Electrospinning is a technique of producing nanofibers from polymer solution/melt solely under the influence of electrostatic forces. In this research, we investigated the formation of nanofibers by melt electrospinning polycaprolactone (PCL). The effect of process parameters such as molecular weight, applied voltage, and electrode separation on the fiber diameter was investigated. Controlling the process parameters could help increase the proportion of ultrafine fibers in the melt electrospun nonwoven mat. The velocity of the straight jets was in the range of 0.2-1 m/s. The melt electrospun fibers were characterized with respect to fiber diameter, distribution, mechanical properties and birefringence. Melt electrospun polycaprolactone fibers had a diameter distribution of the order of 5 -20 μm. The birefringence of the melt electrospun fibers increased with decrease in fiber diameter.

Macroporous cross-linked polymeric dried gels have been obtained by inducing phase separation in a homogeneous poly(divinylbenzene) (PDVB) network formed by organotellurium-mediated living radical polymerization (TERP). The living polymerization reaction of DVB with the coexistence of a non-reactive polymeric agent, poly(dimethylsiloxane) (PDMS), in solvent 1,3,5-trimethylbenzene (TMB) resulted in polymerization-induced phase separation (spinodal decomposition), and the transient structure of spinodal decomposition has been frozen by gelation. Well-defined macroporous monolithic dried gels with bicontinuous structure in the micrometer scale are obtained after removing PDMS and TMB by simple washing and drying. The properties of the macropores have been controlled by changing starting composition.

A chemically adsorbed monolayer containing pyrrolyl group (Pyrrolyl-CAM) was prepared between a plated copper layer and a resin substrate for increasing the adhesion force without roughening a surface of the resin substrate. Although it was not enough to increase the adhesion force between the resin substrate and the copper layer by using only Pyrrolyl-CAM, the sufficient adhesion force was obtained by preparing a polypyrrole thin film between Pyrrolyl-CAM and the copper layer.

Pyrrolyl-CAM and the polypyrrole thin film on the substrate were evaluated by an automat-ic contact angle meter and auger electron spectroscopy in order to analyze the condition of the films between the resin substrate and the copper layer.

The peel strength test was carried out in order to evaluate the adhesion force. The best ad-hesion force was 0.98 [N/mm], and the target value of 0.60 [N/mm] was sufficiently achieved.

This paper reports on the characterization of the charge stability of an amorphous fluoropolymer electret called Cytop. Cytop is a dissolved polymer material, compatible with standard micromachining fabrication technologies. In this study, Cytop layers are deposited and patterned on Pyrex and silicon substrates, followed by the electrical poling of the material by corona discharge using a customized charging station. The long-term performance of Cytop as an electret material is evaluated as a function of several relevant charging parameters. The results reveal highly stable layers, able to keep at least 92% of the initial charge 143 days after the corona charging stored at 23°C.

Thermoresponsive copolymers of poly(N- isopropyl acrylamide) (PNIPAm) and poly(acrylamide) microgels grafted with poly(ethylene glycol)(PEG) chains were synthesized by free-radical photopolymerization. Poly(ethylene glycol) methyl ether methacrylate (PEGMA) macromonomers with varying number-average molecular weights were used (Mn = 300 and 1,000 g/mol). A simple microarray technique coupled with a laser scanning confocal microscope (LSCM) was used to visualize the effect of temperature on the volume phase transition temperatures of the microgels. In general, increasing the concentration of PEGMA in the PNIPAm-co-Am-co-PEGMA copolymers resulted in a broader and higher lower critical solution temperature (LCST) compared to the PNIPAm microgels. We demonstrated that the PEGMA molecular weight and concentration influenced whether it was incorporated as a grafted copolymer or random copolymer in the PNIPAm microgel. The evidence for this is the shift in the LCST as determined by temperature and differential scanning calorimetry (DSC) measurements. This behavior suggests that incorporation of PEGMA in the copolymer depends on its hydrophilicity or water-solubility which in turn influenced the degree at which the copolymer chains collapsed from a coil-to-globule (volume phase transition) with increasing temperature.

