Liu Peng, Li Huang, Wu Jiajun, Wu Xiaowei, Shi Yanqi, Yang Zeyuan, Huang Kerang, Guo Xuetao, Gao Shixiang
Key Laboratory of Plant Nutrition and the Agri-environment in Northwest China, Ministry of Agriculture, College of Natural Resources and Environment, Northwest A & F University, Yangling, 712100, China.
State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University, Nanjing, 210093, China.
Water Res. 2022 May 1;214:118209. doi: 10.1016/j.watres.2022.118209. Epub 2022 Feb 17.
Combined pollution consisted of various types of microplastics (MPs) was extensively detected in the environment; however, little is known about their interaction on degradation behavior during exposure in sunlight. This study investigated the effects of polystyrene (PS) MPs and mechanisms on photodegradation of pure and commercial polypropylene (PP) MPs co-existed in aquatic environment. Results showed that PS MPs significantly accelerated photodegradation of co-existed PP, including faster oxidation and fragmentation. Photodegradation route of PP MPs such as the reaction priority of partial chemical bindings was even altered with the presence of PS MPs, highlighting the important role of PS in photodegradation process of PP. Analysis of leachate and free radical indicated that the critical effects were derived from photosensitization of PS polymer itself and its released dissolved organic matter (PS-DOM); here, more important role of PS itself in initial period and that of PS-DOM in later period. Among generated ROS, OH was the key species for accelerating photodegradation of PP by PS itself and its released DOM, which were generated from the reaction of polymer radical with dissolved oxygen. The findings firstly reveal the important role of PS in photodegradation of co-existed MPs and suggested the shorter duration of (micro)plastics in combined system than that in the single, which provide useful information to assess environmental behavior and fate of MPs more holistically.
环境中广泛检测到由各种类型微塑料(MPs)构成的复合污染;然而,对于它们在阳光照射下对降解行为的相互作用却知之甚少。本研究调查了聚苯乙烯(PS)微塑料在水生环境中与共存的纯聚丙烯(PP)微塑料及商业聚丙烯微塑料光降解的影响及机制。结果表明,PS微塑料显著加速了共存PP的光降解,包括更快的氧化和碎片化。PP微塑料的光降解途径,如部分化学键的反应优先级,甚至因PS微塑料的存在而改变,突出了PS在PP光降解过程中的重要作用。渗滤液和自由基分析表明,关键影响源自PS聚合物本身及其释放的溶解有机物(PS-DOM)的光敏化作用;在此,PS本身在初期起更重要作用,而PS-DOM在后期起更重要作用。在产生的活性氧物种中,OH是PS本身及其释放的DOM加速PP光降解的关键物种,它们是由聚合物自由基与溶解氧反应产生的。这些发现首次揭示了PS在共存微塑料光降解中的重要作用,并表明复合体系中(微)塑料的持续时间比单一体系中更短,这为更全面地评估微塑料的环境行为和归宿提供了有用信息。