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

## TL;DR

This paper presents a new method to create a high-performance carbon material from lignin that effectively removes tetracycline from water.

## Contribution

A novel hydrothermal-phosphoric acid synergistic activation method for producing lignin-derived hierarchical porous carbon with enhanced tetracycline adsorption.

## Key findings

- LPHC achieved a maximum tetracycline adsorption capacity of 219.81 mg·g−1.
- The adsorption process followed the Langmuir isotherm model, indicating monolayer chemical adsorption.
- Multiple interactions, including pore filling and hydrogen bonding, contributed to the adsorption mechanism.

## 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.