Metal oxide precipitation

In the range of pH exhibited by most natural water and in the concentration range greater than millimolar few metal ions exist as simple hydrated cations, and relatively few oxyanions exist as simple monomeric species. The hydrated cations are good buffers toward bases, the metallate ions toward acids. As pH is raised in solutions of many hydrated cations, isopolycations are produced, and ultimately, hydrous metal oxides precipitate. As pH is lowered in solutions of many metallate ions, isopolyanions are produced, and ultimately, hydrous oxides precipitate. Salts of the intermediate isopolyions precipitate in some cases. Where the results are unambiguous, the nature of the intermediate species can be described. Kinetics are thought to have been neglected in studies of such solutions up to the present time. 

Judging from the above, the reason for the increase of catalytic activity is due to the well mixed structure of Cu and ZnO nanocrystals and the increase of surface Cu by MA method. We conclude that MA method is an effective method for obtaining high performance Cu/ZnO catalysts compared with conventional metal oxide precipitation method by wet processing method. 

The molecular-scale structure and chemistry of crystalline and X-ray amorphous metal oxide precipitates... 

Adsorption onto surfaces such as suspended particulates, and carbonate or hydrous metal oxide precipitation. 

We shall now analyse some consequences of the obtained formula, which describes the behaviour of the E-pd dependence in different sections of the potentiometric titration curve. The first consequence concerns the onset of the metal-oxide precipitation the condition... 

As is well known, alkaline-earth metal-oxides possess a limited solubility in molten chlorides at 1000 K. In the saturated solutions of these oxides equilibrium (3.6.1) takes place. Therefore, there are two simultaneous reactions in the carbonate solutions, namely, equations (3.6.1) and (3.7.66), which may result in the precipitation of a solid phase. For equation (3.6.1) all we have said above for the carbonate remains true, i.e. the plateau (Fig. 3.7.23, sections 1-3) may also be a result of alkaline-earth metal-oxide precipitation. 

Group precipitant for several higher-charged metal ions from strongly acid solution. Precipitate ignited to metal oxide. 

Most metals will precipitate as the hydroxide in the presence of concentrated NaOH. Metals forming amphoteric hydroxides, however, remain soluble in concentrated NaOH due to the formation of higher-order hydroxo-complexes. For example, Zn and AP will not precipitate in concentrated NaOH due to the formation of Zn(OH)3 and Al(OH)4. The solubility of AP in concentrated NaOH is used to isolate aluminum from impure bauxite, an ore of AI2O3. The ore is powdered and placed in a solution of concentrated NaOH where the AI2O3 dissolves to form A1(0H)4T Other oxides that may be present in the ore, such as Fe203 and Si02, remain insoluble. After filtering, the filtrate is acidified to recover the aluminum as a precipitate of Al(OH)3. 

Figure 17 summarizes the avadable sol—gel processes (56). The process on the right of the figure involves the hydrolysis of metal alkoxides in a water—alcohol solution. The hydrolyzed alkoxides are polymerized to form a chemical gel, which is dried and heat treated to form a rigid oxide network held together by chemical bonds. This process is difficult to carry out, because the hydrolysis and polymerization must be carefully controlled. If the hydrolysis reaction proceeds too far, precipitation of hydrous metal oxides from the solution starts to occur, causing agglomerations of particulates in the sol. 

Alkali Meta.IPhospha.tes, A significant proportion of the phosphoric acid consumed in the manufacture of industrial, food, and pharmaceutical phosphates in the United States is used for the production of sodium salts. Alkali metal orthophosphates generally exhibit congment solubility and are therefore usually manufactured by either crystallisation from solution or drying of the entire reaction mass. Alkaline-earth and other phosphate salts of polyvalent cations typically exhibit incongment solubility and are prepared either by precipitation from solution having a metal oxide/P20 ratio considerably lower than that of the product, or by drying a solution or slurry with the proper metal oxide/P20 ratio. 

