Sustainable production of Fe-doped MnO2 nanoparticles for accelerated tetracycline antibiotic detoxification

Abstract

Manganese dioxide (MnO2) has been recognized as one of the natural systems' most active mineral oxidants. However, when it comes to catalytic oxidation of antibiotic applications, pure MnO2 falls short in delivering satisfactory performance. Hence, a set of Fe3+-doped porous MnO2 (0.02Fe–MnO2, 0.1Fe–MnO2, and 0.14Fe–MnO2) nanoparticles were synthesized here via a convenient and energy-efficient one-step reaction method. A series of experiments revealed that Fe-doping strategy enhances the properties of MnO2 host by suppressing the crystalline structure, increasing the amount of surface oxygen defects, and modifying the Mn3+/Mn4+ ratio. Specifically, the tetracycline (TC) removal efficiency of 0.14Fe–MnO2 reaches 92% without the need for any additional co-oxidant, representing a 20% improvement over pristine MnO2 nanoparticles. Moreover, this process shows a fast dynamic (achieving 70% of TC removal in just 5 min) and demonstrates pH-resistance, maintaining high TC removal efficiency (≥90%) over a wide pH range of 3.0–9.0. Mechanical studies reveal that the degradation of TC can be attributed to the oxidation by reactive oxygen radicals and Mn3+, with 1O2 being the primary radical involved in the reaction, accounting for 55% of TC removal. Importantly, cytotoxicity testing indicates that the biotoxicity of TC toward organisms can be effectively mitigated using 0.14Fe–MnO2 nanomaterial. This study presents a readily applicable candidate for economically and conveniently eliminating of environmental TC pollution, thereby reducing the threat posed by TC pollution to the ecosystem.