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用于从 ng/L 级别的地表水中和废水中选择性去除 GenX 和短链 PFAS 的阳离子聚合物。

Cationic polymer for selective removal of GenX and short-chain PFAS from surface waters and wastewaters at ng/L levels.

机构信息

Department of Environmental Engineering and Earth Science, Clemson University, Clemson, SC, 29634, USA.

Department of Chemistry, Clemson University, Clemson, SC, 29634, USA.

出版信息

Water Res. 2019 Oct 15;163:114874. doi: 10.1016/j.watres.2019.114874. Epub 2019 Jul 15.

Abstract

The emerging classes of perfluorinated alkyl substances (PFAS) (e.g., Perfluorobutanoic acid (PFBA), perfluorobutane sulfonic acid (PFBS), GenX, ADONA, and F-53B) are persistent and recalcitrant to removal by conventional treatment techniques. Herein, we report on poly (N-[3-(dimethylamino)propyl]acrylamide, methyl chloride quaternary, DMAPAA-Q) hydrogel matrix as an effective sorbent for sequestering PFAS from different water matrices. The selective removal of 16 PFAS from different classes using DMAPAA-Q polymer was confirmed in surface waters and treated wastewater at environmentally relevant concentration (i.e., <1000 ng/L). The results showed fast removal kinetics with equilibrium time of 60-120 min and a higher removal of sulfonated than carboxylic PFAS, regardless of their chain lengths. These observations were in agreement with adsorption energy calculations of short- and long-chain PFAS on poly DMAPAA-Q hydrogel using density functional theory (DFT). No desorption was observed when the experimental time was extended to 24 h, which gives an added advantage of poly DMAPAA-Q hydrogel over previously reported adsorbents in the literature. In addition, the removal efficiency was not affected under a varying pH range of 4-10. The impact of background anions on PFAS removal by poly DMAPAA-Q hydrogel was tested and found to follow an order of SO > Cl > NO. The performance of poly DMAPAA-Q hydrogel was maintained in six consecutive adsorption/regeneration cycles to remove PFAS. The unique fast kinetics and high adsorption activity of poly DMAPAA-Q hydrogel towards PFAS exhibits a great potential for being a promising material for PFAS control.

摘要

新兴的全氟烷基物质(PFAS)类别(例如,全氟丁烷磺酸(PFBS)、全氟丁酸(PFBA)、GenX、ADONA 和 F-53B)具有持久性和抗去除性,常规处理技术无法将其去除。在此,我们报告了聚(N-[3-(二甲氨基)丙基]丙烯酰胺,甲基氯季铵盐,DMAPAA-Q)水凝胶基质作为一种从不同水基质中螯合 PFAS 的有效吸附剂。使用 DMAPAA-Q 聚合物从不同类别中选择性去除 16 种 PFAS 已在地表水中得到证实,在环境相关浓度(即 <1000ng/L)下处理废水。结果表明,无论其链长如何,去除动力学速度都很快,平衡时间为 60-120 分钟,对磺化的去除率高于对羧酸的去除率。这些观察结果与使用密度泛函理论(DFT)对短链和长链 PFAS 在聚 DMAPAA-Q 水凝胶上的吸附能计算结果一致。当实验时间延长至 24 小时时,没有观察到解吸现象,这使得聚 DMAPAA-Q 水凝胶相对于文献中以前报道的吸附剂具有附加优势。此外,在 pH 值范围为 4-10 的变化下,去除效率不受影响。还测试了背景阴离子对聚 DMAPAA-Q 水凝胶去除 PFAS 的影响,发现其去除顺序为 SO42->Cl->NO3-。聚 DMAPAA-Q 水凝胶在六次连续吸附/再生循环中去除 PFAS 的性能得以保持。聚 DMAPAA-Q 水凝胶对 PFAS 具有快速动力学和高吸附活性,这表明它具有成为控制 PFAS 的有前途材料的巨大潜力。

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