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基于生物滤池中铁或锰原位氧化产物的微量磷去除

[Trace Amounts of Phosphorus Removal Based on the in-suit Oxidation Products of Iron or Manganese in a Biofilter].

作者信息

Cai Yan-An, Bi Xue-Jun, Zhang Jia-Ning, Dong Yang, Liu Wen-Zhe

机构信息

School of Environmental and Municipal Engineering, Qingdao University of Technology, Qingdao 266033, China.

出版信息

Huan Jing Ke Xue. 2018 Jul 8;39(7):3222-3229. doi: 10.13227/j.hjkx.201712248.

Abstract

In order to remove trace amounts of phosphorus from water bodies, a lab-scale biofilter was constructed to investigate the capacity of in situ oxidation products of iron or manganese for phosphorus adsorption. SEM, EDS, BET, and zeta technologies were employed to reveal the adsorption mechanisms. The results indicated that phosphorus could be removed by the oxide products generated from the iron or manganese removal process, at 106.28 μg·mg and 77.98 μg·mg, respectively, as shown by the linear relationships between phosphorus removal and the two oxides. SEM, EDS, and BET analysis demonstrated that the BET specific surface areas for the iron- and manganese-rich oxides were 96 m·g and 67 m·g, respectively, with the former accumulated between the pore spaces of the filtering sand and easily washed out of the layer by backwashing, whereas the latter coated the surface of the filtering sand. Thus, backwashing was favorable for phosphorus adsorption in the iron oxidation process to avoid overaccumulation. Moreover, the zero point of charge of the two oxides indicated electrostatic attraction may have occurred between iron-rich oxide and phosphorus; however, inner-sphere complex reactions obviously occurred for the two oxides because the zero point of charge after phosphorus adsorption decreased to a lower level. In addition, other anions were negatively complexed with the phosphorus on the surface of the oxides, it demonstrated that phosphorus adsorption on the surface of the two oxides seemed to be a specific adsorption.

摘要

为了去除水体中的痕量磷,构建了一个实验室规模的生物滤池,以研究铁或锰的原位氧化产物对磷的吸附能力。采用扫描电子显微镜(SEM)、能谱仪(EDS)、比表面积分析仪(BET)和zeta电位技术揭示吸附机制。结果表明,铁或锰去除过程中产生的氧化产物可以去除磷,磷去除量与两种氧化物之间的线性关系表明,铁氧化产物和锰氧化产物对磷的去除量分别为106.28 μg·mg和77.98 μg·mg。SEM、EDS和BET分析表明,富铁氧化物和富锰氧化物的BET比表面积分别为96 m²·g和67 m²·g,前者积聚在滤砂孔隙之间,容易通过反冲洗从滤层中冲出,而后者则覆盖在滤砂表面。因此,反冲洗有利于铁氧化过程中的磷吸附,避免过度积累。此外,两种氧化物的零电荷点表明,富铁氧化物与磷之间可能发生了静电吸引;然而,由于磷吸附后的零电荷点降低到较低水平,两种氧化物明显发生了内层络合反应。此外,其他阴离子与氧化物表面的磷发生负络合,表明两种氧化物表面的磷吸附似乎是一种特异性吸附。

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