On the basis of classical Berthelot reaction, a simple salicylate-spectrophotometric method was developed for quantitative determination of inorganic monochloramine in water samples. With the catalysis of disodium pentacyanonitrosylferrate(III), inorganic monochloramine reacts with salicylate in equimolar to produce indophenol compound which has an intense absorption at 703nm. Parameters that influence method performance, such as pH, dosage of salicylate and nitroprussiate and reaction time, were modified to enhance the method performance. By using this method, inorganic monochloramine can be distinguished from organic chloramines and other inorganic chlorine species, such as free chlorine, dichloramine, and trichloramine. The molar absorptivities of the final products formed by these compounds are below +/-3% of inorganic monochloramine, because of the alpha-N in them have only one exchangeable hydrogen atom, and cannot react with salicylate to produce the indophenol compound. The upper concentrations of typical ions that do not interfere with the inorganic monochloramine determination are also tested to be much higher than that mostly encountered in actual water treatment. Case study demonstrates that the results obtained from this method are lower than DPD-titrimetric method because the organic chloramines formed by chlorination of organic nitrogenous compounds give no response in the newly established method. And the result measured by salicylate-spectrophotometric method is coincident with theoretical calculation.
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http://dx.doi.org/10.1016/j.aca.2008.04.005 | DOI Listing |
Science
November 2024
Center for Environmental Solutions & Emergency Response, Office of Research and Development, US Environmental Protection Agency, Cincinnati, OH 45268, USA.
Inorganic chloramines are commonly used drinking water disinfectants intended to safeguard public health and curb regulated disinfection by-product formation. However, inorganic chloramines themselves produce by-products that are poorly characterized. We report chloronitramide anion (Cl-N-NO) as a previously unidentified end product of inorganic chloramine decomposition.
View Article and Find Full Text PDFWater Res
January 2025
State Key Laboratory of Urban Water Resource and Environment, Shenzhen Key Laboratory of Organic Pollution Prevention and Control, Harbin Institute of Technology, Shenzhen 518055, China. Electronic address:
Aquatic nitrogenous compounds can be classified as dissolved organic nitrogen (DON) and dissolved inorganic nitrogen (DIN), including ammonia, nitrite, nitrate, and inorganic chloramines. The occurrence of nitrogenous disinfection byproducts (N-DBPs) in water, such as haloacetonitriles (HANs), halonitromethanes (HNMs), haloacaetamides (HAcAms), and nitrosamines (NAs), has attracted considerable attention due to their higher toxicity than regulated carbonaceous analogues. While numerous studies have investigated the contributions of DON to N-DBP formation, relatively fewer studies have explored DIN as N-DBP precursors, although DINs are sometimes evaluated as influencing factors.
View Article and Find Full Text PDFWater Res
September 2024
Guangdong Provincial Key Laboratory of Environmental Pollution Control and Remediation Technology, School of Environmental Science and Engineering, Sun Yat-Sen University, Guangzhou, 510275, PR China. Electronic address:
The UV/monochloramine (UV/NHCl) process, while efficiently eliminating micropollutants, produces toxic byproducts. This study utilized Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS) to investigate molecular-level changes in natural organic matter (NOM) and to disclose formation pathways of nitro(so) and chloro byproducts in the UV/NHCl process. The UV/NHCl process significantly increased the saturation and oxidation levels and altered the elemental composition of NOM.
View Article and Find Full Text PDFNat Water
April 2024
Maseeh Department of Civil, Architectural and Environmental Engineering, University of Texas at Austin, Austin, TX, USA.
We demonstrate the application of proton transfer time-of-flight mass spectrometry (PTR-TOF-MS) in monitoring the kinetics of disinfectant decay in water with a sensitivity one to three orders of magnitude greater than other analytical methods. Chemical disinfection inactivates pathogens during water treatment and prevents regrowth as water is conveyed in distribution system pipes, but it also causes formation of toxic disinfection by-products. Analytical limits have hindered kinetic models, which aid in ensuring water quality and protecting public health by predicting disinfection by-products formation.
View Article and Find Full Text PDFWater Res
July 2024
Jiangmen Key Laboratory of Synthetic Chemistry and Cleaner Production, School of Environmental and Chemical Engineering, Wuyi University, Jiangmen, Guangdong Province 529020, China; Institute of Carbon Peaking and Carbon Neutralization, Wuyi University, Jiangmen 529020, Guangdong Province, China. Electronic address:
As an eco-friendly and sustainable energy, solar energy has great application potential in water treatment. Herein, simulated sunlight was for the first time utilized to activate monochloramine for the degradation of environmental organic microcontaminants. Various microcontaminants could be efficiently degraded in the simulated sunlight/monochloramine system.
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