Dissolved organic matter mediated aquatic transport of chlorinated dioxins

The bioavailability and environmental fate of extremely hydrophobic environmental contaminants such as chlorinated dioxins is linked to their solubility characteristics in water. Solubilities of three chlorinated dioxins, viz., 1,2,3,7-T₄CDD, 1,2,3,4,7-P₅CDD, and 1,2,3,4,7,8-H₆CDD, were determined in pure water using a glass bead generator column technique, and their enhanced solubilities in the presence of several dissolved humic fractions quantified at 20, 30 and 40°C. The strengths of these interactions between chlorodioxins and the dissolved humic substances, viz., a fulvic acid, a humic acid, and Aldrich humic acid, were examined using simple thermodynamic calculations. A new partition/association coefficient, K_oc (mobile) is defined.     

Aqueous solubility of polychlorinated dibenzo-p-dioxins determined by high pressure liquid chromatography

Water solubilities (S_W) determined by the HPLC generator column method are reported for a series of chlorinated dibenzo-$\text{p}$-dioxins (PCDDs) with S_W ranging from 0.4 ng/L (ppt) for octa-chlorodibenzo-$\text{p}$-dioxin to 430 ng/L for 1,2,3,7-tetrachlorodibenzo-$\text{p}$-dioxin at 20°C. A correlation is demonstrated between S_W and HPLC capacity factors (k′) for these extremely hydrophobic compounds, allowing calculation of S_W of PCDDs from k′ and melting point data.