Mesoporous sulfur-modified iron oxide as an effective Fenton-like catalyst for degradation of bisphenol A

介孔材料 X射线光电子能谱 催化作用 硫黄 氧化铁 赤铁矿 激进的 反应速率常数 化学 核化学 无机化学 降级(电信) 傅里叶变换红外光谱 比表面积 化学工程 动力学 双酚A 氧化物 矿物学 有机化学 环氧树脂 计算机科学 工程类 物理 电信 量子力学
作者
Jiangkun Du,Jianguo Bao,Xiaoyan Fu,Chenghang Lu,Sang Hoon Kim
出处
期刊:Applied Catalysis B-environmental [Elsevier BV]
卷期号:184: 132-141 被引量:222
标识
DOI:10.1016/j.apcatb.2015.11.015
摘要

A mesoporous sulfur-modified iron oxide (MS-Fe) was prepared as a heterogeneous H2O2 catalyst for degradation of BPA. The physico-chemical properties of MS-Fe and bare M-Fe were characterized by BET surface area measurement, SEM, XRD, FTIR and XPS. Both M-Fe and MS-Fe composites appeared as cubic microparticles with abundant pores and cracks as well as large surface area. As depicted by XRD, EDX and XPS, M-Fe is mainly consisted of hematite while MS-Fe is a kind of S-doped iron oxide with about 5–6% of sulfur element in terms of atomic ratio. In contrast to the poor catalytic activity of bare M-Fe, the MS-Fe composites showed greatly improved efficiencies for H2O2 activation for BPA degradation. The high catalytic activity of this new Fenton-like catalyst can be obtained at different initial pH in range of 3.0–9.0. The time evolution of degradation of BPA followed pseudo-first-order kinetics, and the first-order rate constants showed a linear relationship with parameters of initial pH, catalyst dosage and concentration of BPA. However, the H2O2 dosage showed a dual effect on BPA degradation because excessive H2O2 addition lead to scavenging of hydroxyl radicals (OH). The investigation of working mechanisms of MS-Fe suggested a synergistic effect of homogeneous and heterogeneous degradation reaction, wherein a strong acidic environment, abundant surface-bonded hydroxyl group and electron-mediating effect of sulfur all contributed to fast activation of H2O2. Overall, this new material overcomes the limitation of narrow working pH range and shows a fast oxidation of BPA with a low H2O2 and catalyst dosage, would have a good potential for environmental application.
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
刚刚
MeiFanNao发布了新的文献求助10
刚刚
刚刚
单纯凝雁完成签到,获得积分10
刚刚
刚刚
汉堡包应助子偕采纳,获得10
刚刚
1秒前
1秒前
sawyer完成签到,获得积分10
1秒前
久心完成签到,获得积分20
1秒前
andyyyds完成签到,获得积分10
1秒前
科研通AI6.4应助一个薯片采纳,获得10
2秒前
2秒前
Doppo完成签到,获得积分20
2秒前
2秒前
孙小子完成签到,获得积分20
2秒前
Yy杨优秀发布了新的文献求助20
3秒前
3秒前
莫妮卡发布了新的文献求助10
3秒前
疯狂小硕完成签到,获得积分10
3秒前
moonlight发布了新的文献求助10
4秒前
汉堡包应助孤独的刺猬采纳,获得10
4秒前
4秒前
YONGLI完成签到,获得积分10
4秒前
5秒前
5秒前
耶耶完成签到,获得积分10
5秒前
5秒前
bigpluto完成签到,获得积分0
5秒前
黄鹂完成签到,获得积分10
5秒前
6秒前
HX完成签到,获得积分10
6秒前
keven应助anoxia采纳,获得30
6秒前
大模型应助范范采纳,获得10
6秒前
duoCGA应助阿波采纳,获得10
6秒前
hahacsw发布了新的文献求助10
6秒前
6秒前
今后应助查重采纳,获得10
6秒前
7秒前
7秒前
高分求助中
Principles of Economics, 11th Edition 10000
University Physics with Modern Physics, 16th edition 10000
(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
Matrix Methods in Data Mining and Pattern Recognition 510
Social Skills Improvement System-Rating Scales--Chinese Version 500
Dynamische Polarisation von H-1 und B-11 in (CH-3)-3NBH-3 500
CLSI M07 2024 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 7248505
求助须知:如何正确求助?哪些是违规求助? 8871371
关于积分的说明 18717578
捐赠科研通 6927645
什么是DOI,文献DOI怎么找? 3198390
关于科研通互助平台的介绍 2373952
邀请新用户注册赠送积分活动 2173150