Photocatalytic degradation of methylene blue under UV light irradiation on prepared carbonaceous Ti[O.sub.2].
Currently, the rapid industrialization in developing countries has begun to introduce harmful organic pollutants into the water supply. These effluents are also sourced from the textile industry that consumes a large quantity of water in the process of dyeing and washing of fabrics and the release of huge quantities of dyes . Therefore, the development of inexpensive and green methods to treat and purify contaminated water has been the focal subject in technological developments. Among many strategies, photocatalysis is regarded as the most viable one, especially for treatment of contaminants, due to its usage of sunlight to decompose organic pollutants [2-4]. Titanium dioxide or titania (Ti[O.sub.2]) acts as an agent in this process [5, 6]. However, Ti[O.sub.2] is not without its drawback in the context of photocatalysis, such as its high band gap energy 3.2 eV for anatase , the limitation of photo response only under UV light region, and its high rate of electron and hole recombination. Attempts to address these problems involve doping, nonmetallic elements doping, surface modification, forming composites with narrow semiconductors, using semiconductor polymer as support, and coating with carbon layers to improve and enhance the photocatalytic activity of titanium dioxide.
Current literature shows that activated carbon is gaining attention as it is capable of modifying Ti[O.sub.2] photo catalyst. The work in [8-12] showed that this enhancement is caused by porous structure of activated carbon, which provides a large surface area for photoactive Ti[O.sub.2] particle.
The work in [8, 13-15] found the synergistic effect of the mixture of Ti[O.sub.2] with activated carbon (AC). The improvement of Ti[O.sub.2]/AC composite was explained by the high adsorption of the impurities on the surface of activated carbon and their transfer to the Ti[O.sub.2] surface. In this study, carbonaceous Ti[O.sub.2], namely, Ti[O.sub.2]/activated carbon (AC), Ti[O.sub.2]/carbon (C), and Ti[O.sub.2]/PANi were prepared and evaluated for photocatalytic performance for degradation of methylene blue under UV light irradiation. The carbon and activated carbon/Ti[O.sub.2] were synthesized using polyaniline (PANi) as its carbon source.
2. Experimental and Characterizations
2.1. Preparation of Ti[O.sub.2]/Polyaniline and Ti[O.sub.2]/Carbon. Ti[O.sub.2]/polyaniline (Ti[O.sub.2]/PANi) was synthesized using Ti[O.sub.2] (Sigma Aldrich, 99.9% purity) and aniline hydrochloride (Sigma Aldrich, 99.95%). In order to synthesize Ti[O.sub.2]/PANi, 0.2 mol [cm.sup.-3] aniline hydrochloride solution was prepared by adding 259 mg aniline hydrochloride to 5 mL deionized water and was vigorously stirred for 10 minutes at a temperature of 60[degrees]C. Ti[O.sub.2] powder, with various percentages (5%, 10% and 15%), is added to aniline hydrochloride solution being prepared previously. 0.25 mol [cm.sup.-3] ammonium peroxydisulphate solution was prepared by adding 571 mg ammonium peroxydisulphate (Sigma Aldrich, 98% reagent grade) in 5 mL deionized water. While the mixture above was being stirred, the prepared ammonium peroxydisulphate solution was added to the mixture and was stirred for an additional 10 minutes. The polymerization was completed in about 10 minutes. The solution was then left to dry at room temperature for 48 hours. The precipitate powder was then centrifuged and washed with absolute ethanol, followed by distilled water in order to remove unreacted aniline monomer and its corresponding by-products. The product (Ti[O.sub.2]/PANi) was dried at 65[degrees]C for 24 h. The composite that was the result of the process was labeled as Ti[O.sub.2]/PANi. The product was then pyrolyzed at a temperature of 450[degrees]C for 1 hour in nitrogen flow at a heating rate of 10[degrees]C [min.sup.-1] to produce titania/carbon (Ti[O.sub.2]/C).
