4.7 Article

Drinking water nitrosamines in a large metropolitan region in Brazil

期刊

ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
卷 28, 期 25, 页码 32823-32830

出版社

SPRINGER HEIDELBERG
DOI: 10.1007/s11356-021-12998-4

关键词

Drinking water; Emerging contaminants; Disinfection byproducts; Gas chromatography; Mass spectrometry; Nitrosamines; Solid-phase extraction

资金

  1. Sao Paulo Research Foundation (FAPESP) [2014/24740-6, 17/25490-1]
  2. National Council for Scientific and Technological Development (CNPq) [400182/2016-5, 302748/2018-0]
  3. National Institute of Advanced Analytical Sciences and Technologies (INCTAA)
  4. CNPq [465768/2014-8]
  5. FAPESP [2014/50951-4]
  6. National Council for Scientific and Technological Development (CNPq)
  7. Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) [17/25490-1, 14/50951-4] Funding Source: FAPESP

向作者/读者索取更多资源

This study developed an analytical method for detecting and quantifying nitrosamines in drinking water, with NDMA being the most frequently detected nitrosamine in the Metropolitan Region of Campinas, São Paulo, Brazil. The levels of nitrosamines found in the drinking water samples are of considerable relevance due to the area's expanded industrial and agricultural activities.
Nitrosamines are a concerning group of carcinogens, which have gained increasing attention over the last years, frequently found in drinking and recycled water systems. In this work, an analytical method was developed for the detection and quantification of seven nitrosamines (NDMA, NMEA, NPYR, NDEA, NPIP, NDPA, and NDBA) in drinking water. The method is based on gas chromatography coupled with a single quadrupole mass spectrometer (GC-MS) with electron ionization (EI) mode. Sample enrichment and matrix cleanup by solid-phase extraction (SPE) were performed using the US EPA Method 521 cartridge packed with coconut-based charcoal. The simple method allowed reliable identification and quantification of nitrosamines in the water at nanogram per liter levels. The optimized method was validated at three concentration levels (20, 100, and 200 ng L-1) in ultrapure and drinking water samples. Average recoveries were 63-87% for ultrapure water and 38-79% for drinking water with relative standard deviations (RSD) below 10% for both matrices. Method detection limits were 1.23-3.14 ng L-1. The described method was applied to eighteen drinking water samples collected from 13 cities of the Metropolitan Region of Campinas (Sao Paulo, Brazil). NDMA was the most frequent nitrosamine detected (89% of samples) and had the highest concentration level found (67 ng L-1). The levels of nitrosamines found in drinking water samples are of considerable relevance since the selected area is a major urban center that has amply expanded industrial and agricultural activities over the last few decades. To the best of our knowledge, this is the first evaluation of nitrosamines in drinking water conducted in Brazil to date.

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