4.7 Article

Benignly-fabricated supramolecular poly(amidoxime)-alginate-poly(acrylic acid) beads synergistically enhance uranyl capture from seawater

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 441, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2022.136076

Keywords

Amidoxime; Carboxyl; Supramolecular synergistic; Uranium Extraction; Seawater

Funding

  1. National Natural Science Foundation of China [21705149, 21777159]
  2. Dalian Sci-ence and Technology Bureau Innovation Fund [2020JJ26SN057]
  3. DICP [I202001]
  4. Natural Science Foundation of Liaoning Province [2019-MS-317]

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Designing amidoxime-based adsorbents in a cooperative and synergistic manner, with supramolecular ionic-crosslinking and hydrogen bonding interactions, results in the construction of novel bifunctional poly(amidoxime)-alginate-poly(acrylic acid) (PAO-APAA) composite beads. These beads demonstrate high adsorption capacity for uranium from aqueous solution, excellent selectivity in seawater, and good mechanical and chemical stability, highlighting the importance of efficient sorbent material design for enhanced uranyl capture.
Design of amidoxime-based adsorbents in a cooperative and synergistic manner together with a concept of facile and green fabrication is becoming highly desirable to harvest uranium from seawater. Herein, taking benefit of supramolecular ionic-crosslinking and hydrogen bonding interactions, we have reported a simple and environmentally benign approach to construct novel bifunctional poly(amidoxime)-alginate-poly(acrylic acid) (PAO-APAA) composite beads. As a result of synergistic uranyl binding, the PAO-A-PAA composite beads reached a high adsorption capacity of 735.1 mg g-1 for uranium aqueous solution (36 ppm), which is 2.24 and 1.46 times that of monofunctional Alg-PAA (328.1 mg g-1) and Alg-PAO (502.2 mg g-1), respectively. More importantly, the PAOA-PAA exhibits excellent selectivity towards U(VI) in the presence of natural organic matter and multiple coexisting metal ions in simulated seawater. The XPS analysis reveals the utilization and coordination of both amidoxime and carboxylate ligands of PAO-A-PAA for uranyl binding, which results in energetically more stable synergistic uranyl complexes (Ebinding = -9.45 to -10.34 eV) as proved by the density functional theory study. The adsorption efficiency of PAO-A-PAA is further supported by its ability to extract mu g L-1-level uranium in real seawater (94.7-99.5%). The PAO-A-PAA also demonstrates good mechanical and chemical stability over a wide pH range, as well as good reusability. These findings provide insight into the significance of designing efficient sorbent material for enhanced uranyl capture via a supramolecular strategy.

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