Thị Lan Anh Nguyen, Trần Văn Tám, Minh-Tri Nguyen-Le
2026.1.12Compounds
Abstract
This study investigates the activation mechanism of boron-doped carbon (BMC) catalysts for the degradation of the antibiotic sulfamethoxazole (SMX) via persulfate (PMS) activation. The catalysts were synthesized using a sequential double-melting calcination method, resulting in mesoporous carbon nanosheets characterized by hierarchical macro-mesopores and atomically dispersed dual active sites. Comprehensive characterization was performed using BET, SEM, TEM, FT-IR, XPS, XRD, and Raman techniques. The optimized BMC catalyst demonstrated excellent performance, achieving complete removal of sulfamethoxazole (100%) and a high mineralization rate (~90%) within 45 min. Mechanistic analysis, including electron paramagnetic resonance (EPR), revealed that the degradation predominantly follows a singlet oxygen (1O2)-dominated pathway. The system exhibited broad applicability to various pollutants, along with notable operational stability and robust resistance to common environmental interferents. Persulfate activation was primarily attributed to boron-active sites, while the hierarchical mesoporous structure facilitated both pollutant enrichment and catalytic efficiency.
Citation format
NGUYEN, Thị Lan Anh; TÁM, Trần Văn; NGUYEN-LE, Minh-Tri. Enhanced removal of the antibiotic sulfamethoxazole by a b-doped mesoporous carbon nanosheet/peroxymonosulfate system: Characterization and mechanistic insights. Compounds, 2026, 6(1): 6.