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Journal of Nanoparticles
Volume 2013 (2013), Article ID 507161, 7 pages
Sol-Gel Synthesis of TiO2/SiO2 and ZnO/SiO2 Composite Films and Evaluation of Their Photocatalytic Activity towards Methyl Green
Department of Chemistry, Annamalai University, Annamalai Nagar, Tamil Nadu 608 002, India
Received 31 January 2013; Accepted 2 March 2013
Academic Editor: Amir Kajbafvala
Copyright © 2013 V. L. Chandraboss et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
The TiO2/SiO2 and ZnO/SiO2 composite films were prepared by sol-gel dip coating method. The surface morphology and crystal structure of thin films were characterized by means of scanning electron microscopy (SEM) with elementary dispersive X-ray analysis (EDX) and X-ray diffractometer (XRD). Optical properties of films have been investigated using ultraviolet and visible spectroscopy (UV-visible spectroscopy). The photocatalytic activity was established by testing the degradation and decolorization of methyl green (MG) from aqueous solution with artificial UV-light.
Nanomaterials may provide solutions to scientific and ecological challenges in the areas of catalysis, medicine, solar energy conversion, and water treatment [1, 2]. This increasing demand must be accompanied by “green” synthesis methods. In the global efforts to decrease generated hazardous waste, “green” chemistry and chemical processes are progressively integrating with contemporary developments in science and industry. Implementation of these sustainable processes should adopt the 12 fundamental principles of green chemistry . These principles are gear to guide in minimizing the use of dangerous products and maximizing the efficiency of chemical processes. Hence, any synthetic route or chemical process should address these principles by using environmentally benign solvents and nontoxic chemicals .
From a biological and physiological point of view, the removal of poisonous chemicals from waste water is currently one of the most important subjects in pollution control. MG is a basic triphenylmethane-type dicationic dye, usually used for staining solutions in medicine and biology  and as a photochromophore to sensitize gelatinous films . Triphenylmethane dyes are used widely in the textile industry for dyeing of nylon, wool, cotton, and silk as well as for coloring of waxes, varnish, oil, plastics, and fats.
The application of illuminated semiconductors has been effectively working for the decomposition of variety of organic contaminants in water . The major organic compounds that constitute the industrial wastewater include dyes, phenols, chlorophenols, aliphatic alcohols, aromatics, polymers, and carboxylic acids. Among these, toluene, salicylic acid, and 4-chlorophenol have been identified as a water pollutant arising from numerous sources including paper milling, textile, and cosmetic industries , causing bad odor to the water. Hence, the destruction of organic compounds is of considerable interest. Over the years, a large number of semiconductors have been utilized as photocatalysts. The most commonly studied photocatalysts are TiO2 and ZnO [9, 10].
TiO2 films have been broadly studied in photocatalytic degradation of the dyes, because of their low solubility in wastewater, high oxidation efficiency, ecofriendly properties, and avoiding the need for posttreatment separation in a system. Moreover, the coatings propose a benefit of a strong particle-substrate coupling that allows long-term performance. A variety of methods are obtainable for the preparation of nanostructured TiO2-based photocatalytic films, such as vacuum arc plasma evaporation , electrochemical method [12–14], classical and modified sol-gel methods [15–18], and chemical vapor deposition (CVD) [19, 20].
ZnO has a competitive photocatalytic activity (PA) greater in some cases than TiO2, for example, in the discoloration of Reactive Blue19, a textile anthraquinone dye, in aqueous suspension , and in the oxidation of protocatechuic acid . Furthermore, ZnO thin films have been found to decompose aqueous solutions of reactive dyes [23, 24], as well as phenol and chlorophenol , and other environmental pollutants [26, 27].
ZnO is available at low cost, which gives it an important advantage. However, the solar UV-light reaching the surface of the earth and available to excited TiO2 is relatively small (around 4%), and artificial UV-light sources are somewhat expensive. The biggest advantage of ZnO is that it absorbs over a larger fraction of the solar spectrum than TiO2 [28, 29]. The biggest advantage of ZnO in comparison with TiO2 is that it absorbs over a larger fraction of UV spectrum and the corresponding threshold of ZnO is 425 nm . For this reason, ZnO is the most suitable photocatalyt for photocatalytic degradation of dyes under UV-light irradiation.
