scholarly journals Enhanced Photocatalytic Degradation and Mineralization of Furfural Using UVC/TiO2/GAC Composite in Aqueous Solution

2016 ◽  
Vol 2016 ◽  
pp. 1-10 ◽  
Author(s):  
Bahram Ghasemi ◽  
Bagher Anvaripour ◽  
Sahand Jorfi ◽  
Neematollah Jaafarzadeh
Keyword(s):  
Photocatalytic Degradation ◽  
Removal Efficiency ◽  
Irradiation Time ◽  
Titanium Dioxide Nanoparticles ◽  
Sol Gel ◽  
Total Pore Volume ◽  
Operational Parameters ◽  
Experimental Conditions ◽  
First Order Kinetics ◽  
Initial Ph

Titanium dioxide nanoparticles were immobilized on granular activated carbon (GAC) as a porous and low-density support for photocatalytic degradation of furfural. The TiO2/GAC composite was synthetized using the simple sol-gel method and fully characterized. The effects of the operational parameters of furfural concentration (200–700 mg/L), initial pH (2–12), TiO2/GAC composite dosage (1–3.5 g/L), and irradiation time (20–120 min) were studied. The synthetized TiO2/GAC composite exhibited a total pore volume of 0.13 cm3/g and specific surface area of 35.91 m2/g. Removal efficiency of up to 95% was observed at initial pH of 10, TiO2/GAC dosage of 2.5 g/L, irradiation time of 80 min, and initial furfural concentration of 500 mg/L. The photocatalyst could be reused at least four consecutive times with a mere 2% decrease in furfural removal efficiency. Mineralization efficiency of 94% was obtained within 80 min. Pseudo-first-order kinetics best fit the photocatalytic degradation of furfural under experimental conditions.

scholarly journals Photocatalytic Degradation of a Systemic Herbicide: Picloram from Aqueous Solution Using Titanium Oxide (TiO2) under Sunlight

2020 ◽  
Vol 4 (4) ◽  
pp. 58
Author(s):  
Md. Rakibul Islam ◽  
Jahida Binte Islam ◽  
Mai Furukawa ◽  
Ikki Tateishi ◽  
Hideyuki Katsumata ◽  
...  
Keyword(s):  
Photocatalytic Degradation ◽  
Titanium Oxide ◽  
Irradiation Time ◽  
Degradation Mechanism ◽  
Chloride Ion ◽  
Reaction Rate Constant ◽  
Ammonium Ion ◽  
Light Reaction ◽  
First Order Kinetics ◽  
Initial Ph

The photocatalytic degradation of picloram (4-amino-3,5,6-trichloro-2-pyridincarboxylic acid), which is one of popular acidic herbicide, was investigated with the existence of titanium oxide (TiO2) under sunlight. The total photocatalytic degradation of 20 ppm of picloram was occurred within 30 min irradiation with TiO2, while a negligible degradation was found without TiO2 under sunlight. The influence of various parameters, like TiO2 dosage, solution initial pH, intensity of light, reaction temperature and irradiation time, was found during the photocatalytic degradation of picloram. The mineralization of picloram was proved by the deterioration of total organic carbon (TOC) of the photocatalytic process. The pseudo–first order kinetics of photocatalytic degradation was obtained according to the Langmuir–Hinshelwood model, and the reaction rate constant was 17.6 × 10−2 min−1. Chloride ion, ammonium ion, nitrate ion and CO2 were erected as the final products after completing the photocatalytic degradation of picloram. The intermediate products could not be determined by the GC–MS during the degradation of picloram. Therefore, the degradation mechanism of the picloram was proposed based on the frontier electron density and the point charge at each atom of the picloram molecule. The photocatalytic degradation method, using sunlight, may develop into as a pragmatic technique to purify picloram contaminated wastewater.

scholarly journals Synthesis and characterization of ternary chitosan–TiO2–ZnO over graphene for photocatalytic degradation of tetracycline from pharmaceutical wastewater

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Hossein Asadzadeh Patehkhor ◽  
Moslem Fattahi ◽  
Mohammadreza Khosravi-Nikou
Keyword(s):  
Photocatalytic Degradation ◽  
Irradiation Time ◽  
Sol Gel ◽  
Weight Ratio ◽  
Molar Ratio ◽  
Operational Parameters ◽  
Pharmaceutical Wastewater ◽  
Operational Conditions ◽  
Molar Ratios

