Relation of alpha-naphthol uptake with polarity and aromaticity of sel
ected organic matter surrogates was investigated using batch equilibra
tion. The organic sorbents used were: lignin (organosolv), lignin (alk
ali), collagen, chitin, cellulose, and a collagen-tannic acid mixture
(CTM). These materials represent model input sources for soil organic
matter. Aromaticity of the sorbents was calculated from CPMAS C-13 NMR
spectrum data. Concentration of alpha-naphthol in solution was measur
ed using liquid scintillation counting and elemental composition of th
e sorbents was determined with an elemental analyzer. Hysteresis betwe
en adsorption and desorption was not observed. We infer that uptake of
alpha-naphthol is through partitioning as indicated by linear isother
ms. K(d) values for lignins were 12 to 24 fold higher than that for ch
itin and 130 to 260 fold higher than that for cellulose. The carbon re
ferenced sorption coefficient (K(OC)) decreased from approximately 436
to approximately 3 mLg with increasing polarity index [(O+N)/C] and d
ecreasing aromaticity of organic sorbents. We concluded that the quali
ty of organic sorbents significantly influences partitioning of hydrop
hobic organic chemicals in aqueous systems. If this conclusion holds f
or all hydrophobic organic pollutants, then K(OC) of such xenobiotics
cannot be accurately predicted from its K(OW) or solubility without so
me description of organic sorbent quality such as polarity and degree
of aromaticity.