Abstract

The environmental hazards associated with the presence of antibiotics and dyes in water sources require the development of efficient and appropriate wastewater treatment technologies. In the research, a dual catalytic electrode assisted self-sustained Fe2+ electro-Fenton system was constructed to degrade tetracycline, norfloxacin and methyl orange in wastewater efficiently and economically. The novel titanium mesh based PbO2/SnO2 anode electrode was prepared by electrodeposition with the best oxidation performance at the ratio of Sn to Pb 0.5:1, and silver doped Zinc-based organic framework ([email protected]) mixed crystal cathode catalyst was synthesized by precipitation at room temperature. Meanwhile, a sacrificial iron anode was introduced into the system in an acidic solution without a power supply, realizing the endogenous supply of Fe2+. The results indicated that the process was capable of self-supporting H2O2 and Fe2+ under the optimized conditions of pH range of 3.5–4.0, iron area of 10 cm2 and current intensity of 9 mA. The current efficiency was calculated to be as high as 369.5%. The type of conductive substrate supported cathode catalyst is an important factor determining the performance of the novel coupled electric-Fenton system. Electro-Fenton system using [email protected] catalytic electrode loaded with conductive substrates (stainless steel mesh (SS), carbon felt (CF), and activated charcoal granules (ACG)) was constructed to degrade tetracycline (TC), with the degradation efficiencies of 100% (k = 0.03048), 99.7% (k = 0.01831), 99.7% (k = 0.01421). Moreover, the experiment group of [email protected] electrode had achieved good degradation effects for TC, norfloxacin (NOR), methyl orange (MO), and the degradation efficiency was 99.1%, 92.8% and 100%, respectively. The possible degradation pathways of TC, NOR and MO were proposed by analyzing the intermediates. This work demonstrates the scaling-up potential of the system in the treatment of antibiotics and dye wastewater.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call