the individual data sets, and results in spectra almost identical to those acquired in a conventional manner. This method can potentially be integrated with other new data acquisition and processing schemes for further increases in data acquisition speed.     

3D micron-scale MRI of single biological cells

We report MRI microscopy images of single biological cells with micron-scale resolution in all three dimensions. Sub-cellular organelles are observed, including a spiral-shaped array of chloroplasts on the inner surface of the cell wall of a Spirogyra alga.