Intermittency in the Fisher's droplet model

Intermittent behaviour of fragment multiplicity distributions in the nuclear liquid-gas phase transition is studied in terms of the droplet model of Fisher. The anomalous fractal dimensions are compared with data on heavy ion reactions and classical molecular dynamics simulations. A signature of the transition in the anomalous fractal dimensions is shown.We thank Profs. S. Ayik, M. Di Toro and V. Kondratyev for discussions. One of us (T.K.) acknowledges the support of INFN-LNS.     

Photochemically induced fluorescence investigation of aβ-cyclodextrin: Azure A inclusion complex and determination of analytical parameters

The photooxidation of Azure A and fluorescence properties of Azure A and its photoproduct have been investigated in aqueous media and in the presence of-cyclodextrin (-CD). The fluorescence intensity of the complex formed between the photoproduct and -CD was found to be three times higher than that of the uncomplexed Azure A photoproduct. A complex formation constant of 110±40 M^–1 was calculated using the Benesi-Hildebrand treatment of the fluorescence emission data. Although the stoichiometry of the Azure A photoproduct: -CD complex was found to be 1: 1, it seems that the Azure A structure is only partially included. Calibration graphs were plotted for the free Azure A photoproduct and the photogenerated product included in -CD. The analytical parameters and quantification limits were determined.     

Electrosynthesis,characterization and photoconducting performance of copolymer poly(terthiophene + sexithiophene + TiO<Subscript>2</Subscript>)/ITO composite material

In the present work, a new composite material poly(3T + 6T + TiO₂) was electrochemically synthesized. This composite material was synthesized in a solution of (CH2Cl2/TBAP) containing the monomers (terthiophene), (sexithiophene) and semiconductor (TiO₂) particles. The preparedsamples were characterized electrochemically by cyclic voltamperometry (CV) and spectrometry analysis by scanning electron microscopy (SEM), ultraviolet-visible (UV-Vis) absorption spectroscopy, energy dispersive X-ray spectroscopy (EDX) and fourier transform infrared spectroscopy (FTIR), respectively. The effect of TiO₂ concentration in the solution on dispersed microparticle entity and on the photocurrent response was investigated. The results showed that TiO₂ particles were dispersed and codeposited into the copolymer poly(3T + 6T + TiO₂) matrix, and titanium atom was confirmed by EDX spectra. From SEM images, the TiO₂ has a spherical shape and micrometer size. The FTIR spectrum indicated that titanium dioxide do not show a significant modification in terms of band shape and no interaction between polymers and TiO₂ particles. Furthermore, the results showed that the composite films with different amounts of TiO₂ exhibit good photocurrent properties which imply that these composites films can be used in various fields, such as photoelectrochemical applications as photovoltaic cells.     

Study of Electrical Conductivity of Para-Toluene Sulfonic Acid Doped Polyaniline/Polyester-Based Polyurethane Blends in the S-Band Frequency Range

Conducting polymer blends were prepared using polyaniline doped with para- toluene sulfonic acid (PTSA-PANI) and a polyester polyol-based polyurethane (PU). The morphological, thermal and dielectric properties of the PTSA-PANI/PU blends in the frequency range of 1–5 GHz (S band) were investigated. It was found that the morphology of the samples was affected by the PTSA-PANI loading, resulting in the formation of agglomerates and pathways when above 10 wt%. The thermal stability of the composites was improved with increased PTSA-PANI loading. The electrical conductivity percolation threshold was obtained at 2.5% of PTSA-PANI loading and the electrical conductivity reached the value of 0.13 S/m at a PTSA-PANI loading of 30 wt%. The obtained results for the PTSA-PANI/PU blends prepared indicate a high potential for their successful use in electrical and electromagnetic applications.     

