Removal of polystyrene nanoplastics from water by Cu Ni carbon material: The role of adsorption

吸附 吸热过程 聚苯乙烯 傅里叶变换红外光谱 化学工程 化学 扫描电子显微镜 材料科学 复合材料 有机化学 聚合物 工程类
作者
Guanyu Zhou,Xue Huang,Hao Xu,Qingguo Wang,Meijing Wang,Yunqi Wang,Qiansong Li,Yujian Zhang,Qian Ye,Jing Zhang
出处
期刊:Science of The Total Environment [Elsevier BV]
卷期号:820: 153190-153190 被引量:135
标识
DOI:10.1016/j.scitotenv.2022.153190
摘要

Nanoplastics have attracted wide attention worldwide as a new potentially threatening pollutant, and they can cause harm to the organisms and pose threat to the water environment. Therefore, efficient removal techniques for nanoplastics are urgently needed. In this study, CuNi carbon material (CuNi@C) was prepared by hydrothermal method for the removal of polystyrene (PS) nanoplastics from water. CuNi@C was effectively adsorbed on PS nanoplastics. When the CuNi@C dosage increased from 0.1 g/L to 0.3 g/L, the removal efficiency of PS nanoplastics (10 mg/L) elevated from 32.72% to 99.18%. The images of the scanning electron microscope (SEM) and the Fourier transform infrared spectroscopy (FTIR) spectra of CuNi@C confirmed the adsorption of PS nanoplastics on the CuNi@C. The fitting results of adsorption kinetic models and isotherms equations demonstrated that physical adsorption and monolayer coverage were the predominant mechanisms of the PS nanoplastics adsorption on CuNi@C. Thermodynamics analysis illustrated the adsorption of PS nanoplastics on CuNi@C was a spontaneous and endothermic process. The electrostatic attraction occurred in adsorption progress, and the removal efficiency of PS nanoplastics in the acidic system was generally higher than that in the alkaline system. CuNi@C can be recycled via washing and drying treatment and these CuNi@C comparable PS nanoplastics removal performance to the original ones. After four times cycles, CuNi@C can still remove ~75% of total PS nanoplastics from water. This study reveals that CuNi@C can be used as promising techniques for the removal of PS nanoplastics from the aqueous environment.
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