Antimony trioxide is insoluble in organic solvents and only very slightly soluble in water. The compound does form a number of hydrates of indefinite composition which are related to the hypothetical antimonic(III) acid (antimonous acid). In acidic solution antimony trioxide dissolves to form a complex series of polyantimonic(III) acids freshly precipitated antimony trioxide dissolves in strongly basic solutions with the formation of the antimonate ion [29872-00-2] Sb(OH) , as well as more complex species. Addition of suitable metal ions to these solutions permits formation of salts. Other derivatives are made by heating antimony trioxide with appropriate metal oxides or carbonates. 

In general, hydrated borates of heavy metals ate prepared by mixing aqueous solutions or suspensions of the metal oxides, sulfates, or halides and boric acid or alkali metal borates such as borax. The precipitates formed from basic solutions are often sparingly-soluble amorphous soHds having variable compositions. Crystalline products are generally obtained from slightly acidic solutions. 

Bromine reacts with some metal oxides, eg, thorium oxide, at high temperatures in the presence of reducing agents to form bromides (18). Certain nonhydrated metal haUdes can be formed by precipitation. These include AgBr, CuBr, AuBr, HBr, PbBr2, PtBr2, and Hg2Br2 (19). 

Supports are often prepared first and the catalyst and promoter components added later (60). Metal oxide supports are usually prepared by precipitation from aqueous solutions. Nitrates are commonly used anions alkaUes and ammonium are commonly used cations. Metal oxide supports, eg, sihca and alumina, are prepared in the form of hydrogels. Mixed oxides such as siUca—alumina are made by cogelation. Carefiil control of conditions such as pH is important to give uniform products. 

Nickel plating solutions may contain excess iron and unknown organic contaminants. Iron is removed by peroxide oxidation, precipitation at a pH of about 5, then filtered out. The more complex, less water-soluble organic contaminants along with some trace metals are removed with activated carbon treatments in separate treatment tanks. About 5 g/L of plating-grade activated carbon is mixed in the plating solution for at least 1—2 hours, usually at warmer temperatures. 

With Acyl Halides, Hydrogen Halides, and Metallic Halides. Ethylene oxide reacts with acetyl chloride at slightly elevated temperatures in the presence of hydrogen chloride to give the acetate of ethylene chlorohydrin (70). Hydrogen haUdes react to form the corresponding halohydrins (71). Aqueous solutions of ethylene oxide and a metallic haUde can result in the precipitation of the metal hydroxide (72,73). The haUdes of aluminum, chromium, iron, thorium, and zinc in dilute solution react with ethylene oxide to form sols or gels of the metal oxide hydrates and ethylene halohydrin (74). 

Calcium carbonate makes up the largest amount of deposit in many cooling water systems (Fig. 4.16) and can be easily detected by effervescence when exposed to acid. Deposits are usually heavily stratified, reflecting changes in water chemistry, heat transfer, and flow. Corrosion may be slight beneath heavy accumulations of fairly pure calcium carbonate, as such layers can inhibit some forms of corrosion. When nearly pure, calcium carbonate is white. However, calcium carbonates are often intermixed with silt, metal oxides, and precipitates, leading to severe underdeposit attack. 

Underdeposit corrosion is not so much a single corrosion mechanism as it is a generic description of wastage beneath deposits. Attack may appear much the same beneath silt, precipitates, metal oxides, and debris. Differential oxygen concentration cell corrosion may appear much the same beneath all kinds of deposits. However, when deposits tend to directly interact with metal surfaces, attack is easier to recognize. 

Titanium dioxide used for adhesive applications should contain an inorganic coating to control polarity, improve its ease of dispersion, and improve its weather resistance. The inorganic coating (zirconium dioxide, silica, alumina) is applied in the aqueous sluny by precipitation of one or more hydrated metal oxides and by neutralization of acidic and alkaline compounds. 

The development of electrostatic precipitators soon led to new applications, including the separation of metal oxide fumes. This was followed by various metal manufacturing processes such as the lead blast furnace, ore roaster, and reverberatory furnace. Electrostatic gas cleaning was soon applied also in cement kilns and in several exotic applications, such as recovering valuable metals from exhaust gases. 

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