Investigation into the characteristics of electron beam-aged microplastics and adsorption behavior of dibutyl phthalate

邻苯二甲酸二丁酯 微塑料 吸附 弗伦德利希方程 环境化学 污染物 聚乙烯 化学 化学工程 有机化学 工程类
作者
K.S. Chen,Lei Chen,Haiyang Shao,Jiayuan Li,Hongyong Wang,Chengkai Mao,Gang Xu
出处
期刊:Chemosphere [Elsevier BV]
卷期号:360: 142342-142342 被引量:10
标识
DOI:10.1016/j.chemosphere.2024.142342
摘要

Microplastics are increasingly prevalent in the environment, and their ability to adsorb various organic additives, posing harm to organisms, has attracted growing attention. Currently, there are no effective methods to age microplastics, and there is limited discussion on the subsequent treatment of aged microplastics. This study focuses on micro polyethylene (PE) and employs electron beam technology for aging treatment, investigating the adsorption and leaching behavior between PE and dibutyl phthalate (DBP) before and after aging. Experimental results indicate that with increasing doses of electron beam irradiation, the surface microstructure of PE worsens, inducing the generation of oxygen-containing functional groups on the surface of polyethylene. Comparative evaluations between electron beam aging and existing methods show that electron beam technology surpasses existing aging methods, achieving a level of aging exceeding 0.7 within an extremely short period of one min at doses exceeding 350kGy. Adsorption experiments demonstrate that the adsorption between PE and DBP conforms to pseudo-second-order kinetics and the Freundlich model both before and after aging. The adsorption capacity of microplastics for DBP increases from 76.8 mg·g-1 to 167.0 mg·g-1 after treatment, exceeding that of conventional DBP adsorbents. Electron beam irradiation causes aging of microplastics mainly through the generation of ·OH, which lead to the formation of oxygen-containing functional groups on the microplastics' surface, thereby enhancing their adsorption capacity for DBP. This provides a new perspective for the degradation of aged microplastics and composite pollutants.
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