scholarly journals Photocatalytic Degradation of Organic Dyes by H4SiW6Mo6O40/SiO2Sensitized by H2O2

2013 ◽  
Vol 2013 ◽  
pp. 1-7 ◽  
Author(s):  
Li Yu ◽  
Yongkui Huang ◽  
Yun Yang ◽  
Yulin Xu ◽  
Guohong Wang ◽  
...  
Keyword(s):  
Degradation Rate ◽  
Organic Dyes ◽  
Irradiation Time ◽  
Order Kinetic ◽  
Optimal Conditions ◽  
Basic Fuchsin ◽  
First Order ◽  
Degradation Of Dyes ◽  
Order Kinetic Model ◽  
Catalyst Dosage

H4SiW6Mo6O40/SiO2was sensitized by H2O2solution that significantly improved its catalytic activity under simulated natural light. Degradation of basic fuchsin was used as a probe reaction to explore the influencing factors on the photodegradation reaction. The results showed that the optimal conditions were as follows: initial concentration of basic fuchsin 8 mg/L, pH 2.5, catalyst dosage 4 g/L, and light irradiation time 4 h. Under these conditions, the degradation rate of basic fuchsin is 98%. The reaction of photocatalysis for basic fuchsin can be expressed as the first-order kinetic model. After being used continuously for four times, the catalyst kept the inherent photocatalytic activity for degradation of dyes. The photodegradation of malachite green, methyl orange, methylene blue, and rhodamine B were also tested, and the degradation rate of dyes can reach 90%–98%.

scholarly journals Photocatalytic Degradation of Methyl Violet with TiSiW12O40/TiO2

2013 ◽  
Vol 2013 ◽  
pp. 1-5 ◽  
Author(s):  
Shuijin Yang ◽  
Yulin Xu ◽  
Yongkui Huang ◽  
Guohui Zhou ◽  
Zhiyuan Yang ◽  
...  
Keyword(s):  
Photocatalytic Degradation ◽  
Degradation Rate ◽  
Methyl Violet ◽  
Light Irradiation ◽  
Natural Light ◽  
Order Kinetic ◽  
Solution Ph ◽  
Visible Spectra ◽  
Order Kinetic Model ◽  
Catalyst Dosage

The photocatalytic degradation of methyl violet using TiSiW12O40/TiO2as a novel eco-friendly catalyst under simulated natural light irradiation was investigated. The physical characterizations were carried out by TG/DTA, FT-IR, XRD, and UV-visible spectra. The effects of the initial methyl violet concentration, the solution pH, and catalyst dosage on the photocatalytic degradation rate of methyl violet were also examined. The results demonstrated that at optimal condition (initial concentration of methyl violet is 20 mg/L, catalyst dosage is 0.3 g, and the pH is 5.5), the degradation rate of methyl violet is as high as 82.4% after 3 h under simulated natural light irradiation. The reaction of photocatalysis for methyl violet can be expressed as first-order kinetic model.

Photocatalytic Degradation of Methyl Violet with H3PW6Mo6O40/SiO2 Sensitized by H2O2

2013 ◽  
Vol 709 ◽  
pp. 70-73
Author(s):  
Guo Bin Duan ◽  
Yong Kui Huang ◽  
Li Yu ◽  
Shui Jin Yang
Keyword(s):  
Photocatalytic Degradation ◽  
Degradation Rate ◽  
Sol Gel ◽  
Methyl Violet ◽  
Light Irradiation ◽  
Natural Light ◽  
Order Kinetic ◽  
Initial Concentration ◽  
First Order ◽  
Order Kinetic Model

H3PW6Mo6O40/SiO2 was prepared by sol-gel method, and sensitized by H2O2 solution. The photocatalytic degradation of methyl violet by H3PW6Mo6O40/SiO2 under simulated natural light irradiation was investigated. The results demonstrated that at optimal condition (initial concentration of methyl violet is 10 mg/L, and the pH is 2.5, the dosage of catalyst is 0.5% based on feed stocks), the degradation rate of methyl violet is as high as 88.7 % after 2.5h simulated natural light irradiation. The reaction of photocatalysis for methyl violet can be expressed as first-order kinetic model.

scholarly journals A Highly Efficient Ag Nanoparticle-Immobilized Alginate-g-Polyacrylonitrile Hybrid Photocatalyst for the Degradation of Nitrophenols

