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Conducting polymer polyethylene oxide

The other type is ion-conducting solids [polyethylene oxide) + salt] or gels (polymer + solvent + salt) (p. 314). [Pg.318]

Co-electrospinning has been applied so far for the preparation of polymer core shell fibers, hollow polymer core shell fibers, hollow fibers composed not only of polymers, but also of ceramics, as well as for the immobilization of functional objects in droplets dispersed in the core that are arranged along the fiber axis. Among the examples reported in the literature are core shell fibers spun from polystyrene and polyethylene oxide, two kinds of polyethylene oxide (one with and the other without a chromophore), and core shell fibers with the electrically conductive polymer polyhexathiophene and the insulation polymer polyethylene oxide (Fig. 20). Hollow core shell fibers in which one polymer (polycaprolactone) forms the shell onto which the core material is deposited (polyethylene oxide) as inner wall is another example for the broad spectrum of fiber architectures which can be produced by coelectrospinning. The formation of the two-layer hollow fiber is based on the... [Pg.151]

An example of an ionically conductive polymer is polyethylene oxide containing LiC104, which is used as a solid phase electrolyte in batteries. [Pg.887]

Figure 1. Temperature variation of the conductivity for a cross-section of polymer electrolytes. PESc, poly (ethylene succinate) PEO, polyethylene oxide) PPO, polypropylene oxide) PEI, poly(ethyleneimine) MEEP, poly(methoxyethoxy-ethoxyphosphazene) aPEO, amorphous methoxy-linked PEO PAN, polyacrylonitrile PC, propylene carbonate EC, ethylene carbonate. Figure 1. Temperature variation of the conductivity for a cross-section of polymer electrolytes. PESc, poly (ethylene succinate) PEO, polyethylene oxide) PPO, polypropylene oxide) PEI, poly(ethyleneimine) MEEP, poly(methoxyethoxy-ethoxyphosphazene) aPEO, amorphous methoxy-linked PEO PAN, polyacrylonitrile PC, propylene carbonate EC, ethylene carbonate.
Synthesis of comb (regular graft) copolymers having a PDMS backbone and polyethylene oxide) teeth was reported 344). These copolymers were obtained by the reaction of poly(hydrogen,methyl)siloxane and monohydroxy-terminated polyethylene oxide) in benzene or toluene solution using triethylamine as catalyst. All the polymers obtained were reported to be liquids at room temperature. The copolymers were then thermally crosslinked at 150 °C. Conductivities of the lithium salts of the copolymers and the networks were determined. [Pg.50]

For using lithium batteries (which generally have high energy densities) under extreme conditions, more durable and better conducting electrolytes are necessary. Salt-in-polymer electrolytes discovered by Angell et al. (1993) seem to provide the answer. Polypropylene oxide or polyethylene oxide is dissolved in low melting point mixtures of lithium salts to obtain rubbery materials which are excellent lithium-ion conductors at ambient temperatures. [Pg.436]

The EDLCs, which use all-solid-state ion-conducting polymer [e.g., polyethylene oxide)/LiC104] or polymer gel electrolyte, have also been developed [3],... [Pg.316]

Although the motion of protons does not lead to electrical conduction in the case of benzoic acid, electronic and even ionic conductivity can be found in other molecular crystals. A well-studied example of ionic conduction is a film of polyethylene oxide (PEO) which forms complex structures if one adds alkaline halides (AX). Its ionic conductivity compares with that of normal inorganic ionic conductors (log [cr (Q cm)] -2.5). Other polymers with EO-units show a similar behavior when they are doped with salts. Lithium batteries have been built with this type of... [Pg.389]

The fusion temperature of these polymers is low enough to allow the spinning of fibres and melt pressing of films 263). They can also be blended with normal thermoplastics such as polystyrene or polyethylene oxide)2711. The conductivity shows a percolation threshold of about 16% which is expected for a random distribution of conducting spheres. [Pg.32]

