Electro-Assisted Photocatalytic Degradation of Methyl Orange on TiO2 Film Using NaCl as Electrolyte

2012 ◽  
Vol 457-458 ◽  
pp. 1169-1172
Author(s):  
Wen Jie Zhang ◽  
Mei Ling Hu ◽  
Hong Bo He

Porous and smooth TiO2 film electrodes prepared by sol-gel method were used on methyl orange degradation by an electro-assisted photocatalytic degradation process. When using the applied potential along, there was no obvious degradation of methyl orange whether using TiO2 film electrode prepared using PEG template or not. The largest difference between the two electrodes appears at potential of 0.7 V in 0.05 mol/l NaCl solution, and the porous electrode shows better degradation activity in electro-assisted photocatalytic degradation. When NaCl concentration was 0.07 mol/l, degradation rates on porous and smooth film electrodes were 51.16% and 32.35 %, respectively. After 100 min of irradiation, 90% of the methyl orange degraded on the porous TiO2 film electrode, and 79.87% of the methyl orange degraded on the smooth TiO2 film electrode.

2012 ◽  
Vol 487 ◽  
pp. 635-639
Author(s):  
Wen Jie Zhang ◽  
Hong Liang Xin ◽  
Hong Bo He

Porous and smooth TiO2 film electrodes prepared by sol-gel method were used on methyl orange degradation by an electro-assisted photocatalytic degradation process. Methyl orange cannot be degraded under applied potential solely below 2.0 V. When the applied potential was below 1.3 V, methyl orange degradation rates on porous TiO2 film increased from 5% at 0 V to 65.3% at 1.3 V, and degradation rates on smooth TiO2 film changed from 2.2% at 0 V to 61.1% at 1.3 V. Electro-assisted photocatalytic degradation rate on porous film was better than that on smooth film in the whole electrolyte concentration range. Electro-assisted degradation exhibited the same rising trend along with reaction time on the porous and smooth films.


2012 ◽  
Vol 487 ◽  
pp. 640-643
Author(s):  
Wen Jie Zhang ◽  
Fei Fei Bi ◽  
Hong Bo He

Porous and smooth TiO2 film electrodes prepared by sol-gel method were used on methyl orange degradation by an electro-assisted photocatalytic degradation process. The results indicates that methyl orange was barely degraded under the potential alone, availing that potential under 1.8 V had no noticeable effect on removal of the dye. The porous film electrode showed better electro-assisted photocatalytic activity than the smooth film electrode when the potential was above 0.6 V. The porous film showed better activity than the smooth film in nearly all the concentration range except for the highest one. The porous film exhibited better activity than the smooth one.


Materials ◽  
2019 ◽  
Vol 12 (6) ◽  
pp. 873 ◽  
Author(s):  
Mirta Čizmić ◽  
Davor Ljubas ◽  
Marko Rožman ◽  
Danijela Ašperger ◽  
Lidija Ćurković ◽  
...  

In this paper, nanostructured TiO2 film was prepared by the by sol-gel process and dip-coating technique with titanium tetraisopropoxide as a precursor. After heat treatment at 550 °C, the deposited film was characterized by means of micro-Raman spectroscopy and atomic force microscopy (AFM). It was found that the TiO2 film consisted of only the TiO2 anatase phase and showed a granular microstructure. Photocatalytic degradation of azithromycin by using sol-gel nanostructured TiO2 film was studied to define the most effective degradation process for potential use in wastewater treatment. Different factors were evaluated during photocatalysis, such as pH (3, 7, and 10), water matrix (ultrapure water and synthetic municipal waste water effluent), influence of another pharmaceutically active compound (sulfamethoxazole, one of the most often detected pharmaceutic compounds in waste waters), and radiation sources (low pressure ultraviolet (UV) mercury lamps with a UV-A and UV-C range; a light-emitting diode (LED) lamp with a radiation peak at 365 nm). The most effective degradation process was achieved with the UV-C irradiation source in matrices at pH 10. The water matrix had little effect on the photocatalytic degradation rates of azithromycin. The presence of sulfamethoxazole in the water matrix decreased the degradation rate of azithromycin, however, only in matrices with a pH level adjusted to 10. During the experiments, five azithromycin degradation products were identified and none of them showed toxic properties, suggesting effective removal of azithromycin. LED 365 nm as the irradiation source was not as effective as the UV-C lamp. Nevertheless, considering the cost, energy efficiency, and environmental aspects of the irradiation source, the LED lamp could be a “real-life” alternative.


