首页|磁性碳微球快速芬顿降解苯酚的研究

磁性碳微球快速芬顿降解苯酚的研究

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本研究以可溶性淀粉为碳源,磁性Fe3O4为赋磁剂,采用简单高效的水热碳化法,并在700℃活化,制备磁性碳微球(Fe3O4@CMSs)。并通过傅立叶红外光谱仪、X射线粉末衍射仪、扫描电镜、X射线光电子能谱、比表面积及孔径分析仪等对所得样品进行表征分析。用苯酚溶液模拟有机废液,考察Fe3O4@CMSs的降解性能及可能的降解机理,考察Fe3O4@CMSs的添加量、溶液体系的pH、H2O2用量、温度以及反应时间对苯酚的降解性能影响,研究表明,当苯酚溶液浓度为100mg·L-1,Fe3O4@CMSs的添加量为2 g·L-1,溶液pH为5,H2O2添加量为0。6mL·L-1时,室温下降解5 min,苯酚能够完全降解。通过淬灭实验发现,·O2-、·OH、1O2均参与了反应体系中苯酚的降解,且循环利用实验表明Fe3O4@CMSs循环利用四次后降解率仍有88%以上。
Rapid fenton degradation of phenol by magnetic carbon microspheres
Magnetic carbon microspheres(Fe3O4@CMSs)were prepared by a simple and efficient hydrothermal carbonisation meth-od using soluble starch as a carbon source and magnetic Fe3O4 as a magnetic excipient,and activated at 700 ℃.The resulting sam-ples were also characterised and analysed by Fourier infrared spectrometer,X-ray powder diffractometer,scanning electron micro-scope,X-ray photoelectron spectroscopy,specific surface area and pore size analyser.Phenol solution was used to simulate the or-ganic waste solution to investigate the degradation performance of Fe3O4@CMSs and the possible degradation mechanism,and the effects of the addition of Fe3O4@CMSs,the pH of the solution system,the amount of H2O2,the temperature,and the reaction time on the degradation performance of phenol were investigated.The results showed that phenol could be completely degraded when the concentration of phenol solution was 100 mg·L-1,the addition of Fe3O4@CMSs was 2 g·L-1,the pH of the solution was 5,and the addition of H2O2 was 0.6 mL·L-1,the temperature of the reaction was room temperature,and the time of the reaction was 5 min.The quenching experiments revealed that·O2-,OH,and1O2 were all involved in the degradation of phenol in the reaction system.The recycling experiment showed that the degradation rate of Fe3O4@CMSs was still more than 88%after four times of recycling.

Fe3O4@CMSsphenolhydrothermal methoddegradation

黄云薇、冉源富、肖纯、操江飞

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肇庆学院环境与化学工程学院,广东 肇庆 526061

广东省环境健康与资源利用重点实验室,广东 肇庆 526061

Fe3O4@CMSs 苯酚 水热法 降解

2025

化学研究与应用
四川省化学化工学会 四川大学

化学研究与应用

北大核心
影响因子:0.555
ISSN:1004-1656
年,卷(期):2025.37(1)