AbstractVarious nanocomposites of TiO2–ZnO, TiO2–ZnO/CS, and TiO2–ZnO/CS–Gr with different molar ratios were synthesized by sol–gel and ultrasound-assisted methods and utilized under UV irradiation to enhance the photocatalytic degradation of tetracycline. Characterization of prepared materials were carried out by XRD, FT-IR, FE-SEM, EDX and BET techniques. The TiO2–ZnO with the 1:1 molar ratio supported with 1:2 weight ratio CS–Gr (T1‒Z1/CS1‒Gr2 sample) appeared as the most effective material at the optimized operational conditions including the tetracycline concentration of 20 mg/L, pH = 4, catalyst dosage of 0.5 g/L, and 3 h of irradiation time. As expected, the graphene had a significant effect in improving degradation results. The detailed performances of the T1‒Z1/CS1‒Gr2 were compared with ternary nanocomposites from EDX and BET results as well as from the degradation viewpoint. This novel photocatalyst can be effective in actual pharmaceutical wastewater treatment considering the applied operational parameters.

scholarly journals Simultaneous synthesis-immobilization of nano ZnO on perlite for photocatalytic degradation of an azo dye in semi batch packed bed photoreactor

2012 ◽  
Vol 14 (4) ◽  
pp. 69-76 ◽  
Author(s):  
Ali Khani ◽  
Mahmoud Reza Sohrabi
Keyword(s):  
Photocatalytic Degradation ◽  
Packed Bed ◽  
Acid Orange 7 ◽  
Operational Parameters ◽  
Kinetic Rate Constant ◽  
Nano Zno ◽  
First Order Kinetics ◽  
Initial Ph ◽  
On Line ◽  
Simultaneous Synthesis

Abstract A novel, simple and simultaneous synthesis-immobilization of nano ZnO on perlite (nZnO-P) as a photocatalyst for photocatalytic degradation of Acid orange 7 (AO7) in aqueous solution was investigated. The effect of operational parameters such as initial dye concentration, initial pH, flow rate, photocatalyst granule size, temperature and the kinetic of the removal of AO7 in terms of the Langmuir-Hinshelwood model in a designed semi batch packed bed photoreactor connected to an on-line sampling UV-Vis spectrophotometer was studied. The results showed that AO7 removal efficiency increased with nZnO-P using the designed setup and the proposed photocatalyst was more efficient than TiO2 as a standard catalyst. Our results confirmed the pseudo-first-order kinetics model. The values of the adsorption equilibrium constant, KAO7, the kinetic rate constant of surface reaction, kc, and the activation energy (Ea) were found to be 0.57 (mg.l−1)−1, 0.41 mg.l−1.min−1 and 11.44 kJ/mol, respectively.

scholarly journals Electro-photocatalytic degradation of amoxicillin using calcium titanate

2018 ◽  
Vol 16 (1) ◽  
pp. 949-955 ◽  
Author(s):  
Lvshan Zhou ◽  
Xiaogang Guo ◽  
Chuan Lai ◽  
Wei Wang
Keyword(s):  
Photocatalytic Degradation ◽  
Reaction Rate ◽  
Irradiation Time ◽  
Oxygen Demand ◽  
Reaction Rate Constant ◽  
Calcium Titanate ◽  
Experimental Conditions ◽  
Exponential Factor ◽  
First Order ◽  
First Order Kinetics

AbstractThe electro-photocatalytic degradation of amoxicillin in aqueous solution was investigated using single factor test by the potassium permanganate method for measuring the values of chemical oxygen demand (CODMn). Batch experiments were carried out successfully under different conditions, including initial amoxicillin concentration, calcium titanate dosage, pH, UV irradiation time, electrolyte and temperature. The experimental results show that there is a great difference between electro-photocatalytic and photocatalitic degradation. The maximum electro-photocatalytic degradation efficiency can increase to 79% under the experimental conditions of 200 mL amoxicillin solution (100 mg L-1) with 0.5 g calcium titanate by pH=3 for 120 min irradiation and 0.058 g sodium chloride as electrolyte at 318.5K. In addition, the reaction rate constant of 0.00848~0.01349 min-1, activation energy of 9.8934 kJ mol-1 and the pre-exponential factor of 0.5728 were obtained based on kinetics studies, indicating that the electro-photocatalytic reaction approximately followed the first-order kinetics model.

