Table of Contents Author Guidelines Submit a Manuscript
International Journal of Photoenergy
Volume 2014 (2014), Article ID 503825, 6 pages
Research Article

Photocatalytic Degradation of Anthracene in Closed System Reactor

1Chemistry Department, College of Science, Al-Qadisiya University, Al Deewaniya 58002, Iraq
2Chemistry Department, College of Science, Babylon University, Hilla 51002, Iraq
3Institut für Technische Chemie, Leibniz Universität Hannover, 30167 Hannover, Germany

Received 3 April 2014; Revised 24 May 2014; Accepted 7 June 2014; Published 8 July 2014

Academic Editor: Chuanyi Wang

Copyright © 2014 Faiq F. Karam 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.


Polycyclic aromatic hydrocarbons (PAHs) represent a large class of persistent organic pollutants in an environment of special concern because they have carcinogenic and mutagenic activity. In this paper, we focus on and discuss the effect of different parameters, for instance, initial concentration of Anthracene, temperature, and light intensity, on the degradation rate. These parameters were adjusted at pH 6.8 in the presence of the semiconductor materials (TiO2) as photocatalysts over UV light. The main product of Anthracene photodegradation is 9,10-Anthraquinone which isidentified and compared with the standard compound by GC-MS. Our results indicate that the optimum conditions for the best rate of degradation are 25 ppm concentration of Anthracene, regulating the reaction vessel at 308.15 K and 2.5 mW/cm2 of light intensity at 175 mg/100 mL of titanium dioxide (P25).

1. Introduction

Polycyclic aromatic hydrocarbons (PAHs) constitute an important and hazardous group of priority contaminates [1]. Several researchers determined the concentrations of these compounds by different chromatographic techniques, for instance, HPLC [24], GC-MS/MS in [5], and GC-MS in [6, 7]. The main processes that successfully eliminated PAHs from the environment included the microbiological transformation and degradation, bioaccumulation, biological uptake volatilization, photooxidation, and chemical oxidation [8]. Photolysis and ozonation are the most important methods for transformation for most PAHs adsorbed on natural substances in an environment [9]. Photolysis of PAHs led to the formation of photodimers and photooxidation products [10]. In recent years, the release of toxic and organic contaminants into aquatic environment as a result of human activities has drawn much attention and is considering a baffling problem facing researchers today [11]. Zinc oxide and titanium dioxide are universally considered as the most important photocatalysts due to their lower cost and their considerably low band gap energy (~3.2 eV) [12]. Nanoparticles of titanium dioxide were considered to be more efficient than bulk powder in photocatalytic field [13]. Several previous works used titanium dioxide as catalyst for degradation of different organic pollutants [1416].

Semiconductors have been used for pollutants degradation in water to be less harmful inorganic material. Both catalysts titanium dioxide and zinc oxide have photocatalytic properties which made these catalysts the best for photodegradation of water pollutants [17]. Attention has been focused in the past decade on using nanocrystalline TiO2 as a photocatalyst for the organic pollutants degradation. TiO2 semiconductor has a wide band gap about 3.2 eV, which corresponds to the UV-range radiation. The formation of an electron hole pair occurs within the conduction and valance bands of TiO2 semiconductor after absorption in UV range. Water molecules can be oxidized to hydroxyl radical by positive hole. Scheme 1 shows the mechanism diagram for photodegradation of Anthracene. The hydroxyl is a radical, frequent, and powerful oxidant. The oxidation of organic pollutants seems to be mediated by a series of reactions started by hydroxyl radical on the TiO2 surface. Recombination for the produced hole from valance band and separated electron from conductive band it can appear either in the volume or on the surface of the semiconductor particle accompanied with heat releasing. To this end, both UV light source and TiO2 are necessary for photooxidation reaction to occur [18]. The photodegradation of PAHs compounds in water using TiO2 catalyst has proved high efficiency in [19].

Scheme 1: Mechanism diagram of photocatalytic degradation for Anthracene.

