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Diffusion coefficients of polar organic compounds in agarose hydrogel and water and their use for estimating uptake in passive samplers.
Urík, Jakub; Paschke, Albrecht; Vrana, Branislav.
Afiliação
  • Urík J; RECETOX, Masaryk University, Kamenice 753/5, 625 00, Brno, Czech Republic.
  • Paschke A; UFZ-Department of Ecological Chemistry, Helmholtz-Centre for Environmental Research, Permoserstraße 15, 04318, Leipzig, Germany.
  • Vrana B; RECETOX, Masaryk University, Kamenice 753/5, 625 00, Brno, Czech Republic. Electronic address: branislav.vrana@recetox.muni.cz.
Chemosphere ; 249: 126183, 2020 Jun.
Article em En | MEDLINE | ID: mdl-32088466
Diffusion coefficient (D) is an important parameter for prediction of micropollutant uptake kinetics in passive samplers. Passive samplers are nowadays commonly used for monitoring trace organic pollutants in different environmental matrices. Samplers utilising a hydrogel layer to control compound diffusion are gaining popularity. In this work we investigated diffusion of several perfluoroalkyl substances, currently used pesticides, pharmaceuticals and personal care products in 1.5% agarose hydrogel by measuring diffusion coefficients using two methods: a diffusion cell and a sheet stacking technique. Further, diffusion coefficients in water were measured using Taylor dispersion method. The sheet stacking method was used to measure D at 5, 12, 24, and 33 °C in order to investigate temperature effect on diffusion. Median D values ranged from 2.0 to 8.6 × 10-6 cm2 s-1 and from 2.1 to 8.5 × 10-6 cm2 s-1 for the diffusion cell and sheet stack methods respectively. For most compounds, the variability between replicates was higher than the difference between values obtained by the two methods. Rising temperature from 10 to 20 °C increases the diffusion rate by the factor of 1.41 ± 0.10 in average. In water, average D values ranged from 3.03 to 10.0 × 10-6 cm2 s-1 and were comparable to values in hydrogel, but some compounds including perfluoroalkyl substances with a long aliphatic chain could not be evaluated properly due to sorptive interactions with capillary walls in the Taylor dispersion method. Sampling rates estimated using the measured D values were systematically higher than values estimated from laboratory sampler calibration in our previously published study, by the factor of 2.2 ± 1.0 in average.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sefarose / Poluentes Químicos da Água / Monitoramento Ambiental Tipo de estudo: Prognostic_studies Idioma: En Revista: Chemosphere Ano de publicação: 2020 Tipo de documento: Article País de afiliação: República Tcheca

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sefarose / Poluentes Químicos da Água / Monitoramento Ambiental Tipo de estudo: Prognostic_studies Idioma: En Revista: Chemosphere Ano de publicação: 2020 Tipo de documento: Article País de afiliação: República Tcheca