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Cu(II)对氧代阴离子取代纤铁矿稳定性的影响。

Effect of Cu(II) on the stability of oxyanion-substituted schwertmannite.

机构信息

School of Environment and Energy, South China University of Technology, Guangzhou, 510006, China.

The Key Laboratory of Pollution Control and Ecosystem Restoration in Industry Clusters, Ministry of Education, South China University of Technology, Guangzhou, 510006, China.

出版信息

Environ Sci Pollut Res Int. 2018 Jun;25(16):15492-15506. doi: 10.1007/s11356-018-1773-0. Epub 2018 Mar 22.

Abstract

Schwertmannite, a Fe(III)-oxyhydroxysulfate mineral formed in acidic (pH 3~4), iron- and sulfate-rich acid mine drainage (AMD) environments, tends to undergo phase transformations with changes in pH and redox condition, which may depend on the presence of various trace anions and cations. In the present study, the effects of Cu(II) on the stability of arsenate-, chromate-, and molybdate-substituted schwertmannite were investigated. The release of Fe(III) and sulfate from schwertmannite seems to be accelerated in the presence of Cu(II) at pH ~ 3, while Cu(II) retarded the dissolution of schwertmannite at pH ~ 5. XRD and SEM results showed that pure schwertmannite and chromate-substituted schwertmannite underwent transformation to goethite over a 2-month period, the presence of Cu(II) enhanced the stability of the mineral's structure at both pH 3 and 5. However, the structures of arsenate- and molybdate-substituted schwertmannites showed no significant changes in the presence or absence of Cu(II) at both pH 3 and 5. During the phase transformation process, the amount of released oxyanions followed the sequence of chromate > molybdate > arsenate. Moreover, the release of arsenate and chromate from schwertmannite was retarded in the presence of Cu(II) at pH 5, whereas the release of molybdate was promoted. These results have important environmental implications for the stability of schwertmannite and its potential to immobilize contaminant trace elements under AMD conditions.

摘要

纤铁矿是一种在酸性(pH 34)、富铁和富硫酸盐的酸性矿山排水(AMD)环境中形成的 Fe(III)-氧羟硫酸盐矿物,其结构往往会随着 pH 值和氧化还原条件的变化而发生相变,这可能取决于各种痕量阴离子和阳离子的存在。在本研究中,研究了 Cu(II) 对砷酸盐、铬酸盐和钼酸盐取代纤铁矿稳定性的影响。在 pH3 的条件下,Cu(II) 的存在似乎加速了纤铁矿中 Fe(III) 和硫酸盐的释放,而在 pH5 的条件下,Cu(II) 则减缓了纤铁矿的溶解。XRD 和 SEM 结果表明,纯纤铁矿和铬酸盐取代纤铁矿在 2 个月的时间内转变为针铁矿,Cu(II) 的存在增强了矿物结构在 pH3 和 5 时的稳定性。然而,在 pH3 和 5 时,Cu(II) 的存在或不存在对砷酸盐和钼酸盐取代纤铁矿的结构均没有显著影响。在相变过程中,释放的含氧阴离子的量按铬酸盐>钼酸盐>砷酸盐的顺序排列。此外,在 pH5 的条件下,Cu(II) 的存在会减缓砷酸盐和铬酸盐从纤铁矿中的释放,而钼酸盐的释放则会增强。这些结果对纤铁矿的稳定性及其在 AMD 条件下固定污染物痕量元素的潜力具有重要的环境意义。

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