吸附
水溶液
介孔二氧化硅
化学
选择性
热重分析
单层
朗缪尔吸附模型
铀酰
化学工程
朗缪尔
选择性吸附
无机化学
介孔材料
核化学
红外光谱学
纳米颗粒
表面改性
比表面积
傅里叶变换红外光谱
材料科学
作者
Abdulmalik S. Alshammari,Eid M. Alosime,Ahmed Ali Basfar
出处
期刊:Molecules
[Multidisciplinary Digital Publishing Institute]
日期:2026-10-13
卷期号:31 (20): 3664-3664
标识
DOI:10.3390/molecules31203664
摘要
Uranium(VI) contamination in aquatic environments poses significant environmental and public health concerns, creating a need for efficient and selective adsorbents. In this study, polyphosphate-functionalized poly(glycidyl methacrylate)-grafted mesoporous silica nanoparticles (PP-PGMA/MSNs) were successfully synthesized and evaluated for U(VI) removal from aqueous solutions. A key novelty of this work lies in the incorporation of phosphate-rich functionalities onto PGMA-grafted MSNs prepared via ATRP, together with the systematic investigation of their effects on U(VI) adsorption equilibrium and selectivity in multi-metal systems. Fourier-transform infrared spectroscopy (FTIR), Brunauer–Emmett–Teller (BET), scanning electron microscopy (SEM) and thermogravimetric analysis (TGA) confirmed the successful incorporation of phosphate-containing functional groups onto the MSN surface. The adsorbent exhibited rapid adsorption, reaching equilibrium within 120 min, with optimum performance observed at pH 4–6. A maximum U(VI) removal efficiency of 73.81% was achieved at an initial concentration of 10 mg L−1, while the maximum adsorption capacity reached 114.94 mg g−1. Equilibrium data were well described by the Langmuir isotherm model (R2 = 0.9697), indicating predominantly monolayer adsorption on relatively homogeneous adsorption sites. Despite a substantial reduction in surface area following functionalization, the material maintained a high adsorption capacity, suggesting that uranium uptake is governed primarily by interactions at phosphate-containing active sites. Furthermore, the adsorbent exhibited preferential affinity toward U(VI) in multi-metal systems containing Cr, Ni, Cu, Zn, Cd, and Pb ions, demonstrating enhanced selectivity toward uranyl species. The adsorption behavior suggests that phosphate functionalities serve as the primary binding sites through surface complexation and coordination interactions. These findings demonstrate the potential of PP-PGMA/MSNs as selective adsorbents for U(VI) removal from complex aqueous systems and environmental remediation applications.
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