Microgel particles of poly(2-vinylpyridine) cross linked with 0.5 wt% divinylbenzene were synthesised. Due to differences in the scattering of light, a dispersion of the particles appears opaque milky white above pH 4.5 and transparent below pH 4.5. The pH of a 0.15 wt% dispersion was modified using a poly(aniline) film as a source/sink of protons and a Ag/AgCl electrode as a source/sink of chloride counterions. The absorption of the sample at 400 nm was typically reduced from c.a. 3.5 to c.a. 0.5 in less than 20 minutes and increased to c.a. 3.2 in less than 20 minutes. This system could form the basis for a new type of display device, but it is insufficiently fast or consistent in its current form.

We investigate aromatic polyureas which can be fabricated in the form of thin films through CVD. It was found that the polymer possesses a flat dielectric response (k∼ 4.2 and loss <1%)) to more than 200°C. The frequency-independent dielectric properties in the investigated frequency range(1kHz∼1MHz), low conductance, low dissipation factor (∼0.005), high breakdown strength (>800MV/m), high energy density (>12J/cm3) and high efficiency suggest this polymer can be a good candidate material for high temperature energy storage capacitors. Breakdown strength was analyzed with Weibull model over a broad temperature range (25°C ∼180°C). Experimental results indicate that aromatic polyurea is more like a nonpolar linear dielectric material because of its highly cross-linked structures. The experiment results further show that this polymer maintains its high performance even at high temperatures.

Detection of mercury with high sensitivity and selectivity constitutes a significant research concern. Here, we report an amplified fluorescence turn-on assay for mercury(II) with an improved performance. This sensing system takes advantage of optically amplifying fluorescent conjugated polyfluorene derivatives and DNA immobilized silica nanospheres (NSs) in addition to the specific thymine- mercury(II)-thymine(T- Hg2+-T) interaction. The employment of ion-specific T- Hg2+-T coordination increases the melting temperature (Tm) of the double-stranded DNA (dsDNA) on the hybridized NS surface. After thermal washing at 45 °C, the Hg2+ treated sample (dsDNA-NS) was effectively differentiated from that treated with nonspecific ions through monitoring fluorescence emission of fluorescein (Fl) labeled target DNA remained on the NS surface. Finally, a cationic conjugated polyfluorene derivative (CCP) was introduced to electrostatically associate with the DNA molecules on the NS surface, resulting in an amplified Fl signal via fluorescence resonance energy transfer (FRET) from the CCP to the dye molecule. In comparison with the use of Fl alone as a signal reporter, the presence of CCP significantly enhances the detection fluorescence intensity, reduces false-positive signal, and improves the detection selectivity for mercury(II). Further improvement in the probe design could yield more efficient metal ion sensors, which have the potential to be operated at room temperature and for the detection of other metal ions besides mercury(II).

Water-based polymer latexes have attracted much attention since their invention in the early 1950s. Its advantages for both general health and the environment were recognized as they emit far less volatile organic compounds (VOCs) than their solvent-based counterparts.

The performance of latex paints and coatings is directly proportional to the ease of particle deformation. This is the main driving force for the paints and coatings industry to focus its research efforts towards understanding its mechanism.

In contrast, little has been published with respect to enhancing latex's resistance against deformation despite such needs in applications such as templating porous ceramics for catalysis and biomaterial engineering. Specifically, the latex's resistance to deformation is crucial to retain a network of uniform pores for applications relating to enzyme immobilization and materials reinforcement.

The current study reports increased heat-resistance observed in latexes when synthesized using a rigid surfactant, dimethyl siloxane – ethylene oxide block copolymer (PDMS-PEO). The film formation process for this latex was deduced using atomic force microscopy and subsequent roughness analysis. A comparative study using a non-ionic long-chain hydrocarbon surfactant, morpholine oleate, was also conducted.

