Efficiency and mechanisms of rhodamine B degradation in Fenton-like systems based on zero-valent iron

Abstract

Based on the Fe⁰/H₂O₂ heterogeneous Fenton system, the degradation of rhodamine B (RhB, an organic dye pollutant) was researched in this paper. The effects of initial pH value, concentration of H₂O₂, dosage of zero-valent iron (ZVI), and initial RhB concentration on RhB degradation by Fe⁰/H₂O₂ were studied. The results showed that when the initial pH = 4, dosage of ZVI was 9 mM, and concentrations of H₂O₂ and RhB were 8 mM and 0.1 mM, respectively, the color of RhB could be completely faded within 30 min, and the total organic carbon (TOC) removal percentage was about 63% after 120 min. The dissolved oxygen (DO) content and oxidation–reduction potential (ORP) were monitored during the reaction. Quenching experiments with methanol confirmed that the degradation of the dye was mainly due to oxidation by the ˙OH radical. Besides, the results from UV-Vis spectroscopy showed that the degradation of RhB was mainly due to the destruction of the conjugated oxygen hetero-anthracene in the RhB molecule. The solid-phase characterization of the ZVI samples after reaction confirmed that the original regular and slippery ZVI samples finally were corroded into rough and irregular lepidocrocite and magnetite. Two possible competitive reaction pathways for the degradation of RhB by Fe⁰/H₂O₂ were proposed by GC-MS analysis, which were attributed to the dissociation of ethyl radicals and the degradation of chromophore radicals.