Journal Details
 
Article usage
Total views: 0
[From(publication date):
-- Sep 22, 2014]
Breakdown by view type
HTML page views :
PDF downloads :
XML downloads :
 
 
 
Research Article Open Access
Photodegradation study of Congo Red in Aqueous Solution using ZnO/ UV-A: Effect of pH And Band Gap of other Semiconductor Groups
1DR. Moulay Tahar University, Saida, Algeria
2LCPCE Laboratory, Faculty of sciences, Department of industrial Chemistry, University of the Science and the technology of Oran (USTO M.B). BP 1505 El M'naouar 31000 Oran, Algeria
*Corresponding author: Dr. Elaziouti Abdelkader
LCPCE Laboratory, Faculty of sciences
Department of industrial Chemistry
University of the Science and the technology of Oran (USTO M.B)
BP 1505 El M'naouar 31000 Oran, Algeria
Tel: (213) 0551723590
Fax: (213) 041 56 00 50
E-mail: elaziouti_a@yahoo.com
 
Received March 19, 2011; Accepted May 10, 2011; Published May 13, 2011
 
Citation: Nadjia L, Abdelkader E, Ahmed B (2011) Photodegradation study of Congo Red in Aqueous Solution using ZnO/UV-A: Effect of pH And Band Gap of other Semiconductor Groups. J Chem Eng Process Technol 2:108. doi:10.4172/2157-7048.1000108
 
Copyright: 2011 Nadjia L, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
 
Abstract
 
The photocatalytic degradation of Congo red in aqueous solution was investigated under UVA light at different operating conditions, including irradiation time, pH solution and band gap of MO2 (M=Ti+4 and Ce+4) and M'2O3 (M'=Al+3 and Fe+3) semiconductor groups by UV-spectrophotometric monitoring. The results showed slight stability of 597nmband of CR over the pH range of 6-7, while, it almost completely disappeared at pH higher than 7. Maximum photo degradation was obtained at pH 8 as a result of 95.02% degradation efficiency of CR for 60 min of irradiation time. The photo decomposition efficiency of MO2 (M=Ti+4 and Ce+4) semiconductor group was higher, compared to that of M'2O3 (M'=Al+3 and Fe+3). Photodecomposition reactions correlated with pseudo-first-order kinetic model. These findings can support the design of remediation processes and also assist in predict their fate in the environment.
 
Keywords
 
Kinetics; Photocatalysis; Congo red; Zinc oxide
 
Introduction
 
Heterogeneous photocatalysis oxidations performed with light irradiated semiconductors dispersions has been extensively investigated owing to their highly efficiency to completely mineralize the harmful organic and inorganic ions species to CO2 and water [1]. Most researches has been focalized on the heterogenic systems based on high dispersion TiO2 with a crystalline modification of anatase (Degussa P25, Hombriat UV-100, Aldrich, etc.) as a result of their high photocatalytic activity and widespread uses for large-scale water treatment. However, the relatively elevated intrinsic band gap of anatase TiO2 (3.2 eV), limited their efficiencies under solar light, so that the effective utilization of solar energy is limited to about 4% of total solar spectrum. In order to meet the requirement of future environment and energy technologies, it is necessary to develop highly efficient, non toxic and chemically stable photocatalyst. Various semiconductor catalysts such as MO2 (M=CeO2, ZrO2, SnO2) and M'2O3 (M'=α-Fe2O3, Bi2O3, Al2O3, Sb2O3 etc.) metal oxides and DS (D=Zn, Cd, Pb ect.) metal chalcogenide groups were investigated, but their practical uses have been constrained by their low photocatalytic activity under solar light, short-term stability against photo-and chemical corrosion as well as potential toxicity [2]. Many attempts have been made to study ZnO mediated photocatalytic degradation of organic compounds [3-6]. Semiconductor, on irradiation with photon of sufficient energy, greater than or equal to the band gap energy of the semiconductor (hν=Eg), a free electron (e-) and electronic vacancy-a hole (h+) are generated and recombine or migrate in the semiconductor surface being partially localized on structural defective centers of its crystalline lattice Equation (1). The photogenerated electrons take part in the reduction reaction with dissolved oxygen, producing superoxide anion (O.-2ads), hydroperoxide (HO2ads) radicals and hydrogen peroxide (H2O2ads) Equation (2-4), while the photo generated holes can oxidize either the organic compound directly Equation (5) or both hydroxylic ions and water molecules adsorbed on the photo catalyst surface Equation (6-7) forming the organic cation-radicals (R.+ ads) and hydroxylic radicals (HO. ads). The stepwise photo catalytic mechanism is illustrated below:
 
