Velocity autocorrelation function for the motion of long-chain molecules in the free draining limit

The thermal motion of a long-chain molecule dispersed in a solvent is examined in terms of the velocity autocorrelation, in a reference frame attached to a subunit of the chain.     

High resolution UHV-AFM surface analysis on polymeric materials: Baltic Amber

In this paper we present, for the first time, the results from Atomic Force Microscopy (AFM) surface studies from freshly fractured Baltic Amber samples, carried out under ultrahigh vacuum (UHV) conditions from micrometer to nanometer resolution. The micrometric AFM images provide a structural clue to the birefringent behavior occasionally observed with amber samples. Two-dimensional pair-distance distributions of the nanometric AFM images prove the completely amorphous structure of the material. This, together with the detection of individual motifs such as aromatic rings, supports the notion of amber being an amorphous polymeric organic network, consistent with the accompanying X-Ray Photoelectron spectroscopy (XPS) data. No nanocrystalline inclusions could be found. The results also show that it is possible to obtain atomically resolved AFM images from amorphous dielectric surfaces.     

Laser processing for bio-microfluidics applications (part I)

This paper reviews applications of laser-based techniques to the fabrication of microfluidic devices for biochips and addresses some of the challenges associated with the manufacture of these devices. Special emphasis is placed on the use of lasers for the rapid prototyping and production of biochips in particular for applications in which silicon is not the preferred material base. Part I of this review addresses applications and devices using UV lasers for laser ablation and surface treatment of microchannels, in particular in polymers.     

Flame retardance and thermal stability of carbon nanotube epoxy composite prepared from sol-gel method

Carbon nanotubes (CNTs) are functionalized by vinyltriethoxysilane (VTES) to incorporate the -O-C₂H₅ functional group and become VTES—CNT. The VTES—CNTs are added to the modified DGEBA epoxy resin that contains silicon to induce the sol-gel reaction. The final products are organic/inorganic nanocomposites. Thermogravimetric analysis (TGA) and differential scanning calorimeter (DSC) are used to study the thermal property of nanocomposites. The T_g was increased from 118 to 160 °C and char yield of composites that contained 9 wt% CNT at 750 °C was increased by 46.94%. The integral procedural decomposition temperature (IPDT) was increased from 890 to 1571 °C. The limiting oxygen index (LOI) and UL-94 tests were classified as the flame retardance. The LOI of composites was increased from 22 to 27 and the UL-94 changed from V-1 to V-0 when the contents were increased to 9 wt%. The nanocomposites had a higher char yield and were highly flame retardant. The products can meet to the requirements of halogen-free and phosphorus-free ecological flame retardant.     

Preparation and characterization of carbon nanotubes/epoxy resin nano-prepreg for nanocomposites

The surface carbon nanotubes (CNTs) were modified to generate functional reactors by using the sonicication method to distribute CNTs evenly among epoxy resin, which was prepared into nano-prepreg with carbon fibers. Additionally, based on various proportions of modified and unmodified CNTs, the mechanical properties and conductivities of the composite, as well as, the characteristics of material subjected to various temperature conditions were investigated. Experimental results indicate that increasing CNT content enhances the mechanical strength and electrical properties. At various temperatures, the mechanical strength drops with increase in temperature because different expansion coefficients differ between fiber and epoxy resin. Finally, the failure surface of nanocomposite was examined using scanning electron microscopy (SEM). Finally we provide a discussion of the failure mechanism of the material.     

Luminescence properties of poly(9,9-dioctylfluorene)/polyvinylcarbazole blends: Role of composition on the emission colour stability and electroluminescence efficiency

Light-emitting diodes (LEDs), based on blue-emitting polyfluorenes are usually prone to the appearance of a contaminant green emission (centered around 520 nm), leading to an apparent whitish light emission. We find that, for LEDs based on poly(9,9-dioctylfluorene), PFO, the blending with the hole transporting polyvinylcarbazole, PVK, can suppress such green emission. LEDs based on a PFO/PVK blend with a 1:2 weight ratio and with aluminum cathodes show a quite stable blue emission. This result reveals the important role played by the interchain interactions on the observed contaminant green emission. In addition, we observe that in Al-based devices blending causes a decrease in EL efficiency while in Mg-based devices we obtained higher efficiencies with the blend PFO:3PVK when compared with neat PFO-based devices.     

Influence of the blend compatibility on the morphology of thin polymer blend films

Thin films of incompatible polymer blends can form a variety of structures on preparation. For the polymer blend system consisting of two poly(styrene-co-para-bromo-styrene)s at different degrees of bromination, PBr_xS/PBr_yS, the compatibility can be tuned through a variation of the difference in the degree of bromination. Within this blend system, two series of samples with different compatibilities were investigated at various blend compositions. The surface morphology of the thin films was investigated by atomic force microscopy (AFM) measurements, while diffuse X-ray scattering provided additional depth sensitivity at a comparable lateral resolution. The results are indicative for phase separation lateral, as well as perpendicular, to the sample surface.     

A molecular dynamics study of ion migration in a doped electroactive polymer

Simulating the \hbox{BF}_{4}^{-} -doped poly(3-octylthiophene) lattice by molecular dynamics results in a structure in which dopant ions intercalate as a sandwich between thiophene rings on adjacent polymer chains. The ions occupy sites in channels parallel to the polymer main chain, which retains a high degree of planarity in contrast to the pristine (undoped) polymer. Even when lattice imperfections are created by expanding the cell, Coulomb forces ensure that the intercalation features containing the dopant channels are largely retained. On applying electric fields in the principal directions of the 'perfect lattice' it is found that the ions migrate most readily along the ion-channel directions (the lattice c axis), leaving the lattice undisturbed. Although higher electric fields cause dopant migration to occur perpendicular to the channel directions they destroy the intercalated lattice. In the reduced-order lattice regions substantial motion of the ions are predicted at a critical value of the lattice parameter.     

A study of the activation energy of thermal decomposition of irradiated polymers

The ion irradiation of polymeric solids induces numerous modifications in the polymer properties thus increasing their applicability in various fields. The present work looks into the aspect of thermal modifications induced in the irradiated polymers. The kinetics of thermal decomposition of polymers is investigated by using the thermogravimetric (TG) technique. It has been observed that the degradation of polymers is a multi-step process that involves sequential and competing processes, and obeys the Arrhenius kinetics which allows us to connect the rate constant with the absolute temperature and the activation energy. The activation energy of thermal decomposition has been calculated from the TG curves, and its variation with different irradiation doses has been derived.     

Dynamical study on the stimulated processes of an exciton and a biexciton in a polymer

By applying a femtosecond stimulating pulse, we theoretically study the stimulated processes of an exciton and a biexciton in a polymer within the framework of an extended Su–Schrieffer–Heeger tight-binding model. For an exciton, it is obtained that the stimulated emission and absorption between the intragap levels take place with the same probability, by which we will not get the light amplification. However, the light amplification can be realized by the stimulated emission between the intragap levels in a biexciton, which is found to have two different modes. Finally, effect of the stimulating energy and intensity on the stimulated processes is separately analyzed. These results might be of great importance for further improving the optical applications of polymers, especially for optimizing the polymer laser properties.