4.6 Article

A Series of Polymer-Supported Polyoxometalates as Heterogeneous Photocatalysts for Degradation of Organic Dye

Journal

MOLECULES
Volume 28, Issue 9, Pages -

Publisher

MDPI
DOI: 10.3390/molecules28093968

Keywords

polymer; polyoxometalate; photocatalyst; degradation; methyl red

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Photocatalytic degradation technology has been rapidly developing in the treatment of organic pollutants. In this study, a series of heterogeneous photocatalysts were prepared and characterized. The photocatalytic properties of the photocatalysts for the degradation of methyl red were investigated. The results showed high photodegradation ability of the photocatalysts and their potential as promising candidates for dye degradation.
Photocatalytic degradation technology has developed rapidly in the treatment of organic pollutants due to its high efficiency, mild reaction conditions and easy control. In this paper, a series of heterogeneous photocatalysts, BWZ-en-R (BWZ = [BW(11)Z(H2O)O-39](7-), Z = Zn, Cd, Mn, en = ethylenediamine, R = Merrifield resin), were prepared by using ethanediamine as a linker to immobilize Keggin-type transition elements substituting tungstoborates on Merrifield resin and characterized by Fourier transform infrared spectroscopy, X-ray powder diffraction, scanning electron microscopy and energy-dispersive X-ray spectroscopy. The photocatalytic properties of BWZ-en-R (Z = Zn, Cd, Mn) for the degradation of methyl red (MR) were investigated. The results show that the BWZ-en-R (Z = Zn, Cd, Mn) photocatalysts exhibited high photodegradation ability for MR under the irradiation of ultraviolet light, and were easily separated from the reaction media. The maximum degradation rate (%) of MR (40 mL, 25 mu M, pH = 2) reached 96.4% for the BWMn-en-R photocatalyst (40 mg) after being irradiated for 30 min, making this a promising photocatalyst candidate for dye degradation. Moreover, the influences of some factors, such as the Z-substituted elements in the BWZ, the BWZ-en-R dosage and the MR initial concentration, on the photocatalytic degradation rate of MR were also examined.

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