scholarly journals Photocatalytic Degradation of Diazo Dye over Suspended and Immobilized TiO2 Catalyst in Swirl Flow Reactor: Kinetic Modeling

Processes ◽  
2021 ◽  
Vol 9 (10) ◽  
pp. 1741
Author(s):  
Waleed Jadaa ◽  
Anand Prakash ◽  
Ajay K. Ray

The degradation kinetics of Direct Blue 15 (DB15), a diazo dye, were studied over a suspended and immobilized TiO2 catalyst. For all experiments, the kinetics experiments were performed in a swirl flow photoreactor under the influence of UV light. The effect of different parameters: dye concentration, catalyst loading, and light intensity, on the DB15 kinetics was investigated. The kinetic rates were assessed using apparent ka approach, a single value of reaction rate kr and adsorption constant K, and approach of kr as of variable. The DB15 mineralization was discussed as well. Using a dip-coating device, the P25 catalyst was deposited on a Pyrex glass. The thin film surface characterization was examined. The coated catalyst was evaluated by checking the effect of two variables: initial dye concentration and light intensity on the DB15 kinetics. In terms of the ka approach, the results demonstrated that DB15 degradation is described by the pseudo first-order kinetics model. The Langmuir-Hinshelwood (L-H) model was fitted well with the experimental data for the number of process variables. L-H constant kr was determined as a function of three parameters: initial dye concentration, catalyst loading, and light intensity. The ka values were evaluated and compared with experimental results. In terms of three variables, ka can be expressed as ka=0.15 [C]o−0.69 [W]0.73 I0.91 1 + 0.17 Co  while the empirical model results in the following expression, ka=0.77 Co−1.65 W0.73 Io0.89. It was observed that 83.64% mineralization was achieved after a period of 16 h. In terms of immobilized catalyst, the DB15 degradation kinetics was described by a pseudo first-order model for different dye concentrations. Meanwhile, a power-law model described the impact of light intensity on dye kinetics. In addition, the coated catalyst was successfully reusable with high efficiency for up to four cycles.

2017 ◽  
Vol 14 (3) ◽  
pp. 582-587
Author(s):  
Baghdad Science Journal

In this work, the photocatalytic degradation of indigo carmine (IC) using zinc oxide suspension was studied. The effect of influential parameters such as initial indigo carmine concentration and catalyst loading were studied with the effect of Vis irradiation in the presence of reused ZnO was also investigated. The increased in initial dye concentration decreased the photodegradation and the increased catalyst loading increased the degradation percentage and the reused-ZnO exhibits lower photocatalytic activity than the ZnO catalyst. It has been found that the photocatalytic degradation of indigo carmine obeyed the pseudo-first-order kinetic reaction in presence of zinc oxide. This was found from plotting the relationship between ln (C0/Ct) and irradiation the rate constant of the process.UV- spectrophotometer was used to study the indigo carmine photodegradation.


Catalysts ◽  
2020 ◽  
Vol 10 (12) ◽  
pp. 1418
Author(s):  
Waleed Jadaa ◽  
Anand Prakash ◽  
Ajay K. Ray

Photocatalytic degradation of Direct Blue 15 (DB15), an azo dye, was studied using a swirl-flow monolithic reactor under UV irradiation. The degradation reactions were carried out to investigate effects of initial dye concentration, catalyst loading, and light intensity at an optimal pH. The experiments were designed and mathematically modelled by CCD-RSM (central composite design-response surface methodology) approach. It was found that the selected parameters significantly affect DB15 degradation. In terms of the linear term, catalyst loading and light intensity had a synergistic effect, while dye concentration registered the opposite effect. Strong interaction was observed between catalyst loading and both light intensity and initial dye concentration compared with the interaction of light intensity and initial dye concentration. Based on the experimental results, a quadratic model was developed to predict the percentage removal of DB15. The predicted values of the model were in good agreement with the experimental values (R2 = 0.987), indicating the model fits well for the parameter space for which experiments were performed. According to diagnostic plots, the model credibility was valid because its residuals were distributed normally and exhibited a random pattern based on their examination versus the predicted values. The results revealed that the initial dye concentration and catalyst concentration have a significant effect on the mineralization time.


