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The application of illite supported nanoscale zero valent iron for the treatment of uranium contaminated groundwater

机译:伊利石负载纳米零价铁在铀污染地下水处理中的应用。

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摘要

In this study, nanoscale zero valent iron I-NZVI was investigated as a remediation strategy for uranium contaminated groundwater from the former Cimarron Fuel Fabrication Site in Oklahoma, USA. The 1 L batch-treatment system was applied in the study. The result shows that 99.9% of uranium in groundwater was removed by I-NZVI within 2 h. Uranium concentration in the groundwater stayed around 27 mu g/L, and there was no sign of uranium release into groundwater after seven days of reaction time. Meanwhile the release of iron was significantly decreased compared to NZVI which can reduce the treatment impact on the water environment. To study the influence of background pH of the treatment system on removal efficiency of uranium, the groundwater was adjusted from pH 2-10 before the addition of I-NZVI. The pH of the groundwater was from 2.1 to 10.7 after treatment. The removal efficiency of uranium achieved a maximum in neutral pH of groundwater. The desorption of uranium on the residual solid phase after treatment was investigated in order to discuss the stability of uranium on residual solids. After 2 h of leaching, 0.07% of the total uranium on residual solid phase was leached out in a HNO3 leaching solution with a pH of 4.03. The concentration of uranium in the acid leachate was under 3.2 mu g/L which is below the EPA's maximum contaminant level of 30 mu g/L. Otherwise, the concentration of uranium was negligible in distilled water leaching solution (pH = 6.44) and NaOH leaching solution (pH = 8.52). A desorption study shows that an acceptable amount of uranium on the residuals can be released into water system under strong acid conditions in short terms. For long term disposal management of the residual solids, the leachate needs to be monitored and treated before discharge into a hazardous landfill or the water system. For the first time, I-NZVI was applied for the treatment of uranium contaminated groundwater. These results provide proof that I-NZVI has improved performance compared to NZVI and is a promising technology for the restoration of complex uranium contaminated water resources. (C) 2017 Elsevier Ltd. All rights reserved.
机译:在这项研究中,研究了纳米级零价铁I-NZVI作为来自美国俄克拉荷马州前Cimarron燃料制造基地的铀污染地下水的修复策略。 1 L分批处理系统应用于研究。结果表明,I-NZVI在2小时内去除了地下水中99.9%的铀。反应7天后,地下水中的铀浓度保持在27μg / L左右,并且没有铀释放到地下水中的迹象。同时,与NZVI相比,铁的释放显着降低,这可以减少处理对水环境的影响。为了研究处理系统的背景pH值对铀去除效率的影响,在添加I-NZVI之前将地下水的pH值调整为2-10。处理后,地下水的pH值为2.1至10.7。在地下水的中性pH中,铀的去除效率达到最大。为了研究铀在残余固体上的稳定性,研究了铀在处理后在残余固相上的解吸。浸出2小时后,在pH 4.03的HNO3浸出溶液中浸出残留固相中总铀的0.07%。酸性浸出液中的铀浓度低于3.2μg / L,低于EPA的最大污染物水平30μg / L。否则,在蒸馏水浸出溶液(pH = 6.44)和NaOH浸出溶液(pH = 8.52)中铀的浓度可忽略不计。脱附研究表明,残留物上可接受量的铀可在短期内在强酸条件下释放到水系统中。为了对残余固体进行长期处置管理,需要对渗滤液进行监测和处理,然后将其排入危险的垃圾填埋场或水系统。 I-NZVI首次用于铀污染地下水的处理。这些结果提供了证明,I-NZVI与NZVI相比性能有所提高,并且是用于修复受铀污染的复杂水资源的有前途的技术。 (C)2017 Elsevier Ltd.保留所有权利。

著录项

  • 来源
    《Journal of Environmental Radioactivity》 |2017年第9期|1-6|共6页
  • 作者单位

    Univ Texas Austin, Nucl Engn Teaching Lab, 10,100 Burnet Rd, Austin, TX 78712 USA|China Univ Geosci, Sch Environm Studies, 388 Lumo Rd, Wuhan 430074, Hubei, Peoples R China;

    Univ Texas Austin, Nucl Engn Teaching Lab, 10,100 Burnet Rd, Austin, TX 78712 USA|Enviroklean Prod Dev Inc, 9227 Thomasville Dr, Houston, TX 77064 USA;

    China Univ Geosci, Sch Environm Studies, 388 Lumo Rd, Wuhan 430074, Hubei, Peoples R China;

  • 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

    Supported iron nanoparticles; Uranium; Groundwater; Remediation;

    机译:负载铁纳米粒子;铀;地下水;修复;

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