scholarly journals Optimization of Photocatalytic Degradation of Acid Blue 113 and Acid Red 88 Textile Dyes in a UV-C/TiO2 Suspension System: Application of Response Surface Methodology (RSM)

Catalysts ◽  
2019 ◽  
Vol 9 (4) ◽  
pp. 360 ◽  
Author(s):  
Soroosh Mortazavian ◽  
Ali Saber ◽  
David E. James

Textile industries produce copious amounts of colored wastewater some of which are toxic to humans and aquatic biota. This study investigates optimization of a bench-scale UV-C photocatalytic process using a TiO2 catalyst suspension for degradation of two textile dyes, Acid Blue 113 (AB 113) and Acid Red 88 (AR 88). From preliminary experiments, appropriate ranges for experimental factors including reaction time, solution pH, initial dye concentration and catalyst dose, were determined for each dye. Response surface methodology (RSM) using a cubic IV optimal design was then used to design the experiments and optimize the process. Analysis of variance (ANOVA) was employed to determine significance of experimental factors and their interactions. Results revealed that among the studied factors, solution pH and initial dye concentration had the strongest effects on degradation rates of AB 113 and AR 88, respectively. Least-squares cubic regression models were generated by step-wise elimination of non-significant (p-value > 0.05) terms from the proposed model. Under optimum treatment conditions, removal efficiencies reached 98.7% for AB 113 and 99.6% for AR 88. Kinetic studies showed that a first-order kinetic model could best describe degradation data for both dyes, with degradation rate constants of k1, AB 113 = 0.048 min−1 and k1, AR 88 = 0.059 min−1.

2019 ◽  
Vol 80 (4) ◽  
pp. 685-694 ◽  
Author(s):  
Maryam Dolatabadi ◽  
Saeid Ahmadzadeh

Abstract Presence of emerging contaminants such as pharmaceutical products in aquatic environments has received high concern due to their undesirable effect on wildlife and human health. Current work deals with developing a treatment model based on the electro- Fenton (EF) process for efficient removal of metformin (MET) from an aqueous medium. The obtained experimental results revealed that over the reaction time of 10 min and solution pH of 3, the maximum removal efficiency of 98.57% is achieved where the value of MET initial concentration, current density, and H2O2 dosage is set at 10 mg.L−1, 6 mA.cm−2, and 250 μL.L−1, respectively, which is in satisfactory agreement with the predicted removal efficiency of 98.6% with the desirability of 0.99. The presence of radical scavengers throughout the mineralization of MET under the EF process revealed that the generation of •OH radicals, as the main oxidative species, controlled the degradation mechanism. The obtained kinetics data best fitted to the first order kinetic model with the rate constant of 0.4224 min−1 (R2 = 0.9940). The developed treatment process under response surface methodology (RSM) was employed for modeling the obtained experimental data and successfully applied for efficient removal of the MET contaminant from pharmaceutical wastewater as an adequate and cost-effective approach.


Gels ◽  
2021 ◽  
Vol 7 (4) ◽  
pp. 225
Author(s):  
Katarina Antić ◽  
Antonije Onjia ◽  
Dana Vasiljević-Radović ◽  
Zlate Veličković ◽  
Simonida Lj. Tomić

The adsorption of Ni2+ ions from water solutions by using hydrogels based on 2-hydroxyethyl acrylate (HEA) and itaconic acid (IA) was studied. Hydrogel synthesis was optimized with response surface methodology (RSM). The hydrogel with the best adsorption capacity towards Ni2+ ions was chosen for further experiments. The hydrogel was characterized by Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) and atomic force microscopy (AFM) analysis before and after the adsorption of Ni2+ ions. Batch equilibrium experiments were conducted to investigate the influence of solution pH, hydrogel weight, ionic strength, adsorption time, temperature and initial concentration of nickel ions on the adsorption. Time-dependent adsorption fitted the best to the pseudo-second-order kinetic model. A thermodynamic study revealed that the adsorption was an exothermic and non-spontaneous process. Five isotherm models were studied, and the best fit was obtained with the Redlich–Peterson model. Consecutive adsorption/desorption studies indicated that the HEA/IA hydrogel can be efficiently used as a sorbent for the removal of Ni2+ ions from the water solution. This study develops a potential adsorbent for the effective removal of trace nickel ions.


2017 ◽  
Vol 4 (2) ◽  
pp. 149-160
Author(s):  
Sajad Talebi ◽  
Naz Chaibakhsh Langroudi ◽  
Zeinab Moradi-Shoeili ◽  
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2021 ◽  
Vol 52 (1) ◽  
pp. 204-217
Author(s):  
Mohammed & Mohammed-Ridha

This study was aimed to investigate the response surface methodology (RSM) to evaluate the effects of various experimental conditions on the removal of levofloxacin (LVX) from the aqueous solution by means of electrocoagulation (EC) technique with stainless steel electrodes. The EC process was achieved successfully with the efficiency of LVX removal of 90%. The results obtained from the regression analysis, showed that the data of experiential are better fitted to the polynomial model of second-order with the predicted correlation coefficient (pred. R2) of 0.723, adjusted correlation coefficient (Adj. R2) of 0.907 and correlation coefficient values (R2) of 0.952. This shows that the predicted models and experimental values are in good agreement. The results of the kinetic study showed that the second-order kinetic model was in good agreement with the experimental results and suggested that the mechanism of chemisorption controlled the LVX adsorption. The experimental results indicated that the adsorption of LVX on iron hydroxide flocs follows Sips isotherm with the value of the correlation coefficient (R2) of 0.937. Sips isotherm shows that both homogenous and heterogeneous adsorption can occur.


2015 ◽  
Vol 6 (2) ◽  
pp. 333-344 ◽  
Author(s):  
Neda Khorshidi ◽  
Ali Niazi

We have investigated the biosorption of pyrocatechol violet (PCV) from aqueous solutions by Robinia pseudoacacia tree leaves as a low-cost and eco-friendly biosorbent. A full factorial design was performed for screening the main variables and their interactions, which reduces the large total number of experiments. Results of the full factorial design (24) based on an analysis of variance (ANOVA) demonstrated that the initial PCV concentration, contact time, pH and temperature are statistically significant. Box-Behnken design, a response surface methodology, was used for further optimization of these selected factors. The ANOVA and some statistical tests such as lack-of-fit and coefficient of determination (R2) showed good fit of the experimental data to the second-order polynomial model. The Langmuir and Freundlich isotherm models were used to describe the equilibrium isotherms. Equilibrium data fitted well with the Freundlich isotherm model (R2 > 0.97). In addition, thermodynamic parameters (ΔG°, ΔH° and ΔS°) were calculated, these parameters show that the biosorption process was spontaneous (ΔG° = −2.423) and exothermic (ΔH° = −9.67). The biosorption kinetic data were fitted with the pseudo-second-order kinetic model (R2 > 0.999). These results confirm that R. pseudoacacia leaves have good potential for removal of PCV from aqueous solution.


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