     ZnO + hν → ZnO (e (CB) + h+(VB))                                                                 (1)
 
     O2ads + e → O•−2ads                                                                                     (2)
 
     O•−2ads + H+ → HO2ads                                                                                  (3)
 
     O•− 2ads + 2H+ + e → H2O2ads                                                                     (4)
 
     Rads+ h+ → Rads+                                                                                          (5)
 
     HOads + h+OHads+                                                                                    (6)
 
     H2Oads + h+OHads+ H+                                                                               (7)
 
The hydroxylic, peroxide and hydroperoxide radicals are the main oxidizing agents in the heterogeneous photocatalytic systems used in the water treatment technologies. The heterogeneous photocatalytic processes substantially depend on a variety of environment conditions such as surface charge and electronic structure of catalyst, the nature of surface-active center, the localization degree of photogenerated charges, the amphoteric properties of photocatalyst, pH solution, temperature of system, nature of pollutant, photocongeners, crystalline structure, synthesis method and photoreactor dimension [7]. Aggregation is one of the features of dyes in solution. Based on literature, Congo red tends to aggregate in aqueous and organic solutions leading to dimer formation and sometimes even higher order aggregates due to hydrophobic interactions between aromatic rings of dye molecules. This aggregation phenomenon is more noticed for high Congo red concentrations, at high salinity and/or low pH. The formed aggregates (micelles) separate and precipitate onto solid surfaces.
 
In the present study, the stability of optical properties of the Congo red (CR) in aqueous solutions and upon photodegradation process was investigated at various pH values using UV spectroscopic monitoring. The potential ability of ZnO-assisted photocatalytic degradation of CR, was assessed in terms of evolution of the adsorption and photodecomposition efficiency at different operating parameters such as, pH solution and band gap of MO2 (M=Ti+4 and Ce+4) and M'2O3 (M'=Al+3 and Fe+3) semiconductor groups as a function of irradiation time. The experimental data were quantified by applying the pseudo first order kinetic.
 
Materials and Methods
 
Nanoparticle semiconductors ZnO (BET surface area, S=10 m2/g and particle size D=60 nm, 99.99%), TiO2 (anatase 99.99%), Al2O3 (99.99%), CeO2 (99.99%), and Fe2O3(99.99%), were obtained from Merck, and were used without further purification. Congo red (C.I. 22020, MW=696.67 g mol-1, C32H24N6O6S2. 2Na, pKa=4 and λmax=497 nm). Distilled water was used for preparation of various solutions. The molecular structure of the dye is illustrated in Figure 1.
 
Figure 1: Molecular structure of Congo red (CR)
 
Photocatalytic reactions were carried out inside a (BLX-E365) photoreactor equipped with 6UV-A lamps with an emission maximum at λ of 365 nm. The suspension was irradiated perpendicularly to the surface of solution, and the distance between the UV source and vessel containing reaction mixture was fixed at 15 cm. The experiments were performed at 298 K. In all photocatalytic degradation experiments, 300 mL CR solution of appropriate concentration was taken in photocatalytic reactor vessel of 600 ml capacity. A known quantity of semiconductor was added and mixture was stirred to obtain uniform suspension. The suspension pH values were previous adjusted using NaOH/H2SO4 solutions via pH meter. Before irradiation, photocatalyst/ substrate suspension was stirred in the dark for 30 minutes at 298 K to ensure the adsorption equilibrium was established. Next, the lamp was switched on to initiate the photocatalytic degradation reaction. During irradiation, agitation was maintained by a magnetic stirrer to keep the suspension homogeneous. The suspension was sampled at regular intervals of time and immediately centrifuged using (EBA-Hetlich) at 3500 rpm for 15 min to completely remove photocatalyst particles. The residual concentration of the solution samples was monitored using UV-Vis Spectrophotometer (Shimadzu UV mini-1240) at λ=497 nm as a function of irradiation time.
 
