N-doped coal-based carbon membrane coupling peroxymonosulfate activation for bisphenol A degradation: The role of micro-carbon structure and nitrogen species

化学 热解 三聚氰胺 碳纤维 吸附 双酚A 电子转移 降级(电信) 氮气 化学工程 光化学 有机化学 材料科学 电信 生物化学 复合数 计算机科学 环氧树脂 复合材料 工程类
作者
Huanran Ma,Shuang Xu,Xiao Zhang,Zonglin Pan,Ruisong Xu,Pengcheng Wang,Tianjun Sun,Xinfei Fan,Chengwen Song,Tonghua Wang
出处
期刊:Journal of Cleaner Production [Elsevier BV]
卷期号:423: 138713-138713 被引量:16
标识
DOI:10.1016/j.jclepro.2023.138713
摘要

Herein, a novel N-doped coal-based carbon membrane (N-CCM) was prepared by using melamine as N source with high-temperature pyrolysis assistance. Through reasonable regulation of membrane micro-carbon structure and N species by varying pyrolysis temperature, the N-CCM integrated with peroxymonosulfate (PMS) activation under membrane filtration (MFPA) process showed excellent bisphenol A (BPA) removal of 98.3%. The excellent performance of N-CCM MFPA process was mainly owing to the following reason: For one thing, the more orderly micro-carbon structure of N-CCM possessed high defect density and boundary active sites under suitable pyrolysis temperature (700 °C), contributing to PMS activation (enhanced generation of reactive oxygen species (ROS) and electron transfer). For another, pyrrolic N, pyridinic N and C=C were beneficial to PMS adsorption and facilitate the electrons transfer from BPA to PMS. While C–O and graphitic N were responsible for the generation of ROS (SO4•−, •OH and 1O2). Theoretical calculations showed that the bond length of O–O, O–H and O–S in PMS adsorbed on C atom near N sites was significantly lengthened, corresponding to the generated ROS. Overall, the co-effect of radical process (SO4•− and •OH) and non-radical process (1O2 and electron transfer) achieved efficient BPA degradation in system.
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