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Leveraging the thermoresponsiveness of fluorinated poly(: N -isopropylacrylamide) copolymers as a sensing tool for perfluorooctane sulfonate

Producción científica: Articlerevisión exhaustiva

4 Citas (Scopus)

Resumen

Due to mounting evidence of the negative health effects of persistent perfluoroalkyl acids (PFAAs) with long (i.e., >C7) tails, there is a need for convenient systems capable of sensing these contaminants at dilute aqueous concentrations. To address this concern, a thermoresponsive polymeric network composed of poly(N-isopropylacrylamide) copolymerized with fluorinated comonomers was studied to characterize the gel's physical response to fluorosurfactants in solution. Incorporating fluorinated comonomers into the polymer backbone raised their swelling in fluorocontaminant solutions relative to water-gels synthesized with 10.0 mol% 2,2,2-trifluoroethyl acrylate (TFEA) displayed a heightened maximum water-analyte swelling difference of 3761 ± 147% compared to 3201 ± 466% for non-fluorinated gels in the presence of 1 mM tetraethylammonium perfluorooctane sulfonate (TPFOS). The normalized area under the curve for gels with 12.5 mol% TFEA was further raised to 1.77 ± 0.09, indicating a broadened response window for the contaminant, but at the cost of reducing the overall swelling ratio to 3227 ± 166% and elongating the time required to reach swelling equilibrium. Overall, a copolymer fed with 10.7 mol% TFEA was predicted to maximize both the swelling and response window of the polymer toward TPFOS. Equilibration times followed a logarithmic increase as the percentage of comonomer was raised, noting gradual fluorosurfactant penetration into the gels impeded by initial gel compaction caused by the addition of fluorinated comonomers. Comparative study of gels containing 1H,1H,7H-dodecafluoroheptyl acrylate, TFEA, or 1,1,1,3,3,3-hexafluoroisopropyl acrylate identified careful selection of fluorinated comonomers and their feed ratios as useful tools for tailoring the network's swelling response to TPFOS.

Idioma originalEnglish
Páginas (desde-hasta)3599-3607
Número de páginas9
PublicaciónAnalyst
Volumen146
N.º11
DOI
EstadoPublished - jun 7 2021

Nota bibliográfica

Publisher Copyright:
© 2021 The Royal Society of Chemistry.

Financiación

Research reported was supported by NIEHS/NIH grant P42ES007380. The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIH. Access to characterization instruments and staff assistance was provided by the Electron Microscopy Center at the University of Kentucky, supported in part by the National Science Foundation/EPSCoR Award No. 1355438 and by the Commonwealth of Kentucky.

FinanciadoresNúmero del financiador
National Institutes of Health (NIH)
U.S. Department of Energy Chinese Academy of Sciences Guangzhou Municipal Science and Technology Project Oak Ridge National Laboratory Extreme Science and Engineering Discovery Environment National Science Foundation National Energy Research Scientific Computing Center National Natural Science Foundation of China
National Institutes of Health/National Institute of Environmental Health SciencesP42ES007380
Office of Experimental Program to Stimulate Competitive Research1355438

    ASJC Scopus subject areas

    • Analytical Chemistry
    • Biochemistry
    • Environmental Chemistry
    • Spectroscopy
    • Electrochemistry

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