首页|松木基多孔碳表面重构强化过硫酸盐去除双酚A

松木基多孔碳表面重构强化过硫酸盐去除双酚A

扫码查看
双酚A(BPA)作为最常用的工业化合物之一,在环境中具有持久性,对人类健康及其他微生物造成威胁,因此,开发双酚A高性能去除剂并了解其作用机制具有重要意义.基于此,采用KOH活化策略制备了松木基多孔碳(PC),利用NaBH4对PC进行表面重构获得性能增强的松木基多孔碳(PC-1).随后,采用单因素的实验方法考察了在多孔碳/过硫酸盐系统中松木基多孔碳去除BPA的能力及机制.结果表明,与PC相比,PC-1表面的羟基增加,羰基减少,ID/IG从1.55增至1.60.与PC/PDS系统相比,PC-1/PDS系统在反应温度为25、35及45℃时对BPA的降解效率分别提高了 45%、18%和64%.淬火及电化学实验说明PC及PC-1分别通过自由基及非自由基途径去除BPA.因此,碳的内在缺陷是过硫酸盐活化的活性位点,而含氧官能团则是影响活化途径的关键因素.
Surface reconfiguration of pine-based porous carbon enhanced persulfate for removing bisphenol A
Bisphenol A(BPA),one kind of the most widely-used industrial compounds,is persistent in the environment and poses threat to human health and other microorganisms.Consequently,it is of great significance in developing high-performance removers and understanding their action mechanisms.Based on this,this work used as-prepared pine-based porous carbon(PC)using KOH activation and surface reconstruction for PC using NaBH4 to obtain pine-based porous carbon with enhanced properties(PC-1).Subsequently,a single-factor experimental was used to investigate the ability and mechanism of bisphenol A removal by PC and PC-1 in the persulfate system.Compared to PC,PC-1 exhibited an increase in surface hydroxyl groups,a decrease in carbonyl groups,and an increase in the value of ID1/IG from 1.55 to 1.60.Compared with the PC/PDS system,the PC-1/PDS system improved the degradation efficiency of BPA by 45%,18%,and 64%at 25,35,and 45 ℃,respec-tively.Additionally,quenching and electrochemical experiments illustrated the removal of BPA by PC and PC-1 via radical and non-radical pathways,respectively.The intrinsic defects of carbon were the active sites for persulfate activation,while oxygen-containing functional groups were the key factors in-fluencing the activation pathway.

Bisphenol APorous carbonSurface reconstructionPersulfateRemoval rate

王亮才、陈登宇、周建斌

展开 >

南京林业大学材料科学与工程学院,江苏南京 210037

双酚A 多孔碳 表面重构 过硫酸盐 去除率

国家自然科学基金江苏省研究生科研与实践创新计划

52076112KYCX23_1185

2024

能源环境保护
煤炭科学研究总院杭州环境保护研究所

能源环境保护

影响因子:0.472
ISSN:1006-8759
年,卷(期):2024.38(2)
  • 50