Table of Contents Author Guidelines Submit a Manuscript
Journal of Chemistry
Volume 2015 (2015), Article ID 414269, 5 pages
Research Article

Visible Light Catalytic Degradation of Aniline Wastewater over Multishaped BiOBr Microcrystals

Chemical Engineering & Pharmaceutics School, Henan University of Science & Technology, Luoyang 471023, China

Received 5 September 2015; Revised 23 October 2015; Accepted 2 November 2015

Academic Editor: Davide Vione

Copyright © 2015 Jun Zhang 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 photooxidation process of aniline-containing simulated wastewater under visible light irradiation over BiOBr microcrystal grains with different shapes was studied. The distinctive surface microstructures of the BiOBr microcrystals, like clustered flower petals and quadrate lamellas, were produced by using imidazole ionic liquid and inorganic bromide as Br sources and by solvothermal and hydrothermal route, respectively. The ionic liquid not only can impact the products’ morphology, but also can largely improve the photocatalytic activity of the BiOBr microcrystals due to the soft templating effect. The top degradation ratio of the aniline wastewater photocatalyzed by lamellar BiOBr crystals is 23.71%, but the equivalent value photocatalyzed by flower petal-like BiOBr crystals is almost twice as much; that is, it reaches 46.51%. The photodegradation effect and mechanism over differently shaped BiOBr microcrystals have been compared.

1. Introduction

With the rapid development of photocatalytic theory and technology, photocatalytic oxidation (PCO), which is actually used for pollution abatement, especially for degradation of pollutants [13], has been attracting more and more attention. The PCO technology with such traits as small investment, high efficiency, mild treatment conditions, and no secondary pollution possesses incomparable advantages over other advanced oxidative process (AOPs). Titanium dioxide (TiO2), a semiconductor material with photocatalytic activity found in the 1970s, has been verified to have photodegradation ability for azo dyestuffs, and so forth, but it can only absorb ultraviolet light (ca 4-5% of sunlight) because of its wide band-gap energy ( = 3.2 eV). Poor response to visible light and low utilization efficiency of solar energy have limited its application range. BiOBr is a newly found semiconductor photocatalyst, which has the narrow band-gap energy ( = 2.7 eV) and good visible light response due to its unique lamellar structure made up of alternate overlay of [Bi2O2] and Br atomic layers, and is endowed with better visible light catalytic activity [4, 5]. Hence, the synthesis and application development concerning BiOBr has recently aroused broad interest. Different preparation methods and technological conditions can largely influence the microstructure and morphology of the resulting BiOBr product [6] and then impact its catalytic ability, selectivity, and stability [7]. Ionic liquids possess peculiar composition and structure and not only can be used as reactants, but also can serve as soft templates to regulate and control the product features [8, 9]. Introduction of some ionic liquids into the preparation process of BiOBr microcrystals can be expected to give particular BiOBr product with exceptional shape, property, and photocatalytic ability.

Aniline is a widely used industrial chemical, but it is also one of the recognized contaminants which can badly pollute water and soil. So, intensive study on controlling and removing the aniline-induced pollution is of great importance [10, 11]. Due to its high chemical stability, aniline is hardly degraded by some conventional approaches. To our knowledge, the photocatalysts used to study aniline degradation are mostly transition metal oxides, such as TiO2 [12] and ZnO [13]. In addition, the studies involving TiO2 and ZnO photocatalysis were almost always based on UV light irradiation. Here, we firstly report the research results about visible light catalytic degradation of aniline-containing wastewater over multishaped BiOBr crystal grains, comparing their photodegradation performance.

