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Effects of divalent metal cations and inorganic anions on the transport of tetracycline in saturated porous media: column experiments and numerical simulations

机译:二价金属阳离子和无机阴离子对饱和多孔介质中四环素运输的影响:柱实验与数值模拟

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摘要

Tetracycline is one of the most commonly used antibiotics in the world. Eventually, large amounts of this contaminant will enter into the subsurface environment, where a variety of ions exist. In this study, the effects of divalent metal cations (Mg2+, Ca2+, Pb2+ and Cu2+) and inorganic anions (Cl-, NO3-, SO42- and H2PO4-) on the transport of tetracycline in saturated porous media were investigated. Both batch and column experiments were conducted to determine the interactions between tetracycline and sand. Batch sorption experimental results showed that the presence of divalent metal cations could increase the sorption of tetracycline onto sand due to the cation-bridging mechanism. When Na+ was the counterion in the background solution, anions caused a significant decrease in tetracycline sorption owing to the occupation of some adsorption sites by anions and the decrease of electrostatic attraction. Column experiments indicated that the inhibition effects of divalent cations followed the order of Cu2+ > Pb2+ > Ca2+ approximate to Mg2+; the regular pattern might be related to their different complexing strengths. The presence of inorganic anions enhanced the mobility of tetracycline following the order of H2PO4- > SO42- > NO3- > Cl-. Transport-enhancement effects of anions were ascribed to competition between inorganic anions and tetracycline for deposition sites on sand surfaces. However, when Ca2+ was the counterion, the differences in the breakthrough curve of tetracycline among three inorganic anions (i.e., SO42-, NO3- and Cl-) were very small. In this case, the transport-inhibiting effects of anions could be counterbalanced by the transport-enhancement effects of the cation-bridging effect. Also, the two-site nonequilibrium transport model was applied to analyze the transport data. Findings from this study improve our understanding of the transport of tetracycline in saturated aquifer materials.
机译:四环素是世界上最常用的抗生素之一。最终,大量这种污染物将进入地下环境,其中存在各种离子。在该研究中,研究了二价金属阳离子(Mg2 +,Ca2 +,Pb2 +和Cu2 +)和无机阴离子(Cl-,No3-,SO42-和H2PO4-)对饱和多孔介质中四环素转运的影响。进行两种批次和柱实验以确定四环素和沙子之间的相互作用。分批吸附实验结果表明,由于阳离子桥接机制,二价金属阳离子的存在可能将四环素的吸附在沙子上。当Na +是背景溶液中的抗衡离子时,由于阴离子的一些吸附位点和静电吸引力降低,阴离子导致四环素吸附的显着降低。柱实验表明,二价阳离子的抑制作用遵循Cu 2 +> Pb2 +> Ca2 +近似值的序列+;常规模式可能与其不同的络合强度有关。无机阴离子的存在增强了按照H2PO4-> SO42-> NO 3-> CL-的顺序的四环素的迁移率。阴离子的运输增强效应归因于无机阴离子和四环素之间的竞争,用于砂表面上的沉积位点。然而,当CA2 +是抗衡离子时,三种无机阴离子(即SO42-,NO 3和CL-)中四环素突破曲线的差异非常小。在这种情况下,通过阳离子桥接效果的运输增强效应,可以对阴离子的运输抑制效果进行平衡。此外,应用了双站点非QuiBiRibriaM运输模型来分析传输数据。从本研究中的调查结果改善了我们对饱和含水层饱和含水层中四环素的运输的理解。

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    Henan Univ Coll Chem &

    Chem Engn Henan Joint Int Res Lab Environm Pollut Control M Kaifeng 475004 Peoples R China;

    Henan Univ Coll Chem &

    Chem Engn Henan Joint Int Res Lab Environm Pollut Control M Kaifeng 475004 Peoples R China;

    Nankai Univ Minist Educ Key Lab Pollut Proc &

    Environm Criteria Tianjin 300350 Peoples R China;

    China Met Geol Bur Testing Ctr Shandong Bur Jinan 250014 Shandong Peoples R China;

    Henan Univ Coll Chem &

    Chem Engn Henan Joint Int Res Lab Environm Pollut Control M Kaifeng 475004 Peoples R China;

    Henan Univ Coll Chem &

    Chem Engn Henan Joint Int Res Lab Environm Pollut Control M Kaifeng 475004 Peoples R China;

    Henan Univ Coll Chem &

    Chem Engn Henan Joint Int Res Lab Environm Pollut Control M Kaifeng 475004 Peoples R China;

    Henan Univ Coll Chem &

    Chem Engn Henan Joint Int Res Lab Environm Pollut Control M Kaifeng 475004 Peoples R China;

    Henan Univ Coll Chem &

    Chem Engn Henan Joint Int Res Lab Environm Pollut Control M Kaifeng 475004 Peoples R China;

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  • 正文语种 eng
  • 中图分类 环境质量评价与环境监测;
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