2011 ◽  
Vol 48-49 ◽  
pp. 345-348
Author(s):  
Li Li Yang ◽  
Yan Liang Qu ◽  
Wen Jie Zhang

A co-sol-gel method was used to prepare SiO2-doped TiO2. The amount of ethyl silicate added into the precursor, calcination temperature and time, adsorption equilibrium, and photocatalytic activity of the material were investigated as the factor of degradation efficiency. With the optimum composition of the precursor, the prepared gel calcinated at 500 oC for 3 h showed the highest photocatalytic activity. After 30 min stirring to reach adsorption equilibrium, adsorption contributed less than 2% to the total decoloration of methyl orange on the SiO2-doped TiO2 material. Photocatalytic methyl orange degradation continued with increasing irradiation time. Methyl orange degradation rates after 30 min and 100 min were 31.1% and 96.9%, respectively.


2011 ◽  
Vol 230-232 ◽  
pp. 126-130
Author(s):  
Wen Jie Zhang ◽  
Ke Xin Li

PEG1000 was used as template to prepare porous TiO2 film by sol-gel method. The functions of applied potential and concentration of NaHCO3 to the photoelectrocatalytic degradation of methyl orange on porous and smooth TiO2 films were investigated. Methyl orange degradation rate has two optimal values at the applied potential of 0.8 V and 1.8 V. The addition of PEG may have negative effect on photoelectrocatalytic activity of TiO2 film. The degradation rate increases with increasing NaHCO3 concentration from 0 up to 0.05 mol/l, and then it declines after further increase of electrolyte concentration. After 100 min of reaction, the degradation rates on the films prepared without and with PEG addition are 63.78% and 65.22%, respectively.


2018 ◽  
Vol 2018 ◽  
pp. 1-7 ◽  
Author(s):  
Ghaida H. Munshi ◽  
Amal M. Ibrahim ◽  
Laila M. Al-Harbi

As the need to use green chemistry routes increases, environmentally friendly catalytic processes are a demand. One of the most important and abundant naturally occurring catalysts is chlorophyll. Chlorophyll is the first recognized catalyst; it is a reducing agent due to its electron-rich structure. The effects of spinach on the preparation of zinc oxide nanoparticles and the photocatalytic degradation of methyl orange and paraquat in sunlight and under a UV lamp and photocatalytic degradation in sunlight were studied. Different parameters of the catalytic preparation process and photocatalytic degradation process were studied. Characterization of differently prepared samples was carried out using different analytical techniques such as XRD, SEM, and EDX and finally the photocatalytic activity towards decomposition of methyl orange and paraquat.


2008 ◽  
Vol 11 (2) ◽  
Author(s):  
Suhas R. Patil ◽  
Urška Lavrenčič Štangar ◽  
Silvia Gross ◽  
Ulrich Schubert

AbstractA comparative study of photocatalytic degradation of methyl orange (liquid-solid interface) and methyl stearate (solid-solid interface) was performed with three different kinds of transparent pure and Ag-doped TiO


2014 ◽  
Vol 809-810 ◽  
pp. 860-866 ◽  
Author(s):  
Ce Wang ◽  
Long Gui Peng ◽  
Qiao Qiao Zhang ◽  
Lu Ying Qiu ◽  
Zai Yong Zhang

A intercalated TiO2photocatalyst loaded bentonite was prepared by sol-gel method. The effect of reaction time, reaction temperature,the amount of butyl titanate and other process parameters on prepared material of degradation of methyl orange,as well as the relationship between the concentration of methyl orange on degradation process and illumination time were discussed by single factor method.The results showed : the first absorbance of the intercalated TiO2photocatalyst loaded bentonite material was 0.342 and the average absorbance was respectively 0.7402 through 5 washing after the intercalated TiO2photocatalyst loaded bentonite irradiated at UV-irradiation 1.5h to 20mg/L methyl orange.


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