2012 ◽  
Vol 65 (12) ◽  
pp. 2175-2182
Author(s):  
Abeer S. Elsherbiny ◽  
Sahar H. El-Khalafy ◽  
Michael P. Doyle

The kinetics of the oxidative degradation of an azo dye Metanil Yellow (MY) was investigated in aqueous solution using dirhodium(II) caprolactamate, Rh2(cap)4, as a catalyst in the presence of H2O2 as oxidizing agent. The reaction process was followed by UV/Vis spectrophotometer. The decolorization and degradation kinetics were investigated and both followed a pseudo-first-order kinetic with respect to the [MY]. The effects of various parameters such as H2O2 and dye concentrations, the amount of catalyst and temperature have been studied. The studies show that Rh2(cap)4 is a very effective catalyst for the formation of hydroxyl radicals HO• which oxidized and degraded about 92% of MY into CO2 and H2O after 24 h as measured by total carbon analyzer.


2011 ◽  
Vol 30 (2) ◽  
pp. 229 ◽  
Author(s):  
Shweta Sharma ◽  
Rakshit Ameta ◽  
R. K. Malkani ◽  
Suresh C. Ameta

Different methods have been adopted for the removal and degradation of dyes from effluents of textile, dyeing and printing industries. These methods have their own merits and drawbacks. In the present investigation, bismuth sulfide has been used as a photocatalyst for the degradation of rose Bengal. The effect of different parameters like the pH, concentration of dye solution, amount of semiconductor and light intensity on the rate of reaction has been investigated. The reaction follows pseudo-first order kinetics. The optimum conditions were obtained as: [rose Bengal] = 1.60·10–5 M; Bi2S3 = 0.10 g; pH = 8.5, and light intensity = 50.0 mW·cm–2. The rate constant was 4.68·10–5 sec–1. A mechanism has been proposed for the degradation of rose Bengal involving hydroxyl radicals.


2009 ◽  
Vol 60 (7) ◽  
pp. 1869-1874 ◽  
Author(s):  
D. B. Luiz ◽  
A. K. Genena ◽  
H. J. José ◽  
R. F. P. M. Moreira ◽  
H. Fr. Schröder

In some Brazilian regions, surface water has become scarce, e.g. semi arid climate areas and densely populated and industrial areas, where water over-exploitation and/or fluvial pollution has been more common. Advanced oxidative processes (AOP) provide treated water as a source of reuse water even with the characteristics of drinking water enabling water reuse practices also in food industries. The secondary wastewater of a slaughterhouse was the water source for a tertiary treatment study evaluating the kinetics of the photo-induced degradation of color and UV254 under UV radiation with and without the addition of H2O2. The proximity of the k′ values of color and UV254 degradation by UV indicates that the compounds responsible for color may be the same content measured by UV254. The H2O2/UV treatment was 5.2 times faster than simple UV in removing aromatic compounds. The degradation kinetics of aromatic compounds in both treatments followed a pseudo-first order law. The pseudo-first order constant for H2O2/UV and UV treatments were kUV254′=0.0306 min−1 and kUV254′=0.0056 min−1, respectively.


2004 ◽  
Vol 6 (2) ◽  
pp. 73-80 ◽  
Author(s):  
Ceyda Senem Uyguner ◽  
Miray Bekbolet

The current study was conducted to investigate the photocatalytic degradation kinetics of humic acid at different light intensities using commercialTiO2powders. The pseudo first order kinetic model and Langmuir-Hinshelwood (L-H) rate equation in modified forms were used to compare the photocatalytic activities ofTiO2materials as a function of light intensity. Under constant irradiation conditions, the pseudo first order reaction rates as well as L-H rates were found to be decreasing in the following trend; Degussa P-25, Millennium PC-500 and Millennium PC-100. The pseudo first order rate constants showed the same decreasing trend as the pseudo first order reaction rates while L-H rate constants exhibited a light intensity related change in the ordering of the photocatalysts. At the lowest light intensity, L-H rate constants decreased as follows: Millennium PC-500>Millennium PC-100>Degussa P-25. However, increasing the light intensity changed the order to; Millennium PC-100>Millennium PC-500>Degussa P-25 revealing the significance of the L-H adsorption constant. Under constant irradiation conditions, ionic strength dependent changes in the structure of humic acid did not alter degradation efficiency trend of the photocatalyst specimens and they were ordered such as; Degussa P-25>Millennium PC-500>Hombikat UV-100>Millennium PC-100 > Merck. The results presented in this research also confirmed the effectiveness of Degussa P-25 as a photocatalyst for the degradation of humic acid.


Author(s):  
Chen-Yan Hu ◽  
Si-Cheng Ren ◽  
Yi-Li Lin ◽  
Ji-Chen Zhang ◽  
Ye-Ye Zhu ◽  
...  

