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Proton limiting conductances

H-NMR Using the dependence of the proton-NMR chemical shift on pH, base atom B-2. .. gave a pK of 3.28 0.04. This value is in excellent agreement with die previously-reported value of 3.3 (ref. 122). pK values for cobalamins and cobinamides have been discussed. The limiting conductance of the cyanocobalamin ion is 33 mhos. [Pg.158]

The excess mobihty-vs.-temperature curve was found to exhibit a max-immn at elevated temperatures near 150 °C, achievable at elevated pressure. The magnitude of the proton mobihty in pure water was not addressed in those studies, although attempts to determine it were made by Kohhausch at the end of the 19th centmy [78]. Focus was instead on the conductance of strong acids such as HCl in the Umit of infinite dilution. The difference of the measured conductance and the limiting conductance of a salt of a cation with size similar to that of was attributed to excess proton mobility, based on the assmnption that the hydrodynamic radius of both ions is similar. The excess mobility was taken to represent non-classical proton hops on top of the classical hydrodynamic motion of the HsO". ... [Pg.26]

Similarly, for a given calixarenate anion (common anion), the cation effect is reflected in the different A" values obtained for the various electrolytes. Thus, the limiting conductance decreases significantly ( 6.5 S cm mol" ) from the triethylammonium containing electrolyte to the protonated cryptand salt. This drop in conductance for the latter relative to the former electrolyte is likely to be the result not only of the considerable size increase of the cation but also to the shielding effect of the cryptands on the proton which will undoubtedly reduce the electric field in the vicinity of the ion. [Pg.378]

In Section 8, the material on solubility constants has been doubled to 550 entries. Sections on proton transfer reactions, including some at various temperatures, formation constants of metal complexes with organic and inorganic ligands, buffer solutions of all types, reference electrodes, indicators, and electrode potentials are retained with some revisions. The material on conductances has been revised and expanded, particularly in the table on limiting equivalent ionic conductances. [Pg.1284]

Polymer Electrolyte Fuel Cell. The electrolyte in a PEFC is an ion-exchange (qv) membrane, a fluorinated sulfonic acid polymer, which is a proton conductor (see Membrane technology). The only Hquid present in this fuel cell is the product water thus corrosion problems are minimal. Water management in the membrane is critical for efficient performance. The fuel cell must operate under conditions where the by-product water does not evaporate faster than it is produced because the membrane must be hydrated to maintain acceptable proton conductivity. Because of the limitation on the operating temperature, usually less than 120°C, H2-rich gas having Htde or no ([Pg.578]

Because there are two changes ia material composition near the active region, this represents a double heterojunction. Also shown ia Figure 12 is a stripe geometry that confines the current ia the direction parallel to the length of the junction. This further reduces the power threshold and makes the diffraction-limited spreading of the beam more symmetric. The stripe is often defined by implantation of protons, which reduces the electrical conductivity ia the implanted regions. Many different stmctures for semiconductor diode lasers have been developed. [Pg.10]

The presence of redox catalysts in the electrode coatings is not essential in the c s cited alx)ve because the entrapped redox species are of sufficient quantity to provide redox conductivity. However, the presence of an additional redox catalyst may be useful to support redox conductivity or when specific chemical redox catalysis is used. An excellent example of the latter is an analytical electrode for the low level detection of alkylating agents using a vitamin 8,2 epoxy polymer on basal plane pyrolytic graphite The preconcentration step involves irreversible oxidative addition of R-X to the Co complex (see Scheme 8, Sect. 4.4). The detection by reductive voltammetry, in a two electron step, releases R that can be protonated in the medium. Simultaneously the original Co complex is restored and the electrode can be re-used. Reproducible relations between preconcentration times as well as R-X concentrations in the test solutions and voltammetric peak currents were established. The detection limit for methyl iodide is in the submicromolar range. [Pg.76]

For last few years, extensive studies have been carried out on proton conducting inorganic/organic hybrid membranes prepared by sol-gel process for PEMFC operating with either hydrogen or methanol as a fuel [23]. A major motivation for this intense interest on hybrid membranes is high cost, limitation in cell operation temperature, and methanol cross-... [Pg.80]

Proton, that is, H+ ion, conductors are of importance as potential electrolytes in fuel cells. There are a number of hydroxides, zeolites, and other hydrated materials that conduct hydrogen ions, but these are not usually stable at moderate temperatures, when water or hydroxyl tends to be lost, and so have only limited applicability. [Pg.285]


See other pages where Proton limiting conductances is mentioned: [Pg.244]    [Pg.244]    [Pg.24]    [Pg.18]    [Pg.19]    [Pg.661]    [Pg.91]    [Pg.220]    [Pg.368]    [Pg.174]    [Pg.376]    [Pg.378]    [Pg.574]    [Pg.510]    [Pg.701]    [Pg.361]    [Pg.470]    [Pg.330]    [Pg.114]    [Pg.5]    [Pg.120]    [Pg.519]    [Pg.520]    [Pg.640]    [Pg.102]    [Pg.30]    [Pg.307]    [Pg.151]    [Pg.220]    [Pg.147]    [Pg.305]    [Pg.295]    [Pg.328]    [Pg.121]    [Pg.114]    [Pg.150]   
See also in sourсe #XX -- [ Pg.654 ]




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