Recently, some researchers synthesized TiO2, ZnO thin films, and composite materials for photocatalytic activity of some industrial pollutants and dyes [31–34]. In this context our research group has successfully prepared TiO2/SiO2 and ZnO/SiO2 composite films by sol-gel method. Then, the photocatalytic activity of these composites towards is studied.
2. Materials and Methods
Zinc acetate dihydrate [Zn(CH3COO)2·2H2O], titanium tetraisopropoxide [Ti(iso-OC3H7)4], tetraethyl orthosilicate [TEOS], methyl green, diethanolamine, and ethanol were purchased and used as such. The aqueous solutions were prepared by using double distilled water. All glassware was cleaned with chromic acid followed by thorough washing with distilled water. Chemical structure of MG is shown in Figure 1.
2.2. Preparation of TiO2/SiO2 and ZnO/SiO2 Composite Films
Initially diethanolamine in ethanol was stirred well and then zinc acetate dihydrate was added to the previous solution (solution I). Tetraethyl orthosilicate dissolved in ethanol is taken as another (solution II). The solution II is added to the solution I and stirred (600 rpm) at 65°C for 2 hour. The dip coating was achieved when cleaned glass plates were gradually immersed into the solution. The films were dried at 100°C for 4 hours to evaporate the solvent and to remove the organic residuals. Finally the films were calcinated at 400°C to get uniform ZnO/SiO2 composite film (Scheme 1). The above procedure was also carried out for TiO2-doped SiO2 film.
2.3. Analytical Methods
Scanning electron microscopy (SEM) with elementary dispersive X-ray analysis (EDX) experiments was carried out on an FEI Quanta FEG 200 instrument with EDX analyzer facility at 25°C. X-ray diffraction (XRD) spectra were recorded on the X’PERT PRO model X-ray diffractometer from Pan Analytical instruments operated at a voltage of 40 kV and a current of 30 mA with Cu Kα radiation. UV-visible absorbance spectra were measured over a range of 200–800 nm with a Shimadzu UV-1650PC recording spectrometer using a quartz cell with 10 mm of optical path length.
2.4. Photocatalytic Activity
Photocatalytic studies were carried out in a multilamp photoreactor (HML MP88, supplied by Heber Scientific, India) fitted with eight 8 W mercury UV lamps of wavelength 365 nm. The volume of the reaction solution was maintained as 30 mL. Air was bubbled through the reaction solution for effective stirring. The degradation of MG was followed spectrophotometrically. The solution was diluted to keep the absorbance within the Beer-Lambert law limit.
3. Results and Discussion
3.1. Characterization of TiO2/SiO2 and ZnO/SiO2 Composite Films
3.1.1. SEM with EDX Analysis
The morphology of the TiO2/SiO2 and ZnO/SiO2 composite films was determined by scanning electron microscopy. Figure 2 shows SEM micrograph of TiO2/SiO2 film annealed at 400°C (scale bars of 1 and 0.5 μm) (Figures 2(a) and 2(b)). EDX analysis confirmed the presence of Ti, Si, and O (Figure 2(c)). Figure 3 shows SEM micrograph of ZnO/SiO2 film annealed at 400°C (scale bars of 1 and 0.5 μm) (Figures 3(a) and 3(b)). EDX analysis confirmed the presence of Zn, Si, and O (Figure 3(c)). Uniform morphology of the prepared composite materials has been confirmed from the previous observation.
