scholarly journals Immobilized rGO/TiO2 Photocatalyst for Decontamination of Water

Catalysts ◽  
2019 ◽  
Vol 9 (9) ◽  
pp. 708 ◽  
Author(s):  
Radek Zouzelka ◽  
Monika Remzova ◽  
Jan Plsek ◽  
Libor Brabec ◽  
Jiri Rathousky
Keyword(s):  
Photocatalytic Degradation ◽  
Reaction Rate ◽  
Reaction Rate Constant ◽  
Tio2 Photocatalyst ◽  
Limited Effect ◽  
Environmental Application ◽  
First Order ◽  
Beneficial Effects ◽  
Low Concentrations ◽  
Reduced Graphene

The preparation of immobilized graphene-based photocatalyst layers is highly desired for environmental applications. In this study, the preparation of an immobilized reduced graphene oxide (rGO)/TiO2 composite by electrophoretic deposition (EPD) was optimized. It enabled quantitative deposition without sintering and without the use of any dispersive additive. The presence of rGO had beneficial effects on the photocatalytic degradation of 4-chlorophenol in an aqueous solution. A marked increase in the photocatalytic degradation rate was observed, even at very low concentrations of rGO. Compared with the TiO2 and GO/TiO2 reference layers, use of the rGO/TiO2 composite (0.5 wt% of rGO) increased the first-order reaction rate constant by about 70%. This enhanced performance was due to the increased formation of hydroxyl radicals that attacked the 4-chlorophenol molecules. The direct charge transfer mechanism had only limited effect on the degradation. Thus, EPD-prepared rGO/TiO2 layers appear to be suitable for environmental application.

scholarly journals Immobilized rGO/TiO2 Photocatalyst for Decontamination of Water

2019 ◽  
Author(s):  
Radek Zouzelka ◽  
Monika Remzova ◽  
Jan Plsek ◽  
Libor Brabec ◽  
Jiri Rathousky
Keyword(s):  
Photocatalytic Degradation ◽  
Reaction Rate ◽  
Reaction Rate Constant ◽  
Order Reaction ◽  
Limited Effect ◽  
Environmental Application ◽  
First Order ◽  
Beneficial Effects ◽  
Low Concentrations ◽  
Reduced Graphene

The preparation of immobilized graphene–based photocatalyst layers is highly desired for environmental applications. In this study, the preparation of an immobilized reduced graphene oxide (rGO)/TiO2 composite by electrophoretic deposition (EPD) was optimized. It enabled quantitative deposition without sintering and without the use of any dispersive additive. The presence of rGO had beneficial effects on the photocatalytic degradation of 4-chlorophenol in an aqueous solution. A marked increase in the photocatalytic degradation rate was observed, even at very low concentrations of rGO. Compared with the TiO2 and GO/TiO2 reference layers, use of the rGO/TiO2 composite (0.5 wt% of rGO) increased the first-order reaction rate constant by about 70%. This enhanced performance was due to the increased formation of hydroxyl radicals that attacked the 4-chlorophenol molecules. The direct charge transfer mechanism had only limited effect on the degradation. Thus, EPD-prepared rGO/TiO2 layers appear to be suitable for environmental application.

Photocatalytic Degradation of Antibacterial Sulfanilamide from Aqueous Solution Using TiO2 Nanocatalyst

2017 ◽  
Vol 46 ◽  
pp. 111-122 ◽  
Author(s):  
Hosein Ghahremani
Keyword(s):  
Photocatalytic Degradation ◽  
Uv Irradiation ◽  
Reaction Rate ◽  
Inorganic Salt ◽  
Uv Light ◽  
Kinetic Constant ◽  
Nano Particles ◽  
Order Kinetic ◽  
First Order ◽  
Low Concentrations

Photocatalytic degradation of sulfanilamide (SNM) as a kind of pollutant agent through titanium dioxide nano particles (TiO2) under UV irradiation was evaluated. The effect of different parameters, such as TiO2 and SNM concentrations, amount of pH, inorganic salt and type of light source on the reaction rate was investigated. The results show that SNM was completely removed from the solution after 60 min under UV irradiation. Furthermore, kinetic studied were performed at 25°C over different ranges of SNM concentrations from 100 to 300 ppm, TiO2 concentrations from 0.05 to 1 gL-1 and pH of suspensions from 3 to 11. In this range of concentration of materials, a Langmuir–Hinshelwood kinetic model can describe the process. An overall pseudo-first order kinetic constant was calculated for sulfanilamide conversion. The optimum TiO2 loading, which provides enough surface area for reaction without irradiation loss due to scattering of UV light, was found to be 0.1gL-1, and SNM concentration was100 ppm. Higher degradation efficiency of SNM was observed at pH=9. Finally, the results of this work proved that photocatalysis of SNM is a promising technology to reduce persistent substances even if they are present in low concentrations.

