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Oxidation representation

The N-hydroxy structure (26) was preferred123 to an iV-oxide representation on account of the amphoteric nature of the product and because the derived acetate formed a well-defined hydrochloride salt. Hydrogenation of these N-hydroxyimidazoles over Raney nickel gives imidazoles in 60-94% yields.122 The reaction has been adapted for the preparation of 4-mercaptoimidazoles, using an a-ketothionamide (27) with an aldimine.124... [Pg.129]

Fig. V-3. Schematic representation of (a) the Stem layer (b) the potential-determining ions at an oxide interface (c) the potential-determining and Stem layers together. Fig. V-3. Schematic representation of (a) the Stem layer (b) the potential-determining ions at an oxide interface (c) the potential-determining and Stem layers together.
Figure Bl.22.4. Differential IR absorption spectra from a metal-oxide silicon field-effect transistor (MOSFET) as a fiinction of gate voltage (or inversion layer density, n, which is the parameter reported in the figure). Clear peaks are seen in these spectra for the 0-1, 0-2 and 0-3 inter-electric-field subband transitions that develop for charge carriers when confined to a narrow (<100 A) region near the oxide-semiconductor interface. The inset shows a schematic representation of the attenuated total reflection (ATR) arrangement used in these experiments. These data provide an example of the use of ATR IR spectroscopy for the probing of electronic states in semiconductor surfaces [44]-... Figure Bl.22.4. Differential IR absorption spectra from a metal-oxide silicon field-effect transistor (MOSFET) as a fiinction of gate voltage (or inversion layer density, n, which is the parameter reported in the figure). Clear peaks are seen in these spectra for the 0-1, 0-2 and 0-3 inter-electric-field subband transitions that develop for charge carriers when confined to a narrow (<100 A) region near the oxide-semiconductor interface. The inset shows a schematic representation of the attenuated total reflection (ATR) arrangement used in these experiments. These data provide an example of the use of ATR IR spectroscopy for the probing of electronic states in semiconductor surfaces [44]-...
Fig. 1. Schematic representation of a battery system also known as an electrochemical transducer where the anode, also known as electron state 1, may be comprised of lithium, magnesium, zinc, cadmium, lead, or hydrogen, and the cathode, or electron state 11, depending on the composition of the anode, may be lead dioxide, manganese dioxide, nickel oxide, iron disulfide, oxygen, silver oxide, or iodine. Fig. 1. Schematic representation of a battery system also known as an electrochemical transducer where the anode, also known as electron state 1, may be comprised of lithium, magnesium, zinc, cadmium, lead, or hydrogen, and the cathode, or electron state 11, depending on the composition of the anode, may be lead dioxide, manganese dioxide, nickel oxide, iron disulfide, oxygen, silver oxide, or iodine.
Fig. 9. Schematic representation of a catalyst for ethylene oxide synthesis (not to scale). The porous support particle consists of microparticles held together... Fig. 9. Schematic representation of a catalyst for ethylene oxide synthesis (not to scale). The porous support particle consists of microparticles held together...
Another source of departure from stoichiometry occurs when cations are reduced, as for example in tire reduction of zinc oxide to yield an oxygen-defective oxide. The zinc atoms which are formed in tlris process dissolve in the lattice, Zn+ ions entering interstitial sites and the coiTesponding number of electrons being released from these dissolved atoms in much the same manner as was found when phosphorus was dissolved in the Group IV semiconductors. The Kroger-Viirk representation of dris reduction is... [Pg.225]

Evaluation of catalyst for oxidation of pollutants usually involves an Ignition Curve determination. This is a slightly overused expression, because only heat generation is evaluated, not heat removal. For a true ignition curve representation, heat removal evaluation would also be required. [Pg.103]

In the Fischer convention, the ermfigurations of other molecules are described by the descriptors d and L, which are assigned comparison with the reference molecule glyceraldehyde. In ertqrloying the Fischer convention, it is convenient to use projection formulas. These are planar representations defined in such a w as to convey three-dimensional structural information. The molecule is oriented with the major carbon chain aligned vertically in such a marmer that the most oxidized terminal carbon is at the top. The vertical bonds at each carbon are directed back, away fiom the viewer, and the horizontal bonds are directed toward the viewer. The D and L forms of glyceraldehyde are shown below with the equivalent Fischer projection formulas. [Pg.81]

Fig. 13. Schematic representation of oxygen dissolving froin the oxide into the titanium metal at high temperatures. The interface is weakened with the formation of voids, porosity, and microcracks and with the embrittlement of the interfacial metal region [52). Fig. 13. Schematic representation of oxygen dissolving froin the oxide into the titanium metal at high temperatures. The interface is weakened with the formation of voids, porosity, and microcracks and with the embrittlement of the interfacial metal region [52).
The four oxygen anions in the tetrahedron are balanced by the -i-4 oxidation state of the silicon cation, while the four oxygen anions connecting the aluminum cation are not balanced. This results in -1 net charge, which should be balanced. Metal cations such as Na", Mg ", or protons (H" ) balance the charge of the alumina tetrahedra. A two-dimensional representation of an H-zeolite tetrahedra is shown ... [Pg.70]

