Scholarly article on topic 'Environmental Photocatalysis'

Environmental Photocatalysis Academic research paper on "Chemical engineering"

Share paper
Academic journal
International Journal of Photoenergy
OECD Field of science

Academic research paper on topic "Environmental Photocatalysis"

Hindawi Publishing Corporation International Journal of Photoenergy Volume 2012, Article ID 594214, 4 pages doi:10.1155/2012/594214


Environmental Photocatalysis

Jiaguo Yu,1 Pengyi Zhang,2 Huogen Yu,3 and Christos Trapalis4

1 State Key Laboratory of Advanced Technology for Material Synthesis and Processing, Wuhan University of Technology, Luoshi Road 122, Wuhan 430070, China

2 State Key Joint Laboratory of Environment Simulation and Pollution Control, School of Environment, Tsinghua University, Beijing 100084, China

3 Department of Chemistry, School of Science, Wuhan University of Technology, Wuhan 430070, China

4 Institute of Materials Science, National Centre for Scientific Research "Demokritos," Agia Paraskevi, Attica 15310 Athens, Greece Correspondence should be addressed to Jiaguo Yu,

Received 8 November 2012; Accepted 8 November 2012

Copyright © 2012 Jiaguo Yu 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.

In recent years, semiconductor photocatalytic technology has been demonstrated to be one of the "green" and effective strategies for solving environmental pollution problems. Therefore, environmental photocatalysis, including water disinfection, hazardous waste remediation, air and water purification, deodorization, antibacterial, and self-cleaning, has caused more and more attention in recent years (see the work of J. G. Yu et al. "TiO2 photocatalytic materials" [1-9]). However, owing to low photocatalytic efficiency and activity of photocatalytic materials, the environmental applications of various photocatalytic technologies and materials are still very limited. Thus, more investigations are highly required from the viewpoint of practical use and commerce.

This special issue contains eighteen papers, which mainly deal with environmental photocatalysis. Among them eight papers are related to preparation, characterization, and photocatalytic performance of photocatalytic materials including CeO2-SiO2, BiVO4, mesoporous TiO2, Bi2WO6, Bi2O3-Bi2CrO6, H3PWi2O40/SiO2, Mn-C-codoped TiO2, ZnO, and N-doped TiO2, three papers, are devoted to decolorization and treatment of industrial wastewater, three papers present photocatalytic degradation of dyes, one paper reports on indoor air purification, two papers are related to photo-Fenton and photoelectron-Fenton reactions, and the remaining one deals with photocatalytic degradation of nitrobenzene. Furthermore, in this special issue, 16 papers are research articles and two papers are review articles. We

wish to express our thanks to all the authors who have made this special issue possible. A brief summary of all eighteen papers is presented below.

The article entitled "Comparison between solar and artificial photocatalytic decolorization of textile industrial wastewater" mainly reported the photocatalytic decolorization of industrial wastewater by using TiO2 and ZnO photocatalysts. Heterogeneous photocatalysis applied under natural weathering conditions, in the presence of solar radiation, shows a promising degradation capability. The complete removal of color was achieved in a relatively short time of about 20 minutes when ZnO was used, and about 100 minutes when TiO2 was used under solar irradiation. The results indicated that the photocatalytic decolorization of textile industrial wastewater was obviously influenced by different factors including mass and type of catalyst, reactor, dye concentration, and temperature.

In the article entitled "Synthesis and characterization of CeO2-SiO2 nanoparticles by microwave-assisted irradiation method for photocatalytic oxidation of methylene blue dye," CeO2-SiO2 nanoparticles were prepared for the first time by a facile microwave-assisted irradiation process. The pho-tocatalytic activities were evaluated by the decomposition of methylene blue dye under UV light irradiations. The results showed that all solid samples exhibited mesoporous textures with high specific surface areas, relatively small pore size diameters, and large pore volume. The sample prepared by 30 min microwave irradiation time exhibited the best

photocatalytic activity. The photocatalytic activity of CeO2-SiO2 nanoparticles prepared by 30 min irradiation times was found to have better performance than commercial reference P25.

