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Molecules· 2026Q1

Synthesis of Lignin-Derived Hierarchical Porous Carbon via Hydrothermal–Phosphoric Acid Synergistic Activation for Enhanced Adsorption of Tetracycline

Xin Li, Yipeng Li, Yuhan Li, Mengyu Zhang et al.

Short summary

A novel hierarchical porous carbon derived from lignin (LPHC) achieved a maximum tetracycline adsorption capacity of 219.81 mg·g−1, significantly outperforming previous methods.

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Key points

  • Lignin-derived hierarchical porous carbon (LPHC) synthesized via hydrothermal–phosphoric acid activation.
  • LPHC exhibits a high specific surface area of 1157.25 m2·g−1 and a micro-mesoporous structure.
  • Maximum tetracycline adsorption capacity reached 219.81 mg·g−1.
  • Adsorption is a monolayer process conforming to the Langmuir isotherm model.
  • Multiple interactions, including pore filling and π-π interactions, drive adsorption.

AI-generated from the title and abstract; the full text is not read.

Abstract

Tetracycline is a low-cost broad-spectrum antibiotic and widely used in medicine and aquaculture. Its residues are usually released into the environment through wastewater, which may lead to the spread of antibiotic resistance genes and pose ecological risks. To address this environmental issue, a hierarchical lignin-derived porous carbon (LPHC) was synthesized using renewable biomass lignin as the precursor through a combined phosphoric acid-activated hydrothermal pretreatment. The resulting LPHC was used to effectively remove tetracycline from aqueous solutions. Characterization results indicated that LPHC had a high specific surface area (1157.25 m2·g−1), a well-developed micro-mesoporous structure, and abundant surface oxygen-containing functional groups, which enhanced its interaction with target pollutants. Adsorption experiments showed that LPHC exhibited excellent adsorption performance for tetracycline, with a maximum adsorption capacity of 219.81 mg·g−1. The adsorption process conformed to the Langmuir isotherm model, indicating that monolayer chemical adsorption was dominant. Mechanism analysis further confirmed that the adsorption process was controlled by multiple synergistic interactions, including pore filling, π-π electron donor–acceptor interactions, hydrogen bonding, and electrostatic attraction. This work proposes a feasible strategy to convert waste biomass into high-performance and environmentally friendly adsorbents, which provides technical feasibility for sustainable water purification technologies.

The authors' abstract, as published at the source. Molecules, 2026 · DOI ↗

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