Modeling the Solar Photocatalytic Degradation of Dyes

2006 ◽  
Vol 129 (1) ◽  
pp. 87-93 ◽  
Author(s):  
H. I. Villafán-Vidales ◽  
S. A. Cuevas ◽  
C. A. Arancibia-Bulnes

Background. The calculation of radiation absorption by the catalyst in solar photocatalytic reactors has been addressed by some authors, because it is a necessary step for the modeling of the detoxification of polluted water in these systems. Generally transparent pollutants have been considered, which somewhat simplifies the calculations. However, there has been an increasing interest in the study of solar photocatalytic degradation of dyes. These substances are not transparent to the radiation that the catalyst is able to absorb, and therefore their optical properties must be taken into account in the radiative modeling. Method of Approach. Absorption of radiation by the catalyst suspended in colored water is modeled by using the P1 approximation of radiative transfer theory. The absorption coefficient of the dye is taken into account in these calculations. A kinetic model is used to model degradation rates, based on the results of the radiative calculations. This has to be done through an Euler type method, because the reduction of dye concentration constantly modifies the optical conditions on the reactor, requiring a recalculation of radiation absorption at each step. Also, photocatalytic degradation experiments were carried out in a CPC solar photocatalytic reactor with tubular reaction space. Degradation of the Acid Orange 24 Azo dye was studied. The experimental degradation rates are compared with theoretical predictions. Results. An important influence of dye concentration is observed in the distribution of absorbed radiation, and also this parameter has a notorious effect on the predicted degradation rates. As a function of catalyst concentration, the degradation rate first increases rapidly and then at a smaller pace with an apparent linear trend. The experimental results can be reproduced well by the model. Conclusions. The proposed methodology allows modeling the solar photocatalytic degradation of dyes. The method should be applicable as long as the dye absorption coefficient is not too high in the wavelength region where the catalyst absorbs.

2021 ◽  
Vol 2021 ◽  
pp. 1-8
Author(s):  
Chao Zou ◽  
Qi-Jin Geng ◽  
Jing-Tuo Zhu ◽  
Chen Jing ◽  
Wen Zhong ◽  
...  

To investigate the influence of inorganic salt on the photocatalytic degradation, the effects of KBr and KI at various concentrations and pH values on the photocatalytic degradation of dye W-7G using nanoscaled titanium dioxide as photocatalyst in a bubbling fluidized bed photocatalytic reactor (BFBPR) were studied. The results indicated that the degradation apparent rate constant ( K app ) of the system with KI was clearly higher than that with KBr under acidic or alkaline conditions. And the maximum value of K app (0.01127) appeared at the KI concentration of 0.075 g L-1 with a pH value of 9.37, meaning the highest degradation efficiency. Furthermore, the possible mechanism of photocatalytic degradation of W-7G in the presence of KBr and KI was proposed, which could provide a theoretical support for the further study of inorganic salt effects on the photocatalytic degradation of dyes.


Author(s):  
Nathalie Ho ◽  
Joanne D Gamage ◽  
Zisheng Jason Zhang

Advanced oxidation processes have been investigated as a viable means of treatment for the degradation and removal of dye-containing effluents. In this work, the degradation of an azo dye, Eriochrome black, was studied using a novel photocatalytic reactor in which TiO2 is immobilized on a rotating corrugated drum. The degradation of the dye via the photocatalytic method was confirmed, and degradation rates were compared using different drum designs. Catalyst deactivation was observed, and this process of irreversibility was found to increase with increasing initial dye concentration in the water. A Langmuir-Hinshelwood kinetic analysis was applied, and it was found to agree well with the data in the initial parts of the reaction but diverged with increasing time. The discrepancy was thought to be due to the presence of unquantified reaction intermediates which may only be broken down slowly by the photocatalytic process.


Catalysts ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 624
Author(s):  
Sripriya Dharwadkar ◽  
Linlong Yu ◽  
Gopal Achari

Sulfolane is an emerging industrial pollutant detected in the environments near many oil and gas plants in North America. So far, numerous advanced oxidation processes have been investigated to treat sulfolane in aqueous media. However, there is only a few papers that discuss the degradation of sulfolane using photocatalysis. In this study, photocatalytic degradation of sulfolane using titanium dioxide (TiO2) and reduced graphene oxide TiO2 composite (RGO-TiO2) in a light-emitting diode (LED) photoreactor was investigated. The impact of different waters (ultrapure water, tap water, and groundwater) and type of irradiation (UVA-LED and mercury lamp) on photocatalytic degradation of sulfolane were also studied. In addition, a reusability test was conducted for the photocatalyst to examine the degradation of sulfolane in three consecutive cycles with new batches of sulfolane-contaminated water. The results show that LED-based photocatalysis was effective in degrading sulfolane in waters even after three photocatalytic cycles. UVA-LEDs displayed more efficient use of photon energy when compared with the mercury lamps as they have a narrow emission spectrum coinciding with the absorption of TiO2. The combination of UVA-LED and TiO2 yielded better performance than UVA-LED and RGO-TiO2 for the degradation of sulfolane. Much lower sulfolane degradation rates were observed in tap water and groundwater than ultrapure water.