In the paper entitled "Electrochemical techniques in textile processes and wastewater treatment," the authors review the electrochemical techniques applied to textile industry. In particular, they are an efficient method to remove color of textile effluents. The reuse of the discolored effluent is possible, which implies an important saving of salt and water (i.e., by means of the "UVEC Cell"). Electrochemical reduction reactions are mostly used in sulfur and vat dyeing, but, in some cases, they are applied to effluents discoloration. However, the main applications of electrochemical treatments in the textile sector are based on oxidation reactions. Most of electrochemical oxidation processes involve indirect reactions which imply the generation of hypochlorite or hydroxyl radical in situ. These electrogenerated species are able to bleach indigo-dyed denim fabrics and to degrade dyes in wastewater in order to achieve the effluent color removal.

In the paper entitled "Impact of preparative pH on the morphology and photocatalytic activity of BiVO4," single-crystalline BiVO4 was prepared using aqueous-phase precipitation method by adjusting pH. The effects of pH on structure, surface morphology, visible-light photocatalytic activity, and light absorption performance of BiVO4 were explored and discussed. The highest photocatalytic performance on the degradation of a methylene blue solution was observed under pH = 7.0 for BiVO4 in monoclinic scheelite, which is attributed to its small grain size and marked surface oxygen evolution ability.

In the paper entitled "Mesoporous TiO2 micro-nanometer composite structure: synthesis, optoelectric properties, and photocatalytic selectivity," mesoporous anatase TiO2 micro-nanometer composite structure was prepared using solvothermal method at 180°C, followed by calcination at 400°C for 2h. The photocatalytic activity was characterized by photodegradation of sole rhodamine B (RhB) and sole phenol aqueous solutions under simulated sunlight irradiation and compared with that of Degussa P-25 under the same conditions. The photodegradation preference of this mesoporous TiO2 was also investigated for an RhB-phenol mixed solution. The results showed that the TiO2 composite structure consisted of microspheres with a size of -0.5-2 ^m and irregular aggregates with rough surfaces. The photodegradation activities of this mesoporous TiO2 on both RhB and phenol solutions were higher than those of P25. Moreover, the prepared TiO2 exhibited photodegradation preference on RhB in the RhB-phenol mixture solution.

The article entitled "Rapid decolorization of cobalamin" examined the photocatalytic decolorization of cobalamin in aqueous solution with different types of catalysts including ZnO, TiO2 (Degussa P25), TiO2 (Hombikat UV100), TiO2 (Millennium PC105), and TiO2 (Koronose 2073) under UVA irradiation. The effects of experimental parameters on photocatalytic oxidation were investigated. The results indicated that the photocatalytic decolorization of cobalamin was well described by pseudo-first-order kinetics according

to the Langmuir-Hinshelwood model. The activation energy was calculated according to Arrhenius plot and was found to be 28 ± 1 kJ-mol^1 for ZnO and 22 ± 1 kJ-mol"1 for TiO2 (Degussa P25). The total organic carbon (TOC) analysis indicated that the decolorization rate of dye was faster than the total mineralization. The activity of different types of catalysts used in this study was of the following sequence: ZnO > TiO2 (Degussa P25) > TiO2 (Hombikat UV100) > TiO2 (Millennium PC105) > TiO2 (Koronose 2073).

