Connecting Dynamics and Thermodynamics in Polymer-Resin Cured Systems.

This work connects the calorimetric responses of different rubber-resin blends with varying resin contents with their alpha relaxation dynamics. We used differential scanning calorimetry and broadband dielectric spectroscopy to characterize the calorimetric and dielectric responses of styrene-butadiene, polybutadiene, and polyisoprene with different resin contents. To model the results, we used the Gordon-Taylor equation combined with an extension of the Adam-Gibbs approach.

Approaching Polymer Dynamics Combining Artificial Neural Networks and Elastically Collective Nonlinear Langevin Equation.

The analysis of structural relaxation dynamics of polymers gives an insight into their mechanical properties, whose characterization is used to qualify a given material for its practical scope. The dynamics are usually expressed in terms of the temperature dependence of the relaxation time, which is only available through time-consuming experimental processes following polymer synthesis. However, it would be advantageous to estimate their dynamics before synthesizing them when designing new materials.

AFM based dielectric spectroscopy: extended frequency range through excitation of cantilever higher eigenmodes.

In the last years, a new AFM based dielectric spectroscopy approach has been developed for measuring the dielectric relaxation of materials at the nanoscale, the so called nanoDielectric Spectroscopy (nDS). In spite of the effort done so far, some experimental aspects of this technique remain still unclear. In particular, one of these aspects is the possibility of extending the experimental frequency range, to date limited at high frequencies by the resonance frequency of the AFM cantilever as a main factor.

Determining concentration depth profiles in fluorinated networks by means of electric force microscopy.

By means of electric force microscopy, composition depth profiles were measured with nanometric resolution for a series of fluorinated networks. By mapping the dielectric permittivity along a line going from the surface to the bulk, we were able to experimentally access to the fluorine concentration profile. Obtained data show composition gradient lengths ranging from 30 nm to 80 nm in the near surface area for samples containing from 0.

High pressure dynamics of polymer/plasticizer mixtures.

Plasticizers are usually added to polymers to give them the desired flexibility and processability by changing the dynamical properties of the polymer chains. It is therefore important to give a quantitative description about how the dynamic behavior of a given polymer is modified by the incorporation of a second component. We analyze in this work, by means of dielectric spectroscopy, the dynamics of poly(vinyl acetate)/diethyl phthalate mixtures, at different concentrations, over a broad range of frequency, pressure, and temperature.

Adam-Gibbs based model to describe the single component dynamics in miscible polymer blends under hydrostatic pressure.

We present in this work a new model to describe the component segmental dynamics in miscible polymers blends as a function of pressure, temperature, and composition. The model is based on a combination of the Adam-Gibbs (AG) theory and the concept of the chain connectivity. In this paper we have extended our previous approach [D.

Describing the component dynamics in miscible polymer blends: towards a fully predictive model.

We have recently proposed [D. Cangialosi et al., J.

Glass transition and relaxation processes in supercooled water.

Many of water's peculiar physical properties are still not well understood, and one of the most important unresolved questions is its glass transition related dynamics. The consensus has been to accept a glass transition temperature (T(g)) around 136 K, but this value has been questioned and reassigned to about 165 K. We find evidence that the dielectric relaxation process of confined water that has been associated with the long accepted T(g) of water (130-140 K) must be a local process which is not related to the actual glass transition.

Relaxation dynamics of a polymer in a 2D confinement.

The molecular dynamics of oligomeric poly(propylene glycol) (PPG) liquids (MW=1000, 2000, and 4000 g/mol) confined in a two-dimensional layer-structured Na-vermiculite clay has been studied by broadband dielectric spectroscopy. The alpha-relaxation and the normal mode relaxation processes were studied for all samples in bulk and confinement. The most prominent experimental observation was that for the normal mode process: the relaxation rate in the clay is drastically shifted to lower frequencies compared to that of the bulk material.