Silicone-water partition coefficients determined by cosolvent method for chlorinated pesticides, musks, organo phosphates, phthalates and more
Language English Country England, Great Britain Media print-electronic
Document type Journal Article
PubMed
30031996
DOI
10.1016/j.chemosphere.2018.07.054
PII: S0045-6535(18)31312-2
Knihovny.cz E-resources
- Keywords
- Cosolvent, Hydrophobic organic compounds, Passive sampling, Silicone–water partition coefficient,
- MeSH
- Water Pollutants, Chemical chemistry MeSH
- Chlorobenzenes chemistry MeSH
- Phosphates chemistry MeSH
- Phthalic Acids chemistry MeSH
- Fatty Acids, Monounsaturated MeSH
- Pesticides chemistry MeSH
- Polychlorinated Biphenyls chemistry MeSH
- Flame Retardants MeSH
- Silicones chemistry MeSH
- Water chemistry MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Water Pollutants, Chemical MeSH
- Chlorobenzenes MeSH
- Phosphates MeSH
- Phthalic Acids MeSH
- Fatty Acids, Monounsaturated MeSH
- musk MeSH Browser
- Pesticides MeSH
- phthalic acid MeSH Browser
- Polychlorinated Biphenyls MeSH
- Flame Retardants MeSH
- Silicones MeSH
- Water MeSH
To further support implementation of monitoring by passive sampling, robust sampler-water partition coefficients (Kpw) are required to convert data from passive sampler into aqueous phase concentrations. In this work silicone-water partition coefficients were determined for ∼80 hydrophobic organic contaminants using the cosolvent method. Partition coefficients (Kpm) were measured in pure water and water-methanol mixtures up to a methanol mole fraction of 0.3 (50% v/v). Subsequently, logKpw in pure water was determined as the intercept of linear regression of the logKpm with the corresponding methanol mole fractions. LogKpw were determined for phthalates, musks, organo phosphorus flame-retardants, chlorobenzenes, pesticides, some PCBs and a number of miscellaneous compounds. The median standard error and 95% confidence interval of the measured logKpw was 0.06 and 0.13, respectively. The overall relationship between Kpw and Kow seems insufficient to predict Kpw for unknown compounds. Prediction may work within a group of compounds with similar nature, e.g. homologues but HCH isomers having the same Kow exhibit Kpw ranging over an order of magnitude. Long alkyl-chain phthalates and tris(2-ethylhexyl) phosphate; all having a molecular volume >400 Å3, deviated the most from the Kpw-Kow relationship.
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