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Modifications to EPA Method 3060A to Improve Extraction of Cr(VI) from Chromium Ore Processing Residue-Contaminated Soils

机译:修改EPA方法3060A,以改善铬矿石加工残渣污染土壤中六价铬的提取

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摘要

It has been shown that EPA Method 3060A does not adequately extract Cr(VI) from chromium ore processing residue (COPR). We modified various parameters of EPA 3060A toward understanding the transformation of COPR minerals in the alkaline extraction and improving extraction of Cr(VI) from NIST SRM 2701, a standard COPR-contaminated soil. Aluminum and Si were the major elements dissolved from NIST 2701, and their concentrations in solution were correlated with Cr(Ⅵ). The extraction fluid leached additional Al and Si from the method-prescribed borosilicate glass vessels which appeared to suppress the release of Cr(Ⅵ). Use of polytetrafluoroethylene vessels and intensive grinding of NIST 2701 increased the amount of Cr(VI) extracted. These modifications, combined with an increased extraction fluid to sample ratio of ≥900 mL g~(-1) and 48-h extraction time resulted in a maximum release of 1274 ± 7 mg kg~(-1) Cr(Ⅵ). This is greater than the NIST 2701 certified value of 551 ± 35 mg kg~(-1) but less than 3050 mg kg~(-1) Cr(VI) previously estimated by X-ray absorption near edge structure spectroscopy. Some of the increased Cr(VI) may have resulted from oxidation of Cr(Ⅲ) released from brownmillerite which rapidly transformed during the extractions. Layered-double hydroxides remained stable during extractions and represent a potential residence for unextracted Cr(Ⅵ).
机译:已经证明,EPA方法3060A不能从铬矿石加工残渣(COPR)中充分萃取Cr(VI)。我们修改了EPA 3060A的各种参数,以了解碱性提取中COPR矿物的转化,并改善了从标准COPR污染的土壤NIST SRM 2701中提取六价铬的能力。铝和硅是NIST 2701中溶解的主要元素,它们在溶液中的浓度与Cr(Ⅵ)相关。萃取液从方法规定的硼硅酸盐玻璃容器中浸出了额外的Al和Si,这些容器似乎抑制了Cr(Ⅵ)的释放。使用聚四氟乙烯容器和NIST 2701的强烈研磨可增加提取的Cr(VI)量。这些修饰结合增加的萃取液与样品的比值≥900mL g〜(-1)和48小时的萃取时间,导致最大释放量为1274±7 mg kg〜(-1)Cr(Ⅵ)。该值大于NIST 2701的551±35 mg kg〜(-1)认证值,但小于3050 mg kg〜(-1)Cr(VI)先前通过边缘结构光谱的X射线吸收估计的值。 Cr(VI)的某些增加可能是由于从褐煤中释放出的Cr(Ⅲ)的氧化而引起的,而在提取过程中,其迅速转变。层状双氢氧化物在萃取过程中保持稳定,并代表未萃取的Cr(Ⅵ)的潜在驻留。

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  • 来源
    《Environmental Science & Technology》 |2017年第19期|11235-11243|共9页
  • 作者单位

    U.S. Geological Survey, Crustal Geophysics and Geochemistry Science Center, MS964D, Denver Federal Center, Denver, Colorado 8022S, United States;

    U.S. Geological Survey, Colorado Water Science Center, Denver Federal Center, Denver, Colorado 80225, United States;

    PerkinEImer, Incorporated, 75 Nicholson Lane, San Jose, California 95132, United States;

    U.S. Geological Survey, Geology, Minerals, Energy, and Geophysics Science Center, 345 Middlefield Road, Menlo Park, California 94025, United States;

    U.S. Geological Survey, Crustal Geophysics and Geochemistry Science Center, MS964D, Denver Federal Center, Denver, Colorado 8022S, United States;

    U.S. Geological Survey, Central Mineral and Environmental Resources Science Center, Denver Federal Center, Denver, Colorado 80225, 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
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  • 入库时间 2022-08-17 13:57:48

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