Efficient activation of percarbonate by metal-free carbonylated activated carbon for green groundwater remediation: Performance, mechanism, applicability, and environmental implications

Jun Bo Zhang, Yi Yang, Chaomeng Dai, Jixiang Li, Yucang Liang, Jiajun Hu, Min tian Gao, Xueji You, Xu Jiang, Shunyang Li, Xihua Wang, Zhi Li, Yalei Zhang, Ken Lin Chang, Kah Hon Leong, Yeap Swee Pin

Research output: Contribution to journalArticlepeer-review

Abstract

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.

Original languageEnglish
Article number139679
JournalJournal of Hazardous Materials
Volume497
DOIs
StatePublished - 5 Oct 2025
Externally publishedYes

Keywords

  • Carbonylated activated carbon
  • Electron transfer processes
  • Groundwater remediation
  • Percarbonate activation
  • Reactive oxygen species

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