Photoactivation of peroxymonosulfate by wood pulp cellulose biochar/g-C3N4 composite for diclofenac degradation: the radical and nonradical pathways
Metal-free photocatalysts have attracted growing concern recently. Herein, the composites combining g-C 3 N 4 with wood pulp cellulose biochar (WPBC/g-C 3 N 4 ) were synthesized to effectively activate peroxymonosulfate (PMS) under visible light for the degradation of diclofenac (DCF). The incorpora...
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Veröffentlicht in: | Biochar (Online) 2022-12, Vol.4 (1), p.1-19, Article 35 |
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Sprache: | eng |
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Zusammenfassung: | Metal-free photocatalysts have attracted growing concern recently. Herein, the composites combining g-C
3
N
4
with wood pulp cellulose biochar (WPBC/g-C
3
N
4
) were synthesized to effectively activate peroxymonosulfate (PMS) under visible light for the degradation of diclofenac (DCF). The incorporation of WPBC endowed g-C
3
N
4
with enhanced visible light absorption, improved charge separation capability, reduced electrical conductivity, and increased photocatalytic and PMS activation capability. Based on quenching tests, electron paramagnetic resonance (EPR), electrochemical analysis and solvent exchange experiments, both radical and nonradical mechanisms were proposed. Radical species including ·OH, h
+
, ·O
2
–
were identified to contribute to DCF degradation. The
1
O
2
and electron transfer were the dominant nonradical pathways for DCF degradation. Moreover, the common influencing factors were examined, and DCF concentration was the most influential factor based on principal component analysis. Generally, the composites exhibited good reusability during consecutive runs. Based on HPLC/MS analysis, four intermediates were detected and the possible DCF degradation pathway was proposed. This work provided a potential strategy based on metal-free WPBC/g-C
3
N
4
for the photocatalytic activation of PMS to effectively degrade emerging contaminants in wastewater.
Graphical abstract
Highlights
Wood pulp cellulose biochar (WPBC) improved the catalytic performance of g-C3N4 via both radical and nonradical mechanisms.
The photoelectrical properties and PMS activation capability were improved by WPBC.
WPBC/g-C3N4 presented high stability for multiple runs. |
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ISSN: | 2524-7972 2524-7867 |
DOI: | 10.1007/s42773-022-00155-0 |