Scholarly article on topic 'Effect of Additives on Characterization and Photocatalytic Activity of Tio𝟐/ZnO Nanocomposite Prepared via Sol-Gel Process'

Effect of Additives on Characterization and Photocatalytic Activity of Tio𝟐/ZnO Nanocomposite Prepared via Sol-Gel Process Academic research paper on "Chemical engineering"

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Academic research paper on topic "Effect of Additives on Characterization and Photocatalytic Activity of Tio𝟐/ZnO Nanocomposite Prepared via Sol-Gel Process"

Hindawi Publishing Corporation International Journal of Chemical Engineering Volume 2012, Article ID 215373, 5 pages doi:10.1155/2012/215373

Research Article

Effect of Additives on Characterization and Photocatalytic Activity ofTio2/ZnO Nanocomposite Prepared via Sol-Gel Process

Shahram Moradi,1 Parviz Aberoomand Azar,2 Sanaz Raeis Farshid,1 Saeed Abedini Khorrami,1 and Mohammad Hadi Givianrad2

1 Department of Chemistry, Tehran North Branch, Islamic Azad University, Tehran 1913674711, Iran

2 Department of Chemistry, Science and Research Branch, Islamic Azad University, Tehran, Iran

Correspondence should be addressed to Shahram Moradi, Received 1 December 2011; Accepted 6 January 2012 Academic Editor: Donald L. Feke

Copyright © 2012 Shahram Moradi 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.

TiO2/ZnO nanocomposites were prepared by the sol-gel method with and without addatives such as carboxy methyl cellulose (CMC), poly(ethylene glycol) (PEG), polyvinylpyrrolidon, (PVP), and hydroxylpropylcellulose (HPC). The characteristics of the prepared TiO2/ZnO nanocomposites were identified by IR spectra, X-ray diffraction (XRD), scanning electron microscopy (SEM), and energy dispersive X-ray spectroscopy (EDS) methods. The additives have a significant effect on the particle size distribution and photocatalytic activity of TiO2/ZnO nanocomposites. The photocatalytic activity of the synthesized nanocomposites was investigated for decolorization of methyl orange (MO) in water under UV-irradiation in a batch reactor and the results showed that the photocatalytic activity of the nanocomposites have been increased by CMC, PEG, PVP, and HPC, respectively. SEM has shown that the particle size distribution of TiO2/ZnO nanocomposite in the presence of HPC was better than the other samples.

1. Introduction

Azo dyes constitute the largest group of coloring materials in the textile industry [1-3]. Release of these substances in nature is the largest source of pollution for natural ecosystems. In recent decades, semiconductor photocatalyst TiO2 has been investigated as one of the most promising candidate for a photocatalyst and it has been attracted due to its potential application in removing of all types of organic pollutants in water [4-6]. In order to improve the photocatalytic activity and the response into visible part of the spectrum, TiO2 doping with metal ions or metal oxides has been applied [1, 2].

Several methods on the preparation of TiO2/ZnO were reported, such as solid-state method, impregnation method, and chemical coprecipitation method [7-9]. Another method is the sol-gel method that has significant advantages such as, high purity, good uniformity of the powder microstructure, low-temperature synthesis, and easily controlled reaction condition and therefore it has been used for preparing ofTiO2/ZnO nanocomposite [4, 7, 10-12].

In this work, TiO2/ZnO nanocomposites were prepared by the sol-gel method in presence and absence ofCMC, PEG, PVP, and HPC as additives. The synthesized nanocomposites were characterized by means of XRD, SEM, EDS, and IR spectroscopy. Since the particle size is an important parameter in photocatalytic activity, the effects of mentioned additives have been surveyed on the particle size distribution. The photocatalytic activity of TiO2/ZnO nanocomposites were assessed for decolorization of methyl orange (MO) in water under UV irradiation in a batch reactor.

2. Materials and Methods

2.1. Materials. The chemicals used in this study were Tetra isopropyl orthotitanate (TTIP) (for synthesis), zinc nitrate tetrahydrate, diethanolamine (DEA) (for synthesis), Glacial acetic acid, methyl orange (MO), absolute ethanol, deionized water from Merck Chemical Company, and carboxymethyl cellulose (CMC), poly(ethylene glycol) (PEG), poly vinyl pyrrolidone (PVP), and hydroxylpropyl cellulose (HPC) from Sigma-Aldrich Company.

Table 1: Different samples of TiO2/ZnO.