2. Experimental Section

2.1. Chemicals and Instruments

The chemicals bismuth nitrate (Bi(NO3)3·5H2O), sodium bromide (NaBr), ethylene glycol ((HOCH2)2), and aniline (C6H5NH2), purchased from Shanghai Chemical Reagent Company of China, were of analytically pure grade with purity of more than wt. 99%; the ionic liquid 1-butyl-3-methylimidazolium bromide ([C4mim]Br) was customized product with purity of higher than wt. 98%. The phase composition was characterized on a Bruker D8-advanced X-ray diffractometer. The morphology was observed on a Quanta FEG250 scanning electron microscope. The GC-MS instrument (7890A-5975C) was employed to determine the degradation products under the following GC conditions: chromatographic column of DB-5MS UI (30 m × 0.32 mm × 0.32 μm), temperature programming (35 to 185°C), and MS conditions: electron impact ionization source (70 eV) and scanning range (45~180 amu). The specific surface area was measured on a NOVA 2200e surface area analyzer. A double-beam ultraviolet-visible spectrophotometer (TU-1901) was used for measuring the optical adsorption properties of the degraded mixtures.

2.2. Synthesis of Multishaped BiOBr Microcrystals

Under room temperature and by magnetic stirring, the Br source solution prepared by dissolving 2 mmol [C4mim]Br in 20 mL (HOCH2)2 was slowly dripped into the fully mixed bismuth nitrate solution consisting of 2 mmol Bi(NO3)3·5H2O and 20 mL (HOCH2)2. The initial colorless mixture gradually changed to light yellow suspension containing some insoluble particles. The resulting suspension was poured in a 100 mL teflon-lined autoclave with volumetric filling degree of 80%. After tight sealing, the autoclave was put in a drying oven and kept at 423 K for 12 h. When the solvothermal reaction was over, the autoclave was naturally cooled to ambient temperature. Through centrifugal separation, the isolated solid was in turn washed by water and absolute ethyl alcohol several times, followed by vacuum desiccation at 333 K for 10 h. A faint yellow powder-like product sample was obtained, which was labeled as BiOBr-IL. Analogously, by using NaBr as inorganic Br source to replace ionic liquid [C4mim]Br and water as a substitute for ethylene glycol, the same procedures as above were also carried out so as to prepare BiOBr product. Through such an alternative route, the as-prepared faint yellow powder sample was marked as BiOBr-SB.

2.3. Evaluation of Visible Light Catalytic Performance of the BiOBr Samples

Using BiOBr crystals as catalysts to photocatalytically degrade aniline solution, the related changes of UV-vis absorbance for the reaction mixture can be used for the evaluation of catalytic performance of the BiOBr samples. The photocatalytic degradation reaction was carried out in a photochemical reaction apparatus (BL-GHX-V, Shanghai). A high pressure xenon lamp with adjustable power was used to provide light source, and the nonvisible parts (<420 nm wavelength) were filtered by an optical filter so as to guarantee visible light irradiation. The simulated aniline wastewater with a concentration of 10 mg/L was obtained by mixing aniline with water. The photocatalytic reaction mixture was prepared by putting 0.05 g BiOBr microcrystals in 100 mL aniline wastewater, which was put in the quartz reaction tube in advance, and magnetically stirring for 60 min in dark box so as to reach adsorption equilibrium. At this point, the xenon lamp (adjusted at 500 W) was turned on, and the light-catalyzed reaction was immediately activated. Afterwards, 4 mL reaction solution was sampled every 0.5 h, and the corresponding UV-vis absorption spectrum was measured. According to Lambert-Beer law, the concentration of aniline solution is proportional to absorbance at characteristic absorption wavelength, and the content and degradation ratio of the aniline solution can thereby be quantitatively determined.

3. Result and Discussion

3.1. Phase Composition of the BiOBr Samples

The XRD patterns of the BiOBr samples synthesized by using different Br sources are together exhibited in Figure 1. As shown in the figure, the main diffraction peaks regarding BiOBr-IL and BiOBr-SB are similar with almost same peak positions and intensity, but the peaks of BiOBr-IL show dispersion feature to some extent (Figure 1(b)). By contrast, the diffraction peaks of BiOBr-SB look shaper and more refined (Figure 1(a)), though the positions of the main peaks are consistent with those of the other sample. In the 2θ position of 10.9°, 21.9°, 25.3°, 31.8°, 32.3°, 39.4°, 46.3°, 50.8°, and 57.3°, there appear nine peaks, respectively. By comparing with JCPDS database, it can be identified that these peaks coincide with those of BiOBr crystal (PDF Number 73-2061), corresponding to the crystal faces (001), (002), (011), (012), (110), (112), (020), (014), and (212), respectively, which belongs to tetragonal crystal system with space group P4nmm(129). Moreover, no emergence of extra peaks implies quite elevated purity of as-prepared BiOBr product samples.

