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Selenium Immobilization in Evaporation Pond Sediments by In Situ Precipitation of Ferric Oxyhydroxide

机译:羟基氧化铁的原位沉淀法将硒固定在蒸发池沉积物中

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摘要

Selenium (Se) in agricultural drainage and evaporation pond waters in the semi-arid Central Valley of California can threaten water quality and is toxic to wildlife. This laboratory study focused on the development of an in situ chemical treatment to immobilize soluble Se in drained evaporation pond sediments by amendment with ferrous iron, which forms ferric oxyhydroxide (FeOOH). Three sediment samples from Kesterson Reservoir, Merced County, CA, with elevated levels of Se were characterized by conventional extraction techniques and then subjected to in situ Fe(ll) amendment. Total Se in the three untreated samples ranged from 4 to 29 mg kg~(-1), the majority of which was chemically reduced and insoluble. Soluble (0.25 M KCI-extractable) selenite [Se-(Ⅳ)] was > 90% immobilized in sediment when the added Fe(Ⅱ) was > 50 mmol of Fe(Ⅱ) kg~(-1) sed~(-1) whereas immobilization of soluble selenate [Se(Ⅵ)] was strongly dependent on the initial Se(Ⅵ) concentration. Extraction of Se(Ⅳ) by 0.01 M K_2HPO_4 decreased with increasing Fe(Ⅱ), indicating that Se(Ⅳ) immobilized by the FeOOH precipitation process was not accessible to the PO_4 extra etant. Exchangeable Se(Ⅵ) (0.01 M K_2HPO_4 extra etable) was partially immobilized in sediment depending on the initial Se(Ⅵ) concentration. Both Se(Ⅳ) and Se(Ⅵ) were occluded within FeOOH produced during Fe(Ⅱ) oxidation and hydrolysis. Iron(Ⅱ) salt amendment may be a viable in situ remediation technique for alkaline sediments containing elevated levels of trace elements such as Se.
机译:半干旱的加利福尼亚中央谷地的农业排水和蒸发池水中的硒会威胁水质,并对野生生物有毒。这项实验室研究的重点是开发一种原位化学处理方法,该方法通过用亚铁(形成氢氧化铁(FeOOH))进行改性,将可溶硒固定在排水蒸发池沉积物中。用常规提取技术表征了来自加利福尼亚州默塞德县凯斯特森水库的三个沉积物样品中硒含量的升高,然后对其进行了原位Fe(II)修饰。三个未经处理的样品中的总硒含量为4至29 mg kg〜(-1),其中大多数是化学还原的且不溶的。当添加的Fe(Ⅱ)> 50 mmol Fe(Ⅱ)kg〜(-1)sed〜(-1)时,可溶的(0.25 M KCI可萃取的)亚硒酸盐[Se-(Ⅳ)]> 90%被固定在沉积物中。 ),而可溶性硒酸盐[Se(Ⅵ)]的固定强烈依赖于初始Se(Ⅵ)浓度。随着Fe(Ⅱ)的增加,以0.01 M K_2HPO_4提取Se(Ⅳ)减少,表明POOO_4不能接近FeOOH沉淀过程固定化的Se(Ⅳ)。根据最初的Se(Ⅵ)浓度,可交换的Se(Ⅵ)(0.01 M K_2HPO_4额外可食用)部分固定在沉积物中。在Fe(Ⅱ)氧化和水解过程中产生的FeOOH中都含有Se(Ⅳ)和Se(Ⅵ)。铁(Ⅱ)盐改性剂可能是一种可行的原位修复技术,用于处理含硒等痕量元素含量较高的碱性沉积物。

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  • 来源
    《Environmental Science & Technology》 |1995年第10期|p.2639-2646|共8页
  • 作者

    BRUCE A. MANNING; R. G. BURAU;

  • 作者单位

    USDA-ARS, U.S. Salinity Laboratory, 450 West Big Springs Road, Riverside, CA 92507;

  • 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 环境化学;
  • 关键词

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