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Arsenic Table atmosphere

In the tests described by Tracy, a high-tensile brass suffered severe dezinc-ification (Table 4.11). The loss in tensile strength for this material was 100% and for a non-arsenical 70/30 brass 54% no other material lost more than 23% during 20 years exposure. In Mattsson and Holm s tests the highest corrosion rates were shown by some of the brasses. Dezincification caused losses of tensile strength of up to 32% for a P brass and up to 12% for some of the a-P brasses no other materials lost more than 5% in 7 years. Dezinc-ification, but to a lesser degree, occurred also in the a brasses tested, even in a material with as high a copper content as 92%. Incorporation of arsenic in the a brasses consistently prevented dezincification only in marine atmospheres. [Pg.690]

Table 2.8 Solubility of some arsenic compounds in water at atmospheric pressure. Table 2.8 Solubility of some arsenic compounds in water at atmospheric pressure.
The chemical composition of the Universe is primarily estimated from models of the Big Bang (Delsemme, 1998, 19-42) and spectrographic analyses of nebulas and the atmospheres of stars (Krauskopf and Bird, 1995, 563-564). Currently, hydrogen and helium are the most abundant elements, representing 71% and 28%, respectively, of all known matter in the Universe (Delsemme, 1998, 22). Arsenic has been ranked as the 39th most common element in the Universe with an average concentration of 0.008 mg kg-1 (Matschullat, 2000, 299 Table 3.1). [Pg.73]

Some very fine-grained atmospheric dust is capable of crossing oceans and accumulating on different continents. Dust samples from the Sahara Desert of North Africa (Mali) are known to contain at least 17 mg kg-1 of arsenic and may be responsible for contaminating cisterns as far west as the Caribbean and eastern USA ((Holmes and Miller, 2002 Shinn, 2001) Table 3.17). Dust in one cistern from St. John, US Virgin Islands, contained about 38 mg kg-1 of arsenic ((Holmes and Miller, 2002) Table 3.17). Arsenic from Sahara Desert dust may also accumulate in soils, sediments, water, and plants in Florida and surrounding areas (Holmes and Miller, 2002). [Pg.168]

Table 7.2 Inorganic arsenic removal capacities of various sorbents and ion-exchange media in water. Ambient conditions indicate about one atmosphere pressure and room temperature or about 20-25 °C. [Pg.363]

In thermospray interfaces, the column effluent is rapidly heated in a narrow bore capillary to allow partial evaporation of the solvent. Ionisation occurs by ion-evaporation or solvent-mediated chemical ionisation initiated by electrons from a heated filament or discharge electrode. In the particle beam interface the column effluent is pneumatically nebulised in an atmospheric pressure desolvation chamber this is connected to a momentum separator where the analyte is transferred to the MS ion source and solvent molecules are pumped away. Magi and Ianni (1998) used LC-MS with a particle beam interface for the determination of tributyl tin in the marine environment. Florencio et al. (1997) compared a wide range of mass spectrometry techniques including ICP-MS for the identification of arsenic species in estuarine waters. Applications of HPLC-MS for speciation studies are given in Table 4.3. [Pg.79]

Arsenic is ubiquitous in the Earth s crust arsenic ranks 20th among the elements in abundance. In nature, arsenic is widely but sparsely distributed. It is associated with igneous and sedimentary rocks, particularly with sulfidic ores. Arsenic enters the aquatic environment indirectly from industrial and other air emission, and directly from localized effluent discharges. There is general agreement that most man-caused atmospheric input is due to smelting operations and fossil-fuel combustion. Arsenic emission to the atmosphere was calculated with the factors listed in Table 2 . ... [Pg.727]

TABLE 5. Global emissions (kty" ) of antimony and arsenic to the atmosphere ... [Pg.737]

The physical properties given in Table 75 are for the metallic forms. Arsenic sublimes at the ordinary pressure the m.p. as given is that for 36 atmospheres. [Pg.346]

Final solutions from both pressure and atmospheric leach tests were submitted for chemical analysis, and the results are presented in Table VIA. The concentrations of cobalt, nickel and selenium in the final solutions were not significantly different. Arsenic, antimony and tellurium levels were about the same or lower in the solution generated in pressure leaching (the arsenic concentration was substantially lower in the pressure leach liquor for... [Pg.733]

TABLE 2. Experimental Data for the Molar Magnetic Susceptibility of Glassy Arsenic Chalcogenides Obtained in a Helium Atmosphere... [Pg.147]

Table 3 Estimates atmospheric lifetime of volatile arsenic compounds in moisturized air at a starting concentration of 10 pg m ... Table 3 Estimates atmospheric lifetime of volatile arsenic compounds in moisturized air at a starting concentration of 10 pg m ...

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See also in sourсe #XX -- [ Pg.163 ]




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