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Maximum conductance

Both anatase and mtile are broad band gap semiconductors iu which a fiUed valence band, derived from the O 2p orbitals, is separated from an empty conduction band, derived from the Ti >d orbitals, by a band gap of ca 3 eV. Consequendy the electrical conductivity depends critically on the presence of impurities and defects such as oxygen vacancies (7). For very pure thin films, prepared by vacuum evaporation of titanium metal and then oxidation, conductivities of 10 S/cm have been reported. For both siugle-crystal and ceramic samples, the electrical conductivity depends on both the state of reduction of the and on dopant levels. At 300 K, a maximum conductivity of 1 S/cm has been reported at an oxygen deficiency of... [Pg.121]

As an example of a standard for feed-water for a once-through boiler BS 2486 gives a maximum conductivity of 0-2/iS/cm at 25°C and pH in the... [Pg.849]

The results of an investigation performed upon various salts in PC [207] or MeOH [15] can be summarized as follows. Both the maximum conductivity and the appertaining concentration 41 are determined by the viscosity and ionic radii (nonsolvated ions) or Stokes radii (solvated ions), meaning that electrolytes show a Stokes-Walden behavior, entailing... [Pg.487]

Making use of Eq. (25), the maximum conductivity of a solid electrolyte with monovalent mobile species is given by... [Pg.533]

Suggested maximum conductance values are intended to serve as an alarm for saltwater condenser leaks and can be correlelated with chloride ion content in FW and/or BW. [Pg.575]

On the other hand, Doblhofer218 has pointed out that since conducting polymer films are solvated and contain mobile ions, the potential drop occurs primarily at the metal/polymer interface. As with a redox polymer, electrons move across the film because of concentration gradients of oxidized and reduced sites, and redox processes involving solution species occur as bimolecular reactions with polymer redox sites at the polymer/solution interface. This model was found to be consistent with data for the reduction and oxidation of a variety of species at poly(7V-methylpyrrole). This polymer has a relatively low maximum conductivity (10-6 - 10 5 S cm"1) and was only partially oxidized in the mediation experiments, which may explain why it behaved more like a redox polymer than a typical conducting polymer. [Pg.587]

In the case of linear oUgoethyleneoxy side groups (Table 12), the maximum conductivity increases with the length of the side group from 2.6x10 S cm for x= 1 to 4.8x 10" S cm for x=6. After x=6, the conductivity decreases probably on account of the formation of microcrystalUtes. [Pg.204]

Table 12 Maximum conductivity of the [N=P(0(CH2CH20)xCH3)2]n/LiS03CF3 systems at 25 °C... Table 12 Maximum conductivity of the [N=P(0(CH2CH20)xCH3)2]n/LiS03CF3 systems at 25 °C...
Table 15 Maximum conductivity of the polystyrene derivatives VIII, IX/LiCl04 systems... Table 15 Maximum conductivity of the polystyrene derivatives VIII, IX/LiCl04 systems...
The mechanical properties of X depend partly on the length of the oli-goethyleneoxy groups. The polymers are solid for x=l, highly viscous gums for x=3 and elastomers for x=7.2. The maximum conductivity of these complexes at 30 °C are reported in Table 16. Gel electrolytes have also been obtained by adding propylene carbonate (PC) (10-50 wt%) to these polynorbornene de-... [Pg.209]

Table 16 Maximum conductivity of polynorbornenes bearing cyclotriphosphazenes/lithium salt systems at 30 °C... Table 16 Maximum conductivity of polynorbornenes bearing cyclotriphosphazenes/lithium salt systems at 30 °C...
Multi-armed polymers with a cyclotriphosphazene core XI and XII have been synthesized from the reaction of polyethylene glycol monomethyl ethers with acid chlorides of hexakis(3,5-dicarboxyphenoxy) and hexakis(4-carboxyphe-noxy) cyclotriphosphazenes. Their complexes with LiC104 were investigated, and their maximum conductivities are reported in Table 17 [621]. [Pg.210]

The variations of the conductivity of the corresponding complexes with salt concentration with lithium triflate were similar to those of MEEP, with a passage through a maximum when this concentration increased. The maximum conductivities of these complexes are reported Table 18. [Pg.211]

