微塑料
化学
聚苯乙烯
环境化学
系统间交叉
聚乙烯
氧气
光化学
化学工程
氧化还原
化学转化
共轭体系
聚乳酸
聚对苯二甲酸乙二醇酯
活性氧
氧化磷酸化
羧化
密度泛函理论
高密度聚乙烯
臭氧
有机化学
聚合物
土壤水分
生物降解
非生物石油成因
化学反应
土壤化学
领域(数学)
部分氧化
低密度聚乙烯
作者
Jianyong Wu,Wenhao Yang,Kongyan Luo,Jingcheng Wu,Jie Zeng,Jinsong Guo,Wei Yunmei,Junmin Gao,Jianyong Wu,Wenhao Yang,Kongyan Luo,Jingcheng Wu,Jie Zeng,Jinsong Guo,Wei Yunmei,Junmin Gao
标识
DOI:10.1021/acs.est.5c07624
摘要
Freeze-thaw cycles (FTCs) are a pervasive geochemical force in cold regions, yet their mechanistic role in driving the oxidation of microplastics (MPs) in soil remains unclear. Here, we integrated a 122-day field study, laboratory experiments, and theoretical calculations to elucidate FTC-induced chemical oxidation of MPs in soil. Field observations revealed that only MP-containing conjugated aromatic structures, such as polylactic acid-polybutylene adipate-co-terephthalate (PPAT), polyethylene terephthalate (PET), and polystyrene (PS), underwent oxidative aging during freezing. Using PS MPs as a model, laboratory analyses demonstrated that this selective oxidation was driven by the generation of 1O2 and H2O2 during the initial freezing phase, which progressively altered soil properties over repeated FTCs. In contrast, no 1O2 was detected in soil systems containing MPs lacking aromatic structures (e.g., polyethylene or polyamide). This structural dependence is consistent with density functional theory calculations, which showed that PS possesses a lower excitation threshold and more efficient intersystem crossing than nonaromatic MPs. Notably, the complex reactive oxygen species transformation network within soil-PS systems under FTCs was systematically characterized here for the first time. These findings offer critical insights into freeze-thaw chemistry and open new avenues for decoding MP behavior and its ecological impacts in cold soil ecosystems.
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