Ambivalent photocatalytic strategies for plastic waste conversion: Alkalinized carbon nitride for H2O2 production and complete mineralization

被引:3
|
作者
Son, Sanguk [1 ]
Haider, Zeeshan [1 ,2 ]
Lee, Do-Yeon [1 ]
Kim, Suho [1 ,3 ]
Thai, Nghiem Vinh [1 ]
Kim, Hyoung-il [1 ,4 ]
机构
[1] Yonsei Univ, Dept Civil & Environm Engn, Seoul 03722, South Korea
[2] Incheon Natl Univ, Dept Phys, Incheon 22012, South Korea
[3] Korea Inst Civil Engn & Bldg Technol, Construct Test & Assessment Ctr, Goyang 10223, South Korea
[4] Pohang Univ Sci & Technol POSTECH, Future City Open Innovat Ctr, Pohang 37673, South Korea
来源
APPLIED CATALYSIS B-ENVIRONMENT AND ENERGY | 2025年 / 365卷
基金
新加坡国家研究基金会;
关键词
Plastic; Upcycling; Carbon nitride; Hydrogen peroxide; Photoreforming; Advanced oxidation process; SOLAR HYDROGEN-PRODUCTION; POLYETHYLENE TEREPHTHALATE; H-2; EVOLUTION; PEROXIDE; G-C3N4; DEGRADATION; OXIDATION; ACID; DECOMPOSITION; REDUCTION;
D O I
10.1016/j.apcatb.2024.124847
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Plastic waste poses a significant environmental threat due to its widespread use and disposal, necessitating innovative upcycling methods. Here, we introduce alkalinized carbon nitride (Alk-CN) as an efficient photocatalyst for the solar-driven photoreforming of polyethylene terephthalate (PET) into hydrogen peroxide (H2O2) in alkaline environments. Alk-CN also demonstrates versatility for H2O2 production with other polyester-based plastics, including polybutylene terephthalate and polylactic acid. This study pioneers an innovative dual approach to managing PET waste: (i) photoreforming to produce H2O2 and recover TPA from bulk PET waste and (ii) utilizing an AOP system with in-situ generated H2O2 under UV irradiation for the complete mineralization of trace PET waste in wastewater. These findings offer viable strategies for transforming plastic waste into valuable products or achieving complete mineralization, leveraging solar-driven photocatalytic reactions for environmental remediation and resource recovery.
引用
收藏
页数:11
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