Self-sufficient Fenton-Like Degradation by Cu-TA Encapsulated Melamine Sponge

化学 三聚氰胺 降级(电信) 催化作用 电子顺磁共振 吸附 单宁酸 猝灭(荧光) 核化学 基质(水族馆) 吸收(声学) 激进的 动力学 无机化学 离子 氧气 光化学 多相催化 亚甲蓝 多孔性 化学工程 还原剂 氧化还原 比表面积 海绵
作者
Y. Y. Chen,Peng Zhou,Jiwei Wang,Bei Jiang
出处
期刊: 卷期号:: 100680-100680
标识
DOI:10.1016/j.cjac.2025.100680
摘要

Water contamination is a severe and urgent issue, and advanced oxidation processes (AOPs) offer promising solutions for water purification. Among these, copper-based Fenton-like reaction demonstrate advantages such as rapid reaction kinetics and low reduction potential. However, a major limitation of most Fenton-like reactions is their reliance on externally added H 2 O 2 , which poses risks in transportation, storage, and management. To address this, developing self-sufficient Fenton-like systems with in-situ H 2 O 2 generation is critical. In this study, we conjugated copper ions (Cu 2+ ) and tannic acid (TA) on a melamine sponge (MS) substrate to fabricate a self-sufficient Fenton-like catalyst (MS-Cu-TA). MS exhibits high porosity and absorbency, which facilitate efficient liquid absorption for the degradation process. The H 2 O 2 content generated by a single MS-Cu-TA sponge was determined as ∼0.19 mmol, which was sufficient to sustain the Fenton-like reaction. Methylene Blue (MB) degradation results showed that MS-Cu-TA achieved comparable degradation efficiency (∼60% within 0.5 h) without exogenous H 2 O 2 . Notably, in this specific dye degradation process, adsorption and degradation occurred simultaneously. Results from reactive oxygen species (ROS) quenching tests and electron paramagnetic resonance (EPR) spectroscopic analysis revealed that the dominant ROS generated is •OH, which originates from in-situ formed H 2 O 2 . The in-situ H 2 O 2 generation is likely attributed to the auto-oxidation of TA, which acts as both reducing agent and H 2 O 2 precursor. Concurrently, TA reduces Cu 2+ to Cu + , which catalyzes H 2 O 2 to generate hydroxyl radicals (•OH) via a Fenton-like reaction. This work provides valuable insights for developing self-sufficient Fenton-like systems in wastewater treatment. In this study, we conjugated copper ions (Cu 2+ ) and tannic acid (TA) on a melamine sponge (MS) substrate to fabricate a self-sufficient Fenton-like catalyst (MS-Cu-TA). The in-situ H 2 O 2 generation is likely attributed to the auto-oxidation of TA, which acts as both a reducing agent and H 2 O 2 precursor. Concurrently, TA reduces Cu 2+ to Cu + , which catalyzes H 2 O 2 to generate hydroxyl radicals (•OH) via a Fenton-like reaction.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
1秒前
1秒前
1464565388完成签到,获得积分10
1秒前
冷傲天空发布了新的文献求助10
1秒前
瑾瑜玉完成签到 ,获得积分10
2秒前
领导范儿应助nunu采纳,获得10
3秒前
共享精神应助清风采纳,获得10
4秒前
4秒前
彭于晏发布了新的文献求助10
4秒前
5秒前
yy发布了新的文献求助10
5秒前
wzr887发布了新的文献求助10
6秒前
爆米花应助标致碧曼采纳,获得30
6秒前
西瓜西瓜发布了新的文献求助10
6秒前
琦琦发布了新的文献求助10
7秒前
7秒前
8秒前
行行行完成签到,获得积分10
8秒前
圥忈完成签到,获得积分10
8秒前
111发布了新的文献求助10
8秒前
瑾蘆完成签到 ,获得积分10
9秒前
斯文败类应助喵喵酱采纳,获得10
9秒前
19863737023完成签到,获得积分10
9秒前
桐桐应助吉吉国王采纳,获得10
9秒前
kilig完成签到,获得积分10
9秒前
yang发布了新的文献求助10
10秒前
11秒前
11秒前
v0id应助科研通管家采纳,获得10
11秒前
11秒前
香蕉觅云应助科研通管家采纳,获得10
11秒前
整齐的慕卉应助清蒸鱼采纳,获得10
11秒前
在水一方应助科研通管家采纳,获得10
11秒前
11秒前
苹果不弱完成签到,获得积分10
11秒前
12秒前
天天快乐应助科研通管家采纳,获得10
12秒前
yy完成签到,获得积分10
12秒前
深情安青应助科研通管家采纳,获得10
12秒前
HHHMMM完成签到 ,获得积分10
12秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
APA handbook of comparative psychology: Basic concepts, methods, neural substrate, and behavior 1000
Child and Adolescent Mental Health 600
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
The fast track to determining transfer functions of linear circuits: The student guide 500
Römisch-Germanische Forschungen 500
Electric machines: theory, operating applications, and controls 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7599585
求助须知:如何正确求助?哪些是违规求助? 9175791
关于积分的说明 19646199
捐赠科研通 7175691
什么是DOI,文献DOI怎么找? 3268468
关于科研通互助平台的介绍 2432963
邀请新用户注册赠送积分活动 2262034