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磁性复合材料活化过硫酸盐去除水中双酚A

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将Fe3O4负载于具有二维层状结构的MXene,形成磁性三明治复合材料Fe3O4@MXene,活化过硫酸盐(PMS)去除水中的双酚A(BPA)。探讨了 PMS投加量、Fe3O4@MXene投加量、溶液初始pH值、BPA初始溶液浓度对BPA降解的影响。结果表明,BPA的降解符合准一级反应动力学。在25℃,BPA浓度25mg/L,Fe3O4@MXene投加量0。3g/L,PMS投加量3。3mmol/L,pH=6。0的条件下,反应90min后,BPA的降解率达97。4%。自由基淬灭实验及EPR实验证实,羟基自由基和硫酸根自由基是降解BPA的主导活性氧物种,此外单线氧也参与了降解。经由MXene负载的Fe3O4颗粒大小分布均匀,活性及稳定性均显著提高,MXene表面的Ti原子加速了 Fe(Ⅱ)/Fe(Ⅲ)循环,从而加速了 PMS活化。因此,Fe3O4@MXene可作为理想的过硫酸盐高级氧化过程的非均相催化剂。
Removing bisphenol A with magnetic sandwich composite activated peroxymonosulfate
The magnetic sandwich composite Fe3O4@MXene was prepared to activate peroxymonosulfate(PMS)for removing Bisphenol A(BPA)from water.The effects of PMS dosage,Fe3O4@MXene dosage,initial solution pH value and initial BPA concentration on BPA degradation were investigated.The results show that the degradation of BPA conformed to the quasi-first order reaction kinetics.At 25℃,the combination of Fe3O4@MXene dosage of 0.3g/L,PMS dosage of 1.01g/L and initial pH of 6.0could degrade 97.4%of BPA(25mg/L)after 90-minute,in which hydroxyl radical and sulfate radical were the dominant reactive oxygen species for BPA degradation despite having singlet oxygen involved.The MXene-supported Fe3O4 particles showed a uniform size distribution with obviously improved activity and stability.The Ti atoms on the surface of MXene helped accelerate the Fe(Ⅱ)/Fe(Ⅲ)redox cycle,which thus improved PMS activation.Evidently,the Fe3O4@MXene can be used as an ideal heterogeneous catalyst for the advanced oxidation process of persulfate.

Fe3O4@MXene compositeadvanced oxidationbisphenol Aheterogeneous system

周宇辉、林洋仟、王御豪、杨盈、徐西蒙

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昆明理工大学建筑工程学院,云南昆明 650500

Fe3O4@MXene复合物 高级氧化 双酚A 非均相体系

国家自然科学基金云南省基础研究计划云南省教育厅科研项目

421774641405202102192023Y0430

2024

中国环境科学
中国环境科学学会

中国环境科学

CSTPCDCHSSCD北大核心
影响因子:2.174
ISSN:1000-6923
年,卷(期):2024.44(2)
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