4.7 Article

Synthesis of phosphorylated hyper-cross-linked polymers and their efficient uranium adsorption in water

Journal

JOURNAL OF HAZARDOUS MATERIALS
Volume 419, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.jhazmat.2021.126538

Keywords

Adsorption; Hyper-cross-linked polymers; Phosphorylation; Uranium; Waste water

Funding

  1. Decommissioning of Nuclear Facilities and Special Funds for Radioactive Waste Management [[2017]955]
  2. Natural Science Foundation of Heilongjiang Province, China [B2018003]
  3. Fundamental Research Funds for the Central Universities [3072021CFT1004]
  4. Foundation of Heilongjiang Postdoctoral Science Foundation [LBHZ17050]

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Two novel uranium adsorbents, PHCP-1 and PHCP-2, were synthesized and showed outstanding adsorption performance for uranium, attributed to the complex between phosphate functional groups and U(VI). The high specific surface area and strong complex between phosphate groups and U(VI) contributed to the sorption performance of PHCPs in effective uranium adsorption from water.
Uranium (U) is hazardous and radioactive, wastewater containing U(VI) should be treated before being discharged. Here, two novel uranium adsorbents, phosphorylated hyper-cross-linked bisphenol A (PHCP-1) and fluorene-9-bisphenol (PHCP-2) were separately synthesized via Friedel-Crafts reaction followed by phosphorylation using phosphorus oxychloride. PHCPs had a BET surface area (up to 564 m(2)/g) with pore sizes of 2.2-2.8 nm. These adsorbents were used for the first time for uranium adsorption from water and demonstrated outstanding adsorption performance. PHCP-2 had a great uranium adsorption capacity (297.14 mg/g) and a very fast sorption rate (85% removal rate within 5 min). The adsorption data were well fitted with Freundlich isotherm and the pseudo-second-order kinetic model. PHCPs displayed selective adsorption capacity for U(VI) from solution that including a variety of competing metal ions. The reusability was confirmed through three regeneration cycles. Based on a series of spectroscopic analyses, the mechanism of action between PHCPs and U (VI) is primarily derived from the complex between phosphate functional groups and U (VI). The sorption performance of PHCPs is attributed to their huge specific surface area and the strong complex between phosphate groups and U(VI). These findings suggest that PHCPs could be useful in the effective adsorption of uranium from water.

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