Sample a b c d e

Additive type — CMC PEG PVP HPC

2.2. Preparation ofNanocomposites. In this study, TiO2/ZnO nanocomposite powders were prepared by the sol-gel process. The TiO2 sol was made at room temperature, and TTIP was used as a precursor as follows. In the first stage, additive (CMC or PEG or PVP or HPC = 30g/L) was dissolved in ethanol under fast stirring for 5 minutes. Then TTIP was added into ethanol with a 1:9 molar ratio of TTIP to ethanol and was stirred for 15 minutes, to obtain a precursor solution. After that, a mixture of absolute ethanol, acetic acid, and deionized water with the molar ratio of 10:6:1 was added slowly into the precursor by a fast stirring and it was continuously stirred for 15 minutes to achieve a yellow transparent sol. Here, acetic acid was used as an inhibitor to reduce quick hydrolysis of TTIP, and so the pH value was adjusted on 5.

In the second stage, ZnO sol was prepared as follows. Firstly, zinc nitrate tetrahydrate was dissolved in absolute ethanol with the molar ratio of 0.1:110. After that, stirred for 5 minutes, then a mixture of absolute ethanol, diethanolamine, and deionized water with the molar ratio of 10:2:1 was added slowly into the precursor by a fast stirring and it was continuously stirred for 15 minutes to achieve transparent sol.

The prepared ZnO sol was directly added into the TiO2 acidic sol with the molar ratio of 1: 50 to get TiO2/ZnO sol. This sol aged for 24 hours. After that, the prepared sol was dried in the air, then heat treated at 350°C for 10 minutes and then at 500°C for 5 hours. During this process, the temperature was raised at speed of 5°C/Sec. The samples were naturally cooled after the heat treatment (Table 1) [2, 5, 11, 13, 14].

2.3. Characterization of Nanocomposites. The characteristics of TiO2/ZnO nanocomposites were investigated as follows. FT-IR spectra were obtained as KBr pellets in the wave number range of 400 to 4000 cm"1 using Thermo Nicolet Nexus 870 FT-IR spectroscopy. Phase identification of the nanocomposites was done by XRD from STADIP, STOE with CuKa radiation from 0 to 100 (26) at room temperature. The morphology and microanalysis of the nanocomposites were studied by SEM (SEM-XL30, Philips) and EDS. Additionally; UV-Vis absorption spectrum was obtained by means of Varian UV-Vis spectrophotometer.

2.4. Photocatalytic Activity Measurement. Photocatalytic activity of the nanocomposites was investigated for the decol-orization of MO. All of the experiments were accomplished in a rectangular cube glass reactor with 1 liter capacity. A 15 WUV lamp (Osram) was applied as a light source and it was placed in a quartz tube, which was installed inside the reactor (Figure 1). Initially, 1 g of photocatalyst was added into a 1 liter solution of MO with initial concentration of 5 ppm. Before irradiation, the suspension was stirred for 24

Figure 1: Schematic diagram of the photoreactor system. 1.Water entrance, 2.Water exit, 3.Glass jacket, 4.quartz cover, 5.UV lamp, 6.Stirrer.

3500 3000 2500 20001500 1000 500

Wavenumbers (cm 1) Figure 2: FTIR spectra of powder samples.

hours in darkness, due to elimination of absorption effect of the solution in the catalyst. After that, the lamp was switched on for starting the reaction. During irradiation, the suspensions were sampled at regular intervals and immediately centrifuged to remove catalyst particles [3, 4, 15-17].

3. Results and Discussion

3.1. FT-IR Spectra. FT-IR spectra of samples have been presented in Figure 2 in the wave number range from 400 to 4000 cm"1. Four significant peaks were observed around 650, 800, 1450, and 3450 cm"1. The peak around 650 and 800 cm"1 can be devoted to symmetric stretching vibration of the Ti-O-Ti and vibration mode of Zn-O-Ti groups [8-10]. The peak around 1450cm"1 was ascribed to the vibration mode of Ti-O and Ti-O-C that the Ti-O-C may result from the interaction between the Ti-O network and

the organic polymers (CMC, PEG, PVP, or HPC). The wide peak around 3450 cm-1 which observed in sample b has been assigned to the OH stretching vibration of surface hydroxyl group. During the hydrolysis of TTIP, a large amount of ethanol lead to the appearance of hydroxyl bond [2, 4, 18, 19].

3.2. SEM. The SEM images and EDS analysis on the prepared nanocomposites were carried out and the results were shown in Figure 3.

Sample a without any additives, contains scattered particles which have different sizes. Sample b with CMC, is almost similar to sample a. In sample c, in presence of PEG, particle size becomes small and its distribution is more monotonous than previous samples [5, 9, 11, 20]. In sample d, with

PVP the number and density of particles are increased but the aggregation and the sticking together of the particles are observed. The last sample, e, which contains HPC has the most uniform particle distribution and it shows no agglomeration in comparison with other samples [7, 8, 21].

