ZrO2 nanoparticles confined in metal organic frameworks for highly effective adsorption of phosphate

Chemosphere. 2018 Nov:210:907-916. doi: 10.1016/j.chemosphere.2018.07.085. Epub 2018 Jul 18.

Abstract

Highly dispersed ZrO2 particles confined in the MIL-101 (denoted as MIL-101@Zr(DS)) with varied ZrO2 loading amounts were prepared by the double solvents method. For comparison, ZrO2 loaded MIL-101 samples were synthesized by the conventional impregnation method (denoted as MIL-101@Zr(I)) and the deposition method (denoted as MIL-101@Zr(D)). The characterization results indicated that for MIL-101@Zr(DS), ZrO2 particles were dominantly confined in MIL-101 with a much higher dispersion as compared with MIL-101@Zr(I) and MIL-101@Zr(D). The maximum phosphate adsorption capacity and ZrO2 content normalized phosphate adsorption capacity of the MIL-101@Zr(DS) were 21.28 mg P·g-1 and 1120.0 mg P·g-1, respectively. Additionally, the ZrO2 content normalized phosphate adsorption capacity was significantly larger than that for MIL-101@Zr(I) and MIL-101@Zr(D) as well as the reported values for other Zr-based adsorbents. The effects of solution chemistry on phosphate adsorption to MIL-101@Zr(DS), MIL-101@Zr(I) and MIL-101@Zr(D) were also examined. Compared with MIL-101@Zr(I) and MIL-101@Zr(D), the adsorption of phosphate on MIL-101@Zr(DS) was less affected by the coexistence of anions and dissolved humic acid. Increasing pH from 3 to 12 led to decreased phosphate adsorption capacity of MIL-101@Zr(DS) from 10.38 mg P·g-1 to 2.03 mg P·g-1. Accordingly, used MIL-101@Zr(DS) could be effectively regenerated under alkaline conditions and exhibited stable adsorption-desorption performance.

Keywords: Confinement; Double solvents method; Metal organic frameworks; Phosphate adsorption; ZrO(2).

MeSH terms

  • Adsorption
  • Metal-Organic Frameworks / chemistry*
  • Nanoparticles / chemistry*
  • Phosphates / chemistry*
  • Zirconium / chemistry*

Substances

  • Metal-Organic Frameworks
  • Phosphates
  • Zirconium
  • zirconium oxide