Turning Waste into Treasure: A Magnetic Sludge-Based Biochar for Efficient Co-Removal of Tetracycline and Cu 2+

作者：Leyao Shi, Jiexiong Zhong, Miao Wu, Qun Liu, Yang Liu, Xiaohui Xu, Weixue Wang, Xiaohui Guan, Min Lü · 发表于：Langmuir · 年份：2025 · DOI：10.1021/acs.langmuir.5c05131 · 被引用次数：4 · 研究领域：Adsorption and biosorption for pollutant removal、Advanced oxidation water treatment、Phosphorus and nutrient management

The treatment and disposal of excess sludge, a major solid byproduct of wastewater treatment processes, pose significant environmental and public health challenges, making its rational utilization crucial for promoting resource recycling. This study presents a one-step synthesis of a magnetically responsive bifunctional biochar composite (Fe-SDB 600 ) derived from excess sludge for the simultaneous and enhanced removal of tetracycline (TC) and copper ions (Cu 2+ ) from aqueous solutions. Characterization confirmed the successful loading of nanoscale iron oxide particles onto the biochar surface, resulting in a hierarchical porous structure. Under optimized conditions, Fe-SDB 600 exhibited significantly improved adsorption capacities for TC (269.39 mg/g) and Cu 2+ (271.65 mg/g) compared to the pristine biochar. The composite demonstrated excellent resistance to interference from common coexisting ions and maintained a high TC removal efficiency of 83.28% after four adsorption–desorption cycles, with minimal iron leaching. Adsorption kinetics were best described by the pseudo-second-order model, and isotherm data fitted the Langmuir model, indicating a chemisorption-dominated process. Density functional theory (DFT) calculations provided atomic-level mechanistic validation, confirming the spontaneous coordination of Cu 2+ to surface Fe–OH sites with a high binding energy of −2.05 eV and identifying the A-ring of TC as the dominant moiety for π–π electron donor–acceptor interact...