漂浮型BiOCl/EP光催化剂的原位合成及其光催化降解性能

尹金慧, 王帅, 刘湘

现代化工 ›› 2022, Vol. 42 ›› Issue (2) : 177 -182,187.

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现代化工 ›› 2022, Vol. 42 ›› Issue (2) : 177-182,187. DOI: 10.16606/j.cnki.issn0253-4320.2022.02.036
科研与开发

漂浮型BiOCl/EP光催化剂的原位合成及其光催化降解性能

    尹金慧, 王帅, 刘湘
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In situ synthesis of floating BiOCl/EP photocatalyst and its photocatalytic degradation performance

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摘要

通过原位沉积法将BiOCl负载到膨胀珍珠岩(EP)孔隙表面,制备出新型漂浮型BiOCl/EP光催化剂,并通过一系列手段对样品进行表征。结果表明,在模拟太阳光照射下,BiOCl/EP复合材料在125 min内对100 mL 15 mg/L罗丹明B溶液的降解率可达95.8%,远高于纯BiOCl。光催化活性的提高主要归因于BiOCl/EP复合材料中的Bi—O—Si键可作为电子传输通道促进光生电子-空穴对的分离和迁移、更高效的太阳光能利用率以及活性氧物种产生的效率。经过5次连续循环使用后,该复合物的光催化降解效率仍可达到91.0%。

Abstract

A novel floating BiOCl/EP photocatalyst is prepared by loading BiOCl onto the pores surface of expanded perlite (EP) through in situ deposition method.The prepared BiOCl/EP photocatalyst is characterized by a series of instruments.The results show that the degradation rate of Rhodamine B reaches 95.8% when 100 mL of Rhodamine B solution with a concentration of 15 mg·L-1 has been degraded by BiOCl/EP photocatalyst under simulated solar-light irradiation for 125 min, which is much higher than that by pure BiOCl.The enhancement in photocatalytic activity of BiOCl/EP composite can be mainly attributed to high-efficiency photogenerated electron-hole pair separation and migration via the formed Bi—O—Si bonds in BiOCl/EP, high-efficiency solar-light utilization and more reactive oxygen species (ROSs) production.The photocatalytic efficiency of BiOCl/EP still reaches 91.0% even after it has been used for 5 consecutive cycles.

关键词

BiOCl / 模拟太阳光驱动 / 漂浮型光催化剂 / 膨胀珍珠岩

Key words

BiOCl / simulated solar light driven / floating photocatalyst / expanded perlite

Author summay

尹金慧(1996-),女,硕士研究生,研究方向为铋基光催化材料,yinjinhui0811@qq.com

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漂浮型BiOCl/EP光催化剂的原位合成及其光催化降解性能[J]. 现代化工, 2022, 42(2): 177-182,187 DOI:10.16606/j.cnki.issn0253-4320.2022.02.036

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