Thomas Vad

Novel Carbon Nanotube/Cellulose Composite Fibers As Multifunctional Materials

Electroconductive fibers composed of cellulose and carbon nanotubes (CNTs) were spun using aqueous alkaline/urea solution. The microstructure and physical properties of the resulting fibers were investigated by scanning electron microscopy, Raman microscopy, wide-angle X-ray diffraction, tensile tests, and electrical resistance measurements. We found that these flexible composite fibers have sufficient mechanical properties and good electrical conductivity, with volume resistivities in the range of about 230-1 Ohm cm for 2-8 wt % CNT loading. The multifunctional sensing behavior of these fibers to tensile strain, temperature, environmental humidity, and liquid water was investigated comprehensively. The results show that these novel CNT/cellulose composite fibers have impressive multifunctional sensing abilities and are promising to be used as wearable electronics and for the design of various smart materials.

Structure and dynamics of water in nonionic reverse micelles: A combined time-resolved infrared and small angle x-ray scattering study

We study the structure and reorientation dynamics of nanometer-sized water droplets inside nonionic reverse micelles (water/Igepal-CO-520/cyclohexane) with time-resolved mid-infrared pump-probe spectroscopy and small angle x-ray scattering. In the time-resolved experiments, we probe the vibrational and orientational dynamics of the O-D bonds of dilute HDO:H(2)O mixtures in Igepal reverse micelles as a function of temperature and micelle size. We find that even small micelles contain a large fraction of water that reorients at the same rate as water in the bulk, which indicates that the polyethylene oxide chains of the surfactant do not penetrate into the water volume. We also observe that the confinement affects the reorientation dynamics of only the first hydration layer. From the temperature dependent surface-water dynamics, we estimate an activation enthalpy for reorientation of 45 ± 9 kJ mol(-1) (11 ± 2 kcal mol(-1)), which is close to the activation energy of the reorientation of water molecules in ice.

Structure and dynamics of water in nanoscopic spheres and tubes

We study the reorientation dynamics of liquid water confined in nanometer-sized reverse micelles of spherical and cylindrical shape. The size and shape of the micelles are characterized in detail using small-angle x-ray scattering, and the reorientation dynamics of the water within the micelles is investigated using GHz dielectric relaxation spectroscopy and polarization-resolved infrared pump-probe spectroscopy on the OD-stretch mode of dilute HDO:H2O mixtures. We find that the GHz dielectric response of both the spherical and cylindrical reverse micelles can be well described as a sum of contributions from the surfactant, the water at the inner surface of the reversed micelles, and the water in the core of the micelles. The Debye relaxation time of the core water increases from the bulk value τ(H2O) of 8.2 ± 0.1 ps for the largest reverse micelles with a radius of 3.2 nm to 16.0 ± 0.4 ps for the smallest micelles with a radius of 0.7 nm. For the nano-spheres the dielectric response of the water is approximately ∼6 times smaller than expected from the water volume fraction and the bulk dielectric relaxation of water. We find that the dielectric response of nano-spheres is more attenuated than that of nano-tubes of identical composition (water-surfactant ratio), whereas the reorientation dynamics of the water hydroxyl groups is identical for the two geometries. We attribute the attenuation of the dielectric response compared to bulk water to a local anti-parallel ordering of the molecular dipole moments. The difference in attenuation between nano-spheres and nano-cylinders indicates that the anti-parallel ordering of the water dipoles is more pronounced upon spherical than upon cylindrical nanoconfinement.

Extrusion of CNT-modified Polymers with Low Viscosity - Influence of Crystallization and CNT Orientation on the Electrical Properties

Several polymers were modified with multiwalled carbon nanotubes (CNT) to study the influences of the crystallization in the polymeric matrix and of the CNT orientation during extrusion on the electrical conductivity. Experiments were carried out with common semi-crystalline polymers (polypropylene, polyethylene, polyamide 6) and compared to an amorphous polymer (ethylene vinyl acetate). All polymers were grades with low viscosity, so that the CNT could be oriented well during extrusion. For all materials, the percolation threshold was determined, and the lowest value of 3% was found in polypropylene. The percolation threshold was correlated to the degree of crystallinity of the matrix polymers, so that crystallites could be seen as an excluded volume for CNT. The crystallization itself was analyzed by differential scanning calorimetry (DSC), whereby nucleation effects and changes in the crystallization temperature were found. The shear rate during extrusion had a large influence on the electrical conductivity. This effect was analyzed by transmission electron microscopy (TEM), with which the orientation of CNT in the direction of extrusion was visualized and differences between the polymer matrices were explained.

Novel Melt-Spun Polymer-Optical Poly(methyl methacrylate) Fibers Studied by Small-Angle X-ray Scattering

The structural properties of novel melt-spun polymer optical fibers (POFs) are investigated by small-angle X-ray scattering. The amorphous PMMA POFs were subjected to a rapid cooling in a water quench right after extrusion in order to obtain a radial refractive index profile. Four fiber samples were investigated with small-angle X-ray scattering (SAXS). The resulting distance-distribution functions obtained from the respective equatorial and meridional SAXS data exhibit a real-space correlation peak indicative of periodic cross-sectional and axial variations in the scattering density contrast. Simple model calculations demonstrate how the structural information contained particularly in the equatorial distance distribution function can be interpreted. The respective results are qualitatively verified for one of the fiber samples by comparison of the model curve with the measured SAXS data. Eventually, the study confirms that the cross-sectional variation of the (scattering-) density is the main reason for the formation of radial refractive-index profiles in the POFs.

Noncircular side-emitting fibres for directed lighting

We present a novel fiber type with a trilobal, non-circular cross section. The fiber is designed for illumination purposes with a special shape in order to form a distinct asymmetrical radiation pattern, which can be used to concentrate light on particular locations in order to cure resins or polymers but can also find its applications for illumination purposes.

Communication: Slow proton-charge diffusion in nanoconfined water

We investigate proton-charge mobility in nanoscopic water droplets with tuneable size. We find that the diffusion of confined proton charges causes a dielectric relaxation process with a maximum-loss frequency determined by the diffusion constant. In volumes less than ∼5 nm in diameter, proton-charge diffusion slows down significantly with decreasing size: for diameters <1 nm, the diffusion constant is about 100 times smaller than in bulk water. The low mobility probably results from the more rigid hydrogen-bond network of nanoconfined water, since proton-charge mobility in water relies on collective hydrogen-bond rearrangements.

Gradient-index POF without dopants: how the optical properties can be controlled by sole temperature treatment

In this paper we present a novel melt-spinning fabrication process for graded-index polymer optical fibers that completely avoids additional dopants for the formation of the refractive-index profile. In the presented process the meltspun fiber is rapidly cooled down so that the inner and outer parts of the fiber solidify at different speeds resulting in a density gradient. This density variation leads to a refractive-index profile without any further dopants. We present achieved results for fibers made of PMMA, and also first preliminary results for bio polymers such as TPU.