ICCAS OpenIR
Reaction mechanism of Fe(III) participated photocatalytic degradation of X3B over TiO2
Lu, XJ; Xu, YM; Wang, Z; Zhao, JC; Wu, YD
2004-08-28
Source PublicationACTA CHIMICA SINICA
ISSN0567-7351
Volume62Issue:16Pages:1455-1459
AbstractFerric ions present in an acidic aqueous suspension of TiO2 can promote significantly the photocatalytic degradation of a textile dye X3B upon UV light irradiation (lambdagreater than or equal to320 nm). The initial rate of X3B degradation was observed to increase expotentially with the initial concentration of Fe (III). However, this enhancement disappeared as all ferric species Here transferred into ferrous ions, and after that the degradation of X3B proceeded via a regular pathway of photocatalysis. Several control experiments revealed that the beneficial effect of Fe (III) was attributed mainly to electron trapping at the semiconductor surface, whereas the contribution from homogeneous Fe (III) photolysis, capable of producing hydroxyl radicals, was not significant. In the liquid phase, more than 98.2% of Fe(II) was detected, implying that the involvement of (Photo)-Fenton reaction was less possible. On the other hand, the ferrous ion, once prod iced, exhibited no obvious effect on X3B degradation, but its formation became faster in the presence of X3B, suggesting that hole oxidation of X3B might be involved as well. Both Fe ( III) and X3B were adsorbed strongly on the catalyst surface, allowing efficient separation and utilization of the electron-hole pairs, whereas Fe(II) was hardly adsorbed, which probably was one of the reasons that Fe(II) could not be re-oxidized in situ by hole or other reactive species generated in the system. Moreover, the increase in the initial pH from 1.6 to 3.7 did not affect obviously the initiate rate of X3B degradation, but led to significant decrease in the initial rate of Fe(II) formation. Together with the exponential increase of Fe (II) formation rate with initial Fe ( III) concentration, the primary evidence suggests that the efficiency of electron trapping by Fe(III), similar to Fe(III) photolysis, is also dependent of ferric species polymerization on the surface. The results obtained in this work will be relevant to the study on Fe-doped photocatalyst.
KeywordTitanium Dioxide Ferric Ion Reactive Dye Photocatalysis Mechanism
Indexed BySCI
Language英语
WOS IDWOS:000223627900001
PublisherSCIENCE CHINA PRESS
Citation statistics
Cited Times:10[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.iccas.ac.cn/handle/121111/81674
Collection中国科学院化学研究所
Corresponding AuthorLu, XJ
Affiliation1.Zhejiang Univ, Dept Chem, Hangzhou 310027, Peoples R China
2.Chinese Acad Sci, Inst Chem, Lab Photochem, Beijing 100080, Peoples R China
Recommended Citation
GB/T 7714
Lu, XJ,Xu, YM,Wang, Z,et al. Reaction mechanism of Fe(III) participated photocatalytic degradation of X3B over TiO2[J]. ACTA CHIMICA SINICA,2004,62(16):1455-1459.
APA Lu, XJ,Xu, YM,Wang, Z,Zhao, JC,&Wu, YD.(2004).Reaction mechanism of Fe(III) participated photocatalytic degradation of X3B over TiO2.ACTA CHIMICA SINICA,62(16),1455-1459.
MLA Lu, XJ,et al."Reaction mechanism of Fe(III) participated photocatalytic degradation of X3B over TiO2".ACTA CHIMICA SINICA 62.16(2004):1455-1459.
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