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Efficient decolorization of azo organics by singlet oxygen from activating PMS with octahedral structured FMN-700 |
ZHONG Qing1, YE Xiao-zhen2, ZENG Jing2, CAI Lan-yan2, WANG Yong-quan2, HONG Jun-ming1 |
1. College of Chemical Engineering, Huaqiao University, Fujian Province Engineering Research Center of Industrial Wastewater Biochemical Treatment, Xiamen 361021, China; 2. Xiamen Tobacco Industrial Company Limited, Xiamen 361021, China |
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Abstract A catalytic material containing iron and manganese nitride (FMN-700) was prepared by high-temperature calcination using nitrogen-doped Prussian blue analogue (PBA) as a precursor for the rapid degradation of azo organic compounds by activated peroxymonosulfate (PMS). The catalysts were characterized by scanning electron microscopy (SEM), X-ray powder diffractometer (XRD) and Fourier transform infrared spectroscopy (FTIR), which demonstrated that FMN-700 has a layered stacked ortho-octahedral structure and contains Fe-Mn-nitride. The effects of catalyst dosage, PMS concentration and initial pH on the catalytic degradation of azo organics were investigated. The results showed that 99.5% decolorization of RBK5 at 10mg/L could be achieved within 60min at an initial pH of 7, a catalyst dosing of 0.2g/L and a PMS concentration of 2mmol/L. The quenching experiments and Electron Paramagnetic Resonance (EPR) indicated that 1O2 was the main active substance in the degradation system. X-ray photoelectron spectroscopy (XPS) showed that the Fe(III)/Fe(II) and Mn(III)/Mn(II) ratios increased and the pyridine N content decreased before and after the reaction. This process can induce the production of 1O2. The significant increase of fluorescence intensity of 3D-EEM spectrum showed that the azo bond with fluorescence quenching effect was broken during the degradation process and azo organic compounds were successfully decolorized and degraded.
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Received: 26 April 2023
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About author:: X703.1 |
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