Literature DB >> 24235057

Hydrophobicity of complex organic mixtures.

E M Verbruggen1, W M van Loon, J L Hermens.   

Abstract

Hydrophobicity is an important property in risk assessment of chemicals. A group parameter that reflects the hydrophobicity of technical mixtures is not yet available. However, many substances are complex organic mixtures, for which it is practically impossible to determine each component separately. An experimental procedure to measure the hydrophobicity of organic mixtures without knowledge of the individual components was developed and tested for a mixture of benzene and twelve chlorobenzenes. This procedure is based on separation of the mixture into fractions of increasing hydrophobicity by reversed-phase HPLC, after which the total molar concentration in each fraction is determined by vapour pressure osmometry. The obtained information on hydrophobicity can be used for assessing bioaccumulation and sediment sorption after emission of the mixture to water has occurred.

Entities:  

Year:  1996        PMID: 24235057     DOI: 10.1007/BF02985527

Source DB:  PubMed          Journal:  Environ Sci Pollut Res Int        ISSN: 0944-1344            Impact factor:   4.223


  6 in total

1.  Solubility of organic mixtures in water.

Authors:  S Banerjee
Journal:  Environ Sci Technol       Date:  1984-08-01       Impact factor: 9.028

2.  Surrogate parameter for the baseline toxicity content of contaminated water: simulating the bioconcentration of mixtures of pollutants and counting molecules.

Authors:  H J Verhaar; F J Busser; J L Hermens
Journal:  Environ Sci Technol       Date:  1995-03-01       Impact factor: 9.028

Review 3.  QSAR issues in aquatic toxicity of surfactants.

Authors:  D W Roberts
Journal:  Sci Total Environ       Date:  1991-12       Impact factor: 7.963

4.  Quantitative determination of total molar concentrations of bioaccumulatable organic micropollutants in water using C18 empore disk and molar detection techniques.

Authors:  W M van Loon; F G Wijnker; M E Verwoerd; J L Hermens
Journal:  Anal Chem       Date:  1996-09-01       Impact factor: 6.986

5.  Use of distribution coefficients in quantitative structure-activity relationships.

Authors:  R A Scherrer; S M Howard
Journal:  J Med Chem       Date:  1977-01       Impact factor: 7.446

6.  Differences between retentions of various classes of aromatic hydrocarbons in reversed-phase high-performance liquid chromatography. Implications of using retention data for characterizing hydrophobicity.

Authors:  A Opperhuizen; T L Sinnige; J M van der Steen; O Hutzinger
Journal:  J Chromatogr       Date:  1987-02-06
  6 in total

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