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Field strength metallized

Heterogeneous surface areas consist of anodic regions at corrosion cells (see Section 2.2.4.2) and objects to be protected which have damaged coating. Local concentrations of the current density develop in the area of a defect and can be determined by measurements of field strength. These occur at the anode in a corrosion cell in the case of free corrosion or at a holiday in a coated object in the case of impressed current polarization (e.g., cathodic protection). Such methods are of general interest in ascertaining the corrosion behavior of metallic construction units... [Pg.123]

Fig. 7.31 Partial ligand-field strength for the ligand L in correlation with the isomer shift 5 (relative to Ru metal at 4.2 K) of the nitrosylruthenium (II) compounds [RuL5(NO)]" (L = Br, Cr, NCS, NH3, CN ) (from [124])... Fig. 7.31 Partial ligand-field strength for the ligand L in correlation with the isomer shift 5 (relative to Ru metal at 4.2 K) of the nitrosylruthenium (II) compounds [RuL5(NO)]" (L = Br, Cr, NCS, NH3, CN ) (from [124])...
These results obtained in applied field clearly prove that the ST in the dinuclear compounds under study proceeds via [HS-HS] O [HS-LS] O [LS-LS]. Simultaneous ST in both iron centers of the [HS-HS] pairs, leading directly to [LS-LS] pairs, apparently can be excluded, at least in the systems discussed above. This is surprising in view of the fact that these dinuclear complexes are centrosymmetric, that is, the two metal centers have identical surroundings and therefore, experience the same ligand field strength and consequently, thermal ST is expected to set in simultaneously in both centers. In other dinuclear iron(II) complexes, however, thermally induced direct ST from [HS-HS] to [LS-LS] pairs does occur and, indeed, has been observed by Mossbauer measurements [30, 31]. [Pg.406]

Metal Current density (mA/ cm2) Oxide thickness (nm) Electric field strength (V/nm) t+... [Pg.429]

It is well-established that the molecular and electronic structures of metal complexes of azamacrocycles are greatly affected upon N-alkylation (197). This is mainly due to two factors (a) the decrease of the ligand field strength and (b) the increase in the steric requirements upon going from a secondary to a tertiary amine donor function (251). To examine whether the properties of the dinuclear amine-thiophenolate complexes are affected by the N-alkyl substituents, analogous complexes of the... [Pg.442]


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