Activation of peroxymonosulfate by Co-Mg-Fe layered doubled hydroxide for efficient degradation of Rhodamine B

Reactive species serve as a key to remediate the contamination of refractory organic contaminants in advanced oxidation processes. In this study, a novel heterogeneous catalyst, CoMgFe-LDH layered doubled hydroxide (CoMgFe-LDH), was prepared for an efficient activation of peroxymonosulfate (PMS) to oxidize Rhodamine B (RhB). The characterization results showed that CoMgFe-LDH had a good crystallographic structure. Correspondingly, the CoMgFe-LDH/PMS process exhibited good capacity to remove RhB, which was equivalent to degradation performance as homogeneous Co(II)/PMS process. The RhB oxidation in the CoMgFe-LDH/PMS process was well described with pseudo-first-order kinetic model. Additionally, the oxidation process presented an excellent stability, and only 0.9% leaching rate was detected after six sequential reaction cycles at pH 5.0. The effects of initial pH, CoMgFe-LDH dosage, PMS concentration, RhB concentration, and inorganic anions on the RhB degradation were discussed in detail. Quenching experiments showed that sulfate radicals (SO4 & BULL;-) acted as the dominant reactive species. Further, the removal of RhB from simulated wastewater was explored. The removal efficiency of RhB (90 mu M) could reach 94.3% with 0.8 g/L of catalyst and 1.2 mM of PMS addition at pH 5.0, which indicated the CoMgFe-LDH/PMS process was also effective in degrading RhB in wastewater.

Automated summary

In this study, a novel heterogeneous catalyst CoMgFe-LDH was prepared for efficient activation of PMS to oxidize RhB. The CoMgFe-LDH/PMS process showed good capacity to remove RhB and exhibited excellent stability. Sulfate radicals (SO4-) were found to be the dominant reactive species.