Effects of operational parameters on defluoridation efficiency using electrocoagulation process

2011 ◽  
Vol 6 (1) ◽  
Author(s):  
M. Behbahani ◽  
M.R. Alavi Moghaddam ◽  
M. Arami
Keyword(s):  
Reaction Time ◽  
Anode Material ◽  
Removal Efficiency ◽  
Fluoride Concentration ◽  
Fluoride Removal ◽  
Operational Parameters ◽  
Applied Current ◽  
Initial Ph ◽  
Electrocoagulation Process ◽  
Electrode Connection

The aim of this study is to examine the effect of operational parameters on fluoride removal using electrocoagulation method. For this purpose, various operational parameters including initial pH, initial fluoride concentration, applied current, reaction time, electrode connection mode, anode material, electrolyte salt, electrolyte concentration, number of electrodes and interelectrode distance were investigated. The highest defluoridation efficiency achieved at initial pH 6. In the case of initial fluoride concentration, maximum removal efficiency (98.5%) obtained at concentration of 25mg/l. The increase of applied current and reaction time improved defluoridation efficiency up to 99%. The difference of fluoride removal efficiencies between monopolar and bipolar series and monopolar parallel were significant, especially at reaction time of 5 min. When aluminum used as anode material, higher removal efficiency (98.5%) achieved compared to that of iron anode (67.7%). The best electrolyte salt was NaCl with the maximum defluoridation efficiency of 98.5% compared to KNO3 and Na2SO4. The increase of NaCl had no effect on defluoridation efficiency. Number of electrodes had little effect on the amounts of Al3+ ions released in the solution and as a result defluoridation efficiency. Almost the same fluoride removal efficiency obtained for different interelectrode distances.

Immobilization of Nano-TiO2 on Expanded Perlite for Photocatalytic Degradation of Rhodamine B

2011 ◽  
Vol 110-116 ◽  
pp. 3795-3800 ◽  
Author(s):  
Xiao Zhi Wang ◽  
Wei Wei Yong ◽  
Wei Qin Yin ◽  
Ke Feng ◽  
Rong Guo
Keyword(s):  
Catalytic Activity ◽  
Photocatalytic Degradation ◽  
Rhodamine B ◽  
Degradation Kinetics ◽  
Irradiation Time ◽  
Sol Gel ◽  
Polluted Water ◽  
Order Kinetic ◽  
Expanded Perlite ◽  
Initial Concentration

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.

The Effect of Operational Parameters on the Photocatalytic Mineralization of Indocorn Brilliant Red M5B Using Sol–gel Derived Nanostructured Zinc Titanate as an Efficient Photocatalyst

2012 ◽  
Vol 15 (2) ◽  
Author(s):  
Mohammad Hossein Habibi ◽  
Maryam Mikhak
Keyword(s):  
Azo Dye ◽  
Sol Gel ◽  
Degradation Efficiency ◽  
High Yield ◽  
Operational Parameters ◽  
Solution Ph ◽  
Zinc Titanate ◽  
First Order Kinetics ◽  
Size Uniformity ◽  
One Step

AbstractNanostructured zinc titanate (NZT) was synthesized in high yield via a one-step and template-free sol-gel route. The prepared nanocomposite exhibited good size uniformity and regularity. The enhanced photocatalytic activity of the NZT was evaluated in the degradation and mineralization of Indocorn Brilliant Red (M5B) under metal halide lamp irradiation. The effects of different parameters such as pH of the solution, and initial dye concentration on photodegradation of M5B were analyzed. The degradation of M5B follows pseudo-first order kinetics according to the Langmuir-Hinshelwood model. The experimental results showed that the initial concentration of azo dye in the dye mixture greatly affected the degradation efficiency. At M5B concentrations of 10 mg/L, the optimum conditions for the highest degradation efficiency (94%) of azo dye were a photocatalyst dosage of 0.01 g/L and an initial solution pH of 9. This study provided new insight into the design and preparation of nanomaterial demonstrated an excellent ability to remove organic pollutants in wastewater.

