Oxides hydroxides

Selenious acid, H2Se03. Formed water on Se02. More stable than H2SO3, oxidized to H2Se04, reduced to Se by SO2. Gives selen-ates(IV) with oxides, hydroxides or carbonates. 

Nitrates are prepared by the action of nitric acid on a metal or its oxide, hydroxide or carbonate. All nitrates are soluble in water. On heating, the nitrates of the alkali metals yield only oxygen and the nitrite ... 

Many salt-like halides can be prepared by the action of the hydro-halic acid. HX, on the metal or its oxide, hydroxide or carbonate. The halides prepared by this method are often hydrated, particularly when a less electropositive metal is involved, for example zinc, iron. 

A discussion of the adsorption of water on oxides would be incomplete without some reference to the irreversible effects which are often encountered when samples of oxide, hydroxide or oxide-hydroxide are exposed to the vapour. These effects ( low-temperature ageing ), which manifest themselves in changes in surface area, in pore structure and sometimes in the lattice structure itself, are complex and difficult to reproduce exactly. ... 

Manufacture. Fluoroborate salts are prepared commercially by several different combinations of boric acid and 70% hydrofluoric acid with oxides, hydroxides, carbonates, bicarbonates, fluorides, and bifluorides. Fluoroborate salts are substantially less corrosive than fluoroboric acid but the possible presence of HF or free fluorides cannot be overlooked. Glass vessels and equipment should not be used. 

Manufacture. The transition- and heavy-metal fluoroborates can be made from the metal, metal oxide, hydroxide, or carbonate with fluoroboric acid. Because of the difficulty ia isolating pure crystalline soflds, these fluoroborates are usually available as 40—50% solutions, M(BP. Most... 

Fig. 1. General process operations for hydrothermal synthesis. Feedstocks may be oxides, hydroxides or salts, gels, organic materials, or acids or bases. The atmosphere within the reactor may be oxidising or reducing. To convert MPa to psi, multiply by 145.

Mir-slaked lime contains various proportions of the oxides, hydroxides, and carbonates of calcium and magnesium which result from excessive exposure of quicklime to air that vitiates its quaUty. It is partially or largely decomposed quicklime that has become hydrated and carbonated. 

Magnesium nitrate is prepared by dissolving magnesium oxide, hydroxide, or carbonate in nitric acid, followed by evaporation and crystallization at room temperature. Impurities such as calcium, iron, and aluminum are precipitated by pretreatment of the solution with slight excess of magnesium oxide, followed by filtration. Most magnesium nitrate is manufactured and used on site in other processes. 

Perchlorates. Historically, perchlorates have been produced by a three-step process (/) electrochemical production of sodium chlorate (2) electrochemical oxidation of sodium chlorate to sodium perchlorate and (4) metathesis of sodium perchlorate to other metal perchlorates. The advent of commercially produced pure perchloric acid directly from hypochlorous acid means that several metal perchlorates can be prepared by the reaction of perchloric acid and a corresponding metal oxide, hydroxide, or carbonate. 

Calcium Peroxide. Pure calcium peroxide [1305-79-9] Ca02, has been prepared, but the commercial product is a mixture made by reaction of calcium hydroxide and hydrogen peroxide. Commercial material contains either 60 or 75% Ca02 the remainder is a poorly defined mixture of calcium oxide, hydroxide, and carbonate. A well-defined octahydrate [60762-59-6] 8H20, can be crysta11i2ed from aqueous systems. 

In some cases, a pigment s thermal and chemical resistance can be improved by the encapsulation of the pigment particles by an iasoluble, colorless layer of metal oxide or oxide—hydroxide, eg, siUca, Si02. The function of such a shell is to prevent direct contact and reaction between the pigment surface and the organic matrix ia which the pigment is dispersed (11). 

Iron Oxide Yellows. From a chemical point of view, synthetic iron oxide yellows, also known as iron gelbs, are based on the iron(III) oxide—hydroxide, a-FeO(OH), known as goethite. Color varies from light yellows to dark buffs and is primarily determined by particle size, which is usually between 0.1 and 0.8 p.m. Because of their resistance to alkahes, these are used by the building industry to color cement. Thermally, iron oxide yellows are stable up to 177°C above this temperature they dehydrate to iron(III) oxide ... 

Aluminum [7429-90-5] Al, atomic number 13, atomic weight 26.981, is, at 8.8 wt %, the third most abundant element in the earth s cmst. It is usually found in siUcate minerals such as feldspar [68476-25-5] clays, and mica [12001 -26-2]. Aluminum also occurs in hydroxide, oxide—hydroxide, fluoride, sulfate, or phosphate compounds in a large variety of minerals and ores. 

The CAS registry Hsts 5,037 aluminum-containing compounds exclusive of alloys and intermetaUics. Some of these are Hsted in Table 1. Except for nepheline and alunite in the USSR and Poland, bauxite is the raw material for all manufactured aluminum compounds. The term bauxite is used for ores that contain economically recoverable quantities of the aluminum hydroxide mineral gibbsite or the oxide—hydroxide forms boehmite and diaspore. 

The term alumina hydrates or hydrated aluminas is used in industry and commerce to designate aluminum hydroxides. These compounds are tme hydroxides and do not contain water of hydration. Several forms are known a general classification is shown in Figure 1. The most weU-defined crystalline forms ate the trihydroxides, Al(OH) gibbsite [14762-49-3], bayerite [20257-20-9], and nordstrandite [13840-05-6], In addition, two aluminum oxide—hydroxides, AIO(OH), boelimite [1318-23-6] and diaspote [14457-84-2], have been clearly defined. The existence of several other forms of aluminum hydroxides have been claimed. However, there is controversy as to whether they ate truly new phases or stmctures having distorted lattices containing adsorbed or intedameUar water and impurities. 

