Fluoride deposition

Repeated exposure to excessive concentrations of hydrogen fluoride over a period of years may result in an increased radiographic density of bone and eventually may cause crippling fluorosis (osteosclerosis due to deposition of fluoride in bone)/ The early signs of increased bone density from fluoride deposition are most apparent in the lumbar spine and pelvis and can be detected by X ray. 

The dehalosilylation can be carried out in the gas phase over solid tetra- -butylammo-nium fluoride deposited on glass helices, and even 59 can be transferred to a cold finger and trapped with cyclopentadiene, or as a remarkably stable ene-dimer44,128. 

From a solution of the fluoride in dilute hydrofluoric acid there crystallizes an acid salt, AgF,HF, in brown, deliquescent crystals.7 On cooling, a solution of the fluoride in pure hydrogen fluoride deposits white crystals of the formula AgF,3HF.8... 

Sedimentary formation waters have long been invoked as ore-forming fluids in a number of distinctly different geologic settings. Although ore deposit classification schemes vary, the following have been genetically associated with basinal fluids (i) Mississippi-Valley-type lead, zinc, copper, barium, and fluoride deposits (ii) shale-hosted lead, zinc, and barium deposits (iii) rift-basin and redbed copper deposits ... 

Yu, M.H. and H.-L.S. Hwang. 1986. Influence of protein and ascorbic acid on fluoride-induced changes in blood composition and skeletal fluoride deposition in mice. In Fluoride Research 1985, H. Tsunoda and M.-H. Yu, Eds. Elsevier, Amsterdam, pp. 203-210. 

INTRODUCTION This data sheet applies to freshly evaporated films of magnesium fluoride deposited on glass. ... 

In SMOBC processing, the metal-plated resist is removed to present a flat, clean copper surface for solder mask definition. Tin/lead alloys can be stripped in oxidizing fluoride solutions such as fluoboric acid and hydrogen peroxide or ammonium bifluoride with hydrogen peroxide or nitric acid. (Caution machine construction must be made compatible with fluorides by elimination of titanium and glass components.) Commercial formulations are available to be used inline after the etch machine rinses. Accumulations of spent solution or filtered lead-fluoride deposits must be treated as hazardous waste and have been accepted by solution vendors for treatment and disposal costs. Modern applications usually use lead-free tin plating resists, which can be fluoride containing as previously discussed, or compounds of ferric chloride... 

Fluorination of tungsten and rhenium produces tungsten hexafluoride, WF, and rhenium hexafluoride [10049-17-9J, ReF, respectively. These volatile metal fluorides are used in the chemical vapor deposition industry to produce metal coatings and intricately shaped components (see Thin films,... 

In the geochemistry of fluorine, the close match in the ionic radii of fluoride (0.136 nm), hydroxide (0.140 nm), and oxide ion (0.140 nm) allows a sequential replacement of oxygen by fluorine in a wide variety of minerals. This accounts for the wide dissemination of the element in nature. The ready formation of volatile silicon tetrafluoride, the pyrohydrolysis of fluorides to hydrogen fluoride, and the low solubility of calcium fluoride and of calcium fluorophosphates, have provided a geochemical cycle in which fluorine may be stripped from solution by limestone and by apatite to form the deposits of fluorspar and of phosphate rock (fluoroapatite [1306-01 -0]) approximately CaF2 3Ca2(P0 2 which ate the world s main resources of fluorine (1). 

Molybdenum hexafluoride is used in the manufacture of thin films (qv) for large-scale integrated circuits (qv) commonly known as LSIC systems (3,4), in the manufacture of metallised ceramics (see MetaL-MATRIX COMPOSITES) (5), and chemical vapor deposition of molybdenum and molybdenum—tungsten alloys (see Molybdenumand molybdenum alloys) (6,7). The latter process involves the reduction of gaseous metal fluorides by hydrogen at elevated temperatures to produce metals or their alloys such as molybdenum—tungsten, molybdenum—tungsten—rhenium, or molybdenum—rhenium alloys. 

