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Lead oxide molar volume

For the oxidation of methanol, inhibition by water is assumed by other working groups [23]. In our work however, the results of methanol conversion (Figure 2c) indicate no such inhibition by addition of only small amounts of water in the range of experimental accuracy. The lower conversion in the case of the SCWO may be only a consequence of the lower molar volume of the wato solution. While maintaining the molar ratios and the molar flows constant, expCTiments in carbon dioxide and in wato were carried out with slightly different concentrations of methanol and oxygen simply because of the different molar volume of water and CO2. This should lead to a different conversion. (See also calculations, presented later in this chapto. )... [Pg.444]

Because the molar volumes of oxides differ from those of the corresponding metals, the oxide layers formed are subject to tensile or compressive stress. If sufficiently important, these can lead to cracking or pealing of the oxide films. The PUling-Bedworth Ratio, is a measure of the relative magnitude of the molar volumes of oxides and metals. [Pg.374]

All these oxide phases can be included in the oxides with framework structure. These are oxides (Ma/bO) with composition a/h<0.5 and effective molar volumes bigger than those for the oxides of compact structures (MO2) and the smallest metal content. In these oxides the coordination polyhedra can be identified, connected by corners, edges, etc. Most of these structures can be derived from the structure of the oxide ReQs where the MO octahedrons form a regular lattice. Other cations can easily be included in the structure of this type of oxides. This leads to the stabilization of the structure, and as a result, one can obtain the perovskite-type structures or their variations. [Pg.226]

The mole fractions of aluminium and chromium, as well as the molar volumes, can easily be determined. The diffusion coefficients have been chosen from the literature as given in Table 4.1. Only the solubility of oxygen in iron has not yet been measured without uncertainty [21], because even small levels of impurities lead to adulteration of the results by oxide formation. Thus in this work another method has been chosen. The critical value h has been set to 1/3. From [22] the lowest aluminium contents for the formation of a closed alumina layer on Fe-Al binary alloys have been chosen and the oxygen solubility is then calculated. The result is plotted in Fig. 4.1. The three data points are connected by the best fit straight line Xq = ll%e—kt— Compared... [Pg.70]

Modes of passive degradation are not different from what we can observe in other aqueous media. We may, for example, observe a dissolution at grain boundaries associated with the release of particles and hydrolysis phenomena, sometimes limited to the siuface of the material. In the case of multiphase ceramics, phenomena connected to the transfer of material between phases of different solubility may appear. The release of particles in tissues or biological fluids may sometimes produce inflammatory reactions which we will analyze later. Certain plasma sprayed coatings of calcium phosphate can be associated with small proportions of calcium oxide, whose hydration is accompanied by a large increase in molar volume, leading to the formation of cracks and to a detachment from the metallic substrate. [Pg.509]

On the Figure 9 it appears that the cracks seem to be healed inside the matrix since they cannot be observed after 13h under air at 850 C. Moreover, the oxidation of TiB2 leads to the formation of Ti02 grains (reaction 5) which are covering the matrix surface (due to an increase of 1.64 in the molar volume ) and can act as an environmental barrier. Further characterizations on the self-healing behavior of this material are under progress. [Pg.184]


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See also in sourсe #XX -- [ Pg.60 ]




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