2.2. Chemical Activation of Ti[O.sub.2]/Carbon. In order to produce porous carbon or the so-called activated carbon, the Ti[O.sub.2]/C was treated with 1.0MKOH solution. About 0.3 g Ti[O.sub.2]/C was mixed with 2.5 mL 1.0 M KOH solution. The mixture was then heated at a temperature of 450[degrees]C under nitrogen gas flow for 1 hour. Then the treated sample was washed with deionized water until it was neutral and dried overnight at a temperature of 100[degrees]C and was labeled Ti[O.sub.2]/AC. Since the early photocatalytic performance tests demonstrated better result for the Ti[O.sub.2]/AC prepared from 15% Ti[O.sub.2]/PANi, the characterization was done for 15% Ti[O.sub.2]/PANi and the resulting Ti[O.sub.2]/C and Ti[O.sub.2]/AC (hereafter denoted as Ti[O.sub.2]/PANi, Ti[O.sub.2]/C, and Ti[O.sub.2]/AC, resp.).
2.3. Characterizations. The functionality groups of the samples were determined using FTIR spectra. The morphology and structure of the samples were determined by field emission scanning electron microscope (FESEM, ZEISS Supra VP55) and transmission electron microscope (JEOL JEM-2100). The specific surface area, pore size, pore volume, and pore diameter of the samples were determined by Brunauer-Emmet-Teller (BET) method  using a nitrogen adsorption instrument (Micrometics ASAP 2010). The samples were degassed at 100[degrees]C for 24 hours prior to the analysis. Pore size distribution was calculated from the adsorption desorption of the isotherms using the Barret-Joyner-Halenda (BJH) model , while the crystallinity of the samples was analyzed using Brucker DB-advance X-ray diffractometer (XRD). The analyses were done under the setting of Cu ka radiation at 2 theta, ranging from 10[degrees] to 80[degrees] for a 1-gram sample. The particle size of the sample was calculated by applying Scherrer's equation. Thermal gravimetric analysis (TGA) with a simultaneous TGA-DTG system (model: Mettler Toledo) has been used for investigation of thermal stability of samples. To reduce the influence of the sample quantity on the analyses, 5 [+ or -] 0.2 mg of each sample was used in each analysis with a constant nitrogen (N2) flow 50.0 mL [min.sup.-1] maintained throughout the entire process. To minimize possible differences in the moisture content between samples, all TGA samples were equilibrated at 50[degrees]C for 5 min before being heated to 700[degrees]C at a ramping rate of 5[degrees]C [min.sup.-1].
For investigation of prepared samples recyclability, the used catalyst was separated from reaction mixture by filtration. After that, it is washed with distilled water several times and dried in oven to be reused for next reaction cycle. Then they were used for subsequent cycles under similar reaction conditions as carried out by fresh catalyst.
2.4. Photocatalytic Experimental. The photocatalytic activities of the samples were evaluated via the photocatalytic oxidation of methylene blue (MB) under UV light irradiation. A 15 watt UV bench lamp was used as a light source. Since the photocatalytic test took into account different MB concentrations (0.05, 0.1, and 0.15 mM) and different irradiation times, it showed better results for 0.05 mM and 90 minutes, respectively, and was selected as the test condition (see Section 3.2).
Prior to illumination, 20 mg photocatalyst was added to the MB solution (20 mL, 0.05 mM). The solution was stirred in the dark for 30 minutes in order to reach MB absorption-desorption equilibrium, which will then allow for the commencement of the photocatalytic reaction. The photocatalyst will then be exposed to the UV lamp for 90 minutes in room temperature. The results after this time period will be evaluated after 90 minutes.
The degradation efficiency of MB was analyzed using UV-Vis spectrometer. Peaks were observed to be present between 600 and 700 nm and were assigned as the absorption of the [pi]-system , which was indicative of the degradation of MB. According to Beer-Lambert Law, MB's concentration is directly proportional to its absorbance. This makes it possible to determine the oxidation efficiency of MB using the following equation:
R = ([C.sub.o] - [C.sub.t])/[C.sub.o] x 100%, (1)
where [C.sub.o] is the initial concentration of MB solution and [C.sub.t] is concentration of MB during irradiation.
