Zhang Yi, Lee Cheng-Shiuan, Li Duning, Zheng Size, Hsiao Benjamin S, Venkatesan Arjun K
New York State Center for Clean Water Technology, Stony Brook University, Stony Brook, New York 11794, United States.
Research Center for Environmental Changes, Academia Sinica, Taipei 115, Taiwan.
Environ Sci Technol. 2025 Sep 30;59(38):20761-20771. doi: 10.1021/acs.est.5c03457. Epub 2025 Sep 16.
Hydrophobic ion pairing (HIP) was used as a novel pretreatment approach to enhance the removal of short-chain per- and polyfluoroalkyl substances (PFAS) by granular activated carbon (GAC). The formation of ion pairs between PFAS and cationic surfactants was tested through controlled batch experiments with varying types and dose of HIP (e.g., cetyltrimethylammonium chloride (CTAC)) and surface tension measurements. Interactions between PFAS and CTAC were observed to be disturbed in high ionic strength solution, likely due to competitive electrostatic interactions from the presence of inorganic ions. Addition of CTAC (2 μM) prior to GAC treatment in batch adsorption experiments greatly improved the sorption of short-chain PFAS (<C) by 54-111% but suppressed the sorption of long-chain PFAS (>C) by 23-96%. The changes in sorption capacities were hypothesized to result from the altered physicochemical properties of the formed ion pair complex, thereby affecting its uptake on GAC. Both the linear free energy relationship (LFER) calculation and molecular dynamic (MD) simulation suggested that short-chain PFAS sorption was improved via enhanced hydrophobicity of formed ion pairs with a low self-assembly tendency, while long-chain PFAS sorption was inhibited due to the formation of large complexes with a high self-assembly tendency. Rapid small-scale column tests were performed for tap water spiked with an equal mass of perfluorobutanoate (PFBA), perfluorobutanesulfonate (PFBS), and perfluorooctanesulfonate (PFOS). The bed volume for 50% breakthrough was improved by 350% and 230% for PFBA and PFBS, respectively, in the presence of CTAC and PFOS.
疏水离子对(HIP)被用作一种新型预处理方法,以增强颗粒活性炭(GAC)对短链全氟和多氟烷基物质(PFAS)的去除效果。通过使用不同类型和剂量的HIP(例如十六烷基三甲基氯化铵(CTAC))进行控制批次实验以及表面张力测量,测试了PFAS与阳离子表面活性剂之间离子对的形成。观察到在高离子强度溶液中,PFAS与CTAC之间的相互作用受到干扰,这可能是由于无机离子的存在导致的竞争性静电相互作用。在批次吸附实验中,在GAC处理之前添加CTAC(2 μM)可使短链PFAS(<C)的吸附量大幅提高54 - 111%,但长链PFAS(>C)的吸附量却被抑制了23 - 96%。吸附容量的变化被推测是由于形成的离子对络合物的物理化学性质发生了改变,从而影响了其在GAC上的摄取。线性自由能关系(LFER)计算和分子动力学(MD)模拟均表明,短链PFAS的吸附通过形成具有低自组装倾向的离子对而增强了疏水性得以改善,而长链PFAS的吸附则因形成具有高自组装倾向的大络合物而受到抑制。对添加了等量全氟丁酸(PFBA)、全氟丁烷磺酸(PFBS)和全氟辛烷磺酸(PFOS)的自来水进行了快速小规模柱试验。在存在CTAC的情况下,PFBA和PFBS的50%穿透床体积分别提高了350%和230%。