Figure 3. also demonstrates EDS analysis of TiO2/ZnO nanocomposites in absence and presence of additives. In all of samples, the nanoparticles were composed of Ti and Zn. This proves that Zn was incorporated into the TiO2 nanoparticles to form nanocomposite [9, 14].

3.3. XRD. XRD patterns of all samples have been shown in Figure 4. The peaks were observed at 20 = (25), (27), (31, 48, 57, 63) and (35, 39, 43) which were related to anatase, rutile, zincite, and zinc phases, respectively. As can be seen, anatase

10 20 30 40 50 60 70 80 20

50 60 20

40 50 20

10 20 30 40 50 60 70 80 90 20

10 20 30 40 50 60 70 80 90 20

Figure 4: XRD patterns of powder samples.

phase as the dominant phase has observed in all samples. In all samples; TiO2 and ZnO were not doped, however, separate crystallization of them was observed [5, 18, 20].

The calculated anatase phase percentages of the samples with different additives are between 80-90%. Sample e with 85% anatase phase and 15% rutile phase has showed a good catalytic activity [21-23].

3.4. Photocatalytic Activity. Figure 5. displays photocatalytic activity of the nanocomposites for decolorization of MO as a function of time at X = 465 nm. The photocatalytic activity of the synthesized nanocomposites was investigated for decolorization of MO (5 mgL-1) in water under UV irradiation in a batch reactor. According to Figure 5, the photocatalytic activity is enhanced by using additives [68]. Sample e with HPC has the best photocatalytic activity in comparison of other samples and about 3.5 h after starting the reaction, the absorbance of MO solution has been reached to 0. It indicates that organic polymers have been used as a dispersed factor to avoid accumulation of nanocomposite particles [23-25].

4. Conclusions

Five samples of TiO2/ZnO nanocomposites have been prepared with and without CMC, PEG, PVP, and HPC

—♦- Sample (a) -Ж- Sample (b) -A- Sample (c)

Sample (d) Sample (e)

Figure 5: Decolorization of MO solution under UV radiation.

by the sol-gel method. The XRD results exhibit that in all samples anatase phase has observed as the dominant phase and sample e with 85% anatase phase and 15% rutile phase has showed the best photocatalytic activity. The SEM images indicated that in presence of HPC, density of particles and their size distribution have been improved. It is important for photocatalytic activity that the particle size of the photocatalyst be homogeneous. Finally, all studies show that photocatalytic activity of the nanocomposites has

been enhanced in presence of additives and HPC was more

effective than others.


[1] G. Colon, M. Maicu, M. C. Hidalgo, and J. A. Navio, "Cu-doped TiO2 systems with improved photocatalytic activity," Applied Catalysis B, vol. 67, no. 1-2, pp. 41-51, 2006.

[2] H. Yu, X. J. Li, S. J. Zheng, and W. Xu, "Photocatalytic activity of TiO2 thin film non-uniformly doped by Ni," Materials Chemistry and Physics, vol. 97, no. 1, pp. 59-63, 2006.

[3] P. Aberoomand Azar, S. Moradi Dehaghi, S. Samadi, S. Ka-myar, and M. Saber Tehrani, "Effect of Nd3+, pectin and poly(ethylene glycol) on the photocatalytic activity of TiO2/ SiO2 film," Asian Journal of Chemistry, vol. 22, pp. 1619-1627, 2010.

[4] J. Tian, L. Chen, J. Dai, X. Wang, Y. Yin, and P. Wu, "Preparation and characterization of TiO2, ZnO, and TiO2/ZnO nanofilms via sol-gel process," Ceramics International, vol. 35, no. 6, pp. 2261-2270, 2009.

[5] X. T. Wang, S. H. Zhong, and X. F. Xiao, "Photo-catalysis of ethane and carbon dioxide to produce hydrocarbon oxygenates over ZnO-TiO2/SiO2 catalyst," Journal of Molecular Catalysis A, vol. 229, no. 1-2, pp. 87-93, 2005.

[6] M. H. Liao, C. H. Hsu, and D. H. Chen, "Preparation and properties of amorphous titania-coated zinc oxide nanoparti-cles," Journal of Solid State Chemistry, vol. 179, no. 7, pp. 20202026, 2006.

[7] 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.

[8] J. Tian, L. Chen, Y. Yin et al., "Photocatalyst of TiO2/ZnO nano composite film: preparation, characterization, and photodegradation activity of methyl orange," Surface and Coatings Technology, vol. 204, no. 1-2, pp. 205-214, 2009.

[9] K. Karthik, S. K. Pandian, and N. V. Jaya, "Effect of nickel doping on structural, optical and electrical properties of TiO2 nanoparticles by sol-gel method," Applied Surface Science, vol. 256, no. 22, pp. 6829-6833, 2010.