Furthermore, many researchers dealt with the PAHs in water by photocatalytic degradation for TiO2. Woo et al. in [20] investigated photocatalytically oxidation using TiO2 of 5 selected PAHs, namely, naphthalene, acenaphthylene, phenanthrene, Anthracene, and benzo[a]anthracene. Gu et al. in [21] studied degradation of phenanthrene on soil surfaces photocatalytically with the addition of nanoparticulate anatase TiO2 under UV-irradiation. Vela et al. in [22] discussed photocatalytic processes using semiconductor materials (ZnO and TiO2) to remove the residual concentrations of several PAHs from groundwater. Theurich et al. in [23] reported themechanism of the photocatalytic transformation of naphthalene and Anthracene qualitatively in aqueous suspensions of titanium dioxide. Indeed, catalyst TiO2 can play as efficient photocatalyst in the oxidation of PAHs and convert it to safer compounds especially with Anthracene, Fluorene, and Naphthalene by artificial or sunlight illumination [19, 24]. To this end, our aim in the present paper is to study the effect of photocatalytic reactions on the degradation of Anthracene using titanium dioxide under different experimental conditions.

UV illumination of TiO2 yields valence band holes and conduction band electrons (1), which interact with the surface adsorbed molecular oxygen to give superoxide radical anions, (2), and finally, the water produces radicals of HO (3) [25]. These radicals oxidize target molecule (Anthracene) to Anthraquinone (4):

2. Experimental Procedure

2.1. Chemicals and Reagents

Anthracene was purchased from Sigma Aldrich, Germany, and used without further purification. Acetonitrile (anhydrous, ≥99.98%), Dichloromethane (anhydrous, ≥99.98%), Acetone, ethyl acetate (anhydrous, ≥99.98%), and methanol HPLC-gradient grade were purchased also from Sigma Aldrich, Germany. Titanium dioxide particles were purchased from Degussa (P25), anhydrous Na2SO4 (extra pure Allied Signal, Riedel-de—Germany).

2.2. Preparation of Stock Solution of Anthracene

A set of dilutions of Anthracene solution at the concentration of 100 mg/L were made in the following solvents: methanol, dichloromethane, acetonitrile, ethyl acetate, and acetone. Anthracene solutions in the above solvents were prepared and stored in room temperature (°C) in dark place to keep it from the light degradation. Calibration curve for Anthracene solution has been achieved by preparation several concentrations (0.1, 0.5, 1, 2, 4, 8, 16 and 30) mg/L. All glassware used for experiments was washed in chromic acid mixture for 12 h with methanol, deionized water, and acetone and then dried at 110°C for 3 h.

2.3. Solid Phase Extraction and Sample Preparation

Solid phase extraction (SPE) method was used to extract the Anthracene from the mixture (aqueous solution at different solvents) by Supelcoclean ENV-18 solid phase extraction tube. After passing the specific volume of aqueous solution through extraction column, the extract was treated with anhydrous Na2SO4 to remove all the water content from the extract and then it was concentrated by rotary evaporator (BUCHI-RE121-Swizerland made) in temperatures below 35°C by water bath (BUCHI 461 Metrohm/Swiss made) to be in volume 1 mL. Then samples were analyzed by GC 2010 (Shimadzu, Japan). The study revealed that the Anthracene level had no effect on the percent decrease of the compound during evaporation process for the solvent. The average recovery of analytes for every liquid media and corresponding relative standard deviations RSD () were represented in Table 1. Chromatographic conditions are listed in Table 2.

Table 1: The average recovery of Anthracene and relative standard deviations RSD ().
Table 2: Chromatographic conditions were used for determination Anthracene by GC.
2.4. Photolysis Experiments

The experiments were carried out in glass dual wall reactor closed system type, to keep the temperature constant using chiller (Julabo model EH/Germany) as temperature controller. Agitation of the reaction mixture was provided by a magnetic stirrer (Heidolph-Mr3001). The photoreactor operated in a batch mode. The study was carried out for selected compound Anthracene (Sigma Aldrich) without additional purification. The pH of the reaction solution adjusted about 6.8, pH by adding an exact volume of Sodium hydroxide or sulfuric acid.

2.5. Kinetics of the Photocatalytic Process

Kinetics of Anthracene degradation was calculated by the first-order equation: or where , are the PAH concentration at times (zero and ), respectively, and is the rate constant. First-order degradation rate constants were determined by regression analysis.

3. Results and Discussion

Several parameters were studied to indicate the effect of these degradation rates as follows.

3.1. Effect of the Initial Anthracene Concentrations

The effect of initial Anthracene concentration on the reaction rate is the first parameter studied in this work. Figure 1 shows that Anthracene concentrations decrease with time increases. The rate of degradation increases as the initial concentration increases as well. For photochemical reactions the higher concentration causes a higher light absorption and consequently accelerates the degradation rate [26]. Figure 2 shows the relation between rate constant and initial concentrations of Anthracene.

