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Modelling of the adsorption of chlorinated phenols on polyethylene and polyethylene terephthalate microplastic

机译:聚乙烯与聚对苯二甲酸乙二醇酯氯化酚对氯化酚的吸附建模

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The role of microplastics (MPs) on the fate and transport of various pollutants in water matrices is of major concern, but it is still relatively under investigated. In order to consider the conditions in real aquatic environments, the changes to polyethylene (PE) structure during the fabrication of microplastic particles for specific uses should not be neglected. Thus, this work considers isolated PE from two types of personal care products, which are possible sources of microplastic contamination in aquatic environments. The adsorption affinity of these PE microplastics towards ionisable compounds was compared with those of standards of PE and polyethylene terephthalate (PET), using chlorinated phenols (4-chlorophenol, 2,4-dichlorophenol, 2,4,6-trichlorophenol and pentachlorophenol) as adsorbates. The pseudo-second order kinetic model described well the sorption process for all chlorinated phenols on all four types of MPs (R2 range: 0.900–0.998). The kinetic study showed that sorption rates are mainly controlled by hydrophobic interactions and molecule size. Adsorption isotherms were best described by the Freundlich model for all MPs. The obtained results indicate that MPs could serve for the transport of chlorinated phenols through ambient waters.
机译:微塑料(MPS)对水矩阵中各种污染物的命运和运输的作用具有重要关注,但它仍然在调查中。为了考虑真实水生环境的条件,不应忽略在制备微压颗粒期间对微压颗粒的聚乙烯(PE)结构的变化不应忽略。因此,这项工作考虑了来自两种类型的个人护理产品的隔离体PE,这是水生环境中的微塑性污染源。将这些PE微塑料对离子化合物的吸附亲和力与使用氯化酚(4-氯蛋白,2,4-二氯苯酚,2,4,6-三氯苯酚和五氯苯酚)的PE和聚对苯二甲酸乙二醇酯(PET)的标准物进行比较。吸附物。伪二次阶动力学模型描述了所有四种MPS上所有氯化酚的吸附过程(R2范围:0.900-0.998)。动力学研究表明,吸附率主要由疏水相互作用和分子尺寸控制。所有MPS的Freundlich模型最好地描述吸附等温线。所获得的结果表明,MPS可以通过环境水分离用于氯化酚。

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