Elastic properties and structural studies on lead-boro-vanadate glasses

This paper describes elastic properties and spectroscopic studies on the xPbO-50B₂O₃-(50 - x)V₂O₅ (where x = 20, 25, 30, 35, 40, 45 and 49 mol%) glass system. Elastic moduli and spectroscopic parameters exhibit compositional dependent trends and the existence of characteristic borovanadate groups in these glasses. The bulk modulus and shear modulus increase with the concentration of [BO_4/2]⁻ and [B₂V₂O₉]²⁻ groups, which increases the dimensionality of the network. The scheme of modification of borate and vanadate groups has been explained by considering the Sanderson’s electronegativity principle. Analysis of infrared(IR) and magic angle spinning-nuclear magnetic resonance (MAS-NMR) spectra suggests the presence of characteristic diborovanadate groups also in these glasses. The results are examined in view of the structural groups formed due to the presence of PbO as a modifier.     

Precursors of long-range order and local disorder in colloids

We show the existence of precursors of crystalline and amorphous phases preceding the appearance of freezing and glass transitions in colloidal systems. The formation of crystalline clusters or amorphous local arrangements can be controlled by tuning the parameters of a proposed continuous potential and by changing the packing conditions.     

Well defined transition to gel–like aggregates of attractive athermal particles

In an attempt to extend the range of model jamming transitions, we simulate systems of athermal particles which attract when slightly overlapping. Following from recent work on purely repulsive systems, dynamics are neglected and relaxation performed via a potential energy minimisation algorithm. Our central finding is of a transition to a low-density tensile solid which is sharp in the limit of infinite system size. The critical density depends on the range of the attractive regime in the pair-potential. Furthermore, solidity is shown to be related to the coordination number of the packing according to the approximate constraint-counting scheme known as Maxwell counting, although more corrections need to be considered than with the repulsive-only case, as explained. We finish by discussing how the numerical difficulties encountered in this work could be overcome in future studies.     

Dynamical diversity and metastability in a hindered granular column near jamming

Granular media jam into a panoply of metastable states. The way in which these states are achieved depends on the nature of local and global constraints on grains; here we investigate this issue by means of a non-equilibrium stochastic model of a hindered granular column near its jamming limit. Grains feel the constraints of grains above and below them differently, depending on their position. A rich phase diagram with four dynamical phases (ballistic, activated, logarithmic and glassy) is revealed. The statistics of the jamming time and of the metastable states reached as attractors of the zero-temperature dynamics is investigated in each of these phases. Of particular interest is the glassy phase, where intermittency and a strong deviation from Edwards' flatness are manifest.     

The kinetics of the structural relaxation process in PHEMA-silica nanocomposites based on an equation for the configurational entropy

The enthalpy relaxation of polymer-silica nanocomposites prepared by simultaneous polymerization of poly(2-hydroxyethyl methacrylate) (PHEMA) and tetraethyloxysilane, TEOS, a silica precursor, is investigated. Both the glass transition temperature, T_g, and the temperature interval of the glass transition, ΔT _g , increase as the silica content in the sample does. Structural relaxation experiments show that the temperature interval in which conformational motions take place broadens as the silica content in the hybrid increases. A phenomenological model based on the evolution of the configurational entropy during the structural relaxation process, the SC model, has been used for determining the temperature dependence of the relaxation times during the process. The results show an increase of the fragility of the polymer as the silica content increases, a feature that can be related to the broadening of the distribution of relaxation times characterized by the β parameter of the stretched exponential distribution. On another hand the silica content increase produces a significant change of the relaxation times in the glassy state.     

Nanosecond laser damage resistance of differently prepared semi-finished parts of optical multimode fibers

Optical multimode fibers are applied in materials processing (e.g. automotive industry), defense, aviation technology, medicine and biotechnology. One challenging task concerning the production of multimode fibers is the enhancement of laser-induced damage thresholds. A higher damage threshold enables a higher transmitted average power at a given fiber diameter or the same power inside a thinner fiber to obtain smaller focus spots.In principle, different material parameters affect the damage threshold. Besides the quality of the preform bulk material itself, the drawing process during the production of the fiber and the preparation of the fiber end surfaces influence the resistance. Therefore, the change of the laser-induced damage threshold of preform materials was investigated in dependence on a varying thermal treatment and preparation procedure.Single and multi-pulse laser-induced damage thresholds of preforms (F300, Heraeus) were measured using a Q-switched Nd:YAG laser at 1064 nm wavelength emitting pulses with a duration of 15 ns, a pulse energy of 12 mJ and a repetition rate of 10 Hz. The temporal and spatial shape of the laser pulses were controlled accurately.Laser-induced damage thresholds in a range from 150 J cm⁻² to 350 J cm⁻² were determined depending on the number of pulses applied to the same spot, the thermal history and the polishing quality of the samples, respectively.     

A quantum field theory of the liquid-glass transition in multi-component liquids

An established unified theory of the liquid-glass transition in one-component liquids is extended to multi-component liquids. The universal features such as the Kauzmann paradox, the Vogel-Tamman-Fulcher (VTF) law on the relaxation times and the transport coefficients, the jump of the specific heat at the glass transition temperature and the Boson peaks are elucidated. The Kauzmann entropy in a form of a Curie law with a negative sign comes from the mixing between the sound and the intra-band fluctuation entropies, where the critical temperature corresponds to the sound instability temperature at a reciprocal particle distance. The VTF law is constructed from the Einstein relation on entropy and probability so that the Kauzmann entropy is included as a normal form in exponent of the VTF law. The Kauzmann entropy explains the Kauzmann paradox and the jump of the specific heat so that the universal features of the glass transition are elucidated consistently.     

Role of Viscosity Stratification and Insoluble Surfactant in Instability of Two-Layer Channel Flow

We study, for the case of the two layer plane Poiseuille flow, the effect of viscosity stratification and interracial surfactant on the flow instability. Considering a normal mode of the streamwise wave number α, both the linear and energy analyses are presented. The expressions of perturbation energy supplied at the interface are derived. The result demonstrates that the jumps of horizontal velocity and tangential stress of the perturbed flow across the interface could be induced by the presence of viscosity stratification and surfactant. This is expected to be responsible for the Yih and Marangoni instability.     

Equilibration of fluid-phase coexistence in polydisperse particle systems with short- and moderate-range depletion attractions

Gibbs ensemble Monte Carlo (GEMC) simulations have been done on polydisperse systems of particles interacting via the Asakura-Oosawa depletion potential. On restricting the range of the depletion attraction particles aggregate forming long-lived, unequilibrated structures and it becomes increasingly difficult to sample phase space. It is found that by simply equilibrating systems sequentially starting at longer ranges of attraction, the equilibrium fluid-fluid phase coexistence can be determined down to polymer-colloid size ratios approaching 10%. For such short ranges of the depletion interaction it becomes difficult to obtain reliable estimates of chemical potentials due to occasional particle insertions resulting in very low energies. The results show that full equilibrium is not reached at a polymer-colloid size ratio of 10% in spite of lengthy simulations due to persistent structures in the dense-fluid phase dominated by particles belonging to the larger size fraction. Free-volume theory with a polydisperse colloid component, modeled as a three-component mixture, is used for qualitative comparison with some of the results of the computer simulations.