Abstract

Porous silicate supported micro-nano zero-valent iron (PSi@ZVI) was prepared from copper slag (CS) through carbothermal reduction technology, and used as a persulfate (PS) activator for removing organic contaminants. Results showed that the properties of the activator were greatly affected by the preparation conditions. Calcination for 20 min at 1100 °C with 20% anthracite was considered the optimum preparation condition for degradation of orange G (OG). The removal rate of OG was improved by increasing the dosages of PSi@ZVI or PS and raising the reaction temperature. Moreover, PSi@ZVI exhibited excellent PS activator ability in a wide range of initial pH, good degradation capability for eosin Y, methyl orange, acid fuchsine, and methylene blue. The reusability and safety of PSi@ZVI were verified. Electron paramagnetic resonance and radical quenching tests indicated that sulfate radical (SO4−) was the main active species in the PSi@ZVI/PS system. The X-ray diffraction results indicated that a high calcination temperature (1100 °C) was beneficial to the reduction of iron-bearing minerals to ZVI. Scanning electron microscopy and energy-dispersive spectroscopy results revealed that the formation of porous structure of PSi@ZVI and the generation of nano to micro-sized ZVI particles on the surface of the silicate holes. The X-ray photoelectron spectra showed that ZVI was first convert into Fe(II), which mainly activated PS and generated Fe(III) in the PSi@ZVI/PS system. Furthermore, the intermediates of OG were detected using gas chromatography–mass spectrometry, and the possible degradation pathway of OG was proposed. This study provides a novel approach for reuse of CS as a heterogeneous activator to effectively activate PS.

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