Electrical conductance, stability

The expansion of the areas of application for carbon fibers is stimulated by their attractive properties, not found in other materials, such as strength, electrical conductivity, stability on exposure to reactive media, low density, low-to-negative coefficient of thermal expansion, and resistance to shock heating. The most representative applications of carbon fibers and element carbon fibers are as sorption materials, electrostatic discharge materials, catalysts, and reinforcement materials in composites. 

The selection of a suitable chemical route depends primarily on two factors (1) the availability of a counter functionality for the desired reactant, and (2) the influence of the posttreatment on the desired properties of the carbon material (e.g., electrical conductivity, stability, wettability). 

Whilst the conductivity of these polymers is generally somewhat inferior to that of metals (for example, the electrical conductivity of polyacetylenes has reached more than 400 000 S/cm compared to values for copper of about 600 000 S/cm), when comparisons are made on the basis of equal mass the situation may be reversed. Unfortunately, most of the polymers also display other disadvantages such as improcessability, poor mechanical strength, poor stability under exposure to common environmental conditions, particularly at elevated temperatures, poor storage stability leading to a loss in conductivity and poor stability in the presence of electrolytes. In spite of the involvement of a number of important companies (e.g. Allied, BASF, IBM and Rohm and Haas) commercial development has been slow however, some uses have begun to emerge. It is therefore instructive to review briefly the potential for these materials. 

Many liquid alloys, in particular, the alkali-group IV alloys, exhibit (Zintl) anion clustering and show strong effects of compound formation. A typical example of such Zintl systems are sodium-tin alloys. In the solid NaSn crystal the Zintl anions Sn appear [1]. An interesting question is the stability of these anions in the liquid. Furthermore, the electrical conductivity of these alloys shows a strong dependence on composition [2] For the limiting (sodium-rich or tin-rich) cases a metallic (small) conductivity appears, but for the nearly equimolar compositions a semi-metallic behavior - with a considerably smaller conductivity - is observed. 

From the obtained trajectories the following structural and electronic properties were extracted (i) structure factors, (ii) stability of Sn complexes, in particular, the Zintl anions, and (iii) the electrical conductivities - which yield answers to the questions mentioned in the first paragraph. 

Steam-turbine lubricants Lubricants in steam turbines are not exposed to such arduous conditions as those in engines. The main requirement is for high oxidation stability. However, they may be exposed to aqueous condensate or, in the case of marine installations, to sea water contamination, so they have to be able to separate from water easily and to form a rustpreventing film on ferrous surfaces, and it is usual to employ rust inhibitors. The problem of tin oxide formation on white-metal bearings is associated with the presence of electrically conducting water in lubricants and can be over-come by keeping the lubricant dry . 

In Chapter 5 we identified metals by their high electrical conductivity. Now we can explain why they conduct electric current so well. It is because there are some electrons present in the crystal lattice that are extremely mobile. These conduction electrons move throughout the metallic crystal without specific attachment to particular atoms. The alkali elements form metals because of the ease of freeing one electron per atom to provide a reservoir of conduction electrons. The ease of freeing these conduction electrons derives from the stability of the residual, inert gas-like atoms. 

Ionic bond, 287, 288 dipole of, 288 in alkali metal halides, 95 vs. covalent, 287 Ionic character, 287 Ionic crystal, 81, 311 Ionic radius, 355 Ionic solids, 79, 81, 311 electrical conductivity, 80 properties of, 312 solubility in water, 79 stability of, 311... 

Filler or Reinforcement Chcmicul Resistance i 8 u i i Electrical Insulation Impact Strength Tensile Strength Dimensional Stability Stiffness Hardness Lubricity Electrical Conductivity Thermal Conductivity 1 8 C s TS 1 X I I h 11... 

An electric conductive rubber base containing carbon black is laminated with an electric conductive cover layer of phosphoric acid ester plasticizer and other ionic surfactants to prepare antistatic mats, where the covers have colors other than black. It is also reported that alkyl acid phosphates act as color stabilizer for rubber. Small amounts of phosphate esters are helpful in restoring reclaimed rubber to a workable viscosity [284,290]. Esters of phosphoric acid are used in the production of UV-stable and flame-retarded alkylbenzenesulfonate copolymer compositions containing aliphatic resins and showing a high-impact strength... 

For the support material of electro-catalysts in PEMFC, Vulcan XC72(Cabot) has been widely used. This carbon black has been successfully employed for the fuel cell applications for its good electric conductivity and high chemical/physical stability. But higher amount of active metals in the electro-catalysts, compared to the general purpose catalysts, make it difficult to control the metal size and the degree of distribution. This is mainly because of the restricted surface area of Vulcan XC72 carbon black. Thus complex and careM processes are necessary to get well dispersed fine active metal particles[4,5]. 

The composition of the electrolyte is quite important in controlling the electrolytic deposition of the pertinent metal, the chemical interaction of the deposit with the electrolyte, and the electrical conductivity of the electrolyte. In the case of molten salts, the solvent cations and the solvent anions influence the electrodeposition process through the formation of complexes. The stability of these complexes determines the extent of the reversibility of the overall electroreduction process and, hence, the type of the deposit formed. By selecting a suitable mixture of solvent cations to produce a chemically stable solution with strong solute cation-anion interactions, it is possible to optimize the stability of the complexes so as to obtain the best deposition kinetics. In the case of refractory and reactive metals, the presence of a reasonably stable complex is necessary in order to yield a coherent deposition rather than a dendritic type of deposition. 

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