Removing forever chemicals via amphiphilic functionalized membranes

被引:12
|
作者
Johnson, James K. [1 ]
Salerno, K. Michael [1 ]
Schlesinger, Danielle R. [1 ]
Le, Nam Q. [1 ]
Ko, Jesse S. [1 ]
Xia, Zhiyong [1 ]
机构
[1] Johns Hopkins Univ, Appl Phys Lab, 11100 Johns Hopkins Rd, Laurel, MD 20723 USA
关键词
POLYFLUOROALKYL SUBSTANCES PFASS; GRANULAR ACTIVATED CARBON; PERFLUOROALKYL SUBSTANCES; ADSORPTION; REMEDIATION; GROUNDWATER; EFFICIENT; RELEVANT; GASES; SCALE;
D O I
10.1038/s41545-022-00193-y
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Per- and poly-fluoroalkyl species (PFAS) remain ever-present drinking water contaminants. While some physical adsorption technologies for PFAS removal have been implemented on a large scale, they are limited by high cost and low effectiveness. In this work, an amphiphilic coating was developed and used to functionalize an aluminum oxide hydroxide membrane. Dynamic filtration of challenge water containing eighteen PFAS demonstrated >99% removal of eleven of eighteen PFAS as defined in EPA 537.1. Comparable performance was observed under gravity filtration conditions with >90% removal of fifteen of the eighteen PFAS. A comparison of breakthrough rates using amphiphilic silanes versus granular activated carbon (GAC), the commonly used filtration technology, was performed. Filters with the new amphiphilic coating outperformed GAC under dynamic filtration conditions by more than an order of magnitude for the perfluorooctanoic acid adsorption capacity and even greater for perfluorooctane sulfonic acid. Molecular dynamics simulations were used to compute the free energy, enthalpy, and entropy of interactions between coatings and six PFAS contaminants. Computed interaction free-energy (FE) values agree with experimental filtration performance across contaminants. The ability to use simulated FE values to predict filtration efficiency presents an opportunity for future in-silico rational design with overall reduced cost and development time.
引用
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页数:6
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