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Oxygen and the Oxides

Predict the ionic or molecular character of the products in Example 5-7. [Pg.193]

Reaction (a) is a reaction between hydrogen and another nonmetal. The product, HI, must be molecular. Reaction (b) is the reaction of hydrogen with an active Group 1A metal. Thus, KH must be ionic. The products of reaction (c) are molecular H2(g) and the strong base, NaOH, which is ionic. [Pg.193]

Oxygen was discovered in 1774 by an English minister and scientist, Joseph Priestley (1733-1804). He observed the thermal decomposition of mercury(II) oxide, a red powder, to form liquid Hg and a colorless gas  [Pg.193]

Oxygen atoms, or radicals, are intermediates in this exothermic decomposition of O3 to O2. They act as strong oxidizing agents in such applications as destroying bacteria in water purification. [Pg.193]

The ozone molecule is angular and has two oxygen-oxygen bond lengths (1.28 A) that are identical. This is intermediate between typical single and donble bond lengths between oxygen atoms. [Pg.193]


In all these cases, the electrode potential will be determined by a mixed reaction resulting from the reduction of oxygen and the oxidation of the... [Pg.94]

The mixed-potential model demonstrated the importance of electrode potential in flotation systems. The mixed potential or rest potential of an electrode provides information to determine the identity of the reactions that take place at the mineral surface and the rates of these processes. One approach is to compare the measured rest potential with equilibrium potential for various processes derived from thermodynamic data. Allison et al. (1971,1972) considered that a necessary condition for the electrochemical formation of dithiolate at the mineral surface is that the measmed mixed potential arising from the reduction of oxygen and the oxidation of this collector at the surface must be anodic to the equilibrium potential for the thio ion/dithiolate couple. They correlated the rest potential of a range of sulphide minerals in different thio-collector solutions with the products extracted from the surface as shown in Table 1.2 and 1.3. It can be seen from these Tables that only those minerals exhibiting rest potential in excess of the thio ion/disulphide couple formed dithiolate as a major reaction product. Those minerals which had a rest potential below this value formed the metal collector compoimds, except covellite on which dixanthogen was formed even though the measured rest potential was below the reversible potential. Allison et al. (1972) attributed the behavior to the decomposition of cupric xanthate. [Pg.9]

Under aerobic conditions, the glycolytic pathway becomes the initial phase of glucose catabolism (fig. 13.2). The other three components of respiratory metabolism are the tricarboxylic acid (TCA) cycle, which is responsible for further oxidation of pyruvate, the electron-transport chain, which is required for the reoxidation of coenzyme molecules at the expense of molecular oxygen, and the oxidative phosphorylation of ADP to ATP, which is driven by a proton gradient generated in the process of electron transport. Overall, this leads to the potential formation of approximately 30 molecules of ATP per molecule of glucose in the typical eukaryotic cell. [Pg.283]

Yttrium stabilized zirconia (Zr02-Y203) as an electrolyte for reduction of molecular oxygen at elevated temperatures (400-800°C) has been already discussed in Section 6.23.4. In fact, both the reduction of oxygen and the oxidation of the oxide ion at the Pt/zirconia interface is reversible and the transport of both species in zirconia is so rapid it is possible to construct an electrochemical oxygen pump, which is the heart of the limiting current oxygen sensor described in this chapter (Saji, 1987). The overall electrochemical reaction that takes place at the porous Pt electrode is... [Pg.232]

Kimble ML, Castleman AW Jr, Mitric R, Biirgel C, Bonacic-Koutecky V (2004) Reactivity of atomic gold anions toward oxygen and the oxidation of CO Experiment and theory. J Am Chem Soc 126 2526... [Pg.315]

Oxygen and the Oxides Oxygen and Ozone Reactions of Oxygen and the Oxides... [Pg.235]

As described in Section 21.3.2, the H2 addition promotes the oxidation of hydrocarbon to surface oxygenates and the oxidation of NO to nitrates. It is clear, that the co-presence of protons and reduced Ag species is indispensable for reductive oxidation of 02 to yield reactive oxygen species (02 ). This clearly explains why CO is not effective as a co-reductant and why the formation of Ag clusters is not sufficient to improve the catalytic activity. Over 0.5 wt.% Ag/Al203, showing no activity for NO reduction, monomeric Ag+ species are not reduced to clusters, and 02 is not produced because of the absence of reduced Ag species. The co-presence of CO leads to the formation of Ag clusters, though the condition is not sufficient because of the absence of protons. The co-presence of both the dissociated hydrogen as acidic proton and Ag cluster are indispensable for the 02 activation. [Pg.139]

Both oxidation pathways, the NOs catalysed oxidation of S(IV) by molecular oxygen and the oxidation of S(IV) by peroxy nitric acid lead to the formation of sulphate anions and further studies are required to decide, which of the two pathways is the mot important (or... [Pg.258]

The photochemical oxidation of PC can be characterized by the increase in absorbance at 3470 cm 1 versus irradiation time, as shown on Fig. 15.3. Oxidation occurred rapidly for uncoated PC. A decrease in the rate of oxidation was observed in the case of the coated samples. The more the ZnO layer is thick, the less is the oxidation rate. Similar conclusions were drawn when the absorbance was measured at 400 nm. The screening effect reduces therefore the PC photodegradation produced by the direct absorption of sunlight radiations. In addition, we have shown that the grain size and the density increase with the coating thickness. The coatings are denser and have lower micro voids. Consequently, they are more impermeable to oxygen and the oxidation is limited. [Pg.586]


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Oxygen and oxidation

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