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Aggregation and stability of nanoscale plastics in aquatic environment

机译:纳米塑料在水环境中的聚集和稳定性

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The widespread use and release of plastics in nature have raised global concerns about their impact on public health and the environment. While much research has been conducted on macro- and micro-sized plastics, the fate of nanoscale plastics remains unexplored. In this study, the aggregation kinetics and stability of polyethylene and polystyrene nanoscale plastics were investigated over a wide range of aquatic chemistries (pH, salt types (NaCl, CaCl2, MgCl2), ionic strength) relevant to the natural environment. Results showed that salt types and ionic strength had significant effects on the stability of both polyethylene and polystyrene nanoscale plastics, while pH had none. Aggregation and stability of both polyethylene and polystyrene nanoscale plastics in the aquatic environment followed colloidal theory (DLVO theory and Schulze-Hardy rule), similar to other colloidal particles. The critical coagulation concentration (CCC) values of polyethylene nanoscale plastics were lower for CaCl2 (0.1 mM) compared to NaCl (80 mM) and MgCl2 (3 mM). Similarly, CCC values of polystyrene nanospheres were 10 mM for CaCl2, 800 mM for NaCl and 25 mM for MgCl2. It implies that CaCl2 destabilized both polyethylene and polystyrene nanoscale plastics more aggressively than NaCl and MgCl2. Moreover, polystyrene nano spheres are more stable in the aquatic environment than polyethylene nanoscale plastics. However, natural organic matter improved the stability of polyethylene nanoscale plastics in water primarily due to steric repulsion, increasing CCC values to 0.4 mM, 120 mM and 8 mM for CaCl2, NaCl and MgCl2 respectively. Stability studies with various water conditions demonstrated that polyethylene nanoscale plastics will be fairly stable in the natural surface waters. Conversely, synthetic surface water, wastewater, seawater and groundwater rapidly destabilized polyethylene nanoscale plastics. Overall, our findings indicate that significant aqueous transport of nanoscale plastics will be possible in natural surface waters. (C) 2019 Elsevier Ltd. All rights reserved.
机译:自然界中塑料的广泛使用和释放引起了全球对其塑料对公共卫生和环境影响的关注。尽管已经对宏观和微观尺寸的塑料进行了大量研究,但纳米级塑料的命运仍待探索。在这项研究中,研究了聚乙烯和聚苯乙烯纳米级塑料在与自然环境有关的各种水生化学(pH,盐类(NaCl,CaCl2,MgCl2),离子强度)中的聚集动力学和稳定性。结果表明,盐类型和离子强度对聚乙烯和聚苯乙烯纳米级塑料的稳定性都有显着影响,而pH值则没有。聚乙烯和聚苯乙烯纳米级塑料在水生环境中的聚集和稳定性均遵循胶体理论(DLVO理论和Schulze-Hardy法则),类似于其他胶体颗粒。与NaCl(80 mM)和MgCl2(3 mM)相比,CaCl2(0.1 mM)的聚乙烯纳米级塑料的临界凝结浓度(CCC)值较低。同样,聚苯乙烯纳米球的CCC值对于CaCl2为10 mM,对于NaCl为800 mM,对于MgCl2为25 mM。这表明,CaCl2比NaCl和MgCl2更能破坏聚乙烯和聚苯乙烯纳米级塑料的稳定性。而且,聚苯乙烯纳米球在水生环境中比聚乙烯纳米级塑料更稳定。但是,天然有机物主要是由于空间排斥作用,提高了聚乙烯纳米级塑料在水中的稳定性,将CaCl2,NaCl和MgCl2的CCC值分别提高到0.4 mM,120 mM和8 mM。在各种水条件下的稳定性研究表明,聚乙烯纳米级塑料在天然地表水中将相当稳定。相反,合成地表水,废水,海水和地下水使聚乙烯纳米级塑料迅速失稳。总体而言,我们的发现表明,在天然地表水中,纳米塑料的大量水传输将成为可能。 (C)2019 Elsevier Ltd.保留所有权利。

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