3.1.2. XRD Analysis
Figure 4(a) shows XRD of TiO2-doped SiO2 composite film. The peaks at 23.5°, 27.0°, 38.0°, 42.4°, and 48.8° are the diffractions of the TiO2 (1 0 1), SiO2 (1 0 1), TiO2 (1 1 2), SiO2 (2 0 0), and TiO2 (2 0 0). The diffractogram consists of broad diffraction peaks of TiO2 anatase phase (JCPDS file no. 84-1286). Figure 4(b) shows XRD of ZnO-doped SiO2 composite film. The peaks at 26.5°, 31.7°, 33.3°, 36.0°, 49.4°, and 68.9° are the diffractions of the SiO2 (1 0 1), ZnO (1 0 0), ZnO (0 0 2), ZnO (1 0 1), SiO2 (1 1 2), and ZnO (2 0 1). The diffractogram consists of broad diffraction peaks of ZnO (JCPDS file no. 36-1451).
3.1.3. Optical Transmittance Analysis
Optical transmittance spectra of TiO2/SiO2 and ZnO/SiO2 composite films annealed at different temperatures (100°C, 150°C, 200°C, 250°C, and 300°C) are shown in Figure 5. When the films were heated at different temperatures, the transmittance of the films becomes lower as the temperature increases. Transmittance of the ZnO/SiO2 film was slightly lower than the TiO2/SiO2 with increasing temperature (Figures 5(a) and 5(b)).
3.2. Photodegradation and Decolorization of MG
3.2.1. Photodegradation of Methyl Green with Artificial UV Light
The photodegradation of MG in aqueous medium in the presence of atmospheric air on TiO2/SiO2 and ZnO/SiO2 composite films was studied using multilamp photoreactor with mercury UV lamps of wavelength 365 nm. The reference wavelength of MG reaction solution is 630 nm. Initially the dye solution is dark green in color; after the photodegradation and decolorization the color of the solution becomes pale green. The reaction time affords the photodegradtation and decolorization of MG.
3.2.2. Photocatalytic Activity of TiO2/SiO2 and ZnO/SiO2 Composite Films
The absorption spectrum of MG in the presence of TiO2/SiO2 and ZnO/SiO2 is shown in Figures 6(a) and 6(b), respectively. The absorption spectrum shows the decrease in intensity with respect to time. The rapid decrease in the intensity of ZnO/SiO2 is noted in the photocatalysis compared with TiO2/SiO2. The enhanced photocatalytic activity shown by ZnO/SiO2 is compared with TiO2/SiO2 composites.
3.2.3. Effect of Dye Concentration
The progress of the photodegradation of MG represents increases with light intensity in the presence of TiO2/SiO2 and ZnO/SiO2 composite films. Different concentrations of MG were prepared and used for the photodegradation process. At lower concentration, the degradation and decolorization of MG are high but at higher concentration, the photocatalytic activity is low (Figure 7). The photodegradation of TiO2/SiO2 and ZnO/SiO2 is shown in Figures 7(a) and 7(b), respectively. From these figures, it is concluded that the degradation efficiency of ZnO/SiO2 composite film is higher than TiO2/SiO2 composites only at lower concentration of MG.
TiO2/SiO2 and ZnO/SiO2 composite films were prepared by the sol-gel method. The prepared films were characterized by SEM with EDX, XRD, and optical transmittance studies. TiO2/SiO2 and ZnO/SiO2 films were used for the photodegradation of MG under UV-light irradiation. The photodegradation of MG on TiO2/SiO2 and ZnO/SiO2 composite films in aqueous medium has been studied as a function of dye concentration. ZnO/SiO2 composite film exhibited reasonable activity under UV-light and had much better activity when compared to that of TiO2/SiO2 composite films.
S. Senthilvelan is highly thankful to UGC, New Delhi, for granting a major research project (F. no. 39-771/2010(SR)).
- J. A. Dahl, B. L. S. Maddux, and J. E. Hutchison, “Toward greener nanosynthesis,” Chemical Reviews, vol. 107, no. 6, pp. 2228–2269, 2007.
- J. E. Hutchison, “Greener nanoscience: a proactive approach to advancing applications and reducing implications of nanotechnology,” ACS Nano, vol. 2, no. 3, pp. 395–402, 2008.
- J. M. DeSimone, “Practical approaches to green solvents,” Science, vol. 297, no. 5582, pp. 799–803, 2002.
- P. Raveendran, J. Fu, and S. L. Wallen, “Completely “Green” synthesis and stabilization of metal nanoparticles,” Journal of the American Chemical Society, vol. 125, no. 46, pp. 13940–13941, 2003.