Boehmite (OC-Aluminum Oxide-Hydroxide). Boehmite, the main constituent of bauxite deposits in Europe, is also found associated with gibbsite in tropical bauxites in Africa, Asia, and Austraha. Hydrothemial transformation of gibbsite at temperatures above 150 °C is a common method for the synthesis of weU-cry stalhzed boehmite. Higher temperatures and the presence of alkali increase the rate of transfomiation. Boehmite ciy stals of 5—10 ]liii size (Fig. 3) are produced by tliis method. Fibrous (acicular) boehmite is obtained under acidic hydrothemial conditions (6). Excess water, about 1% to 2% higher than the stoichiometric 15%, is usually found in hydrothemiaHy produced boehmite. 

Fig. 3. Aluminum oxide—hydroxide hydrothemiaHy prepared boehmite, x2,000.

Diaspore (P-Aluminum Oxide Hydroxide). Diaspore, found in bauxites of Greece, Cliina, and the USSR, can also be obtained by hydrothemial transfomiation of gibbsite and boehmite. Higher (>200°) temperatures and pressure (>15 AlPa-150bar) are needed for synthesis and the presence of diaspore seed cry stals helps to avoid boehmite fomiation. 

Under equiUbrium vapor pressure of water, the crystalline tfihydroxides, Al(OH)2 convert to oxide—hydroxides at above 100°C (9,10). Below 280°—300°C, boehmite is the prevailing phase, unless diaspore seed is present. Although spontaneous nucleation of diaspore requires temperatures in excess of 300 °C and 20 MPa (200 bar) pressure, growth on seed crystals occurs at temperatures as low as 180 °C. For this reason it has been suggested that boehmite is the metastable phase although its formation is kinetically favored at lower temperatures and pressures. The ultimate conversion of the hydroxides to comndum [1302-74-5] AI2O2, the final oxide form, occurs above 360°C and 20 MPa. 

Many of the procedures used for technical analysis of aluminum hydroxides are readily available from the major producers of aluminum hydroxides. Phase Composition. Weight loss on ignition (110°—1200°C) can differentiate between pure (34.5% Al(OH)2) ttihydroxides and oxide—hydroxides (15% Al(OH)2). However, distinction between individual ttihydroxides and oxide —hydroxides is not possible and the method is not useful when several phases are present together. X-ray powder diffraction is the most useful method for identifying and roughly quantifying the phase composition of hydroxide products. 

The carboxyl group reacts with metal oxides, hydroxides, or salts to form rosin soaps or salts (resinates). The soaps of alkah metals, such as sodium and potassium, are usehil in paper sizing and as emulsifiers in mbber polymerization. 

Sodium is commonly shipped in 36- to 70-t tank cars in the United States. Smaller amounts are shipped in 16-t tank tmcks or ISO-tanks. Sodium is also available in 104- and 190-kg dmms, and in bricks (0.5—5 kg). A thin layer of oxide, hydroxide, or carbonate is usually present. Sodium is also marketed in small lots as a dispersion in an inert hydrocarbon, or produced in-process via high pressure injection into a pumped stream of inert carrier fluid, such as toluene or mineral oil. 

Strontium Oxide, Hydroxide, and Peroxide. Strontium oxide, SrO, is a white powder that has a specific gravity of 4.7 and a melting point of 2430°C. It is made by heating strontium carbonate with carbon in an electric furnace, or by heating celestite with carbon and treating the sulfide formed with caustic soda and then calcining the product (10). It reacts with water to form strontium hydroxide [18480-07-4] and is used as the source of strontium peroxide [1314-18-7],... 

Sulfamates. Sulfamates are formed readily by the reaction of sulfamic acid and the appropriate metal or its oxide, hydroxide, or carbonate. Approximate heats of neutraH2ation are —54.61 kJ/mol(—13.05 kcal/mol) for the NaOH reaction and —47.83 kJ/mol (—11.43 kcal/mol) for NH OH at... 

Hydrated Titanium Oxides. Hydroxides of Ti(Il) (black) and Ti(Ill) (brown) are precipitated when an alkaU metal hydroxide is added to a solution of the corresponding salt. These precipitates, though difficult to purify (45), are powerful reduciag agents and readily oxidize ia air to form a hydrated titanium dioxide. 

Stibonic and Stibinic Acids. The stibonic acids, RSbO(OH)2, and stibinic acids, R2SbO(OH), are quite different in stmcture from their phosphoms and arsenic analogues. The stibonic and stibinic acids are polymeric compounds of unknown stmcture and are very weak acids. lUPAC classifies them as oxide hydroxides rather than as acids. Thus CgH3SbO(OH)2 is named phenyl antimony dihydroxide oxide [535-46-6], the Chemical Abstracts n.2ixn.e is dihydroxyphenylstibine oxide [535-46-6], CgH OgSb. 

Electrodes. A number of different types of nickel oxide electrodes have been used. The term nickel oxide is common usage for the active materials that are actually hydrated hydroxides at nickel oxidation state 2+, in the discharged condition, and nickel oxide hydroxide [12026-04-9] NiO OH, nickel oxidation state 3+, in the charged condition. Nickelous hydroxide [12034-48-7J, Ni(OH)2, can be precipitated from acidic solutions of bivalent nickel... 

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