The effect of initial pH on the photocatalytic degradation of Congo red was researched over a range of pH values from 6 to 10 for avoiding dye aggregation. The experiments were also performed by replacing ZnO catalyst by MO2 (M=Ti+4 and Ce+4) and M'2O3 (M'=Al+3 and Fe+3) semiconductor groups. The data obtained from the photocatalytic degradation experiments were then used to calculate the degradation efficiency η (%) of the substrate Equation (8):
 
                                                                                            (8)
 
where Ci: dye initial concentration (mgL-1) and Cf : dye residual concentration after certain intervals (mgL-1). To calculate the corresponding energy at UV-A wavelength. The energy of an electrovolt, E (eV), at a given wavelength, λ (nm), is given by Equation (9):
 
                                                                                                          (9)
 
where h is Planck's constant (6.626x10-34 J s); c is the speed of light (3x108 m/s); and j is the number of electro-volt per joule (joule=1.6 10-19 electro-volt). The corresponding light energy at UV-A wavelength (λ UV-A=365 nm) was estimated to EλUV-A =3.4 eV.
 
The photocatalytic degradation efficiency of ZnO catalyst for the degradation CR was quantified by measurement of dye apparent first order rate constants under operating parameters.
 
Surface catalyzed reactions can often be adequately described by a monomolecular Langmuir-Hinshelwood mechanism, in which an adsorbed substrate with fractional surface coverage θ is consumed at an initial rate given as follow Equation (10) [8]:
 
                                                                            (10)
 
where K1 is a specific rate constant that changes with photocatalytic activity, K2 the adsorption equilibrium constant, and Co is the initial concentration of the substrate (Benzopurpurine 4B in our case). Inversion of the above rate equation is given by Equation (11):
 
                                                                                          (11)
 
Thus, a plot of reciprocal of the apparent first order rate constant 1/Kapp against initial concentration of the dye Co should be a straight line with a slope of 1/K1 and an intercept of 1/K1K2. Such analysis allows one to quantify the photocatalytic activity of ZnO catalyst through the specific rate constant K1 (with larger K1 values corresponding to higher photocatalytic activity) and adsorption equilibrium constant K2 (K2 expresses the equilibrium constant for fast adsorption-desorption processes between surface of catalyst and substrates). The integrated form of the above equation (Equation 10) yields to the following Equation (12):
 
                                                                               (12)
 
where t is the time in minutes required for the initial concentration of the dye Co to decrease to C. Since the dye concentration is very low, the second term of the expression becomes small when compared with the first one and under these conditions the above equation reduces to Equation (13).
 
                                                                                            (13)
 
where kapp is the apparent pseudo-first order rate constant, C and Co are the concentration at time 't' and 't=0', respectively. The plot of ln Co/C against irradiation time t should give straight lines, whose slope is equal to Kapp.
 
The half-life of dye degradation at various process parameters was raised from Equation (14).
 
                                                                                             (14)
 
where half-life time, t1/2, is defined as the amount of time required for the photocatalytic degradation of 50% of CR dye in a aqueous solution by ZnO catalyst.
 
