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Adsorption of chlorophenols on polyethylene terephthalate microplastics from aqueous environments: Kinetics, mechanisms and influencing factors

机译:从含水环境中吸附氯酚对聚对苯二甲酸乙二醇酯微塑料的:动力学,机制和影响因素

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摘要

Microplastics have received growing attention as carriers of organic pollutants in the water environment. To better understand the contribution of hydrophobic interaction, hydrogen-bonding interaction, pi-pi interaction and electrostatic interaction on the adsorption of hydrophilic compounds on microplastics and their adsorption behavior in natural waters, polyethylene terephthalate (PET, 150 mm) was used as an adsorbent and 4-chlorophenol (MCP), 2,4-dichlorophenol (DCP) and 2,4,6-trichlorophenol (TCP) were used as adsorbates. The results of batch adsorption experiments showed that chlorophenols (CPs) reached adsorption sites of PET through film diffusion and intra-particle diffusion. pH greatly affected the adsorption capacity. Hydrophobic interaction was the main adsorption mechanism of undissociated CPs on PET. Hydrogen-bonding interaction was also an adsorption mechanism between undissociated CPs and PET, and the contribution of hydrogen-bonding interaction to adsorption decreased with the increase of chlorine content. Meanwhile, the increase of chlorine content was favorable to the hydrophobic interaction between undissociated CPs and PET. However, higher chlorine content CPs with lower pK(alpha) values tended to dissociate at neutral pH condition and resulted in stronger electrostatic repulsion with PET. The increase of solution ionic strength and fulvic acid content negatively affected the adsorption of DCP and TCP on PET, but did not show significant impacts on MCP adsorption. Similarly, the adsorption capacity obtained using Taihu lake water and Bohai seawater as matrices was much lower than that using laboratory water for both DCP and TCP, while the adsorption coefficient (K-d) of MCP remained at approximately 10.6 L/kg to 11.4 L/kg in the three different solution matrices. The K-d values exhibited using natural water matrices consistently followed the order of DCP MCP TCP. This study provides insights into the fate of CPs in the presence of microplastics and suggests that the potential risks posed by CPs and microplastics to aqueous ecosystems merit further investigation. (C) 2020 Elsevier Ltd. All rights reserved.
机译:微塑料塑料受到水环境中有机污染物的载体的关注。为了更好地了解疏水性相互作用的贡献,氢键相互作用,PI-PI相互作用和静电相互作用对微塑料的亲水化合物的吸附及其在天然水域中的吸附行为,使用聚对苯二甲酸乙二醇酯(PET,<150mM)作为一种吸附剂和4-氯苯酚(MCP),2,4-二氯苯酚(DCP)和2,4,6-三氯苯酚(TCP)用作吸附物。批量吸附实验的结果表明,氯酚(CPS)通过薄膜扩散和颗粒 - 颗粒扩散达到PET的吸附位点。 pH极大地影响了吸附能力。疏水性相互作用是未分化的CPS在PET上的主要吸附机制。氢键相互作用也是未加化的CPS和PET之间的吸附机理,并且随着氯含量的增加,氢键相互作用对吸附的贡献降低。同时,氯含量的增加有利于未加入的CPS和PET之间的疏水相互作用。然而,具有较低PK(α)值的较高氯含量CPS倾向于在中性pH条件下解离,并导致宠物较强的静电排斥。溶液离子强度和富含酸含量的增加对DCP和TCP的吸附性产生负面影响,但对MCP吸附没有显示出显着影响。同样,使用太湖水和渤海海水获得的吸附能量远低于DCP和TCP的实验水,而MCP的吸附系数(KD)保持在约10.6L / kg至11.4L / kg。在三种不同的解决方案矩阵中。使用天然水矩阵展出的K-D值一致地跟随DCP> MCP> TCP的顺序。本研究提供了在微薄的存在下进入CPS的命运的见解,并表明CPS和微塑料与水性生态系统所带来的潜在风险优异的研究。 (c)2020 elestvier有限公司保留所有权利。

著录项

  • 来源
    《Environmental Pollution》 |2020年第1期|114926.1-114926.10|共10页
  • 作者单位

    Southeast Univ Sch Civil Engn Dept Municipal Engn Nanjing 210096 Jiangsu Peoples R China;

    Southeast Univ Sch Civil Engn Dept Municipal Engn Nanjing 210096 Jiangsu Peoples R China;

    Southeast Univ Sch Civil Engn Dept Municipal Engn Nanjing 210096 Jiangsu Peoples R China;

    Southeast Univ Sch Civil Engn Dept Municipal Engn Nanjing 210096 Jiangsu Peoples R China;

    Southeast Univ Sch Civil Engn Dept Municipal Engn Nanjing 210096 Jiangsu Peoples R China;

    Southeast Univ Sch Civil Engn Dept Municipal Engn Nanjing 210096 Jiangsu Peoples R China;

  • 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
  • 关键词

    Microplastics; Adsorption; Chlorophenols; Diffusion; NOM;

    机译:微塑料;吸附;氯酚物;扩散;NOM;

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