吸附
环境化学
自然(考古学)
沸石
环境科学
化学
天然有机质
废物管理
水处理
环境工程
吸附
地质学
有机化学
工程类
催化作用
古生物学
作者
Nathaniel Sheehan,Charles A Ponge,Abe Pankratz,Justin M. Hutchison,Brian B. Laird,Nuong P. Nguyen,Mark B. Shiflett,Deepak Timalsina,M. Wang,Edward Peltier
出处
期刊:Chemosphere
[Elsevier BV]
日期:2025-04-15
卷期号:378: 144414-144414
被引量:1
标识
DOI:10.1016/j.chemosphere.2025.144414
摘要
Per- and polyfluoroalkyl substances (PFAS) are emerging anthropogenic pollutants of concern and are associated with potential human and environmental health concerns. PFAS removal can be achieved using adsorbents such as activated carbon and ion exchange resins. Recently, zeolites have been identified as another potential adsorption technology with increased selectivity and product regenerability that is not currently achieved with other adsorbents. Zeolite CP814E∗ (BEA) was tested in batch reactions for PFAS removal in different water matrix characteristics, including pH, select cations, humic acids (HA), fulvic acids (FA), and natural organic matter (NOM). In synthetic EPA waters, BEA performance increased compared to ultrapure water testing. BEA performance also significantly increased in the presence of Na+, Ca2+, and Mg2+ ions compared to ultrapure waters. PFOA and PFOS sorption did not vary significantly in the 6-9 pH range. HA, FA, and NOM did not significantly impact the sorption of PFOA and PFOS on the BEA at 1 g/L zeolite loading. One organic interferent, Suwannee River humic acids, did reduce PFOA sorption when the ratio of adsorbent to liquid was reduced to 0.1 mg/L. BEA retained sorption capacity over seven thermal regeneration cycles, and a BEA test with a real water demonstrated PFOA, PFOS and PFHxS adsorption at the parts per trillion level.
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