Developing a solar photothermal method for peroxydisulfate activation for water purification: Taking degradation of sulfamethoxazole as an example

过氧二硫酸盐 过硫酸盐 水溶液 光热治疗 化学 活性炭 降级(电信) 饮用水净化 过硫酸钠 光化学 吸附 化学工程 猝灭(荧光) 光热效应 催化作用 水处理 核化学 材料科学 环境工程 纳米技术 荧光 有机化学 工程类 物理 电信 量子力学 计算机科学
作者
Hanchao Zhang,Pu-Can Guo,Xin Zhang,Guo‐Ping Sheng
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:403: 126324-126324 被引量:46
标识
DOI:10.1016/j.cej.2020.126324
摘要

Persulfate activation is a promising advanced oxidation processes to remove micropollutants for the water purification. Persulfate could be activated by heat efficiently, but the continuous energy input limited its application. In this study, a novel photothermal method was developed to activate peroxydisulfate (PDS) to degrade sulfamethoxazole, a widely detected antibiotic in aqueous environments, for water purification. Using the carbon black as the photothermal conversion agent, both heating rate and equilibrium temperature of the solution were enhanced under the simulated sunlight, which was beneficial for PDS activation. By using the developed photothermally-activated PDS method, about 95% of sulfamethoxazole in the aqueous solution could be removed within 180 min, which was 3.28 times faster than that using the individual PDS activated by solar irradiation. Quenching experiment and the electron paramagnetic resonance proved that ·OH and SO4·- were the main species for pollutant degradation, and PDS decomposition at high temperature was the main mechanism for the PDS activation by photothermal method. In addition, this photothermally-activated PDS method also showed a great capacity for degrading SMX in the actual water. This work provides a novel and low cost persulfate activation technology for the contaminant removal from the aqueous solution, which shows a great application potential for water purification.
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
兴奋的天蓉完成签到,获得积分10
1秒前
2秒前
薯条发布了新的文献求助10
2秒前
Altria发布了新的文献求助10
3秒前
Altria发布了新的文献求助10
3秒前
li发布了新的文献求助10
4秒前
5秒前
姝涵完成签到 ,获得积分10
5秒前
6秒前
6秒前
冷酷冬卉完成签到,获得积分10
6秒前
ZHAO完成签到,获得积分10
7秒前
SunJay发布了新的文献求助10
7秒前
9秒前
11秒前
12秒前
sywang完成签到,获得积分10
12秒前
慕青应助有内涵采纳,获得10
12秒前
14秒前
机灵的芷珊完成签到,获得积分10
15秒前
盛夏完成签到,获得积分10
16秒前
17秒前
18秒前
18秒前
19秒前
英姑应助山海采纳,获得10
20秒前
21秒前
22秒前
郭莹莹发布了新的文献求助10
24秒前
Yang完成签到 ,获得积分10
24秒前
24秒前
24秒前
25秒前
26秒前
27秒前
科研通AI6.2应助小伙子采纳,获得10
28秒前
28秒前
科研菜鸟发布了新的文献求助30
29秒前
29秒前
我3发布了新的文献求助10
30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 7600102
求助须知:如何正确求助?哪些是违规求助? 9176216
关于积分的说明 19648242
捐赠科研通 7176215
什么是DOI,文献DOI怎么找? 3268572
关于科研通互助平台的介绍 2433042
邀请新用户注册赠送积分活动 2262187