Silicates chlorides

By besting sodium in s current of the vapour of silicic chloride.—... 

Preparation.-—By heating jduminium Tery strongly in a current of the vapour of silicic chloride. The aluminic chloride which is formed volatilizes, leaving the adamantine silicon bc-hind —... 

For many years after the Joosten Process was proven in the field, the term chemical grout was synonymous with the Joosten Process and sodium silicate. However, sodium silicate is the basis for many chemical grout formulations in addition to the silicate-chloride two-shot injection. In a similar marmer to the way the techniques of cement grouting could not be cost effectively applied to chemical grouting, the techniques of using high viscosity silicates did not transfer well to the low viscosity materials coming on the market. 

Sodium silicate Chloride Schweinitz et al. (1942) Dechema Werk (1%5)... 

Brunauer and co-workers [129, 130] found values of of 1310, 1180, and 386 ergs/cm for CaO, Ca(OH)2 and tobermorite (a calcium silicate hydrate). Jura and Garland [131] reported a value of 1040 ergs/cm for magnesium oxide. Patterson and coworkers [132] used fractionated sodium chloride particles prepared by a volatilization method to find that the surface contribution to the low-temperature heat capacity varied approximately in proportion to the area determined by gas adsorption. Questions of equilibrium arise in these and adsorption studies on finely divided surfaces as discussed in Section X-3. 

Heavy water, see Hydrogen[ H] oxide Heazlewoodite, see rn-Nickel disulfide Hematite, see Iron(III) oxide Hermannite, see Manganese silicate Hessite, see Silver telluride Hieratite, see Potassium hexafluorosilicate Hydroazoic acid, see Hydrogen azide Hydrophilite, see Calcium chloride Hydrosulfite, see Sodium dithionate(III)... 

A general method for preparing acetals by treating aldehydes or ketones with the appropriate tetra-alkyl silicate, using dry hydrogen chloride as the catalyst. Helferich and Hausen, Ber. 57, 795 (1924). 

The condensing steam turbine has a relatively low thermal efficiency because about two-thirds of the steam enthalpy is lost to cooling water in the condenser. Expensive boiler feedwater treatment is required to remove chlorides, salts, and silicates, which can be deposited on the blades causing premature failure. The blades are already under erosion conditions because of water drops present in the condensing steam. Even with these disadvantages, the condensing turbine is still selected, especially in a process that requires very large compressor drivers and relatively low amounts of process steam. 

Ethyl chloride Ethyl ether Ethyl formate 2-Ethyl hexanol Ethyl mercaptan Ethyl silicate Ethylene... 

Coagulation involves the addition of chemicals to alter the physical state of dissolved and suspended solids. This facilitates their removal by sedimentation and filtration. The most common primary coagulants are alum ferric sulfate and ferric chloride. Additional chemicals that may be added to enhance coagulation include activate silica, a complex silicate made from sodium silicate, and charged organic molecules called polyelectrolytes, which include large-molecular-weight polyacrylamides, dimethyl-diallylammonium chloride, polyamines, and starch. 

Alternatively, as described in U.S. Patent 3,341,557, 6-dehydro-17-methyltestosterone may be used as the starting material. A mixture of 0.4 g of cuprous chloride, 20 ml of 4 M methylmagnesium bromide in ether and 60 ml of redistilled tetrahydrofuran was stirred and cooled in an ice bath during the addition of a mixture of 2.0 g of 6-dehydro-l 7-methyl-testosterone, 60 ml of redistilled tetrahydrofuran and 0.2 g of cuprous chloride. The ice bath was removed and stirring was continued for four hours. Ice and water were then carefully added, the solution acidified with 3N hydrochloric acid and extracted several times with ether. The combined ether extracts were washed with a brine-sodium carbonate solution, brine and then dried over anhydrous magnesium sulfate, filtered and then poured over a 75-g column of magnesium silicate (Florisil) packed wet with hexanes (Skellysolve B). The column was eluted with 250 ml of hexanes, 0.5 liter of 2% acetone, two liters of 4% acetone and 3.5 liters of 6% acetone in hexanes. 

A mixture of iron, ferric chloride and water is added to the toluene solution. The mixture is heated to reflux and concentrated hydrochloric acid is added dropwise at a rate calculated to keep the mixture refluxing vigorously. After the hydrochloric acid Is all added, the refluxing is continued by the application of heat for several hours. A siliceous filter aid is then added to the cooled reaction mixture and the material is removed by filtration. The filter cake is washed four times, each time with 90 ml of benzene. The organic layer is then separated from the filtrate. The water layer is acidified to a pH of 2 and extracted three times with 90 ml portions of benzene. 

