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!

New functionalization approach synthesis of Sulfur doped, Nitrogen doped and Co-doped porous carbon: Superior metal-free Carbocatalyst for the catalytic oxidation of aqueous organics pollutants

表面改性 催化作用 杂原子 化学 碳纤维 硫黄 石墨氮化碳 热解 三聚氰胺 化学工程 兴奋剂 硫脲 无机化学 材料科学 有机化学 光催化 复合材料 物理化学 工程类 复合数 戒指(化学) 光电子学
作者
Zakaria Anfar,Abdellah Ait El Fakir,Mohamed Zbair,Zakaria Hafidi,Abdallah Amedlous,Mohammed Majdoub,Salaheddine Farsad,Asma Amjlef,Amane Jada,Noureddine El Alem
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:405: 126660-126660 被引量:69
标识
DOI:10.1016/j.cej.2020.126660
摘要

New green synthesis methods of novel commercially applicable carbocatalysts suitable for the catalytic oxidation of organic pollutants, remain a challenge. Herein, Nitrogen doped (N-PC), Sulfur doped (S-PC) and Co-doped (N, S-PC) porous carbon, were synthesized via a new facile environmentally functionalization approach followed by pyrolysis. Thus, Almond Shell (AS) as Bio-sourced material was used for porous carbon (PC) preparation as support. Thereafter, the introduction of Melamine, Diphenyl Disulfide and Thiourea on the PC matrix with high -COCl− and -CCl− groups facilitated the surface functionalization, and allowed us the introduction of high N and S heteroatoms contents in the PC networks surface. It was found that the optimized carbocatalysts could effectively activate PS, and exhibited excellent catalytic performances for the organic pollutants degradation, with an exceptionally low activation energy and fast kinetic reaction. Based on a systematic comparison, it was found that the N-PC exhibited the superior catalytic activity for activating the PS and degrading various organic pollutants. Such superior catalytic activity of the N-PC Carbocatalyst resulted from its high surface area, its low defect degree with the higher content of Graphitic-N. In addition, all experimental and theoretical investigations demonstrated the critical role of graphitic–N for the PS activation. It is expected that the doping process by N will significantly break the chemical inertness of the PC network and will make the N-PC surface more positively charged accelerating hence its interaction with the negatively charged S2O82−. Furthermore, the 1O2 was found to be the predominant reactive oxygen species (ROS) as assessed by radical scavenging tests and EPR experiments. The carbocatalysts were not easily influenced by the water aqueous phase, which give us more obvious advantages over the PS activation.

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
酷波er应助科研通管家采纳,获得10
21秒前
blenx完成签到,获得积分0
31秒前
大橘完成签到 ,获得积分10
34秒前
chenchen完成签到,获得积分10
1分钟前
wyx完成签到,获得积分10
1分钟前
chenchen发布了新的文献求助10
1分钟前
1分钟前
nono发布了新的文献求助10
1分钟前
甜瓜123完成签到,获得积分10
1分钟前
SciGPT应助nono采纳,获得10
1分钟前
领导范儿应助坚强雨双采纳,获得10
2分钟前
zicong发布了新的文献求助10
2分钟前
molihuakai应助科研通管家采纳,获得20
2分钟前
脆蜜金桔应助科研通管家采纳,获得10
2分钟前
doctorwan完成签到 ,获得积分10
2分钟前
zicong完成签到 ,获得积分10
2分钟前
2分钟前
战钺蟠龙发布了新的文献求助10
4分钟前
优秀的流沙完成签到,获得积分10
4分钟前
5分钟前
lk发布了新的文献求助10
5分钟前
6分钟前
6分钟前
小怪兽发布了新的文献求助10
6分钟前
nono发布了新的文献求助10
6分钟前
开放的乐驹完成签到 ,获得积分10
6分钟前
Demi_Ming完成签到,获得积分10
7分钟前
香蕉觅云应助7749采纳,获得10
7分钟前
JEREMIAH完成签到,获得积分10
7分钟前
nono完成签到,获得积分10
7分钟前
8分钟前
坚强雨双发布了新的文献求助10
8分钟前
坚强雨双完成签到,获得积分10
8分钟前
咖啡酸醋冰完成签到,获得积分10
8分钟前
成就书雪完成签到,获得积分10
8分钟前
9分钟前
7749发布了新的文献求助10
9分钟前
Sherry发布了新的文献求助10
9分钟前
斯文麦片完成签到 ,获得积分10
9分钟前
小马甲应助7749采纳,获得10
9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
晶种分解过程与铝酸钠溶液混合强度关系的探讨 8888
Chemistry and Physics of Carbon Volume 18 800
The Organometallic Chemistry of the Transition Metals 800
Leading Academic-Practice Partnerships in Nursing and Healthcare: A Paradigm for Change 800
The formation of Australian attitudes towards China, 1918-1941 640
Signals, Systems, and Signal Processing 610
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 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6427032
求助须知:如何正确求助?哪些是违规求助? 8244143
关于积分的说明 17527635
捐赠科研通 5482132
什么是DOI,文献DOI怎么找? 2894859
邀请新用户注册赠送积分活动 1870937
关于科研通互助平台的介绍 1709553