Biomedical subjects

A Arbe

Publications and source records attributed to A Arbe.

16 recordsLinked to original sources

PubMed2005

Dynamics of poly(ethylene oxide) in a blend with poly(methyl methacrylate): a quasielastic neutron scattering and molecular dynamics simulations study.

In this paper, we have addressed the question of the dynamic miscibility in a blend characterized by very different glass-transition temperatures, Tg, for the components: poly(ethylene oxide) and poly(methyl methacrylate) (PEO/PMMA). The combination of quasielastic neutron scattering with isotopic labeling and fully atomistic molecular dynamics simulations has allowed us to selectively investigate the dynamics of the two components in the picosecond-10 nanoseconds scale at temperatures close and above the Tg of the blend. The main focus was on the PEO component, i.e., that of the lowest Tg, but first we have characterized the dynamics of the other component in the blend and of the pure PEO homopolymer as reference. In the region investigated, the dynamics of PMMA in the blend is strongly affected by the alpha-methyl rotation; an additional process detected in the experimental window 65 K above the blend-Tg can be identified as the merged alphabeta process of this component that shows strong deviations from Gaussian behavior. On the other hand, pure PEO displays entropy driven dynamics up to very large momentum transfers. Such kind of motion seems to freeze when the PEO chains are in the blend. There, we have directly observed a very heterogeneous and moreover confined dynamics for the PEO component. The presence of the hardly moving PMMA matrix leads to the creation of little pockets of mobility where PEO can move. The characteristic size of such confined islands of mobility might be estimated to be of approximately 1 nm. These findings are corroborated by the simulation study, which has been an essential support and guide in our data analysis procedure.

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PubMed2005

Sub-Tg dynamics in polycarbonate by neutron scattering and its relation with secondary gamma relaxation.

We have investigated the dynamics of phenylene rings in glassy bisphenol-A (BPA) polycarbonate (PC) by means of quasielastic neutron scattering. Taking advantage of selective deuteration of the samples, we have studied the incoherent scattering of hydrogens in phenylene rings on the one hand, and on the other hand the coherent quasielastic scattering of all the atoms in the sample. Two different types of neutron spectrometers, time of flight and backscattering, were used in order to cover a wide dynamic range, which extends from microscopic (approximately 10(-13) s) to mesoscopic (approximately 10(-9) s) times. Moreover, neutron-diffraction experiments with polarization analysis were carried out in order to characterize the structural features, and the relative coherent and incoherent contributions of the samples investigated. In contrast with previous studies of phenylene ring dynamics in BPA polysulfone performed by us also by neutron scattering, phenylene rings in BPA PC exhibit an "extra" motion in addition to those found for BPA polysulfone's phenylene rings. This extra motion of the rings in PC perfectly correlates with the main carbonate group motion followed by dielectric spectroscopy and allows us to (i) consistently interpret the PC's gamma relaxation in terms of two different motions; and (ii) experimentally confirm the relation between the motion of phenylene rings and carbonate groups within BPA PC formerly predicted by computational methods.

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PubMed2004

Hydrogen motions in the alpha-relaxation regime of poly(vinyl ethylene): a molecular dynamics simulation and neutron scattering study.

The hydrogen motion in poly(vinyl ethylene) (1,2-polybutadiene) in the alpha-relaxation regime has been studied by combining neutron spin echo (NSE) measurements on a fully protonated sample and fully atomistic molecular dynamics simulations. The almost perfect agreement between experiment and simulation results validates the simulated cell. A crossover from Gaussian to non-Gaussian behavior is observed for the intermediate scattering function obtained from both NSE measurements and simulations. This crossover takes place at unusually low Q values, well below the first maximum of the static structure factor. Such anomalous deviation from Gaussian behavior can be explained by the intrinsic dynamic heterogeneity arising from the differences in the dynamics of the different protons in this system. Side group hydrogens show a markedly higher mobility than main chain protons. Taking advantage of the simulations we have investigated the dynamic features of all different types of hydrogens in the sample. Considering each kind of proton in an isolated way, deviations from Gaussian behavior are also found. These can be rationalized in the framework of a simple picture based on the existence of a distribution of discrete jumps underlying the atomic motions in the alpha process.