Polythiophene films can be electrochemically cycled from the neutral to the conducting state with coulombic efficiencies in excess of 95% [443], with little evidence of decomposition of the material up to + 1.4 V vs. SCE in acetonitrile [37, 54, 56, 396,400] (the 3-methyl derivative being particularly stable [396]), but unlike polypyrrole, polythiophene can be both p- and n-doped, although the n-doped material has a lower maximum conductivity [444], Cyclic voltammetry shows two sets of peaks corresponding to the p- and n-doping reactions, with E° values at approximately + 1.1 V and — 1.4 V respectively (vs. an Ag+/Ag reference electrode)... [Pg.57]

For an ideal conductor, no scattering occurs, and the transmission is given by T = 1. The quantum of conductance Go is obtained, indicating a maximum conductance. In other words, a perfect single-channel conductor between two electrodes has a finite, non-zero resistance. The exact interpretation of this result was provided by Imry [177], who associated the finite resistance with resistance arising at the interface between leads and the electrodes. [Pg.134]

The maximum conductivity of fluorite-structured oxygen ion conductors is not only a function of dopant concentration, but also of dopant radius [9], For stabilized zirconia, the conductivity increases as the radius becomes close to that of Zr4 (rvm = 0.084 nm). The best value is reached for Sc3+ (rvlll = 0.087 nm) with a conductivity of 0.1 Scnr1 at 800°C for (ScjC o. ZrO o. ). For the sake of comparison,... [Pg.4]

The ratio of the integrated currents for the first reduction wave of V2+ and the oxidation wave of the polythiophene from 0.4 V to 1.0 V vs. Ag+/Ag is about 4. This value means that upon oxidation of poly(I) one electron is withdrawn from four repeat units in the backbone of the polymer upon scanning to +1.0 V vs. Ag+/Ag. At this potential, the polythiophene achieves its maximum conductivity (vide infra). The level of oxidation to achieve maximum conductivity is consistent with the result reported by Gamier and co-workers (31-33) that the doping level of oxidized polythiophene is about 25%, but the Garnier work did not establish that the 25% doping level corresponds to maximum conductivity. Scheme III illustrates the electrochemical processes of poly(I) showing reversible oxidation of the polythiophene backbone and reversible reduction of the pendant V2+ centers. [Pg.414]

Electrochemical oxidation of X produces a polymer film with polythiophene as the backbone and viologen centers as pendant redox groups. The electrochemical properties of the polymer are the combination of polythiophene and viologen. Using viologen subunits as the internal standard (one per repeat unit of the polymer), the "doping level" of the oxidized polythiophene backbone at its maximum conductivity can be measured and is about 25%. The charge transport via the pendant V2+/+ of poly(l) has been studied by... [Pg.427]

The situation at the end of the ionogenic reaction (maximum conductivity and D424) is complicated, in that the reaction mixture then contains ester, saturated and unsaturated... [Pg.665]

A concern for alkaline as well as solid polymer electrolysers should be the sensitivity of the electrolysers to contaminants in the feed water. The minimum required water quality of an industrial solid polymer electrolyzer is ASTM type II water [48], which contains at maximum 5 pg L 1 of sodium and chlorine, and 3 pg L 1 Si02 [52], It should have a maximum conductivity of 0.25 pS cm 1. Clean drinking water meeting Dutch standards contains around 60 mg L 1 of... [Pg.317]

With t taking experimental values in the range 1-5 for both CNTs and graphene [26,27,28]. The upper limit of equation (8.4) is ct0, which has been experimentally found to be as high as around 104 S/m for both CNTs [24] and graphene [29]. These values can be taken as indicators of the maximum conductivities attainable by dispersing nanocarbons in polymer matrices. [Pg.233]


See other pages where Maximum conductance is mentioned: [Pg.418]    [Pg.43]    [Pg.43]    [Pg.285]    [Pg.186]    [Pg.486]    [Pg.600]    [Pg.572]    [Pg.207]    [Pg.209]    [Pg.210]    [Pg.211]    [Pg.648]    [Pg.180]    [Pg.433]    [Pg.116]    [Pg.47]    [Pg.506]    [Pg.48]    [Pg.15]    [Pg.23]    [Pg.34]    [Pg.148]    [Pg.156]    [Pg.427]    [Pg.112]   


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