Abstract
The reliable quantification of perfluoroalkyl carboxylic acids (PFCAs) in environmental samples like surface water by using gas chromatography (GC) remains challenging because the polar PFCAs call for derivatization before injection and problems involving the integration of sample pretreatment and derivatization procedures. Here we proposed a cost-effective method for the GC based determination of C4–C12 PFCAs in surface water samples by integrating solid phase extraction and PFCAs anilide derivatization. First, we assessed the performance of different PFCAs derivatization methods, namely esterification and amidation. Esterification was unable to derivatize C4–C6 PFCAs. On the contrary, amidation procedures by using 2,4-difluoroaniline (DFA) and N,N′-dicyclohexylcarbodiimide (DCC) could successfully transform all the PFCA analogs to produce anilide derivatives, which could be easily detected by GC. Then the reaction conditions in the amidation approach were further optimized by using orthogonal design experiments. After optimizing the instrumental parameters of GC, the limits of detection (LOD) of this derivatization method were determined to be 1.14–6.32 μg L−1. Finally, in order to establish an intact method for the quantification of PFCAs in surface water samples, solid phase extraction (SPE) was used for extraction and cleanup, which was further integrated with the subsequent amidation process. The SPE-amidation-GC method was validated for application, with good accuracy and precision reflected by the PFCAs recoveries and derivatization of triplicates. The method reported here could provide a promising and cost-effective alternative for the simultaneous determination of C4–C12 PFCAs in environmental water samples.
Highlights
Perfluoroalkyl acids (PFAAs) refer to a series of aliphatic acids with all the H atoms in theC–H bonds replaced by F atoms
The responses of the peaks by iso-propanol were much lower compared with those generated by methanol and ethanol, probably due to the relatively lower esterification efficiency caused by the steric hindrance in the molecular structure of iso-propanol [29,30]
It can be concluded that the perfluoroalkyl carboxylic acids (PFCAs) esters approach was only feasible for the derivatization of PFCAs with a longer carbon chain (>C6), but inadequate for short-chained PFCAs, such as PFBA and PFPeA
Summary
Perfluoroalkyl acids (PFAAs) refer to a series of aliphatic acids with all the H atoms in the. According to different functional groups, they are mainly divided into two categories: perfluoroalkyl carboxylic acids (PFCAs) and perfluoroalkyl sulfonates (PFSAs) [1,2]. PFAAs and their precursors are widely used as a surfactant in metal plating, ingredients of polytetrafluoroethylene and polyvinylidene fluoride plastics, surface coatings for textile and paper, components of fire-fighting foam, cosmetics, textiles, carpets, and leather [3,4,5]. It has been reported that PFAAs are environmentally-persistent, long-distance migratory, bio-accumulative, Int. J. Res. Public Health 2020, 17, 100; doi:10.3390/ijerph17010100 www.mdpi.com/journal/ijerph
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