ZIF-67衍生Co3O4/g-C3N4复合材料光催化降解盐酸四环素废水的研究

梁月明, 董海山, 王栋, 刘航

现代化工 ›› 2024, Vol. 44 ›› Issue (4) : 186 -190.

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现代化工 ›› 2024, Vol. 44 ›› Issue (4) : 186-190. DOI: 10.16606/j.cnki.issn0253-4320.2024.04.035
科研与开发

ZIF-67衍生Co3O4/g-C3N4复合材料光催化降解盐酸四环素废水的研究

    梁月明, 董海山, 王栋, 刘航
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Photocatalytic degradation of tetracycline hydrochloride-containing wastewater by ZIF-67 derived Co3O4/g-C3N4 composites

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摘要

将ZIF-67与g-C3N4按一定质量比复合制备Co3O4/g-C3N4复合光催化材料,并以此来提高Co3O4的光催化性能。利用XRD、SEM和FT-IR对复合材料结构、性能和元素分布进行表征。结果表明,当盐酸四环素(TC-HCl)质量浓度为 3 mg/L、质量分数为3%的Co3O4/g-C3N4投加量为15 mg且pH为中性时,催化剂光催化性能最佳,90 min降解盐酸四环素效率达到了91.1%。3% Co3O4/g-C3N4复合光催化剂重复使用5次后,其降解率仍可达到88.5%,表明该材料具有一定的光催化稳定性和重复利用性。体系自由基捕获实验证明,产生了·O-2、h+、·OH 3种自由基,其中·O-2在Co3O4/g-C3N4光催化降解TC-HCl中发挥主要作用。

Abstract

To improve the photocatalytic performance of Co3O4,a Co3O4/g-C3N4 composite photocatalytic material is prepared from ZIF-67 and g-C3N4 through calcining ZIF-67 with MOF template.The structure,properties and elements distribution of the prepared samples are characterized by means of XRD,SEM and FT-IR.The results show that the catalyst exhibits the best photocatalytic performance with a degradation efficiency of 91.1% in 90 min when the concentration of tetracycline hydrochloride is 3 mg·L-1,the dosage of Co3O4/g-C3N4 with a mass ratio of 3% is 15 mg and pH is neutral.The degradation rate can still reach 88.5% after the 3% Co3O4/g-C3N4 composite photocatalyst has been reused for 5 times,indicating a certain photocatalytic stability and reusability.It is verified through system radical capture experiments that three kinds of free radicals including ·O2-,h+ and ·OH are produced,among them ·O2- plays a major role in the photocatalytic degradation of tetracycline hydrochloride by Co3O4/g-C3N4.

关键词

光催化 / MOFs / Co3O4 / 盐酸四环素

Key words

photocatalysis / MOFs / Co3O4 / tetracycline hydrochloride

Author summay

梁月明(1998-),女,硕士生,研究方向为水污染控制工程,2970501848@qq.com;董海山(1975-),男,博士,副教授,研究方向为水污染控制工程,通讯联系人,1305080092@qq.com。

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ZIF-67衍生Co3O4/g-C3N4复合材料光催化降解盐酸四环素废水的研究[J]. 现代化工, 2024, 44(4): 186-190 DOI:10.16606/j.cnki.issn0253-4320.2024.04.035

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