Photocatalytic degradation of methyl orange by polyoxometalates supported on yttrium-doped TiO2

Yajun Wang*, Kecheng Lu, Changgen Feng

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

76 Citations (Scopus)

Abstract

A series of novel photocatalysts, H3PW12O 40-Y-TiO2 nanocomposites with different H 3PW12O40 loading levels (10-40) were prepared by impregnation method. And the Y-TiO2 support, doped with yttrium, was synthesized via sol-gel technique. The prepared catalysts were characterized by Fourier transform infrared spectroscopy (FT-IR), powder X-ray diffraction (XRD), nitrogen adsorption-desorption analysis and scanning electron microscopy (SEM). The processes allowed obtaining Keggin structure and crystallized anatase with large BET surface area as well as uniform distribution. The effects of H3PW12O40 loadings, catalyst dose, initial pH and concentration of dye solution on the degradation kinetics of methyl orange under UV light (λ≥ 365 nm) were discussed. Kinetics studies showed that the photocatalytic degradation of methyl orange fitted the apparent first-order reaction. Methyl orange was totally degraded in 21 min under optimum conditions: 20 loading, 0.03 g dose and pH 1.0. The catalyst was stable and easily to be separated from reaction system for recovery.

Original languageEnglish
Pages (from-to)866-871
Number of pages6
JournalJournal of Rare Earths
Volume29
Issue number9
DOIs
Publication statusPublished - Sept 2011

Keywords

  • azo dyes
  • kinetics
  • photocatalytic degradation
  • polyoxometalates
  • rare earths
  • titanium dioxide

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