Yang Yicheng, Qiu Junjie, Zhang Hua, He Pinjing, Lü Fan
Institute of Waste Treatment & Reclamation, College of Environmental Science and Engineering, Tongji University, Shanghai, 200092, China.
Shanghai Institute of Pollution Control and Ecological Security, Shanghai, 200092, China.
Environ Sci Ecotechnol. 2025 Jun 24;26:100590. doi: 10.1016/j.ese.2025.100590. eCollection 2025 Jul.
Approximately half of plastic waste ends up in landfills, where fragmentation leads to the leakage of microplastics, nanoplastics, and petrogenic carbon back into ecosystems. However, the timeframe for plastic re-entry into the geological carbon cycle remains unknown. Using landfill-derived field data, we developed a model predicting fragmentation of various polymers into macroplastics, microplastics, fine microplastics, and nanoplastics. We find total waste plastic concentrations range from 85 to 414 mg g, with microplastic, fine microplastic, and nanoplastic generation rates of 2-69, 0.5-36.8, and 0.04-1.9 mg per g of plastic, respectively. Plastic distribution depends more on landfill depth than disposal age. Polyethylene terephthalate fragments faster than polypropylene or polyethylene. Our model predicts peak microplastic and fine microplastic fractions within 157-382 and 412-2118 years, respectively, with approximately half of the plastic-derived carbon available for geological cycling in 80-208 years. This research helps clarify the environmental fate of pervasive plastic pollution.
大约一半的塑料垃圾最终进入垃圾填埋场,在那里塑料破碎会导致微塑料、纳米塑料和石油源碳泄漏回生态系统。然而,塑料重新进入地质碳循环的时间框架仍不清楚。利用来自垃圾填埋场的实地数据,我们开发了一个模型,预测各种聚合物破碎成大塑料、微塑料、细微塑料和纳米塑料的情况。我们发现总废弃塑料浓度范围为85至414毫克/克,微塑料、细微塑料和纳米塑料的生成速率分别为每克塑料2至69毫克、0.5至36.8毫克和0.04至1.9毫克。塑料分布更多地取决于垃圾填埋深度而非处置年限。聚对苯二甲酸乙二酯比聚丙烯或聚乙烯破碎得更快。我们的模型预测微塑料和细微塑料的峰值比例分别在157至382年和412至2118年出现,约一半的塑料源碳在80至208年内可用于地质循环。这项研究有助于阐明普遍存在的塑料污染的环境归宿。