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Oxygen spatial distribution

Figure 5 Oxygen-oxygen spatial distribution functions g r) for a 3 1 water-methanol solution at 25 °C. Above Water-water correlations for g f) = 2.0. Below Methanol-oxygen density around water for an iso-surface threshold of 1.75. Figure 5 Oxygen-oxygen spatial distribution functions g r) for a 3 1 water-methanol solution at 25 °C. Above Water-water correlations for g f) = 2.0. Below Methanol-oxygen density around water for an iso-surface threshold of 1.75.
If, however, it is assumed from Eq. (2-40) that the protection current density corresponds to the cathodic partial current density for the oxygen reduction reaction, where oxygen diffusion and polarization current have the same spatial distribution, it follows from Eq. (2-47) with = A0/7 ... [Pg.161]

Figure 2.14. The molecular orbitals of gas phase carbon monoxide, (a) Energy diagram indicating how the molecular orbitals arise from the combination of atomic orbitals of carbon (C) and oxygen (O). Conventional arrows are used to indicate the spin orientations of electrons in the occupied orbitals. Asterisks denote antibonding molecular orbitals, (b) Spatial distributions of key orbitals involved in the chemisorption of carbon monoxide. Barring indicates empty orbitals.5 (c) Electronic configurations of CO and NO in vacuum as compared to the density of states of a Pt(lll) cluster.11 Reprinted from ref. 11 with permission from Elsevier Science. Figure 2.14. The molecular orbitals of gas phase carbon monoxide, (a) Energy diagram indicating how the molecular orbitals arise from the combination of atomic orbitals of carbon (C) and oxygen (O). Conventional arrows are used to indicate the spin orientations of electrons in the occupied orbitals. Asterisks denote antibonding molecular orbitals, (b) Spatial distributions of key orbitals involved in the chemisorption of carbon monoxide. Barring indicates empty orbitals.5 (c) Electronic configurations of CO and NO in vacuum as compared to the density of states of a Pt(lll) cluster.11 Reprinted from ref. 11 with permission from Elsevier Science.
A different situation arises with a preliminary reduced surface. In this case the measured value of y is within lO - 10 2, and as the temperature increases, the y grows by the Arrhenius Law (Equation) with the activation energy of 5.2 kcal/mole. In addition, there is dependence of y upon the triplet oxygen pressure in the set-up, though the experiment conditions allow us to neglect a priori the impact of homogeneous processes on the spatial distribution of 02( A ) molecules. Prolonged... [Pg.311]

Raman spectroscopy has been successfully applied to the investigation of oxidic catalysts. According to Wachs, the number of Raman publications rose to about 80-100 per year at the end of the nineties, with typically two thirds of the papers devoted to oxides [41]. Raman spectroscopy provides insight into the structure of oxides, their crystallinity, the coordination of metal oxide sites, and even the spatial distribution of phases through a sample when the technique is used in microprobe mode. As the frequencies of metal-oxygen vibrations found in a lattice are typically between a few hundred and 1000 cm 1 and are thus difficult to investigate in infrared, Raman spectroscopy is clearly the indicated technique for this purpose. [Pg.235]

The sensor covalently joined a bithiophene unit with a crown ether macrocycle as the monomeric unit for polymerization (Scheme 1). The spatial distribution of oxygen coordination sites around a metal ion causes planarization of the backbone in the bithiophene, eliciting a red-shift upon metal coordination. They expanded upon this bithiophene structure by replacing the crown ether macrocycle with a calixarene-based ion receptor, and worked with both a monomeric model and a polymeric version to compare ion-binding specificity and behavior [13]. The monomer exhibited less specificity for Na+ than the polymer. However, with the gradual addition of Na+, the monomer underwent a steady blue shift in fluorescence emission whereas the polymer appeared to reach a critical concentration where the spectra rapidly transitioned to a shorter wavelength. Scheme 2 illustrates the proposed explanation for blue shift with increasing ion concentration. [Pg.396]

A spatial distribution of Pb centres (g = 2.0029, g — 2.0086) has been revealed in porous silicon formed by anodic etching of crystalline silicon in hydrofluoric acid.144 Oxygen ions were also implanted using accelerator at 2 MeV and compared with photoluminescence. [Pg.24]

Figure 12. Steady-state spatial distribution of different oxygen uptake rates in a... Figure 12. Steady-state spatial distribution of different oxygen uptake rates in a...
Lipschultz et al. (1985) documented the light inhibition of NH3 oxidation in the Delaware River and concluded that this effect influenced the spatial distribution of nitrification in the estuary. Depending on their depth, light is not usually a problem for nitrification in sediments. In shallow sediments, light may have an indirect positive effect on nitrification rates by increasing photosynthesis, and thus increasing oxygen supply to the sediments (Lorenzen et al., 1998). [Pg.239]

Bao H., Thiemens M. H., and Heine K. (2001) Oxygen-17 excesses of the Central Namib gypcretes spatial distribution. Earth Planet. Sci. Lett. 192, 125-135. [Pg.2289]

Figure 2 Spatial distribution functions displayed as three-dimensional maps showing the local oxygen density in liquid water. Above TIP4P water at ambient conditions Below PPC water along the co-existence line at 2U0 C. The iso-surfaces shown are for — 1.3 where the surfaces have been cf)k>ied according to their separation from the central molecule, as discu.sse Figure 2 Spatial distribution functions displayed as three-dimensional maps showing the local oxygen density in liquid water. Above TIP4P water at ambient conditions Below PPC water along the co-existence line at 2U0 C. The iso-surfaces shown are for — 1.3 where the surfaces have been cf)k>ied according to their separation from the central molecule, as discu.sse<l in the text.

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Spatial distributions

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