Figure 1: The changes of ln() with irradiation times on different Anthracene concentrations by TiO2.
Figure 2: Effects of initial Anthracene concentrations at a rate constant.
3.2. Effect of Temperature

The oxidation of Anthracene molecule was studied at different temperatures, to indicate the best one at which the degradation rate is fastest. Figure 3 shows the effect of temperature on the concentration of Anthracene with time of reaction. Figure 4 illustrates the Arrhenius plot for the relation between and , activation energy calculated by Arrhenius equation.

Figure 3: Effect of temperature on the degradation rate of Anthracene.
Figure 4: Arrhenius plot for photocatalytic degradation of Anthracene on TiO2 at (278.15–308.15) K.

The influence of temperature on the degradation rate is typical. The greatest increase of the rate of degradation about two times can be achieved after about 180 min at 308.15 K; initial rates within the first 30 min appear to increase with increasing the temperature. This phenomenon is related to the effect of temperature on the stability of Anthracene molecule. Luo et al. [27] reported that higher temperature slightly enhances the rate constant of Pyrene.

3.3. Effect of Light Intensity

UV light intensity has an important role in the process of photocatalytic degradation. Figure 5 shows effect of light intensity on the degradation rate of Anthracene molecule. This figure indicates that the reactions followed pseudo-first-order rate constant with increasing UV light intensity from 1–2.5 mW/cm2. The results indicate the perfect degradation at light value: 2.5 mW/cm2.

Figure 5: Effect of light intensity on the degradation rate of Anthracene.

Therefore, when light intensity increases the number of photons increases which means that the formation of electrons and holes increases, and hence, electron-hole recombination is negligible. However, at the lower light intensity, electron and hole pair separation competes with recombination which in turn decreases the formation of free radicals [28], causing less effect on the rate of degradation of the Anthracene as shown in Figure 6.

Figure 6: The effect of initial light intensity on the rate constant.
3.4. Photodegradation Products of Anthracene

The major product for photodegradation of Anthracene is 9,10-Anthraquinone. Anthraquinone is characterized by GC-MS (2010-SHIMADZU). Standard solution 25 ppm of 9,10-Anthraquinone (Sigma Aldrich) was prepared and compared with that produced by oxidation. Figures 7 and 8 illustrate that there are no differences between them. The proposed degradation pathway of Anthracene is as in Figure 11.

Figure 7: Chromatogram of GC-MS for standard 9,10-Anthraquinone and produced by oxidation of Anthracene before exposure to UV light.
Figure 8: Mass spectra for standard 9,10-Anthraquinone before exposure to UV light.

During the photocatalytic degradation experiments with Anthracene only 9,10-Anthraquinone was detected as an intermediate, in agreement with Theurich et al. [23]. Figures 9 and 10 show the GC chromatogram and mass spectra for 9,10-Anthraquinone after exposure to the light intensity in the same environment of perfect conditions for Anthracene degradation.

Figure 9: Chromatogram of GC-MS for standard 9,10-Anthraquinone after exposure to UV light.
Figure 10: Mass spectra for standard 9,10-Anthraquinone after exposure to UV light.
Figure 11: Proposed pathway degradation of Anthracene.

4. Conclusions

The photocatalytic degradation of Anthracene using artificial UV light has been achieved. The observations of these investigations demonstrate the importance of selecting the optimum parameters for degradation to obtain a high degradation rate, which is considered essential for any application of photocatalytic oxidation processes. The experimental work in controlled pH media at closed system reactor has found that the main product of oxidation of Anthracene is 9,10-Anthraquinone, which is safer for environment than Anthracene. The rate of photodegradation in present UV light has been found to be maximum in neutral medium with optimum concentration of 25 ppm of Anthracene. The optimum temperature for degradation is 308.15 K. The optimum light intensity is 2.5 mW/cm2 at pH 6.8. The degradation of Anthracene increases with the increase of light intensity. Nevertheless, the increase of light intensity leads to the increase of the number of electron-hole pairs and increases the degradation of Anthracene.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.


The authors are gratefully acknowledging the financial support provided by the Arab Science and Technology Foundation (ASTF) without which this research would not have been possible. The authors also express sincere appreciation to all the staff working at ASTF, Baghdad Office. The authors thank Dr. Amir Hakki for his assistance in the experimental phases of the research.


