Protocol for the Derivation of Environmental and Human ... - CCME
Protocol for the Derivation of Environmental and Human ... - CCME
Protocol for the Derivation of Environmental and Human ... - CCME
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Part C, Section 5<br />
GEOCHEM (Mattigod <strong>and</strong> Sposito 1979), MINTEQ (Brown <strong>and</strong> Allison 1987)}. A generic,<br />
straight<strong>for</strong>ward, <strong>and</strong> quantitative treatment <strong>of</strong> metal contaminant partitioning is not available at this time.<br />
An alternative approach to <strong>the</strong> problem <strong>of</strong> metal mobility in soils has been to develop guidelines <strong>for</strong> soil<br />
conditions that restrict movement. For most metals, soils <strong>of</strong> moderate pH <strong>and</strong> high redox potential<br />
restrict movement. Waterlogged <strong>and</strong>/or strongly alkaline or acidic soils fail to attenuate different classes<br />
<strong>of</strong> metals. This "restrictive range" approach will be used pending review <strong>and</strong> evaluation <strong>of</strong> <strong>the</strong> potential<br />
<strong>for</strong> application <strong>of</strong> speciation models to guideline development.<br />
Recommended soil conditions <strong>for</strong> application <strong>of</strong> generic guidelines <strong>for</strong> <strong>the</strong> common contaminant metals<br />
are described in "Evaluation <strong>and</strong> Distribution <strong>of</strong> Master Variables Affecting Solubility <strong>of</strong> Contaminants in<br />
Canadian Soils" (Alder et al. 1994). For certain metals, notably cadmium, cobalt, nickel, zinc, <strong>and</strong><br />
some oxyanions, significant deviations from <strong>the</strong> assumed conditions must be considered during <strong>the</strong><br />
development <strong>of</strong> site-specific objectives.<br />
Organic Contaminants<br />
In contrast to metals, partitioning <strong>of</strong> non-polar organic contaminants in soils depends mainly on <strong>the</strong><br />
organic matter content <strong>and</strong> can be described by a simple iso<strong>the</strong>rm (Hamaker <strong>and</strong> Thompson 1972):<br />
C s = K d × C w<br />
1/n<br />
[1]<br />
where<br />
C s = concentration in solid phase (mg/kg)<br />
K d = distribution coefficient<br />
C w = concentration in aqueous phase (mg/L)<br />
n = empirical constant<br />
For most nonionic organics n = 1 <strong>and</strong> sorption is a linear function <strong>of</strong> equilibrium solution concentration<br />
up to 60% to 80% <strong>of</strong> its water solubility (Hassett <strong>and</strong> Banwart 1989).<br />
Over a broad range <strong>of</strong> soil types <strong>the</strong> distribution coefficient is directly related to <strong>the</strong> organic matter<br />
content:<br />
K d = f oc × K oc [2]<br />
where f oc = fraction <strong>of</strong> organic carbon in soil<br />
K oc = sorption coefficient <strong>for</strong> soil organic carbon<br />
A particular chemical's K oc can be measured or predicted by correlating with <strong>the</strong> water solubility (S) or<br />
n-octanol/water partition coefficient, K ow .<br />
The relationship between total soil concentration <strong>of</strong> an organic contaminant <strong>and</strong> its concentration in pore<br />
water is (Appendix C):<br />
103