[10] J. Wang, J. Li, Y. Xie et al., "Investigation on solar pho-tocatalytic degradation of various dyes in the presence of Er3+ : YAlO3/ZnO-TiO2 composite," Journal of Environmental Management, vol. 91, no. 3, pp. 677-684, 2010.

[11] C. Chen, Z. Wang, S. Ruan, B. Zou, M. Zhao, and F. Wu, "Photocatalytic degradation of C.I. Acid Orange 52 in the presence of Zn-doped TiO2 prepared by a stearic acid gel method," Dyes and Pigments, vol. 77, no. 1, pp. 204-209, 2008.

[12] Z. Zhang, Y. Yuan, Y. Fang, L. Liang, H. Ding, and L. Jin, "Preparation of photocatalytic nano-ZnO/TiO2 film and application for determination of chemical oxygen demand," Talanta, vol. 73, no. 3, pp. 523-528, 2007.

[13] Z. Liu, Z. Jin, W. Li, and J. Qiu, "Preparation of ZnO porous thin films by sol-gel method using PEG template," Materials Letters, vol. 59, no. 28, pp. 3620-3625, 2005.

[14] C. Hariharan, "Photocatalytic degradation of organic contaminants in water by ZnO nanoparticles: revisited," Applied Catalysis A, vol. 304, no. 1-2, pp. 55-61, 2006.

[15] Y. Jiang, M. Wu, X. Wu, Y. Sun, and H. Yin, "Low-temperature hydrothermal synthesis of flower-like ZnO microstructure and nanorod array on nanoporous TiO2 film," Materials Letters, vol. 63, no. 2, pp. 275-278, 2009.

[16] S. Janitabar-Darzi and A. R. Mahjoub, "Investigation of phase transformations and photocatalytic properties of sol-gel prepared nanostructured ZnO/TiO2 composites," Journal of Alloys and Compounds, vol. 486, no. 1-2, pp. 805-808, 2009.

[17] S. Rengaraj, S. Venkataraj, J. W. Yeon, Y. Kim, X. Z. Li, and G. K. H. Pang, "Preparation, characterization and application of Nd-TiO2 photocatalyst for the reduction of Cr(VI) under UV light illumination," Applied Catalysis B, vol. 77, no. 1-2, pp. 157-165, 2007.

[18] Z. Zhang, Y. Yuan, L. Liang, Y. Cheng, G. Shi, and L. Jin, "Preparation and photoelectrocatalytic activity of ZnO nanorods embedded in highly ordered TiO2 nanotube arrays electrode for azo dye degradation," Journal of Hazardous Materials, vol. 158, no. 2-3, pp. 517-522, 2008.

[19] A. Abdel Aal, M. A. Barakat, and R. M. Mohamed, "Elec-trophoreted Zn-TiO2-ZnO nanocomposite coating films for photocatalytic degradation of 2-chlorophenol," Applied Surface Science, vol. 254, no. 15, pp. 4577-4583, 2008.

[20] C. C. Chan, C. C. Chang, W. C. Hsu, S. K. Wang, and J. Lin, "Photocatalytic activities of Pd-loaded mesoporous TiO2 thin films," Chemical Engineering Journal, vol. 152, no. 2-3, pp. 492-497, 2009.

[21] J. Chen, N. Yao, R. Wang, and J. Zhang, "Hydrogenation of chloronitrobenzene to chloroaniline over Ni/TiO2 catalysts prepared by sol-gel method," Chemical Engineering Journal, vol. 148, no. 1, pp. 164-172, 2009.

[22] B. A. Sava, A. Diaconu, M. Elisa, C. E. A. Grigorescu, I. C. Vasiliu, and A. Manea, "Structural characterization of the sol-gel oxide powders from the ZnO-TiO2-SiO2 system," Superlattices and Microstructures, vol. 42, no. 1-6, pp. 314-321, 2007.

[23] S. Liao, H. Donggen, D. Yu, Y. Su, and G. Yuan, "Preparation and characterization of ZnO/TiO2, SO4 2-/ZnO/TiO2 photocatalyst and their photocatalysis," Journal of Photochemistry and Photobiology A, vol. 168, no. 1-2, pp. 7-13, 2004.

[24] M. D. Snel, F. Snijkers, J. Luyten, A. Kodentsov, andG. de With, "Tape casting and reaction sintering of titanium-titanium oxide-nickel oxide mixtures," Journal of the European Ceramic Society, vol. 28, no. 6, pp. 1185-1190, 2008.

[25] J. Qiu, Z. Jin, Z. Liu et al., "Fabrication of TiO2 nanotube film by well-aligned ZnO nanorod array film and sol-gel process," Thin Solid Films, vol. 515, no. 5, pp. 2897-2902, 2007.

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