This paper presents the results of a study of the gas transfer and selective properties of PMP hollow fibres (HFs) produced by melt spinning technology. The HFs are characterized by WAXD, SEM and DSC methods. Transport and separation properties have been determined in relation to N2, CO2, methane, butane and different mixtures in the temperature range from -10 to 80 degrees C. It has been shown that the permeance of methane in mixture with N2 and CO2 is similar to the pure methane transport, whereas the presence of butane changes PMP properties and influence transport of methane. An increase in the activity of butane in a mixture with methane led to a significant increase in the permeation flux of both butane and methane through the walls of the HFs. It was shown that PMP changes properties from methane-selective at low butane activities to butane -selective at higher butane activities. The changing of butane and methane permeance in a mixture was found well described by an exponential dependence on the activity of butane. The values of permeance parameters were determined by different methods and found to be in good agreement between each other. Discovered effect for methane/butane mixture transfer in PMP HFs allows to perform the simulation of hydrocarbons separation taking into account changing of membrane properties and discovering of promising areas and conditions of practical application for the new PMP HFs.

The structural properties, mainly the spatial variation of density and chain interaction, of melt-spun polymer optical fibres (POFs) are investigated by small-angle X-ray scattering (SAXS) and compared to Monte-Carlo polymer simulations. The amorphous PMMA POFs had been subjected to a rapid cooling in a water quench right after extrusion in order to obtain a radial refractive-index profile. Four fibre samples with different processing parameters are investigated and the SAXS data analysed via Guinier approach. Distance-distribution functions from the respective equatorial and meridional SAXS data are computed to extract the fibres’ nanostructures in the equatorial plane and along the fibre axis, respectively. Temperature profiles of the cooling process are simulated for different locations within the fibre and taken as input for Monte-Carlo simulations of the polymer structure. The simulation results agree with the SAXS measurements in terms of the cooling profile’s strong influence on the structural properties of the fibre: slower cooling in the centre of the fibre leads to stronger interchain interaction, but also results in a higher density and more homogenous materials with less optical scattering.

The structural properties of PMMA, which has been melt-spun and treated using a specific cooling profile, is investigated in order to evoke desired optical and mechanical properties. Several PMMA fibres, which had been melt spun and subsequently processed with different temperature profiles, were analysed by small-angle X-ray scattering (SAXS) measurements. These results will be compared to a combination of numerical models, which consider the quenching of a filamentary PMMA polymer melt in water. This multi-scale simulation considers macroscopically the cooling process in the water and within the fiber. The spatially resolved cooling rates, which have been simulated at different locations serve as input for a 3D-Monte-Carlo polymer simulation model, which takes, among others, the Lennard-Jones, the bending and bond potentials into account in order to predict the resulting PMMA structure of the fabricated fiber These simulated structures are then evaluated in order to analyse their macroscopic properties. These comprise for instance the polymer entanglement, which describes the interaction of neighboring polymer chains leading to stronger, but stiffer fibers. Entanglement will also affect the glass-transition temperature, which determines the maximum operation temperature. But this can also lead to increased optical scattering, which will be subject to investigations, as well.

Designing hollow fiber (HF) membrane modules occupies one of the key positions in the development of efficient membrane processes for various purposes. In developing HF membrane modules, it is very important to have a uniform HF distribution and flow mixing in the shell side to significantly improve mass transfer and efficiency. This work suggests the application of different textile 3D HF structures (braided hoses and woven tape fabrics). The 3D structures consist of melt-spun, dense HFs based on poly(4-methyl-1-pentene) (PMP). Since the textile processing of HFs can damage the wall of the fiber or close the fiber bore, the membrane properties of the obtained structures are tested with a CO2/CH4 mixture in the temperature range of 0 to 40 °C. It is shown that HFs within the textile structure keep the same transport and separation characteristics compared to initial HFs. The mechanical properties of the PMP-based HFs allow their use in typical textile processes for the production of various membrane structures, even at a larger scale. PMP-based membranes can find application in separation processes, where other polymeric membranes are not stable. For example, they can be used for the separation of hydrocarbons or gas mixtures with volatile organic compounds.

In this article, the melt spinning behavior of poly(4-methyl-1-pentene) (PMP) hollow fibers (HF) is examined. The melt spinning trials are carried out on a pilot scale melt spinning plant with different settings while a 10-hole 2c-shaped spinneret is used. It is found that the winding speed mainly affects the outer fiber diameter. The influence of different melt spinning parameters is investigated, in particular temperatures, take-up velocities, and the use of quench air. For this purpose, the shape and crystalline structure of the fibers are analyzed using a light microscope, a scanning electron microscope, and wide-angle X-ray scattering. The shape of the fibers is mainly influenced by the temperature settings in the melt spinning process. As a reasonable lower limit, a melt spinning temperature of 280 degrees C is identified. Concerning the crystallinity, a saturation going along with a slight reduction of the polymer chain orientation is observed at elevated take-up velocities.

ABSTRACT We present a novel type of side‐light‐emitting fibre with trilobal cross‐section. The fibre is especially designed for indirect illumination applications and the special shape of the filament cross‐section permits the formation of a distinct asymmetric radiation pattern. These fibres can focus the radially emitted light on particular locations, e.g. in order to cure resins or polymers at well‐defined positions, or may be used as indirect illumination sources in car interiors. The polymer material is commercial optical‐grade poly(methyl methacrylate) (PMMA) that is compounded with different concentrations of a TiO 2 ‐nanofiller‐modified PMMA. © 2018 Society of Chemical Industry

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.

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.

The increase of fibre abrasion properties aims at the lifecycle improvement of technical textiles containing abrasion resistant fibres. Furthermore, the improvement of fibre abrasion properties is - presumably - the key to higher productivity and reduction of energy costs. Especially the fibre composites made of Nylon 6 and two-dimensional particles as organoclays or graphene platelets bear high potentials to achieve increased abrasion properties compared to virgin Nylon 6 fibres. The problems to be solved within this research were the transfer of positive effects known from bulk polymers, the guarantee of stable multifilament spinning and the loss of fibre properties by using additives. The effect of two-dimensional particles was visualised with the analysis of the tribological behaviour and mechanical properties. In order to gain the insight into the relationship among the processing conditions, material composition and resulting material properties, Wide Angle X-ray scattering experiments were performed.

An overview of the most important materials and fabrication methods for polymer optical fibers is given. In addition to conventional fabrication methods a newly developed continuous melt spinning process for graded-index fibers is presented that uses rapid cooling in a water quench for the profile formation. The approaches presented are divided into continuous and discontinuous processes for step- and graded-index profile fibers as well as microstructured polymer optical fibers. The methods are described in detail and discussed concerning their efficiency, quality of produced fibers and scalability. © 2014 Society of Chemical Industry

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.

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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.