Perfluorooctane sulfonate (PFOS), a persistent and bioaccumulative perfluoroalkyl substance, poses significant environmental and human health risks due to the extraordinary stability of its C–F bonds. Conventional remediation strategies largely fail to achieve mineralization, instead transferring contamination or producing secondary waste streams. In this study, we investigate neutron irradiation as a potential destructive approach for PFOS remediation in both solid and aqueous matrices. Samples were exposed to thermal neutrons (flux: 3.2 × 109 n·cm−2·s−1, 0.0025 eV) at the Argonauta reactor for 6 h. Raman and FTIR spectroscopy revealed that PFOS in powder form remained largely resistant to degradation, with only minor structural perturbations observed. In contrast, aqueous PFOS solutions exhibited pronounced spectral changes, including attenuation of C–F and S–O vibrational signatures, the emergence of carboxylate and carbonyl functionalities, and enhanced O–H stretching, consistent with radiolytic oxidation and partial defluorination. Notably, clear peak shifts were predominantly observed for PFOS in aqueous solution after irradiation (overall displacement toward higher wavenumbers), whereas in powdered PFOS the main spectral signature of irradiation was the attenuation of CF2 and S–O related bands with comparatively limited band relocation. To evaluate the biological relevance of these structural alterations, cell viability assays (MTT) were performed using human umbilical vein endothelial cells. Non-irradiated PFOS induced marked cytotoxicity at 100 and 50 μg/mL (p < 0.0001), whereas neutron-irradiated PFOS no longer exhibited significant toxicity, with cell viability comparable to the control. These findings indicate a matrix-dependent response: neutron scattering in solids yields negligible molecular breakdown, whereas radiolysis-driven pathways in water facilitate measurable PFOS transformation. The cytotoxicity assay demonstrates that neutron irradiation promotes sufficient molecular degradation of PFOS in aqueous media to suppress its cytotoxic effects. Although complete mineralization was not achieved under the tested conditions, the combined spectroscopic and biological evidence supports neutron-induced radiolysis as a promising pathway for perfluoroalkyl detoxification. Future optimization of neutron flux, irradiation duration, and synergistic catalytic systems may enhance mineralization efficiency. Because PFOS concentration, fluoride release (F−), and TOC were not quantified in this study, remediation was assessed through spectroscopic fingerprints of transformation and the suppression of cytotoxicity, rather than by mass-balance mineralization metrics. This study highlights neutron irradiation as a promising strategy for perfluoroalkyl destruction in contaminated water sources.
Souza et al. (Sun,) studied this question.