深入了解传统和新型全氟及多氟烷基物质(PFASs)在各种阴离子交换树脂上的吸附行为
Insights into the Understanding of Adsorption Behaviors of Legacy and Emerging Per- and Polyfluoroalkyl Substances (PFASs) on Various Anion-Exchange Resins.
作者信息
Tan Hong-Ming, Pan Chang-Gui, Yin Chao, Yu Kefu
机构信息
Guangxi Laboratory on the Study of Coral Reefs in the South China Sea, School of Marine Sciences, Guangxi University, Nanning 530004, China.
School of Resources, Environment and Materials, Guangxi University, Nanning 530004, China.
出版信息
Toxics. 2023 Feb 9;11(2):161. doi: 10.3390/toxics11020161.
Per- and polyfluoroalkyl substances (PFASs) have received extensive attention due to their various harmful effects. In this study, the adsorptive removal of 10 legacy and emerging PFASs by four anion-exchange resins (including gel and macroreticular resins) were systematically investigated. Our results showed that the capacities of resins absorbing PFASs were ranked in the following order: gel strong base HPR4700 (297300 μg/g) ≈ macroreticular strong base S6368 (294300 μg/g) ≈ macroreticular weak base A111S (289300 μg/g) > gel weak base WA10 (233297 μg/g). Adsorption kinetic results indicated that the adsorption process might involve chemical and Henry regime adsorption or reaction control. Intraparticle diffusion was probably the major removal step. Co-existing fulvic acid (0.5, 1, 5 mg/L) and inorganic anions (5 mg/L of sulfate, carbonate, bicarbonate) would hinder the PFAS removal by resins with WA10 showing the highest inhibition rate of 17% and 71%, respectively. The adsorption capacities of PFBA decreased from 233 μg/g to 194 μg/g, and from 233 μg/g to 67 μg/g in the presence of fulvic acid and inorganic anions, respectively. PFASs were more easily removed by HPR4700, S6368, and A111S under neutral and alkaline environment. Moreover, WA10 was not able to remove PFASs under an alkaline medium. This study offered theoretical support for removing PFASs from aqueous phases with various resins.
全氟和多氟烷基物质(PFASs)因其各种有害影响而受到广泛关注。在本研究中,系统地研究了四种阴离子交换树脂(包括凝胶型和大孔型树脂)对10种传统和新型PFASs的吸附去除情况。我们的结果表明,树脂对PFASs的吸附容量排序如下:凝胶型强碱HPR4700(297300μg/g)≈大孔型强碱S6368(294300μg/g)≈大孔型弱碱A111S(289300μg/g)>凝胶型弱碱WA10(233297μg/g)。吸附动力学结果表明,吸附过程可能涉及化学吸附和亨利定律吸附或反应控制。颗粒内扩散可能是主要的去除步骤。共存的富里酸(0.5、1、5mg/L)和无机阴离子(5mg/L的硫酸根、碳酸根、碳酸氢根)会阻碍树脂对PFASs的去除,其中WA10表现出最高的抑制率,分别为17%和71%。在富里酸和无机阴离子存在的情况下,PFBA的吸附容量分别从233μg/g降至194μg/g和从233μg/g降至67μg/g。在中性和碱性环境下,HPR4700、S6368和A111S更容易去除PFASs。此外,WA10在碱性介质中无法去除PFASs。本研究为使用各种树脂从水相中去除PFASs提供了理论支持。
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