scholarly journals Effect of Process Parameters on the Photocatalytic Degradation of Phenol in Oilfield Produced Wastewater using ZnO/Fe2O3 Nanocomposites.

2019 ◽  
Vol 15 (1) ◽  
pp. 128-136 ◽  
Author(s):  
Omer Al Haiqi ◽  
Abdurahman Hamid Nour ◽  
Rushdi Bargaa ◽  
Bamidele Victor Ayodele
Keyword(s):  
Solar Radiation ◽  
Photocatalytic Degradation ◽  
Calcination Temperature ◽  
Process Parameters ◽  
Batch Reactor ◽  
Phenol Degradation ◽  
Phenol Concentration ◽  
Catalyst Loading ◽  
Nanocomposite Catalyst ◽  
Initial Phenol Concentration

The upstream processing of crude oil is often associated with the presence of phenolic compounds when not properly treated could result in adverse effects on human health. The objective of the study was to investigate the effect of process parameters on the photocatalytic degradation of phenol. The ZnO/Fe2O3 nanocomposite photocatalyst was prepared by sol-gel method and characterized using various instrument techniques. The characterized ZnO/Fe2O3 nanocomposite displayed suitable physicochemical properties for the photocatalytic reaction. The ZnO/Fe2O3 nanocomposite was employed for the phenol degradation in a cylindrical batch reactor under solar radiation. The photocatalytic runs show that calcination temperature of the ZnO/Fe2O3 nanocomposite, catalyst loading, initial phenol concentration and pH of the wastewater significantly influence the photocatalytic degradation of phenol. After 180 min of solar radiation, the highest phenol degradation of 92.7% was obtained using the ZnO/Fe2O3 photocatalyst calcined at 400 ºC. This study has demonstrated that phenol degradation is significantly influenced by parameters such as calcination temperature of the ZnO/Fe2O3 nanocomposite, catalyst loading, initial phenol concentration and pH of the wastewater resulting in highest phenol degradation using the ZnO/Fe2O3 nanocomposite calcined at 400 ºC, initial phenol concentration of 0.5 mg/L, catalyst loading of 3 mg/L and pH of 3. Copyright © 2020 BCREC Group. All rights reserved

scholarly journals Phenol Removal by a Novel Non-Photo-Dependent Semiconductor Catalyst in a Pilot-Scaled Study: Effects of Initial Phenol Concentration, Light, and Catalyst Loading

2014 ◽  
Vol 2014 ◽  
pp. 1-8
Author(s):  
Xiao Chen ◽  
Yan Liang ◽  
Xuefei Zhou ◽  
Yanling Zhang
Keyword(s):  
Titanium Dioxide ◽  
Uv Radiation ◽  
Phenol Degradation ◽  
Phenol Concentration ◽  
Catalyst Loading ◽  
Phenol Removal ◽  
Operational Parameters ◽  
Initial Concentration ◽  
Light Area ◽  
Initial Phenol Concentration

A novel non-photo-dependent semiconductor catalyst (CT) was employed to degrade phenol in the present pilot-scaled study. Effect of operational parameters such as phenol initial concentration, light area, and catalyst loading on phenol degradation, was compared between CT catalyst and the conventional photocatalyst titanium dioxide. CT catalyst excelled titanium dioxide in treating and mineralizing low-level phenol, under both mild UV radiation and thunder conditions of nonphoton. The result suggested that CT catalyst could be applied in circumstances when light is not easily accessible in pollutant-carrying media (e.g., particles, cloudy water, and colored water).

scholarly journals Photocatalytic Degradation of Acid Yellow 36 Using Zinc Oxide Photocatalyst in Aqueous Media

2013 ◽  
Vol 2013 ◽  
pp. 1-6 ◽  
Author(s):  
Sajjad Khezrianjoo ◽  
Hosakere Doddarevanna Revanasiddappa
Keyword(s):  
Photocatalytic Degradation ◽  
Catalyst Concentration ◽  
Heterogeneous Medium ◽  
Batch Reactor ◽  
Aqueous Media ◽  
Electrical Energy ◽  
Degradation Process ◽  
Active Species ◽  
Catalyst Loading ◽  
Order Of Magnitude

