N-nitrosodimethylamine (NDMA) formation from the ozonation of model compounds. (1st April 2015)
- Record Type:
- Journal Article
- Title:
- N-nitrosodimethylamine (NDMA) formation from the ozonation of model compounds. (1st April 2015)
- Main Title:
- N-nitrosodimethylamine (NDMA) formation from the ozonation of model compounds
- Authors:
- Marti, Erica J.
Pisarenko, Aleksey N.
Peller, Julie R.
Dickenson, Eric R.V. - Abstract:
- Abstract: Nitrosamines are a class of toxic disinfection byproducts commonly associated with chloramination, of which several were included on the most recent U.S. EPA Contaminant Candidate List. Nitrosamine formation may be a significant barrier to ozonation in water reuse applications, particularly for direct or indirect potable reuse, since recent studies show direct formation during ozonation of natural water and treated wastewaters. Only a few studies have identified precursors which react with ozone to form N -nitrosodimethylamine (NDMA). In this study, several precursor compound solutions, prepared in ultrapure water and treated wastewater, were subjected to a 10 M excess of ozone. In parallel experiments, the precursor solutions in ultrapure water were exposed to gamma radiation to determine NDMA formation as a byproduct of reactions of precursor compounds with hydroxyl radicals. The results show six new NDMA precursor compounds that have not been previously reported in the literature, including compounds with hydrazone and carbamate moieties. Molar yields in deionized water were 61–78% for 3 precursors, 12–23% for 5 precursors and <4% for 2 precursors. Bromide concentration was important for three compounds (1, 1-dimethylhydrazine, acetone dimethylhydrazone and dimethylsulfamide), but did not enhance NDMA formation for the other precursors. NDMA formation due to chloramination was minimal compared to formation due to ozonation, suggesting distinct groups ofAbstract: Nitrosamines are a class of toxic disinfection byproducts commonly associated with chloramination, of which several were included on the most recent U.S. EPA Contaminant Candidate List. Nitrosamine formation may be a significant barrier to ozonation in water reuse applications, particularly for direct or indirect potable reuse, since recent studies show direct formation during ozonation of natural water and treated wastewaters. Only a few studies have identified precursors which react with ozone to form N -nitrosodimethylamine (NDMA). In this study, several precursor compound solutions, prepared in ultrapure water and treated wastewater, were subjected to a 10 M excess of ozone. In parallel experiments, the precursor solutions in ultrapure water were exposed to gamma radiation to determine NDMA formation as a byproduct of reactions of precursor compounds with hydroxyl radicals. The results show six new NDMA precursor compounds that have not been previously reported in the literature, including compounds with hydrazone and carbamate moieties. Molar yields in deionized water were 61–78% for 3 precursors, 12–23% for 5 precursors and <4% for 2 precursors. Bromide concentration was important for three compounds (1, 1-dimethylhydrazine, acetone dimethylhydrazone and dimethylsulfamide), but did not enhance NDMA formation for the other precursors. NDMA formation due to chloramination was minimal compared to formation due to ozonation, suggesting distinct groups of precursor compounds for these two oxidants. Hydroxyl radical reactions with the precursors will produce NDMA, but formation is much greater in the presence of molecular ozone. Also, hydroxyl radical scavenging during ozonation leads to increased NDMA formation. Molar conversion yields were higher for several precursors in wastewater as compared to deionized water, which could be due to catalyzed reactions with constituents found in wastewater or hydroxyl radical scavenging. Graphical abstract: Highlights: New precursors were identified for the formation of NDMA due to ozonation. Wastewater constituents may enhance or catalyze NDMA formation. Molecular ozone dominates NDMA formation as compared to hydroxyl radicals. NDMA ozonation precursors have low molar yields with monochloramine. Transformation products after ozonation may be NDMA chloramination precursors. … (more)
- Is Part Of:
- Water research. Volume 72(2015)
- Journal:
- Water research
- Issue:
- Volume 72(2015)
- Issue Display:
- Volume 72, Issue 2015 (2015)
- Year:
- 2015
- Volume:
- 72
- Issue:
- 2015
- Issue Sort Value:
- 2015-0072-2015-0000
- Page Start:
- 262
- Page End:
- 270
- Publication Date:
- 2015-04-01
- Subjects:
- N-Nitrosodimethylamine -- NDMA -- ozone -- Nitrosamine -- Disinfection byproduct -- Potable reuse
Water -- Pollution -- Research -- Periodicals
363.7394 - Journal URLs:
- http://catalog.hathitrust.org/api/volumes/oclc/1769499.html ↗
http://www.sciencedirect.com/science/journal/00431354 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.watres.2014.08.047 ↗
- Languages:
- English
- ISSNs:
- 0043-1354
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 9273.400000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 7297.xml