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SELENIUM IN SELENIFEROUS ENVIRONMENTS 35 <br />vapors are discharged as aerosols to the atmosphere, only to enter the ter- <br />restrial and aquatic environment by wet or dry deposition. <br />A Se mass balance study was conducted at the Allen Steam Plant in Mem- <br />phis, TN (Andren et al., 1975). This plant was equipped with ahigh-efficiency <br />electrostatic precipitator that allowed only 0.5% of the total incoming fly <br />ash to be exhausted to the atmosphere. However, as much as 15 to 20% of <br />the 0.1 to 0.5 µm MMAD particles and a very large portion of the <0.1 <br />µm MMAD particles were lost as aerosols. Of the 2.2 mg Se/kg coal enter- <br />ing the boiler, 0.3010 exited with the slag, 68% was with the precipitated fly <br />ash particles, and the remaining 32010 was associated with the vapor phase. <br />The Se in the slag, fly ash, and vapor phases was identified as elemental Se. <br />However, some of this Se must occur as or eventually become bioavailable, <br />because fly ash is a good source of Se for higher plants (see section on Bio- <br />availability of Fly Ash Selenium, below). <br />An estimated 6 x 10 ~ 1 and 28 x 1011 kg of coal (having about 11 % <br />ash) are combusted annually in the USA and world, respectively (Andren <br />et al., 1975). Perhaps coal consumption has been reduced or data were cal- <br />culated differently, because Eisenberg et al. (1986) quoted a figure of 4.5 <br />x 1010 kg of fly ash produced in the USA in 1980. <br />Upon combustion, about 40010 of the ash occurs as bottom ash or slag, <br />60010 as fly ash, and < 1% as aerosols that escape to the atmosphere (Eisen- <br />berg et al., 1986). These proportions may differ for other coal-boiler plants, <br />because of design and operating conditions. Selenium concentrations in these <br />components at the Allen Steam Plant were 2.2, 0.08, 28, and 88 mg Se/kg <br />for the bulk coal, slag, fly ash, and aerosol fractions, respectively. <br />Selenium Enrichment Factors in Aerosols, Particulates, and Precipitation <br />The Se enrichment of a given fraction relative to crustal rocks provides <br />a useful index to follow the preferential movement of Se (or other elements) <br />in the environment. The enrichment factor (EF) for Se is calculated as follows: <br />EF = (Se/Al)aerosol/(Se/Al)crust <br />The term (Se/Al)aerosol is the ratio of the Se concentration to that of Al <br />in the aersol and the (Se/A1)crust is the ratio of the elements in igneous rocks <br />of the upper continental crust (Wedepohl, 1971). This approach assumes that <br />AI is conserved in the combustion process and thus the EF for Al is 1.0. The <br />EF values could also be calculated for the Se enrichment in the ash or other <br />carrier. Similar EF values of 84 and 132 were calculated for Se in ash from <br />11 coal-fired power plants in the United Kingdom and 23 in the USA, respec- <br />tively (Wadge et al., 1986; Furr et al., 1977). <br />Wadge et al. (1986) separated fly ash into size fractions ranging from <br />1.25 to 76 µm MMAD. Most of the particles were <20 µm MMAD. The <br />Se concentrations in the bulk ash from the 11 plants ranged from 2 to 26 <br />mg Se/kg ash with a mean of 5.4 mg Se/kg. These researchers reported that <br />Se concentrations were inversely related to particle size and further that the <br />