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Nonequilibrium sorption and transport of neutral and ionized chlorophenols

Journal Article · · Environmental Science and Technology; (United States)
DOI:https://doi.org/10.1021/es00016a018· OSTI ID:5185805
; ;  [1]
  1. Univ. of Florida, Gainesville (United States)
For a series of chlorophenols sorption nonequilibrium was assessed by fitting a bicontinuum sorption model to breakthrough curves measured by miscible displacement techniques. A single log-log inverse relationship was observed between the desorption rate coefficient (k{sub 2}, h{sup {minus}1}) and the equilibrium sorption constant (K{sub p}, mL/g) for all chlorophenols as well as for a series of chlorobenzenes. This suggests that approach to sorption equilibrium for neutral and ionized chlorophenols is constrained in a manner similar to that for nonpolar hydrophobic organic chemicals. For neutral pentachlorophenol (PCP), K{sub p} values decreased log-linearly with increasing volume fraction methanol (f{sub c}), with successful extrapolation of these data to aqueous systems. A log-linear relationship was observed between k{sub 2} and f{sub c} in good agreement with independent estimates. For a series of ionized chlorophenols, the fraction of instantaneous sorption domains (F) increased with increasing solute hydrophobicity, while F decreased with increasing f{sub c} for neutral PCP.
OSTI ID:
5185805
Journal Information:
Environmental Science and Technology; (United States), Journal Name: Environmental Science and Technology; (United States) Vol. 25:4; ISSN ESTHA; ISSN 0013-936X
Country of Publication:
United States
Language:
English