4.7 Article

Sensitive determination of salicylate and benzophenone type UV filters in water samples using solid-phase microextraction, derivatization and gas chromatography tandem mass spectrometry

Journal

ANALYTICA CHIMICA ACTA
Volume 638, Issue 1, Pages 36-44

Publisher

ELSEVIER
DOI: 10.1016/j.aca.2009.02.015

Keywords

UV filters; Water samples; Solid-phase microextraction; Derivatization; Gas chromatography

Funding

  1. Spanish Government
  2. Xunta de Galicia
  3. E.U. FEDER [DGICT CTQ2006-03334, PGIDIT06PX1B237039PR]
  4. Spanish Ministry of Science and Innovation

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A sensitive procedure for the determination of three UV filters: ethylhexyl salicylate (EHS), 3,3,5-trimethylcyclohexyl salicylate (Homosalate, HMS), 2-hydroxy-4-methoxybenzophenone (BP-3) and two related hydroxylated benzophenones (2.4-dihydroxybenzophenone, BP-1 and 2,2'-dihydroxy-4-methoxybenzophenone, BP-8) in water samples is presented. Analytes were first concentrated on the coating of a solid-phase microextraction (SPME) fibre. on-fibre silylated and then determined using gas chromatography combined with tandem mass spectrometry (GC-MS/MS). Factors affecting the performance of extraction and derivatization steps are thoroughly evaluated and their effects on the yield of the sample preparation discussed. Under final working conditions, a PDMS-DVB coated SPME fibre was exposed directly to 10 ml of water. adjusted at pH 3, for 30 min. After that, the fibre was placed in the headspace (HS) of a 1.5 mL vial containing 20 mu L of N-methyl-N-(trimethylsilyl)-trifluoroacetamide (MSTFA). On-fibre silylation of hydroxyl groups contained in the structure of target compounds was performed at 45 C 10 min, The whole sample preparation process was completed in 40 min, providing limits of quantification from 0.5 to 10 ng L-1 and acceptable precision (RSDS under 13%) for samples spiked at different concentrations. All compounds could be accurately determined in river and treated wastewater (relative recoveries from 89 to 115%) using standards in ultrapure water, whereas standard addition is recommended to quantify their levels in untreated wastewater. Analysis of wastewater revealed the systematic presence of BP-3 and BP-1 in raw samples with maximum concentrations close to 500 and 250 ng L-1, respectively. (c) 2009 EIsevier B.V. All rights reserved.

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