微塑料
吸附
聚苯乙烯
水溶液
聚对苯二甲酸乙二醇酯
朗缪尔吸附模型
单层
化学工程
碳化
傅里叶变换红外光谱
材料科学
朗缪尔
废水
化学
惰性
炭黑
活性炭
X射线光电子能谱
低密度聚乙烯
环境污染
气凝胶
纳米复合材料
碳纤维
双酚A
作者
Ge Bai,Chen Wang,Baolin Wang,Peerapong Promcharoen,Peerapong Chumkaeo,Ekasith Somsook
标识
DOI:10.1021/acssuschemeng.5c02073
摘要
This study transformed polyethylene terephthalate (PET) waste into activated carbon (PET-C) by means of direct carbonization and subsequent KOH activation, without inert gases. PET-C was characterized and evaluated for microplastic (MP) removal, specifically targeting polystyrene (PS). Adsorption experiments revealed a maximal adsorption capacity of 139.57 mg·g–1 (0.5 g/L, 12 h, 298 K), and monolayer chemical adsorption was indicated by the Langmuir isotherm and pseudo-second-order kinetics fitting. The process occurred spontaneously and exothermically with robust pH stability. Removal mechanisms included π–π interactions, hydrogen bonding, hydrophobic interactions, and electrostatic interactions supported by Fourier transform infrared spectroscopy (FTIR), X-Ray photoelectron spectroscopy (XPS), and density functional theory (DFT) calculations. PET-C demonstrated high efficiency in diverse water matrices with minimal anion interference and >80% removal efficiency retention after five cycles. This work offered a sustainable strategy for transforming PET waste into a high-performance adsorbent, addressing plastic waste management and microplastic pollution for environmental remediation and wastewater treatment.
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