scholarly journals Application of Heterogeneous Catalytic Ozonation for Refractory Organics in Wastewater

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.

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.


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

2021 ◽  
Vol 2021 ◽  
pp. 1-18
Author(s):  
Eid H. Alosaimi ◽  
Nadia Azeem ◽  
Noor Tahir ◽  
Asim Jilani ◽  
Muhammad Zahid ◽  
...  

The rapid population growth and economic development have largely contributed to environmental pollution. Various advanced oxidation processes have been used as the most viable solution for the reduction of recalcitrant pollutants and wastewater treatment. Heterogeneous photocatalysis is one of the broadly used technologies for wastewater treatment among all advanced oxidation processes. Graphitic carbon nitride alone or in combination with various other semiconductor metal oxide materials acts as a competent visible light active photocatalyst for the removal of recalcitrant organic pollutants from wastewater. Rational designing of an environment-friendly photocatalyst through a facile synthetic approach encounters various challenges in photocatalytic technologies dealing with semiconductor metal oxides. Doping in g-C3N4 and subsequent coupling with metal oxides have shown remarkable enhancement in the photodegradation activity of g-C3N4-based nanocomposites owing to the modulation in g-C3N4 bandgap structuring and surface area. In the current study, a novel ternary Fe-doped g-C3N4/Ag2WO4 visible light active photocatalyst was fabricated through an ultrasonic-assisted facile hydrothermal method. Characterization analysis included SEM analysis, FTIR, XRD, XPS, and UV-Visible techniques to elucidate the morphology and chemical structuring of the as-prepared heterostructure. The bandgap energies were assessed using the Tauc plot. The ternary nanocomposite (Fe-CN-AW) showed increased photodegradation efficiency (97%) within 120 minutes, at optimal conditions of pH = 8, catalyst dose = 50 mg/100 ml, an initial RhB concentration of 10 ppm, and oxidant dose 5 mM under sunlight irradiation. The enhanced photodegradation of rhodamine B dye by ternary Fe-CN-AW was credited to multielectron transfer pathways due to insertion of a Fe dopant in graphitic carbon nitride and subsequent coupling with silver tungstate. The data were statistically assessed by the response surface methodology.


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.


2019 ◽  
Vol 125 ◽  
pp. 03003
Author(s):  
Elin Marlina ◽  
Purwanto

Electro-Fenton is part of electrochemical advanced oxidation processes (EAOPs) which have been widely used to treat various types of waste such as color, drugs, phenol compounds, leachate, surfactants, and others. This article focuses on the effects of various operating parameters and recent developments in the electro-Fenton process, and then their optimum ranges for maximum pollutant removal and various pollutants removed by this process is observed.


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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