Fenton-like degradation of rhodamine B over highly durable Cu-embedded alumina: Kinetics and mechanism

被引:56
|
作者
Sheng, Yiyi [1 ]
Sun, Yang [1 ]
Xu, Jing [1 ]
Zhang, Jie [2 ]
Han, Yi-Fan [2 ]
机构
[1] East China Univ Sci & Technol, State Key Lab Chem Engn, Shanghai 200237, Peoples R China
[2] Zhengzhou Univ, Sch Chem Engn & Energy, Res Ctr Heterogeneous Catalysis & Engn Sci, Zhengzhou 450001, Henan, Peoples R China
基金
美国国家科学基金会;
关键词
Fenton-like catalyst; Cu-embedded alumina; dynamic structure; RhB degradation; hydroxyl radicals; kinetics; VISIBLE-LIGHT IRRADIATION; WET PEROXIDE OXIDATION; HETEROGENEOUS FENTON; PHOTOCATALYTIC DEGRADATION; CATALYTIC-ACTIVITY; MESOPOROUS CARBON; AQUEOUS-SOLUTIONS; WASTE-WATER; AZO-DYE; IRON;
D O I
10.1002/aic.15937
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Cu-embedded mesoporous alumina, as a Fenton-like catalyst prepared via a sol-gel method, showed excellent activity and durability for the degradation of refectory compounds. The origin of active sites for the generation of hydroxyl radicals (center dot OH) were thoroughly studied using multitechniques. Cu, as the only active element, could be penetrated into the bulk of alumina and some Cu atoms were embedded into the framework. The dynamic structure of surface Cu species (the variety of Cu+/Cu2+ ratio) during the reaction were determined as well. Furthermore, the structure plasticity of catalyst has proved by optimizing preparation and reaction conditions. A 98.53% degradation of RhB was recorded within 30 min, following a pseudo-first-order reaction rate expression. Electron spin resonance spectra and center dot OH scavenging experiments have confirmed that center dot OH is the main reactive oxidant for the elimination of RhB. By the surface-enhanced Raman spectroscopy and gas chromatography-mass spectrometer results, plausible pathways of RhB degradation were elaborated. (c) 2017 American Institute of Chemical Engineers AIChE J, 64: 538-549, 2018
引用
收藏
页码:538 / 549
页数:12
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