Photocatalytic degradation of azo dye in TiO2 suspended solution

2001 ◽  
Vol 43 (2) ◽  
pp. 313-320 ◽  
Author(s):  
C.-H. Hung ◽  
P.-C. Chiang ◽  
C. Yuan ◽  
C.-Y. Chou

The photocatalysis of azo dye, Orange G, by P-25 anatase TiO2 was investigated in this research. The experiments were conducted in a batch reactor with TiO2 powder suspension. Four near-UV lamps were used as the light source. The experimental variables included solution pH level, amount of TiO2, illumination light intensity, and reaction time. A pseudo-first order reaction kinetic was proposed to simulate the photocatalytic degradation of Orange G in the batch reactor. More than 80% of 10 mg/L Orange G decomposition in 60-minute reaction time was observed in this study and fast decomposition of Orange G only occurred in the presence of both TiO2 and suitable light energy. Faster degradation of Orange G was achieved under acid conditions. The degradation rates of Orange G at pH = 3.0 were about two times faster than those at pH = 7.0. Faster degradation of azo dye was observed for greater irradiated light intensity and more TiO present during the reaction. The reaction rates were proportional to TiO2concentration and light intensity with the power order of 0.726 and 0.734, respectively.

2004 ◽  
Vol 6 (2) ◽  
pp. 73-80 ◽  
Author(s):  
Ceyda Senem Uyguner ◽  
Miray Bekbolet

The current study was conducted to investigate the photocatalytic degradation kinetics of humic acid at different light intensities using commercialTiO2powders. The pseudo first order kinetic model and Langmuir-Hinshelwood (L-H) rate equation in modified forms were used to compare the photocatalytic activities ofTiO2materials as a function of light intensity. Under constant irradiation conditions, the pseudo first order reaction rates as well as L-H rates were found to be decreasing in the following trend; Degussa P-25, Millennium PC-500 and Millennium PC-100. The pseudo first order rate constants showed the same decreasing trend as the pseudo first order reaction rates while L-H rate constants exhibited a light intensity related change in the ordering of the photocatalysts. At the lowest light intensity, L-H rate constants decreased as follows: Millennium PC-500>Millennium PC-100>Degussa P-25. However, increasing the light intensity changed the order to; Millennium PC-100>Millennium PC-500>Degussa P-25 revealing the significance of the L-H adsorption constant. Under constant irradiation conditions, ionic strength dependent changes in the structure of humic acid did not alter degradation efficiency trend of the photocatalyst specimens and they were ordered such as; Degussa P-25>Millennium PC-500>Hombikat UV-100>Millennium PC-100 > Merck. The results presented in this research also confirmed the effectiveness of Degussa P-25 as a photocatalyst for the degradation of humic acid.


RSC Advances ◽  
2015 ◽  
Vol 5 (25) ◽  
pp. 19675-19685 ◽  
Author(s):  
Fatemeh Khodam ◽  
Zolfaghar Rezvani ◽  
Ali Reza Amani-Ghadim

A facile and effective approach for assembling ZnO/MMO/CNT nanohybrid with excellent photodegradation performance under visible light is reported.


2018 ◽  
Vol 25 (29) ◽  
pp. 29493-29504 ◽  
Author(s):  
Nesrin Ozmen ◽  
Sema Erdemoglu ◽  
Abbas Gungordu ◽  
Meltem Asilturk ◽  
Duygu Ozhan Turhan ◽  
...  

2006 ◽  
Vol 6 (2) ◽  
pp. 77-85 ◽  
Author(s):  
C.-H. Hung

This study investigated photocatalysis of MTBE via both UV/TiO2 and H2O2-UV/TiO2 processes. Several experimental parameters including pH level, H2O2 concentration, TiO2 dosage and light intensity were investigated. The experimental results demonstrated the degradation of MTBE following a pseudo first-order reaction in both reaction systems. Faster degradation rates were observed in alkaline solution for the UV/TiO2 system, but for the H2O2-UV/TiO2 system, faster degradation rates were detected in acidic solution. More dosage of TiO2 and irradiated light intensity were beneficial for the photocatalysis of MTBE. However, a peak reaction rate was observed at a TiO2 concentration of about 500 mg/L. The experimental results also indicated that the degradation rate of MTBE was enhanced by the addition of H2O2. H2O2 could be a more efficient electron acceptor than oxygen for retarding recombination of electron–hole pairs. The degradation rate in the H2O2-UV/TiO2 system was about 2.8 times faster than that in the UV/TiO2 system for solution pH below 5, and the rate increased 30% for solution pH above 6. In addition, it is observed that the reaction rate of MTBE increased quickly with H2O2 concentration at low H2O2 dosages, but the rate was independent of H2O2 dosage when adding too much H2O2.


2019 ◽  
Vol 246 ◽  
pp. 211-220 ◽  
Author(s):  
Jean-Baptiste Tarkwa ◽  
Elie Acayanka ◽  
Bo Jiang ◽  
Nihal Oturan ◽  
Georges Y. Kamgang ◽  
...  

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