The majority of the fluorine ia the earth s cmst is present in the form of the phosphoms fluoride fluoroapatite [1306-05 ] Ca (P0 2F- Phosphate rock deposits contain an average concentration of 3.5 wt % fluorine. During phosphate processing these fluorine values are partially recovered as by-product fluorosihcic acid. The amount of fluorosiUcic acid recovered has grown steadily, in part because of environmental requirements (see Phosphoric acid and THE phosphates). 

Fused Salt Electrolysis. Only light RE metals (La to Nd) can be produced by molten salt electrolysis because these have a relatively low melting point compared to those of medium and heavy RE metals. Deposition of an alloy with another metal, Zn for example, is an alternative. The feed is a mixture of anhydrous RE chlorides and fluorides. The materials from which the electrolysis cell is constmcted are of great importance because of the high reactivity of the rare-earth metals. Molybdenum, tungsten, tantalum, or alternatively iron with ceramic or graphite linings are used as cmcible materials. Carbon is frequently used as an anode material. 

A typical example might involve use of a krypton fluoride excimer laser operating at 249 nm with a pulse duration around 100 nanoseconds and a pulse repetition rate which can be varied up to 200 Hz. For metal deposition, energy densities in the range from 0.1 to 1 J/cm per pulse are typical. 

According to Faraday s law, one Faraday (26.80 Ah) should deposit one gram equivalent (8.994 g) of aluminum. In practice only 85—95% of this amount is obtained. Loss of Faraday efficiency is caused mainly by reduced species ( Al, Na, or A1F) dissolving or dispersing in the electrolyte (bath) at the cathode and being transported toward the anode where these species are reoxidized by carbon dioxide forming carbon monoxide and metal oxide, which then dissolves in the electrolyte. Certain bath additives, particularly aluminum fluoride, lower the content of reduced species in the electrolyte and thereby improve current efficiency. 

Piebaked anodes aie produced by molding petroleum coke and coal tar pitch binder into blocks typically 70 cm x 125 cm x 50 cm, and baking to 1000—1200°C. Petroleum coke is used because of its low impurity (ash) content. The more noble impurities, such as iron and siUcon, deposit in the aluminum whereas less noble ones such as calcium and magnesium, accumulate as fluorides in the bath. Coal-based coke could be used, but extensive and expensive prepurification would be required. Steel stubs seated in the anode using cast iron support the anodes (via anode rods) in the electrolyte and conduct electric current into the anodes (Fig. 3). Electrical resistivity of prebaked anodes ranges from 5-6 Hm anode current density ranges from 0.65 to 1.3 A/crn. ... 

Optical Coatings. Thin surface coatings are appHed to optical components to improve performance. Wideband antireflection coatings for the visible and ir regions need materials with a refractive iadex of for the best efficieacy. Cerium fluoride, a stable material resistant to humidity damage, has a suitable iadex, 1.63 ia the visible, 1.59 ia the iafrared, and is transparent over the range 0.5 p.m to 5 p.m. It is one of the compounds used to build up the multilayers deposited on lenses, sensors, and the like. 

The most common plafing bath uses fluoride to complex the fin. A typical solution contains 45 g/L staimous chloride, 300 g/L nickel chloride hexahydrate, and 55 g/L ammonium bifluofide. It is operated at pH 2.0—2.5 usiag ammonium hydroxide temperature is 65—75°C and current about 200 A/m. The bath has excellent throwing power. Air agitation is avoided. The deposit is bright without additives. Anodes are cast nickel, and the fin is replenished by additions of staimous chloride. AHoy anodes of 72% fin have been used to a much lesser extent. Tia-nickel deposits are covered by ASTM (136) and ISO (137) specifications. One other bath based on pyrophosphate has appeared ia the Hterature, but does not seem to be ia commercial use. 

Air pollutants that present a hazard to livestock, therefore, are those that are taken up by vegetation or deposited on the plants. Only a few pollutants have been observed to cause harm to animals. These include arsenic, fluorides, lead, mercury, and molybdenum. 

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