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Oxidation State and Size of Fe Controlled by Organic Matter in Natural Waters

机译:天然水中有机质控制的铁的氧化态和尺寸

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摘要

In a well mixed-stream, in which the iron/organic carbon (OC) ratio varied from 0.333 to 0.05 with sampling point and discharge, 40-70% of the Fe load was found to be present as lightly bound Fe(II). In laboratory simulations of streamwater, after 24 h of aeration at pH 6.5, and with an Fe/OC concentration ratio of 0.417,97% of Fe(II) was converted to Fe(III) (hydr)oxides, while at a ratio of 0.083, 87% of Fe(II) remained unoxidized. The particle size distribution of Fe contained < 0.2μm fractions only when 0C was present, and comparison of Fe and 0C size distributions suggested that there was more than one mechanism by which colloidal Fe was produced. At high Fe/ OC ratios, < 0.2μm fractions may be predominantly Fe(III) (hydr)oxides stabilized by 0C, but at low ratios, they must consist of otherwise soluble Fe(II) attached to <0.2μm OC. The recognition in the field of the consequences of processes demonstrated in the laboratory suggests that OC may be a predominant control of both size and oxidation state of Fe in many natural waters.
机译:在一个良好的混合流中,其中铁/有机碳(OC)的比值随采样点和放电而从0.333变为0.05,发现有40-70%的Fe负载作为轻结合的Fe(II)存在。在实验室模拟的流水中,在pH 6.5曝气24小时后,Fe / OC浓度比为0.417,97%的Fe(II)转化为Fe(III)(氢)氧化物,而0.083,仍有87%的Fe(II)未被氧化。仅当存在0C时,Fe的粒径分布才包含<0.2μm的级分,Fe与0C尺寸分布的比较表明,胶体Fe的产生机理不止一种。在高的Fe / OC比下,<0.2μm的馏分可能主要是被0°C稳定的Fe(III)(氢氧化)氧化物,但是在低的比例下,它们必须由附着在<0.2μmOC上的可溶Fe(II)组成。在实验室中对过程结果的认识表明,在许多天然水中,OC可能是铁的尺寸和氧化态的主要控制因素。

著录项

  • 来源
    《Environmental Science & Technology》 |2008年第10期|p.3575-3581|共7页
  • 作者单位

    School of Earth, Atmospheric, and Environmental Sciences, University of Manchester, Manchester M13 9PL, United Kingdom;

  • 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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