  1. S. Ledakowicz, J. S. Miller, and D. Olejnik, “Oxidation of PAHs in water solution by ozone combined with ultraviolet radiation,” International Journal of Photoenergy, vol. 3, no. 2, pp. 95–101, 2001. View at Publisher · View at Google Scholar · View at Scopus
  2. F. J. López-Jiménez, A. Ballesteros-Gómez, and S. Rubio, “Determination of polycyclic aromatic hydrocarbons (PAH4) in food by vesicular supramolecular solvent-based microextraction and LC-fluorescence detection,” Food Chemistry, vol. 143, pp. 341–347, 2014. View at Publisher · View at Google Scholar · View at Scopus
  3. M. Ciecierska and M. W. Obiedziński, “Polycyclic aromatic hydrocarbons in the bakery chain,” Food Chemistry, vol. 141, no. 1, pp. 1–9, 2013. View at Publisher · View at Google Scholar · View at Scopus
  4. T. Payanan, N. Leepipatpiboon, and P. Varanusupakul, “Low-temperature cleanup with solid-phase extraction for the determination of polycyclic aromatic hydrocarbons in edible oils by reversed phase liquid chromatography with fluorescence detection,” Food Chemistry, vol. 141, no. 3, pp. 2720–2726, 2013. View at Publisher · View at Google Scholar · View at Scopus
  5. J. Pincemille, C. Schummer, E. Heinen, and G. Moris, “Determination of polycyclic aromatic hydrocarbons in smoked and non smoked black teas and tea infusion,” Food Chemistry, vol. 145, pp. 807–813, 2014. View at Google Scholar
  6. A. L. V. Escarrone, S. S. Caldas, E. B. Furlong, and V. L. Menghetti, “Polycyclic aromatic hydrocarbons in rice grain dried by different processes: evaluation of quick, easy, cheap, effective, rugged and safe extraction method,” Food Chemistry, vol. 146, pp. 597–602, 2014. View at Publisher · View at Google Scholar
  7. A. M. R. Machado, M. G. Cardoso, H. S. Dorea et al., “Contamination of cachaca by PAHs from storage containers,” Food Chemistry, vol. 146, pp. 65–70, 2014. View at Google Scholar
  8. L. Zhang, P. Li, Z. Gong, and A. Oni Adeola, “Photochemical behavior of benzo[a]pyrene on soil surfaces under UV light irradiation,” Journal of Environmental Sciences, vol. 18, no. 6, pp. 1226–1232, 2006. View at Publisher · View at Google Scholar · View at Scopus
  9. J. Ma, Y. Liu, Q. Ma, C. Liu, and H. He, “Heterogeneous photochemical reaction of ozone with anthracene adsorbed on mineral dust,” Atmospheric Environment, vol. 72, pp. 165–170, 2013. View at Publisher · View at Google Scholar · View at Scopus
  10. R. Debestani, K. J. Ellis, and M. E. Sigman, “Photodecomposition of anthracene on dry surfaces: products and mechanism,” Journal of Photochemistry and Photobiology A: Chemistry, vol. 86, no. 1–3, pp. 231–239, 1995. View at Publisher · View at Google Scholar · View at Scopus
  11. N. A. Mir, M. M. Haque, A. Khan, M. Muneer, and C. Boxall, “Photoassisted degradation of a herbicide derivative, dinoseb, in aqueous suspension of titania,” The Scientific World Journal, vol. 2012, Article ID 251527, 8 pages, 2012. View at Publisher · View at Google Scholar · View at Scopus
  12. F. H. Hussein, “Comparison between solar and artificial photocatalytic decolorization of textile industrial wastewater,” International Journal of Photoenergy, vol. 2012, Article ID 793648, 10 pages, 2012. View at Publisher · View at Google Scholar · View at Scopus
  13. L. M. Ahmed, I. Ivanova, F. H. Hussein, and D. W. Bahnemann, “Role of platinum deposited on TiO2 in photocatalytic methanol oxidation and dehydrogenation reactions,” International Journal of Photoenergy, vol. 2014, Article ID 503516, 9 pages, 2014. View at Publisher · View at Google Scholar
  14. F. H. Hussein, “Effect of photocatalytic treatment on physical and biological properties of textile dyeing wastewater,” Asian Journal of Chemistry, vol. 25, no. 16, pp. 9387–9392, 2013. View at Google Scholar
