Comparative study of reactive oxygen species and tetracycline degradation pathways in catalytic peroxodisulfate activation by asymmetric mesoporous TiO2 and the corresponding controlled-release materials

Abstract

The removal of trace amounts of antibiotics from water environments while simultaneously avoiding potential environmental hazards during the treatment is still a challenge. In this work, green, harmless, and novel asymmetric mesoporous TiO₂ (A-mTiO₂) was combined with peroxodisulfate (PDS) as active components in a controlled-release material (CRM) system for the degradation of tetracycline (TC) in the dark. The formation of reactive oxygen species (ROS) and the degradation pathways of TC during catalytic PDS activation by A-mTiO₂ powder catalysts and the CRMs were thoroughly studied. Due to its asymmetric mesoporous structure, there were abundant Ti³⁺/Ti⁴⁺ couples and oxygen vacancies in A-mTiO₂, resulting in excellent activity in the activation of PDS for TC degradation, with a mineralization rate of 78.6%. In CRMs, ROS could first form during PDS activation by A-mTiO₂ and subsequently dissolve from the CRMs to degrade TC in groundwater. Due to the excellent performance and good stability of A-mTiO₂, the resulting constructed CRMs could effectively degrade TC in simulated groundwater over a long period (more than 20 days). From electron paramagnetic resonance analysis and TC degradation experiments, it was interesting to find that the ROS formed during PDS activation by A-mTiO₂ powder catalysts and CRMs were different, but the degradation pathways for TC were indeed similar in the two systems. In PDS activation by A-mTiO₂, besides the free hydroxyl radical (·OH), singlet oxygen (¹O₂) worked as a major ROS participating in TC degradation. For CRMs, the immobilization of A-mTiO₂ inside CRMs made it difficult to capture superoxide radicals (·O₂^-), and continuously generate ¹O₂. In addition, the formation of sulfate radicals (·SO₄^-), and ·OH during the release process of CRMs was consistent with PDS activation by the A-mTiO₂ powder catalyst. The eco-friendly CRMs had a promising potential for practical application in the remediation of organic pollutants from groundwater.

Keywords: Asymmetric mesoporous TiO(2); Controlled-release materials; Peroxodisulfate activation; Reactive oxygen species; Tetracycline.