Vacuum-assisted sorbent extraction: An analytical methodology for the determination of ultraviolet filters in environmental samples.

Environmental analysis Gas chromatography Mass spectrometry Ultraviolet filters Vacuum-assisted sorbent extraction

Journal

Talanta
ISSN: 1873-3573
Titre abrégé: Talanta
Pays: Netherlands
ID NLM: 2984816R

Informations de publication

Date de publication:
01 Feb 2020
Historique:
received: 31 07 2019
revised: 24 09 2019
accepted: 24 09 2019
entrez: 11 12 2019
pubmed: 11 12 2019
medline: 11 12 2019
Statut: ppublish

Résumé

Vacuum-assisted sorbent extraction (VASE) has been applied in combination with gas chromatography-mass spectrometry for the determination of UV filters in water samples. VASE is a variant of headspace extraction which was developed in conjunction with the sorbent pen (SP) technology. This technique combines the advantages of both stir-bar assisted extraction and headspace solid-phase microextraction. The SP traps allowed both reduced pressure in-vial extraction and direct thermal desorption via a unique gas chromatographic injection port. The main parameters that affect the performance of VASE, including both extraction and desorption conditions, were extensively optimized. Under optimum conditions, extraction required 10 mL of sample within 40 mL vials, pH 3.5, ~30 s of air-evacuation, 14 h incubation at 70 °C, stirring at 200 rpm, and a final water management step conducted at ~ -17 °C for 15 min. Optimal thermal desorption required preheating at 260 °C for 2 min followed by desorption at 300 °C for 2 min. The beneficial effect of reduced-pressure extraction was demonstrated by comparing the UV filter extraction time profiles collected using VASE to an analogous atmospheric pressure procedure, resulting in up to a 3-fold improvement under optimized conditions. The VASE methodology enabled simultaneous extractions using different SPs without compromising the method reproducibility, which increases the overall sample throughput. The method was characterized by low limits of detection, from 0.5 to 80 ng L

Identifiants

pubmed: 31816753
pii: S0039-9140(19)31023-9
doi: 10.1016/j.talanta.2019.120390
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

120390

Informations de copyright

Copyright © 2019 The Authors. Published by Elsevier B.V. All rights reserved.

Auteurs

María J Trujillo-Rodríguez (MJ)

Department of Chemistry, Iowa State University, Ames, IA, 50011, USA.

Jared L Anderson (JL)

Department of Chemistry, Iowa State University, Ames, IA, 50011, USA. Electronic address: andersoj@iastate.edu.

Sage J B Dunham (SJB)

Entech Instruments Inc., Simi Valley, CA, 93065, USA.

Victoria L Noad (VL)

Entech Instruments Inc., Simi Valley, CA, 93065, USA.

Daniel B Cardin (DB)

Entech Instruments Inc., Simi Valley, CA, 93065, USA.

Classifications MeSH