A detailed investigation of photocatalytic degradation of Acid Yellow 36 (AY36) has been carried out in aqueous heterogeneous medium containing ZnO as photocatalyst in a batch reactor. The effects of some parameters such as pH, catalyst loading, and ethanol concentration were examined. Solutions with initial concentration of 50 mg L−1 of dye, within the range of typical concentration in textile wastewaters, were treated at natural pH of 6.93 and catalyst concentration of 1 g L−1 after 180 min irradiation. Investigations on the active species indicated that hydroxyl radicals play the major role in the process. Experiments showed that the most efficient pH on the removal of the dye with photocatalytic degradation process was 8; however, acidic pH was favored for the dark surface adsorption. Electrical energy consumption per order of magnitude for photocatalytic degradation of AY36 has been also determined.

scholarly journals Phenol Photocatalytic Degradation by Advanced Oxidation Process under Ultraviolet Radiation Using Titanium Dioxide

2013 ◽  
Vol 2013 ◽  
pp. 1-9 ◽  
Author(s):  
Ali Nickheslat ◽  
Mohammad Mehdi Amin ◽  
Hassan Izanloo ◽  
Ali Fatehizadeh ◽  
Seyed Mohammad Mousavi
Keyword(s):  
Titanium Dioxide ◽  
Photocatalytic Degradation ◽  
Uv Radiation ◽  
Removal Efficiency ◽  
Quartz Glass ◽  
Contact Time ◽  
Phenol Concentration ◽  
Solution Ph ◽  
Glass Tubes ◽  
Initial Phenol Concentration

Background. The main objective of this study was to examine the photocatalytic degradation of phenol from laboratory samples and petrochemical industries wastewater under UV radiation by using nanoparticles of titanium dioxide coated on the inner and outer quartz glass tubes.Method. The first stage of this study was conducted to stabilize the titanium dioxide nanoparticles in anatase crystal phase, using dip-coating sol-gel method on the inner and outer surfaces of quartz glass tubes. The effect of important parameters including initial phenol concentration, TiO2catalyst dose, duration of UV radiation, pH of solution, and contact time was investigated.Results. In the dip-coat lining stage, the produced nanoparticles with anatase crystalline structure have the average particle size of 30 nm and are uniformly distributed over the tube surface. The removal efficiency of phenol was increased with the descending of the solution pH and initial phenol concentration and rising of the contact time.Conclusion. Results showed that the light easily passes through four layers of coating (about 105 nm). The highest removal efficiency of phenol with photocatalytic UV/TiO2process was 50% at initial phenol concentration of 30 mg/L, solution pH of 3, and 300 min contact time. The comparison of synthetic solution and petrochemical wastewater showed that at same conditions the phenol removal efficiency was equal.

scholarly journals Photocatalytic Degradation of Phenolics by N-Doped Mesoporous Titania under Solar Radiation

2012 ◽  
Vol 2012 ◽  
pp. 1-10 ◽  
Author(s):  
Priti A. Mangrulkar ◽  
Sanjay P. Kamble ◽  
Meenal M. Joshi ◽  
Jyotsna S. Meshram ◽  
Nitin K. Labhsetwar ◽  
...  
Keyword(s):  
Photocatalytic Degradation ◽  
Phenol Degradation ◽  
Catalyst Loading ◽  
Operating Parameters ◽  
Mesoporous Titania ◽  
Templating Method ◽  
Initial Concentration ◽  
Nitrogen Doped ◽  
Coexisting Ions

