吸附
材料科学
铜
共价键
超短脉冲
金属有机骨架
化学工程
离子
金属
无机化学
扩散
共价有机骨架
纳米技术
水溶液中的金属离子
水溶液
污染
动力学
选择性吸附
水准点(测量)
工作(物理)
配体(生物化学)
选择性
作者
Zifeng You,Ying Yue,Zhiyuan Zhang,Mao Yi,Junhua Wang,Yuhan Liu,Chen Li,Qiao Zhao,Baiyan Li
标识
DOI:10.1021/acsami.5c21794
摘要
Copper ion (Cu(II)) contamination poses a serious threat to water quality and public health due to its high toxicity and nonbiodegradability. Herein, we develop for the first time high-density salicylaldehyde-hydrazone covalent organic frameworks (COFs) for ultrafast and highly efficient Cu(II) removal. The resulting DhaTGCl-COF exhibits excellent adsorption performance, achieving a record-high adsorption kinetics (k2 = 160.58 mg·g–1·min–1) and one of the highest capacities of 569 mg·g–1 among all adsorbents reported to date. Notably, the material also demonstrates the lowest residual Cu(II) concentration (0.01 ppm) within 30 min. The outstanding performance is attributed to the uniform distribution of high-density, strong-affinity tridentate N,N,O-chelating moieties derived from salicylaldehyde-hydrazone within the well-aligned two-dimensional pore channels, which facilitate rapid diffusion and coordination of Cu(II) to the binding sites and ensure exceptional adsorption efficiency even for trace-level Cu(II). This work not only sets a new benchmark for Cu(II) adsorbents but also opens a promising avenue for the design of high-performance COFs for heavy metal ion removal.
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