微塑料
石英晶体微天平
纳米技术
化学
纳米力学
单层
粘附
吸附
环境修复
环境友好型
分子间力
纳米尺度
原子力显微镜
地下水修复
聚苯乙烯
水溶液
纳米颗粒
涂层
化学工程
合理设计
生物污染
疏水效应
材料科学
分子动力学
环境化学
力谱学
自组装
帽状体
堆积
电动现象
作者
Lin Yang,Yuanyuan Wang,Yongxiang Sun,Xingyang Qiu,Pan Huang,Qiongyao Peng,Yifu Chu,Qi Zhou,Ziqian Zhao,Matthew S. Macauley,Lingyun Chen,Hongbo Zeng
标识
DOI:10.1021/acs.est.5c16655
摘要
Microplastic (MP) pollution poses escalating environmental and health risks, yet the molecular mechanisms governing the interactions between environmentally aged microplastics (MPs) and engineered surfaces remain largely unresolved, hindering the rational design of remediation materials. Herein, we quantitatively elucidate the interaction forces between aged polystyrene MPs (PSMPs) and self-assembled monolayer (SAM)-functionalized surfaces at the solid/water interface using colloidal probe atomic force microscopy (AFM), complemented by quartz crystal microbalance (QCM) analysis. The results reveal that adhesion forces are strongly influenced by aqueous salinity and pH, with π–π stacking and electrostatic/cation−π interactions likely contributing predominantly on phenyl- and amino-terminated surfaces, respectively. A robust correlation between nanoscale adhesion forces and macroscopic adsorption capabilities is established, enabling predictive understanding of aged MP–surface interactions. Guided by these mechanistic insights, a tannic acid-modified chitosan biomaterial integrating amino and phenyl functionalities is developed, achieving over 92.1% removal efficiency for aged PSMPs across diverse water chemistries at an environmentally relevant initial MP concentration of 1 mg L–1. This work provides an intermolecular force–driven design paradigm that bridges nanoscale intermolecular interaction mechanisms with macroscopic material performance, offering theoretical and practical guidance for next-generation remediation strategies targeting environmentally aged MPs.
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