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.

scholarly journals Determination of exothermic batch reactor specific model parameters

2019 ◽  
Vol 292 ◽  
pp. 01063
Author(s):  
Lubomír Macků
Keyword(s):  
Rate Constant ◽  
Reaction Rate ◽  
Batch Reactor ◽  
Specific Model ◽  
Reaction Rate Constant ◽  
Order Reaction ◽  
First Order Reaction ◽  
Model Parameters ◽  
Reactor Model ◽  
First Order

An alternative method of determining exothermic reactor model parameters which include first order reaction rate constant is described in this paper. The method is based on known in reactor temperature development and is suitable for processes with changing quality of input substances. This method allows us to evaluate the reaction substances composition change and is also capable of the reaction rate constant (parameters of the Arrhenius equation) determination. Method can be used in exothermic batch or semi- batch reactors running processes based on the first order reaction. An example of such process is given here and the problem is shown on its mathematical model with the help of simulations.

Estimation of Effective Moisture Diffusivity in Starchy Materials Following Hydrothermal Treatments

2011 ◽  
Vol 312-315 ◽  
pp. 364-369 ◽  
Author(s):  
Seyed Amir Bahrani ◽  
Catherine Loisel ◽  
Jean Yves Monteau ◽  
Sid Ahmed Rezzoug ◽  
Zoulikha Maache-Rezzoug
Keyword(s):  
Reaction Rate ◽  
Effective Diffusivity ◽  
Moisture Diffusivity ◽  
Reaction Model ◽  
Reaction Rate Constant ◽  
Diffusivity Coefficient ◽  
Maize Starch ◽  
First Order ◽  
Melting Phenomenon ◽  
Treatment Processes

Two hydrothermal treatment processes (DV-HMT and DIC treatment) were investigated on standard maize starch for three processing temperatures; 100, 110 and 120°C. The gravimetric change of starch powder during the treatment was analyzed by a simultaneous water diffusion and starch reaction model. The effective diffusivity coefficient (Deff) and reaction rate constant (k) were estimated by minimizing the error between experimental and analytical results. The values of Deff and k clearly increased with temperature. The degree of starch melting was evaluated for the two treatments using the first-order reaction model as a function of processing time. The results suggest that the absorption process is controlled by water–starch reactivity that induces melting phenomenon of starch crystallites, which progresses when temperature increases. The two hydrothermal treatments considerably differ: DIC being more prone to water absorption as demonstrated by the values of Deff and k.

scholarly journals The alcoholysis of 1,2,2-trimethylpropyl-methylfluorophosphonate

2000 ◽  
Vol 65 (12) ◽  
pp. 857-866
Author(s):  
Mladjen Micevic ◽  
Slobodan Petrovic
Keyword(s):  
Kinetic Data ◽  
Reaction Rate ◽  
Frequency Factor ◽  
Reaction Rate Constant ◽  
Order Reaction ◽  
Activation Entropy ◽  
Second Order Reaction ◽  
Third Order ◽  
First Order ◽  
Kinetics Of

The alcoholysis of 1,2,2-trimethylpropyl-methylfluorophosphonate (soman) was examined with a series of alkoxides and in corresponding alcohols: methanol, ethanol, 1-propanol, 2-propanol, 2-methoxyethanol and 2-ethoxyethanol. Soman reacts with the used alkoxides in a second order reaction, first order in each reactant. The kinetics of the reaction between 1,2,2-trimethylpropyl-methylfluorophosphonate and ethanol in the presence of diethylenetriamine was also examined. A third order reaction rate constant was calculated, first order in each reactant. The activation energy, frequency factor and activation entropy were determined on the basis of the kinetic data.

scholarly journals Sheet-on-belt branched TiO2(B)/rGO powders with enhanced photocatalytic activity

