The role of nanoparticulate agglomerates in TiO2 photocatalysis: degradation of oxalic acid

被引:16
作者
Ivanova, Irina [1 ]
Mendive, Cecilia B. [2 ]
Bahnemann, Detlef [1 ,3 ]
机构
[1] Leibniz Univ Hannover, Inst Tech Chem, Callinstr 3, D-30167 Hannover, Germany
[2] Univ Nacl Mar del Plata, Fac Ciencias Exactas & Nat, Dept Quim, Dean Funes 3350, RA-7600 Mar Del Plata, Buenos Aires, Argentina
[3] St Petersburg State Univ, Lab Photoact Nanocomposite Mat, Ulyanovskaya Str 1, St Petersburg 198504, Russia
关键词
Semiconductor nanoparticles; Deaggregation; Photocatalysis; TiO2; Oxalic acid; SURFACE SCIENCE; ADSORPTION; SEMICONDUCTORS; MECHANISM; ISOTHERM; KINETICS; OXALATE; WATER;
D O I
10.1007/s11051-016-3495-x
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The simultaneous bimodal study of the photocatalytic oxalic acid degradation by aqueous TiO2 suspensions revealed that particular systems possess the capacity to protect a certain amount of oxalic acid from oxidation, thus hindering, to some extent, the photocatalytic reaction. While measurements of the oxalic acid concentration in the bulk liquid phase indicated full photocatalytic degradation; in situ pH-stat measurements allowed the quantification of the amount of oxalic acid remaining in the part of the nanoparticulate agglomerates where light could apparently not access. An explanation for this phenomenon takes into account the possibility of the formation of TiO2 agglomerates in which these molecules are hidden from the effect of the light, thus being protected from photocatalytic degradation. Studies of different TiO2 materials with different particle sizes allowed a deeper exploration of this phenomenon. In addition, because this property of encapsulating pollutant molecules by photocatalytic systems is found to be a reversible phenomenon, P25 appears to be more convenient and advantageous as compared to the use of large surface area photocatalysts. Fig.: Deaggregation of TiO2 particle agglomerates upon UV illumination.
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页数:13
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