scholarly journals Photocatalytic degradation of the herbicide imazapyr: do the initial degradation rates correlate with the adsorption kinetics and isotherms?

2018 ◽  
Vol 8 (4) ◽  
pp. 985-995 ◽  
Author(s):  
M. Faycal Atitar ◽  
Asmae Bouziani ◽  
Ralf Dillert ◽  
Mohamed El Azzouzi ◽  
Detlef W. Bahnemann

The Langmuir–Hinshelwood mechanism applies to the photocatalytic degradation of imazapyr only when assuming the occurence of light-induced changes of the photocatalyst surface affecting the adsorption of the probe molecule.

Langmuir ◽  
2021 ◽  
Author(s):  
Lídia Kunz Lazzari ◽  
Daniele Perondi ◽  
Ademir José Zattera ◽  
Ruth Marlene Campomanes Santana

Catalysts ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 624
Author(s):  
Sripriya Dharwadkar ◽  
Linlong Yu ◽  
Gopal Achari

Sulfolane is an emerging industrial pollutant detected in the environments near many oil and gas plants in North America. So far, numerous advanced oxidation processes have been investigated to treat sulfolane in aqueous media. However, there is only a few papers that discuss the degradation of sulfolane using photocatalysis. In this study, photocatalytic degradation of sulfolane using titanium dioxide (TiO2) and reduced graphene oxide TiO2 composite (RGO-TiO2) in a light-emitting diode (LED) photoreactor was investigated. The impact of different waters (ultrapure water, tap water, and groundwater) and type of irradiation (UVA-LED and mercury lamp) on photocatalytic degradation of sulfolane were also studied. In addition, a reusability test was conducted for the photocatalyst to examine the degradation of sulfolane in three consecutive cycles with new batches of sulfolane-contaminated water. The results show that LED-based photocatalysis was effective in degrading sulfolane in waters even after three photocatalytic cycles. UVA-LEDs displayed more efficient use of photon energy when compared with the mercury lamps as they have a narrow emission spectrum coinciding with the absorption of TiO2. The combination of UVA-LED and TiO2 yielded better performance than UVA-LED and RGO-TiO2 for the degradation of sulfolane. Much lower sulfolane degradation rates were observed in tap water and groundwater than ultrapure water.


2011 ◽  
Vol 2011 ◽  
pp. 1-5
Author(s):  
Peng Bing ◽  
Wang Jia ◽  
Chai Li-yuan ◽  
Wang Yun-yan ◽  
Mao Ai-li

The photocatalytic degradation rates of methyl orange and antibacterial properties of nano-Ag/TiO2 thin film on ceramics were investigated in this study. XRD was used to detect the structure of film to clarify the impacts on the rates and properties. The effect of film layers, heating temperature, heating time, and embedding of Ag+ on the degradation rates and antibacterial properties were ascertained. The nano-Ag/TiO2 film of 3 layers with AgNO3 3% embedded and treated at 350°C for 2 h would exhibit good performance.


2013 ◽  
Vol 726-731 ◽  
pp. 2829-2832
Author(s):  
Yong Shu Tian ◽  
Run Xin Hou

Photocatalyst of Fe-Sm-Yb modified TiO2 loaded on clay brick was prepared for degradation of NH3-N in coking water. The influence factors of NH3-N degradation rates were discussed by single factor experiment and orthogonal experiment. The optimum process conditions of photocatalytic degradation NH3-N in coking water were confirmed. The results show that NH3-N degradation rates 82.23% were highest in the conditions of pH 6.5, photocatalyst charge of 1.4 g, illumination for 6h, reaction at 55°C, calcination at 500°C.


2013 ◽  
Vol 58 (1-2) ◽  
pp. 273-280 ◽  
Author(s):  
Aylin Atakan ◽  
Gerrit Fueldner ◽  
Gunther Munz ◽  
Stefan Henninger ◽  
Melkon Tatlier

2001 ◽  
Vol 43 (2) ◽  
pp. 313-320 ◽  
Author(s):  
C.-H. Hung ◽  
P.-C. Chiang ◽  
C. Yuan ◽  
C.-Y. Chou

The photocatalysis of azo dye, Orange G, by P-25 anatase TiO2 was investigated in this research. The experiments were conducted in a batch reactor with TiO2 powder suspension. Four near-UV lamps were used as the light source. The experimental variables included solution pH level, amount of TiO2, illumination light intensity, and reaction time. A pseudo-first order reaction kinetic was proposed to simulate the photocatalytic degradation of Orange G in the batch reactor. More than 80% of 10 mg/L Orange G decomposition in 60-minute reaction time was observed in this study and fast decomposition of Orange G only occurred in the presence of both TiO2 and suitable light energy. Faster degradation of Orange G was achieved under acid conditions. The degradation rates of Orange G at pH = 3.0 were about two times faster than those at pH = 7.0. Faster degradation of azo dye was observed for greater irradiated light intensity and more TiO present during the reaction. The reaction rates were proportional to TiO2concentration and light intensity with the power order of 0.726 and 0.734, respectively.


2007 ◽  
Vol 20 (2) ◽  
pp. 163-172 ◽  
Author(s):  
Razika Zouaghi ◽  
Abdennour Zertal ◽  
Bernard David ◽  
Sylvie Guittonneau

Abstract The photocatalytic degradation of two phenylurea herbicides, monolinuron (MLN) and linuron (LN), was investigated in an aqueous suspension of TiO2 using simulated solar irradiation. The objective of the study was to compare their photocatalytic reactivity and to assess the influence of various parameters such as initial pesticide concentration, catalyst concentration and photonic flux on the photocatalytic degradation rate of MLN and LN. A comparative study of the photocatalytic degradation kinetics of both herbicides showed that these two compounds have a comparable reactivity with TiO2/simulated sun light. Under the operating conditions of this study, the photocatalytic degradation of MLN and LN followed pseudo first-order decay kinetics. The kobs values indicated an inverse dependence on the initial herbicide concentration and were fitted to the Langmuir-Hinshelwood equation. Photocatalytic degradation rates increased with TiO2 dosage, but overdoses did not necessarily increase the photocatalytic efficiency. The degradation rate of MLN increased with radiant flux until an optimum at 580 W m‑2 was reached and then decreased. Under these conditions, an electron-hole recombination was favored. Finally, the photocatalytic degradation rate depended on pH, where an optimum was found at a pH value close to the pH of the point of zero charge (pH = 6).


2020 ◽  
Vol 1008 ◽  
pp. 97-103
Author(s):  
Mahmoud Samy ◽  
Mona G. Ibrahim ◽  
Mohamed Gar Alalm ◽  
Manabu Fujii

Methylene blue (MB) is one of the commonly used dyes in the textile industry and can be used as a model pollutant for the textile industry wastewater. In this work, the photocatalytic degradation of MB by synthesized nanoparticles of lanthanum vanadate (LaVO4) was assessed. The effects of pH, initial MB concentration and catalyst dose on the removal performance of MB were investigated and measuring the optimum values of these operational conditions was performed using response surface methodology (RSM). Catalyst dose of 0.43 g/L, initial MB concentration of 5.0 mg/L, and pH of 6.86 were found to be the optimum conditions in reaction time of 60 min. A mathematical model was formed to relate the removal efficiency of MB to the aforementioned operating parameters. The removal efficiency of MB was 91% without any scavengers at a catalyst dose of 0.3 g/L, pH of 7 and initial MB concentration of 10 mg/L. The trapping experiments confirmed the participation of different reactive species in the photo-degradation process. The degradation rates of MB were 91%, 86%, 81%, 77.70% and 72% in five successive runs using LaVO4.


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