Abstract In this study, we studied the degradation kinetics of a common iodine contrast agent, diatrizoate, by ozone and the formation of disinfection by-products (DBPs) in the sequential chlorination. Effects of ozone concentration, solution pH, and bromide concentration on diatrizoate degradation were evaluated. The results indicate that diatrizoate can be effectively degraded (over 80% within 1 h) by ozone, and the degradation kinetics can be well described using the pseudo-first-order kinetic model. The pseudo-first-order rate constant (kobs) of diatrizoate degradation significantly increased with increasing ozone concentration and decreasing bromide concentration. The kobs kept increasing with the increase of pH value and reached a maximum of 6.5 (±0.05) × 10−2 min−1 at pH 9. As the ozone concentration gradually increased from 0.342 to 1.316 mg/L, the corresponding kobs of diatrizoate degradation increased from 1.76 (±0.20) × 10−3 to 4.22 (±0.3) × 10−2 min−1. The bromide concentration exhibited a strong inhibitory effect on diatrizoate degradation because of the competition for ozone with diatrizoate. Trichloromethane was the only detected DBP in the subsequent chlorination in the absence of bromide. However, in the presence of bromide, six other DBPs were detected, and bromochloroiodomethane and tribromomethane became the major products with concentrations 1–2 orders higher than those of the other DBPs. In order to provide safe drinking water to the public, water should be maintained at circumneutral pH values and low bromine concentrations (<5 μM) before reaching the chlorine disinfection process to effectively control the formation of DBPs.


2012 ◽  
Vol 441 ◽  
pp. 549-554
Author(s):  
Ying Jie Cai ◽  
Xiao Jun Yang ◽  
Dong Sheng Xia ◽  
Qing Fu Zeng

Abstract. Degradation of reactive brilliant red X-3B (X-3B) by a UV/Mn2+/H2O2/micro- aeration method was investigated. The influencing factors of degradation of X-3B including UV irradiation, aeration, pH value, H2O2 concentration and X-3B concentration were examined. The results show that X-3B was effectively degraded by the UV/Mn2+/H2O2/micro-aeration method. The degradation rate of X-3B was obtained from weighted linear least squares analysis of the experimental data, and accorded with the pseudo-first order kinetics equation.


2019 ◽  
Vol 79 (5) ◽  
pp. 911-920 ◽  
Author(s):  
Jiamin Hu ◽  
Jing Zhang ◽  
Qingguo Wang ◽  
Qian Ye ◽  
Hao Xu ◽  
...  

Abstract In this study, the difference in oxidative capacity for removing antibiotics and the mechanism between the Cu(II)/peroxymonosulfate (PMS)/UV and Cu(II)/persulfate (PDS)/UV systems were compared under various conditions. The optimal Cu(II) concentration in the Cu(II)/PMS/UV system was 30 μM, and in the Cu(II)/PDS/UV system was 50 μM. With the PMS or PDS concentration increasing, higher tetracycline (TC) degradation in these two systems occurred. Investigation on the mechanism revealed that •OH was the primary radical in the Cu(II)/PMS/UV system, while SO4−• was the primary radical in the Cu(II)/PDS/UV system where •OH also played an important role. In these two systems, it was observed that Cu(I) was generated by PMS or PDS activated via UV illumination; however, oxygen alone could not promote TC removal. The degradation of TC was increased with the increasing pH level. In addition, TC degradation in the Cu(II)/PMS/UV system followed the pseudo-first-order kinetics model during the entire reaction period. It was found that the TC degradation kinetics in the Cu(II)/PDS/UV system can be divided into two parts (0 to 7 min and 10 to 50 min) and these two parts had good agreement with the pseudo-first-order kinetics model, respectively.


2020 ◽  
Vol 32 (9) ◽  
pp. 2143-2148
Author(s):  
JAYANTI SAMOTA ◽  
SURAJ SHARMA ◽  
SHIPRA BHARDWAJ ◽  
KUMUD INTODIA

In present work, a photocatalytic degradation of Erythrosin-B has been studied using cadmium cobaltite. The impact of different parameters such as pH, amount of cadmium cobaltite, concentration of Erythrosin-B and light intensity have been observed on the reaction rate. Radical quenching experiments revealed that hydroxyl radicals are primarily responsible for the degradation of Erythrosin-B. The progress of reaction monitored spectrophotometrically and it followed pseudo first-order kinetics. An experimental mechanism is proposed for the photochemical degradation of Erythrosin-B.


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