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Aerosol heavy metal

Preconditioning for Particulates Heavy particulate loading of the inlet gas with dust, grease, oils, or other aerosols can be very dam-aging to the pore structure of the filter bed, resulting in an eventual pressure-drop increase. Oils and heavy metals that are deposited on the filter bed can be poisonous to the microorganisms that live within the biofilm. Particulate APC equipment such as fabric filters and venturi scrubbers are generally adequate for this level of particulate removal. [Pg.2192]

For exposure of reasons of observable discrepancy of results of the analysis simulated experiment with application synthetic reference samples of aerosols [1]. The models have demonstrated absence of significant systematic errors in results XRF. While results AAA and FMA depend on sort of chemical combination of an elements, method of an ashing of a material and mass of silicic acid remaining after an ashing of samples. The investigations performed have shown that silicic acid adsorbs up to 40 % (rel.) ions of metals. The coefficient of a variation V, describing effect of the indicated factors on results of the analysis, varies %) for Mn and Fe from 5 up to 20, for Cu - from 10 up to 40, for Pb - from 10 up to 70, for Co the ambassador of a dry ashing of samples - exceeds 50. At definition Cr by a method AAA the value V reaches 70 %, if element presences an atmosphere in the form of Cr O. At photometric definition Cr (VI) the value V is equal 40%, when the element is present at aerosols in the form of chromates of heavy metals. [Pg.207]

The name dust , is used in a variety of ways, and with different meanings. These range from the material that accumulates on the earth s surface, such as on streets and in living and working environments, to the particulate material suspended in the atmosphere. In this paper I wish to consider these two materials in terms of their chemical composition, sources and relationship between them. The names used for the two materials will be surface dust and atmospheric dust . The word aerosol may also be used for atmospheric dust but it more properly applies to the finer particles of atmospheric dust and includes liquid aerosol (i). Botfi surface and atmospheric dusts are increasingly seen to be a hazard to human beings as they are a source of intake of toxic materials such as heavy metals. For this reason study is important of the composition and sources of the dusts. [Pg.117]

If low volatility agent aerosols or metal fumes have been released, all foodstuffs in the area should be considered contaminated. Unopened items packaged in glass, metal, or heavy duty plastic may be used after decontamination of the container. Opened or unpackaged items, or those packaged only in paper or cardboard, should be destroyed. [Pg.267]

As a rule, simulations consider emissions of heavy metals from anthropogenic and natural sources, transport in the atmosphere and deposition to the underlying surface (Figure 6). It is assumed that lead and cadmium are transported in the atmosphere only as a part of aerosol particles. Besides, chemical transformations of these metals do not change removal properties of their particles-carriers. On the contrary, mercury enters the atmosphere in different physical and chemical forms and undergoes numerous transformations during its pathway in the atmosphere (Ilyn et al., 2002 2004 Ilyin and Travnikov, 2003). [Pg.364]

These methods, when applied to the downtown Phoenix aerosol sample, produced a satisfying range of particle types and left unasslgned only about MJ of the particles (Table I). The major particle type was quartz whldi accounted for 19> of the particles. Various alumino-silicate types were the next most abundant. Easily identifiable types included clusters rich in only one to three elements, including iron (7il), calciun Oil), calciun-silicon-lron (4H), calciun-sulfur (1J), lead OS), lead-chloride-bromide OS) and titanium (2S). The abundances of these particle types, indicated in parentheses, vary widely from site to site. Many particles rich in heavy metals were found in the unassigned group at this point. [Pg.127]

Konradova V. 1968. The ultrastructure of the tracheal epithelium in rabbits following inhalation of aerosols of colloidal solutions of heavy metals. II. Signs of cell alteration in the epithelium after 8 hour inhalation of colloidal solutions of iron and silver. Folia Morphol (Praha) 16 265-271. [Pg.151]

Kelley, J.A., Jaffe, D.A., Baklanov, A. and Mahura, A. (1995) Heavy metals on the Kola Peninsula aerosol size distribution. Science of the Total Environment, 160-161, 135-38. [Pg.214]

Malm, W.C. and Sisler, J.F. (2000) Spatial patterns of major aerosol species and selected heavy metals in the United States. Fuel Processing Technology, 65, 473-501. [Pg.217]

Although pure sulfuric acid droplets are used almost exclusively in controlled exposures, ambient acid aerosols are chemically complex and are proposed to be composed of a core consisting of carbon, minerals, or heavy metals surrounded by acidic (sulfuric or nitric acid) surface material. Thus, knowing which chemical species is responsible for acid aerosol-induced adverse health effects is fundamental in developing proper control strategies for reducing air pollutants at their source. [Pg.2056]

