Zhu Sidi, Xu Haihua, Khan M Shahnawaz, Xia Mingzhu, Wang Fengyun, Chen Yexiang
School of Chemistry and Chemical Engineering, Nanjing University of Science and Technology, Nanjing, 210094, PR China; Department of Chemical and Biomolecular Engineering, College of Design and Engineering, National University of Singapore, 4 Engineering Drive 4, Singapore 117585, Singapore.
School of Chemistry and Chemical Engineering, Nanjing University of Science and Technology, Nanjing, 210094, PR China.
Water Res. 2025 Mar 15;272:122997. doi: 10.1016/j.watres.2024.122997. Epub 2024 Dec 17.
While technological advancements in treating electroplating wastewater continue, removing high concentrations of Ni and Co remains a challenge. Surface functionalization of clay has emerged as a pivotal approach for effectively removing heavy metals, rivaling intercalation modification in its effectiveness. This study investigated the adsorption performance and mechanisms of a phosphonate-modified layered double hydroxide material, employing batch experiments and simulation calculations to elucidate the impact of surface modification on adsorption behavior. Briefly, various characterization techniques confirmed that the layered double hydroxide synthesized through co-precipitation exhibited a sheet-like morphology, with phosphonate groups anchoring onto the clay surface following functionalization. Under optimal conditions (pH=6.0, t = 60 min, and C=300 mg/L), the material demonstrated high uptake capacities for Ni (198.01 mg/g) and Co (180.18 mg/g), surpassing most previously reported adsorbents. The adsorption kinetics for Ni and Co on the modified material followed a pseudo-second-order model, and the isotherms conformed to the Langmuir equation, indicating a monolayer chemical adsorption process. Moreover, after five adsorption-desorption cycles, the adsorbent demonstrated exceptional reusability and stability, and its potential for practical application preliminarily assessed using electroplating wastewater containing Ni. To further clarify the adsorption mechanism, a molecular dynamics simulation employing the CLAYFF-CVFF force field was conducted to examine the electrostatic interaction of modifiers at the clay surface. Wavefunction analyses derived from quantum chemical calculations provided insights into interactions, identified molecular reactive sites, and elucidated orbital interactions within chelation complexes. This research presents a feasible approach for developing high-performance materials for wastewater remediation in practical applications.
随着电镀废水处理技术的不断进步,去除高浓度的镍和钴仍然是一项挑战。粘土的表面功能化已成为有效去除重金属的关键方法,其有效性可与插层改性相媲美。本研究通过批量实验和模拟计算,研究了膦酸盐改性层状双氢氧化物材料的吸附性能和机制,以阐明表面改性对吸附行为的影响。简而言之,各种表征技术证实,通过共沉淀合成的层状双氢氧化物呈现片状形态,功能化后膦酸基团锚定在粘土表面。在最佳条件下(pH = 6.0,t = 60分钟,C = 300毫克/升),该材料对镍(198.01毫克/克)和钴(180.18毫克/克)表现出高吸附容量,超过了大多数先前报道的吸附剂。镍和钴在改性材料上的吸附动力学遵循准二级模型,等温线符合朗缪尔方程,表明是单层化学吸附过程。此外,经过五次吸附-解吸循环后,吸附剂表现出优异的可重复使用性和稳定性,并使用含镍电镀废水初步评估了其实际应用潜力。为了进一步阐明吸附机制,采用CLAYFF-CVFF力场进行了分子动力学模拟,以研究改性剂在粘土表面的静电相互作用。量子化学计算得出的波函数分析提供了相互作用的见解,确定了分子反应位点,并阐明了螯合配合物中的轨道相互作用。本研究为在实际应用中开发用于废水修复的高性能材料提供了一种可行的方法。