Carbon Dot Integrated Cellulose-Based Green-Fluorescent Aerogel for Detection and Removal of Copper Ions in Water

气凝胶 荧光 纤维素 碳纤维 离子 材料科学 纳米技术 化学工程 化学 有机化学 冶金 复合材料 光学 物理 工程类 复合数
作者
Guanyan Fu,Chenzhan Peng,Jian Yu,Jiafeng Cao,Shilin Peng,Tian Zhao,Dong Xu
出处
期刊:Gels [Multidisciplinary Digital Publishing Institute]
卷期号:11 (8): 655-655 被引量:1
标识
DOI:10.3390/gels11080655
摘要

Industrial pollution caused by Cu(II) ions remains one of the most critical environmental challenges worldwide. A novel green-fluorescent aerogel has been successfully developed for simultaneous sensing and adsorption of Cu(II) through the cross-linking of carboxymethyl nanocellulose and carbon dots (C dots) using epichlorohydrin as a linker. The C dots were synthesized by heating glucose and aspartate mixed solutions at 150 °C. Under UV illumination, the aerogel exhibited intense homogeneous green fluorescence originating from the uniformly dispersed C dots, whose emission can be efficiently quenched by Cu(II) ions. By leveraging smartphone-based imaging, the concentration of Cu(II) was quantified within the range of 5-200 µg/L, with a detection limit of 3.7 µg/L. The adsorption isotherm of Cu(II) onto the aerogel strictly conformed to the Freundlich isotherm model (fitting coefficient R2 = 0.9992), indicating a hybrid adsorption mechanism involving both physical adsorption and chemical complexation. The maximum adsorption capacity reached 149.62 mg/g, a value surpassing many reported adsorbents. X-ray photoelectron spectroscopy and Fourier-transform infrared spectroscopy analyses confirmed that the interactions between the aerogel and Cu(II) involved chelation and redox reactions, mediated by functional groups such as hydroxyl, amino, and carboxyl moieties. The straightforward fabrication process of the aerogel, coupled with its low cost, abundant raw materials, facile synthesis, and superior Cu(II) removal efficiency, positions this bifunctional fluorescent material as a promising candidate for large-scale environmental remediation applications.
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