Related Experiment Video
Updated: Aug 6, 2026

Removal of Arsenic Using a Cationic Polymer Gel Impregnated with Iron Hydroxide
Published on: June 28, 2019
Fabrication of a tripolyphosphate-modified chitosan-sodium alginate composite for highly efficient uranium adsorption
Xingyu Zhong1, Fang Yang1, Lihong Lu1
1School of Chemistry and Molecular Engineering, East China University of Science and Technology, Shanghai, 200237, PR China.
Abstract:
The preparation of composite materials with excellent adsorption capacity for uranium in water remains a topic of great interest. In this work, a novel composite adsorbent, tripolyphosphate-modified chitosan-sodium alginate (PCSSA), was successfully prepared by incorporating sodium alginate into tripolyphosphate-modified chitosan via chemical cross-linking. The resulting material exhibited excellent adsorption capacity for U(VI) in aqueous solutions. Within the chitosan matrix, amino, alkyl, and phosphate groups act synergistically to form amino-alkyl phosphate ligands (NH2-CH2-PO43-) with chelating functionality, providing abundant adsorption sites for efficient U(VI) removal. SEM and EDS characterization revealed a rugged, plate-like surface morphology, loaded with functional groups such as phosphate and carboxyl/hydroxyl groups. Systematic adsorption experiments indicated that the U(VI) adsorption behavior of PCSSA follows the Langmuir isotherm and the Elovich kinetic model. Under optimal conditions (pH = 3, 298.15 K, adsorbent dose = 30 mg), the maximum adsorption capacity reached 561.86 mg·g-1. In real water samples with a low U(VI) concentration (30 mg·L-1), the removal efficiency was as high as 88%, outperforming many similar bio-based adsorbents. FTIR and XPS analyses suggested that the phosphate groups interact with UO22+ through multiple mechanisms, including electrostatic attraction, ligand exchange, and complexation. The PCSSA composite is environmentally friendly and straightforward to prepare, showing promising potential for application in water pollution control.
