The effects of ultraviolet/H2O2 advanced oxidation on the content and characteristics of groundwater natural organic matter

2014 ◽  
Vol 15 (1) ◽  
pp. 34-41 ◽  
Author(s):  
J. Molnar ◽  
J. Agbaba ◽  
A. Tubić ◽  
M. Watson ◽  
M. Kragulj ◽  
...  

This work investigates the effects of ultraviolet (UV)/H2O2 advanced oxidation on the content and characteristics of natural organic matter (NOM) originating from two different groundwaters (3.03–9.69 mg/L total organic carbon (TOC), 2.71–4.31 Lmg−1m−1 specific ultraviolet absorbance (SUVA)). Application of UV irradiation resulted in a minor reduction in the total content of NOM. Using UV/H2O2 advanced oxidation led to a significant reduction of the aromatic character of NOM (SUVA was reduced by up to 80%) and an increase in the hydrophilic character of the residual NOM, with the optimal UV/H2O2 treatment conditions depending on the water type. In addition, fluctuations in trihalomethane formation potential (THMFP) were observed depending on the UV/H2O2 process conditions, with a maximal reduction of about 40% achieved for both waters.

2009 ◽  
Vol 9 (6) ◽  
pp. 643-651 ◽  
Author(s):  
K. Lekkerkerker ◽  
J. Scheideler ◽  
S. K. Maeng ◽  
A. Ried ◽  
J. Q. J. C. Verberk ◽  
...  

Dunea, the drinking water company for The Hague and surroundings, has as objective the production of drinking water of impeccable quality, particularly with respect to organic micropollutants. As organic micropollutants are only a minor part of the total natural organic matter, a challenge is posed in targeting the removal of a very small, specific part of the DOC, without removing all of the natural organic matter. In addition, organic micropollutants encompass a broad range of physicochemical properties, which make their removal by a single treatment step impossible. Combining AOP with artificial recharge and recovery, two complementary processes are expected to provide a hybrid system for organic micropollutant removal, according to the Dutch multiple barrier approach. Pilot-scale experiments with O3 and different advanced oxidation processes (UV/H2O2, UV/O3 and O3/H2O2) were carried out in cooperation between Dunea and ITT Wedeco. The pilot installation had a capacity of about 0.5–2.0 m3/h, with a varying LP-UV-dose, ozone dose and peroxide dose. Atrazine, isoproturone, carbamazepine, diclofenac and ibuprofen are well removed by UV/H2O2 as well as by O3/H2O2. In general, O3/H2O2 is a more energy efficient process compared to UV/H2O2. MTBE is best removed by O3/H2O2, Amidotrizoic acid and iohexol are best removed by UV/H2O2.


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.


2020 ◽  
Vol 55 (2) ◽  
pp. 155-166
Author(s):  
Mehrnaz Sadrnourmohammadi ◽  
Kenneth Brezinski ◽  
Beata Gorczyca

Abstract The effect of ozonation on the structural and chemical characteristics of natural organic matter (NOM) and its isolated humic fractions, humic acid (HA) and fulvic acid, were studied using Fourier transform infrared coupled to attenuated total reflectance (FTIR-ATR), ultraviolet/visible (UV/Vis) spectroscopy, and synchronous scanning fluorescence (SSF) spectroscopy. The results were linked to the effect of ozonation on trihalomethane formation potential (THMfp) reduction for water standards with high THM precursors. Results showed that ozonation at a dose of 1 mg ozone/mg dissolved organic carbon (DOC) was capable of reducing DOC, UV absorbance at 254 nm (UV254), and THMfp by up to 42%, 95%, and 89% for the HA water standard, respectively. The study of UV/Vis, FTIR-ATR, and SSF revealed trends showing that ozone can alter the composition of DOC in the water standards, causing a significant reduction in aromaticity. The reduction of UV254 for each ozonated sample also affirms that ozone mainly targets aromatic moieties contained in NOM. FTIR-ATR results showed that the reduction of unsaturated functional groups, including aromatic rings and C = C bonds in the water standards tested, were the main components impacted by ozone application. SSF results also revealed that ozonation decreases the fluorescence intensity of the maximum peak – as well as the whole spectra.


2014 ◽  
Vol 15 (1) ◽  
pp. 75-83 ◽  
Author(s):  
J. Agbaba ◽  
J. Molnar ◽  
A. Tubić ◽  
M. Watson ◽  
S. Maletić ◽  
...  

In this study the influence of water matrix and oxidation treatment by ozone on natural organic matter (NOM) fractionation and corresponding disinfection by-products formation was investigated. Three water types were selected, based on their different NOM contents (5.16–9.85 mg/L dissolved organic carbon (DOC)) and structures (42–79% proportion of hydrophobic NOM fraction). It was determined that increasing the ozone dose (0.2–0.8 mg O3/mg DOC) generally led to reductions in DOC (2–26%) and trihalomethane formation potential values (4–58%). Results of NOM fractionation showed that the reactivity of all the individual NOM fractions towards trihalomethane formation decreased after ozone oxidation (0.8 mg O3/mg DOC) by 47–69%, relative to the raw waters.


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