Chloride oxide

Higher chlorides, Si2Cle to Si6Cl,4 (highly branched - some cyclic) are formed from SiCU plus Si or a silicide or by amine catalysed disproportionations of Si2Cl,5, etc. Partial hydrolysis gives oxide chlorides, e.g. CUSiOSiCla. SiCU is used for preparation of silicones. 

Sulphur tetrachloride, SCI4, m.p. 30 C. Stable only in the solid. The oxide chloride of sulphur(lV) is SOCI2, thionyl chloride. ... 

Sulphur(Vl) forms the oxide chloride S02C12, sulphuryl chloride see sulphuryl halides). 

Titaniufn(iy) chloride, T1CI4, m.p. — 25"C, b.p. 136°C, d 1-76. Colourless liquid, important intermediate in Ti production (TiOi plus C plus CI2). Hydrolysed via oxide chlorides to Ti02- Forms many complexes including [TiCUP. ... 

Copper. Some 15 copper compounds (qv) have been used as micronutrient fertilizers. These include copper sulfates, oxides, chlorides, and cupric ammonium phosphate [15928-74-2] and several copper complexes and chelates. Recommended rates of Cu appHcation range from a low of 0.2 to as much as 14 kg/hm. Both soil and foHar appHcations are used. 

Uses. The principal use of magnesium hydroxide is in the pulp (qv) and paper (qv) industries (52). The main captive use is in the production of magnesium oxide, chloride, and sulfate. Other uses include ceramics, chemicals, pharmaceuticals, plastics, flame retardants/smoke suppressants, and the expanding environmental markets for wastewater treatment and SO removal from waste gases (87). 

In the initial thiocyanate-complex Hquid—Hquid extraction process (42,43), the thiocyanate complexes of hafnium and zirconium were extracted with ether from a dilute sulfuric acid solution of zirconium and hafnium to obtain hafnium. This process was modified in 1949—1950 by an Oak Ridge team and is stiH used in the United States. A solution of thiocyanic acid in methyl isobutyl ketone (MIBK) is used to extract hafnium preferentially from a concentrated zirconium—hafnium oxide chloride solution which also contains thiocyanic acid. The separated metals are recovered by precipitation as basic zirconium sulfate and hydrous hafnium oxide, respectively, and calcined to the oxide (44,45). This process is used by Teledyne Wah Chang Albany Corporation and Western Zirconium Division of Westinghouse, and was used by Carbomndum Metals Company, Reactive Metals Inc., AMAX Specialty Metals, Toyo Zirconium in Japan, and Pechiney Ugine Kuhlmann in France. 

Chelated complexes such as sodium zirconium lactate [15529-67-6] or ammonium zirconium carbonate [22829-17-0] and acidic forms such as zirconium hydroxy oxide chloride [18428-88-1] have been used in preparations in deodorants or for treatment for poison oak and poison ivy dermatitis. In such occasions, when the skin had been cut or abraded, a few users developed granulomas which have been identified as a delayed hypersensitivity to zirconium (99). These may take several weeks to develop, and commonly persist for 6 months to over a year. 

Hydroxyl Compounds. The aqueous chemistry of zirconium is complex, and in the past its understanding was compHcated by differing interpretations. In a study of zirconium oxide chloride and zirconium oxide bromide, the polymeric cation [Zr4(OH)g (H20)jg was identified (189) the earlier postulated moiety [Zr=0] was discarded. In the tetramer, the zirconium atoms are coimected by double hydroxyl bridges (shown without the coordinating water molecules) ... 

Oxide Chlorides. Zirconium oxide dichloride, ZrOCl2 -8H2 0 [13520-92-8] commonly called zirconium oxychloride, is really a hydroxyl chloride, [Zr4(OH)g T6H2 0]Clg T2H2O (189). Zirconium oxychloride is produced commercially by caustic fusion of zircon, followed by water washing to remove sodium siUcate and to hydrolyze the sodium zirconate the wet filter pulp is dissolved in hot hydrochloric acid, and ZrOCl2 -8H2 O is recovered from the solution by crystallization. An aqueous solution is also produced by the dissolution and hydrolysis of zirconium tetrachloride in water, or by the addition of hydrochloric acid to zirconium carbonate. 

Anhydrous zirconium oxide chloride, ZrOCl2 [7699-43-6] has been prepared by the reaction of dichlorine oxide with a zirconium tetrachloride suspension in carbon tetrachloride starting at —30° C and slowly rising to room temperature. The white soHd is extremely hygroscopic and decomposes to ZrCl and Zr02 at 250°C (200). 

Although zirconium phosphate is insoluble in acids, it is easily hydrolyzed in excess caustic to give hydrous zirconium oxide. Zirconium phosphate forms soluble complexes with a large excess of zirconium oxide chloride, and therefore separation of phosphoms from zirconium oxide chloride solutions is difficult (215). 

Dissolve 1 g zirconium(IV) oxide chloride octahydrate (zirconyl chloride) in 50 ml methanol. 

SbOF and SbOCl can be obtained as polymeric solids by controlled hydrolysis of SbX3. Several other oxide chlorides can be obtained by varying the conditions, e.g. ... 

Zinnozyd, n. tin oxide, specif, stannic oxide, tin(IV) oxide, -chlorid, n. stannic chloride, tin(IV) chloride, -hydrat, n. stannic hydroxide, tin(IV) hydroxide, -natron, n. sodium stannate. -salz, n. stannic salt, tin(IV) salt. 

Spray solution Dissolve 2 to 25 g zirconium(IV) oxide chloride octahydrate in 100 ml methanol [1], ethanol — water (55 + 15) [5] or water [4]. 

Many years ago, geochemists recognized that whereas some metallic elements are found as sulfides in the Earth s crust, others are usually encountered as oxides, chlorides, or carbonates. Copper, lead, and mercury are most often found as sulfide ores Na and K are found as their chloride salts Mg and Ca exist as carbonates and Al, Ti, and Fe are all found as oxides. Today chemists understand the causes of this differentiation among metal compounds. The underlying principle is how tightly an atom binds its valence electrons. The strength with which an atom holds its valence electrons also determines the ability of that atom to act as a Lewis base, so we can use the Lewis acid-base model to describe many affinities that exist among elements. This notion not only explains the natural distribution of minerals, but also can be used to predict patterns of chemical reactivity. 

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