scholarly journals Identification of Degradation By-Products of Selected Pesticides During Oxidation and Chlorination Processes

2019 ◽  
Vol 26 (3) ◽  
pp. 571-581 ◽  
Author(s):  
Edyta Kudlek

Abstract Advanced oxidation processes (AOPs) are considered to be one of the most effective methods for the decomposition of a wide range of hardly-biodegradable organic compounds, including pesticides. The implementation of such processes in the water streams treatment often leads to the formation of decomposition by-products of micropollutants occurring in water. These compounds, even in concentrations of a few ng/dm3, may negatively affect the water quality. Therefore, there is a need for detailed analyses that will allow to identify intermediates found in the AOP solutions and to assess their impact on the aquatic environment. The paper presents an attempt to identify by-products of three pesticides: triclosan, triallat and oxadiazon during ozonation, chlorination and UV irradiation of their water solutions. The identification of compounds was performed based on the results of the GC-MS analysis using the NIST v17 mass spectral library. It has been shown that during all of tested advanced oxidation processes, incomplete degradation of pesticides occurs. The number of micropollutant decomposition by-products increases with the increase of the applied ozone dose and UV exposure time. During the chlorination process Cl− atoms were added to the tested compound molecules. In the case of triclosan, it led to the generation of compounds containing four or five chlorine atoms in their structure. The toxicological analysis performed by the use of the Microtox® and Lemna sp. Growth Inhibition Test showed the toxic nature of post-process solutions. The decomposition by-products of triclosan and triallate, generated during the UV irradiation process, were highly toxic against the test organisms (toxic effect > 75 %). This makes it impossible to drain these solutions into the natural environment.

2017 ◽  
pp. 147
Author(s):  
Naser Jamshidi ◽  
Farzad Nezhad Bahadori ◽  
Ladan Talebiazar ◽  
Ali Akbar Azimi

Today, advanced oxidation processes (AOPs) is considered as a key and effective method for environment preservation from pollutions. In this study , advanced photochemical oxidation processes using O3/H2O2 and O3/H2O2/UV systems were investigated batch photolytic reactor in lab-scale for the degradation of bisphenol A (BPA). In ozone generator source, air, as of the initial instrument feed, changes to ozone after electrical action and reaction. The UV irradiation source was a medium-pressure mercury lamp 300 W that was immerse in the wastewater solution with in 1.5 liter volume reactor. The reaction was influenced by the pH, the input concentration of H2O2, the input concentration of BPA, ozone dosage, chemical oxidation demand (COD) and UV irradiation time. Results showed that at initial bisphenol A concentration of 100 mg/l will completely degrade after 60 minutes by using O3/H2O2 in the pH range from 9.8 to 10 and by adding UV, it will happen in less than 36 minutes in the pH range of 3 to 10. The O3/H2O2/UV process reduced COD to 75 percents.


Catalysts ◽  
2020 ◽  
Vol 10 (6) ◽  
pp. 612 ◽  
Author(s):  
Juan José Rueda-Márquez ◽  
Irina Levchuk ◽  
Manuel Manzano ◽  
Mika Sillanpää

The application of Fenton-based advanced oxidation processes (AOPs), such as photo-Fenton or electro-Fenton for wastewater treatment have been extensively studied in recent decades due to its high efficiency for the decomposition of persistent organic pollutants. Usually Fenton-based AOPs are used for the degradation of targeted pollutant or group of pollutants, which often leads to the formation of toxic by-products possessing a potential environmental risk. In this work, we have collected and reviewed recent findings regarding the feasibility of Fenton-based AOPs (photo-Fenton, UVC/H2O2, electro-Fenton and galvanic Fenton) for the detoxification of real municipal and industrial wastewaters. More specifically, operational conditions, relevance and suitability of different bioassays for the toxicity assessment of various wastewater types, cost estimation, all of which compose current challenges for the application of these AOPs for real wastewater detoxification are discussed.


Author(s):  
James R. Bolton ◽  
Keith G. Bircher ◽  
William Tumas ◽  
Chadwick A. Tolman

AbstractAdvanced oxidation processes (AOPs), which involve the in-situ generation of highly potent chemical oxidants such as the hydroxyl radical (•OH), have recently emerged as an important class of technologies for accelerating the oxidation and hence destruction of a wide range of organic contaminants in polluted water and air. We propose generally applicable standard figures-of-merit for comparing these waste treatment technologies. These figures-of-merit are based on electrical energy consumption within two phenomenological kinetic order regimes: one for high contaminant concentrations (electrical energy per mass, EE/M) and one for low concentrations (electrical energy per order of magnitude per m


2010 ◽  
Vol 10 (1) ◽  
pp. 51-57 ◽  
Author(s):  
R. Mosteo ◽  
N. Miguel ◽  
P. Ormad Maria ◽  
J. L. Ovelleiro

Any nonylphenol compounds found in water have to be removed since they are endocrine disruptors. In this study, natural water from the river Ebro fortified with nonylphenol compounds (4n-nonylphenol and technical nonylphenol) is used as a sample in order to simulate a real situation in drinking water treatment plants. The aim is to compare conventional disinfection with advanced oxidation processes (O3, O3/H2O2, O3/TiO2 and O3/H2O2/TiO2) used for the removal of nonylphenol compounds present in natural water. Furthermore, a study is carried out of the by-products (THMs) generated as a consequence of the presence of natural organic matter. Preoxidation by chlorine completely oxidizes 4n-nonylphenol and technical nonylphenol. It can be seen that the best of the advanced oxidation processes is the O3/H2O2, achieving an average oxidation of 55%, although the differences among the processes were not very significant. Furthermore, the use of post-chlorination guarantees the total removal of nonylphenol compounds.


2018 ◽  
Vol 19 (5) ◽  
pp. 1388-1395 ◽  
Author(s):  
Jelena Molnar Jazić ◽  
Jasmina Agbaba ◽  
Aleksandra Tubić ◽  
Malcolm Watson ◽  
Tajana Đurkić ◽  
...  

Abstract This study evaluates the effect of photochemical advanced oxidation processes (AOPs) (O3/UV, H2O2/UV and O3/H2O2/UV) on the formation potential (FP) of emerging disinfection by-products including nitrogenous by-products (N-DBPs) and haloketones (HKs) in groundwater from part of the Pannonian Basin (AP Vojvodina, Republic of Serbia). Among the N-DBPs, the haloacetonitrile (HAN) precursor contents were 9.83 ± 0.59 μg/L while precursors of halonitromethanes, particularly trichloronitromethane (TCNM) were not detected. Similarly, precursors of HKs as carbonaceous DBPs were also not detected in raw water. Ozonation alone and the H2O2/UV process with a lower UV dose maximally decomposed HAN precursors (about 70%) while during O3-based AOPs, HANFP varied significantly. Application of UV photolysis and H2O2/UV processes with increasing UV dose doubled the HANFP. Ozone alone, O3/UV and H2O2/UV slightly increased HK formation potential, particularly 1,1-dichloro-2-propanone FP (0.93 ± 0.21 to 2.01 ± 0.37 μg/L). None of the investigated treatments influenced the formation of TCNM precursors. The effect of the applied treatments on bromide incorporation was most evident for HANs.


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