Study on the Efficiency and Mechanism of a Novel Copper-Based Composite Material Activated by Supramolecular Self-Assembly for Degrading Reactive Red 3BS
To address the challenge of treating refractory organic dyes in textile wastewater, this study synthesized a novel copper-based composite material (designated MEL-Cu-6HNA) via a supramolecular self-assembly-pyrolysis pathway. Its core component consists of CuO/Cu<sub>2</sub>O(SO<sub>4</sub>), which was applied to efficiently degrade the Reactive Red 3BS dye within a sodium bicarbonate-activated hydrogen peroxide (BAP) system. This material was applied to degrade the Reactive Red 3BS dye using a sodium bicarbonate-activated hydrogen peroxide system. The morphology, crystal structure, and surface chemistry of the material were systematically characterized using scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and X-ray photoelectron spectroscopy (XPS). Electron paramagnetic resonance (EPR) was employed to identify reactive species generated during the reaction. The effects of dye concentration, H<sub>2</sub>O<sub>2</sub> concentration, MEL-Cu-6HNA dosage, and coexisting substances in water on degradation efficiency were systematically investigated, with active species identified via EPR. This study marks the first application of the supramolecular self-assembled CuO/Cu<sub>2</sub>O(SO<sub>4</sub>)<sub>2</sub> composite material MEL-Cu-6HNA, prepared via pyrolysis, in a sodium bicarbonate-activated hydrogen peroxide system. It achieved rapid and efficient decolorization of the recalcitrant Reactive Red 3BS dye. The three-dimensional sulfate framework and dual Cu<sup>2+</sup> sites of the material significantly enhanced the degradation efficiency. MEL-Cu-6HNA achieved rapid and efficient decolorization of the recalcitrant Reactive Red 3BS in a sodium bicarbonate-activated hydrogen peroxide system. The material's three-dimensional sulfate framework and dual Cu<sup>2+</sup> sites significantly enhanced interfacial electron transfer and Cu<sup>2+</sup>/Cu<sup>+</sup> cycling activation capacity. ·OH served as the primary reactive oxygen species (ROS), with SO<sub>4</sub><sup>2-</sup>, <sup>1</sup>O<sub>2</sub>, and ·O<sub>2</sub><sup>-</sup> contributing to sustained radical generation. This system achieved 95% decolorization within 30 min, demonstrating outstanding green treatment potential and providing a reliable theoretical basis and practical pathway for efficient, low-energy treatment of dyeing wastewater.
Authors
- Bo Chen (ORCID: https://orcid.org/0000-0001-7605-9453)
- Xinrong Wang
- Jiangming Dai
- Liang Chen
Institutions
- Ministry of Public Security of the People's Republic of China (CN)
- Zhejiang Wanli University (CN)
- Shanghai Public Health Clinical Center (CN)
Publication Details
- Journal
- Nanomaterials
- Published
- 2026-01-15
- DOI
- https://doi.org/10.3390/nano16020111
- Primary Topic
- Environmental remediation with nanomaterials
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Natural Science Foundation of China