Voltammetric Selectivity in Detection of Ionized Perfluoroalkyl Substances at Micro-Interfaces between Immiscible Electrolyte Solutions

Widespread contamination by per- and polyfluoroalkyl substances (PFAS) and concern about their health impacts require the availability of rapid sensing approaches. In this research, four PFAS, perfluorooctanoic acid (PFOA), perfluorobutanesulfonic acid (PFBS), perfluorohexanesulfonic acid (PFHxS), and perfluorooctanesulfonic acid (PFOS), were studied at micropipette-based interfaces between two immiscible electrolyte solutions (mu ITIES) to assess the potentiality for their detection by ion transfer voltammetry. All four PFAS substances were detected by ion transfer voltammetry at the mu ITIES, with half-wave transfer potentials (E-1/2 vs Ag/AgCl) for PFOS, PFHxS, PFBS, and PFOA of 0.34, 0.32, 0.2S, and 0.23 V, respectively. The selectivity of the mu ITIES for detection of PFAS mixtures was investigated. Among the six combinations of the four compounds, most combinations were detectable, except PFOA + PFBS and PFHxS + PFOS, because of unresolved ion transfer voltammograms. These findings provide a basis for the design of new PFAS sensing strategies based on ion transfer voltammetry.

Automated summary

This research investigates the detection of four PFAS substances using ion transfer voltammetry at micropipette-based interfaces between two immiscible electrolyte solutions (mu ITIES). The study finds that all four PFAS substances can be detected by ion transfer voltammetry at the mu ITIES, with selectivity for detecting most combinations of the compounds. These findings provide a basis for the design of new PFAS sensing strategies based on ion transfer voltammetry.