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Composite particles carbon black-polymers

In carbon black-polymer composites, the value of Xc varies from about 40 vol.% in the case of spherical CB (e.g., N990) particles [51] to about 5 vol.% (e.g., for XC-72 [51] and Ketjenblack [52]) following the increase of the aspect ratio of the particles to the order of 10 [34]. The latter result is in excellent agreement with the excluded volume theory that predicts such a dependence of Xc on the aspect ratio (see Eq. (5.11)) if we identify the shell thickness d with a critical average distance, dc, that the tuimeling electrons should cross [29], This trend is continued when we consider the x values for CNTs [43], where x values on the order of 1 vol.% are observed for aspects ratios on the order of 10, and 0.1 vol.% for aspect ratios on the order of lO -lO. ... [Pg.160]

Electrical conductivity measurements have been reported on a wide range of polymers including carbon nanofibre reinforced HOPE [52], carbon black filled LDPE-ethylene methyl acrylate composites [28], carbon black filled HDPE [53], carbon black reinforced PP [27], talc filled PP [54], copper particle modified epoxy resins [55], epoxy and epoxy-haematite nanorod composites [56], polyvinyl pyrrolidone (PVP) and polyvinyl alcohol (PVA) blends [57], polyacrylonitrile based carbon fibre/PC composites [58], PC/MnCli composite films [59], titanocene polyester derivatives of terephthalic acid [60], lithium trifluoromethane sulfonamide doped PS-block-polyethylene oxide (PEO) copolymers [61], boron containing PVA derived ceramic organic semiconductors [62], sodium lanthanum tetrafluoride complexed with PEO [63], PC, acrylonitrile butadiene [64], blends of polyethylene dioxythiophene/ polystyrene sulfonate, PVC and PEO [65], EVA copolymer/carbon fibre conductive composites [66], carbon nanofibre modified thermotropic liquid crystalline polymers [67], PPY [68], PPY/PP/montmorillonite composites [69], carbon fibre reinforced PDMS-PPY composites [29], PANI [70], epoxy resin/PANI dodecylbenzene sulfonic acid blends [71], PANI/PA 6,6 composites [72], carbon fibre EVA composites [66], HDPE carbon fibre nanocomposites [52] and PPS [73]. [Pg.110]

The conductivity of the sample containing 0.05% PANI-CSA is approximately 10 S/cm, several orders of magnitude higher than the typical values of conductivity obtained in filled polymer composites containing similar volume fractions of carbon black [222-224 H. B. Brom, personal communication, 1994.) or graphite particles [225. 226]. Although percolation thresholds as low as0.1 vol % [222,223 H. B. Brom, personal communication] and 0.4 wt % [224] have been reported for carbon black/polymer composites, the conductivity near the percolation threshold for those samples is less than 10 S/cm. [Pg.72]

The TEM is one of the most generally useful microscopes many thousands of them ate in daily use throughout the world. They ate appHcable to the study of ultrafine particles (eg, pigments abrasives and carbon blacks) as well as microtomed thin sections of plant and animal tissue, paper, polymers, composites of all kinds, foods, industrial materials, etc. Even metals can be thinned to sections thin enough for detailed examination. [Pg.332]

Composite structures that consist of carbon particles and a polymer or plastic material are useful for bipolar separators or electrode substrates in aqueous batteries. These structures must be impermeable to the electrolyte and electrochemical reactants or products. Furthermore, they must have acceptable electronic conductivity and mechanical properties. The physicochemical properties of carbon blacks, which are commonly used, have a major effect on the desirable properties of the conductive composite structures. Physicochemical properties such as the surface... [Pg.237]

A composite consisting of a mixture of carbon particles (e.g., carbon black or graphite) and a polymer binder such as polyethylene or polypropylene with a surface layer of a carbon-black or carbon-felt... [Pg.241]

The Emerman model described in the previous section is hardly applicable to the carbon black-filled CCM as the black particles have sizes of hundreds angstrom and such a composite, compared with the molding channel size, may be considered as a homogeneous viscous fluid. Therefore, the polymer structure, crystallinity and orientation play an important role for such small particles. The above-given example of manufacture of the CCM demonstrates the importance of these factors being considered during processing of a composite material to and article with the desired electrical properties. [Pg.136]

At the other extreme, in the formation of composite materials, especially filled polymers, fine particles must be dispersed into a highly viscous Newtonian or non-Newtonian liquid. The incorporation of carbon black powder into rubber is one such operation. Because of the large surface areas involved, surface phenomena play an important role in such applications. [Pg.275]

Note 6 Electric conductance of a nonconducting polymer can be achieved by dispersing conducting particles (e.g., metal, carbon black) in the polymer. The resulting materials are referred to as conducting polymer composites or solid polymer-electrolyte composites. [Pg.245]

Among the two ionic polymerization techniques mentioned above, a living anionic polymerization should show the best possible control of polymer architecture and composition. Mono dispersed homopolymers, complex-block, graft, star, and miktoarm architectures have been accessible primarily by anionic polymerization methods [22]. They have been used to grow polymer brushes from various small particles such as silica gels graphite,carbon black, and flat surfaces [23-26]. Recent results have been reported on living anionic polymerizations on clay [27] and silica nanoparticles [28,29]. [Pg.113]

Composite-based PTC thermistors are potentially more economical. These devices are based on a combination of a conductor in a semicrystalline polymer—for example, carbon black in polyethylene. Other fillers include copper, iron, and silver. Important filler parameters in addition to conductivity include particle size, distribution, morphology, surface energy, oxidation state, and thermal expansion coefficient. Important polymer matrix characteristics in addition to conductivity include the glass transition temperature, Tg, and thermal expansion coefficient. Interfacial effects are extremely important in these materials and can influence the ultimate electrical properties of the composite. [Pg.595]

Although a majority of these composite thermistors are based upon carbon black as the conductive filler, it is difficult to control in terms of particle size, distribution, and morphology. One alternative is to use transition metal oxides such as TiO, VO2, and V2O3 as the filler. An advantage of using a ceramic material is that it is possible to easily control critical parameters such as particle size and shape. Typical polymer matrix materials include poly(methyl methacrylate) PMMA, epoxy, silicone elastomer, polyurethane, polycarbonate, and polystyrene. [Pg.596]

The electrical conductivity of two-phase, incompatible polymer blends containing carbon black has been shown to depend on the relative affinity of the conductive particles to each of the polymer components in the blend, the concentration of carbon black in the filler-rich phase, and the structural continuity of this phase [82]. Hence, by judicious manipulation of the phase microstructure, these three-phase filled composites can exhibit double percolation behaviour. [Pg.180]

Next 129Xe experiments on an EPDM terpolymer, which is present as the elastomer component in a composite material with carbon black will be discussed. The question investigated for these materials is whether the existence of any polymer-filler interaction can be detected by 129Xe NMR. This interaction influences the mobility of the elastomer chains in a relatively large shell around the filler particles. This fraction is called the bound rubber fraction. It is generally believed that the bound rubber fraction influences the mechanical and frictional properties of the filled elastomer [17, 18]. [Pg.474]


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