Oxidation of natural organic matter with processes involving O3, H2O2and UV light: formation of oxidation and disinfection by-products

RSC Advances ◽  
2016 ◽  
Vol 6 (89) ◽  
pp. 86212-86219 ◽  
Author(s):  
Jasmina Agbaba ◽  
Jelena Molnar Jazić ◽  
Aleksandra Tubić ◽  
Malcolm Watson ◽  
Snežana Maletić ◽  
...  

This study investigates the effects of UV photolysis, ozonation and different advanced oxidation processes (O3/UV, H2O2/UV and O3/H2O2/UV) on the oxidation of groundwater natural organic matter (NOM) and by-product formation.

2004 ◽  
Vol 4 (4) ◽  
pp. 113-119 ◽  
Author(s):  
C.A. Murray ◽  
S.A. Parsons

Advanced oxidation processes have been reported to have the potential to remove natural organic matter from source waters. Of these Fenton's reagent, photo-Fenton's reagent and titanium dioxide photocatalysis are the three most promising processes. Compared to conventional coagulation/flocculation processes they have higher removal efficiencies in terms of both dissolved organic carbon and UV254 absorbance. Under optimum reaction conditions all three remove over 80% dissolved organic carbon and 0% UV254 absorbance. In addition the enhanced removal of natural organic matter leads to a corresponding reduction in the formation of disinfection by-products following chlorination of the treated water. Advanced oxidation processes give enhanced removal of organic species ranging from low to high molecular weight while coagulation/flocculation is inefficient at removing low molecular weight species. One additional benefit is all three processes produce less residuals compared to conventional coagulation, which is advantageous as the disposal of such residuals normally contributes a large proportion of the costs at water treatment works.


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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