Photo-Fenton reaction of supported cationic cyclopentadienyl iron complexes of arene and application as heterogeneous catalysts in photodegradation of dyes under visible light

被引:8
作者
Chen, Yu [2 ]
Jin, Shao [2 ]
Liu, Jiqiang [2 ]
Zhao, Baodong [2 ]
Wang, Tao [1 ,2 ]
机构
[1] Beijing Univ Chem Technol, Coll Sci, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China
[2] Beijing Univ Chem Technol, Dept Organ Chem, Coll Sci, Beijing 100029, Peoples R China
基金
中国国家自然科学基金;
关键词
Cationic cyclopentadienyl iron complexes; Electron transfer; Photo-Fenton; Visible light; Organic dye; AZO-DYE; ORANGE-II; NICKEL(II) COMPLEXES; MOLECULAR-OXYGEN; FE-NANOCOMPOSITE; DEGRADATION; OXIDATION; DECOLORIZATION; MINERALIZATION; DISCOLORATION;
D O I
10.1016/j.ica.2013.07.005
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Cationic cyclopentadienyl iron complexes of arene ([CpFeAr](+)) were successfully loaded on silica gel (SiO) by physical absorption. The supported [CpFeAr](+) ([CpFeAr](+)/SiO) catalysts were characterized by SEM-EDX, FT-IR and UV-Vis spectra. The catalysts show strong and broad absorptions from 200 to 550 nm. [CpFeAr](+)/SiO carries out an effective photo-Fenton reaction with H2O2 under visible light for the photodegradations of organic dyes. Nearly total decolorations of rhodamine B (RhB) and crystal violet (CV) dyes were achieved by using [CpFeAr](+)/SiO as the heterogeneous catalyst. Hydroxyl radicals (center dot OH) were found in the photodegradation system of [CpFeAr](+)/SiO, H2O2 and dyes under visible light. The negative Delta G(el) values of CV/[CpFeAr](+) and RhB/[CpFeAr](+) systems indicate that the electron transfer processes for the dye/CpFe+ Ar systems are thermodynamically allowed. The possible mechanism for the degradation process of organic dyes in photo-Fenton reaction of [CpFeAr](+)/SiO with H2O2 is proposed. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:37 / 43
页数:7
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