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Sorption of non-polar organic compounds by micro-sized plastic particles in aqueous solution

机译:微米级塑料颗粒在水溶液中吸附非极性有机化合物

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The presence of microscale polymer particles (i.e., microplastics) in the environment has become a major concern in recent years. Sorption of organic compounds by microplastics may affect the phase distribution within both sediments and aqueous phases. To investigate this process, isotherms were determined for the sorption of seven aliphatic and, aromatic organic probe sorbates by four polymers with different physico-chemical properties. Sorption increased in the order polyamide < polyethylene < polyvinylchloride < polystyrene. This order does not reflect the particle sizes of the investigated microplastics within the aqueous dispersions, indicating the influence of additional factors (e.g., pi-pi-interactions) on the sorption of aromatic compounds by polystyrene. Linear isotherms by polyethylene suggested that sorbate uptake was due to absorption into the bulk polymer. In contrast, non-linear isotherms for sorption by PS, PA, and PVC suggest a predominance of adsorption onto the polymer surface, which is supported by the best fit of these isotherms using the Polanyi-Manes model. A strong relationship between the sorption coefficients of the microplastics and the hydrophobicity of the sorbates suggests that hydrophobic interactions are of major importance. (C) 2016 Elsevier Ltd. All rights reserved.
机译:近年来,环境中微米级聚合物颗粒(即,微塑料)的存在已成为主要关注点。微塑料对有机化合物的吸附可能会影响沉积物和水相中的相分布。为了研究该过程,确定了四种具有不同物理化学性质的聚合物对七种脂肪族和芳香族有机探针吸附剂的吸附等温线。吸附性按聚酰胺<聚乙烯<聚氯乙烯<聚苯乙烯的顺序增加。该顺序没有反映出水性分散体中所研究的微塑料的粒径,表明了其他因素(例如,π-π-相互作用)对聚苯乙烯吸附芳族化合物的影响。聚乙烯的线性等温线表明,山梨酸酯的吸收是由于吸收到本体聚合物中。相反,用于PS,PA和PVC吸附的非线性等温线表明,在聚合物表面上的吸附占优势,这通过使用Polanyi-Manes模型的这些等温线的最佳拟合得到了支持。微塑料的吸附系数与被吸附物的疏水性之间的密切关系表明,疏水性相互作用至关重要。 (C)2016 Elsevier Ltd.保留所有权利。

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