Characteristics and mechanisms of dissolved organic matter leached by photodegradation of polyethylene microplastics: role of adsorbed antibiotics

微塑料 化学 光降解 聚乙烯 吸附 溶解有机碳 环境化学 X射线光电子能谱 分馏 光化学 有机质 红外光谱学 腐植酸 紫外线 激进的 光敏剂 核化学 傅里叶变换红外光谱 紫外可见光谱 聚合物 浸出(土壤学) 光谱学 降级(电信) 水处理 无机化学 水消毒 氧气
作者
Yanan Chen,Yunkun Qian,Fan Liu
出处
期刊:Environmental Science: Processes & Impacts [Royal Society of Chemistry]
卷期号:28 (2): 624-634
标识
DOI:10.1039/d5em00805k
摘要

The photoaging of polyethylene microplastics (PE MPs) and their interactions with co-contaminants such as ofloxacin (OFL) play a critical role in shaping the composition and characteristics of dissolved organic matter (DOM) in aquatic environments. This study systematically investigates the characteristics and leaching mechanisms of DOM from pristine PE and PE-adsorbed OFL (PE-OFL) under prolonged ultraviolet irradiation. Molecular weight (MW) fractionation revealed that UV exposure significantly enhanced DOM release from pristine PE, with low-MW fractions (<1k Da) dominating (75.6-98.3% of total DOM). In contrast, PE-OFL initially released high-MW compounds (44.9-51.8% > 1k Da), which transitioned to low-MW dominance. Two-dimensional correlation spectroscopy of FTIR spectra indicated that photolytic degradation of pristine PE primarily involved -CH2 groups, while C-O groups were dominant in PE-OFL, reflecting OFL-induced alterations in photolytic pathways. Energy-dispersive X-ray spectroscopy and X-ray photoelectron spectroscopy demonstrated that OFL adsorption substantially increased surface oxidation, with a 2.4-fold elevation in O/C ratios and enhanced carboxylation (77.5% CO content vs. 32.8% in PE). These findings elucidate that OFL acts as both a photosensitizer and an electron shuttle, accelerating PE backbone scission via reactive oxygen species generation while temporarily stabilizing high-MW intermediates. Overall, the findings highlights that contaminant-laden MPs exhibit distinct DOM profiles compared to pristine MPs, emphasizing the necessity of considering co-pollutant interactions in environmental risk assessments.
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