Results
 
Effect of UV irradiation and ZnO nanoparticle
 
Figure 2 illustrated the photocatalytic degradation kinetics of 20 mg/L of CR in aqueous solution under different experimental conditions under UV-A alone, dark/ ZnO and UV-A/ZnO. The degradation rate was found to increase with increase in irradiation time and 95.02% of degradation were achieved within 60 min at pH of 8 (curve CR/ZnO/ UV-A). When 20 mg/L of both dye along with ZnO were magnetically stirred for the same optimum irradiation times in the absence of light, lower (20.78%) degradation was observed (curve CR/ZnO), whereas, disappearance of dyes was negligible (0.49%) in the direct photolysis (curve CR/UV-A) indicating that the observed high decomposition of the dye in the UV/ZnO process is exclusively attributed to the photocatalytic reaction of the semiconductor particles. Similar results have been reported for ZnO-assisted photocatalytic degradation of azo dyes such as Congo red [9] and Reactive Black 5 [10].
 
Figure 2: Photocatalytic degradation kinetics of CR under different experimental conditions ([ZnO]= 0.5g/L, [CR]=20mg/L, pH=8, T=298K, λmax=365 nm and I=90 J /cm>2).
 
Effect of pH solution
 
Qualitative study: The evolution of maxima absorption bands of CR in aqueous solution and upon ZnO-mediated photocatalytic degradation under UV-A light at various pH: Figure 3 illustrated UV visible spectra of CR in aqueous solution at various pH solutions. The position and the evolution of the maxima absorption bands of CR in aqueous solution and upon ZnO-mediated photocatalytic degradation of substrate CR in aqueous solution were displayed in Table 1. Congo red in aqueous solution exhibited a main band at 497nm (C0=20 mg/L and natural pH=8), assigned to the absorption band of anionic monomer, and associated with two absorption bands in the ultraviolet region appeared at 235 and 347 nm, attributed to the benzoic and naphthalene rings, respectively. As seen in Table 1, the CR monomers have nearly constant absorption bands and absorbance intensities over a range of pH values of 6 to10, while they are most sensitive to the pH solution under acidic medium (pH<6). The main band of CR monomer at 497 nm (in aqueous solution) gradually shifted to the longer wavelengths, almost reaching 595.5 and 537.5 nm at pH 2 and 4 respectively. The intensity decrease and red shift of CR monomer bands are attributed to the partially self-association of CR monomers as anionic dimers in face-to-face arrangement to minimize their hydrophobic interaction with water. For that reason, the adsorption and photocatalytic degradation conditions were conducted only within neutral and alkali pH range.
 
Figure 3: UV visible spectra of CR in aqueous solution as a function of pH ([CR]=20mg/l and T=298K)
 
Table 1: The position of the absorption bands of CR in aqueous solution and during the ZnO-mediated photocatalytic degradation of dye as a function of pH ([ZnO] =0.5g/L, [CR]=20mg/l, T=298K, λmax=365 nm, I=90 J /cm2 and irradiation time =60min)
 
The adsorption equilibrium of CR on ZnO catalyst in dark for 30 min at different pH values (Table 1) showed that CR monomers have nearly constant absorption bands, while a slight decrease in the absorbance intensities over the pH values in the range of 6 and 10 was observed.
 
On the other hand, the behavior of the maxima absorption bands of CR during the ZnO-mediated photocatalytic degradation as a function of pH solution differ in certain aspects from those of CR in aqueous solution and adsorbed on ZnO catalyst surface. As elucidated Table 1, the photodecomposition profile of CR was accompanied by a blue shift of the main bands of CR monomers, compared to those in aqueous solutions.
 
The maxima bands became visible at 497, 481, 492, 481 and 488 nm at pH 6, 7, 8, 9 and 10 respectively as the light illumination time was increased up to 40 minutes. However, they remained nearly constant at pH 6 and 7 and completely disappeared within 60 minutes of irradiation time at pH beyond of 7. The shift does not exceed 10nm over the pH in the range of 6 and 10. These results are consistent with the destruction of CR chromophoric structure in the vicinity of the azo-linkage. Additionally, this shift was accompanied by a parallel decrease in the intensities of bands in the ultraviolet region located at 235 and 347 nm, ascribed to the benzoic and naphthalene rings, respectively. No new absorption bands appeared in either the visible or the ultraviolet spectra regions.
 