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PubMed2004

Phenylene ring dynamics in bisphenol-A-polysulfone by neutron scattering.

We have investigated the dynamics of phenylene rings in a glassy polysulfone (bisphenol-A-polysulfone) by means of quasielastic neutron scattering. Nowadays it is well known that these molecular motions are directly connected with the mechanical properties of engineering thermoplastics in general. The particular system investigated by us has the advantage that by selective deuteration of the methyl groups, the neutron scattering measured is dominated by the incoherent contribution from the protons in the phenylene rings. In this way, the dynamics of such molecular groups can be experimentally isolated. Two different types of neutron spectrometers: time of flight and backscattering, were used in order to cover a wide dynamic range, which extends from microscopic (10(-13) s) to mesoscopic (10(-9) s) times. Moreover, neutron diffraction experiments with polarization analysis were also carried out in order to characterize the structural features of the sample investigated. Fast oscillations of increasing amplitude with temperature and pi-flips are identified for phenylene rings motions. Due to the structural disorder characteristic of the amorphous state, both molecular motions display a broad distribution of relaxation times, which spreads over several orders of magnitude. Based on the results obtained, we propose a model for phenylene rings dynamics, which combines the two kinds of molecular motions identified. This model nicely describes the neutron scattering results in the whole dynamic range investigated.

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PubMed2003

Experimental evidence by neutron scattering of a crossover from Gaussian to non-Gaussian behavior in the alpha relaxation of polyisoprene.

We report incoherent quasielastic neutron scattering experiments exploring the alpha-relaxation range in polyisoprene over an unprecedented range in momentum transfer Q. The data corroborate and validate earlier molecular dynamics simulations and reveal the existence of a crossover from Gaussian to non-Gaussian character of the main chain protons self-correlation function in the alpha-relaxation regime. The real challenge of the experiment was to push the neutron techniques to cover a Q range as wide as possible. By combining two neutron spin echo spectrometers and a backscattering instrument, we have been able to study the dynamics in a Q range of 0.1 < or = Q < or = 4.7 A(-1). In the low-Q regime the shape of the relaxation function was found to be related to the dispersion of the relaxation times as predicted by the Gaussian assumption. At short distances or large Q, this relationship is strongly violated indicating a non-Gaussian regime. We have performed a detailed comparison between the experiments and simulations at different temperatures and found, apart from a temperature shift, complete agreement. Combining experiments and simulations led to a consistent interpretation in terms of a distribution of jumps underlying the diffusive motion of protons in the alpha process. This model leads to a time-dependent non-Gaussianity parameter that agrees nearly quantitatively with the simulations and exhibits all features resolved so far from various simulations.

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PubMed2002

Non-Gaussian nature of the alpha relaxation of glass-forming polyisoprene.

We report quasielastic neutron scattering experiments exploring the alpha relaxation in polyisoprene over an unprecedented range in momentum transfer. Corroborating and validating earlier molecular dynamics simulations, the measurements reveal a crossover from a Gaussian regime of sublinear diffusion to a strongly non-Gaussian regime at short distances. We show that a consistent interpretation in terms of a distribution of finite jumps underlying the alpha process is possible. This model leads to a time-dependent non-Gaussian parameter exhibiting all features revealed so far from various simulations.

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PubMed2002

Intermediate length scale dynamics of polyisobutylene.

We report on a neutron spin echo investigation of the intermediate scale dynamics of polyisobutylene studying both the self-motion and the collective motion. The momentum transfer (Q) dependences of the self-correlation times are found to follow a Q(-2/beta) law in agreement with the picture of Gaussian dynamics. In the full Q range of observation, their temperature dependence is weaker than the rheological shift factor. The same is true for the stress relaxation time as seen in sound wave absorption. The collective times show both temperature dependences; at the structure factor peak, they follow the temperature dependence of the viscosity, but below the peak, one finds the stress relaxation behavior.

