亲爱的研友该休息了!由于当前在线用户较少,发布求助请尽量完整地填写文献信息,科研通机器人24小时在线,伴您度过漫漫科研夜!身体可是革命的本钱,早点休息,好梦!

One-step synthesis of mixed valence FeOX nanoparticles supported on biomass activated carbon for degradation of bisphenol A by activating peroxydisulfate

过氧二硫酸盐 双酚A 活性炭 化学 纳米颗粒 煅烧 X射线光电子能谱 扫描电子显微镜 碳化 材料科学 催化作用 结晶度 化学工程 碳纤维 核化学 复合数 有机化学 纳米技术 复合材料 吸附 环氧树脂 工程类
作者
Xin Li,Shengxiao Zhang,Mingming Zhang,Mingwu Yu,Hou Chen,Huawei Yang,Qiang Xu
出处
期刊:Journal of Hazardous Materials [Elsevier BV]
卷期号:409: 124990-124990 被引量:50
标识
DOI:10.1016/j.jhazmat.2020.124990
摘要

Abstract A novel FeOX nanoparticles supported biomass activated carbon (BAC/FeOX) composite was prepared through one-pot calcination method with FeCl3 and cherry stone powder as precursors. The carbonization of biomass, reduction of Fe3+, and FeOX anchored on carbon substrate could be achieved at the same time. Characterization with transmission electron microscope (TEM) and scanning electron microscope indicated that nanoscale FeOX distributed uniformly on carbon substrate, and X-ray photoelectron spectroscopy, X-ray diffraction, and high resolution TEM characterization proved that the loaded FeOX was high crystallinity of Fe3O4 and α-Fe0. Bisphenol A (BPA) was used to investigate the degradation performance of BAC/FeOX activating peroxydisulfate (PDS). The ratio of raw materials affected degradation efficiency of BPA intensively through the content, valence state, and dispersibility of FeOX nanoparticles, and the optimal material could degrade 20 mg/L BPA completely in 5 min at 0.1 g/L in the presence of 1 g/L PDS. Free radical determination and quenching experiments indicated that both SO4•− and •OH were involved in BPA degradation. The degradation pathway was proposed based on the identification of degradation intermediates. The facile synthesis method, high activation efficiency, and low-cost and environmental friendly raw materials made the BAC/FeOX-50 an alternative catalyst for organic pollution water treatment.
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
Nole应助Alex013采纳,获得10
1秒前
大大完成签到 ,获得积分10
4秒前
斯文败类应助科研通管家采纳,获得10
7秒前
Kao应助科研通管家采纳,获得10
7秒前
Kao应助科研通管家采纳,获得10
7秒前
Ava应助科研通管家采纳,获得10
8秒前
Kao应助科研通管家采纳,获得10
8秒前
13秒前
听听发布了新的文献求助10
18秒前
李木头完成签到,获得积分10
20秒前
香蕉觅云应助饱满如风采纳,获得10
38秒前
听听完成签到,获得积分10
40秒前
无奈的琦完成签到,获得积分10
43秒前
44秒前
44秒前
复杂鸵鸟完成签到,获得积分10
45秒前
蓝朱发布了新的文献求助30
48秒前
饱满如风发布了新的文献求助10
50秒前
irene完成签到,获得积分10
53秒前
李爱国应助陈运气采纳,获得10
58秒前
睡不醒发布了新的文献求助10
58秒前
1分钟前
1分钟前
陈运气发布了新的文献求助10
1分钟前
清脆的惜萍完成签到,获得积分10
1分钟前
1分钟前
神勇千秋完成签到,获得积分10
1分钟前
1分钟前
平常以云完成签到 ,获得积分10
1分钟前
2分钟前
小蘑菇应助KKSun采纳,获得10
2分钟前
2分钟前
Kao应助科研通管家采纳,获得10
2分钟前
Kao应助科研通管家采纳,获得10
2分钟前
Kao应助科研通管家采纳,获得10
2分钟前
谦让的鹤轩完成签到,获得积分10
2分钟前
活力傲柏完成签到,获得积分10
2分钟前
Owen应助昏睡的金毛采纳,获得10
2分钟前
2分钟前
2分钟前
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
China Pluperfect I: Epistemology of Past and Outside in Chinese Art 520
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
Cosmos as Art Object: Studies in Plato's Timaeus and Other Dialogues 500
What is the Future of Psychotherapy in Digital Age? Technology, AI Bots, and Psychotherapy after Covid 444
Management and the Arts 310
Teaching Social and Emotional Learning in Physical Education 300
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 7633712
求助须知:如何正确求助?哪些是违规求助? 9207872
关于积分的说明 19748106
捐赠科研通 7202236
什么是DOI,文献DOI怎么找? 3274994
关于科研通互助平台的介绍 2436914
邀请新用户注册赠送积分活动 2271826