The autofocusing system of the IMAT neutron camera.

In this paper, we present the autofocusing system of the imaging instrument to be used on IMAT, a new neutron-imaging facility under construction at the ISIS (UK) target station 2. We have compared 16 different autofocus algorithms to select the one with the best performance. The algorithms have been evaluated by using both a qualitative analysis and a quantitative one. An overall score has been computed and the "contrast based" algorithm has been selected for the autofocusing system. The adopted setup together with the described autofocusing system makes the camera a user-friendly imaging device allowing the optimization of beam time use.

Enhancement of electrorheological effect by particle-fluid interaction.

The influence of interactions between particle surface and host fluids in electrorheological suspensions is explored. It is observed that dispersions of nanosized particles of titania in octanoid acid exhibit an anomalously large electrorheologic effect when compared with a similar dispersion of micrometric particles or with a more conventional colloidal suspension of silica in silicone oil. The effect is interpreted as originated by the formation of a thin layer of octanoid acid molecules with the surface of the titania solid particle. The experimental data are fitted with the outcomes of a modified version of conductive models existing in the literature. It is suggested that anomalous large electrorheological effect is mainly originated by the increasing of the effective radius of the nanometric particles, which results in an increasing of the effective volume fraction of the dispersed phase. It is also shown that the deformation of the soft shell around the solid particles, induced by Coulombic force, plays a not negligible role. Some hints for tailoring electrorheologic fluids suitable for different applications are proposed.

High-frequency propagating density fluctuations in deeply supercooled water: evidence of a single viscous relaxation.

We performed a Brillouin scattering experiment on deeply supercooled water and compared the results with similar literature data obtained both at the same and at higher values of the exchanged wave vector. The whole set of available experimental data can be well reproduced with the use of the generalized hydrodynamic model where all the involved thermodynamic parameters are fixed to their literature values. On the contrary, the model based on the memory function approach generates the wrong estimates for measurables when the same values of the thermodynamic parameters are used. This result confirms our recent criticisms against the utilization of models originating from linear response theory [Phys. Rev. E 84, 051202 (2011)]. The inconsistency between models explains apparent discrepancies between the different conclusions on water acoustic behavior which may be found in the literature. We demonstrate that the observed behavior can be explained by assuming only a single relaxation process that is typical of any viscoelastic system. With all thermodynamics quantities fixed, the hydrodynamic description needs only two parameters to model the experimental data, namely, the relaxation time and the high-frequency limit of the sound velocity. The whole body of the experimental data can be well reproduced when the relaxation time behaves in an Arrhenian manner and the difference between the relaxed and not relaxed sound velocities is a constant. The high-frequency sound velocity is never higher than 2200 m/s. We conclude that, at least from experiments performed within the hydrodynamic regime, there is no indication for a fast sound close to the hypersonic velocity observed in ice.

Low-energy vibrational dynamics of cesium borate glasses.

Low-temperature specific heat and inelastic light scattering experiments have been performed on a series of cesium borate glasses and on a cesium borate crystal. Raman measurements on the crystalline sample have revealed the existence of cesium rattling modes in the same frequency region where glasses exhibit the boson peak (BP). These localized modes are supposed to overlap with the BP in cesium borate glasses affecting its magnitude. Their influence on the low frequency vibrational dynamics in glassy samples has been considered, and their contribution to the specific heat has been estimated. Evidence for a relation between the changes of the BP induced by the increased amount of metallic oxide and the variations of the elastic medium has been provided.

Collective acoustic modes in liquids: a comparison between the generalized-hydrodynamics and memory-function approaches.

The most familiar approaches used to describe the dynamical structure factor from adiabatic density fluctuations in liquids are based on generalized hydrodynamics and on the memory function, respectively. We show that, contrary to the common belief, the two approaches are not fully equivalent. In particular, models based on the memory function of a normalized damped oscillator fail in reproducing the correct experimental spectral profiles of systems close to the relaxation process. The discrepancy is due to misleading interpretation of the theoretical memory-function expressions, producing an unavoidable mixing of spectral contribution at different wave vectors when the theory is forced beyond its limits of validity.

Communication: An extended model of liquid bridging.

Recent phenomenological studies have drawn attention to an appealing effect, observed for the first time in 1893, today known as water-bridge. The phenomenon has been ascribed to unknown properties of water. We report some experimental results showing that, contrary to a widely common belief, the phenomenon is not to be related with water neither with a property of hydrogen bonded networks. Using a very simple model, we show that the liquid bridge phenomenon is originated by electrostatic effects and can be reproduced in any dense fluid with no respect of its peculiar molecular properties. This basic approach is able to reproduce many of the experimentally observed features of the bridge formation. In perspective of future investigations, the possible phenomena responsible of the bridge stability, after its formation, are briefly discussed.

A mean field analysis of the O-H stretching Raman spectra in methanol/carbon tetrachloride mixtures.

The O-H stretching region of the Raman spectra obtained from methanol/carbon tetrachloride mixtures of different compositions is analyzed. The various components of the spectra associated with methanol molecules with different H-binding states (i.e., non-H-bonded, chain-end, and doubly bonded) are quantitatively related with the alcohol cluster distribution derived by means of a simple lattice model. This comparison allows for the estimate of the mean overall hydrogen bonding energy by means of a best fitting procedure on the Raman data obtained at low-to-moderate alcohol contents; the solvation energy contribution of carbon tetrachloride is then also included. The result (approximately 3 kcal/mol) is found to be in agreement with the estimates from calorimetric and dielectric measurements.

Near-field Raman imaging of morphological and chemical defects in organic crystals with subdiffraction resolution.

In this study we report on the application of an aperture near-field optical microscope for Raman imaging of organic materials. Spectral analysis and detailed Raman imaging are performed with integration times of 100 ms per point, without the aid of field enhancement effects. The studied samples consist of two high Raman-efficiency molecular samples: a 7,7',8,8'-tetracyanoquinodimethane crystal showing surface defects and a 7,7',8,8'-tetracyanoquinodimethane thin film characterized by the presence of submicrometre-sized organometallic copper-salt complexes. In the first case, the effect of the surface deformation was studied, whereas in the second sample we were able to chemically image the formation of salt complexes. Subdiffraction resolution was achieved in both studies.

Single-particle dynamics of water molecules confined in a lecithin-based gel.

We present experimental measurements, obtained by a quasielastic neutron scattering experiment, of the self-diffusion coefficient of water confined in the dense structure of lecithin-based gels. The inelastic neutron scattering (INS) technique was also used to monitor the dynamic state of water molecules involved in the gel structure. It is shown that, at least in highly concentrated systems, the diffusional properties of water can be related with the growth process of worm-like aggregates. However, an interpretation of our data consistent with a number of experimental results in the literature and with INS indications requires the adoption of a model in which the gel structure is better described in terms of percolating aggregates rather than the usually described polymer-like entangled (not interconnected) network. In such a way, we are pointing out the existence of an interpretative controversy calling for further investigation to be disentangled. The source of the inconsistencies is found in the commonly accepted basic assumption of the existence of a simple scaling law, relating the average micellar length to the concentration.