Quantitative study: The evolution of photocatalytic degradation rate of CR in aqueous solution by ZnO under UV-A irradiation at various pH: It is commonly accepted that in photocatalyst/aqueous systems, the potential of the surface charge is determined by the activity of ions (e.g. H+ or pH). A convenient index of the tendency of a surface to become either positively or negatively charged as a function of pH is the value of the pH required to give zero net charge (pHZPC) [11-12]. pHZPC is a critical value for determining the sign and magnitude of the net charge carried on the photocatalyst surface during adsorption and photocatalytic degradation process. Most of the semiconductor oxides are amphoteric in nature, can associate (Equation 15) or dissociate (Equation 16) proton. To explain the relationship between the layer charge density and the adsorption, so called models of surface complexation (SCM) was developed [13], which consequently affects the sorption-desorption processes and the separation and transfer of the photogenerated electron-hole pairs at the surface of the semiconductor particles. In the 2-pK approach we assume two reactions for surface protonation. The zero point charge pHZPC for ZnO is 9.0. For pH values lower than the pHZPC of ZnO, the surface becomes positively charged, according to the following reaction Equation (15):
 
     Zn-OH+ H+ → ZnOH2 + pH< pHZPC                                                                 (15)
 
ZnO surface becomes negatively charged for pH values higher than pHpzc, given by the following reaction Equation (16):
 
     Zn-OH + OH- → ZnO- +H2O pH> pHZPC                                                         (16)
 
The experimental data revealed that higher degradation rate of CR was observed in acidic medium (Figure 4 and Table 1). Since CR is an anionic dye, its adsorption mainly performed via an electrostatic interactions between the positive ZnO surface and CR anions, leading to a maximum extent at pH 6. Thus, a high adsorption (18.19%) can lead to a decrease in the active centers on the catalyst surface, which results in decrease in the absorption of the light quanta by the catalyst and consequently to a reducing of the kinetic reaction. As a result, the high degradation efficiency cannot be ascribed to the photocatalytic oxidation of the CR dye, but to catalyst behavior under strong acid pH. ZnO nanoparticles can undergo photo-corrosion through selfoxidation at pH lower than 4 Equation (17). In particular, ZnO can be photo-oxidized with decreasing the pH Equation (18).
 
     ZnO + 2h+(VB) → Zn2+ + 1/2O2                                                                      (17)
 
     ZnO + 2H+ → Zn2+ + H2O (acidic issolution)                                                  (18)
 
Photocatalytic activity of anionic dyes (mainly sulfonated groups) such as CR reaches a maximum value (95.02%) in lower pHZPC (i.e. pH=8). At alkaline mediums, excess of hydroxyl anions facilitate photogeneration of OH radicals which is accepted as primary oxidizing species responsible for photocatalytic degradation, resulting in enhancement of the efficiency of the process. Furthermore we found that, where the adsorption of dye was weak, degradation scarcely occurred. The adsorption affects strongly the accessibility of the surface reducing species to the CR reduction kinetics. However, adsorption is not the only factor that controls the photocatalytic degradation of dye. Although the adsorption extents of the dye were lower, the degradation rates were in the reverse order (Figure 4 and Table 2).
 
Figure 4: Adsorption and photocatalytic degradation of CR as a function of initial pH ([ZnO]= 0.5g/L, [CR]= 20mg/L, T=298K, λmax=365 nm and I=90 J /cm2).
 
Table2: Kinetic parameters of the photocatalytic degradation of CR as a function of initial pH ([ZnO]= 0.5g/L, [CR]= 20mg/l, T=298K, λmax=365 nm and I=90 J /cm2).
 
At pH higher than pHZPC value (i.e. pH=9-10), a dramatically decrease in the degradation efficiency could be explained on the basis of amphoteric behaviors of ZnO catalyst. The negatively surface of ZnO catalyst (highly concentration of hydroxide ions) and the great negatively charged CR dye anions results in electrostatic repulsion electrostatic.
 