3. Results and Discussions
The existence of polyaniline on the Ti[O.sub.2] surface particle was verified by IR spectra. The characteristic bands of Ti[O.sub.2], polyaniline (made in the same way for comparison purpose only), Ti[O.sub.2]/PANi, and Ti[O.sub.2]/AC are shown in Figures 1(a), 1(b), 1(c), and 1(d), respectively. The FTIR spectrum of polyaniline was clearly observed in Ti[O.sub.2]/PANi sample. The spectra display the two bands at 1490 and 1585 [cm.sup.-1], which were assigned to benzenoid and quinoide rings. The band at 1300 [cm.sup.-1] is related to C-N stretching of a secondary aromatic amine, while the band at 1140 [cm.sup.-1] is attributed to the vibration mode of the polymer. These bands reveal the existence of PANi in the synthesized Ti[O.sub.2]/PANi sample. In Ti[O.sub.2] and Ti[O.sub.2]/AC spectra, peaks around 3400 [cm.sup.-1] were assigned to -OH stretching, while those at 1600 [cm.sup.-1] were assigned to -OH vibration. These peaks can be attributed to the adsorbed water from the environment.
The morphologies and size of the prepared nanoparticles were studied by variable pressure scanning electron microscope (VPSEM) and transmission electron microscopy (TEM) (Figures 2 and 3).
From the TEM image of Figure 3(a), it was shown that bare Ti[O.sub.2] particles are uniform in shape, with sizes ranging from 25 to 30 nm. Figure 3(b) shows Ti[O.sub.2]/PANi composite, where the sizes range from 30 to 40 nm. Both TEM and FESEM photographs show that there is no significant difference of particle size of the samples Ti[O.sub.2]/C and Ti[O.sub.2]/AC (before and after chemical activation of KOH solution) (40-80 nm). This agrees with previous studies, which reported that the sintering effect did not occur for Ti[O.sub.2]/carbon after being heated at temperatures below 700[degrees]C .
The XRD patterns of the prepared samples were shown in Figure 4. The main diffraction peaks were at 25.3[degrees], 37.8[degrees], 48[degrees], 54[degrees], and 62.6[degrees], assigned to the diffraction planes of (1 0 1), (0 0 4), (2 0 0), (1 0 5), and (2 0 4) for anatase (JCPDS number 021-1272), respectively. Other crystal phases corresponding to the peaks at 27.4 and 36.1[degrees] were assigned to the diffraction peaks of (110) and (10 1) of rutile (JCPDS number 021-1276), respectively. The XRD patterns revealed the diffraction peaks of a mixture of anatase and rutile in the prepared samples, which is favorable for photocatalytic reactions [20-23]. XRD also showed that the preparation of Ti[O.sub.2] composites did not affect the crystal structure of Ti[O.sub.2], but the peaks intensity became lower and its shape got wider, especially in the case of Ti[O.sub.2]/PANi. This can be attributed to certain crystalline structure in PANi overlapping Ti[O.sub.2] peaks, but this effect is less pronounced in Ti[O.sub.2]/C and Ti[O.sub.2]/AC. The anatase content (/(A)) was determined from the integrated intensity of the anatase diffraction line (1 0 1), [I.sub.A], and that of the rutile diffraction line (1 1 0), [I.sub.R], using the following equation  and the results are listed in Table 1:
f(A)= 1/1 + 12.6 ([I.sub.A]/[I.sub.R]). (2)
The f(A) values showed that the rutile phase is dominant in all of the prepared samples. Besides that, the crystallite size of the samples was calculated by applying the Scherrer equation on the plane (101) diffraction peak of anatase and (110) diffraction peak of rutile, as listed in Table 1. The BET surface area, pore size, micropore area, and volumes are listed in Table 1 as well. The results showed that the specific surface area adhered to the following order: Ti[O.sub.2]/AC > Ti[O.sub.2]/C > Ti[O.sub.2]/PANi >Ti[O.sub.2] (179 >134 > 54 > 9 [m.sup.2] [g.sup.-1]). This suggests that the characteristics of the composited catalyst were enhanced, as it provided more active sites for photocatalytic reactions to take place.
