Synergistic optimization of Pb(II) adsorption from aqueous solutions by manganese-doped carbon aerogels
In this study, a novel carbon aerogel adsorbent (Mn-PA-CS) was synthesized through a one-step calcination-activation method using manganese acetate as the precursor. Unlike conventional phytic acid-activated carbons, this work introduces manganese doping as an effective strategy to tailor the pore structure and surface chemistry. The resulting material features enriched surface P/O functional groups and a significantly increased proportion of micropores (0.7–0.8 nm), which closely match the hydration diameter of Pb(II) ions, alongside elevated defect density (ID/IG = 0.94). These modifications synergistically promote adsorption through micropore filling, electrostatic attraction, and surface complexation. The optimized Mn-PA-CS, prepared with 100 mg of manganese acetate, exhibited a high Pb(II) uptake capacity of 302.88 mg·g −1 , which represents a 132.43 % improvement compared to the undoped material. The adsorption behavior followed pseudo-second-order kinetics and the Freundlich isotherm, suggesting a spontaneous, endothermic, and multilayer chemisorption process. This study indicates that transition metal doping is a promising strategy for regulating the adsorption performance of bio-derived carbon materials.
Authors
- Yirong Zhang (ORCID: https://orcid.org/0000-0001-8585-2197)
- Sheng Cai (ORCID: https://orcid.org/0000-0003-1456-8134)
- Luming Tian (ORCID: https://orcid.org/0009-0007-2801-8762)
- Zhi Liu (ORCID: https://orcid.org/0000-0002-8973-6561)
- Xing Yan (ORCID: https://orcid.org/0000-0002-6538-9227)
- Ruirui Zhu
- D. He
Institutions
- Hunan University (CN)
- Ministry of Ecology and Environment (CN)
- Early Warning (United States) (US)
Publication Details
- Journal
- Colloids and Surfaces A Physicochemical and Engineering Aspects
- Published
- 2025-09-05
- DOI
- https://doi.org/10.1016/j.colsurfa.2025.138259
- Primary Topic
- Adsorption and biosorption for pollutant removal
- Type
- article
- Field-Weighted Citation Impact
- 0.00