359,223 research outputs found

    Embedding of fibre optic sensors within flexible host

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    This work deals with the establishment of a UV polymerisation procedure combined with moulding technology towards the development of a mass production technology for the fabrication of flexible polymers with optical fibres embedded. The concept is to provide an artificial sensing skin based on fibre optic sensors which can be applied to irregular or moveable surfaces for distributed pressure applications, as for instance in structural monitoring or rehabilitation. The selected polymers for such an application are here reviewed and their composition adjusted in order to accommodate the required flexibility. As compared to other techniques, UV polymerisation advantages are pointed out when moving towards industrial applications and large scale productions. Meanwhile, curing tests to embed optical fibres in the developed polymers are carried out with an in house developed glass mould set-up and the results are presented. Laser ablation of polymers is also discussed in order to reply the demand of complex fibre layout as for example meandering or curved shape patterns

    High performance polymer development

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    The term high performance as applied to polymers is generally associated with polymers that operate at high temperatures. High performance is used to describe polymers that perform at temperatures of 177 C or higher. In addition to temperature, other factors obviously influence the performance of polymers such as thermal cycling, stress level, and environmental effects. Some recent developments at NASA Langley in polyimides, poly(arylene ethers), and acetylenic terminated materials are discussed. The high performance/high temperature polymers discussed are representative of the type of work underway at NASA Langley Research Center. Further improvement in these materials as well as the development of new polymers will provide technology to help meet NASA future needs in high performance/high temperature applications. In addition, because of the combination of properties offered by many of these polymers, they should find use in many other applications

    Design of fibre reinforced PV concepts for building integrated applications

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    Fibre reinforced polymers present an interesting encapsulation medium for PV-modules. Glass fibres can provide increased strength and stiffness to thin polymer layers overcoming the brittleness and limited deformability of glass-panes. Glass fibre reinforced polymers allows for transparency over a broad range of the solar spectrum while the material properties and integral production processes create possibilities for novel product concepts with embedded PV technology. To explore such possibilities, innovative design methods were used to design novel PV product concepts for applications in the build environment.\ud In our paper three conceptual designs are presented; (1) a thin film module with an adjoining interconnection system functioning as structural element for geodetic roofing structures, (2) a PV lamella with single-axis tracking utilizing a linear concentration effect caused by the geometry of the product and the materials applied, and (3) a prepreg PV-material which allows for easy shaping during the production of PV modules with complex geometries. Each concept employs a specific PV technology and demonstrates a possible application aimed at a specific market. In this way we show the potential of integration of PV technology in fibre reinforced composites. The paper will be illustrated by concept renderings

    Plasma functionalized surface of commodity polymers for dopamine detection

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    We have fabricated potentially generalizable sensors based on polymeric-modified electrodes for the electrochemical detection of dopamine. Sensitive and selective sensors have been successfully obtained by applying a cold-plasma treatment during 1–2 min not only to conducting polymers but also to electrochemically inert polymers, such as polyethylene, polypropylene, polyvinylpyrrolidone, polycaprolactone and polystyrene. The effects of the plasma in the electrode surface activation, which is an essential requirement for the dopamine detection when inert polymers are used, have been investigated using X-ray photoelectron spectroscopy. Results indicate that exposure of polymer-modified electrodes to cold-plasma produces the formation of a large variety of reactive species adsorbed on the electrode surface, which catalyse the dopamine oxidation. With this technology, which is based on the application of a very simple physical functionalization, we have defined a paradox-based paradigm for the fabrication of electrochemical sensors by using inert and cheap plastics.Peer ReviewedPostprint (author's final draft

    Equilibrium kinetics of self-assembling, semi-flexible polymers

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    Self-assembling, semi-flexible polymers are ubiquitous in biology and technology. However, there remain conflicting accounts of the equilibrium kinetics for such an important system. Here, by focusing on a dynamical description of a minimal model in an overdamped environment, I identify the correct kinetic scheme that describes the system at equilibrium in the limits of high bonding energy and dilute concentration.Comment: 12 pages, 4 figure

