微塑料
降级(电信)
光催化
聚乙烯
环境化学
动能
化学
光化学
化学工程
环境科学
催化作用
有机化学
物理
工程类
量子力学
电信
作者
Daniel Aragón,Carmen Barquín,Eugenio Bringas,Inmaculada Ortíz,Marı́a J. Rivero
标识
DOI:10.1016/j.cej.2025.166672
摘要
The accumulation of plastic debris in water bodies requires urgent remediation. Significant research efforts are being made for the effective capture of microplastics (MPs), but a technology to achieve the complete degradation is still a must. Photocatalysis of MPs mediated by the action of semiconductor materials under light irradiation deserves attention due to its advantageous environmental and energetic characteristics. Here, we aim to contribute to this field by a detailed experimental analysis of the photocatalytic degradation of polyethylene (PE) microspheres, selected as target MPs, with TiO 2 P25 as the photocatalyst. Dark and photolysis experiments do not achieve significant degradation yields. Additionally, under the experimental conditions and after 8 h of treatment the photocatalytic degradation is evidenced by: i) gravimetric analysis that resulted in a 34.0 ± 1.4 % of mass loss, ii) chemical transformation quantified through a 58.5 % increase in the carbonyl index, and iii) particle size reduction, from an initial size of 234 ± 12 μm to an average diameter of 185 ± 13 μm. Furthermore, changes in the dissolved organic carbon, detection of short-chain acids in solution and CO 2 in the gas phase, confirm the degradation of the initial MPs. It is noteworthy that the implementation of consecutive cycles contributes to increase the degradation yield, increasing the mass loss to 54 % after 5 cycles. Photocatalysis phytotoxicity analysis in different water matrices demonstrates that treated water is suitable for irrigation. This research represents a step forward in the analysis of the photocatalytic degradation of MPs in water. • Heterogeneous photocatalysis is able to degrade polyethylene microplastics (MPs). • Major photocatalytic degradation is obtained with a TiO 2 /MPs ratio of 1:1. • Successive photocatalytic cycles exhibit increased degradation performance. • Acetic and formic acids are observed after the treatment. • CO 2 in the gas phase evidences the photocatalytic degradation of MPs.
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