scholarly journals Advances in Treatment of Brominated Hydrocarbons by Heterogeneous Catalytic Ozonation and Bromate Minimization

Molecules ◽  
2019 ◽  
Vol 24 (19) ◽  
pp. 3450
Author(s):  
Asogan N. Gounden ◽  
Sreekantha B. Jonnalagadda

The formation of carcinogenic bromate ions is a constraint when ozone is used for the remediation of water containing brominated organic materials. With its strong oxidizing ability, ozone rapidly transforms bromide in aqueous media to bromate, through a series of reactions involving hydroxyl radicals. Several strategies, such as limiting the ozone concentration, maintaining pH < 6, or the use of ammonia or hydrogen peroxide were explored to minimize bromate generation. However, most of the above strategies had a negative effect on the ozonation efficiency. The advanced oxidation processes, using catalysts together with ozone, have proven to be a promising technology for the degradation of pollutants in wastewater, but very few studies have been conducted to find ways to minimize bromate formation during this approach. The proposed article, therefore, presents a comprehensive review on recent advances in bromate reduction in water by catalytic ozonation and proposes reaction mechanisms associated with the catalytic process. The main aim is to highlight any gaps in the reported studies, thus creating a platform for future research and a quest to find environment friendly and efficacious catalysts for minimizing bromate formation in aqueous media during ozonation of brominated organic compounds.

Catalysts ◽  
2019 ◽  
Vol 9 (3) ◽  
pp. 241 ◽  
Author(s):  
Bing Wang ◽  
Huan Zhang ◽  
Feifei Wang ◽  
Xingaoyuan Xiong ◽  
Kun Tian ◽  
...  

Catalytic ozonation is believed to belong to advanced oxidation processes (AOPs). Over the past decades, heterogeneous catalytic ozonation has received remarkable attention as an effective process for the degradation of refractory organics in wastewater, which can overcome some disadvantages of ozonation alone. Metal oxides, metals, and metal oxides supported on oxides, minerals modified with metals, and carbon materials are widely used as catalysts in heterogeneous catalytic ozonation processes due to their excellent catalytic ability. An understanding of the application can provide theoretical support for selecting suitable catalysts aimed at different kinds of wastewater to obtain higher pollutant removal efficiency. Therefore, the main objective of this review article is to provide a summary of the accomplishments concerning catalytic ozonation to point to the major directions for choosing the catalysts in catalytic ozonation in the future.


2015 ◽  
Vol 44 ◽  
pp. 1-9 ◽  
Author(s):  
Manhal Abouzlam ◽  
Régis Ouvrard ◽  
Driss Mehdi ◽  
Florence Pontlevoy ◽  
Bertrand Gombert ◽  
...  

2019 ◽  
Vol 9 (13) ◽  
pp. 2652 ◽  
Author(s):  
Jéssica Martini ◽  
Carla A. Orge ◽  
Joaquim L. Faria ◽  
M. Fernando R. Pereira ◽  
O. Salomé G. P. Soares

The degradation of sulfamethoxazole (SMX) by several advanced oxidation processes (AOPs) is carried out in the presence of different catalysts. The catalysts used consisted of carbon nanotubes (CNT), titanium dioxide (TiO2), a composite of carbon nanotubes and titanium dioxide (TiO2/CNT), and iron supported on carbon nanotubes (Fe/CNT). SMX removal was evaluated by catalytic ozonation, photocatalysis, catalytic oxidation with hydrogen peroxide, and combinations of these processes. The evolution of the SMX concentration during reaction time, the mineralization degree, the toxicity of the treated solution, and the formation of organic intermediates and ions were monitored. Ozonation catalyzed by Fe/CNT and CNT and photocatalytic ozonation in the presence of CNT presented the fastest degradation of SMX, whereas photocatalytic ozonation with CNT showed the best results in terms of organic matter removal (92% of total organic carbon (TOC) depletion). Total mineralization of the solution and almost complete reduction of toxicity was only achieved in the photocatalytic ozonation with H2O2 and Fe/CNT catalysts. The compound 3-amino-5-methylisoxazole was one of the first intermediates formed during SMX degradation. p-Benzoquinone was only formed in photocatalysis. Oxalic and oxamic acids were also detected and in most of the catalytic processes they appeared in small amounts. Ion concentrations increased with the reaction time.