Polymers ◽  
2020 ◽  
Vol 12 (12) ◽  
pp. 3049
Author(s):  
Imran Hasan ◽  
Charu Shekhar ◽  
Walaa Alharbi ◽  
Maymonah Abu Khanjer ◽  
Rais Ahmad Khan ◽  
...  
Keyword(s):  
Irradiation Time ◽  
Analytical Techniques ◽  
Order Rate Constant ◽  
Order Kinetic ◽  
Ag Nps ◽  
Reaction Conditions ◽  
First Order ◽  
Order Kinetic Model ◽  
Pseudo First Order

Herein, we report PAN-g-Alg@Ag-based nanocatalysts synthesis via in situ oxidative free-radical polymerization of acrylonitrile (AN) using Alg@Ag nanoparticles (Alg@Ag NPs). Various analytical techniques, including FTIR, XRD, SEM, TEM, UV–Vis, and DSC, were employed to determine bonding interactions and chemical characteristics of the nanocatalyst. The optimized response surface methodology coupled central composite design (RSM–CCD) reaction conditions were a 35-min irradiation time in a 70-mg L−1 2,4-dinitrophenol (DNP) solution at pH of 4.68. Here, DNP degradation was 99.46% at a desirability of 1.00. The pseudo-first-order rate constant (K1) values were 0.047, 0.050, 0.054, 0.056, 0.059, and 0.064 min−1 with associated half-life (t1/2) values of 14.74, 13.86, 12.84, 12.38, 11.74, 10.82, and 10.04 min that corresponded to DNP concentrations of 10, 20, 30, 40, 50, 60, and 70 mg L−1, respectively, in the presence of PAN-g-Alg@Ag (0.03 g). The results indicate that the reaction followed the pseudo-first-order kinetic model with an R2 value of 0.99. The combined absorption properties of PAN and Alg@Ag NPs on copolymerization on the surface contributed more charge density to surface plasmon resonance (SPR) in a way to degrade more and more molecules of DNP together with preventing the recombination of electron and hole pairs within the photocatalytic process.

scholarly journals Removal of Ibuprofen From Synthetic Wastewater Using Photocatalytic Method in the Presence of Feo Photocatalyst Supported on Modified Iranian Clinoptilolite

2021 ◽  
Author(s):  
Majid Mohadesi ◽  
Ashkan Gouran ◽  
Kiarash Seifi
Keyword(s):  
Iron Oxide ◽  
Synthetic Wastewater ◽  
Process Time ◽  
Order Kinetic ◽  
Optimal Conditions ◽  
Initial Concentration ◽  
First Order ◽  
Order Kinetic Model ◽  
Ft Ir ◽  
Good Agreement

Abstract This study investigated the removal of an organic drug called ibuprofen from the wastewater containing this drug. Iron oxide supported on modified Iranian clinoptilolite was used as the photocatalyst in the presence of the light of a solar lamp. XRD, SEM, EDAX and FT-IR analyses were performed to detect the prepared photocatalyst. The results of photocatalytic identification analyses proved the suitable loading of iron oxide supported on modified Iranian clinoptilolite. This study investigated the effect of initial concentration of ibuprofen (5–25 mg/L), photocatalyst concentration (100–300 mg/L), and process time (10–240 min) on the removal from ibuprofen from wastewater containing this drug. The experiments were performed in a setup in the presence of a solar lamp with a flux of 300 W/m2. The results indicated that with the initial ibuprofen concentration of 25 mg/L, photocatalyst concentration of 300 mg/L, and time of 210 min, the highest percentage of ibuprofen removal was 99.80%. Kinetic modeling was then performed using the Langmuir-Hinshelwood model, and a quasi-first-order kinetic model showed a good agreement with the results obtained. Finally, the recovery of the photocatalyst was investigated and the results showed that under optimal conditions about 91% of ibuprofen was removed after five re-uses of the photocatalyst.

scholarly journals Paracetamol degradation by photo-activated peroxydisulfate process (UV/PDS): kinetic study and optimization using central composite design

2020 ◽  
Vol 82 (7) ◽  
pp. 1404-1415 ◽  
Author(s):  
Karima Dibene ◽  
Idris Yahiaoui ◽  
Lamia Yahia Cherif ◽  
Salima Aitali ◽  
Abdeltif Amrane ◽  
...  
Keyword(s):  
Reaction Time ◽  
Central Composite Design ◽  
Degradation Rate ◽  
Degradation Efficiency ◽  
Order Kinetic ◽  
Optimal Conditions ◽  
Order Kinetic Model ◽  
Pseudo Second Order ◽  
Central Composite ◽  
Optimal Ph

