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老化对可生物降解和石油基微塑料中二-(2-乙基己基)邻苯二甲酸酯向土壤中释放的影响。

Effect of aging on the release of di-(2-ethylhexyl) phthalate from biodegradable and petroleum-based microplastics into soil.

机构信息

School of Environmental and Chemical Engineering, Shanghai University, Shanghai 200444, China.

School of Environmental and Chemical Engineering, Shanghai University, Shanghai 200444, China.

出版信息

Ecotoxicol Environ Saf. 2024 Mar 1;272:116006. doi: 10.1016/j.ecoenv.2024.116006. Epub 2024 Jan 31.

Abstract

Due to microplastics (MPs) being widely distributed in soil, the use of advanced oxidation to remediate organic-contaminated soils may accelerate the aging of MPs in soil and impact the release of di-(2-ethylhexyl) phthalate (DEHP), a potential carcinogen used as a plasticizer in plastics, from MPs. In this study, persulfate oxidation (PO) and temperature treatment (TT) were used to treat biodegradable and petroleum-based MPs, including polylactic acid (PLA), polyvinyl chloride (PVC), and polystyrene (PS). The methods used for evaluating the characteristics changes of MP were X-ray diffraction (XRD) analysis and water contact angle measurement. The effects of aging on DEHP release from MPs were investigated via soil incubation. The results showed PO and TT led to increased surface roughness, oxygen-containing functional group content, and hydrophilicity of the MPs with prolonged aging, consequently accelerating the release of DEHP from the MPs. Interestingly, PLA aged faster than PVC and PS under similar conditions. After 30 days of PO treatment, DEHP release from PLA into the soil increased 0.789-fold, exceeding the increase from PVC (0.454-fold) and PS (0.287-fold). This suggests that aged PLA poses a higher ecological risk than aged PVC or PS. Furthermore, PO treatment resulted in the oxidation and degradation of DEHP on the MP surface. After 30 days of PO treatment, the DEHP content in PLA, PVC, and PS decreased by 19.1%, 25.8%, and 23.5%, respectively. Specifying the types of MPs studied and the environmental conditions would provide a more precise context for the results. These findings provide novel insights into the fate of biodegradable and petroleum-based MPs and the potential ecotoxicity arising from advanced oxidation remediation in contaminated soils.

摘要

由于微塑料(MPs)广泛分布于土壤中,因此使用高级氧化法修复有机污染土壤可能会加速 MPs 在土壤中的老化,并影响作为增塑剂用于塑料的邻苯二甲酸二(2-乙基己基)酯(DEHP)从 MPs 中的释放。在这项研究中,过硫酸盐氧化(PO)和热处理(TT)被用于处理可生物降解和石油基 MPs,包括聚乳酸(PLA)、聚氯乙烯(PVC)和聚苯乙烯(PS)。用于评估 MPs 特征变化的方法是 X 射线衍射(XRD)分析和水接触角测量。通过土壤培养研究了老化对 MPs 中 DEHP 释放的影响。结果表明,随着老化时间的延长,PO 和 TT 导致 MPs 的表面粗糙度、含氧官能团含量和亲水性增加,从而加速了 MPs 中 DEHP 的释放。有趣的是,在相似条件下 PLA 的老化速度快于 PVC 和 PS。经过 30 天的 PO 处理,PLA 向土壤中释放的 DEHP 增加了 0.789 倍,超过了 PVC(0.454 倍)和 PS(0.287 倍)的增加量。这表明老化的 PLA 比老化的 PVC 或 PS 具有更高的生态风险。此外,PO 处理导致 MPs 表面 DEHP 的氧化和降解。经过 30 天的 PO 处理,PLA、PVC 和 PS 中 DEHP 的含量分别减少了 19.1%、25.8%和 23.5%。具体说明所研究的 MPs 类型和环境条件将为结果提供更精确的背景。这些发现为可生物降解和石油基 MPs 的命运以及污染土壤中高级氧化修复引起的潜在生态毒性提供了新的见解。

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