Photocatalytic Activity of Bismuth Ferrite Nanoparticles Synthesized via Sol-Gel Route

2019 ◽  
Vol 233 (5) ◽  
pp. 595-607 ◽  
Author(s):  
Mohsin Siddique ◽  
Noor Muhammad Khan ◽  
Muhammad Saeed
Keyword(s):  
Visible Light ◽  
Photocatalytic Degradation ◽  
Irradiation Time ◽  
Bismuth Ferrite ◽  
Sol Gel ◽  
Reaction System ◽  
Light Conditions ◽  
X Ray Diffraction ◽  
Light Region ◽  
Gel Technique

Abstract Nanosized, magnetically separable bismuth ferrite (BFO) nanoparticles, pertaining a crystallite size in the range of 14–15 nm were prepared via facile sol-gel technique. The product was characterized by scanning electron microscopy, X-ray diffraction, and Fourier-transform infrared spectroscopy. The product was explored for the photocatalytic mineralization of rhodamine B (RB) dye in aqueous medium. The effect of different investigational parameters such as amount of photocatalyst, initial dye concentration and irradiation time on the photocatalytic degradation of RB was studied. The results reveal that the catalyst shows good degrading ability under normal pH and visible light conditions. BFO nanoparticles demonstrated a strong absorption ability in the visible-light region, which lead to efficient photocatalytic degradation of RB dye The reaction system was heterogeneous in nature in which the catalyst can be separated by a normal magnet.

Influence of Operational Parameters on Photocatalytic Degradation of Linuron in Aqueous TiO2 Pillared Montmorillonite Suspension

2021 ◽  
Vol 16 (3) ◽  
pp. 673-685
Author(s):  
D. Hadj Bachir ◽  
Hocine Boutoumi ◽  
H. Khalaf ◽  
Pierre Eloy ◽  
J. Schnee ◽  
...  
Keyword(s):  
Photocatalytic Degradation ◽  
Physicochemical Characterization ◽  
Operating Conditions ◽  
Cod Removal ◽  
Pollutant Concentration ◽  
Catalyst Loading ◽  
Operational Parameters ◽  
X Ray ◽  
Pillared Montmorillonite ◽  
Initial Ph

TiO2 pillared clay was prepared by intercalation of titan polyoxocation into interlamelar space of an Algerian montmorillonite and used for the photocatalytic degradation of the linuron herbicide as a target pollutant in aqueous solution. The TiO2 pillared montmorillonite (Mont-TiO2) was characterized by X-ray photoelectron spectroscopy (XPS), X-Ray diffraction (XRD), X-Ray fluorescence (XRF), scanning electronic microscopy (SEM), thermogravimetry and differential thermal analysis (TG-DTA), Fourier transformed infra-red (FT-IR), specific area and porosity determinations. This physicochemical characterization pointed to successful TiO2 pillaring of the clay. The prepared material has porous structure and exhibit a good thermal stability as indicated by its surface area after calcination by microwave. The effects of operating parameters such as catalyst loading, initial pH of the solution and the pollutant concentration on the photocatalytic efficiency and COD removal  were evaluated. Under initial pH of the solution around seven, pollutant concentration of 10 mg/L and 2.5 g/L of catalyst at room temperature, the degradation efficiency and COD removal of linuron was best then the other operating conditions. It was observed that operational parameters play a major role in the photocatalytic degradation process. Copyright © 2021 by Authors, Published by BCREC Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0). 

scholarly journals Synthesis and characterization of La1-xCexNiO3 with enhanced visible light photocatalytic activities

2019 ◽  
Vol 118 ◽  
pp. 01005
Author(s):  
Ying-ying Li ◽  
Jin-zhou Li ◽  
Yong-chun Liu
Keyword(s):  
Methyl Orange ◽  
Visible Light ◽  
Irradiation Time ◽  
Xylenol Orange ◽  
Sol Gel ◽  
Operational Parameters ◽  
X Ray Diffraction ◽  
Alizarin Red ◽  
Alizarin Yellow ◽  
Photocatalytic Activities

A series of La1-xCexNiO3 photocatalysts with different content of cerium element have been synthesized by sol-gel method. The as-prepared products were characterized by powder X-ray diffraction (XRD) and scanning electron microscopy (SEM). The photocatalytic activities of these La1-xCexNiO3 composites under visible-light irradiation were evaluated by the degradation of methyl orange (MO). The effect of important operational parameters such as catalyst amount, reaction temperature, irradiation time, and comparison of photocatalytic activity with different dyes including methyl orange, alizarin red, alizarin yellow, xylenol orange were also studied. The results revealed that the La0.8Ce0.2NiO3 (LCNO) composites exhibited much higher photocatalytic activities than pure LaNiO3 (LNO).

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