College of Energy and Environment, Shenyang Aerospace University, No.37 Daoyi South Avenue, Shenbei New Area, Shenyang 110136, China.
College of Energy and Environment, Shenyang Aerospace University, No.37 Daoyi South Avenue, Shenbei New Area, Shenyang 110136, China.
Sci Total Environ. 2022 Dec 10;851(Pt 1):158174. doi: 10.1016/j.scitotenv.2022.158174. Epub 2022 Aug 19.
A novel adsorbent of carbon@chitosan@montmorillonite nanosheet (C@CS@ MTN) was successfully fabricated layer-by-layer assembly method to deal with cationic dye wastewater. Batch adsorption experiments showed that the adsorption capacities of MB and RhB were higher than 325 mg·g and 236 mg·g, respectively, indicating that C@CS@MTN exhibited an excellent adsorption performance. Through quantum chemistry simulations, the molecular electrostatic potential, electron density, differential charge density, molecular orbital distribution and adsorption binding energy were analyzed to reveal the adsorption reaction mechanism between C@CS@MTN and cationic dyes. The results indicated that SiO tetrahedron ring and AlO octahedron ring released from montmorillonite with inherent periodic structure was beneficial to electrostatic attraction, while cation-π interaction benefitted from the interaction between Al atoms of AlO octahedron ring and benzene ring. It was noteworthy that the electron transfer direction of electrostatic attraction was from O atoms of SiO tetrahedron ring to the benzene ring of dye molecules, but the electron transfer direction of cation-π interaction was from benzene ring of dye molecules to Al atoms of AlO octahedron ring. These results provide fundamental theoretical support for the functional design of mineral-based adsorbents and the efficient removal of cationic dyes.
一种新型的碳@壳聚糖@蒙脱石纳米片(C@CS@MTN)吸附剂通过层层组装方法成功制备,用于处理阳离子染料废水。批量吸附实验表明,C@CS@MTN 对 MB 和 RhB 的吸附容量分别高于 325 mg·g 和 236 mg·g,表明 C@CS@MTN 具有优异的吸附性能。通过量子化学模拟,分析了分子静电势、电子密度、差分电荷密度、分子轨道分布和吸附结合能,揭示了 C@CS@MTN 与阳离子染料之间的吸附反应机制。结果表明,蒙脱石中具有固有周期性结构的 SiO 四面体环和 AlO 八面体环的释放有利于静电吸引,而阳离子-π 相互作用则得益于 AlO 八面体环中的 Al 原子与苯环之间的相互作用。值得注意的是,静电吸引的电子转移方向是从 SiO 四面体环的 O 原子到染料分子的苯环,而阳离子-π 相互作用的电子转移方向是从染料分子的苯环到 AlO 八面体环的 Al 原子。这些结果为基于矿物的吸附剂的功能设计和阳离子染料的有效去除提供了基础理论支持。