The article entitled "Feasibility of carbonaceous nano-material-assisted photocatalysts calcined at different temperatures for indoor air applications" examined the characteristics and photocatalytic activity of multiwall carbon nanotube-assisted TiO2 (MWNT-TiO2) nanocomposites and their potential indoor air applications. The results indicated that the MWNT-TiO2 composites calcined at low temperatures showed higher photocatalytic activity for decomposition of aromatic hydrocarbons at indoor concentrations than those calcined at high temperatures. The mean rates for the decomposing benzene, toluene, ethyl benzene, and o-xylene (BTEX) by the composite calcined at 300°C were 32%, 70%, 79%, and 79%, respectively, whereas they were 33%, 71%, 78%, and 78% for the composite calcined at 400° C, respectively. In contrast, the rates decreased to close to zero when the calcination temperature increased to 600°C. Moreover, the MWNT-TiO2 exhibited superior photocatalytic performance for the decomposition ofindoor air pollutants compared to pure TiO2 under conventional UV-lamp irradiations.

The article entitled "Heterogeneous photo-Fenton reaction catalyzed by nanosized iron oxides for water treatment" reviewed the recent developments in the heterogeneous photo-Fenton reaction which utilized nanosized iron oxides as catalysts for maximizing the activity due to the enhanced physical and chemical properties caused by the unique structures. This paper also summarized the fundamentals of the Fenton reaction, which determined the inherent drawbacks and associated advances, to address the advantages of iron oxides and nanosized iron oxides.

In the paper entitled "UV-irradiated photocatalytic degradation of nitrobenzene by titania binding on quartz tube," a new method for UV-irradiated degradation of nitrobenzene by titania photocatalysts was presented. Titania nanoparticles were coated on a quartz tube by the addition of tetraethyl orthosilicate into the matrix. The dependence of nitrobenzene photodegradation on pH, temperature, concentration, and air feeding was discussed, and the physical properties such as the activation energy, entropy, enthalpy, adsorption constant, and rate constant were acquired by conducting the reactions in a variety of experimental conditions. The optimum efficiency of the photodegradation with the nitrobenzene residue as low as 8.8% was obtained and the photodegradation mechanism was also investigated by HPLC, GC/MS, ion chromatography (IC), and chemical oxygen demand (COD) analyses.

In the paper entitled "Hydrothermal synthesis of iodine-doped Bi2WO6 nanoplates with enhanced visible and ultraviolet-induced photocatalytic activities," the iodine-doped

BÍ2WO6 (I-BWO) photocatalyst was prepared by a hyline-breakdrothermal method using KI as the source of iodine. The photocatalytic activity of I-BWO for the degr-adation of rhodamine B (RhB) was higher than that of pure BWO and I2-loaded Bi2WO6 (I2-BWO) sample regardless of visible light (>420nm) or ultraviolet light (<400nm) irradiation. The results of DRS analysis showed that the I-BWO and I2-BWO catalysts had narrower band gaps. XPS analysis proved that the multivalent iodine species including I0 and I~ were coadsorbed on the defect surface of Bi2WO6 in I-BWO. The enhanced photocatalytic activity of I-BWO for degradation of RhB was due to the synergetic effect of a small crystalline size, a narrow band gap, and plenty of oxygen vacancies.

The article entitled "Synthesis and photocatalytic properties of one-dimensional composite Bi2O3-Bi2CrO6 nano-wires" reported preparation of one-dimensional composite Bi2O3-Bi2CrO6 nanowires by a simple microwave-assistant hydrothermal method. The diameter of the nanowires varied from 30 to 100 nm and the length was a few micrometers. Methylene blue (MB) solutions were used to evaluate the visible light photocatalytic activities of the prepared samples. Compared with Bi2O3, the Bi2O3-Bi2CrO6 composite nanowires showed enhanced performance in oxidization of MB under visible light.