Particulate emissions are by-products of fuel combustion, industrial processes, and motor vehicles and are believed to have a significant potential for causing adverse health effects. Carbonaceous material present in atmospheric aerosols is a combination of elemental carbon and organic and inorganic compounds. Particulate matter may also consist of fly ash, minerals, or road dust and contain traces of a number of heavy metals. Population-based studies have consistently found that the association between adverse respiratory effects and particulate concentrations occurs in a number of regions throughout the United States. This association is strongest for PM]o and PM2.5 indices (particulate matter less than 10 and 2.5 pm in diameter, respectively). The observed adverse effects include increases in total mortality, mortality due to respiratory and cardiovascular causes, chronic bronchitis, and hospital visits and admissions for asthma. Elderly or unhealthy individuals and infants appear to comprise subpopulations that are most sensitive to the adverse health effects of PM. [Pg.2056]

The first measurements of Pb isotopes in Greenland snow were reported in 1993 (45). The samples were taken from a 10.7 m long, 10.5 cm diameter, snow core drilled at Summit, central Greenland, in 1989 (72°35 N, 37°38 W, mean annual accumulation rate 21.5 g cm year ). Cores were drilled with a polycarbonate auger to minimise the Pb contamination. The core contained snow deposited between the years 1967 and 1988. The 3.23 km elevation of the site provided representative samples of free tropospheric aerosols. An expanded data set and a more complete description and interpretation of these data were later reported by Rosman et al. (46). The latter included samples from the upper part of a 70 m snow core including snow deposited between 1960 and 1974. Data on all four Pb isotopes were given for these samples ( Pb/ Pb, ° Pb/ ° Pb and Pb/ °" Pb). Aliquots of these samples were also analysed for heavy metals by Boutron et al. (47) who showed there was a reduction in the Pb concentration in Greenland snow after 1970, which they attributed mainly to the reduction in the use of alkyl-leaded petrol. [Pg.94]

N. Radlein, K. G. Heumann, Trace analysis of heavy metals in aerosols over the Atlantic Ocean from Antarctica to Europe, Int. J. Anal. Chem., 48 (1992), 127-150. [Pg.360]

In 1998, there were 7 monitoring stations for regional air pollution monitoring, characterized as pollution of a rural type. The measurement programme includes SO2, NO2 and heavy metal concentrations in atmospheric aerosol PM, Pb, Mn, Cu, Cd, Zn, Ni, V, Cr. [Pg.328]

The trace-metal concentrations in streams are controlled not only by input from the weathering of rocks and from aerosols, but also by the chemical reactions occurring within the streams. The evidence from studies utilizing °Pb as a tracer for heavy-metal behavior in streams indicates rapid scavenging by particles associated with the flowing water (Bennin-... [Pg.131]

Beside "classical" applications of surface flow properties, like increased stability of disperse systems, the damping of surface disturbances and influence of small particles flows near gas bubbles, the complex actions of surface forces modified by surfactants appear to be responsible for the presence and the enrichment of micro-flotable components in marine aerosols (Loglio et al. 1985). Loglio et al. (1986a) also define the action of rising bubbles on heavy-metal enrichment at the sea surface. [Pg.95]

The chemical composition of aerosol particles was also determined. Analysis of one typical haze sample gave the following results in % of aerosol mass C = 70.0, H = 4.0, N = 2.8, S = 4.7, Cl = 1.0, K = 19.6, Na = 3.3, Ca = 5.4, Mg = 0.05, Fe = 0.24, and Zn = 19.4. Some heavy metals like As, Cd, Ni, V, and Hg were also present but their mass percentages were generally < 0.01 of the total aerosol mass. This chemical composition of haze reflects the relevant chemical composition ofburning biomass in the tropical forests. [Pg.125]

Lowest concentrations of trace elements have been found in the Antarctic (Cunningham and Zoller 1981), and very low levels in the maritime atmosphere over the Pacific ocean (Gordon etal. 1978 Duce etal. 1983 Farrington and Zoller 1984). A series of elements (V, Cr, Mn, Cu, Zn, Co, Ag, Cd, Ba, Pb, Bi, U) have been measured by Planchon et al. (2002) in snow samples collected at remote, low accumulation sites in Coats Land, Antarctica. Heavy metal concentrations were found to be extremely low, down to 3 pgkg confirming the high purity of Antarctic snow. A review of the data on heavy metals in aerosols over... [Pg.25]

Shevchenko V, Lisitzin A, Vinogradova A and Stein R (2003) Heavy metals in aerosols over the seas of the Russian Arctic. Sci Total Environ 306 11-25. [Pg.49]

Chesselet, R., Buat-Menard, P., Lesty, M. and Jehanno, C., 1976. Heavy metals in oceanic microlayer-derived aerosols. Abstracts of papers. Joint Oceanographic Assembly, Edinburgh, September, 1976. FAO, Rome. [Pg.296]


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See also in sourсe #XX -- [ Pg.21 ]




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