Journal
WATER RESEARCH
Volume 220, Issue -, Pages -Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.watres.2022.118650
Keywords
GenX; Adsorptive photocatalyst; Adsorption; Photocatalysis; Defluorination; PFAS
Funding
- Strategic Environmental Research and Development Program (SERDP) [ER18-1515]
- National Science Foundation [CBET-2041060]
- Alabama Research & Development Fund [1ARDEF20 01]
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In this study, a novel adsorptive photocatalyst Bi/TNTs@AC was developed for efficient adsorption and solid-phase photodegradation of GenX. The material mainly consists of activated carbon, anatase, and bismuth nanoparticles with a metallic bismuth core covered by an amorphous Bi2O3 shell. Through analysis and calculations, it was found that Bi/TNTs@AC can degrade GenX into shorter-chain fluorinated compounds through a stepwise defluorination mechanism. The results suggest that Bi/TNTs@AC holds potential for more cost-effective degradation of GenX.
GenX, the ammonium salt of hexafluoropropylene oxide dimer acid, has been used as a replacement for perfluorooctanoic acid. Due to its widespread uses, GenX has been detected in waters around the world amid growing concerns about its persistence and adverse health effects. As relevant regulations are rapidly evolving, new technologies are needed to cost-effectively remove and degrade GenX. In this study, we developed an adsorptive photocatalyst by depositing a small amount (3 wt.%) of bismuth (Bi) onto activated-carbon supported titanate nanotubes, Bi/TNTs@AC, and tested the material for adsorption and subsequent solid-phase photodegradation of GenX. Bi/TNTs@AC at 1 g/L was able to adsorb GenX (100 mu g/L, pH 7.0) within 1 h, and then degrade 70.0% and mineralize 42.7% of pre-sorbed GenX under UV (254 nm) in 4 h. The efficient degradation also regenerated the material, allowing for repeated uses without chemical regeneration. Material characterizations revealed that the active components of Bi/TNTs@AC included activated carbon, anatase, and Bi nanoparticles with a metallic Bi core and an amorphous Bi2O3 shell. Electron paramagnetic resonance spin-trapping, UV-vis diffuse reflectance spectrometry, and photoluminescence analyses indicated the superior photoactivity of Bi/TNTs@AC was attributed to enhanced light harvesting and generation of charge carriers due to the UV-induced surface plasmon resonance effect, which was enabled by the metallic Bi nanoparticles. (OH)-O-center dot radicals and photogenerated holes (h(+)) were responsible for degradation of GenX. Based on the analysis of degradation byproducts and density functional theory calculations, photocatalytic degradation of GenX started with cleavage of the carboxyl group and/or ether group by (OH)-O-center dot, h(+), and/or e(aq)(-), and the resulting intermediates were transformed into shorter-chain fluorochemicals following the stepwise defluorination mechanism. Bi/TNTs@AC holds the potential for more cost-effective degradation of GenX and other per- and polyfluorinated alkyl substances.
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