The thermal stability of the prepared Ti[O.sub.2]/PANi and Ti[O.sub.2]/AC was investigated and the TG-DTA analysis results are shown in Figure 5. The first weight loss took place in the range of temperature 50-120[degrees]C for Ti[O.sub.2]/PANi, which is 6.5% decrease from the original weight. The weight loss is due to the loss of moisture or water content, the evaporation of solvents such as ethanol and small molecules from the polymer matrix . The second loss was determined at temperatures between 310 and 700[degrees]C. During this step, the weight loss was attributed to the degradation of polyaniline main chain (about 54%) [26-28]. At a temperature of about 700[degrees]C, the PANi molecule was completely decomposed to carbon. The result showed that Ti[O.sub.2]/AC has significantly improved thermal stabilities compared to Ti[O.sub.2]/PANi.
3.1. Evaluation of Photocatalytic Performance. The degradation of methylene blue (MB) was used in this work in order to evaluate the photocatalytic activity of the prepared samples. The effect of different loading percentages of Ti[O.sub.2] in activated carbon on photocatalytic activity has been investigated as well (Figure 6). The results showed that increasing the content of Ti[O.sub.2] improves photocatalytic performances. From the tests, it was determined that the 15% Ti[O.sub.2] loading was to be further tested.
It is known that the concentration of methylene blue influences the photocatalytic performance of the samples . Therefore, in this study, the photocatalytic activity of Ti[O.sub.2]/PANi and Ti[O.sub.2]/AC (0.05 mM) using different concentrations of MB within 90 minutes irradiation time was studied. It can be seen that Ti[O.sub.2]/activated carbon demonstrated superior photocatalytic activity for all different concentrations of MB (Figure 7).
The photocatalytic activity was also evaluated using irradiation time acting as its parameter (Figure 8). The result show rapid increase in MB degradation from 0 to 30 minutes which becomes slower after 30 minutes for both samples. The much higher MB degradation rate for Ti[O.sub.2]/AC proves its better performance compared to Ti[O.sub.2]/PANi. Ti[O.sub.2]/AC showed almost complete degradation of MB after 90 minutes of irradiation.
Figure 9 presents the result of the degradation of MB for bare Ti[O.sub.2], Ti[O.sub.2]/PANi, Ti[O.sub.2]/C, and Ti[O.sub.2]/AC. The experiment was carried out in 90-minute irradiation, and the concentration of methylene blue was 0.05 mM for all samples. The degradation of MB without catalyst was used as a reference.
The results can be explained using texture properties of the prepared samples, as shown in Table 1. The specific surface area, micropore area, and volume adhered to the trend Ti[O.sub.2]/AC > Ti[O.sub.2]/C > Ti[O.sub.2]/PANi >Ti[O.sub.2], which is similar to photocatalytic performance. This is attributed to the higher porosity of the activated carbon compered to others, which provide high adsorption capacity and more active sites for the reacting species during chemical reaction, which agrees with previous studies [8, 9, 19, 30-32]. It was noted that the surface area of Ti[O.sub.2]/AC is larger compared to the ones reported in the literature, which used polystyrene (PS) as a carbon source . It also shows that PANi is a better source for the preparation of highly porous activated carbon.
On top of the synergistic effect for the mixture of Ti[O.sub.2] with activated carbon and highly porous structures, the high photocatalytic performance could be the result of the mixture of anatase and rutile phase of Ti[O.sub.2] in this work (Table 1). This can be explained by the synergic effect between anatase and rutile in Ti[O.sub.2] particles that are approximately close to each other, thus enhancing the activity . This finding is in agreement with other studies reporting that the photocatalytic activity was enhanced when anatase and rutile were mixed [34, 35].
3.2. Recyclability of Ti[O.sub.2]/AC. Recyclability test was carried out for Ti[O.sub.2]/AC to up to five cycles. The results are depicted in Figure 10, demonstrating good recyclability for the prepared composite.
Regarding the possibility of photocatalytic improvement using a composite of Ti[O.sub.2], a different form of modified Ti[O.sub.2], namely, Ti[O.sub.2]/activated carbon (AC), Ti[O.sub.2]/Carbon (C), and Ti[O.sub.2]/PANi, were synthesized and characterized, and their catalytic performance have been studied. The effect of Ti[O.sub.2] loading, irradiation time, and MB concentration has been studied. Ti[O.sub.2]/AC showed the highest porosity and photocatalytic performance compared to other composites. On top of considering the synergistic effect for the mixture of Ti[O.sub.2] with activated carbon and its high porosity, this high performance can also be attributed to the anatase and rutile mixture. Meanwhile, PANi demonstrated better AC source compared to previous works, and the recyclability test demonstrated excellent performance for the synthesized composite.
