|
|
Kinetics of hydrogen peroxide quenching following UV/H2O2 advanced oxidation by thiosulfate, bisulfite, and chlorine in drinking water treatment |
Tianyi Chen, Lizbeth Taylor-Edmonds, Susan Andrews, Ron Hofmann( ) |
Department of Civil and Mineral Engineering, University of Toronto, Toronto, Ontario M5S 1A4, Canada |
|
|
Abstract ● H2O2 quenching rates by Cl/S-based chemicals were measured ● Chlorine takes seconds-to-minutes to quench H2O2 at common water pH ● The form of chlorine (gas vs . hypochlorite) affects the H2O2 quenching rate ● H2O2 quenching rates by chlorine in different conditions were predicted Residual H2O2 from UV/H2O2 treatment can be quenched by thiosulfate, bisulfite, and chlorine, but the kinetics of these reactions have not been reported under the full range of practical conditions. In this study, the rates of H2O2 quenching by these compounds were compared in different water matrices, temperatures, pH, and when using different forms of bisulfite and chlorine. In general, it was confirmed that thiosulfate would be too slow to serve as a quenching agent in most practical scenarios. At pH 7–8.5, chlorine tends to quench H2O2 more than 20 times faster than bisulfite in the various conditions tested. An important observation was that in lightly-buffered water (e.g., alkalinity of 20 mg/L as CaCO3), the form of chlorine can have a large impact on quenching rate, with gaseous chlorine slowing the reaction due to its lowering of the pH, and hypochlorite having the opposite effect. These impacts will become less significant when water buffer capacity (i.e., alkalinity) increases (e.g., to 80 mg/L as CaCO3). In addition, water temperature should be considered as the time required to quench H2O2 by chlorine at 4 °C is up to 3 times longer than at 20 °C.
|
Keywords
UV/H2O2
H2O2 quenching
Chlorine type
Water alkalinity
Temperature
|
Corresponding Author(s):
Ron Hofmann
|
Issue Date: 17 July 2023
|
|
1 |
L Breytenbach, W van Pareen, J J Pienaar, R van Eldik. (1994). The influence of organic acids and metal ions on the kinetics of the oxidation of sulfur(IV) by hydrogen peroxide. Atmospheric Environment, 28(15): 2451–2459
https://doi.org/10.1016/1352-2310(94)90396-4
|
2 |
A D Dotson, V S Keen, D Metz, K G Linden. (2010). UV/H2O2 treatment of drinking water increases post-chlorination DBP formation. Water Research, 44(12): 3703–3713
https://doi.org/10.1016/j.watres.2010.04.006
|
3 |
A M Held, D J Halko, J K Hurst. (1978). Mechanisms of chlorine oxidation of hydrogen peroxide. Journal of the American Chemical Society, 100(18): 5732–5740
https://doi.org/10.1021/ja00486a025
|
4 |
M R Hoffmann, J O Edwards. (1975). Kinetics of the oxidation of sulfite by hydrogen peroxide in acidic solution. Journal of Physical Chemistry, 79(20): 2096–2098
https://doi.org/10.1021/j100587a005
|
5 |
Y Huang, Z Nie, C Wang, Y Li, M Xu, R Hofmann. (2018). Quenching H2O2 residuals after UV/H2O2 oxidation using GAC in drinking water treatment. Environmental Science. Water Research & Technology, 4(10): 1662–1670
https://doi.org/10.1039/C8EW00407B
|
6 |
E Kan, C I Koh, K Lee, J Kang. (2015). Decomposition of aqueous chlorinated contaminants by UV irradiation with H2O2. Frontiers of Environmental Science & Engineering, 9(3): 429–435
https://doi.org/10.1007/s11783-014-0677-6
|
7 |
