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Metal oxides in water

Solution phase deposition of metal oxides is less established than deposition of metal sulfides. The chemical process for the formation of metal oxides in water can be considered to be hydrolysis of metal cations and dehydration of intermediate hydroxides, for divalent cations described as... [Pg.53]

The corresponding normal sulfates are completely converted to the hydrogen sulfates and formally they are analogous to the metal oxides in water (37). [Pg.395]

T24.il A very good starting point for tiiis research is Guo, J., Chen, X. (2012). Solar Hydrogen Generation Transition Metal Oxides in Water Photoelectrolysis. New York McGraw-Hill Professional. [Pg.222]

LAVOISIER. After the fall of the Phlogiston Theory and the discovery of oxygen, Lavoisier studied the combustion of carbon, sulfur and phosphorus in 1777. By dissolving the resulting non-metallic oxides in water, he found that all these solutions show acidic effects. Based on these examples, he defined acids as substances composed of a non-metal and oxygen. In addition, he found out that acids, combined with the bases , the metal oxides, result in well-known salts carbon dioxide forms the carbonates, sulfuric acid the sulfates, phosphoric acid the phosphates - the combination system of acids and bases was discovered ... [Pg.13]

Does the reaction of a main-group metal oxide in water produce an acidic solution or a basic solution Write a balanced equation for the reaction of a Group 2A(2) oxide with water. [Pg.266]

Another aspect of this topic is the colloidal stability of nanoparticles, mainly in metal oxides. In water, the most common liquid medium, metal oxide surface chemistry is controlled by the surface hydroxyl groups [42-44]. The following surface equilibrium condition must therefore be considered ... [Pg.37]

Table 9.23 Selected physico-chemico properties of metal oxides in water (Tengvall and Lundstrom, 1992)... [Pg.451]

In general, the reaction and dissolving of the Group 2 metal oxides in water is described by the following ionic equation ... [Pg.176]

Perhaps the simplest case of reaction of a solid surface is that where the reaction product is continuously removed, as in the dissolving of a soluble salt in water or that of a metal or metal oxide in an acidic solution. This situation is discussed in Section XVII-2 in connection with surface area determination. [Pg.282]

In mixtures of nonpolar solvents with little water, surfactants form spherical reverse micelles. They have a reversed orientation of the molecules with the hydrophilic groups in the interior and a drop of enclosed water in the middle. Starting from a precursor material, metal oxides in the form of uniform nanosized spheres can be obtained by hydrolysis under controlled conditions (pH, concentration, temperature). For example, titanium oxide spheres are obtained from a titanium alkoxide, Ti(OR)4 + 2 H20 —t Ti02 + 4 ROH. [Pg.245]

Zinc hydroxy double salts are layered materials similar to layered double hydroxides which show intercrystalline reactivity and incorporate organic compounds between layers.337 Hydroxy double salts of high crystallinity can be obtained by reacting ZnO with organic metal salts in water. Zinc oxide crystals could then be prepared by thermal treatment of hydroxy zinc acetate.338... [Pg.1173]

Ionic metal oxides contain the oxide ion, which is a very strong base. Therefore, the addition of a metal oxide to water will result in a basic solution as a result of the reaction... [Pg.301]

In groundwater, hexavalent chromium tends to be mobile due to the lack of solubility constraints and the low adsorption of CH6 anion species by metal oxides in neutral to alkaline waters (Calder 1988). Above pH 8.5, no CH6 adsorption occurs in groundwater Cr adsorption increases with decreasing pH. Trivalent chromium species tend to be relatively immobile in most groundwaters because of the precipitation of low-solubility Cr 3 compounds above pH 4 and high adsorption of the Cr+3 ion by soil clay below pH 4 (Calder 1988). [Pg.81]

Transition metal oxides (in absence of water) are therefore essential catalysts for many chemical processes such as oxidation (e.g., oxidation of CO in emission control), dehydrogenation (e.g., production of aldehydes from alcohol), and selective reduction (e.g., reduction of NO). Usually, activation of an oxide by heating is a pre-... [Pg.38]

For metal oxide electrodes, the iso-electric point pH p is also located midway between the unitary acidic proton level and the unitary basic proton level of adsorbed water. Table 9-1 shows the iso-electric point pHi, of several metal oxides in aqueous solutions. [Pg.322]

Moisture acts as a debonding agent through one of or a combination of the following mechanisms 1) attack of the metallic surface to form a weak, hydrated oxide interface, 2) moisture assisted chemical bond breakdown, or 3) attack of the adhesive. (2 ) A primary drawback to good durability of metal/adhesive bonds in wet environments is the ever present substrate surface oxide. Under normal circumstances, the oxide layer can be altered, but not entirely removed. Since both metal oxides and water are relatively polar, water will preferentially adsorb onto the oxide surface, and so create a weak boundary layer at the adhesive/metal interface. For the purposes of this work, the detrimental effects of moisture upon the adhesive itself will be neglected. The nitrile rubber modified adhesive used here contains few hydrolyzable ester linkages and therefore will be considered to remain essentially stable. [Pg.181]

Stone TA, Morgan JJ (1987) Reductive dissolution of metal oxides. In W Stumm (ed) Aquatic surface chemistry Chemical processes at the particle water interface. WUey, New York pp 221-254... [Pg.407]

Macdonald, D.D., Rummery, T.E. and Tomlinson, M., "Stability and Solubility of Metal Oxides in High Temperature Water", proceedings of the IAEA Symposium on the Thermodynamics of Nuclear Materials, Vol. II, pl23. International Atomic Energy Agency IAEA-SM-190/19, Vienna (1975). [Pg.345]


See other pages where Metal oxides in water is mentioned: [Pg.32]    [Pg.4364]    [Pg.596]    [Pg.467]    [Pg.4363]    [Pg.199]    [Pg.32]    [Pg.4364]    [Pg.596]    [Pg.467]    [Pg.4363]    [Pg.199]    [Pg.90]    [Pg.117]    [Pg.374]    [Pg.145]    [Pg.390]    [Pg.125]    [Pg.436]    [Pg.186]    [Pg.81]    [Pg.152]    [Pg.276]    [Pg.412]    [Pg.404]    [Pg.111]    [Pg.364]    [Pg.63]    [Pg.456]    [Pg.440]    [Pg.103]    [Pg.90]    [Pg.117]    [Pg.100]    [Pg.298]    [Pg.305]    [Pg.257]   
See also in sourсe #XX -- [ Pg.89 ]




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