Vacuum behavior in two-dimensional scalar electrodynamics

The vacuum properties in two-dimensional scalar electrodynamics are investigated by calculating the one-loop contribution to the effective lagrangian for a constant electric field.     

Acoustic voice analysis in patients with essential tremor

To quantify several acoustic features of the voice in patients with essentialtremor (ET), 28 patients and 28 age- and sex-matched controls were studied. ET severity was assessed with the rating scale for tremor of Fahn, Tolosa, and Marín. The Computerized Speech Lab 4300 program (Kay Elemetrics) was used. Two-second samples of a sustained /a/ and a sentence were captured with a microphone and laryngograph equipment. Measures included fundamental frequency (F₀), frequency perturbation (fitter, Koike algorithm), intensity perturbation (shimmer, Horii algorithm), and harmonic-to-noise ratio (H/N, Yumoto algorithm) of the vowel /a/, and the frequency and intensity variability of the sentence, phonational range, and dynamic range at the natural frequency, maximum phonational time, and s/z ratio. All subjects underwent indirect laryngoscopy and/or laryngeal fibroscopy. When compared with controls, ET patients showed higher jitter, lower H/N ratio (the last one only with laryngographic signal), of the vowel /a/, lower frequency variability in the microphonc signal, lower intensity variability in the laryngographic signal of the sentence, and significantly lower dynamic range at natural frequency of phonation. ET patients reported higher frequency of the presence of high voice intensity, tremor, and struggle. Several acoustic parameters were influenced by the severity of the disease, including shimmer, jitter, H/N ratio, frequency variability of the sentence, and s/z ratio, although neither of the acoustic analysis values or the phonetometric measurements were affected by the presence of voice tremor or by a successful pharmacological treatment of ET.     

Electrical conductivity of cationic polyelectrolytes in aqueous solution

Four different fluoride, chloride, bromide, and nitrate cationic polyelectrolytes were prepared. Their electrolytic conductivity in aqueous dilute solution was investigated. The results show a remarkable increase, with dilution being practically constant down to limiting concentration. The limiting equivalent conductivity Λ° follows the order The distances between neighboring charges calculated from experimental data are in good agreement with those calculated geometrically according to Manning's definition. The results are mainly dependent on the assumption that Br^? and NO₃^? interact in a similar manner with the cationic charges on the polyion. This phenomenon also has been observed in cationic micelles.     

Critical contribution of nonlinear chromatography to the understanding of retention mechanism in reversed-phase liquid chromatography

The retention of most compounds in RPLC proceeds through a combination of several independent mechanisms. We review a series of recent studies made on the behavior of several commercial C18-bonded stationary phases and of the complex, mixed retention mechanisms that were observed in RPLC. These studies are essentially based on the acquisition of adsorption isotherm data, on the modeling, and on the interpretation of these data. Because linear chromatography deals only with the initial slope of the global, overall, or apparent isotherm, it is unable fully to describe the complete adsorption mechanism. It cannot even afford clues as to the existence of several overlaid retention mechanisms. More specifically, it cannot account for the consequences of the surface heterogeneity of the packing material. The acquisition of equilibrium data in a wide concentration range is required for this purpose. Frontal analysis (FA) of selected probes gives data that can be modeled into equilibrium isotherms of these probes and that can also be used to calculate their adsorption or affinity energy distribution (AED). The combination of these data, the detailed study of the best constants of the isotherm model, the determination of the influence of experimental parameters (e.g., buffer pH and pI, temperature) on the isotherm constants provide important clues regarding the heterogeneity of the adsorbent surface and the main properties of the adsorption mechanisms. The comparison of similar data obtained for the adsorption of neutral and ionizable compounds, treated with the same approach, and the investigation of the influence on the thermodynamics of phase equilibrium of the experimental conditions (temperature, average pressure, mobile phase composition, nature of the organic modifier, and, for ionizable compounds, of the ionic strength, the nature, the concentration of the buffer, and its pH) brings further information. This review provides original conclusions regarding retention mechanisms in RPLC.     

