Silicon solution-precipitation

The red cake can be further purified by dissolving it in an aqueous solution of Na2C02- The iron, aluminum, and silicon impurities precipitate from the solution upon pH adjustment. Ammonium metavanadate then precipitates upon the addition of NH Cl and is calcined to give vanadium pentoxide of greater than 99.8% purity. 

Melendez-Martinez, J J., Gomez-Garcla, D., and Dominguez-Rodriguez, A., Acritical analysis and a recent improvement of the two-dimensional model for solution-precipitation creep application to silicon nitride ceramics , Phil. Mag., 2004, 84, 2305-16. 

The test and standaid samples are irradiated in a nuclear reactor. After dissolution in the presence of 12 mmol fluorine carrier, the solution is adjusted to pH 8-9. The hydrated silicon dioxide precipitate is filtered and the acidity of the filtrate is adjusted to IM nitric add. Then it is passed through a column packed with hydrated tin dioxide. The radioactivity of the column is measured. The oxygen content is calculated from the activities of the test and standard samples. This method is easy and quick, and is suitable for determinations of trace amounts of oxygen. 

Silicon nitride powder particles are contaminated by layers of silica on their surfaces. Oxide additives MxOy mixed with silicon nitride react with this silica and some of the nitride itself at sintering temperatures to form an oxynitride liquid which promotes liquid phase sintering and densification by solution-precipitation [1, 6, 10]. The a-Si3N4 dissolves in the liquid and is... 

Modifications to Precipitates. Silicon is sometimes added to Al—Cu—Mg alloys to help nucleate S precipitates without the need for cold work prior to the elevated temperature aging treatments. Additions of elements such as tin [7440-31-5] Sn, cadmium [7440-43-9] Cd, and indium [7440-74-6] In, to Al—Cu alloys serve a similar purpose for 9 precipitates. Copper is often added to Al—Mg—Si alloys in the range of about 0.25% to 1.0% Cu to modify the metastable precursor to Mg2Si. The copper additions provide a substantial strength increase. When the copper addition is high, the quaternary Al CuMg Si Q-phase must be considered and dissolved during solution heat treatment. 

Copper—chromium and copper—nickel—silicon—chromium alloys are also precipitation hardenable. The precipitates are nickel sdicides, chromium silicides, and elemental chromium. If conductivity is critical, the chromium—silicon ratio should be held at 10 1 so that appreciable amounts of either element are not left in soHd solution in the copper after aging. Lithium can be used as a deoxidizer in copper alloys when conductivity is important. For a discussion of the principle of age- or precipitation-hardening copper alloys, see Copperalloys,wrought copperalloys. 

Aluminum is the most abundant metallic element in the Earth s crust and, after oxygen and silicon, the third most abundant element (see Fig. 14.1). However, the aluminum content in most minerals is low, and the commercial source of aluminum, bauxite, is a hydrated, impure oxide, Al203-xH20, where x can range from 1 to 3. Bauxite ore, which is red from the iron oxides that it contains (Fig. 14.23), is processed to obtain alumina, A1203, in the Bayer process. In this process, the ore is first treated with aqueous sodium hydroxide, which dissolves the amphoteric alumina as the aluminate ion, Al(OH)4 (aq). Carbon dioxide is then bubbled through the solution to remove OH ions as HCO and to convert some of the aluminate ions into aluminum hydroxide, which precipitates. The aluminum hydroxide is removed and dehydrated to the oxide by heating to 1200°C. 

The luminescence of macrocrystalline cadmium and zinc sulfides has been studied very thoroughly The colloidal solutions of these compounds also fluoresce, the intensity and wavelengths of emission depending on how the colloids were prepared. We will divide the description of the fluorescence phenomena into two parts. In this section we will discuss the fluorescence of larger colloidal particles, i.e. of CdS particles which are yellow as the macrocrystalline material, and of ZnS particles whose absorption spectrum also resembles that of the macrocrystals. These colloids are obtained by precipitating CdS or ZnS in the presence of the silicon dioxide stabilizer mentioned in Sect. 3.2, or in the presence of 10 M sodium polyphosphate , or surfactants such as sodium dodecyl sulfate and cetyldimethylbenzyl-ammonium... 

Coprecipitation is a partitioning process whereby toxic heavy metals precipitate from the aqueous phase even if the equilibrium solubility has not been exceeded. This process occurs when heavy metals are incorporated into the structure of silicon, aluminum, and iron oxides when these latter compounds precipitate out of solution. Iron hydroxide collects more toxic heavy metals (chromium, nickel, arsenic, selenium, cadmium, and thorium) during precipitation than aluminum hydroxide.38 Coprecipitation is considered to effectively remove trace amounts of lead and chromium from solution in injected wastes at New Johnsonville, Tennessee.39 Coprecipitation with carbonate minerals may be an important mechanism for dealing with cobalt, lead, zinc, and cadmium. 

In 1978, on the basis of a few measurements of urine calcium and phosphate excretion as well as an awareness of the previously mentioned work regarding the amounts of calcium and phosphate normally accreted in utero and postnatally, it became apparent that the demineralization, fractures and rickets we were seeing in our infants were caused by calcium deficiency. Consequently we increased the amount of calcium added to the parenteral alimentation solutions. If more than 12.5 mM of the calcium were added to a liter of hyperalimentation solution, gross precipitation would occur in the feeding solution. If 10 mM of calcium were added per liter, crystalline precipitated began to build up on the inside of our barium-impregnated silicone rubber central venous catheters. This crystalline precipitate resulted in gradual occlusion and functional loss of these lines. After several false starts and six lost catheters, chemical and crystal analysis showed that the precipitate inside these catheters was CaHPO. ... 

The product of the fusion of silica with sodium carbonate, sodium silicate (strictly called sodium poly trioxosilicate but usually metasilicate), dissolves in water to give a clear, viscous solution known as waterglass . It hydrolyses slowly and silica is precipitated. Besides the metasilicate, other silicates of sodium are known, e.g. the poly-tetroxosilicate (orthosilicate), Na4Si04. Only the silicates of the alkali metals are soluble in water. Other silicates, many of which occur naturally, are insoluble, and in these substances the polysilicate anions can have highly complicated structures, all of which are constructed from a unit of one silicon and four oxygen atoms arranged tetrahedrally (cf. the structure of silica). Some of these contain aluminium (the aluminatesilicates) and some have import ant properties and uses. 

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