2018 ◽  
Vol 9 ◽  
pp. 1550-1557 ◽  
Author(s):  
Huan Xing ◽  
Wei Wen ◽  
Jin-Ming Wu
Keyword(s):  
Photocatalytic Activity ◽  
Graphene Oxide ◽  
Reduced Graphene Oxide ◽  
Charge Separation ◽  
Reaction Rate ◽  
Uv Light ◽  
Three Dimensional ◽  
Reaction Rate Constant ◽  
Light Illumination ◽  
Reduced Graphene

TiO2(B) is usually adopted to construct phase junctions with anatase TiO2 for applications in photocatalysis to facilitate charge separation; its intrinsic photocatalytic activity, especially when in the form of one- or three-dimensional nanostructures, has been rarely reported. In this study, a sheet-on-belt branched TiO2(B) powder was synthesized with the simultaneous incorporation of reduced graphene oxide (rGO). The monophase, hierarchically nanostructured TiO2(B) exhibited a reaction rate constant 1.7 times that of TiO2(B)/rGO and 2.9 times that of pristine TiO2(B) nanobelts when utilized to assist the photodegradation of phenol in water under UV light illumination. The enhanced photocatalytic activity can be attributed to the significantly increased surface area and enhanced charge separation.

Bisulfite Degrades Aflatoxin: Effect of Temperature and Concentration of Bisulfite

1978 ◽  
Vol 41 (10) ◽  
pp. 774-780 ◽  
Author(s):  
M. P. DOYLE ◽  
E. H. MARTH
Keyword(s):  
Rate Constant ◽  
Aflatoxin B1 ◽  
Reaction Rate ◽  
Reaction Rates ◽  
Reaction Rate Constant ◽  
Effect Of Temperature ◽  
Kcal Mole ◽  
First Order ◽  
Potassium Acid Phthalate ◽  
Acid Phthalate

Bisulfite reacted with aflatoxin B1 and G1 resulting in their loss of fluorescence. The reaction was first order with rate depending on bisulfite (or the bisulfite and sulfite) concentration(s). Aflatoxin G1 reacted more rapidly with bisulfite than did aflatoxin B1. In the presence of 0.035 M potassium acid phthalate-NaOH buffer (pH 5.5) plus 1.3% (vol/vol) methanol at 25 C, the reaction rate constant for degradation of aflatoxin G1 was 2.23 × 10−2h− and that for aflatoxin B1 was 1.87 × 10−2h− when 50 ml of reaction mixture contained 1.60 g of K2SO3. Besides bisulfite concentrations, temperature influenced reaction rates. The Q10 for the bisulfite-aflatoxin reaction was approximately 2 while activation energies for degrading aflatoxin B1 and aflatoxin G1 were 13.1 and 12.6 kcal/mole, respectively. Data suggest that treating foods with 50 to 500 ppm SO2 probably would not effectively degrade appreciable amounts of aflatoxin. Treating foods with 2000 ppm SO2 or more and increasing the temperature might reduce aflatoxin to an acceptable level.

scholarly journals Effects of HRT on the efficiency of denitrification and carbon source release in constructed wetland filled with bark

2017 ◽  
Vol 75 (12) ◽  
pp. 2908-2915 ◽  
Author(s):  
Yinghe Jiang ◽  
Yao Li ◽  
Ying Zhang ◽  
Xiangling Zhang
Keyword(s):  
Carbon Source ◽  
Removal Efficiency ◽  
Constructed Wetland ◽  
Reaction Rate ◽  
Reaction Rate Constant ◽  
Municipal Sewage ◽  
First Order ◽  
N Removal ◽  
Carbon Release ◽  
The Relationship

Constructed wetland is widely used to treat municipal sewage. However, lack of carbon source always constraints the application of constructed wetland in advanced tailwater treatment process. Bark was used as the filler and external carbon source of constructed wetland in the study, and the effects of hydraulic retention time (HRT) on NO3−−N removal efficiency and carbon release velocity were explored. Results showed that the NO3−−N removal process was steady in the constructed wetland filled with bark without additional carbon source. The NO3−−N removal efficiency and NO3−−N concentration presented a first-order reaction. The reaction rate constant k was 0.4 day−1. The relationship between NO3−−N removal efficiency (η) and HRT (t) was η = 1-e−0.4t, and η was increased with increasing of HRT. η reached a maximum of 77% at HRT of 4.48 days. η obtained the minimum of 20% at HRT of 0.75 days. The relationship between the carbon source releasing velocity (v) by bark and HRT was v = 0.53(1.62/t-1/t2) + 0.32. v increased first and then decreased with HRT increasing. The maximum v was detected at t = 1.12 days.

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