Biomedical subjects

F Sette

Publications and source records attributed to F Sette.

At least 37 records · Page 2Linked to original sources

PubMed2000

Nature of the short wavelength excitations in vitreous silica: An X-Ray brillouin scattering study

The dynamical structure factor [ S(Q,E)] of vitreous silica has been measured by inelastic x-ray scattering varying the exchanged wave vector ( Q) at fixed exchanged energy ( E)-an experimental procedure that, contrary to the usual one at constant Q, provides spectra with much better identified inelastic features. This allows us to obtain the first direct evidence of Brillouin peaks in the S(Q,E) of SiO2 at energies above the boson peak (BP) energy, a finding that excludes the possibility that the BP marks the transition from propagating to localized dynamics in glasses.

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PubMed2000

Experimental evidence of the acousticlike character of the high frequency excitations in glasses

The dynamic structure factor S(Q,E) of glassy glycerol has been measured by inelastic x-ray scattering as a function of momentum transfer Q and at constant energy transfer E. This allows one to establish independently from specific models of S(Q,E) the following: (i) Propagating collective excitations exist in glasses at high Q. (ii) Their dispersion up to E higher than E(BP) (the boson peak energy) confirms that E(BP) is not the onset of modes localization. (iii) The observation of an almost Q independent plateau on the high Q side of the Brillouin peak supports numerical simulations on glasses, describing the vibrational eigenvectors in terms of acousticlike and "random" components.

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PubMed2000

Relaxation processes in harmonic glasses?

A relaxation process, with the associated phenomenology of sound attenuation and sound velocity dispersion, is found in a simulated harmonic Lennard-Jones glass. We propose to identify this process with the so-called microscopic (or, instantaneous) relaxation process observed in real glasses and supercooled liquids. A model based on the memory function approach accounts for the observation and allows one to relate to each other (1) the characteristic time and strength of this process, (2) the low frequency limit of the dynamic structure factor of the glass, and (3) the high frequency sound attenuation coefficient, with its observed quadratic dependence on the momentum transfer.

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PubMed2000

Determination of the short-wavelength propagation threshold in the collective excitations of liquid ammonia

The dynamics structure factor S(Q,E) of liquid ammonia l-NH3 at T = 200 K and at its vapor pressure has been measured by inelastic x-ray scattering (IXS) in the 1-15 nm(-1) momentum transfer ( Q) range. Contrary to previous IXS studies on other associated liquids and glasses, in l-NH3 a large inelastic signal is observed up to Q = 15 nm(-1). This, enabling S(Q,E) measurements as a function of Q at constant E transfer, allows us to demonstrate experimentally the transition from a propagating dynamics regime, where the acoustic excitation energy linearly disperses with Q, to a high-Q regime, where it is no longer possible to observe a dominant excitation in the S(Q,E).

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PubMed2000

Analysis of inelastic x-ray scattering spectra of low-temperature water

We analyze a set of high-resolution inelastic x-ray scattering (IXS) spectra from H2O measured at T=259, 273, and 294 K using two different phenomenological models. Model I, called the "dynamic cage model," combines the short time in-cage dynamics described by a generalized Enskog kinetic theory with a long-time cage relaxation dynamics described by an alpha relaxation. This model is appropriate for supercooled water where the cage effect is dominant and the existence of an alpha relaxation is evident from molecular-dynamics (MD) simulation data of extended simple point charge (SPC/E) model water. Model II is essentially a generalized hydrodynamic theory called the "three effective eigenmode theory" by de Schepper et al. 11. This model is appropriate for normal liquid water where the cage effect is less prominent and there is no evidence of the alpha relaxation from the MD data. We use the model I to analyze IXS data at T=259 K (supercooled water). We successfully extract the Debye-Waller factor, the cage relaxation time from the long-time dynamics, and the dispersion relation of high-frequency sound from the short time dynamics. We then use the model II to analyze IXS data at all three temperatures, from which we are able to extract the relaxation rate of the central mode and the damping of the sound mode as well as the dispersion relation for the high-frequency sound. It turns out that the dispersion relations extracted from the two models at their respective temperatures agree with each other giving the high-frequency sound speed of 2900+/-300 m/s. This is to be compared with a slightly higher value reported previously, 3200+/-320 m/s, by analyzing similar IXS data with a phenomenological-damped harmonic oscillator model 22. This latter model has traditionally been used exclusively for the analysis of inelastic scattering spectra of water. The k-dependent sound damping and central mode relaxation rate extracted from our model analyses are compared with the known values in the hydrodynamic limit.

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PubMed1999

Viscoelastic behavior of water in the terahertz-frequency range: an inelastic x-ray scattering study.

High-resolution, inelastic x-ray scattering measurements of the dynamic structure factor S(q,omega) of liquid water in the THz frequency range have been performed as a function of wave vector q (1-7 nm(-1)) and temperature T (273-473 K), using pressure (0-1.5 kbar) to keep the density at rho approximately 1 g/cm(3). We show that, for q 2 nm(-1), we find that the viscoelastic contribution to the memory function becomes q dependent. Thus this work provides a view on the evolution of the collective dynamics of water across the q region where the continuum approximation inherent in the hydrodynamic formulation begins to fail. The physical consequences of such a result are discussed in some detail.

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PubMed1999

Brillouin and Umklapp scattering in polybutadiene: comparison of neutron and x-ray scattering.

We report a comparison of high resolution inelastic x-ray Brillouin scattering to coherent inelastic neutron scattering for amorphous deuterated polybutadiene, done for one temperature in the glass phase and another one in the melt. The x-ray scattering proves to be by far the better technique for such a polymer within its present resolution bounds. The neutron scattering allows one to extend these measurements to a much better resolution, showing an additional quasielastic signal in the melt. The results suggest x-ray measurements at higher momentum transfer, to see whether they are complementary to neutrons.

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PubMed1996