Multibubble sonoluminescence in aqueous salt solutions

The sonoluminescence from aqueous solutions containing various salts in the concentration range of 0 to 7 M has been examined using 3.5 ms pulses of 515 kHz ultrasound. In almost all cases the sonoluminescence intensity recorded increased with increasing salt level until a critical concentration (in the range of 1-2 M) was reached. At salt levels above the critical concentration the signal intensity decreased sharply with increasing salt concentration. It is not possible to satisfactorily account for the trends in terms of changes in solution viscosity, rate of bubble coalescence, water vapour pressure, air/water interfacial tension or ionic strength. However, a good correlation of the increase in the signal with the extent of gas solubilisation in the solutions with changing salt concentration was observed. Possible reasons for the signal increase with the addition of salts and the marked decrease at high salt concentrations are discussed.     

The mechanism of sonochemical degradation of a cationic surfactant in aqueous solution

The sonochemical degradation of the cationic surfactant, laurylpyridinium chloride (LPC), in water was studied at concentrations of 0.1-0.6 mM, all below its critical micelle concentration (15 mM). It has been found that the initial step in the degradation of LPC occurs primarily by a pyrolysis pathway. Chemical analysis of sonicated solutions by gas chromatography, electrospray mass spectrometry, and high performance liquid chromatography reveals that a broad range of decomposition products, hydrocarbon gases and water-soluble species, are produced. Propionamide and acetamide were identified as two of the degradation intermediates and probably formed as the result of the opening of the pyridinium ring following OH radical addition. Most of the LPC is eventually converted into carboxylic acids. The complete mineralization of these carboxylic acids by sonolysis is however a comparatively slow process due to the hydrophilic nature of these low molecular weight products.     

On a new condition distinguishing Weyl and Lorentz space-times

The paper is concerned with the derivability of a Lorentz instead of only a Weyl manifold as space-time structure from postulates about free fall and light propagation. For this purpose it identifies a property distinguishing both kinds of space-times. The property is one of a particular metric of the conformal class of the Weyl manifold. viz. that in suitably chosen locally geodesic coordinates theg _i4 components,i=1, 2, 3 vanish along the time axis. Although seemingly somewhat hidden, one is led to this property in looking for a metric which can play a distinguished role. We demonstrate that for a Lorentzian manifold such a condition is always given; thus it is a necessary one. It is sufficient since for a Weyl space it has the consequence that the metric connection of the selectedg is projectively equivalent to the Weyl connection. Thus, if a Weyl space-time complies with it, it is a reducible one. The results of this paper lay the ground for deriving in a second step this condition from a simple, empirically testable postulate about free-fall worldlines and “radar” measurements by light signals.     

Quantitative assessment of solid oxide electrochemical doping

Quantitative analysis of metal cation doping by solid oxide electrochemical doping (SOED) has been performed under galvanostatic doping conditions. A M–β″-Al₂O₃ (M=Ag, Na) microelectrode (contact radius: about 10 μm) was used as cation source to attain a homogeneous solid–solid contact between the β″-Al₂O₃ and doping target. In Ag doping into alkali borate glass, the measured dopant amount closely matched the theoretical value. High Faraday efficiencies of above 90% were obtained. This suggests that the dopant amount can be precisely controlled on a micromole scale by the electric charge during electrolysis. On the other hand, current efficiencies of Na doping into Bi₂Sr₂CaCu₂O_y (BSCCO) ceramics depended on the applied constant current. Efficiencies of above 80% were achieved at a constant current of 10 μA (1.6 A cm⁻²). The relatively low efficiencies were explained by the saturation of BSCCO grain boundaries with Na. By contrast, excess Na was detected on the anodic surface of ceramics at a constant current of 100 μA (16 A cm⁻²). In the present study, we demonstrate that SOED enables micromole-scale control over dopant amount.     

Electron-impact dissociation and transient properties of a stored LiH2 - beam

The fragmentation of LiH₂ ^- anions after electron impact was investigated at the heavy-ion storage ring TSR. The main reaction channel was found to be electron detachment followed by a breakup into LiH + H. In the first ms after production of the molecular ions in a cesium sputtering ion source, additional contributions were observed in the Li + H₂ and Li^- + H₂ channels, hinting at an initial population of a short-lived state of the anion. To gain a better understanding of the mechanisms underlying the observed behavior of the system, ab initio calculations of relevant potential energy surfaces were performed at selected geometries. The experimental findings are discussed in the light of these calculations.     

On the changes in the microwave dielectric spectrum of aqueous phospholipid bilayer solutions at the ordered-fluid phase transition

The microwave part of the dielectric spectrum (ν ? 1 GHz) is considered of aqueous phospholipid solutions in the limit of high water content. A continuum model is presented which allows to calculate in the water relaxation region the frequency-dependent complex permittivity of solutions in which the bilayers form globular single-walled vesicles as well as multilamellar liposomes. The model is not only capable of explaining the strikingly small values of the extrapolated static permittivity and of the main dielectric relaxation time which became evident in many measurements on colloidal aqueous solutions of phospholipids. It also allows the positive and negative step-like changes in the dielectric properties of solutions, which have been found at the main (order-disorder) phase transition temperature of the bilayers, to be explained by dimensional changes as resulting from vesicle growth and fusion.     

Non-interferometric transient quantitative phase microscopy for ultrafast engineering

Lead-free piezoelectric ceramics Bi_0.5(Na_1-x-yK_xAg_y)_0.5TiO₃ [BNKAT(x/y)] have been synthesized by the mixed oxide method. The effects of the amount of K⁺ and Ag⁺ on the electrical properties were examined. X-ray diffraction patterns indicate that K⁺ and Ag⁺ ions partially substitute for the Na⁺ ions in Bi_0.5Na_0.5TiO₃ and form a solid solution during sintering. At room temperature, the ceramics exhibit good performances with piezoelectric constant d₃₃=189 pC/N, electromechanical coupling factor k_p=35.0%, remanent polarization P_r=39.5 μC/cm², and coercive field E_c=3.3 kV/mm, respectively. The curves of the dielectric constant ε_r and loss tangent tan δ versus temperature show that the transition temperature from ferroelectric to anti-ferroelectric phase decreases with increasing the K⁺ content for the compositions researched. The dependencies of k_p and polarization versus electric (P–E) hysteresis loops on temperature reveal that the depolarization temperature T_d of BNKAT(0.15/0.015) ceramics, which have good piezoelectric properties (d₃₃=134 pC/N, k_p=32.5%) and strong ferroelectricity (P_r=39.5 μC/cm², E_c=4.1 kV/mm) at room temperature, is above 160 °C. PACS 77.22.-d; 77.65.Bn; 77.80.Bh; 77.80.Dj; 77.84.Dy     

Experimental results on neutrino-electron scattering

A determination of sin² θ _w based on measurements of elastic scattering of muon-neutrinos and muon-anti-neutrinos on atomic electrons is described. These purely leptonic processes were studied using the CHARM calorimeter exposed to neutrino and antineutrino wide-band beams at the CERN super proton synchrotron. A total of 83±16 neutrino-electron and 112±21 antineutrino-electron events have been detected. From the measurement of the ratio of muon-neutrino and muon-antineutrino cross-sections a value of sin² θ _w =0.211±0.037 was obtained.