Redox-active rGO-nZVI nanohybrid-catalyzed chain shortening of perfluorooctanoic acid (PFOA) and perfluorooctane sulfonic acid (PFOS)
Redox-active rGO-nZVI nanohybrid-catalyzed chain shortening of perfluorooctanoic acid (PFOA) and perfluorooctane sulfonic acid (PFOS)
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DOI:
10.1016/j.hazl.2020.100007
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发表时间:
2020-12
影响因子:
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通讯作者:
Arvid Masud;M. G. Guardian;S. C. Travis;Nita G. Chavez Soria;Mourin Jarin;D. Aga;Nirupam Aich
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文献类型:
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作者:
Arvid Masud;M. G. Guardian;S. C. Travis;Nita G. Chavez Soria;Mourin Jarin;D. Aga;Nirupam Aich
Per- and polyfluoroalkyl substances (PFASs) are exceptionally stable chemicals due to their strong Csingle bondF bonds. Nanoscale zero-valent iron (nZVI) particles have the potential to remove and degrade PFASs through redox activity. In this study, we deposited nZVI onto two-dimensional reduced graphene oxide (rGO) nanosheets and tested these synthesized rGO-nZVI nanohybrid (NH) for the treatment of a mixture of short- and long-chain PFASs in water with and without H2O2. All PFASs were removed at a higher efficiency by the rGO-nZVI NH than by the parent materials rGO and nZVI. Notably, the long-chain PFASs were removed at a faster rate than the short-chain PFASs. After a 10 min exposure to the rGO-nZVI NH without H2O2, the long-chain PFASs (perfluorooctane sulfonic acid (PFOS) and perfluorooctanoic acid (PFOA)) were removed by 85 % and 39 %, respectively, while short-chain PFASs (perfluoropentane sulfonic acid and perfluoropentanoic acid) were removed by 19 % and 18 %, respectively. The addition of H2O2enhanced the PFAS treatment performance by 10–18 %, which can be attributed to the generation of reactive oxygen species by the rGO-nZVI NH. Liquid chromatography high-resolution mass spectrometry analysis confirmed the formation of unique shorter chain and partially defluorinated PFAS-Fe complexes from both PFOS and PFOA.