Figure 1: The XRD patterns of as-prepared BiOBr product samples. (a) BiOBr-SB; (b) BiOBr-IL.

According to Scherrer formula: , where , , and are X-ray wavelength, Bragg diffraction angle, and half peak width of (012) face, respectively, the mean particle diameter () of both BiOBr powders can be calculated: BiOBr-SB ( = 516 nm), BiOBr-IL (127 nm), which basically agree with the SEM observation. Obviously, assistance of the ionic liquid could make the BiOBr crystal grains become smaller, verifying the regulating action of the ionic liquid in this inorganic synthesis [14]. Besides, for BiOBr-IL and BiOBr-SB, the diffraction peak strength ratios for crystal faces (110) to (012) are 2.71 and 0.98, respectively, indicating that the ionic liquid contributes to orienting the growth of crystal face (110) in the BiOBr crystal growth process.

3.2. Morphology and Specific Surface Area of the BiOBr Samples

The SEM images of the BiOBr samples prepared by using different Br sources are shown in Figure 2. The BiOBr-SB crystals mostly show square sheets with about 2 μm edge length and 50 nm thickness. In contrast, the shape of the BiOBr-IL crystals reveals much difference, displaying a spherically porous structure with a hole on it, just like clustered flower petals. This further proves that the ionic liquid has considerable impact on the morphology of as-prepared BiOBr products. The particular microstructure of BiOBr-IL crystals with higher porosity may be partly attributed to higher dielectric constant () and good hydrophilicity of the ionic liquid [C4mim]Br, which could effectively retard conglomeration among the nascent BiOBr crystalline grains. Referring to the formation mechanism of CuS hollow spheres [15], it is conceivable for us to speculate the reason while a little hole was formed on the surface of the BiOBr-IL globoids. The speculation is based on the fact that the ionic liquid [C4mim]Br preferentially clusters together according to a special pattern to form the “crystal nucleus,” on which the BiOBr crystalline plates grow. During washing and cooling, the template could escape from the inside of the core-shell structure, leaving an irregular hole on the outside.

Figure 2: The SEM images of as-prepared BiOBr samples. (a) BiOBr-SB; (b) BiOBr-IL.

The measurements of specific surface area for BiOBr-IL and BiOBr-SB are 14.71 m2/g and 6.36 m2/g, respectively.

3.3. Photocatalytic Degradation of Aniline over Both BiOBr Samples

The removal or degradation of the aniline in wastewater via visible light catalytic action of both BiOBr microcrystals has been experimentally determined. Just as shown in Figure 3, in the absence of any catalyst, the degradation ratio (ratio between the aniline concentration decrease at a given time and the initial concentration) of the aniline solution is almost negligible despite the sufficiently long visible light irradiation time. This means that suitable catalyst for the degradation reaction is necessary. The BiOBr-SB microcrystals have been found to possess visible light catalytic activity to some degree, but the degradation ratio of aniline is not satisfactory. At reaction times of 1 h and 4 h, the degradation ratios in the presence of BiOBr-SB microcrystals were 13.60% and 23.71%, respectively. Compared to BiOBr-SB, the visible light catalytic activity of BiOBr-IL microcrystals was significantly higher. During the same reaction time as BiOBr-SB, the corresponding degradation ratios in the presence of BiOBr-IL reached 27.04% and 46.51%, respectively, of which the top degradation ratio is nearly twice that of BiOBr-SB. In consideration of the measurement results of SEM and specific surface area, we can deduce the reason for the difference of catalytic ability of the two BiOBr crystals. The larger specific surface area of the clustered flower petal BiOBr-IL could provide more active sites in comparison with lamellar BiOBr-SB, which should be the main reason for the difference in catalytic activity. What is more, the porous and dispersive microstructure of the BiOBr-IL crystals could make visible light scattered or reflected, leading to extension of the light propagation path, thus generating more photoelectrons and vacancies [16].

