TY - JOUR
T1 - Efficient activation of percarbonate by metal-free carbonylated activated carbon for green groundwater remediation
T2 - Performance, mechanism, applicability, and environmental implications
AU - Zhang, Jun Bo
AU - Yang, Yi
AU - Dai, Chaomeng
AU - Li, Jixiang
AU - Liang, Yucang
AU - Hu, Jiajun
AU - Gao, Min tian
AU - You, Xueji
AU - Jiang, Xu
AU - Li, Shunyang
AU - Wang, Xihua
AU - Li, Zhi
AU - Zhang, Yalei
AU - Chang, Ken Lin
AU - Leong, Kah Hon
AU - Pin, Yeap Swee
N1 - Publisher Copyright:
© 2025 Elsevier B.V.
PY - 2025/10/5
Y1 - 2025/10/5
N2 - Sodium percarbonate (SPC)-based advanced oxidation processes (AOPs) hold great promise for in-situ groundwater remediation. However, most existing studies have focused on the metal-carbon composite activation systems, facing the risk of secondary pollution from metal ion leaching. Herein, this study innovatively prepared metal-free carbonylated activated carbon (CAC) by regulating the conversion of oxygen-containing functional groups on carbon materials to activate SPC efficiently. The results showed that the removal of 1-naphthoic acid (1-NA) by the CAC/SPC system reached 100.0 % within 60 min, with kobs of 0.5188 min−1, which was 6.84–11.85 times higher than that without carbonyl-modified carbon materials. Mechanistic studies revealed that the abundant carbonyl and graphitic carbon-like structures in CAC could activate SPC and promote 1-NA degradation through synergistic reactive oxygen species (1O2 > CO3•– > •OH) and electron transfer processes. The static/dynamic groundwater simulation experiments confirmed that the system maintained efficient degradation performance under a wide range of pH (3–10), complex inorganic anions (Cl⁻, HPO42⁻), and coexisting organics (humic acid, surfactant), showing strong adaptability to real groundwater environments. Moreover, the CAC/SPC system exhibited universal degradation of phenol (100.0 %), sulfamethoxazole (83.5 %), and carbamazepine (65.3 %), further highlighting its application potential. Notably, the CAC/SPC system was environmentally safe: the toxicity of degradation products was obviously lower than 1-NA; the carbon leaching of CAC (1.2 mg L−1) was much lower than from other carbon materials (68.5–80.9 mg L−1), and there was no risk of metal ions leaching; the pH (around 7.6) buffering of SPC degradation products (CO32⁻/HCO3⁻) prevented acidification of groundwater. This study provides an efficient, safe, and adaptable green technology solution for the remediation of organic contaminated groundwater.
AB - Sodium percarbonate (SPC)-based advanced oxidation processes (AOPs) hold great promise for in-situ groundwater remediation. However, most existing studies have focused on the metal-carbon composite activation systems, facing the risk of secondary pollution from metal ion leaching. Herein, this study innovatively prepared metal-free carbonylated activated carbon (CAC) by regulating the conversion of oxygen-containing functional groups on carbon materials to activate SPC efficiently. The results showed that the removal of 1-naphthoic acid (1-NA) by the CAC/SPC system reached 100.0 % within 60 min, with kobs of 0.5188 min−1, which was 6.84–11.85 times higher than that without carbonyl-modified carbon materials. Mechanistic studies revealed that the abundant carbonyl and graphitic carbon-like structures in CAC could activate SPC and promote 1-NA degradation through synergistic reactive oxygen species (1O2 > CO3•– > •OH) and electron transfer processes. The static/dynamic groundwater simulation experiments confirmed that the system maintained efficient degradation performance under a wide range of pH (3–10), complex inorganic anions (Cl⁻, HPO42⁻), and coexisting organics (humic acid, surfactant), showing strong adaptability to real groundwater environments. Moreover, the CAC/SPC system exhibited universal degradation of phenol (100.0 %), sulfamethoxazole (83.5 %), and carbamazepine (65.3 %), further highlighting its application potential. Notably, the CAC/SPC system was environmentally safe: the toxicity of degradation products was obviously lower than 1-NA; the carbon leaching of CAC (1.2 mg L−1) was much lower than from other carbon materials (68.5–80.9 mg L−1), and there was no risk of metal ions leaching; the pH (around 7.6) buffering of SPC degradation products (CO32⁻/HCO3⁻) prevented acidification of groundwater. This study provides an efficient, safe, and adaptable green technology solution for the remediation of organic contaminated groundwater.
KW - Carbonylated activated carbon
KW - Electron transfer processes
KW - Groundwater remediation
KW - Percarbonate activation
KW - Reactive oxygen species
UR - https://www.scopus.com/pages/publications/105014609281
U2 - 10.1016/j.jhazmat.2025.139679
DO - 10.1016/j.jhazmat.2025.139679
M3 - 文章
AN - SCOPUS:105014609281
SN - 0304-3894
VL - 497
JO - Journal of Hazardous Materials
JF - Journal of Hazardous Materials
M1 - 139679
ER -