Fundamental considerations on the mechanisms of silver cementation onto zinc particles in the Merril-Crowe process

Studies on the Merrill-Crowe process as applied to silver recovery have shown that one half of the used zinc powder is wasted in water reduction at high cyanide concentrations, while the other half reduces silver ions from the cyanide solution. However, the cementation mechanisms as an electrochemical process taking place on the zinc surface do not explain the split of the electric current resulting from the anodic dissolution of zinc into two equal values. This study demonstrates that the mechanism for silver precipitation at high and low cyanide concentrations differs considerably. At low cyanide concentrations cementation is essentially an electrochemically-controlled process following a shrinking-core behavior. At high cyanide concentrations, the process seems not to be electrochemically controlled. The areas for zinc dissolution and silver deposition are not connected by an electrical-conducting medium and reduction of silver-cyano complex ions takes place by hydrogen adsorbed onto silver growing outward from the cementing zinc particles. The results are based on scanning electron microscopy of solids recovered from cementations in stirred reactors and in situ observations by optical microscopy of the cementation process on the edge of thin zinc disks in cyanide solutions.     

Orienting the Demixion of a Diblock‐copolymer Using 193 nm Interferometric Lithography for the Controlled Deposition of Nanoparticles

DUV interferometric lithography and diblock copolymer self‐organization have successfully been combined to provide a simple and highly collective nanopatterning technique enabling the organization of nanoparticles over several orders of magnitude, from nanometre to millimetre. The nanostructural changes at the surface of the polymer film after thermal annealing have been monitored by AFM and the process parameters optimized for obtaining a long‐range organization of the lamellar domains. In particular, the impact of the annealing conditions and geometric parameters of the substrate patterns have been investigated. The nanopatterns resulting from the lamellar demixion of (PS‐b‐MMA) were used for a controlled deposition of nanoparticles. The affinity of the hydrophobic particles for the PS block was demonstrated, opening new doors towards the preparation of high‐density arrays of nanoparticles with potential applications in data storage.

     

Energy level and band alignment for GaAs-alkylthiol monolayer-Hg junctions from electrical transport and photoemission experiments

A series of p- and n-GaAs-S-C(n)H(2n+1) || Hg junctions are prepared, and the electronic transport through them is measured. From current-voltage measurements, we find that, for n-GaAs, transport occurs by both thermionic emission and tunneling, with the former dominating at low forward bias and the latter dominating at higher forward bias. For p-GaAs, tunneling dominates at all bias voltages. By combining the analysis of the transport data with results from direct and inverse photoemission spectroscopy, we deduce an energy band diagram of the system, including the tunnel barrier and, with this barrier and within the Simmons tunneling model, extract an effective mass value of 1.5-1.6m(e) for the electronic carriers that cross the junctions. We find that transport is well-described by lowest unoccupied and highest occupied states at 1.3-1.4 eV above and 2.0-2.2 eV below the Fermi level. At the same time, the photoemission data indicate that there are continua of states from the conduction band minimum and the valence band maximum, the density of which varies with energy. On the basis of our results, it appears likely that, for both types of junctions, electrons are the main carrier type, although holes may contribute significantly to the transport in the p-GaAs system.     

Galactose Oxidase models: 19F NMR as a powerful tool to study the solution chemistry of tripodal ligands in the presence of copper(II)

In copper(ii) complexes of tripodal ligands, the protonation state of the phenol moiety, and its position (axial vs. equatorial), are easily assessed by (19)F NMR.     

Asymptotic-Preserving Particle-In-Cell method for the Vlasov–Poisson system near quasineutrality

This paper deals with the numerical resolution of the Vlasov–Poisson system in a nearly quasineutral regime by Particle-In-Cell (PIC) methods. In this regime, Classical PIC methods are subject to stability constraints on the time and space steps related to the small Debye length and large plasma frequency. Here, we propose an “Asymptotic-Preserving” PIC scheme which is not subjected to these limitations. Additionally, when the plasma period and Debye length are small compared to the time and space steps, this method provides a consistent PIC discretization of the quasineutral Vlasov equation. We perform several one-dimensional numerical experiments which provide a solid validation of the method and its underlying concepts, and compare the method with Classical PIC and Direct-Implicit methods.