In:
Environmental Toxicology and Chemistry, Wiley, Vol. 36, No. 2 ( 2017-02), p. 329-336
Abstract:
To predict the fate and potential effects of organic contaminants, information about their hydrophobicity is required. However, common parameters to describe the hydrophobicity of organic compounds (e.g., octanol–water partition constant [ K OW ]) proved to be inadequate for ionic and nonionic surfactants because of their surface‐active properties. As an alternative approach to determine their hydrophobicity, the aim of the present study was therefore to measure the retention of a wide range of surfactants on a C 18 stationary phase. Capacity factors in pure water ( k ′ 0 ) increased linearly with increasing number of carbon atoms in the surfactant structure. Fragment contribution values were determined for each structural unit with multilinear regression, and the results were consistent with the expected influence of these fragments on the hydrophobicity of surfactants. Capacity factors of reference compounds and log K OW values from the literature were used to estimate log K OW values for surfactants (log ). These log values were also compared to log K OW values calculated with 4 computational programs: KOWWIN, Marvin calculator, SPARC, and COSMO ThermX . In conclusion, capacity factors from a C 18 stationary phase are found to better reflect hydrophobicity of surfactants than their K OW values. Environ Toxicol Chem 2017;36:329–336. © 2016 The Authors. Environmental Toxicology and Chemistry Published by Wiley Periodicals, Inc. on behalf of SETAC.
Type of Medium:
Online Resource
ISSN:
0730-7268
,
1552-8618
Language:
English
Publisher:
Wiley
Publication Date:
2017
detail.hit.zdb_id:
2027441-5
SSG:
12
