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Oxidative Measurement of Perfluoroalkyl Acid Precursors: Implications for urban runoff management and remediation of AFFF-contaminated groundwater and soil.

机译:全氟烷基酸前体的氧化测量:对城市径流管理和被AFFF污染的地下水和土壤的修复的意义。

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摘要

Perfluoroalkyl acids (PFAAs) are used to impart oil- and water-repellant and surfactant properties to numerous products, and they are among the most persistent chemicals to ever enter commerce. PFAAs are detected in the blood of humans all over the world. The two 8-carbon PFAAs, perfluorooctanoate (PFOA) and perfluorooctane sulfonate (PFOS), have been associated with a number of adverse health outcomes. In this research, a new oxidation-based technique of PFAA precursor measurement was developed for aqueous and solid samples. Along with other analytical tools, this precursor assay was used to gain insight into the occurrence and fate of PFAA precursors in two sources: urban runoff and soil and groundwater impacted by firefighting materials known as aqueous film forming foams (AFFF).;The occurrence of PFAA precursors in urban runoff was investigated to determine the extent to which runoff could serve as a source of PFAAs to drinking water supplies during storage in aquifers or reservoirs. An indirect technique of measuring PFAA precursors was developed for urban runoff samples by exposing samples to a high concentration of hydroxyl radicals and converting precursors to measureable perfluorinated carboxylate products (Chapter 2). By comparing perfluorinated carboxylate concentrations before and after oxidation, the total concentration of PFAA precursors was inferred. Analysis of thirty-three urban runoff samples collected from locations around the San Francisco Bay, CA indicated that C8 forms of PFAAs and C6 forms of PFAA precursors were predominant in runoff. The assay demonstrated that commonly measured PFAA precursors represented only a small fraction (<25%) of the total concentration of precursors present in runoff, confirming the utility of the precursor assay.;To assess the persistence of AFFF-derived PFAA precursors, groundwater, soil, and aquifer solids were obtained in 2011 from an unlined firefighter training area at a U.S. Air Force Base where AFFF was regularly used between 1970 and 1990 (Chapter 3). To measure the total concentration of PFAA precursors in archived AFFF formulations and AFFF-impacted environmental samples, the oxidation-based assay developed in Chapter 2 was adapted for these media. This precursor assay was employed along with direct measurement of twenty-two precursors found in AFFF and a suite of other poly- and perfluoroalkyl substances (PFASs). On a molar basis, precursors accounted for 41% to 100% of the total concentration of PFASs in archived AFFF formulations. In the training area, precursors measured by the precursor assay accounted for an average of 23% and 28% of total PFASs in groundwater and solids samples, respectively. Thus, much of the mass of precursors released at the site appeared to be converted to perfluorinated carboxylates and sulfonates over a residence time of twenty years or more.;In order to elucidate the conditions most amenable to AFFF-derived PFAA precursor transformation, microcosms were constructed with soil and sediment inocula and were incubated under different redox conditions with two different types of AFFF (Chapter 4). Live microcosms amended with AFFF manufactured by 3M demonstrated an ability to utilize the carbon in AFFF, but no changes in PFAS concentrations were observed over 60- to 90-day incubation periods. The main precursor in AFFF manufactured by Ansul, 6:2 fluorotelomer thioamido sulfonate (6:2 FtTAoS), was transformed in both aerobic and anaerobic live incubations. Application of the precursor assay to microcosm slurries suggested that all unquantifiable biological transformation products under aerobic conditions were partitioned to the microcosm slurry. In the anaerobic microcosms, the precursor assay indicated that unidentified biological transformation products were either sufficiently volatile to leave the slurry or unable to be oxidized to perfluorinated carboxylates. Transformation products reported in soil and groundwater beneath many U.S. military firefighter training areas (Chapter 3) are consistent with the aerobic transformation products observed in Ansul AFFF-amended microcosm. (Abstract shortened by UMI.).
机译:全氟烷基酸(PFAA)用于赋予许多产品以拒油和拒水和表面活性剂的特性,它们是有史以来进入市场的最持久的化学品之一。在全世界人类的血液中都检测到PFAA。两种8碳全氟辛烷磺酸全氟辛酸酯(PFOA)和全氟辛烷磺酸(PFOS)与许多不良健康后果有关。在这项研究中,针对水性和固态样品,开发了一种新的基于氧化的PFAA前体测量技术。与其他分析工具一起,使用该前体测定方法来深入了解PFAA前体在以下两个来源中的发生和命运:城市径流以及受称为水成膜泡沫(AFFF)的消防材料影响的土壤和地下水。对城市径流中的PFAA前体进行了研究,以确定在蓄水层或水库中储存过程中,径流在多大程度上可以作为饮用水中PFAA的来源。通过将样品暴露于高浓度的羟基自由基并将前体转化为可测量的全氟羧酸盐产品,开发了一种用于测量城市径流样品的间接测量PFAA的技术(第2章)。通过比较氧化前后的全氟羧酸盐浓度,可以推断出PFAA前体的总浓度。对从加利福尼亚州旧金山湾附近地区收集的33个城市径流样品进行的分析表明,径流中主要是C8型的PFAA和C6型的PFAA前体。该分析表明,常用的PFAA前体仅占径流中前体总浓度的一小部分(<25%),证实了该前体测定法的实用性;为了评估AFFF衍生的PFAA前体,地下水, 2011年,从美国空军基地一个没有衬砌的消防员训练区获得了土壤和含水层固体,1970年至1990年之间经常使用AFFF(第3章)。为了测量存档的AFFF配方和AFFF影响的环境样品中PFAA前体的总浓度,将第2章中开发的基于氧化的分析方法适用于这些介质。该前体测定法与直接测量AFFF中发现的22种前体以及一系列其他聚和全氟烷基物质(PFAS)一起使用。以摩尔计,前体占归档AFFF配方中PFAS总浓度的41%至100%。在培训区域,通过前体测定法测量的前体分别分别占地下水和固体样品中总PFAS的23%和28%。因此,在该位点释放的大量前体在超过20年或更长时间的停留时间内似乎已转化为全氟化的羧酸盐和磺酸盐。为了阐明最适合AFFF衍生的PFAA前体转化的条件,用土壤和沉​​积物接种物构建,并在不同的氧化还原条件下与两种不同类型的AFFF一起孵育(第4章)。用3M制造的AFFF修正的活微观世界证明了能够利用AFFF中的碳,但是在60至90天的温育期中未观察到PFAS浓度的变化。 Ansul生产的AFFF的主要前体,即6:2氟调聚物硫代酰胺基磺酸盐(6:2 FtTAoS),在需氧和厌氧条件下均进行了温育。将前体分析应用于缩微浆液表明,在好氧条件下所有无法量化的生物转化产物都被分配到了缩微浆液中。在厌氧性微观世界中,前体测定表明,未鉴定的生物转化产物要么具有足够的挥发性,以致无法离开浆液,要么无法被氧化成全氟化的羧酸盐。在许多美国军事消防员训练区下方的土壤和地下水中报告的转化产物(第3章)与在Ansul AFFF修订的缩影中观察到的有氧转化产物一致。 (摘要由UMI缩短。)。

著录项

  • 作者

    Houtz, Erika Frances.;

  • 作者单位

    University of California, Berkeley.;

  • 授予单位 University of California, Berkeley.;
  • 学科 Engineering Environmental.
  • 学位 Ph.D.
  • 年度 2013
  • 页码 148 p.
  • 总页数 148
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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