- F. J. Green, The Sigma–Aldrih Handbook of Stains, Dyes, and Indicators, Aldrich Chemical, Milwaukee, Wis, USA, 1990.
- T. Geethakrishnan and P. K. Palanisamy, “Degenerate four-wave mixing experiments in Methyl green dye-doped gelatin film,” Optik, vol. 117, no. 6, pp. 282–286, 2006.
- M. A. Behnajady, N. Modirshahla, and R. Hamzavi, “Kinetic study on photocatalytic degradation of C.I. Acid Yellow 23 by ZnO photocatalyst,” Journal of Hazardous Materials, vol. 133, no. 1–3, pp. 226–232, 2006.
- A. Mills, C. E. Holland, R. H. Davies, and D. Worsely, “Photo mineralization of salicylic acid: a kinetic study,” Journal of Photochemistry and Photobiology A, vol. 83, pp. 257–263, 1994.
- S. K. Kansal, M. Singh, and D. Sud, “Studies on photodegradation of two commercial dyes in aqueous phase using different photocatalysts,” Journal of Hazardous Materials, vol. 141, no. 3, pp. 581–590, 2007.
- Y. Wei, Y. Huang, J. Wu, et al., “Synthesis of hierarchically structured ZnO spheres by facile methods and their photocatalytic deNOx properties,” Journal of Hazardous Materials, vol. 248, pp. 202–210, V.
- T. Miyata, S. Tsukada, and T. Minami, “Preparation of anatase TiO2 thin films by vacuum arc plasma evaporation,” Thin Solid Films, vol. 496, no. 1, pp. 136–140, 2006.
- S. Wang, X. Wu, W. Qin, and Z. Jiang, “TiO2 films prepared by micro-plasma oxidation method for dye-sensitized solar cell,” Electrochimica Acta, vol. 53, no. 4, pp. 1883–1889, 2007.
- X. H. Wu, Z. H. Jiang, L. H. Liu, X. D. Li, and X. G. Hu, “TiO2 ceramic films prepared by micro-plasma oxidation method for photodegradation of rhodamine B,” Materials Chemistry and Physics, vol. 80, no. 1, pp. 39–43, 2003.
- S. Karuppuchamy, N. Suzuki, S. Ito, and T. Endo, “Enhanced efficiency of dye sensitized solar cells by UV-O3 treatment of TiO2 layer,” Current Applied Physics, vol. 9, pp. 243–248, 2009.
- D. L. Liao, C. A. Badour, and B. Q. Liao, “Preparation of nanosized TiO2/ZnO composite catalyst and its photocatalytic activity for degradation of methyl orange,” Journal of Photochemistry and Photobiology A, vol. 194, no. 1, pp. 11–19, 2008.
- X. Zhang and Q. Liu, “Preparation and characterization of titania photocatalyst co-doped with boron, nickel, and cerium,” Materials Letters, vol. 62, no. 17-18, pp. 2589–2592, 2008.
- L. Andronic and A. Duta, “The influence of TiO2 powder and film on the photodegradation of methyl orange,” Materials Chemistry and Physics, vol. 112, no. 3, pp. 1078–1082, 2008.
- I. Stambolova, V. Blaskov, I. N. Kuznetsova, N. Kostova, and S. Vassilev, “Effect of the thermal treatment on the morphology and optical properties of nanosized TiO2 films,” Journal of Optoelectronics and Advanced Materials, vol. 13, pp. 381–386, 2011.
- B. H. Kim, J. Y. Lee, Y. H. Choa, M. Higuchi, and N. Mizutani, “The effect of target density and its morphology on TiO2 thin films,” Materials Science and Engineering B, vol. 107, pp. 289–294, 2004.
- T. K. Ghorai, D. Dhak, S. K. Biswas, S. Dalai, and P. Pramanik, “Photocatalytic oxidation of organic dyes by nano-sized metal molybdate incorporated titanium dioxide () (M = Ni, Cu, Zn) photocatalysts,” Journal of Molecular Catalysis A, vol. 273, no. 1-2, pp. 224–229, 2007.
