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首页> 外文期刊>Environmental Science & Technology >Enhanced Recovery of Per- and Polyfluoroalkyl Substances (PFASs) from Impacted Soils Using Heat Activated Persulfate
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Enhanced Recovery of Per- and Polyfluoroalkyl Substances (PFASs) from Impacted Soils Using Heat Activated Persulfate

机译:使用热活化过硫酸盐从受冲击的土壤中增强恢复的每氟氟烷基物质(PFASS)

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摘要

Varying transport potential of cationic, zwitterionic, and anionic per- and polyfluoroalkyl substances (PFASs) may pose challenges for remediation of aqueous film forming foam (AFFF) impacted sites, particularly during groundwater extraction. Slow desorption of stronger sorbing, zwitterionic, and cationic PFASs may cause extended remediation times and rebound in aqueous PFAS concentrations. Persulfate oxidation has the potential to convert a complex mixture of PFASs into a simpler and more recoverable mixture of perfluoroalkyl acids (PFAAs). AFFF-impacted soils were treated with heat-activated persulfate in batch reactors and subjected to 7-day leaching experiments. Soil and water were analyzed using a combination of targeted and high resolution liquid chromatography mass spectrometry techniques as well as the total oxidizable precursors assay. Following oxidation, total PFAS composition showed the expected shift to a higher fraction of PFAAs, and this led to higher total PFAS leaching in pretreated reactors (108-110%) vs control reactors (62-90%). In both pretreated and control soils, precursors that remained following leaching experiments were 61 - 100% cationic and zwitterionic. Results suggest that persulfate pretreatment of soils has promise as an enhanced recovery technique for remediation of total PFASs in impacted soils. They also demonstrate that PFAS distribution may have been altered at sites where in situ chemical oxidation was applied to treat co-occurring contaminants of concern.
机译:不同的阳离子,两性离子和阴离子和聚氟烷基物质(PFASS)的运输潜力可能造成用于修复含水膜(AFFF)的受冲击位置的挑战,特别是在地下水提取过程中。较强的吸附,两性离子和阳离子PFASS的慢吸附可能导致延长的修复时间和在PFAS浓度水溶液中反弹。过硫酸盐氧化具有将施用的复杂混合物转化为全氟烷基酸(PFAAs)的更简单和更高的可回收混合物。在分批反应器中用热活化过硫酸盐处理过的抗冲击土壤并进行7天的浸出实验。使用靶向和高分辨率的高分辨率液相色谱质谱技术的组合分析土壤和水,以及总可氧化的前体测定。在氧化之后,总PFAS组合物显示预期转变为更高的PFAAs偏移,并且这导致预处理反应器中的更高总PFA浸出(108-110%)VS对照反应器(62-90%)。在预处理和对照土壤中,浸出实验后保持的前体为61-100%阳离子和两性离子。结果表明,未经硫酸盐的土壤预处理有望作为一种增强的恢复技术,用于修复受影响的土壤中的总纸币。他们还证明,在施用原位化学氧化以治疗令人关注的共同污染物的位置,PFAs分布可能已改变。

著录项

  • 来源
    《Environmental Science & Technology》 |2021年第14期|9805-9816|共12页
  • 作者单位

    Department of Civil Environmental and Construction Engineering Texas Tech University Lubbock Texas 79409 United States;

    Department of Civil Environmental and Construction Engineering Texas Tech University Lubbock Texas 79409 United States;

    Department of Civil Environmental and Construction Engineering Texas Tech University Lubbock Texas 79409 United States;

    Department of Civil Environmental and Construction Engineering Texas Tech University Lubbock Texas 79409 United States;

    Engineering and Management Clarkson University Potsdam New York 13699 United States;

    Department of Civil Environmental and Construction Engineering Texas Tech University Lubbock Texas 79409 United States;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    soil; groundwater; remediation; chemical oxidation; precursors;

    机译:土壤;地下水;修复;化学氧化;前体;

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