Nguyen Thi Hai Anh

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.

Rice husk (RH) is a widely available lignocellulosic residue for biohydrogen production but requires effective pretreatment to overcome lignin-related recalcitrance. This study investigates the kinetics of lignin removal from RH using 3% sodium hydroxide (NaOH) and water pretreatments at high temperatures between 100 and 129 °C (25 °C control) with short reaction times (15–60 min) in an autoclave system. Biomass composition, solid yield, delignification efficiency, and enzymatic hydrolysis for glucose production were evaluated. NaOH pretreatment achieved up to 72.72% lignin removal at 129 °C after 60 min, significantly outperforming water pretreatment, which reached a maximum delignification of 20.24% under the same conditions. Kinetic analysis revealed first-order reaction behavior, with the kinetic rate constants varying between 5.14 × 10⁻⁵ and 4.31 × 10⁻³ with water pretreatment and from 3.73 × 10⁻⁴ to 2.46 × 10⁻² with NaOH and activation energies of 42.61 kJ mol⁻¹ K⁻¹ and 39.31 kJ mol⁻¹ K⁻¹ for water and NaOH pretreatment, respectively. Enhanced lignin removal improved cellulose accessibility, resulting in glucose yields from enzymatic hydrolysis of up to 52.13 mg/g for NaOH-treated samples, double those obtained with water pretreatment (26.97 mg/g). While NaOH pretreatment achieved higher lignin removal efficiency and glucose yield, it exhibited significantly higher environmental impacts across multiple categories, including global warming potential and terrestrial ecotoxicity, based on the life cycle assessment (LCA). Even water-based pretreatment showed considerable burdens; thus, both pretreatment methods impose high life cycle impacts when applied to RH, which makes it an unsustainable feedstock for glucose production under the evaluated conditions. Alternative feedstocks or improved process integration strategies are required for environmentally viable biohydrogen production.