Figure 3: The plot of aniline degradation ratio versus reaction time.

In the process of photocatalytic reaction, the color of the aniline solution changed from colorless to brownish yellow, visually depicting the degradation course of aniline. The serial changes of absorption spectra of the aniline solution catalyzed by BiOBr-IL crystals during different reaction times are shown in Figure 4. Evidently, the intensity of the characteristic absorption peaks (λ = 230 nm, λ = 280 nm) gradually weakens with the prolonging of reaction time, suggesting a gradual reduction of aniline concentration. By measuring the intermediate products during different reaction stages we have verified the existence of such species by GC-MS measurements: aminophenol, nitrobenzene, and azobenzene, and the concentration relationship of these species follows: aminophenol > nitrobenzene > azobenzene. In addition, we also detected inorganic species like and through ion chromatography (ICS-900, Dionex, USA). Referring to related report [11], we suggest a possible 4-step mechanism for aniline degradation: (1) reactive species, such as radicals, stemming from reaction of photogenerated vacancies with H2O oxidize aniline to generate azobenzene, nitrobenzene, and aminophenol; (2) the intermediates turn to hydroxyl derivatives via electrophilic addition; (3) the aromatic rings of aromatic species break to form 6-carbon aldehydes and acids; (4) the 6-carbon intermediates further degrade to mineralization species: , .

Figure 4: The changing relation of UV-vis absorption spectra during the aniline degradation process.

4. Conclusions

(1) Through hydrothermal and solvothermal approach, the square sheet-like and clustered flower petal-like BiOBr microcrystals were synthesized. The XRD and SEM measurements show that ionic liquid [C4mim]Br not only acts as reactant to provide a Br source, but also more importantly can play the role of soft template to fabricate the morphologies of the resulting products. (2) The as-prepared BiOBr products with both different kinds of morphologies all have visible light catalytic activity in varying degrees, but, in the case of aqueous aniline degradation, the photocatalytic activity of the clustered flower petal-like BiOBr-IL microcrystals was much larger than that of the quadrate lamellar BiOBr-SB products.

Conflict of Interests

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


The authors gratefully acknowledge the financial support from the National Natural Science Foundation of China (21576073) and Key Laboratory Construction Project for Chemical Engineering of Mineral Resources of Luoyang City (1003016A).


