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通过加速光氧化,从原生和含添加剂的聚丙烯中分离纳米和微塑料碎片。

Fragmentation of nano- and microplastics from virgin- and additive-containing polypropylene by accelerated photooxidation.

机构信息

Korea Institute of Ocean Science and Technology, Geoje-shi, 53201, South Korea.

Korea Institute of Ocean Science and Technology, Geoje-shi, 53201, South Korea; University of Science and Technology, Daejeon, 34113, South Korea.

出版信息

Environ Pollut. 2023 Jun 15;327:121590. doi: 10.1016/j.envpol.2023.121590. Epub 2023 Apr 6.

Abstract

Plastic is ubiquitous in the environment, where it gradually weathers and fragments into nanoplastics (NPs) and microplastics (MPs); however, the weathering process and fragmentation rate are poorly understood. In this study, we quantitatively determined the abundances and size distributions of NPs and MPs produced from virgin polypropylene (PP) and additive-containing PP (PPa) sheets via photooxidation with water in a simulated sunlight chamber followed by vortexing. The fragmentation rate of PP and PPa were approximately 1.1 × 10 particles/cm and 1.0 × 10 particles/cm, respectively, during 176 days of exposure in the chamber (corresponding to 2.7 years of exposure in an outdoor environment in the Republic of Korea). However, quadratic regression analysis of the relationship between total particles produced and exposure duration revealed that the PP fragmentation rate was faster than the PPa fragmentation rate after a sunlight exposure duration equivalent to 2.7 years. Furthermore, the mechanical stress of vortexing after photooxidation played an important role in the production of MPs; it had a smaller role in the production of NPs. The sizes of fragmented particles produced by photooxidation and mechanical stress followed a power law distribution, with a scaling exponent of α = 2.87 ± 0.15, which was similar to a three-dimensional fragmentation pattern. This study provides valuable insights into the weathering and fragmentation processes of plastics. Further studies on the environmental fate and impact of NP and MP production from plastic weathering and fragmentation, as well as the potential influence of plastic additives on these processes.

摘要

塑料在环境中无处不在,会逐渐风化并碎裂成纳米塑料(NPs)和微塑料(MPs);然而,其风化过程和碎裂速率还了解甚少。在这项研究中,我们通过模拟阳光室中的水光氧化作用定量测定了由原生聚丙烯(PP)和含添加剂的聚丙烯(PPa)薄片产生的 NPs 和 MPs 的丰度和粒径分布,然后通过涡旋混合。在室内暴露 176 天(相当于在韩国户外环境中暴露 2.7 年)期间,PP 和 PPa 的碎裂速率分别约为 1.1×10 个颗粒/cm 和 1.0×10 个颗粒/cm。然而,对总颗粒生成量与暴露时间的关系进行二次回归分析表明,在相当于 2.7 年的阳光暴露时间之后,PP 的碎裂速率快于 PPa 的碎裂速率。此外,光氧化后涡旋产生的机械应力在 MPs 的生成中起着重要作用;在 NPs 的生成中作用较小。光氧化和机械应力产生的碎裂颗粒的尺寸遵循幂律分布,标度指数 α=2.87±0.15,与三维碎裂模式相似。本研究为塑料的风化和碎裂过程提供了有价值的见解。进一步研究塑料风化和碎裂产生的 NP 和 MP 的环境归宿和影响,以及塑料添加剂对这些过程的潜在影响。

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