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首页> 外文期刊>Journal of Contaminant Hydrology >In situ testing of metallic iron nanoparticle mobility and reactivity in a shallow granular aquifer
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In situ testing of metallic iron nanoparticle mobility and reactivity in a shallow granular aquifer

机译:浅颗粒含水层中金属铁纳米颗粒迁移率和反应性的原位测试

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摘要

This paper describes the results of a series of single well push-pull tests conducted to evaluate the in situ transport of carboxymethyl cellulose (CMC) stabilized nanoscale zero-valent iron (ZVI) particles in saturated sediments and their reactivity toward chlorinated ethenes. CMC-stabilized nanoscale ZVI particles were synthesized on site by reducing ferrous ions with borohydride in water in the presence of CMC. Nanoscale ZVI and bimetallic ZVI-Pd nanoparticle suspensions were prepared and injected into depth-discrete aquifer zones during three push-pull tests. The injected nanoparticle suspensions contained a conservative tracer (Br~-) and were allowed to reside in the aquifer pore space for various time periods prior to recovery by groundwater extraction. The comparison between Br~- and Fe concentrations in extracted groundwater samples indicated that the CMC-stabilized nanoscale ZVI particles were mobile in the aquifer but appeared to lose mobility with time, likely due to the interactions between particles and aquifer sediments. After 13 h in the aquifer, the nanoscale ZVI particles became essentially immobilized. During the push-pull test with injection of Fe-Pd nanoparticles, ethane concentrations increased from non-detectable to 65 ug/L in extracted groundwater within less than 2 h of reaction time, indicating the rapid abiotic degradation of chlorinated ethenes. The amount of total chlorinated ethene mass destroyed was low presumably because the injected solutions "pushed" the dissolved chlorinated ethenes away from the injection well, without substantial mixing, and because stationary (sorbed) chlorinated ethene mass on the aquifer sediments was low. In situ remediation programs using highly reactive metallic nanoparticles should incorporate delivery methods that maintain high groundwater pore velocities during injection to increase advective transport distances (e.g. groundwater circulation wells). Also, source zones with abundant stationary contaminant mass that is accessible by advective transport should be targeted for remediation with the nanoparticles, as opposed to portions of dissolved plumes, in order to maximize the in situ destruction of contaminants.
机译:本文介绍了一系列单井推挽试验的结果,以评估羧甲基纤维素(CMC)稳定的纳米级零价铁(ZVI)颗粒在饱和沉积物中的原位运输及其对氯化乙烯的反应性。 CMC稳定的纳米级ZVI颗粒是通过在CMC存在下在水中用硼氢化物还原亚铁离子现场合成的。制备了纳米级ZVI和双金属ZVI-Pd纳米颗粒悬浮液,并在三个推挽测试过程中将其注入到离散的含水层区域。注入的纳米颗粒悬浮液含有保守的示踪剂(Br-),在通过地下水萃取回收之前,可以在含水层孔隙空间中停留不同的时间。提取的地下水样品中Br和Fe的浓度比较表明,CMC稳定的纳米级ZVI颗粒在含水层中可移动,但随着时间的流逝似乎失去了流动性,这可能是由于颗粒与含水层沉积物之间的相互作用所致。在含水层中放置13小时后,纳米级ZVI颗粒已基本固定。在注入Fe-Pd纳米颗粒的推挽试验过程中,在不到2小时的反应时间内,提取的地下水中乙烷浓度从检测不到的乙烷增加到65 ug / L,表明氯化乙烯的快速非生物降解。据估计,破坏的总氯乙烯总量很低,这是因为注入的溶液将注入的溶解的氯乙烯从注入井中“冲出”而没有大量混合,并且含水层沉积物上固定的(吸附的)氯乙烯质量较低。使用高反应性金属纳米颗粒的原位修复程序应结合使用输送方法,以在注入过程中保持较高的地下水孔隙速度,以增加对流传输距离(例如地下水循环井)。同样,与溶解的羽流部分不同,应该通过平流运输接近具有大量固定污染物质量的源区,以利用纳米颗粒进行修复,以最大程度地就地消除污染物。

著录项

  • 来源
    《Journal of Contaminant Hydrology》 |2010年第4期|P.35-46|共12页
  • 作者单位

    AMEC Geomatrix, 2101 Webster Street, 12th Floor, Oakland, CA 94612, United States;

    rnEnvironmental Engineering Program, Department of Civil Engineering, Auburn University, Auburn, AL 36849, United States;

    rnEnvironmental Engineering Program, Department of Civil Engineering, Auburn University, Auburn, AL 36849, United States;

    rnAMEC Geomatrix, 3711 S. Mopac Expressway, Building 1 Suite 100, Austin, TX 78746, United States;

    rnAMEC Geomatrix, 2101 Webster Street, 12th Floor, Oakland, CA 94612, 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

    chlorinated solvents; groundwater remediation; nanoparticle; push-pull test; transport; zero-valent iron; ZVI;

    机译:氯化溶剂;地下水修复;纳米粒子推挽测试运输;零价铁ZVI;

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