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PubMed2002

Self-motion and the alpha relaxation in a simulated glass-forming polymer: crossover from Gaussian to non-Gaussian dynamic behavior.

We present fully atomistic molecular dynamics simulations for a realistic model of a glass-forming polymer: polyisoprene. The simulations are carried out at 363 K and extend until 20 ns. We calculate the self-part of the Van Hove correlation function G(s)(r,t), the mean-squared displacement , the second-order non-Gaussian parameter alpha(2)(t), and the incoherent intermediate scattering function F(s)(Q,t) for the main chain protons. In addition, we also calculate the density-density correlation function F(Q,t)/F(Q,0) and the second-order autocorrelation function M2(t) for different C-H bonds of the main chain. alpha(2)(t) shows a broad maximum centered at a time t(*) approximately 4 ps, which corresponds to the intermediate region of between microscopic dynamics and sublinear diffusion. The analysis of F(s)(Q,t), F(Q,t)/F(Q,0), and M2(t) focuses on the second slow step which is associated to the alpha relaxation. Following the usual experimental procedure this decay is described in terms of a Kohlrausch-Williams-Watts (KWW) function: A exp[-(t/tau)(beta)]. In the Q range below Q(max), where Q(max) is the value at which the static structure factor shows its first maximum, the Q dependence of the KWW relaxation time of F(s)(Q,t) follows a law tau approximately Q(-2/beta). This kind of Q dependence corresponds to a Gaussian behavior of G(s)(r,t) and F(s)(Q,t). This law has been experimentally found in this Q range for different polymers. In the higher Q range-not easily accessible experimentally-strong deviations from the Gaussian behavior manifest. This crossover from Gaussian to non-Gaussian behavior can be understood in the framework of the mode coupling theory as well as in terms of a crossover from homogeneous to heterogeneous dynamics. This last interpretation opens a possible way of rationalizing the apparent contradiction between the neutron scattering and relaxation techniques results concerning dynamical heterogeneity of the alpha relaxation.

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PubMed2000

Origin of dynamic heterogeneities in miscible polymer blends: A quasielastic neutron scattering study

In order to investigate the origin of the often invoked nanoheterogeneities in miscible polymer blends, we have performed quasielastic neutron scattering experiments on the component dynamics within the miscible polymer blend polyisoprene/polyvinyl ether including the pure components as a reference. We find that the apparent local heterogeneities observed by spectroscopic techniques originate from the chain specific crossover properties between entropy driven and local chain dynamics and are, thus, a purely dynamical phenomenon.

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PubMed1998

Investigation of the Dielectric beta-Process in Polyisobutylene by Incoherent Quasielastic Neutron Scattering.

Recently by dielectric spectroscopy a new secondary relaxation process in polyisobutylene (PIB) was detected showing all the signatures of a Johari-Goldstein relaxation [Richter, D; Arbe, A.; Colmenero, J.; Monkenbusch, M.; Farago, B.; Faust, R. Macromolecules 1998, 31, 1133]. Using high resolution neutron backscattering, we investigated the quasielastic neutron spectra from protonated PIB which are related to this process as a function of momentum transfer and temperature. In addition we studied the elastically scattered intensity over a wide temperature range. After multiple scattering corrections all results can be described consistently in terms of a local jump process with the distribution parameters from the dielectric beta-relaxation. The spatial extent of the associated protonic motion was determined to be d = 2.7 Å. A comparison with the existing body of data for PIB leads to the conclusion that the dielectric beta-process and the earlier found delta-process must be identical, thereby revising the assignment of the delta-process as due to methyl group rotation. Finally, we remark on aspects of the relation between quasielastic coherent and incoherent scattering and address the seemingly contradictory result of different length scales revealed for the same process with the two techniques.

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PubMed1996