M Kerker. (1957). The ionization of sulfuric acid. Journal of the American Chemical Society, 79(14): 3664–3667
https://doi.org/10.1021/ja01571a015
|
8 |
J C Kruithof, P C Kamp, B J Martijn. (2007). UV/H2O2 treatment: a practical solution for organic contaminant control and primary disinfection. Ozone Science and Engineering, 29(4): 273–280
https://doi.org/10.1080/01919510701459311
|
9 |
J Lagrange, C Pallares, G Wenger, P Lagrange. (1993). Electrolyte effects on aqueous atmospheric oxidation of sulphur dioxide by hydrogen peroxide. Atmospheric Environment. Part A, General Topics, 27(2): 129–137
https://doi.org/10.1016/0960-1686(93)90342-V
|
10 |
M W Lister. (1952). The decomposition of hypochlorous acid. Canadian Journal of Chemistry, 30(11): 879–889
https://doi.org/10.1139/v52-107
|
11 |
W Liu, S A Andrews, M I Stefan, J R Bolton. (2003). Optimal methods for quenching H2O2 residuals prior to UFC testing. Water Research, 37(15): 3697–3703
https://doi.org/10.1016/S0043-1354(03)00264-1
|
12 |
S Lu, N Wang, C Wang. (2018). Oxidation and biotoxicity assessment of microcystin-LR using different AOPs based on UV, O3 and H2O2. Frontiers of Environmental Science & Engineering, 12(3): 12
https://doi.org/10.1007/s11783-018-1030-2
|
13 |
Y Lu, Q Gao, L Xu, Y Zhao, I R Epstein. (2010). Oxygen-sulfur species distribution and kinetic analysis in the hydrogen peroxide-thiosulfate system. Inorganic Chemistry, 49(13): 6026–6034
https://doi.org/10.1021/ic100573a
|
14 |
F Maaß, H Elias, K J Wannowius. (1999). Kinetics of the oxidation of hydrogen sulfite by hydrogen peroxide in aqueous solution. Atmospheric Environment, 33(27): 4413–4419
https://doi.org/10.1016/S1352-2310(99)00212-5
|
15 |
P M Mader. (1958). Kinetics of the hydrogen peroxide-sulfite reaction in alkaline solution. Journal of the American Chemical Society, 80(11): 2634–2639
https://doi.org/10.1021/ja01544a009
|
16 |
V K Sharma, X Yu, T J McDonald, C Jinadatha, D D Dionysiou, M Feng. (2019). Elimination of antibiotic resistance genes and control of horizontal transfer risk by UV-based treatment of drinking water: a mini review. Frontiers of Environmental Science & Engineering, 13(3): 37
https://doi.org/10.1007/s11783-019-1122-7
|
17 |
M I Stefan (2017). Chapter 2: UV/Hydrogen Peroxide Process. Advanced Oxidation Processes for Water Treatment: Fundamentals and Application, 7–123
|
18 |
C Wang, M Hofmann, A Safari, I Viole, S Andrews, R Hofmann. (2019). Chlorine is preferred over bisulfite for H2O2 quenching following UV-AOP drinking water treatment. Water Research, 165(15): 115000
https://doi.org/10.1016/j.watres.2019.115000
|
19 |
T X Wang, D W Margerum. (1994). Kinetics of reversible chlorine hydrolysis: temperature dependence and general-acid/base-assisted mechanisms. Inorganic Chemistry, 33(6): 1050–1055
https://doi.org/10.1021/ic00084a014
|
20 |
N van Klassen, D Marchington, H C E McGowan. (1994). H2O2 Determination by the I3− method and by KMnO4 Titration. Analytical Chemistry, 66(18): 2921–2925
https://doi.org/10.1021/ac00090a020
|
21 |
J van McArdle, M R Hoffmann. (1983). Kinetics and mechanism of the oxidation of aquated sulfur dioxide by hydrogen peroxide at low pH. Journal of Physical Chemistry, 87: 5425–5429
https://doi.org/10.1021/j150644a024
|
|
Viewed |
|
|
|
Full text
|
|
|
|
|
Abstract
|
|
|
|
|
Cited |
|
|
|
|
|
Shared |
|
|
|
|
|
Discussed |
|
|
|
|