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McKay, Donald. "Front matter" Multimedia Environmental Models ...

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includes an excellent treatment of human exposure. It was originally designed to<br />

assess exposure to chemicals present in hazardous waste sites. The environmental<br />

fate equations are formulated using fugacities. Maddalena et al. (1995) compared<br />

the output of and ChemCAN and found similar results, indicating that both<br />

models were using similar predictive equations.<br />

The reader should consult the Trent website for current versions of the model<br />

software described in this text.<br />

8.3.1 Introduction<br />

©2001 CRC Press LLC<br />

8.3 AN AIR-WATER EXCHANGE MODEL<br />

Air-water exchange process calculations are useful when estimating chemical<br />

loss from treatment lagoons, ponds, and lakes; for estimating deposition rates of<br />

atmospheric contaminants, and for interpreting observed air and water concentrations<br />

to establish the direction and rate of transfer. The complexity of the several processes<br />

and the widely varying physical chemical properties of chemicals of interest leads<br />

to situations in which chemical behavior is not necessarily intuitively obvious. The<br />

simple model derived here provides a rational method of estimating exchange characteristics<br />

and exploring the sensitivity of the results to assumed values of the various<br />

chemical and environmental parameters. Bidleman (1988) gives an excellent review<br />

of atmospheric processes treated by the model.<br />

An elegant application of the fugacity concept to elucidating chemical exchange<br />

in the air-water system is that of Jantunen and Bidleman (1997). Samples of air and<br />

surface water from the Bering and Chukchi Seas (between Alaska and Russia) were<br />

analysed for a-hexachlorocyclohexane (a-HCH) over a multiyear period, and the<br />

ratios of air to water fugacities were deduced using the Henry’s law constant for<br />

seawater at the appropriate temperature. Initially, in the mid 1980s, this ratio was<br />

greater than 1, indicating that a-HCH was being absorbed by the ocean. This is<br />

consistent with the source of a-HCH being evaporation of technical lindane following<br />

application in South East Asia, India, and China, with subsequent atmospheric<br />

transport. Later, in the mid 1990s, after the use of technical lindane was greatly<br />

reduced, the fugacity ratio became less than 1 (because of the drop in air fugacity),<br />

and net volatilization of a-HCH started. Essentially, the ocean acted first as a<br />

“sponge,” absorbing a-HCH, then it desorbed the a-HCH in response to changes<br />

in the concentration in air. Interpretation of data using of the fugacity ratio illustrated<br />

this clearly. It is an example to be followed in cases where there is doubt about the<br />

direction of net transport of chemicals between air and water.<br />

8.3.2 Process Description<br />

The situation treated here, and the resulting model, are largely based on the<br />

study of air- -water exchange by Mackay et al. (1986) as is depicted in Figure 8.1.<br />

The water phase area and depth (and hence volume) are defined, it being assumed<br />

that the water is well mixed. The water contains suspended particulate matter, to

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