Moreover, the stability of ZnO may not be guaranteed at this high pH due to possibility of alkaline dissolution of ZnO Equation (19):
 
     ZnO + H2O+ 2OH- → Zn(OH)4+ alkaline dissolution                                       (19)
 
The linearity of the plots of lnC/Co against irradiation time t for the photocatalytic degradation process of CR by ZnO catalyst at low dye concentrations and under various pH solutions adsorption (Figure 5, Table 2) suggest that the adsorption data were satisfactorily described by pseudo-second order model (R2=0.747-0.968).
 
Figure 5: Pseudo first order kinetics of photocatalytic degradation of CR as a function of initial pH ([ZnO]= 0.5g/L, [CR]= 20mg/L, T=298K, λmax=365 nm and I=90 J /cm2).
 
Effect of band gap of semiconductor
 
The photocatalytic degradation reactions were further performed in two semiconductor groups MO2 (M=Ti+4 and Ce+4) and M'2O3 (M'=Al+3 and Fe+3) having different band gap values. Figure 5 depict the plot of C/Co versus irradiation time CR on ZnO catalys. It is evident that the photocatalytic degradation of dye greatly depends on the electronic structure and properties of semiconductor surface/solvent. The results exposed in Figure 6 shows that the highest degradation efficiency of 95.02% was obtained for ZnO catalyst. The photo decomposition process profiles under the same optimized conditions (pH=5, C=20 mg/L CR, m/v=0.5g/L ZnO and irradiation time of 60min) were different for both MO2 and M'2O3 semiconductor groups in comparison with that of ZnO catalyst. As elucidated Figure 5, the best result of photocatalytic degradation process was observed for MO2 group. TiO2 catalyst exhibited high degradation efficiency of 93.34%, whereas, only 14.95% of CR was degraded for CeO2 semiconductor. On the other hand, the M'2O3 (M'=Al+3 and Fe+3) semiconductors group showed lower (4.20 and 5.15 % for Al2O3 and Fe2O3 respectively) degradation of CR.
 
Figure 6: Photocatalytic degradation kinetics of CR as a function of band gap of semiconductors ([CR]= 20mg/L, [Catalyst]= 0.5g/L, pH =8, T=298K, λmax=365 nm and I=90 J /cm2).
 
Generally, semiconductor on irradiation with light energy greater or equal than band gap energy of the semiconductor (hV≥Eg), a free electron (e-) and electronic vacancy-a hole (h+) are formed and recombine or migrate in the semiconductor surface. Probability of electron transfer in the semiconductor/substrrate system is determined by a relative position of the valence band, the photocatalyst conductance band and the value of the oxidation-reduction potential (ORP) of the oxidant and the substrate. The photogeneration of electrical charge is in dynamic equilibrium with their recombination substantially reducing the quantum yield of the photocatalytic process. The ORP of water oxidation, hydroxylic ions, and most of organic compounds below of reducing photogenerated holes within a wide interval of the pH due to which the formation of hydroxylic radicals and organic cation-radicals of photocatalyst surface are thermodynamically possible processes. It has already reported that semiconductors such as ZnO and TiO2 having band gaps larger than 3 eV are excellent photocatalysts. Obviously, MO2 (M=Ti+4) semiconductor exhibits a higher degradation activity than that of the other systems because its band gap (Eg=3.3 eV) is slightly equal to that of UV-A irradiation source (EUV-A=3.4 eV). The photogenerated electron (e-) hole (h+) pairs can be easily separated and transferred to the semiconductor/adsorbate interface efficiently, consequently improving the photocatalytic activity. The minimum energy required for excitation of an electron from the valence band to conductance band for the semiconductor such as MO2 (M=Ce+4) is 2.6 eV. The photodecomposition process of CR by CeO2 system was much lower than that of the other catalysts, although it band gap being smaller than of EUV-A light energy. The CeO2 system might reduce the life of electron-hole pairs, and enhance the opportunities of their recombination [14]. On the other hand, M'2O2 (M'=Al+3 and Fe+3) catalysts showed lower activity for the photocatalytic of CR than ZnO since their conductance bands of 5.6 and 3.7 eV respectively, are much higher than of the EUV-A light irradiation as a result of low light energy conversion efficiency, so the photogenerated electrical charge in semiconductor cannot efficiently transfer in the surface and are lost due to recombination.
 