In the paper entitled "Pretreatment of color filter wastewater towards biodegradable by Fresnel-lens-assisted solar TiO 2 photocatalysis," the experimental design of response surface methodology (RSM) was employed to assess the effect of critical process parameters (including initial pH, TiO2 dosage, and reaction time) on pretreatment performance in terms of BOD5/COD, COD, and TOC removal efficiency. Appropriate reaction conditions were established as an initial pH of 7.5, a TiO2 dosage of 1.5 g/L with a reaction time of 3 h for increasing the BOD5/COD ratio to 0.15, which implied that the treated wastewater would be possibly biodegradable. Meanwhile, the rates of COD and TOC removals reached 32.9% and 24.4%, respectively. With the enhancement of Fresnel lens, the required reaction time for improving the biodegradability of wastewater to 0.15 was 1h only. Moreover, the rates of COD and TOC removals were promoted to 37.4% and 25.8%, respectively. This was mainly due to the concentrated effect of Fresnel lens for solar energy, including an increase of 2 times of solar irradiation and a increase of 15-20° C of wastewater temperature. Consequently, solar TiO2 photocatalytic process with the use of a PMMA Fresnel lens could offer an economical and practical alternative for the pretreatment of industry wastewater containing diversified biorefractory pollutants with a high concentration of COD such as color filter wastewater.

In the paper entitled "Photocatalytic degradation of rhodamine B with H3PWi2O4o/SiO2 sensitized by H2O2," the Keggin-type H3PW12O40 was loaded on the surface of SiO2 by the sol-gel method and sensitized by H2O solution. The photocatalytic degradation of rhodamine B (RhB) byH3PW12O40/SiO2 (x) under simulated natural light irradiation was investigated. The results indicated that at optimal condition (initial concentration of methyl orange is 10 mg/L, catalyst dosage is 0.8 g, and the pH is 2.5) the degradation rate of RhB was as high as 97.7% after 2 h

under simulated natural light irradiation. The photocatalytic reaction of RhB could be expressed as a first-order kinetic model.

In the paper entitled "Synthesis and characterization of Mn-C-codoped TiO2 nanoparticles and photocatalytic degradation of methyl orange dye under sunlight irradiation," novel visible-light-driven Mn-C-TiO2 nanoparticles were synthesized by sol-gel method using polyoxyethylenes orbitan monooleate (Tween 80) as template and carbon precursor and manganese acetate as manganese precursor. The pho-tocatalytic activity of synthesized catalyst was evaluated by photocatalytic oxidation of methyl orange (MO) solution under the sunlight irradiation. The results showed that Mn-C-TiO2 nanoparticles had higher activity than other samples under sunlight, which was due to their high specific surface area, smaller particle size, and lower band gap energy.

The article entitled "Photocatalytic performance of ZnO: Al films under different light sources" reported preparation ofZnO and Al doped ZnO films by spray pyrolysis. Their photocatalytic activity was evaluated by the decomposition of the methyl orange dye using different light sources: ultraviolet light, artificial white light, and direct sunlight. The Al doped ZnO films presented a very high degradation rate not only under UV and sunlight (100% degradation), but also under white light (90% degradation after the same irradiation time). An unexpected high degradation was also obtained in the dark, which indicated that a nonphotonic process took place parallel to the photocatalytic process. This was due to the extra electrons—provided by the aluminum atoms—that migrated to the surface and produced O2 radicals favoring the decomposition process even in the dark. The high activity achieved by the ZnO : Al films under natural conditions could be potentially applied to water treatment processes.

The article entitled "Supported nanosized a-FeOOH improves efficiency of photoelectro-Fenton process with reaction-controlled pH adjustment for sustainable water treatment" demonstrated that the overall efficiency of photoelectro-Fenton process was improved by rapidly recycling the iron substance. Nanosized iron oxide was prepared and employed to ensure such rapid recycling. SEM and XRD results showed that the as-prepared iron oxide was a-FeOOH with 20 nm in size. The experimental results of dimethyl phthalate (DMP) degradation indicated that diatomite-supported a-FeOOH (N-a-FeOOH/diatomite) could reduce the DMP concentration and total organic carbon. Furthermore, compared with Fe3+, the N-a-FeOOH/diatomite saved 160 min for iron settlement at 20mgL_1 DMP concentration. Also, with increasing the initial DMP concentration, extra energy consumed by the individual step of PE-Fenton reaction using the N-a-FeOOH/diatomite became negligible compared with that using free iron ions with increasing the initial DMP concentration.

