Interface engineering strategy of a Ti4O7 ceramic membrane via graphene oxide nanoparticles toward efficient electrooxidation of 1,4-dioxane

材料科学 石墨烯 电化学 氧化物 化学工程 极化(电化学) 纳米颗粒 化学 电极 纳米技术 冶金 物理化学 工程类
作者
Wei Li,Runlin Xiao,Jiale Xu,Hui Lin,Kui Yang,Wei Li,Kuanchang He,Longxiang Tang,Jie Chen,Yiping Wu,Sihao Lv
出处
期刊:Water Research [Elsevier BV]
卷期号:216: 118287-118287 被引量:62
标识
DOI:10.1016/j.watres.2022.118287
摘要

Although Ti4O7 ceramic membrane has been recognized as one of the most promising anode materials for electrochemical advanced oxidation process (EAOP), it suffers from relatively low hydroxyl radical (•OH) production rate and high charge-transfer resistance that restricted its oxidation performance of organic pollutants. Herein, we reported an effective interface engineering strategy to develop a Ti4O7 reactive electrochemical membrane (REM) doped by graphene oxide nanoparticles (GONs), GONs@Ti4O7 REM, via strong GONs-O-Ti bonds. Results showed that 1% (wt%) GON doping on Ti4O7 REM significantly reduced the charge-transfer resistance from 73.87 to 8.42 Ω compared with the pristine Ti4O7 REM, and yielded •OH at 2.5-2.8 times higher rate. The 1,4-dioxane (1,4-D) oxidation rate in batch experiments by 1%GONs@Ti4O7 REM was 1.49×10-2 min-1, 2 times higher than that of the pristine Ti4O7 REM (7.51×10-3 min-1) and similar to that of BDD (1.79×10-2 min-1). The 1%GONs@Ti4O7 REM exhibited high stability after a polarization test of 90 h at 80 mA/cm2, and within 15 consecutive cycles, its oxidation performance was stable (95.1-99.2%) with about 1% of GONs lost on the REM. In addition, REM process can efficiently degrade refractory organic matters in the groundwater and landfill leachate, the total organic carbon was removed by 54.5% with a single-pass REM. A normalized electric energy consumption per log removal of 1,4-D (EE/O) was observed at only 0.2-0.6 kWh/m3. Our results suggested that chemical-bonded interface engineering strategy using GONs can facilitate the EAOP performance of Ti4O7 ceramic membrane with outstanding reactivity and stability.
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
Twistti完成签到,获得积分10
刚刚
xxx完成签到,获得积分10
1秒前
QQQ秋发布了新的文献求助10
1秒前
共享精神应助章半仙采纳,获得10
1秒前
大萌完成签到,获得积分10
1秒前
华仔应助nano采纳,获得10
1秒前
SESAME复合体完成签到,获得积分10
1秒前
一一发布了新的文献求助10
2秒前
传奇3应助hongzhihu采纳,获得10
2秒前
Twistti发布了新的文献求助10
2秒前
落樱幻梦染星尘完成签到,获得积分10
3秒前
酸甜完成签到,获得积分10
3秒前
共享精神应助时辰采纳,获得10
3秒前
biu发布了新的文献求助10
4秒前
迅速雨琴发布了新的文献求助10
4秒前
无情的芹关注了科研通微信公众号
4秒前
4秒前
zhu完成签到,获得积分10
5秒前
qiyr完成签到,获得积分10
5秒前
ZX612发布了新的文献求助10
5秒前
李健的粉丝团团长应助zsq采纳,获得10
5秒前
科研通AI6.4应助QQQ秋采纳,获得10
5秒前
5秒前
李爱国应助李不乐采纳,获得10
6秒前
852应助bijialcl采纳,获得100
6秒前
lcy666llll发布了新的文献求助50
6秒前
6秒前
dd完成签到,获得积分10
6秒前
6秒前
hi_traffic发布了新的文献求助10
7秒前
小二郎应助kk采纳,获得10
7秒前
陈腿毛完成签到,获得积分10
8秒前
ayoubeibei完成签到,获得积分10
8秒前
任性的雁风关注了科研通微信公众号
9秒前
9秒前
小呵点发布了新的文献求助10
9秒前
10秒前
QQQ秋完成签到,获得积分10
10秒前
小蘑菇应助迅速雨琴采纳,获得10
10秒前
陆可完成签到 ,获得积分10
10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
An Introduction to Foreign Language Learning and Teaching 750
China Pluperfect I: Epistemology of Past and Outside in Chinese Art 520
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
Les chinois de jakarta: temples et vie collective 500
The fast track to determining transfer functions of linear circuits: The student guide 500
What is the Future of Psychotherapy in Digital Age? Technology, AI Bots, and Psychotherapy after Covid 444
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 7628265
求助须知:如何正确求助?哪些是违规求助? 9202658
关于积分的说明 19732289
捐赠科研通 7197919
什么是DOI,文献DOI怎么找? 3273952
关于科研通互助平台的介绍 2436259
邀请新用户注册赠送积分活动 2270145