Polyphosphate-Functionalized PGMA-Grafted Mesoporous Silica Nanoparticles for Selective U(VI) Removal from Aqueous Solutions

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.

Authors

Institutions

Publication Details

Journal
Molecules
Published
2026-10-13
DOI
https://doi.org/10.3390/molecules31203664
Primary Topic
Radioactive element chemistry and processing
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Polyphosphate-Functionalized PGMA-Grafted Mesoporous Silica Nanoparticles for Selective U(VI) Removal from Aqueous Solutions

Eid M. Alosime, Ahmed Ali Basfar, Abdulmalik S. Alshammari
Molecules
Radioactive element chemistry and processing
article

Polyphosphate-Functionalized PGMA-Grafted Mesoporous Silica Nanoparticles for Selective U(VI) Removal from Aqueous Solutions

Eid M. Alosime, Ahmed Ali Basfar, Abdulmalik S. Alshammari
article en

Abstract

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.

MoleculesVol. 31(20)
King Abdulaziz City for Science and Technology (SA), King Saud University (SA)
King Saud University
Openalex Percentile: Top 28%
Radioactive element chemistry and processing
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.