Non-linear structure of the light-intensity-output versus pump-input characteristics in self-pulsing lasers

This paper is intended to show that laser-intensity-output versus excitation characteristics of bad-cavity configured lasers deviate from the linearly expected evolution when these are driven beyond the instability threshold. These deviations result in collapsed curves with marked and discernible intensity-reduction at the onset of instability. Such behaviors are shown to be rooted in the fundamental and intrinsic aspects of both the single mode homogeneously-broadened laser and the inhomogeneously-broadened system. In addition, we clarify, for the first example, the physical origin of a hysteresis effect which is known to occur when the pump-input power is scanned from levels above to levels below the instability threshold. As for the inhomogeneous case, a lateral hole-burning effect, which takes place in the spectral profile at high excitations, is shown to shift the output-intensity towards higher levels, with respect to the steady-state values. Simple theoretical elements are put forward to identify the physical origin of these features.     

A new approach to A,B-difunctionalisation of cyclodextrins using bulky 1,3-bis[bis(aryl)chloromethyl]benzenes as capping reagents

1,3-Bis[bis(4-tert-butylphenyl)chloromethyl]benzene and 1,3-bis[bis(4-anisyl)chloromethyl]benzene were employed as regioselective capping reagents for the preparation of C-6A,C-6B-bridged, permethylated alpha- and beta-CD derivatives; isolated yields up to 55% of proximally capped, methylated CDs were obtained, thus opening the way to the straightforward preparation of a wide range of A,B-functionalised CDs. As revealed by a single crystal X-ray diffraction study, the benzene-1,3-bis[bis(4-tert-butylphenyl)methyl] spacer is perfectly suited for A,B-capping of beta-cyclodextrin.     

Performance of hydrodynamic journal bearing under the combined influence of textured surface and journal misalignment: A numerical survey

A wisely chosen geometry of micro textures with the favorable relative motion of lubricated surfaces in contacts can enhance tribological characteristics. In this paper, a computational investigation related to the combined influence of bearing surface texturing and journal misalignment on the performances of hydrodynamic journal bearings is reported. To this end, a numerical analysis is performed to test three texture shapes: square “SQ”, cylindrical “CY”, and triangular “TR”, and shaft misalignment variation in angle and degree. The Reynolds equation of a thin viscous film is solved using a finite differences scheme and a mass conservation algorithm (JFO boundary conditions), taking into account the presence of textures on both full film and cavitation regions. Preliminary results are compared with benchmark data and are consistent with a positive enhancement in misaligned bearing performances (load carrying capacity and friction). The results suggest that the micro-step bearing mechanism is a key parameter, where the micro-pressure recovery action present in dimples located at the second angular part of the bearing (from 180° to 360°) can compensate for the loss on performances caused by shaft misalignment, while the micro-pressure drop effect at the full film region causes poor performances. Considering the right arrangement of textures on the contact surface, their contours geometries can have a significant impact on the performance of misaligned journal bearings, particularly at high eccentricity ratios, high misalignment degrees and when the misalignment angle α approaches to $0\mathrm{°}$ or $180\mathrm{°}$.     

Hydrogen bonding interactions between α-, β-glucose,and methacrylic acid

Intermolecular interactions between α-, β-glucose, and methacrylic acid (MAA) have been investigated. Twenty-two possible conformations have been optimized at the DFT(B3LYP) level of theory with the 6-31G(d) basis set. The geometrical parameters for the most stable configurations of hydrogen bonding sites in the optimized systems have been determined. The binding energies ΔE _bind have been calculated at the MP2/6-311++G(d,p) level of approximation taking into account the basis set superposition error (BSSE) and the zero-point vibrational energies corrections. Results indicate that the most stabilized complexes form hydrogen bonds either through carboxylic and hemiacetal oxygen atoms acting as proton acceptors. Both, α- and β-anomers are studied in the pyranose six-membered ring. In all complexes, the nuclear quadrupole coupling constants (χ) for ¹⁷O nuclei were obtained about 10.0 MHz, while for the ²H atoms they vary from ≈200.0 to ≈350.0 kHz.