Fig. 10. Representation of the mechanism of redox driven K + transport using an electron and a cation carrier. (59-Ni°) and (59-Ni ) are the oxidized and reduced form of the electron carrier, the nickel bis-dithiolene complex 59 [] and [K+] are dicyclohexyl-18-crown-6 and its K+ complex. (Cited from Ref. 59>)... Fig. 10. Representation of the mechanism of redox driven K + transport using an electron and a cation carrier. (59-Ni°) and (59-Ni ) are the oxidized and reduced form of the electron carrier, the nickel bis-dithiolene complex 59 [] and [K+] are dicyclohexyl-18-crown-6 and its K+ complex. (Cited from Ref. 59>)...
The elements carbon and silicon form oxides with similar empirical formulas CO2 and SiOi. The former sublimes at —78.5°C and the latter melts at about 1700°C and boils at about 2200°C. From this large difference, propose the types of solids involved. Draw an electron dot or orbital representation of the bonding in C02 that is consistent with your answer. [Pg.318]

Two types of redox systems (Fig. 7) are used for batteries [14]. The standard potential (E°) of MnO 2 should be a good representation of the total energy of the oxide. For two-phase systems such as Pb02, Ag20, HgO, etc., the initial potential (E ) and middle potential (Em ) are equal to E°, from which we can calculate AF (-nFE°). For MnOz, a one-phase system, as shown in Fig. 7(A), the E (initial potential) cannot be used as E°. Ko-zawa proposed the middle potential (Em) of the S-shaped curve to be used as the E°... [Pg.118]

The reaction for the oxidation of sulphoxides by peracids in an alkaline medium is probably best described as shown in equation (16). Here the addition step is usually much slower than the latter step due to the low O—O bond energy which allows easy bond fission. For the reaction in acidic media, equation (17) is probably a good representation. [Pg.975]

Figure 39. Semilogarithmic representation of / vs. anodic potential from a series of potential steps. Each series was performed between a cathodic potential and different anodic potentials in a 0.1 M UClCtyPC solution. (Reprinted from T. F. Otero, H.-J. Grande, and J. Rodriguez, A new model for electrochemical oxidation of polypyrrole under conformational relaxation control. 7. Electroanal. Chem. 394,211, 1995, Figs. 2-5. Copyright 1995. Reprinted with permission from Elsevier Science.)... Figure 39. Semilogarithmic representation of / vs. anodic potential from a series of potential steps. Each series was performed between a cathodic potential and different anodic potentials in a 0.1 M UClCtyPC solution. (Reprinted from T. F. Otero, H.-J. Grande, and J. Rodriguez, A new model for electrochemical oxidation of polypyrrole under conformational relaxation control. 7. Electroanal. Chem. 394,211, 1995, Figs. 2-5. Copyright 1995. Reprinted with permission from Elsevier Science.)...
Figure 4.42. Ethylene epoxidation on Ag/p"-Al203.101 Steady-state effect of catalyst potential on the selectivity to ethylene oxide at various levels of gas-phase dichloroethane (a) and 3-dimensional representation of the effect of dichloroethane concentration, catalyst potential and corresponding Na coverage on the selectivity to ethylene oxide (b).101 Reprinted with permission from Academic Press. Figure 4.42. Ethylene epoxidation on Ag/p"-Al203.101 Steady-state effect of catalyst potential on the selectivity to ethylene oxide at various levels of gas-phase dichloroethane (a) and 3-dimensional representation of the effect of dichloroethane concentration, catalyst potential and corresponding Na coverage on the selectivity to ethylene oxide (b).101 Reprinted with permission from Academic Press.
FIGURE 12.12 A schematic representation of the electrolytic cell used in the Dow process for magnesium. The electrolyte is molten magnesium chloride. As the current generated by the external source passes through the cell, magnesium ions are reduced to magnesium metal at the cathode and chloride ions are oxidized to chlorine gas at the anode. [Pg.630]

FIGURE 12.14 A schematic representation showing the electrolytic process for refining copper. The anode is impure copper. The Cu2 ions produced by oxidation of the anode migrate to the cathode, where they are reduced to pure copper metal. A similar arrangement is used for electroplating objects. [Pg.632]

Figure 2-2. Schematic representation of the radial waveforms for 3d, 45 and 4p orbitals in first row transition-metal ions of intermediate oxidation state (Werner-type complexes). Figure 2-2. Schematic representation of the radial waveforms for 3d, 45 and 4p orbitals in first row transition-metal ions of intermediate oxidation state (Werner-type complexes).

See other pages where Oxidation representation is mentioned: [Pg.40]    [Pg.116]    [Pg.404]    [Pg.218]    [Pg.2409]    [Pg.288]    [Pg.267]    [Pg.18]    [Pg.102]    [Pg.238]    [Pg.291]    [Pg.613]    [Pg.434]    [Pg.706]    [Pg.72]    [Pg.1305]    [Pg.459]    [Pg.460]    [Pg.431]    [Pg.1052]    [Pg.219]    [Pg.225]    [Pg.430]    [Pg.448]    [Pg.211]    [Pg.345]    [Pg.397]    [Pg.193]    [Pg.180]    [Pg.129]    [Pg.94]   
See also in sourсe #XX -- [ Pg.152 ]




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