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生态学杂志 ›› 2025, Vol. 44 ›› Issue (12): 4144-4151.doi: 10.13292/j.1000-4890.202512.028

• 研究报告 • 上一篇    下一篇

溶液化学条件对全氟辛酸迁移行为的复合影响及其机制

邢颖娜,李琪*,季蕾,傅晓文,张强,王加宁   

  1. (齐鲁工业大学(山东省科学院), 山东省科学院生态研究所, 山东省应用微生物重点实验室, 济南 250013)

  • 出版日期:2025-12-10 发布日期:2025-12-11

Complex effects and mechanisms of solution chemical conditions on the migration of perfluorooctanoic acid.

XING Yingna, LI Qi*, JI Lei, FU Xiaowen, ZHANG Qiang, WANG Jianing   

  1. (Shandong Province Key Laboratory of Applied Microbiology, Ecology Institute of Shandong Academy of Sciences, Qilu University of Technology (Shandong Academy of Sciences), Jinan 250013, China).

  • Online:2025-12-10 Published:2025-12-11

摘要: 全氟辛酸(PFOA)及其盐类是一类兼具疏水、疏油特性的新型持久性有机污染物,广泛存在于土壤和地下水环境,威胁人类健康和生态安全。本研究通过饱和柱迁移实验揭示了溶液离子强度、pH、溶解性有机质(DOM)以及阳离子类型对PFOA迁移行为的影响,利用对流扩散方程拟合穿透曲线,并探讨了其中的关键机制。结果表明,PFOA具有极强的迁移能力,在背景电解质为NaCl时,溶液离子强度和pH对PFOA的最大穿透比(C/C0max)没有显著影响,并且其穿透率保持在100%左右,但酸性条件下PFOA与孔隙介质间的静电斥力减弱,迁移速率较慢。当背景电解质为CaCl2时,PFOA迁移特征发生显著变化,离子强度升高,使PFOA的穿透率降低了8.3%,pH降低使其穿透率降低了23.4%。此外,DOM具有抑制PFOA迁移的能力,并且Ca2+对该能力有促进作用。孔隙溶液中的多价阳离子可以通过桥接等作用改变PFOA与孔隙介质之间的相互作用,从而改变PFOA迁移行为对溶液化学条件变化的响应,在PFOA的迁移过程中发挥关键作用。这些结果为PFOA环境行为的预测和环境风险管控提供重要的科学基础。


关键词: 全氟化合物, 迁移, 溶液化学条件, 溶解性有机质, 多价阳离子

Abstract: Perfluorooctanoic acid (PFOA) and its salts are a group of emerging persistent organic pollutants with both hydrophobic and oleophobic properties. Their widespread presence in soil and groundwater threatens human health and ecological safety. In this study, we investigated the effects of solution ionic strength, pH, dissolved organic matter (DOM), and cation type on the migration of PFOA through saturated column experiments. The breakthrough curves were fitted by the convection-diffusion equation, and the key mechanisms were discussed. Results showed that PFOA had a high mobility. When the background electrolyte was NaCl, the ionic strength and pH of the solution did not affect the maximum relative concentration (C/C0max) of PFOA, and its breakthrough rate remained at about 100%. However, the electrostatic repulsion between PFOA and the porous media was weakened, leading to a slow migration velocity under acidic conditions. When the background electrolyte was CaCl2, the migration characteristics of PFOA significantly changed. The increase in ionic strength and the decrease in pH reduced the breakthrough rate of PFOA by 8.3% and 23.4%, respectively. In addition, DOM had the ability to inhibit the migration of PFOA, which was enhanced by Ca2+. Multivalent cations in the pore solution could alter the interaction between PFOA and the pore medium by bridging. This alteration could change the response of PFOA transport behavior to variations in solution chemical conditions and play a crucial role in its migration. These results provide an important scientific basis for predicting the environmental transport behavior and managing the migration risk associated with PFOA.


Key words: perfluorinated compound, transport, solution chemical condition, dissolved organic matter, multivalent cation