Thermal transformation of carbonized materials to functional activated carbon (AC) is a simplified, economical and eco-friendly strategy, which has great potential in the practical applications of water purification. Herein, a… Click to show full abstract
Thermal transformation of carbonized materials to functional activated carbon (AC) is a simplified, economical and eco-friendly strategy, which has great potential in the practical applications of water purification. Herein, a Fe/S codoped activated carbon (S/Fe@AC) with only 0.90 wt% S and 0.76 wt% Fe was creatively fabricated by one synchronous method of physical activation, carbothermal reduction and sulfidation in the solid phase. The formed iron sulfide shell significantly enhances the antioxidation ability of nanoscale zero-valent iron (NZVI, >180 d) and dramatically improves the hydrophobicity of the composite. Meanwhile, the doped thiophenic S in AC enhances the hydrophobicity and increases the specific surface area to 1194.14 m2 g-1. Incorporating with AC in turn greatly strengthens the dispersibility and stability of SNZVI particles. Compared to NZVI@AC, AC and NZVI, the removal capacity of S/Fe@AC for the representative hydrophobic contaminant-triclosan increases to 519.68 mg g-1 by 66.60%, 78.60% and 981.21%, respectively, outperforming most of the previously reported materials. The strong hydrophobic and π-π interactions, and weak hydrogen bonding and electrostatic repulsion are responsible for the excellent removal performance for TCS. More importantly, the improved chemical property (29.38%) of the composite caused by the doped Fe/S has a greater effect on TCS removal compared with the changed physical structure (14.56%). Furthermore, the stable S/Fe@AC shows strong anti-interference capability and exceptional regenerability. These intriguing discoveries provide new insights into the design of advanced and sustainable adsorbing materials for emerging contaminants.
               
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