Table 3 records the kinetic parameters of photodecomposition of CR by ZnO in aqueous solution at various band gaps of semiconductors. The results showed that the decolorization process for ZnO as well as TiO2 catalysts could be described by the pseudo-first-order kinetic model. The plots of the experimental data (lnC/Co against t, Figure 8) yielding to a straight line with relatively high regression coefficients R2=0.944 and 0.985 for ZnO and TiO2 respectively. However, the regression coefficients, R2, (given in Table 3) for the pseudo-first- order model for semiconductors such as CeO2, Al2O3 and Fe2O3 did not exceed 0.49, 0.887 and 0.34 respectively. These results suggested that the photodegradation process of CR by CeO2, Al2O3 and Fe2O3 semiconductors did not follow the pseudo-first-order.
 
Figure 7: Adsorption and photocatalytic degradation rates of CR a function of band gap of semiconductors ([CR]= 20mg/L, [Catalyst]= 0.5g/L, pH=8, T=298K, λmax=365 nm and I=90J/cm2).
 
Figure 8: Pseudo first order kinetics of photocatalytic degradation of CR as a function of band gap of semiconductors ([CR]= 20mg/L, [Catalyst]= 0.5g/L, pH=8, T=298K, λmax=365 nm and I=90 J /cm2).
 
Table 3: Kinetic parameters of photocatalytic degradation of CR as a function of band gap of semiconductors ([CR]= 20mg/L, [Catalyst]= 0.5g/L, pH=8, T=298K, λmax=365 nm and I=90 J /cm2).
 
Comparative study
 
Table 4 gives clear assessment chart of photocatalytic degradation of Congo red on ZnO and TiO2 catalysts compared to those of prior work of ZnO and TiO2 photocatalytic systems for dye degradation applications.
 
Table 4: Comparative chart of photocatalytic degradation of Congo red on various catalysts.
 
Conclusion
 
The photocatalytic degradation of Congo red in aqueous solution was investigated under UVA light at different operating conditions, including irradiation time, pH solution and band gap of other semiconductor groups by UV-spectrophotometric monitoring. The results showed slight stability of 597 nm-band of CR over the pH range of 6-7, while, it almost completely disappeared beyond pH 7. The highest photodecomposition was obtained at pH 8 as a result of 95.02% degradation efficiency of CR for 60 min exposure of irradiation time. The photodegradation rate of MO2 (M=Ti+4 and Ce+4) semiconductor group was higher, compared to that of M'2O3 (M'=Al+3 and Fe+3). Photodecomposition process profiles were satisfactory correlated with pseudo-first-order kinetic model. These findings suggest that the degradation of Congo red mainly occurred by the attack of OH radical [15].
 
Acknowledgements
 
We greatly acknowledge the material support obtained from DR T.M. University
 
References
 


















 
 
 
This article
DOWNLOAD
» XML (80 kB)
» PDF (1,800 kB)
»
Export citation
»
Blog this article
   
CONTRIBUTE
» Write a response
» Read other responses
» Publishing with OPG
   
SHARE
» E-mail this article
» Print this article
» Rights and permissions
   
Share
EXPLORE
Related article at
» Pubmed
» DOAJ
» Scholar Google
 
 
 
Untitled Document
| More
 
OMICS Publishing Group is the member of / publishing partner of/source content provider to
       
OMICS Publishing Group, An Open Access Publisher and Scientific Events Organizer for the Advancement of Science & Technology. All Published content, except where otherwise noted, is licensed under a Creative Commons Attribution License
Please ensure that you are using the latest version of Adobe reader. If you do not have this software installed on your system, you can download the free Adobe Reader by simply clicking on the following link: http://www.adobe.com/products/acrobat/readstep2.html
Best viewed in Mozilla Firefox | Google Chrome | Above IE 7.0 version Copyright 2013 OMICS Group, All Rights Reserved.