The segmental and chain relaxation modes in high-cis-polyisoprene as studied by thermally stimulated currents.

The technique of Thermally Stimulated Currents is used to study the slow molecular mobility in a series of poly (1,4-cis-isoprene) samples with different molecular weights, Mw, and low polydispersity. The technique revealed a high resolution power, particularly useful in the study of the lower molecular weight samples where the chain and the segmental relaxations strongly overlap. The dynamic crossover that is reported for the normal mode by varying the molecular weight is clearly revealed by the thermally stimulated depolarization currents results through the temperature location, TMn, of the normal mode peak, the values of the relaxation time at TMn, τ(TMn), and the value of the fragility index of the normal mode, mn. The kinetic features of the glass transition relaxation of polyisoprene have also been determined.

Influence of the Solvent Quality on Ring Polymer Dimensions.

We present a systematic investigation of well-characterized, experimentally pure polystyrene (PS) rings with molar mass of 161 000 g/mol in dilute solutions. We measure the ring form factor at θ- and good-solvent conditions as well as in a polymeric solvent (linear PS of roughly comparable molar mass) by means of small-angle neutron scattering (SANS). Additional dynamic light scattering (DLS) measurements support the SANS data and help elucidate the role of solvent quality and solution preparation. The results indicate the increase of ring dimensions as the solvent quality improves. Furthermore, the experimental form factors in both θ-solvent and linear matrix behave as ideal rings and are fully superimposable. The nearly Gaussian conformations of rings in a melt of linear chains provide evidence of threading of linear chains through rings. The latter result has implications for the dynamics of ring-linear polymer mixtures.

Compact structure and non-Gaussian dynamics of ring polymer melts.

We present a neutron scattering analysis of the structure and dynamics of PEO polymer rings with a molecular weight 2.5 times higher than the entanglement mass. The melt structure was found to be more compact than a Gaussian model would suggest. With increasing time the center of mass (c.o.m.) diffusion undergoes a transition from sub-diffusive to diffusive behavior. The transition time agrees well with the decorrelation time predicted by a mode coupling approach. As a novel feature well pronounced non-Gaussian behavior of the c.o.m. diffusion was found that shows surprising analogies to the cage effect known from glassy systems. Finally, the longest wavelength Rouse modes are suppressed possibly as a consequence of an onset of lattice animal features as hypothesized in theoretical approaches.

Viscosity of ring polymer melts.

We have measured the linear rheology of critically purified ring polyisoprenes, polystyrenes and polyethyleneoxides of different molar masses. The ratio of the zero-shear viscosities of linear polymer melts η0,linear to their ring counterparts η0,ring at isofrictional conditions is discussed as function of the number of entanglements Z. In the unentangled regime η0,linear/η0,ring is virtually constant, consistent with the earlier data, atomistic simulations, and the theoretical expectation η0,linear/η0,ring=2. In the entanglement regime, the Z-dependence of rings viscosity is much weaker than that of linear polymers, in qualitative agreement with predictions from scaling theory and simulations. The power-law extracted from the available experimental data in the rather limited range 1

Ion jelly: a tailor-made conducting material for smart electrochemical devices.

We present a new concept for the design of a polymeric conducting material that combines the chemical versatility of an organic salt (ionic liquid) with the morphological versatility of a biopolymer (gelatin); the resulting 'ion jelly' can be applied in electrochemical devices, such as batteries, fuel cells, electrochromic windows or photovoltaic cells.

Molecular motions in amorphous ibuprofen as studied by broadband dielectric spectroscopy.

The molecular mobility of amorphous ibuprofen has been investigated by broadband dielectric relaxation spectroscopy (DRS) covering a temperature range of more than 200 K. Four different relaxation processes, labeled as alpha, beta, gamma, and D, were detected and characterized, and a complete relaxation map was given for the first time. The gamma-process has activation energy E a = 31 kJ.mol (-1), typical for local mobility. The weak beta-relaxation, observed in the glassy state as well as in the supercooled state was identified as the genuine Johari-Goldstein process. The temperature dependence of the relaxation time of the alpha-process (dynamic glass transition) does not obey a single VFTH law. Instead two VFTH regimes are observed separated by a crossover temperature, T B = 265 K. From the low temperature VFTH regime, a T g (diel) (tau =100 s) = 226 K was estimated, and a fragility or steepness index m = 93, was calculated showing that ibuprofen is a fragile glass former. The D-process has a Debye-like relaxation function but the temperature dependence of relaxation time also follows the VFTH behavior, with a Vogel temperature and a pre-exponential factor which seem to indicate that its dynamics is governed by the alpha-process. It has similar features as the Debye-type process observed in a variety of associating liquids, related to hydrogen bonding dynamics. The strong tendency of ibuprofen to form hydrogen bonded aggregates such as dimers and trimers either cyclic or linear which seems to control in particular the molecular mobility of ibuprofen was confirmed by IR spectroscopy, electrospray ionization mass spectrometry, and MD simulations.

Changes in molecular dynamics upon formation of a polymer dispersed liquid crystal.

The molecular dynamics during the formation of a polymer dispersed liquid crystal (PDLC) was followed by dielectric relaxation spectroscopy in the frequency range from 10(-1) to 2 x 10(6) Hz and over the temperature range from 158 to 273 K. The composite was produced by thermal polymerization induced phase separation of a mixture of triethyleneglycol dimethacrylate and the nematic liquid crystal, E7, in the proportion of 60:40 w/w. Both monomer and liquid crystal vitrify upon cooling having glass transition relaxation processes already characterized by some of us; yet E7 was previously studied in a narrower frequency range, so the present work updates its dielectric behavior. The starting mixture exhibits a rather complex dielectric spectrum due to the detection of multiple processes occurring simultaneously in the monomer and liquid crystal constituents. The PDLC formation occurs by mobility changes essentially in the liquid crystal tumbling motion, while the main relaxation of the monomer depletes upon polymerization. A low intense secondary process of E7 hardly detected in the bulk material is enhanced in both starting mixture and final composite allowing its characterization.