The residue was redissolved in methylene chloride and chromatographed over 500 g of Florisil anhydrous magnesium silicate. The column was eluted with 1 liter portions of hexanes (Skelly-solve B) containing increasing proportions of acetone. There was so eluted 6a-fIuoro-9/3,1113-epoxy-16a-methy 1-17a,21 -d I hydroxy-1, 4-pregnad ene-3,20-dione-21-acetate which was freed of solvent by evaporation of the eluates. 

This reaction mixture is kept between 0°C and -i-5°C for six hours, with agitation and under an inert atmosphere, then 5 cc of a 0.2N solution of acetic acid in toluene are added. The mixture is extracted with toluene, and the extracts are washed with water and evaporated to dryness. The residue is taken up in ethyl acetate, and then the solution Is evaporated to dryness in vacuo, yielding a resin which is dissolved in methylene chloride, and the solution passed through a column of 40 g of magnesium silicate. Elution is carried out first with methylene chloride, then with methylene chloride containing 0.5% of acetone, and 0.361 g Is thus recovered of a crude product, which is dissolved in 1.5 cc of isopropyl ether then hot methanol Is added and the mixture left at 0°C for one night. 

The methyl benzoate thus formed is eliminated by steam distillation, and 2.140 g of crude product are obtained, which are dissolved in 20 cc of methylene chloride. This solution is passed through 10 parts of magnesium silicate, elution being performed with 250 cc of methylene chloride containing 5% of acetone. After evaporation of the solvent 2.050 g of product is recovered, which is recrystallized from isopropyl ether. 

The poor efficiencies of coal-fired power plants in 1896 (2.6 percent on average compared with over forty percent one hundred years later) prompted W. W. Jacques to invent the high temperature (500°C to 600°C [900°F to 1100°F]) fuel cell, and then build a lOO-cell battery to produce electricity from coal combustion. The battery operated intermittently for six months, but with diminishing performance, the carbon dioxide generated and present in the air reacted with and consumed its molten potassium hydroxide electrolyte. In 1910, E. Bauer substituted molten salts (e.g., carbonates, silicates, and borates) and used molten silver as the oxygen electrode. Numerous molten salt batteiy systems have since evolved to handle peak loads in electric power plants, and for electric vehicle propulsion. Of particular note is the sodium and nickel chloride couple in a molten chloroalumi-nate salt electrolyte for electric vehicle propulsion. One special feature is the use of a semi-permeable aluminum oxide ceramic separator to prevent lithium ions from diffusing to the sodium electrode, but still allow the opposing flow of sodium ions. 

Beryllium is extracted from the main source mineral, the alumino-silicate beryl, by conversion to the hydroxide and then through either the fluoride or the chloride to the final metal. If the fluoride is used, it is reduced to beryllium by magnesium by a Kroll-type reaction. The raw metal takes the form of pebble and contains much residual halides and magnesium. With the chloride on the other hand, the pure metal is extracted by electrolysis of a mixture of fused beryllium chloride and sodium chloride. The raw beryllium is now dendritic in character, but still contains residual chloride. 

Woods contain from 0-2 to 4% of mineral ash. This consists largely of calcium, potassium and magnesium as carbonate, phosphate, silicate and sulphate. Aluminium, iron, sodium and chloride are also present. Sulphate contributes 1 to 10% by weight, usually 2 to 4%, and chloride 01 to 5%. 

Significant figure A meaningful digit in a measured quantity, 9,20-2 lq ambiguity in, 10 in inverse logarithms, 645-647 in logarithms, 645-647 Silicate lattices, 243 Silicon, 242-243 Silver, 540-541 Silver chloride, 433,443-444 Simple cubic cell (SC) A unit cell in which there are atoms at each comer of a cube, 246... 

For analytical purposes silicates may be conveniendy divided into the following two classes (a) those ( soluble silicates) which are decomposed by acids, such as hydrochloric acid, to form silicic acid and the salts (e.g. chlorides) of the metals present and (b) those ( insoluble silicates) which are not decomposed by any acid, except hydrofluoric acid. There are also many silicates which are partially decomposed by acids for analytical purposes these will be included in class (b). 

---