Single-wall and multi-wall carbon nanotube blends (0 to 0.5 vol% ) with polyvinylidene fluoride (PVDF) have been prepared using solution cast method and characterized. By acid treatment, it has been observed that nanotube has been well functionalized and uniformly dispersed into the polymer. X-ray diffraction analysis coupled with differential scanning calorimetry (DSC) has revealed that carbon nanotube alters the crystallinity of PVDF and thereby enhances the β-phase in PVDF. Experimental results have demonstrated that enhancement of β-phase is a function of carbon nanotube concentration.

In an extension of earlier work, the temperature dependent parameters of PVDF operating in the length mode have been measured at frequencies useful in air ultrasound (20kHz to 100kHz) over a -45°C to +65°C temperature range. The length mode resonance of PVDF strips of different lengths was excited by mechanically clamping samples at the mid point during dielectric impedance testing conducted in a desiccated thermal chamber. Material properties were extracted from the impedance magnitude and phase angle data at temperature, and the various sample lengths allowed a range of resonant frequencies to be studied. Overall results generally confirm the visco-elastic behavior of PVDF. Testing was conducted on samples with both thin sputtered metal electrodes (∼60nm) and thicker elastomeric silver ink electrodes (∼8μm) to assess the performance difference. Silver ink is preferred in production as sputtered metal has current density an other limitations, but it causes a serious loss in performance at high frequencies.

LC-NANOP is an ESF EUROCORES SONS Collaborative Research Project that is addressing an innovative approach to self-organized nanostructures by combination of a variety of organic, inorganic and metal scaffolds with the unique self-organization properties of liquid crystals to obtain liquid crystal nano-particles. LC-NANOP is concerned with the synthesis, analysis, characterization, modeling and physico-chemical properties of super- and supra-molecular systems which are formed from a nano-particle as a central scaffold, surrounded by a layer of liquid crystal. The self-organization properties of the liquid crystal coating is the driving force leading to the self-assembly of the nano-particles into secondary or tertiary hierarchical structures, with emphasis on the systematic variation of nano-particle size, chirality, shape and functionality. This bottom-up approach to nano-structuring is very powerful as it combines the extraordinary variety of morphologies that liquid crystals present with the combination of functional entities, relevant for chemical, biological, optoelectronic, and photonic tasks, etc, to create ordered nano-structures that can be controlled by external stimuli.

Transparent organic-inorganic hybrid aerogels and aerogel-like xerogels have been prepared from methyltrimethoxysilane (MTMS) respectively by supercritical drying (SCD) and ambient pressure drying (APD). The new aerogels and xerogels significantly deform without collapsing on uniaxial compression and almost fully relax when unloaded. This elastic behavior, termed as “gspring-back”, allows APD without noticeable shrinkage and cracking. The flexible network composed of lower cross-linking density (up to three bonds per every silicon atom) compared to silica gels (up to four bonds) and repulsion between hydrophobic methyl groups bonded to every silicon atom largely contributes to the pronounced deformability and relaxing, respectively. Lower surface silanol group density also plays a crucial role for the “gspring-back” behavior.

Based on solution casting method, a ceramic [CaCu3Ti4O12 (CCTO)]-Polymer [P(VDF-TrFE)] composite with flexibility has been synthesized and its dielectric response has been studied. The CCTO ceramic powders were prepared by traditional sintering method and were milled with a relative uniform size. The dielectric properties of these films with micro-size and nano-size CCTO particle, as well as different polymer matrixes were determined. The process was optimized by hot pressing and surface modification to achieve high dielectric constant. A dielectric constant about 175 for one layer composite with high flexibility using silane coupling agent was obtained at 1 kHz at room temperature.