In this study, nitrogen-doped mesoporous titania was synthesized by templating method using chitosan. This biopolymer chitosan plays the dual role of acting as a template (which imparts mesoporosity) and precursor for nitrogen. BET-SA, XRD, UV-DRS, SEM, and FTIR were used to characterize the photocatalyst. The doping of nitrogen into TiO2lattice and its state was substantiated and measured by XPS. The photocatalytic activity of the prepared N-doped mesoporous titania for phenol ando-chlorophenol degradation was investigated under solar and artificial radiation. The rate of photocatalytic degradation was observed to be higher foro-chlorophenol than that of phenol. The photodegradation ofo-chlorophenol was 98.62% and 72.2%, while in case of phenol, degradation to the tune of 69.25% and 30.58% was achieved in solar and artificial radiation. The effect of various operating parameters, namely, catalyst loading, pH, initial concentration and the effect of coexisting ions on the rate of photocatalytic degradation were studied in detail.

scholarly journals Photocatalytic Degradation of Phenol Using ImmobilizedTiO2Nanotube Photocatalysts

2011 ◽  
Vol 2011 ◽  
pp. 1-9 ◽  
Author(s):  
Chung Leng Wong ◽  
Yong Nian Tan ◽  
Abdul Rahman Mohamed
Keyword(s):  
Photocatalytic Activity ◽  
Photocatalytic Degradation ◽  
Silica Gel ◽  
Batch Reactor ◽  
Phenol Degradation ◽  
Reaction Medium ◽  
Photogenerated Electron ◽  
Electron Hole ◽  
Operating Cycles ◽  
Excellent Stability

TiO2nanotubes immobilized on silica gel were used in the photocatalytic degradation of phenol in a batch reactor. The highest rate of photocatalytic activity was observed when the ratios of TiO2nanotubes: silica gel: colloidal silica were 3 : 2 : 20. The optimal air flow rate for phenol degradation was 0.3 L/min while pH 3 was optimal for the reaction medium. Decreasing the initial phenol concentration led to an increase in phenol degradation efficiency due to more hydroxyl radicals being presented on the catalyst surface. Immobilized TiO2nanotubes showed higher photocatalytic activity than that of the pure TiO2which only achieved 87% degradation. Compared with pure TiO2, the immobilized TiO2nanotubes benefited from a larger specific surface area and a low recombination rate of photogenerated electron-hole pairs. After three operating cycles, the decrease in photocatalytic activity of the immobilized TiO2nanotubes was slight, indicating that the immobilized TiO2nanotubes have excellent stability and reusability.

Photocatalytic degradation of methylene blue from aqueous solutions using nanopillars-TiO2 thin films: Batch reactor studies

2018 ◽  
Vol 18 (3) ◽  
pp. 81-91 ◽  
Author(s):  
C. Lalhriatpuia
Keyword(s):  
Thin Films ◽  
Methylene Blue ◽  
Photocatalytic Activity ◽  
Organic Carbon ◽  
Photocatalytic Degradation ◽  
Batch Reactor ◽  
Tio2 Thin Films ◽  
Initial Concentration ◽  
Bet Specific Surface Area ◽  
Interfering Ions

Nanopillars-TiO2 thin films was obtained on a borosilicate glass substrate with (S1) and without (S2) polyethylene glycol as template. The photocatalytic behaviour of S1 and S2 thin films was assessed inthe degradation of methylene blue (MB) dye from aqueous solution under batch reactor operations. The thin films were characterized by the SEM, XRD, FTIR and AFM analytical methods. BET specific surface area and pore sizes were also obtained. The XRD data confirmed that the TiO2 particles are in its anatase mineral phase. The SEM and AFM images indicated the catalyst is composed with nanosized pillars of TiO2, evenly distributed on the surface of the substrate. The BET specific surface area and pore sizes of S1 and S2 catalyst were found to be 5.217 and 1.420 m2/g and 7.77 and 4.16 nm respectively. The photocatalytic degradation of MB was well studied at wide range of physico-chemical parameters. The effect of solution pH (pH 4.0 to 10.0) and MB initial concentration (1.0 to 10.0 mg/L) was extensively studied and the effect of several interfering ions, i.e., cadmium nitrate, copper sulfate, zinc chloride, sodium chloride, sodium nitrate, sodium nitrite, glycine, oxalic acid and EDTA in the photocatalytic degradation of MB was demonstrated. The maximum percent removal of MB was observed at pH 8.0 beyond which it started decreasing and a low initial concentration of the pollutant highly favoured the photocatalytic degradation using thin films and the presence of several interfering ions diminished the photocatalytic activity of thin films to some extent. The overall photocatalytic activity was in the order: S2 > S1 > UV. The photocatalytic degradation of MB was followed the pseudo-first-order rate kinetics. The mineralization of MB was studied with total organic carbon measurement using the TOC (total organic carbon) analysis.

