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J Hazard Mater. 2013 Dec 15;263 Pt 2:600-9. doi: 10.1016/j.jhazmat.2013.10.022. Epub 2013 Oct 18.

Could microwave induced catalytic oxidation (MICO) process over CoFe2O4 effectively eliminate brilliant green in aqueous solution?

Author information

1
South China Institute of Environmental Science, Ministry of Environmental Protection (MEP), Guangzhou 510655, PR China. Electronic address: juyongming@scies.org.

Abstract

In this study, we adopted the chemical co-precipitation (CP) method and sol-gel method followed by calcination at temperatures of 100-900°C for 12h to synthesize CoFe2O4 materials, which were further characterized by TEM, XRD and XPS techniques. The properties of CoFe2O4 materials were evaluated in a microwave (MW) induced catalytic oxidation (MICO) process for the elimination of brilliant green (BG). The results showed that: (1) the removal rates of BG gradually decreased over a series of CoFe2O4 materials prepared by CP method and calcinated with 100-700°C (except 900°C) for 12h within three reuse cycles; for comparison, no removal of BG was obtained over CoFe2O4 synthesized by sol-gel method and CoFe2O4-900 (CP); (2) no hydroxyl radicals were captured with salicylic acid used as molecular probe in the MICO process; (3) MW irradiation enhanced the release of residual NaOH within the microstructure of CoFe2O4 and further discolored BG, because BG is sensitive to pH; (4) granular activated carbon (GAC), an excellent MW-absorbing material possessing higher dielectric loss tangent compared to that of a series of CoFe2O4 materials, could not remove BG in suspensions at a higher efficiency, even if the loading amount was 20 g L(-1). Accordingly, MICO process over CoFe2O4 materials and GAC could not effectively eliminate BG in suspensions.

KEYWORDS:

Brilliant green; CoFe(2)O(4); Dielectric loss tangent; Microwave induced catalytic oxidation (MICO); Wastewater treatment

PMID:
24220199
DOI:
10.1016/j.jhazmat.2013.10.022
[Indexed for MEDLINE]
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