Photodegradation of rhodamine B with molecular oxygen catalyzed by a novel unsymmetrical iron porphyrazine under simulated sunlight

被引:15
作者
Zhang, Zehui [1 ]
Wen, Xiaoye
Deng, Kejian
Zhang, Bingguang
Lv, Kangle
Sun, Jie
机构
[1] South Cent Univ Nationalities, Dept Chem, Key Lab Catalysis & Mat Sci, State Ethn Affairs Commiss, Wuhan, Peoples R China
基金
中国国家自然科学基金;
关键词
VISIBLE-LIGHT IRRADIATION; PHOTOCATALYTIC DEGRADATION; OXIDATIVE-DEGRADATION; CHLORINATED PHENOLS; POLLUTANTS; TIO2; COMPLEXES; DYE; PHOTOOXIDATION; TRANSFORMATION;
D O I
10.1039/c3cy20879f
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A novel unsymmetric biomimetic catalyst iron(II) (1,4-dithiin)(3)-4-pentyloxyphenyl-porphyrazine [abbreviated as FePzPh(1,4-dithiin)(3)] was successfully synthesized by a template method. Its photocatalytic activity was evaluated by the degradation of rhodamine B under solar-simulating Xe lamp irradiation. A high degradation ratio and TOC removal were achieved in 97.3% and 70%, respectively, at pH 9.18 in 100 min. Wavelength filter experiments demonstrated that the small portion of light with the wavelength shorter than 420 nm played a significant role in the activation of molecule oxygen to degrade RhB. The photocatalytic activity of this unsymmetric catalyst FePzPh(1,4-dithiin)(3) is higher than its symmetric matrix. Hydroxyl radicals were detected as a main reactive oxidative species, and a possible mechanism of the activation of molecular oxygen catalyzed by FePzPh(1,4-dithiin)(3) was proposed.
引用
收藏
页码:1415 / 1422
页数:8
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