Accelerated Phenol Removal by Amplifying the Metabolic Pathway with a Recombinant Plasmid Encoding Catechol 2, 3 Oxygenase

1992 ◽  
Vol 26 (9-11) ◽  
pp. 2191-2194 ◽  
Author(s):  
M. Fujita ◽  
M. Ike ◽  
T. Kamiya
Keyword(s):  
Metabolic Pathway ◽  
Recombinant Plasmid ◽  
Removal Rate ◽  
Phenol Degradation ◽  
Wild Strain ◽  
Phenol Concentration ◽  
Phenol Removal

The metabolic pathway of the phenol degradation in Pseudomonasputida BH was amplified by introducing the recombinant plasmid containing catechol 2,3 oxygenase gene isolated fron the chromosome of BH. This strain could degrade phenol and grow much faster than the wild strain at the phenol concentration of 100mg/L. This strain seems to accelerate the phenol removal rate if it is applied to the treatment of wastewater containing phenol.

Use of Nanopillars-TiO2 Thin Films in the Photocatalytic Degradation of Bromophenol Blue from Aqueous Solution

2018 ◽  
Vol 6 (1) ◽  
pp. 22-30
Author(s):  
C. Lalhriatpuia ◽  
◽  
Thanhming liana ◽  
K. Vanlaldinpuia
Keyword(s):  
Thin Films ◽  
Aqueous Solution ◽  
Photocatalytic Activity ◽  
Photocatalytic Degradation ◽  
Batch Reactor ◽  
Bromophenol Blue ◽  
Tio2 Thin Films ◽  
Initial Concentration ◽  
Bet Specific Surface Area ◽  
Interfering Ions

The photocatalytic activity of Nanopillars-TiO2 thin films was assessed in the degradation of Bromophenol blue (BPB) dye from aqueous solution under batch reactor operations. The thin films were characterized by the XRD, SEM and AFM analytical methods. BET specific surface area and pore sizes were also obtained. The XRD data showed anatase phase of TiO2 particles with average particle size of 25.4 and 21.9 nm, for S1 and S2 catalysts respectively. The SEM and AFM images indicated the catalyst composed with Nanosized pillars of TiO2, evenly distributed on the surface of the substrate. The average height of the pillars was found to be 180 and 40 nm respectively for the S1 and S2 catalyst. The BET specific surface area and pore sizes of S1 and S2 catalyst were found to be 5.217 and 1.420 m2/g and 7.77 and 4.16 nm respectively. The photocatalytic degradation of BPB using the UV light was studied at wide range of physico-chemical parametric studies to determine the mechanism of degradation as well as the practical applicability of the technique. The batch reactor operations were conducted at varied pH (pH 4.0 to 10.0), BPB initial concentration (1.0 to 20.0 mg/L) and presence of several interfering ions, i.e., cadmium nitrate, copper sulfate, zinc chloride, sodium chloride, sodium nitrate, sodium nitrite, glycine, oxalic acid and EDTA in the photocatalytic degradation of BPB. The maximum percent removal of BPB was observed at pH 6.0 and a low initial concentration of the pollutant highly favours the photocatalytic degradation using thin films. The presence of several interfering ions suppressed the photocatalytic activity of thin films to some extent. The time dependence photocatalytic degradation of BPB was demonstrated with the pseudo-first-order rate kinetics. Study was further extended with total organic carbon measurement using the TOC (Total Organic Carbon) analysis. This demonstrated an apparent mineralization of BPB from aqueous solutions.

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