Ion implantation process was used to fabricate ultra-thin conducting films in inert polymers and to tailor the surface electrical properties for strain gauge applications. To this aim, polycarbonate substrates were irradiated at room temperature with low energy Cu+ ions of 60 keV at 1 μA/cm2 and with doses ranging from 1×1016 to 1×1017 ions/cm2. XRD and TEM measurements on the nanocomposite surfaces demonstrated the spontaneous precipitation of Cu nanocrystals at 1×1016 ions/cm2 fluence. These nanocrystals were located at about 50 nm - 80 nm below the polymer surface in accordance with TRIM calculations. Optical absorption spectra exhibited a surface plasmon resonance (SPR) at 2 eV, in accordance with the formation of Cu nanoparticles. For doses of 5×1016 ions/cm2 the formation of a continuous nanocrystalline Cu subsurface film occurred and a well pronounced SPR peak was observed. Otherwise, for higher doses (1×1017 ions/cm2) a damaged and structurally disordered film was obtained and the SPR peak was smeared out. Electrical conductivity measurements clearly indicated a reduced electrical resistance for the samples implanted with a doses up to 5×1016 ions/cm2, whereas higher doses (1×1017 ions/cm2) resulted detrimental for the electrical properties, probably due to the radiation induced damage. The dependence of electrical resistance from surface load was evaluated during compression tests up to 3 MPa. A significant linear variation of the electrical resistance with the surface load was found and could be related to the changes in the spatial distribution of nanoparticles inside the copper film.

Conducting polymers such as polypyrrole, polythiophene and polyaniline are currently studied as novel biologically inspired actuators. The actuation mechanism of these materials depends upon the motion of ions in and out of the polymer film during electrochemical cycling. The diffusion of ions into the bulk of the film causes the dynamic mechanical compliance (or modulus) of the material to change during the actuation process. The mechanism of this change in compliance is not fully understood as it can depend on many different factors such as oxidation state, solvation of the film and the level of counter ion swelling. In-situ measurement of the dynamic compliance of polypyrrole as a function of charge is difficult since the compliance depends upon the excitation frequency as well as the electrochemical stimulus. Pytel et al [1] studied the effect of the changing elastic modulus in-situ at a fixed frequency. In this study we describe a technique to measure the compliance response of polypyrrole as a function of frequency and electrochemistry. A voltage input and a simultaneous stress input was applied to polypyrrole actuated in neat 1-butyl-3-methylimidazolium hexaflourophosphate. The stress input was a stochastic force with a bandwidth of 30 Hz and it allows us to compute the mechanical compliance transfer function of polypyrrole as function of the electrochemistry. Our studies show that the low frequency compliance changes by 50% as charge was injected into the polymer. The compliance changes reversibly as ions diffuse in and out of the film which indicates that the compliance depends upon the level of counter ion swelling.

Bromoform absorption on crystalline polyvinylidene fluoride with 30% of trifluoroethylene, P(VDF-TrFE 70:30) was investigated by photoemission and inverse photoemission and found to be associative and reversible. Molecular bromoform adsorption appears to be an activated process at 120 K with enhanced adsorption following the initial adsorption of bromoform. Strong intermolecular interactions are also implicated in the presence of a weak shake off or screened photoemission final state.

Colloidal lithography is a popular, non-conventional process that uses two–dimensional self-assembled monolayer arrays of colloidal nanoparticles as masks for techniques such as etching or sputtering. Initiated Chemical Vapor Deposition (iCVD) is a surface controlled process which offers unprecedented opportunity for producing polymeric layers grafted to substrates with dangling vinyl bonds and patterned through a colloidal template. We demonstrate a generic “bottom-up” process as an inexpensive and simple technique for creating well-ordered arrays of functional patterned polymeric nanostructures. These patterns were produced from thin polymer films of p(butyl acrylate) and p(hydroxyethyl methacrylate), and are robustly tethered to the underlying substrate, as demonstrated by their ability to withstand aggressive solvents. Furthermore, using capillary force lithography, we created topographical templates for large-scale orientation of the nanoparticle assembly. Through this “top-down” approach, for assisting the bottom-up assembly, we present a process for multi-scale patterning of functional polymeric materials, without the need for expensive lithography tools.