- I. Poulios, D. Makri, and X. Prohaska, “Photocatalytic treatment of olive milling wastewater: oxidation of protocatechuic acid,” GLOBAL NEST, vol. 1, pp. 55–62, 1999.
- S. Sakthivel, B. Neppolian, M. V. Shankar, B. Arabindoo, M. Palanichamy, and V. Murugesan, “Solar photocatalytic degradation of azo dye: comparison of photocatalytic efficiency of ZnO and TiO2,” Solar Energy Materials and Solar Cells, vol. 77, no. 1, pp. 65–82, 2003.
- C. A. K. Gouvêa, F. Wypych, S. G. Moraes, N. Durán, N. Nagata, and P. Peralta-Zamora, “Semiconductor-assisted photocatalytic degradation of reactive dyes in aqueous solution,” Chemosphere, vol. 40, no. 4, pp. 433–440, 2000.
- C. Lizama, J. Freer, J. Baeza, and H. D. Mansilla, “Optimized photodegradation of reactive blue 19 on TiO2 and ZnO suspensions,” Catalysis Today, vol. 76, no. 2–4, pp. 235–246, 2002.
- S. Lathasree, A. N. Rao, B. Sivasankar, V. Sadasivam, and K. Rengaraj, “Heterogeneous photocatalytic mineralisation of phenols in aqueous solutions,” Journal of Molecular Catalysis A, vol. 223, no. 1-2, pp. 101–105, 2004.
- L. B. Khalil, W. E. Mourad, and M. W. Rophael, “Photocatalytic reduction of environmental pollutant Cr(VI) over some semiconductors under UV/visible light illumination,” Applied Catalysis B, vol. 17, no. 3, pp. 267–273, 1998.
- Y. Huang, Y. Wei, J. Wu, et al., “Low temperature synthesis and photocatalytic properties of highly oriented ZnO/TiO2−xNy coupled photocatalysts,” Applied Catalysis B, vol. 123, pp. 9–17, 2012.
- S. Sakthivel, B. Neppolian, M. Palanichamy, B. Arabindoo, and V. Murugesan, “Photocatalytic degradation of leather dye, Acid green 16 using ZnO in the slurry and thin film forms,” Indian Journal of Chemical Technology, vol. 6, no. 3, pp. 161–165, 1999.
- I. Poulios and I. Tsachpinis, “Photodegradation of the textile dye Reactive Black 5 in the presence of semiconducting oxides,” Journal of Chemical Technology and Biotechnology, vol. 74, pp. 349–357, 1999.
- S. S. Shinde, P. S. Shinde, C. H. Bhosale, and K. Y. Rajpure, “Zinc oxide mediated heterogeneous photocatalytic degradation of organic species under solar radiation,” Journal of Photochemistry and Photobiology B, vol. 104, no. 3, pp. 425–433, 2011.
- I. Stambolova, M. Shipochka, V. Blaskov, A. Loukanovb, and S. Vassilevc, “Sprayed nanostructured TiO2 films for efficient photocatalytic degradation of textile azo dye,” Journal of Photochemistry and Photobiology B, vol. 117, pp. 19–26, 2012.
- G. Torres Delgado, C. I. Zúñiga Romero, S. A. Mayén Hernández, R. Castanedo Péreza, and O. Zelaya Angel, “Optical and structural properties of the sol– gel-prepared ZnO thin films and their effect on the photocatalytic activity,” Solar Energy Materials and Solar Cells, vol. 93, no. 1, pp. 55–59, 2009.
- X. Zhang and H. Zheng, “Synthesis of TiO2-doped SiO2 composite films and its applications,” Bulletin of Materials Science, vol. 32, pp. 787–790, 2008.
- A. Mahyar, M. A. Behnajady, and N. Modirshahla, “Enhanced photocatalytic degradation of C.I. Basic violet 2 using TiO2-SiO2 composite nanoparticles,” Photochemistry and Photobiology, vol. 87, no. 4, pp. 795–801, 2011.