Abstract In this study, peroxydisulfate (PDS) was successfully activated by UV-irradiation for the degradation of paracetamol (PCT) frequently detected in the environment. Results showed that increasing the initial PDS concentration from 5 to 20 mM promote the removal of PCT from 49.3% to 97.5% after 240 min of reaction time. As the initial PCT concentration increased from 0.066 to 0.132 mM, the degradation efficiency of PCT decreased from 98% to 73% after 240 min of reaction time, while the optimal pH was found to be 6. It is apparent that the degradation rate of PCT was favored by the lamp power regardless of the initial PCT concentration, for 0.132 mM of PCT, the degradation efficiency increased from 73% to 95% when the lamp power increased from 9 to 30 W, respectively. The kinetic of degradation of the PCT was described by a pseudo-second order kinetic model. The model obtained by central composite design led to the following optimal conditions for PCT degradation: 0.132 mM initial PCT concentration, 20 mM PDS dose, pH solution 6 and lamp power 30 W led to the removal of 92% of PCT at 25 °C within 240 min of reaction time.

scholarly journals Photocatalytic Degradation of Rhodamine B with H3PW12O40/SiO2Sensitized by H2O2

2012 ◽  
Vol 2012 ◽  
pp. 1-6 ◽  
Author(s):  
Shuijin Yang ◽  
Yongkui Huang ◽  
Yunzhi Wang ◽  
Yun Yang ◽  
Mingbo Xu ◽  
...  
Keyword(s):  
Photocatalytic Degradation ◽  
Rhodamine B ◽  
Degradation Rate ◽  
Sol Gel ◽  
Light Irradiation ◽  
Natural Light ◽  
Order Kinetic ◽  
Solution Ph ◽  
Order Kinetic Model ◽  
Catalyst Dosage

In order to remove aquatic organic dye contaminants by utilizing the inexpensive and inexhaustible solar energy, the Keggin-type H3PW12O40was loaded on the surface of SiO2with the sol-gel method and sensitized by H2O2solution. The photocatalytic degradation of rhodamine B (RhB) by H3PW12O40/SiO2(x) under simulated natural light irradiation was investigated. The effects of the initial RhB concentration, the solution pH, and catalyst dosage on the photocatalytic degradation rate of RhB were also studied. The results demonstrated that at optimal condition (initial concentration of methyl orange is 10 mg/L, catalyst dosage is 0.8 g, and the pH is 2.5) the degradation rate of RhB is as high as 97.7% after 2 h under simulated natural light irradiation. The reaction of photocatalysis for RhB can be expressed as a first-order kinetic model.

Kinetics of bioactive compounds in functional spice Jiangpo during thermal processing

2012 ◽  
Vol 8 (3) ◽  
Author(s):  
Xiaoyan Dai ◽  
Chenhuan Yu ◽  
Qiaofeng Wu
Keyword(s):  
Kinetic Parameters ◽  
Bioactive Compounds ◽  
Thermal Processing ◽  
Order Rate Constant ◽  
Heat Processing ◽  
Order Kinetic ◽  
Time Intervals ◽  
First Order ◽  
Order Kinetic Model ◽  
Kinetics Of

Abstract Jiangpo is an increasingly popular East Asian spice which is made from Mangnolia officinalis bark and ginger juice. Since it induces bioactive compounds decomposition and has influence on final flavor and fragrance, cooking is regarded as the key operation in preparation of Jiangpo. To evaluate the bioactive compounds content changes of Jiangpo during thermal processing, kinetic parameters including reaction order, rate constant, T1/2 and activation energy of bioactive markers namely honokiol, magnolol and curcumin were determined. Cooking was set at temperatures 60, 90 and 120 °C for selected time intervals. Results displayed the thermal kinetic characteristics of the three compounds. Thermal degradation of Honokiol and magnolol both followed first order kinetic model and the loss of curcumin fitted second order. A mathematical model based on the obtained kinetic parameters has also been developed to predict the degradation of honokiol, magnolol and curcumin in non-isothermal state. All the information in this paper could contribute necessary information for optimizing the existing heat processing of Jiangpo.

scholarly journals Municipal Leachate Treatment by Fenton Process: Effect of Some Variable and Kinetics

2013 ◽  
Vol 2013 ◽  
pp. 1-6 ◽  
Author(s):  
Mohammad Ahmadian ◽  
Sohyla Reshadat ◽  
Nader Yousefi ◽  
Seyed Hamed Mirhossieni ◽  
Mohammad Reza Zare ◽  
...  
Keyword(s):  
Reaction Time ◽  
Color Removal ◽  
Molar Ratio ◽  
Order Kinetic ◽  
Fenton Process ◽  
Solution Ph ◽  
Leachate Treatment ◽  
First Order ◽  
Order Kinetic Model ◽  
Better Than

