化学
离子交换
环境化学
降级(电信)
卤水
矿化(土壤科学)
溶剂
氟化物
总有机碳
核化学
离子
无机化学
有机化学
计算机科学
电信
氮气
作者
Mark E. Fuller,Yuwei Zhao,Paul C. Hedman,Paul G. Koster van Groos,Anthony Soto,Francis Boodoo,Jord Yniguez,Erica R. McKenzie
标识
DOI:10.1016/j.jhazmat.2024.134291
摘要
One of the primary technologies currently being deployed for the removal of per- and polyfluoroalkyl substance (PFAS) from water is ion exchange (IX). For regenerable IX resins, concentrated PFAS in the resulting spent brine and/or still bottoms requires further treatment. This research demonstrated that PFAS in spent brine and still bottoms can be effectively degraded sonochemically at 1000 kHz. Overall, PFAS degradation was negatively impacted by high total organic carbon (TOC) and residual methanol (MeOH) solvent (up to 50 g/kg; 5% w:w), but was enhanced by the high chloride. The addition of caustic (up to 1 N NaOH) partially mitigated the inhibition by TOC and MeOH. Sonochemical degradation of individual PFAS compounds resulted in significant mineralization to form inorganic fluoride, but small quantities of volatile organic fluorine species (VOF) were noted. This is believed to be the first report of sonochemical degradation of PFAS in ion exchange regeneration wastes, and indicates the possibility for the application of this technology as part of a complete PFAS capture and destruction treatment train.
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