首页|尿素改性Bi2MoO6摩擦催化氧化降解罗丹明B

尿素改性Bi2MoO6摩擦催化氧化降解罗丹明B

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通过水热法制备了尿素改性Bi2MoO6(Urea-Bi2MoO6)催化剂,借助SEM,XRD,XPS,BET等技术表征了其微观结构。经过尿素改性的Bi2MoO6结晶度提高,具有优异的摩擦催化性能。在转速为700r/min,RhB浓度为5mg/L,催化剂投加量为1g/L,35mm PTFE磁子的条件下,反应300min,RhB的降解率达99。02%。Urea-Bi2MoO6摩擦催化氧化降解RhB符合一级反应动力学方程。Urea-Bi2MoO6循环利用5次以后,RhB降解率仍在91。6%以上。EPR证实Urea-Bi2MoO6摩擦催化过程中产生了 h+,O2-和·OH自由基,自由基猝灭实验证实h+是导致RhB降解的主要物质,Urea-Bi2MoO6受到摩擦刺激,产生电子(e-)-空穴(h+)对。h+与游离的OH-反应生成·OH,e-与水中的O2生成·O2-,三者协同降解RhB。
Urea-modified Bi2MoO6 friction-catalyzed oxidative degradation of rhodamine B
Urea modified Bi2MoO6(Urea-Bi2MoO6)catalyst was prepared by a hydrothermal method,and its microstructure was characterized by SEM,XRD,XPS,BET,etc.The crystallinity of Bi2MoO6 modified by urea was improved,and it exhibited excellent frictional catalytic performance.Under the conditions of a rotational speed of 700r/min,RhB initial concentration of 5mg/L,catalyst dosage of 1g/L,and 35mm PTFE magnetic particles,the degradation of RhB reached 99.02%after 300min.The friction catalyzed oxidation degradation of RhB by Urea-Bi2MoO6 followed first-order reaction kinetics equation After 5cycles of Urea-Bi2MoO6 friction catalysis,RhB degradation remained above 91.6%.EPR confirmed that h+,·O2-,and·OH radicals were generated during the friction catalytic process of Urea Bi2MoO6.And scavenger test for radicals confirmed that h+was the main substance causing RhB to be degraded.Urea-Bi2MoO6 is stimulated by friction,producing electron(e)-hole(h+)pairs.H+reacts with OH-to generate·OH,and e reacts with O2 in water to generate·O2-,then RhB is degraded by them.

RhBtribocatalysisBi2MoO6urea modification

邢玉鲁、薛怡然、陈柠、史焕鑫、徐浩、高博、张留科、马丙瑞、赵宝秀、李金成

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青岛理工大学环境与市政工程学院,山东 青岛 266525

罗丹明B 摩擦催化 Bi2MoO6 尿素改性

国家自然科学基金资助项目国家自然科学基金资助项目山东省自然科学基金山东省自然科学基金山东省自然科学基金

5217433620709026ZR2019MEE097ZR2020ME256ZR2021MB051

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(10)