Conflict of Interests
The authors declare that there is no conflict of interests regarding the publication of this paper.
The authors would like to acknowledge the financial support of the work by the Universiti Kebangsaan Malaysia for funding this project under the research Grants of Dana Impak Perdana (DLP-2013-015 and FRGS/1/2012/TK07/UKM/3/4) from Ministry of Higher Education (MOHE), Malaysia, and Centre of Research and Innovation Management (CRIM), UKM.
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Zatil Amali Che Ramli, (1) Nilofar Asim, (1) Wan N. R. W. Isahak, (2) Zeynab Emdadi, (1) Norasikin Ahmad-Ludin, (1) M. Ambar Yarmo, (2) and K. Sopian (1)
(1) Solar Energy Research Institute, Universiti Kebangsaan Malaysia, 43600 Bangi, Selangor, Malaysia
(2) School of Chemical Science & Food Technology, Faculty of Science and Technology, Universiti Kebangsan Malaysia, 43600 Bangi, Selangor, Malaysia
Correspondence should be addressed to Nilofar Asim; firstname.lastname@example.org
Received 6 February 2014; Accepted 7 May 2014; Published 11 June 2014
Academic Editor: Liqiang Jing
TABLE 1: Texture properties of the Ti[O.sub.2], Ti[O.sub.2]/PANi, Ti[O.sub.2]/C, and Ti[O.sub.2]/AC composites. Physical properties Ti[O.sub.2] Ti[O.sub.2]/PANi Surface area ([m.sup.2]/g) 8.55 53.73 Pore size (nm) 9.48 13.8 Micropore area ([m.sup.2]/g) 3.34 8.22 Microporevolume ([cm.sup.3]/g) 0.001 0.004 Crystallite size (a) (nm) anatase 25 14 Crystallite size (a) (nm) rutile 48 19 f(A) (b) 0.135 0.061 Physical properties Ti[O.sub.2]/C Ti[O.sub.2]/AC Surface area ([m.sup.2]/g) 134 178.57 Pore size (nm) 9.26 6.79 Micropore area ([m.sup.2]/g) 29.33 76.62 Microporevolume ([cm.sup.3]/g) 0.015 0.037 Crystallite size (a) (nm) anatase -- 11 Crystallite size (a) (nm) rutile -- 20 f(A) (b) 0.087 0.092 (a) Calculated by applying Scherrer's equation. (b) Anatase content calculated using (2). FIGURE 6: Effect of Ti[O.sub.2] loading (%) on degradation of MB (under 90 minutes of UV light irradiation in room temperature). Ti[O.sub.2] loading (%) 1 87.27 5 95.83 10 96.64 15 98.24 Note: Table made from bar graph. FIGURE 7: Effect of MB concentration on photocatalytic activity for Ti[O.sub.2]/PANi and Ti[O.sub.2]/AC. Concentration Ti[O.sub.2] Ti[O.sub.2] of MB (mM) /PANi /AC 0.15 54 94.54 0.1 63 95.73 0.05 69 98.24 Note: Table made from bar graph. FIGURE 8: Photocatalytic activity: effect of irradiation time in degradation of MB. 15%-Ti[O.sub.2] 15%-Ti[O.sub.2] /AC /PANi 39% 22% 55% 29% 70% 34% 88% 46% 94.64% 55% 96.48% 61% 98.24% 69% 98.30% 73% Note: Table made from line graph. FIGURE 10: Recyclability of Ti[O.sub.2]/AC was carried out for 5 cycles used. 1st time 98 2nd time 97 3rd time 95 4th time 88 5th time 83 Note: Table made from bar graph.
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|Title Annotation:||Research Article|
|Author:||Ramli, Zatil Amali Che; Asim, Nilofar; Isahak, Wan N.R.W.; Emdadi, Zeynab; Ahmad-Ludin, Norasikin; Y|
|Publication:||The Scientific World Journal|
|Date:||Jan 1, 2014|
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