Bika Panagiota, Ioannidis Nikolaos, Tsipas Polychronis, Papagiannis Stefanos, Gatou Maria-Anna, Pavlatou Evangelia A, Karydas Andreas Germanos, Stergiopoulos Thomas, Dallas Panagiotis
Institute of Nanoscience and Nanotechnology, NCSR Demokritos, 15341 Athens, Greece.
National Institute of Materials Physics, Atomistilor 405A, Magurele 077125, Romania.
ACS Omega. 2025 May 21;10(21):21755-21766. doi: 10.1021/acsomega.5c01393. eCollection 2025 Jun 3.
Commercial melamine sponges were modified with a functional covalent organic framework (COF), and they were evaluated as adsorbents of divalent copper cations from aqueous solutions. A phosphazene unit successfully covered the surface of the melamine sponge, and the organic framework was subsequently formed through the nucleophilic substitution with 4,4' bipyridine. The covalent organic framework functionalized on the melamine sponge can detect and effectively adsorb copper compounds in aqueous solutions. Its selectivity toward the adsorption of copper was demonstrated through the presence of different metal salts. Four competitive metal cations, i.e., copper, nickel, iron, and calcium, were selected to confirm the preferential binding of copper on the COF-functionalized sponge. The outcome was determined through the studies of X-Ray Fluorescence elemental analysis, X-Ray Photoelectron Spectroscopy (XPS), and Electron Paramagnetic Resonance experiments. XRF reported a copper sorption capacity of 293 μg cm, which is nearly nine times higher than the performance of the pristine sponge. Q-band EPR measurements demonstrated the presence of different coordination sites with different substituents for copper on the modified sponges, when the adsorption took place in an aqueous solution containing exclusively copper cations, while only one coordination, the favorable trigonal bipyramidal geometry, was obtained in the presence of additional metals.
商用三聚氰胺海绵用功能性共价有机框架(COF)进行了改性,并将其作为水溶液中二价铜阳离子的吸附剂进行了评估。磷腈单元成功覆盖了三聚氰胺海绵的表面,随后通过与4,4'-联吡啶的亲核取代反应形成了有机框架。三聚氰胺海绵上功能化的共价有机框架能够检测并有效吸附水溶液中的铜化合物。通过存在不同金属盐证明了其对铜吸附的选择性。选择了四种竞争性金属阳离子,即铜、镍、铁和钙,以确认铜在COF功能化海绵上的优先结合。通过X射线荧光元素分析、X射线光电子能谱(XPS)和电子顺磁共振实验研究确定了结果。XRF报告铜吸附容量为293μg/cm,几乎是原始海绵性能的九倍。Q波段EPR测量表明,当在仅含铜阳离子的水溶液中发生吸附时,改性海绵上存在不同取代基的铜的不同配位位点,而在存在其他金属的情况下,仅获得一种配位,即有利的三角双锥几何构型。