  1. E. S. Aazam and R. M. Mohamed, “Environmental remediation of direct blue dye solutions by photocatalytic oxidation with cuprous oxide,” Journal of Alloys and Compounds, vol. 577, pp. 550–555, 2013. View at Publisher · View at Google Scholar · View at Scopus
  2. M. A. Nasalevich, E. A. Kozlova, T. P. Lyubina, and A. V. Vorontsov, “Photocatalytic oxidation of ethanol and isopropanol vapors on cadmium sulfide,” Journal of Catalysis, vol. 287, pp. 138–148, 2012. View at Publisher · View at Google Scholar · View at Scopus
  3. V. Píšťková, M. Tasbihi, M. Vávrová, and U. L. Štangar, “Photocatalytic degradation of β-blockers by using immobilized titania/silica on glass slides,” Journal of Photochemistry and Photobiology A, vol. 305, pp. 19–24, 2015. View at Publisher · View at Google Scholar
  4. D. Zhang, M. Wen, B. Jiang, G. Li, and J. C. Yu, “Ionothermal synthesis of hierarchical BiOBr microspheres for water treatment,” Journal of Hazardous Materials, vol. 211-212, pp. 104–111, 2012. View at Publisher · View at Google Scholar · View at Scopus
  5. E. Brillas, E. Mur, R. Sauleda et al., “Aniline mineralization by AOP's: anodic oxidation, photocatalysis, electro-Fenton and photoelectro-Fenton processes,” Applied Catalysis B: Environmental, vol. 16, no. 1, pp. 31–42, 1998. View at Publisher · View at Google Scholar · View at Scopus
  6. Z. Liu, B. Wu, D. Xiang, and Y. Zhu, “Effect of solvents on morphology and photocatalytic activity of BiOBr synthesized by solvothermal method,” Materials Research Bulletin, vol. 47, no. 11, pp. 3753–3757, 2012. View at Publisher · View at Google Scholar · View at Scopus
  7. J. Henle, P. Simon, A. Frenzel, S. Scholz, and S. Kaskel, “Nanosized BiOX (X = Cl, Br, I) particles synthesized in reverse microemulsions,” Chemistry of Materials, vol. 19, no. 3, pp. 366–373, 2007. View at Publisher · View at Google Scholar · View at Scopus
  8. J.-S. Xu, Y.-J. Zhu, and F. Chen, “Microwave-assisted solvothermal ionic liquid rapid synthesis of aluminum fluorohydroxide single-crystalline octahedra,” Materials Letters, vol. 94, pp. 104–107, 2013. View at Publisher · View at Google Scholar · View at Scopus
  9. L. Wu, L. Liao, G. Lv, F. Qin, and Z. Li, “Microstructure and process of intercalation of imidazolium ionic liquids into montmorillonite,” Chemical Engineering Journal, vol. 236, pp. 306–313, 2014. View at Publisher · View at Google Scholar · View at Scopus
  10. Y. Huang, Y. Xu, Q. He, Y. Cao, and B. Du, “Rapid removal of aniline from contaminated water by a novel polymeric adsorbent,” Water Environment Research, vol. 86, no. 1, pp. 20–27, 2014. View at Publisher · View at Google Scholar · View at Scopus
  11. C. D. Wu, J. Y. Zhang, L. Wang, and M. H. He, “Removal of aniline and phenol from water using raw and aluminum hydroxide-modified diatomite,” Water Science and Technology, vol. 67, no. 7, pp. 1620–1626, 2013. View at Publisher · View at Google Scholar · View at Scopus
  12. A. Kumar and N. Mathur, “Photocatalytic degradation of aniline at the interface of TiO2 suspensions containing carbonate ions,” Journal of Colloid and Interface Science, vol. 300, no. 1, pp. 244–252, 2006. View at Publisher · View at Google Scholar · View at Scopus
  13. B. Pare, V. S. Solanki, and P. Singh, “Photocatalytic degradation of Acridine Yellow G and Aniline Blue B dyes in a slurry batch reactor using visible light and ZnO suspension,” Journal of the Indian Chemical Society, vol. 88, no. 10, pp. 1533–1540, 2011. View at Google Scholar · View at Scopus
  14. G. Wang, Z. Ling, C. Li, Q. Dong, B. Qian, and J. Qiu, “Ionic liquid as template to synthesize carbon xerogels by coupling with KOH activation for supercapacitors,” Electrochemistry Communications, vol. 31, pp. 31–34, 2013. View at Publisher · View at Google Scholar · View at Scopus
  15. L. Ge, X.-Y. Jing, J. Wang et al., “Ionic liquid-assisted synthesis of CuS nestlike hollow spheres assembled by microflakes using an oil-water interface route,” Crystal Growth & Design, vol. 10, no. 4, pp. 1688–1692, 2010. View at Publisher · View at Google Scholar · View at Scopus
  16. J. G. Yu, Y. R. Su, and B. Cheng, “Template-free fabrication and enhanced photocatalytic activity of hierarchical macro-/mesoporous titania,” Advanced Functional Materials, vol. 17, no. 12, pp. 1984–1990, 2007. View at Publisher · View at Google Scholar · View at Scopus