  15. F. H. Hussein, “Chemical properties of treated textile dyeing wastewater,” Asian Journal of Chemistry, vol. 25, no. 16, pp. 9393–9400, 2013. View at Google Scholar
  16. F. H. Hussein and A. F. Halbus, “Rapid decolorization of cobalamin,” International Journal of Photoenergy, vol. 2012, Article ID 495435, 9 pages, 2012. View at Publisher · View at Google Scholar · View at Scopus
  17. A. J. Attia, S. H. Kadhim, and F. H. Hussein, “Photocatalytic degradation of textile dyeing wastewater using titanium dioxide and zinc oxide,” E-Journal of Chemistry, vol. 5, no. 2, pp. 219–223, 2008. View at Publisher · View at Google Scholar · View at Scopus
  18. W.-Y. Wang, A. Irawan, and Y. Ku, “Photocatalytic degradation of Acid Red 4 using a titanium dioxide membrane supported on a porous ceramic tube,” Water Research, vol. 42, no. 19, pp. 4725–4732, 2008. View at Publisher · View at Google Scholar · View at Scopus
  19. L. Zhang, P. Li, Z. Gong, and X. Li, “Photocatalytic degradation of polycyclic aromatic hydrocarbons on soil surfaces using TiO2 under UV light,” Journal of Hazardous Materials, vol. 158, no. 2-3, pp. 478–484, 2008. View at Publisher · View at Google Scholar · View at Scopus
  20. O. T. Woo, W. K. Chung, K. H. Wong, A. T. Chow, and P. K. Wong, “Photocatalytic oxidation of polycyclic aromatic hydrocarbons: intermediates identification and toxicity testing,” Journal of Hazardous Materials, vol. 168, no. 2-3, pp. 1192–1199, 2009. View at Publisher · View at Google Scholar · View at Scopus
  21. J. Gu, D. Dong, L. Kong, Y. Zheng, and X. Li, “Photocatalytic degradation of phenanthrene on soil surfaces in the presence of nanometer anatase TiO2 under UV-light,” Journal of Environmental Sciences, vol. 24, no. 12, pp. 2122–2126, 2012. View at Publisher · View at Google Scholar · View at Scopus
  22. N. Vela, M. Martínez-Menchón, G. Navarro, G. Pérez-Lucas, and S. Navarro, “Removal of polycyclic aromatic hydrocarbons (PAHs) from groundwater by heterogeneous photocatalysis under natural sunlight,” Journal of Photochemistry and Photobiology A: Chemistry, vol. 232, pp. 32–40, 2012. View at Publisher · View at Google Scholar · View at Scopus
  23. J. Theurich, D. W. Bahnemann, R. Vogel, F. E. Ehamed, G. Alhakimi, and I. Rajab, “Photocatalytic degradation of naphthalene and anthracene: GC-MS analysis of the degradation pathway,” Research on Chemical Intermediates, vol. 23, no. 3, pp. 247–274, 1997. View at Publisher · View at Google Scholar · View at Scopus
  24. S. Das, M. Muneer, and K. R. Gopidas, “Photocatalytic degradation of wastewater pollutants. Titanium-dioxide-mediated oxidation of polynuclear aromatic hydrocarbons,” Journal of Photochemistry and Photobiology A: Chemistry, vol. 77, no. 1, pp. 83–88, 1994. View at Publisher · View at Google Scholar · View at Scopus
  25. N. A. Laoufi, D. Tassalit, and F. Bentahar, “The degradation of phenol in water solution by TiO2 photocatalysis in helical reactor,” Global NEST Journal, vol. 10, no. 3, pp. 404–418, 2008. View at Google Scholar
  26. J. S. Miller and D. Olejnik, “Photolysis of polycyclic aromatic hydrocarbons in water,” Water Research, vol. 35, no. 1, pp. 233–243, 2001. View at Publisher · View at Google Scholar · View at Scopus
  27. Z. Luo, K. Katayama-Hirayama, T. Akitsu, and H. Kaneko, “Photocatalytic degradation of pyrene in porous Pt/TiO2 -SiO2 photocatalyst suspension under UV irradiation,” Nano, vol. 3, no. 5, pp. 317–322, 2008. View at Publisher · View at Google Scholar · View at Scopus
  28. D. Dong, P. Li, X. Li, Q. Zhao, Y. Zhang, and C. Jia, “Investigation on the photocatalytic degradation of pyrene on soil surfaces using nanometer anatase TiO2 under UV irradiation,” Journal of Hazardous Materials, vol. 174, no. 1–3, pp. 859–863, 2010. View at Publisher · View at Google Scholar · View at Scopus