    Improving the mechanical recycling and reuse of mixed plastics and polymer composites

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    This is a post-print version of the chapter.In this chapter we will explore the possibilities and viability of commercially recycling and reusing of composites and mixed polymer based waste that is difficult and expensive to separate into individual generic polymers for subsequent recycling. The chapter will also attempt to cover legislations that hinder and drive this technology and give sources of information for further examples of polymer recycling in action

    Controlled Nanoparticle Formation by Diffusion Limited Coalescence

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    Polymeric nanoparticles (NPs) have a great application potential in science and technology. Their functionality strongly depends on their size. We present a theory for the size of NPs formed by precipitation of polymers into a bad solvent in the presence of a stabilizing surfactant. The analytical theory is based upon diffusion-limited coalescence kinetics of the polymers. Two relevant time scales, a mixing and a coalescence time, are identified and their ratio is shown to determine the final NP diameter. The size is found to scale in a universal manner and is predominantly sensitive to the mixing time and the polymer concentration if the surfactant concentration is sufficiently high. The model predictions are in good agreement with experimental data. Hence the theory provides a solid framework for tailoring nanoparticles with a priori determined size.Comment: 4 pages, 3 figure

    Nonlinear optical polymers for electro-optic signal processing

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    Photonics is an emerging technology, slated for rapid growth in communications systems, sensors, imagers, and computers. Its growth is driven by the need for speed, reliability, and low cost. New nonlinear polymeric materials will be a key technology in the new wave of photonics devices. Electron-conjubated polymeric materials offer large electro-optic figures of merit, ease of processing into films and fibers, ruggedness, low cost, and a plethora of design options. Several new broad classes of second-order nonlinear optical polymers were developed at the Navy's Michelson Laboratory at China Lake, California. Polar alignment in thin film waveguides was achieved by electric-field poling and Langmuir-Blodgett processing. Our polymers have high softening temperatures and good aging properties. While most of the films can be photobleached with ultraviolet (UV) light, some have excellent stability in the 500-1600 nm range, and UV stability in the 290-310 nm range. The optical nonlinear response of these polymers is subpicosecond. Electro-optic switches, frequency doublers, light modulators, and optical data storage media are some of the device applications anticipated for these polymers

    Formulation/cure technology for ultrahigh molecular weight silphenylene-siloxane polymers

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    Molecular weights above one million were achieved for methylvinylsilphenylene-siloxane terpolymers using a two-stage polymerization technique which was successfully scaled up to 200 grams. The resulting polymer was vulcanized by two different formulations and compared to an identically formulated commercial methylvinyl silicone on the basis of ultimate strength, Young's modulus, percent elongation at failure, and tear strength. Relative thermal/oxidative stabilities of the elastomers were assessed by gradient and isothermal thermogravimetric analyses performed in both air and nitrogen. The experimental elastomer exhibited enhanced thermal/oxidative stability and possed equivalent or superior mechanical properties. The effect of variations in prepolymer molecular weight on mechanical properties was also investigated

    Globalisation of Stone Tools and Beginnings of Mechanical Processing of Polymers

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    Based on research on influence of rubber and plastics on globalization, an interesting question arose: can we define the first globalization way of material culture? Manufacturing of first stone tools can be seen at the site of Gona, Ethiopia (dated to 2,6 million years ago), followed by several sites including the evidence from West Turkana in Kenya (2,74 - 1.94 million years ago), Olduvai in Tanzania and Sterkfontain in South Africa (2 - 1,6 million years ago). The products found at the sites were simple stone choppers, chopping tools and flakes. We used synthesiological approach and combined the knowledge from archaeology, production technology and the field of polymers in order to approach the interesting question relating to the aforementioned finds: for which purpose these tools were used? Firstly, the manufactured stone tools were used for procedures such as breaking of the natural polymers: e.g. crushing of the larger bones in order to obtain the marrow, and for butchering of animals.globalisation, Stone tools Road, mechanical processing, natural polymers
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