On the other hand, polyphosphazene 3.79 and its variants are non-crystalline. Then-ionic conductivities at room temperature are 1,000 times or more greater than that of polyethylene oxide).164 166 For battery type applications, 3.79 must be cross-linked lightly to prevent slow liquid-like flow, but this can be accomplished by radiation techniques without lowering the conductivity. An analogous type of polymer, with a poly-siloxane backbone and oligoether side groups, is being studied for similar applications. [Pg.117]

Ionically conducting polymers and their relevance to lithium batteries were mentioned in a previous section. However, there are several developments which contain both ionically conducting materials and other supporting agents which improve both the bulk conductivity of these materials and the properties of the anode (Li)/electrolyte interface in terms of resistivity, passivity, reversibility, and corrosion protection. A typical example is a composite electrolyte system comprised of polyethylene oxide, lithium salt, and A1203 particles dispersed in the polymeric matrices, as demonstrated by Peled et al. [182], By adding alumina particles, a new conduction mechanism is available, which involved surface conductivity of ions on and among the particles. This enhances considerably the overall conductivity of the composite electrolyte system. There are also a number of other reports that demonstrate the potential of these solid electrolyte systems [183],... [Pg.54]

To improve the properties of PLA, plasticizers, special additives such as chain-extenders, polymer blends, and composites are commonly investigated. Martin and Averous (10) have studied the effects of various plasticizers on the properties of PLA. Pilla et al. (11-12) have investigated the effects of chain-extenders on the foaming properties of PLA. In addition, a vast number of studies have been conducted to enhance the properties of PLA by blending it with various polymers such as polyethylene oxide (PEO), polypropylene oxide (PPO), polyvinyl acetate, polyolefins, polystyrene, HIPS (high impact polystyrene), polyacetals, polycarbonate, and acrylonitrile butadiene styrene (ABS) (13-26). [Pg.251]

Figure 4. Backbone structures of salt-solvating polymers. The figure shows the similarity of backbone structure, with optimal spacing between electron-donating oxygens, of polymers that form ion-conducting salt complexes. PPL-poly-3-propiolac-tone PEO polyethylene oxide PPO 1,2- polypropylene oxide.18... Figure 4. Backbone structures of salt-solvating polymers. The figure shows the similarity of backbone structure, with optimal spacing between electron-donating oxygens, of polymers that form ion-conducting salt complexes. PPL-poly-3-propiolac-tone PEO polyethylene oxide PPO 1,2- polypropylene oxide.18...
Haidar, B., Singru, R.M., Maurya, K.K., Chandra, S. (1996) Temperature dependence of positron-annihilation lifetime, free volume, conductivity, ionic mobility, and number of charge carries in a polymer electrolyte polyethylene oxide complexed with NH4CIO4 . Phys. Rev. B. 54, 7143. [Pg.391]

As a result of the advances in catalyst discovery for aqueous ethylene polymerization, silica-polyethylene nancomposites have been prepared with structures that vary with changing catalyst structure and silica composition." It is likely that many more advances in the area of high-tech composites with potential biological and nanotechnology applications will be made in the next few years through aqueous polymerization processes. In addition to free radical polymerizations and catalytic polymerizations, it should be noted that oxidative polymerizations can also be performed in aqueous media to yield conducting polymers. Recently, this has been used to prepare polypyrrole-coated latex particles that are expected to be interesting synthetic mimics for micrometeorites. [Pg.61]

In experiments conducted to obtain controlled sizes of filler particles formed in a matrix, several polymers were used as the matrix. Copolymers were synthesized from polyethylene oxide (does not interact with CaCOs) and poly(methacrylic acid) (reacts with in situ crystallizing CaCOj). In the presence of polyethylene oxide, crystals grew to similar sizes as without any polymer. The presence of the poly(methacrylic acid) crystal size of CaCOa was reduced by a factor 5 to 10 depending on the concentration of the filler precursor. [Pg.493]


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