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.
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