Due to complex composition of leachate, the comprehensive leachate treatment methods have been not demonstrated. Moreover, the improper management of leachate can lead to many environmental problems. The aim of this study was application of Fenton process for decreasing the major pollutants of landfill leachate on Kermanshah city. The leachate was collected from Kermanshah landfill site and treated by Fenton process. The effect of various parameters including solution pH, Fe2+and H2O2dosage, Fe2+/H2O2molar ratio, and reaction time was investigated. The result showed that with increasing Fe2+and H2O2dosage, Fe2+/H2O2molar ratio, and reaction time, the COD, TOC, TSS, and color removal increased. The maximum COD, TOC, TSS, and color removal were obtained at low pH (pH: 3). The kinetic data were analyzed in term of zero-order, first-order, and second-order expressions. First-order kinetic model described the removal of COD, TOC, TSS, and color from leachate better than two other kinetic models. In spite of extremely difficulty of leachate treatment, the previous results seem rather encouraging on the application of Fenton’s oxidation.

Performance of poly-o-phenylenediamine and its carbon dot composite electrode in the removal of Cu2+ from its aqueous solution

2021 ◽  
pp. 2151037
Author(s):  
Yu Meng ◽  
Qing Zhong ◽  
Arzugul Muslim
Keyword(s):  
Aqueous Solution ◽  
Electrochemical Reduction ◽  
Composite Electrode ◽  
Reduction Process ◽  
Order Kinetic ◽  
Carbon Dot ◽  
First Order ◽  
Oxidation Reduction ◽  
Order Kinetic Model ◽  
Optimal Ph

Because −NH2 and −NH− in poly-[Formula: see text]-phenylenediamine (P[Formula: see text]PD) can interact strongly with the empty orbitals of Cu to show unique electrochemical activity, P[Formula: see text]PD is suitable for the removal of Cu[Formula: see text] by electrochemical oxidation–reduction process. In this study, with P[Formula: see text]PD and its carbon dot composite (CDs/P[Formula: see text]PD) as working electrodes, the electrochemical reduction and removal of Cu[Formula: see text] in the aqueous solution were carried out with the potentiostatic method. According to effects of voltage, pH of the solution, initial concentration of Cu[Formula: see text], and electrochemical reduction time on the Cu[Formula: see text] removal, the Cu[Formula: see text] removal ratios of P[Formula: see text]PD and CDs/P[Formula: see text]PD were up to 64.69% and 73.34%, respectively, at −0.2 V and the optimal pH. Additionally, results showed that these processes were in line with the quasi-first order kinetic model. Both P[Formula: see text]PD and CDs/P[Formula: see text]PD showed good reproducibility in six cycles. After five times of repeated usage, the regeneration efficiencies of P[Formula: see text]PD and CDs/P[Formula: see text]PD dropped to 77.04% and 79.36%, respectively.

scholarly journals Enhanced photocatalytic activity of wool-ball-like TiO2 microspheres on carbon fabric and FTO substrates

2018 ◽  
Vol 38 ◽  
pp. 02014
Author(s):  
Yu Zhang ◽  
Jian Gu ◽  
Mengqi Zhang
Keyword(s):  
Hydrothermal Method ◽  
Order Kinetic ◽  
Carbon Fabric ◽  
Facile Hydrothermal Method ◽  
Sem Images ◽  
First Order ◽  
Good Crystallinity ◽  
Degradation Rate Constant ◽  
Order Kinetic Model ◽  
Pseudo First Order

The wool-ball-like TiO2 microspheres on carbon fabric (TiO2-CF) and FTO substrates (TiO2-FTO) have been synthesized by a facile hydrothermal method in alkali environment, using commercial TiO2 (P25) as precursors. The XRD results indicate that the as-prepared TiO2 have good crystallinity. And the SEM images show that the wool-ball-like TiO2 microspheres with a diameter of 2-3 μm are composed of TiO2 nanowires, which have a diameter of ~50 nm. The photocatalytic behavior of the wool-ball-like TiO2 microspheres, TiO2-CF and TiO2-FTO under ultraviolet light was investigated by a pseudo first-order kinetic model, using methyl orange (MO) as pollutant. The wool-ball-like TiO2 microspheres obtained a degradation rate constant (Kap) of 6.91×10-3 min-1 . The Kap values of TiO2-FTO and TiO2-CF reach 13.97×10-3 min-1 and 11.80×10-3 min-1, which are 2.0 and 1.7 times higher than that of pristine wool-ball-like TiO2 microspheres due to the “sum effect” between TiO2 and substrates. This study offers a facile hydrothermal method to prepare wool-ball-like TiO2 microspheres on CF and FTO substrates, which will improve the recyclability of phtocatalysts and can be extended to other fields.

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