The article entitled "Photocatalytic degradation of organic dyes under visible light on N-doped TiO2 photocatalysts" focused on the application of white and blue light emitting diodes (LEDs) as light sources for the photocatalytic degradation of organic dyes in liquid phase with visible light. The photocatalytic activity of N-doped TiO2, synthesized

by direct hydrolysis of titanium tetraisopropoxide with ammonia, was evaluated by means of a batch photoreactor. The bandgap energy of TiO2 was moved into the visible range from 3.3 eV to 2.5 eV. The results demonstrated that the right selection of operating conditions was allowed to effectively degrade different dyes with the N-doped TiO2 photocatalysts irradiated with visible light emitted by LEDs.

In the paper entitled "Photocatalytic treatment of rhodamine 6G in wastewater using photoactive ZnO," the photocatalytic activity of zinc oxide, prepared by precipitation followed by calcinations, was tested using rhodamine 6G as an organic pollutant. The results were compared with those obtained on P-25 titania and one of the samples had similar performances in terms of dye degradation degree, but needed higher pH values to prevent the photocatalyst degradation.

The above synopsis of the articles collected in this special issue on environmental photocatalysis indicates that this area of research is continuously expanding. Our hope is this special issue will stimulate further developments in the field of environmental photocatalysis.

Jiaguo Yu Pengyi Zhang Huogen Yu Christos Trapalis


[1] J. G. Yu, M. Jaroniec, H. G. Yu, and W. H. Fan, "Synthesis, characterization, properties, and applications of nanosized photocatalytic materials," Journal of Nanomaterials, vol. 2012, Article ID 783686, 3 pages, 2012.

[2] Q. J. Xiang, J. G. Yu, and M. Jaroniec, "Graphene-based semiconductor photocatalysts," Chemical Society Reviews, vol. 41, pp. 782-796, 2012.

[3] Q. J. Xiang, J. G. Yu, and M. Jaroniec, "Synergetic effect of MoS2 and graphene as cocatalysts for enhanced photocatalytic H2 production activity of TiO2 nanoparticles," Journal of the American Chemical Society, vol. 134, pp. 6575-6578, 2012.

[4] X. M. Zhou, G. Liu, J. G. Yu, and W. H. Fan, "Surface plas-mon resonance-mediated photocatalysis by noble metal-based composites under visible light," Journal of Materials Chemistry, vol. 22, pp. 21337-21354, 2012.

[5] S. W. Liu, J. G. Yu, and M. Jaroniec, "Anatase TiO2 with dominant high-energy 001 facets: synthesis, properties, and applications," Chemistry of Materials, vol. 23, pp. 4085-4093, 2011.

[6] S. Liu, J. Yu, and M. Jaroniec, "Tunable photocatalytic selectivity of hollow TiO2 microspheres composed of anatase polyhedra with exposed 001 facets," Journal of the American Chemical Society, vol. 132, no. 34, pp. 11914-11916, 2010.

[7] W. G. Wang, J. G. Yu, Q. J. Xiang, and B. Cheng, "Enhanced photocatalytic activity of hierarchical macro/mesoporous TiO2-graphene composites for photodegradation of acetone in air," Applied Catalysis B, vol. 119-120, pp. 109-116, 2012.

[8] J. Yu and X. Yu, "Hydrothermal synthesis and photocatalytic activity of zinc oxide hollow spheres," Environmental Science and Technology, vol. 42, no. 13, pp. 4902-4907, 2008.

[9] J. Yu, Y. Su, and B. Cheng, "Template-free fabrication and enhanced photocatalytic activity of hierarchical macro-/me-soporous titania," Advanced Functional Materials, vol. 17, no. 12, pp. 1984-1990, 2007.

Copyright of International Journal of Photoenergy is the property of Hindawi Publishing Corporation and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use.