Biochar-Driven Synergistic Adsorption and Catalytic Degradation of Triazine Herbicides in Aquatic Systems: Mechanisms, Pathways, and Sustainable Water Remediation

In recent decades, triazine herbicides (THs), one of the most widely used agrochemicals, have been extensively applied to enhance crop yields. However, their persistent nature and high mobility have resulted in pervasive contamination of aquatic ecosystems, posing significant risks to non-target organisms and human health through bioaccumulation and endocrine disruption. Addressing THs pollution in water bodies has thus emerged as a critical environmental challenge. This study reviews the efficacy of biochar, a carbon-rich material derived from biomass pyrolysis, for TH removal due to its high surface area, hierarchical porosity, and tunable surface functionality. The maximum reported adsorption capacities are up to 260.5 mg·g−1; with degradation efficiencies, they can exceed 99.5% in advanced oxidation systems. Mechanistic investigations reveal that TH removal primarily involves π–π interactions, hydrogen bonding, pore filling, and electrostatic attraction during adsorption, while degradation proceeds via radical pathways (e.g., •OH, SO4•−) and nonradical routes (e.g., 1O2, direct electron transfer) in processes such as persulfate activation, photocatalysis, and Fenton-like reactions. By analyzing degradation intermediates and pathways, this review underscores the necessity of coupling adsorption with advanced oxidation to achieve complete mineralization and mitigate secondary ecological risks. Furthermore, it emphasizes the importance of tailoring biochar’s physicochemical properties through feedstock selection, pyrolysis conditions, and chemical modifications to optimize THs’ removal performance. This work advocates for the integration of biochar-based technologies into sustainable water treatment frameworks, aligning with carbon neutrality goals and circular economy principles. Future research should prioritize scalable synthesis methods, long-term stability assessments, and field-scale validations to translate laboratory insights into practical solutions for safeguarding global water resources. However, realizing this potential requires that we overcome challenges related to matrix interference, catalyst deactivation, and incomplete mineralization, which are often overlooked in laboratory-scale studies.

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Processes
Published
2026-04-16
DOI
https://doi.org/10.3390/pr14081270
Primary Topic
Advanced oxidation water treatment
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article
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article

Biochar-Driven Synergistic Adsorption and Catalytic Degradation of Triazine Herbicides in Aquatic Systems: Mechanisms, Pathways, and Sustainable Water Remediation

Liang Yuan, Haoming Sun
Processes
Advanced oxidation water treatment
article

Biochar-Driven Synergistic Adsorption and Catalytic Degradation of Triazine Herbicides in Aquatic Systems: Mechanisms, Pathways, and Sustainable Water Remediation

Liang Yuan, Haoming Sun
article en

Abstract

In recent decades, triazine herbicides (THs), one of the most widely used agrochemicals, have been extensively applied to enhance crop yields. However, their persistent nature and high mobility have resulted in pervasive contamination of aquatic ecosystems, posing significant risks to non-target organisms and human health through bioaccumulation and endocrine disruption. Addressing THs pollution in water bodies has thus emerged as a critical environmental challenge. This study reviews the efficacy of biochar, a carbon-rich material derived from biomass pyrolysis, for TH removal due to its high surface area, hierarchical porosity, and tunable surface functionality. The maximum reported adsorption capacities are up to 260.5 mg·g−1; with degradation efficiencies, they can exceed 99.5% in advanced oxidation systems. Mechanistic investigations reveal that TH removal primarily involves π–π interactions, hydrogen bonding, pore filling, and electrostatic attraction during adsorption, while degradation proceeds via radical pathways (e.g., •OH, SO4•−) and nonradical routes (e.g., 1O2, direct electron transfer) in processes such as persulfate activation, photocatalysis, and Fenton-like reactions. By analyzing degradation intermediates and pathways, this review underscores the necessity of coupling adsorption with advanced oxidation to achieve complete mineralization and mitigate secondary ecological risks. Furthermore, it emphasizes the importance of tailoring biochar’s physicochemical properties through feedstock selection, pyrolysis conditions, and chemical modifications to optimize THs’ removal performance. This work advocates for the integration of biochar-based technologies into sustainable water treatment frameworks, aligning with carbon neutrality goals and circular economy principles. Future research should prioritize scalable synthesis methods, long-term stability assessments, and field-scale validations to translate laboratory insights into practical solutions for safeguarding global water resources. However, realizing this potential requires that we overcome challenges related to matrix interference, catalyst deactivation, and incomplete mineralization, which are often overlooked in laboratory-scale studies.

ProcessesVol. 14(8)
Suzhou University of Science and Technology (CN)
Openalex Percentile: Top 17%
Advanced oxidation water treatment
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