2021 ◽  
Author(s):  
Ali Kamel H. Al jibouri

Industrial wastewater is one of the largest environmental challenges of this century. Most of these wastewaters contain non-biodegradable pollutants which need special treatment methods. Advanced oxidation processes (AOP’s), such as, ozonation, catalytic ozonation and ozone/ hydrogen peroxide have proved their effectiveness on the degradation of bio-recalcitrant pollutants. The main drawback in these processes is the high operating cost. The objective of this study was to develop innovative continuous ozonation and ozone based processes that can effectively degrade industrial non-biodegradable pollutants. Naphthenic acids (NAs) was used as the model pollutant in this study due to its importance as a major pollutant in oil and oil sands industries. The target was to convert bio-recalcitrant NAs into biodegradable substances with minimum consumption of ozone gas (operating cost). These processes can be followed by the biodegradation process to fully remove the rest of the pollutants. This research passed through several stages including screening of operating parameters, kinetic studies, and modeling, followed by optimal control of these processes. It was found that ozone concentration had the most significant effect on the NAs degradation compared to other parameters. The kinetics of direct and indirect (radical) ozonation of NAs were investigated and rate constants and activation energies of these reactions were determined. Catalytic ozonation of NAs was explored using alumina supported metal oxides and unsupported catalysts. Activated carbon was found to be the most effective catalyst. The addition of hydrogen peroxide into the ozonation systems significantly improved the removal of NAs compared with the ozonation only process. Models based on mass balance for the ozonation and ozone/ hydrogen peroxide processes were developed to predict the concentration profiles of reacting species. Optimal control policies of ozone/oxygen gas flow rate versus time were developed and validated to minimize NAs concentration in the liquid outlet stream from the continuous ozonation and ozone/ hydrogen peroxide processes. The experimental results demonstrated that the optimal control policies successfully minimized NAs concentration in the outlet stream. At the same time, ozone gas consumption was reduced to its minimum, i.e., just enough to minimize the concentration of NAs in the outlet stream.


2021 ◽  
Vol 8 (4) ◽  
pp. 20218407
Author(s):  
Sofia M. Tikhanova ◽  
Lev A. Lebedev ◽  
Svetlana A. Kirillova ◽  
Maria V. Tomkovich ◽  
Vadim I. Popkov

Photo-Fenton-like oxidation of organic substances is one of the key advanced oxidation processes based on the reversible Fe2+↔Fe3+ transition and the generation of a strong oxidant ·OH in the presence of H2O2 and is currently considered as a promising method for the purification of polluted aqueous media. However, the absence of effective and stable photocatalysts of this process, operating under the action of visible light, necessitates the exploratory studies, mainly among iron oxides and ferrites of various compositions and structures. In this work, using the method of solution combustion followed by heat treatment in air the heterojunction nanocomposites based on ytterbium orthoferrite and cerium dioxide of the composition o-YbFeO3/h-YbFeO3/CeO2 (0–20 mol.%) with high absorption in the visible region and advanced photo-Fenton-like activity were obtained. The nanocomposites were studied by EDS, SEM, XRD, BET, and DRS methods. The photo-Fenton-like activity of the nanocomposites was investigated during the degradation of methyl violet under the action of visible (λmax = 410 nm) radiation. As a result, the formation of I-type heterojunction based on stable rhombic (55.4–79.0 nm) and metastable hexagonal (19.5–24.0 nm) modifications of ytterbium orthoferrite (o-YbFeO3 and h-YbFeO3, respectively) and cubic cerium dioxide CeO2 (13.2–19.2 nm) nanocrystals was established. It was shown that the obtained nanocomposites had foamy morphology and were characterized by a specific surface in the range of 9.1–25.0 m2/g, depending on the CeO2 content. It was found that nanocrystalline components were chemically and phase-pure, uniformly spatially distributed over the nanocomposite, and had multiple contacts with each other. Based on this fact and the established electronic structure of the nanocomposite components, the formation of I-type heterojunction with the participation of o-YbFeO3 (Eg = 2.15 eV), h-YbFeO3 (Eg = 2.08 eV), and CeO2 (Eg = 2.38 eV) was shown, the presence of which increased photocatalytic activity of the resulting nanocomposite. The optimal content of CeO2 in the nanocomposite was 5%, and the o-YbFeO3/h-YbFeO3/CeO2–5% sample was characterized by the highest rate constant of photo-Fenton-like degradation of methyl violet under the action of visible light equal to k = 0.138 min–1, which was 2.5 to 5 times higher than for nanocomposites based on ytterbium orthoferrite. The obtained results obtained indicate that the developed nanocomposites can be considered as a promising basis for the advanced oxidation processes for the purification of aqueous media from organic pollutants.


