Extended abiotic incubation and alkaline hydrolysis of chlorinated high molecular weight (HMW) organics (>400D) isolated from bleached kraft mill effluents (BKME) were used to release bound Chlorophenolics. Incubation experiments showed a temperature dependent slow release of 4,5-dichloroguaiacol (4,5-DCG), 3,4,5-trichloroguaiacol (3,4,5-TCG), 4,5,6-trichloroguaiacol (4,5,6-TCC), tetrachloroguaiacol (TeCG), 6-chlorovanillin (6-CVa) and 5,6-dichlorovanillin (5,6-DCVa) from HMW material. Alkaline hydrolysis of HMW with 2 M NaOH at 50 and 100°C released significantly higher concentrations of Chlorophenolics and also 4,6-dichioroguaiacol (4,6-DCG), 3,4-dichloroguaiacol (3,4-DCG) 3,4,5-trichlorocatechol (3A5-TCC) and tetrachlorocatcchol (TeCC) which were not observed during the incubation period. However, chlorocatechols were found to be unstable during alkaline hydrolysis. Chlorophenolic organic carbon partiton coefficients (K oe ) from the solvent extractable (free) and the alkaline hydrolysis released (bound) concentrations were compared to estimated and reported literature values. Measured primary treated effluent KOC values were in agreement with estimated values for 2,4,6-trichlorophenol (2,4,6-TCP), 2,3,4,6-tetrachlorophenol (2,3,4,6-TeCP), pentachlorophenol (PCP), 3,4,5-TCG, 4,5,6-TCG and TeCG but significantly different for 4,5-DCG. Primary and secondary treated effluent chlorophenolic K«c values of 3,4-DCG, 4,5-DCG, 6-CVa, 5,6-DCVa, 2-chlorosyringaldehyde (2-CSAld) and 2,6-dichlorosyringaldehyde (2,6-DCSAld) did not agree with their measured chlorophenolic KOC values. These results suggest that simple hydrophobic interaction does not account for the high concentrations of these Chlorophenolics bound to HMW material.