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Chemical lead fluoride

Stannous and lead fluoborates are the source of metal.Their concentrations and ratio must be strictly maintained, as they will directly affect alloy composition. Fluoboric acid increases the conductivity and throwing power of the solutions. Boric acid prevents the formation of lead fluoride. Additives promote smooth, fine-grained, tree-free deposits. Excess peptone (three to four times too much) may cause pinholes (volcanoes) in deposit when reflowed. Testing by Hull cell and periodic carbon treatments is indicated.The peptone add rate is about 1 to 2 qt per week for a 400 gal tank. Only DI water and contamination-free chemicals should be used—for example, <10 ppm iron-free and <100 ppm sulfate-free fluoboric add. A clear solution is maintained by constant filtration. [Pg.710]

Ionic conductivity is electrical conductivity due to the motion of ionic charge. Elementary science introduces this phenomenon as a property of liquid electrolyte solutions. In the solid state, ionic conductivity has recently been somewhat overshadowed by electronic, but nevertheless was recognized by Faraday, who observed electrical conductivity in solid lead fluoride at high temperature. The conductivity in this case was due to the motion of fluoride anions within the structure. This type of conductivity in solids has long been of fundamental interest as well as being applied in the interpretation of corrosion. More recently, applications have been found in energy conversion devices and chemical sensors. ... [Pg.669]

Gr. aktis, aktinos, beam or ray). Discovered by Andre Debierne in 1899 and independently by F. Giesel in 1902. Occurs naturally in association with uranium minerals. Actinium-227, a decay product of uranium-235, is a beta emitter with a 21.6-year half-life. Its principal decay products are thorium-227 (18.5-day half-life), radium-223 (11.4-day half-life), and a number of short-lived products including radon, bismuth, polonium, and lead isotopes. In equilibrium with its decay products, it is a powerful source of alpha rays. Actinium metal has been prepared by the reduction of actinium fluoride with lithium vapor at about 1100 to 1300-degrees G. The chemical behavior of actinium is similar to that of the rare earths, particularly lanthanum. Purified actinium comes into equilibrium with its decay products at the end of 185 days, and then decays according to its 21.6-year half-life. It is about 150 times as active as radium, making it of value in the production of neutrons. [Pg.157]

Chemica.1 Lasers. Chemical lasers (44) produce a population inversion by a chemical reaction that leaves the product in an excited state. One example is the set of reactions leading to production of excited-state hydrogen fluoride [7664-39-3], HE, according to... [Pg.11]

Zirconium tetrafluoride [7783-64-4] is used in some fluoride-based glasses. These glasses are the first chemically and mechanically stable bulk glasses to have continuous high transparency from the near uv to the mid-k (0.3—6 -lm) (117—118). Zirconium oxide and tetrachloride have use as catalysts (119), and zirconium sulfate is used in preparing a nickel catalyst for the hydrogenation of vegetable oil. Zirconium 2-ethyIhexanoate [22464-99-9] is used with cobalt driers to replace lead compounds as driers in oil-based and alkyd paints (see Driers and metallic soaps). [Pg.433]

The principal constituents of the paniculate matter are lead/zinc and iron oxides, but oxides of metals such as arsenic, antimony, cadmium, copper, and mercury are also present, along with metallic sulfates. Dust from raw materials handling contains metals, mainly in sulfidic form, although chlorides, fluorides, and metals in other chemical forms may be present. Off-gases contain fine dust panicles and volatile impurities such as arsenic, fluorine, and mercury. [Pg.132]

FAS is normally characterized by growth retardation, anomalies of the head and face, and psychomotor dysfunctions. Excessive consumption of ethyl alcohol may lead to malformations of the heart, extremities, and kidneys. Since consumption of ethyl alcohol is socially acceptable and prevalent even in pregnant women, the risks associated with the use of ethyl alcohol are remarkable. However, it should be kept in mind that there are several chemical compounds in tlie occupational environment that may also cause malformations even at low doses. The oc-cupationally-important known human teratogens include methyl mercury, ethyl alcohol, PCB compounds, tobacco smoke, lead, TCDD, 2,4,5- F, carbon monoxide, nitrogen dioxide, gasoline, and fluoride. [Pg.316]

C03-0067. Write chemical formulas for these compounds (a) sodium sulfate (b) potassium sulfide (c) potassium dihydrogen phosphate (d) cobalt(II) fluoride tetrahydrate (e) lead(IV) oxide (Q sodium hydrogen carbonate and (g) lithium perbromate. [Pg.187]

Although the chemical shifts of most commonly encountered orga-nofluorine compounds are upheld of CFC13 and thus have negative values, there are a number of structural situations for fluorine that lead to positive chemical shifts (downfield from CFC13). These include acyl and sulfonyl fluorides as well as the fluorines of SF5 substituents. [Pg.27]

The typical chemical shift for primary n-alkyl fluorides is -219, but the values for primary alkyl fluorides vary between -212 for ethyl fluoride and -226 for 2-ethyl-l-fluorobutane (Scheme 3.1). As mentioned above, alkyl branching leads to shielding of fluorine nuclei. [Pg.49]

Vinylidine fluoride (CF2 = CH2) exhibits a 19F chemical shift of -82 ppm. As seen in Scheme 4.43, one alkyl substitution at the 2-position leads to about 10 ppm of shielding, with two alkyl groups providing 6-7 ppm more. The two-bond F—F coupling constant in such AB systems is typically around 50 Hz. Modest shielding of the Z-fluorine is generally observed relative to the E-fluorine of 1,1-difluoroalkenes. [Pg.135]


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See also in sourсe #XX -- [ Pg.203 ]




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