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Unpolarized metal

In conclusion, Ecorr and icorr can be determined from an Evans diagram for an unpolarized metal since icon- = ia = -ic at E = Ecoor- On... [Pg.86]

Measuring electrodes for impressed current protection are robust reference electrodes (see Section 3.2 and Table 3-1) which are permanently exposed to seawater and remain unpolarized when a small control current is taken. The otherwise usual silver-silver chloride and calomel reference electrodes are used only for checking (see Section 16.7). All reference electrodes with electrolytes and diaphragms are unsuitable as long-term electrodes for potential-controlled rectifiers. Only metal-medium electrodes which have a sufficiently constant potential can be considered as measuring electrodes. The silver-silver chloride electrode has a potential that depends on the chloride content of the water [see Eq. (2-29)]. This potential deviation can usually be tolerated [3]. The most reliable electrodes are those of pure zinc [3]. They have a constant rest potential, are slightly polarizable and in case of film formation can be regenerated by an anodic current pulse. They last at least 5 years. [Pg.408]

Fig. 10. Unpolarized Raman spectra (T = 300 K) for solid Ceo, KaCeo, RbsCeo, NaeCeo, KaCco, RbeCeo and CseCeo [92, 93], The tangential and radial modes of Ag symmetry are identified, as are the features associated with the Si substrates. From the insensitivity of these spectra to crystal structure and specific alkali metal dopant, it is concluded that the interactions between the Cao molecules are weak, as are also the interactions between the Cao anions and the alkali metal cations. Fig. 10. Unpolarized Raman spectra (T = 300 K) for solid Ceo, KaCeo, RbsCeo, NaeCeo, KaCco, RbeCeo and CseCeo [92, 93], The tangential and radial modes of Ag symmetry are identified, as are the features associated with the Si substrates. From the insensitivity of these spectra to crystal structure and specific alkali metal dopant, it is concluded that the interactions between the Cao molecules are weak, as are also the interactions between the Cao anions and the alkali metal cations.
Magnetic hyperfine splitting in Ru Mossbauer spectra was observed in the 1960s by Kistner [110, 143] for an absorber of 2.3 at% ruthenium dissolved in metallic iron. The spectra obtained with an unpolarized absorber (a) and with polarized absorbers, i.e., magnetization parallel to incident y-rays (b), and magnetization perpendicular to incident y-rays (c) are shown in Fig. 7.35. The stick spectra on top... [Pg.281]

Fig. 7.35 Ru Mossbauer spectra of Ruo.023Feo.977 at 4.2 K (source Rh in Ru metal), (a) unpolarized absorber (b) absorber magnetized parallel and (c) perpendicular to incident y-rays (from [110])... Fig. 7.35 Ru Mossbauer spectra of Ruo.023Feo.977 at 4.2 K (source Rh in Ru metal), (a) unpolarized absorber (b) absorber magnetized parallel and (c) perpendicular to incident y-rays (from [110])...
A comparison of weight loss during unpolarized immerision tests in various electrolytes [85, 89] for Ebonex and titanium metal electrodes is given below. [Pg.141]

The unpolar solvent required rather long reaction times, but allowed one to identify a Rh(I) intermediate, [Rh(CO)2]2(OEP), which carries two Rh(CO)2 groups on both sides on the porphyrin ring and is a typical example of a bimetallic porphyrin [8]. A photochemical variant of this insertion in benzene/tetrachloromethane [58] accelerates the reaction and gives a 50% yield of RhCl(OEP)H20. Aoyama, Ogoshi et al. [59] used [RhCl(CO)2]2 and carefully purified benzene. The solution of the porphyrin with the metal carrier was... [Pg.11]

The origin of the characteristic colors of alkali metal suboxides has been investigated by reflectometry in the range 1.4-6.2eV (900-200 nm). (63) Investigations have been confined to those samples which could be obtained as homogeneous mirrors on quartz glass. Measurements with unpolarized light and vertical incidence are shown in Fig. 23. [Pg.112]

Aggregation adversely affects metalation reactivity. With 2CHLi TMED in toluene at 25°C and 820 mm hydrogen the rate at 0AM was only one-fifth that at 0.025M (46). One possible explanation is that this is related to the increased formation of separated ion pairs in the aggregates. One could rationalize more facile hydrogenolysis in a contact ion pair via a four center reaction mechanism with lithium participation than in a simple anionic attack on unpolarized hydrogen. [Pg.17]

The relations given for both dielectrics and metals are for unpolarized incident radiation if polarization is important, then more detailed analysis must be used (see Refs. 1, 3,18,19). Also, the refractive index and absorption index may show spectral dependence, in which case the computed radiative properties will also be spectral in nature. [Pg.535]

For a few combinations of less reactive dienes and dienophiles, transition metal catalyzed variants of the Diels Alder reaction have been developed. An example is the cycloaddition of an unpolar diene and an unactivated alkyne however, except when the reaction is catalyzed with iron, nickel, cobalt, or rho-dium(I) complexes, the temperature required often causes competing decomposition, even for the intramolecular version. [2] Wilkinson s catalyst [3] - tris(triphenylphosphane)rho-dium(I) chloride - frequently used for hydrogenations and for decarbonylations, permits the cyclization of 4 to the annelated cyclo-hexadiene 5 in excellent yield in only 15 minutes at 55 °C in trifluoroethanol as solvent (Scheme 2). [2c]... [Pg.103]

In the study of the nature of atmosphereless solar system bodies it is also necessary to pay attention to the presence of circular polarization at large (> 120 ) phase angles. Non-zero circular polarization is typical of surface layers having small amounts of metallic particles [12]. Circular polarization can be observed even when the surface is illuminated with unpolarized light. [Pg.372]

Whereas the insertion of ynamines into a metal-alkynylcarbene bond to give 18 is initiated by a nucleophilic attack at the carbene carbon atom, [21] the less nucleophilic ( softer ) 3-acyl enamine 19 rather adds to the ( softer ) P-carbon of the alkynylcarbene ligand to give l-metala-l,3,5-hexatriene 20 which upon thermolysis in unpolar solvents undergoes cyclization and demetala-tion to homopyrrole 21 (Scheme 11). [22]... [Pg.238]


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See also in sourсe #XX -- [ Pg.86 ]




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