Sorption of benzo(a)pyrene and of a complex mixture of petrogenic polycyclic aromatic hydrocarbons onto polystyrene microplastics

Ignacio Martínez-Álvarez, K. Le Ménach, M. Devier, M. Cajaraville, A. Orbea, H. Budzinski
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引用次数: 2

Abstract

Microplastics (MPs) largely occur in aquatic ecosystems due to degradation of larger plastics or release from MP-containing products. Due to the hydrophobic nature and large specific surface of MPs, other contaminants, such as polycyclic aromatic hydrocarbons (PAHs), can potentially sorb onto MPs. Several studies have addressed the potential impact of MPs as vectors of PAHs for aquatic organisms. Therefore the role of MPs as sorbents of these compounds should be carefully investigated. The present study aimed to determine the sorption capacity of benzo(a)pyrene (B(a)P), as a model pyrolytic PAH, to polystyrene (PS) MPs of different sizes (4.5 and 0.5 μm). In addition, the sorption of PAHs present in the water accommodated fraction (WAF) of a naphthenic North Sea crude oil to 4.5 μm MPs was also studied as a model of a complex mixture of petrogenic PAHs that could appear in oil-polluted environments. The results indicated that 0.5 μm MPs showed higher maximum sorption capacity (Qmax) for B(a)P (145–242.89 μg/g) than 4.5 μm MPs (30.50–67.65 μg/g). From the WAF mixture, naphthalene was sorbed at a higher extent than the other PAHs to 4.5 μm MPs but with weak binding interactions (Kf = 69.25 L/g; 1/n = 0.46) according to the analysis of the aqueous phase, whereas phenanthrene showed stronger binding interactions (Kf = 0.24 L/g; 1/n = 0.98) based on the analysis of the solid phase. Sorption of PAHs of the complex WAF mixture to 4.5 μm MPs was relatively limited and driven by the hydrophobicity and initial concentration of each PAH. Overall, the results indicate that sorption estimations based solely on the analysis of the aqueous phase could overestimate the capacity of MPs to carry PAHs. Therefore, controlled laboratory assays assessing the “Trojan Horse effect” of MPs for aquatic organisms should consider these findings in order to design accurate and relevant experimental procedures. GRAPHICAL ABSTRACT
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苯并(a)芘和含岩多环芳烃的复杂混合物在聚苯乙烯微塑料上的吸附
由于较大塑料的降解或含MP产品的释放,微塑料(MP)主要出现在水生生态系统中。由于MPs的疏水性和大的比表面积,其他污染物,如多环芳烃(PAHs),可能会吸附在MPs上。一些研究已经解决了MP作为多环芳烃载体对水生生物的潜在影响。因此,应仔细研究MPs作为这些化合物吸附剂的作用。本研究旨在测定苯并(a)芘(B(a)P)作为热解PAH的模型,对不同尺寸(4.5和0.5μm)的聚苯乙烯(PS)MPs的吸附能力。此外,还研究了北海环烷原油的水容馏分(WAF)中存在的PAHs在4.5μm MPs中的吸附,作为可能出现在石油污染环境中的成因PAHs的复杂混合物的模型。结果表明,0.5μm的MPs对B(a)P(145–242.89μg/g)的最大吸附容量(Qmax)高于4.5μm的MP(30.50–67.65μg/g)。从WAF混合物中,萘比其他PAHs以更高的程度吸附到4.5μm MPs,但根据水相分析,萘具有较弱的结合相互作用(Kf=69.25 L/g;1/n=0.46),而菲根据固相分析显示出较强的结合相互作用力(Kf=0.24 L/g;1/n=0.98)。复合WAF混合物对4.5μm MPs的PAHs吸附相对有限,并受每种PAHs的疏水性和初始浓度的驱动。总体而言,结果表明,仅基于水相分析的吸附估计可能高估了MPs携带PAHs的能力。因此,评估MPs对水生生物的“特洛伊木马效应”的受控实验室分析应考虑这些发现,以便设计准确和相关的实验程序。图形摘要
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