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BiOCl/g-C3N4-Br光催化降解罗丹明BOA北大核心CSTPCD

Photocatalytic degradation of RhB by BiOCl/g-C3N4-Br

中文摘要英文摘要

采用原位生长法制备了二元异质结光催化剂BiOCl/g-C3N4-Br,运用多种技术手段对其进行了表征,考察了BiOCl/g-C3N4-Br在模拟可见光照射下对罗丹明(RhB)的光催化降解性能.表征结果显示,BiOCl附着在g-C3N4-Br表面,二者之间形成了Z-scheme异质结.实验结果表明:BiOCl/g-C3N4-Br催化剂比g-C3N4-Br和BiOCl具有更高的光催化活性,在RhB质量浓度20 mg/L、BiOCl/2%-g-C3N4-Br(g-C3N4-Br质量分数为2%)加入量0.5 g/L的条件下,经日光灯(14 W)照射90 min后,RhB去除率可达98%;经过4次循环实验后,RhB去除率从98%逐渐降低至90%,表现出良好的稳定性和可重复利用性.BiOCl/2%-g-C3N4-Br光催化降解RhB过程中发生的氧化还原反应分别在BiOCl和g-C3N4-Br的表面进行,BiOCl与g-C3N4-Br之间高度紧密的接触面形成了Z-scheme异质结,实现了电子和空穴的快速分离,降低了二者在催化剂内部的复合速率,提高了催化性能.

A binary heterojunction photocatalyst,BiOCl/g-C3N4-Br,was synthesized by in-situ growth method and characterized by XRD,SEM,FTIR,XPS,and UV-vis DRS.The photocatalytic degradation activity of BiOCl/g-C3N4-Br to RhB under simulated visible light irradiation was investigated.The experimental results show that:Compared to g-C3N4-Br and BiOCl alone,BiOCl/g-C3N4-Br exhibits significantly improved photocatalytic activity,and under the conditions of RhB mass concentration 20 mg/L,BiOCl/2%-g-C3N4-Br amount 5 g/L,fluorescent lamp power 40 W,and irradiation time 90 min,the RhB removal rate can reach 98%;After 4 cycles of reusing,the RhB removal rate gradually decreases from 98%to 90%,demonstrating good stability and reusability of the photocatalyst.The oxidation-reduction reactions in the photocatalytic degradation process occur on the surface of BiOCl and g-C3N4-Br,respectively.The Z-scheme heterojunction formed on the highly compact interface between BiOCl and g-C3N4-Br achieves rapid separation of electrons and holes and reduces their recombination rate inside the catalyst,thereby enhancing the catalytic performance.

孙天奇;陈勇号;巫衡;朱雨婷;董延茂;赵丹

苏州科技大学 环境科学与工程学院 城市生活污水资源化利用技术国家地方联合工程实验室,江苏 苏州 215009苏州科技大学 化学与生命科学学院,江苏 苏州 215009

环境科学

光催化异质结石墨相氮化碳氯氧化铋罗丹明B

photocatalysisheterojunctiongraphitic phase carbon nitride(g-C3N4)bismuth oxychloride(BiOCl)Rhodamine B(RhB)

《化工环保》 2024 (002)

196-204 / 9

苏州区域水质改善和水生态安全技术与综合示范项目(2017ZX07205);苏州市产业化前瞻项目(SYG201744).

10.3969/j.issn.1006-1878.2024.02.006

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