2015 ◽  
Vol 7 (4) ◽  
pp. 1569-1578 ◽  
Author(s):  
Khan Mamun Reza ◽  
ASW Kurny ◽  
Fahmida Gulshan

2011 ◽  
Vol 110-116 ◽  
pp. 3795-3800 ◽  
Author(s):  
Xiao Zhi Wang ◽  
Wei Wei Yong ◽  
Wei Qin Yin ◽  
Ke Feng ◽  
Rong Guo

Expanded perlite (EP) modified titanium dioxide (TiO2) with different loading times were prepared by Sol-Gel method. Photocatalytic degradation kinetics of Rhodamine B (RhB) in polluted water by the materials (EP-nanoTiO2), as well as the effects of different loading times and the initial concentration of RhB on photocatalysis rate were examined. The catalytic activity of the regenerated photocatalyst was also tested. The results showed that photocatalyst modified three times with TiO2had the highest catalytic activity. Degradation ratio of RhB by EP-nanoTiO2(modified three times) under irradiation for 6 h were 98.0%, 75.6% and 63.2% for 10 mg/L, 20 mg/L and 30 mg/L, respectively.The photocatalyst activity has little change after the five times recycling, and the degradation rate of RhB decreased less than 8%. The reaction of photocatalysis for RhB with irradiation time can be expressed as first-order kinetic mode within the initial concentration range of RhB between 10mg/L and 30 mg/L. EP-nanoTiO2photocatalyst has a higher activity and stability to degrade RhB in aqueous solution.


Catalysts ◽  
2018 ◽  
Vol 8 (12) ◽  
pp. 604 ◽  
Author(s):  
Robert Arthur ◽  
John Ahern ◽  
Howard Patterson

Bismuth oxyhalides have recently gained attention for their promise as photocatalysts. Due to their layered structure, these materials present fascinating and highly desirable physicochemical properties including visible light photocatalytic capability and improved charge separation. While bismuth oxyhalides have been rigorously evaluated for the photocatalytic degradation of dyes and many synthesis strategies have been employed to enhance this property, relatively little work has been done to test them against pharmaceuticals and pesticides. These persistent organic pollutants are identified as emerging concerns by the EPA and effective strategies must be developed to combat them. Here, we review recent work directed at characterizing the nature of the interactions between bismuth oxyhalides and persistent organic pollutants using techniques including LC-MS/MS for the determination of photocatalytic degradation intermediates and radical scavenging to determine active species during photocatalytic degradation. The reported investigations indicate that the high activity of bismuth oxyhalides for the breakdown of persistent organic pollutants from water can be largely attributed to the strong oxidizing power of electron holes in the valence band. Unlike conventional catalysts like TiO2, these catalysts can also function in ambient solar conditions. This suggests a much wider potential use for these materials as green catalysts for industrial photocatalytic transformation, particularly in flow chemistry applications.


2013 ◽  
Vol 20 (6) ◽  
pp. 3570-3581 ◽  
Author(s):  
R. Byberg ◽  
J. Cobb ◽  
L. Diez Martin ◽  
R. W. Thompson ◽  
T. A. Camesano ◽  
...  

2014 ◽  
Vol 2014 ◽  
pp. 1-3 ◽  
Author(s):  
Alka Garg ◽  
Monika Tomar ◽  
Vinay Gupta

Bismuth iodide is a potentially active material for room temperature radiation detector, as it is well reported in the literature that it has both wide energy band gap and high atomic absorption coefficient. Crystalline films of high atomic number and high radiation absorption coefficient can absorb the X-rays and convert them directly into electrical charges which can be read by imaging devices. Therefore, it was proposed to grow thin films of Bismuth iodide on glass substrate using thermal evaporation technique in vacuum to avoid the inclusion of impurities in the films. The structural studies of the films were carried out using XRD and optical absorption measurement was carried out in the UV/VIS region using spectrophotometer. All Bismuth iodide films grown at room temperature are polycrystalline and show X-ray diffraction peaks at angles reported in research papers. The optical transmission spectra of BiI3 films show a high transmission of about 80% in visible region with a sharp fall near the fundamental absorption at 650 nm. Resistivity of the as-grown film was found to be around 1012 ohm-cm suitable value for X-ray detection application. Films were subjected to scanning electron microscopy to study the growth features of both as-grown and annealed films.


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