4.6 Article

Evaluation of passive samplers with neutral or ion-exchange polymer coatings to determine freely dissolved concentrations of the basic surfactant lauryl diethanolamine: Measurements of acid dissociation constant and organic carbon-water sorption coefficient

Journal

JOURNAL OF CHROMATOGRAPHY A
Volume 1315, Issue -, Pages 8-14

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.chroma.2013.09.041

Keywords

SPME-fibers; Cationic surfactant; Cation-exchange; pK(a); Sorption; Humic acid

Funding

  1. European Oleochemicals and Allied Products Group (APAG)
  2. European Chemical Industry Council (CEFIC) sector groups
  3. Environmental Risk Assessment and Management (ERASM)
  4. China Scholarship Council (CSC)
  5. Unilever [CH-2012-0078]

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A passive sampler tool (solid-phase microextraction, SPME) was optimized to measure freely dissolved concentrations (C-w,C-free) of lauryl diethanolamine (C12-DEA). C12-DEA can be protonated and act as a cationic surfactant. From the pH-dependent sorption to neutral SPME coatings (polyacrylate and PDMS), a pK(a) of 8.7 was calculated, which differs more than two units from the value of 6.4 reported elsewhere. Polyacrylate coated SPME could not adequately sample largely protonated C12-DEA in humic acid solutions of pH 6. A new hydrophobic SPME coating with cation-exchange properties (C-18/SCX) sorbed C12-DEA 100 fold stronger than polyacrylate, because it specifically sorbs protonated C12-DEA species. The C-18/SCX-SPME fiber showed linear calibration isotherms in a concentration range of <1 nM-1 mu M (well below the CMC). Using the C-18/SCX-SPME fibers, linear sorption isotherms to Aldrich humic acid at pH 6 (ionic strength 0.015 M) were measured over a broad concentration range with a sorption coefficient of 10(5.3). (C) 2013 Elsevier B.V. All rights reserved.

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