The synergistic effect of typical chiral organic acids and solution chemistry conditions on the transport of 2-arylpropionic acid chiral derivatives in porous media

The hazards of man-made chiral compounds are of great public concern, with reports of worrying stereoselective compounds and an urgent need to assess their transport. This study evaluated the transport of 2-arylpropionic acid derivatives enantiomers (2-APA) in porous media under a variety of solutio...

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Veröffentlicht in:Environmental pollution (1987) 2024-06, Vol.351, p.124059, Article 124059
Hauptverfasser: Xu, Duo, Ji, Yantian, Du, Bowen, He, Bo, Chen, Hongyang, Sun, Huimin, Yin, Xianqiang
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Sprache:eng
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Zusammenfassung:The hazards of man-made chiral compounds are of great public concern, with reports of worrying stereoselective compounds and an urgent need to assess their transport. This study evaluated the transport of 2-arylpropionic acid derivatives enantiomers (2-APA) in porous media under a variety of solution chemistry conditions via column packing assays. The results revealed the introduction of Malic acid (MA) enantiomers enhanced the mobility of 2-APA enantiomers, but the enhancement effect was different for different 2-APA enantiomers. Batch sorption experiments confirmed that the MA enantiomers occupied the sorption site of the quartz sand, thus reducing the deposition of the 2-APA enantiomer. Homo- or heterochirality between 2-APA and MA dominates the transport of 2-APA enantiomers, with homochirality between them triggering stronger retention and vice versa. Further evaluating the effect of solution chemistry conditions on the transport of 2-APA enantiomers, increased ionic strength attenuated the mobility of 2-APA enantiomers, whereas introduced coexisting cations enhanced the retention of 2-APA enantiomers in the column. The redundancy analyses corroborated these solution chemistry conditions were negatively correlated with the transport of 2-APA enantiomers. The coupling of pH and these conditions reveals electrostatic forces dominate the transport behavior and stereoselective interactions of 2-APA enantiomers. Distinguishing the transport of enantiomeric pair helps to understand the difference in stereoselectivity of enantiomers and promises to remove the more hazardous one. [Display omitted] •Stereoselectivity force of 2-APA and MA depend on homo- or heterochirality among them.•Increased ISs and introduction of coexisting cations weaken chiral interactions.•Enhanced electrostatic forces weaken chiral interactions and guide transport of 2-APA.•Divalent ions increase the retention of 2-APA in the column via bridging effects.
ISSN:0269-7491
1873-6424
1873-6424
DOI:10.1016/j.envpol.2024.124059