Author(s):  
Alysson S. Martins ◽  
Vanessa M. Vasconcelos ◽  
Tanare C. R. Ferreira ◽  
Edenir R. Pereira-Filho ◽  
Marcos R. V. Lanza

AbstractPesticides are often reported in aquatic environments contamination as being a result of soil leaching and improper disposal of agricultural packages. Advanced oxidation processes have been studied as alternatives to treat such compounds in aqueous media. The aim of this study was to determine the best concentrations of H


Author(s):  
Alex Leandro Lucena ◽  
Rayany Magali da Rocha Santana ◽  
Marcos André Oliveira ◽  
Luciano Costa Almeida ◽  
Marta Maria Bezerra Duarte Duarte ◽  
...  

The presence of pharmaceutical contaminants in nature is an environmental problem generating increasing concerns. Due to this, it is necessary to evaluate treatments that are capable of degrading these contaminants, such as the advanced oxidation processes (AOP). In this work, the photoperoxidation and photo-Fenton AOP were applied to degrade a mixture of the drugs lamivudine and zidovudine, in aqueous medium and synthetic effluent (SE). To this end, a bench reactor (UV-C; UV-A and sunlight irradiations) was built. The AOP treatments efficiency was evaluated by ultraviolet/visible spectrophotometry. The tests involved the application of the irradiations individually and combined. The best operational conditions were [H2O2] of 600 mg.L-1 and [Fe] of 0.5 mg.L-1, for both matrices, with degradations of 90.53% and 89.32% for the photoperoxidation and photo-Fenton processes in aqueous media and 88.69% and 85.79% in SE. Kinetic studies showed a good fit for two pseudo-first order models with R2 > 0.93. Toxicity tests involving the application of lettuce, carrot, and tomato seeds showed an inhibition for the three seeds when submitted to solutions after treatment, for both matrices, this fact is corroborated by the HPLC analysis, in which the formation of small peaks was verified, suggestive of the formation of by-products. Thus, it can be affirmed that both photo-Fenton and photoperoxidation processes are efficient to degrade the drug mixture when applying UV-C radiation.


2021 ◽  
Author(s):  
Ali Kamel H. Al jibouri

Industrial wastewater is one of the largest environmental challenges of this century. Most of these wastewaters contain non-biodegradable pollutants which need special treatment methods. Advanced oxidation processes (AOP’s), such as, ozonation, catalytic ozonation and ozone/ hydrogen peroxide have proved their effectiveness on the degradation of bio-recalcitrant pollutants. The main drawback in these processes is the high operating cost. The objective of this study was to develop innovative continuous ozonation and ozone based processes that can effectively degrade industrial non-biodegradable pollutants. Naphthenic acids (NAs) was used as the model pollutant in this study due to its importance as a major pollutant in oil and oil sands industries. The target was to convert bio-recalcitrant NAs into biodegradable substances with minimum consumption of ozone gas (operating cost). These processes can be followed by the biodegradation process to fully remove the rest of the pollutants. This research passed through several stages including screening of operating parameters, kinetic studies, and modeling, followed by optimal control of these processes. It was found that ozone concentration had the most significant effect on the NAs degradation compared to other parameters. The kinetics of direct and indirect (radical) ozonation of NAs were investigated and rate constants and activation energies of these reactions were determined. Catalytic ozonation of NAs was explored using alumina supported metal oxides and unsupported catalysts. Activated carbon was found to be the most effective catalyst. The addition of hydrogen peroxide into the ozonation systems significantly improved the removal of NAs compared with the ozonation only process. Models based on mass balance for the ozonation and ozone/ hydrogen peroxide processes were developed to predict the concentration profiles of reacting species. Optimal control policies of ozone/oxygen gas flow rate versus time were developed and validated to minimize NAs concentration in the liquid outlet stream from the continuous ozonation and ozone/ hydrogen peroxide processes. The experimental results demonstrated that the optimal control policies successfully minimized NAs concentration in the outlet stream. At the same time, ozone gas consumption was reduced to its minimum, i.e., just enough to minimize the concentration of NAs in the outlet stream.


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