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一种将亚铁生物氧化与铁化学还原相结合以促进模拟酸性矿山排水中生物矿化的新方法。

A novel approach coupling ferrous iron bio-oxidation and ferric iron chemo-reduction to promote biomineralization in simulated acidic mine drainage.

作者信息

Wang Ning, Fang Di, Zheng Guanyu, Liang Jianru, Zhou Lixiang

机构信息

College of Resources and Environmental Sciences, Nanjing Agricultural University Nanjing 210095 P. R. China

出版信息

RSC Adv. 2019 Feb 11;9(9):5083-5090. doi: 10.1039/c8ra09887e. eCollection 2019 Feb 5.

Abstract

A novel -mediated approach coupling biological oxidation and chemical reduction for treating acid mine drainage (AMD) was investigated. The results showed that controlled addition of zero valent iron (ZVI) into the coupling system did not exhibit a significant adverse influence on the bacterial activity of but markedly increased the formation of secondary Fe-minerals. Nutrition did not affect the efficiency of coupling process, except for the bacteria density of . 2 days cyclic treatment performed better than that of 4 and 8 days. After 14 cycles of the coupling process, 89.4% of total iron (2.23 g L) was transferred into Fe-minerals finally. In addition, the combined system was highly effective in removing sulfate (63%) from a simulated AMD that contained soluble Cu, Zn, Al, and Mn. Valuable iron-sulfate material schwertmannite was formed with little co-precipitation of other metals. Therefore, the integration of into the reduction by ZVI may have considerable potential in the enhancement of biomineralization efficiency, which may further decrease soluble TFe and sulfate loads in AMD before lime neutralization.

摘要

研究了一种通过生物氧化和化学还原耦合处理酸性矿山排水(AMD)的新型方法。结果表明,向耦合系统中控制性添加零价铁(ZVI)对[具体细菌名称未给出]的细菌活性没有显著不利影响,但显著增加了次生铁矿物的形成。营养物质除了对[具体细菌名称未给出]的细菌密度有影响外,不影响耦合过程的效率。2天循环处理比4天和8天的处理效果更好。经过14个循环的耦合过程后,最终89.4%的总铁(2.23 g/L)转化为铁矿物。此外,该组合系统对模拟的含可溶性铜、锌、铝和锰的AMD中的硫酸盐(63%)具有高效去除能力。形成了有价值的硫酸铁物质施氏矿物,其他金属的共沉淀很少。因此,将[具体细菌名称未给出]整合到ZVI还原过程中可能在提高生物矿化效率方面具有相当大的潜力,这可能会在石灰中和之前进一步降低AMD中可溶性总铁和硫酸盐的负荷。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19ea/9060654/649e99c9ba26/c8ra09887e-f3.jpg

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