63 ratios can be calculated and is presented in Table 5-8. The study shows phenol suffered the greatest loss of adsorption capacity when mixed with other phenolic compounds, and indicates that the loss of adsorption capacity was predominantly caused by competitive adsorption effects. Table 5-8. Ratios of Freundlich sorption coefficients for phenolic compounds in single and multiple compound systems. Ratio of KFA: Soil Soil+sludge organic carbon Phenol 3.05 2.88 2.66 2,4-DCP 1.22 1.47 1.66 PCP 1.51 1.42 1.38 In general, Freundlich sorption coefficients for phenolic compounds increase as the level of chlorination increases. The less-than-unity values of the Freundlich exponent, b, indicate the adsorption was not linear, and higher concentrations resulted in a proportionately less amount of adsorption. These values of the Freundlich exponent are in good agreement with the ones reported by Boyd (1982) (b=0.79 for phenol and b=0.67 for 2,4-DCP), Lagas (1988) (b=0.86 for PCP), and Laquer and Manahan (1987) (b=0.65 for phenol). The calculated K values (Table 5-4 and Table 5-7) are oc closer to those predicted by Equation (3-5), which are 2.99 for phenol, 4.03 for 2,4-DCP and 5.86 for PCP. A least squares linear regression reveals a good correlation between the log of water solubility (in umole/l) and log of Ko oc