4.7 Article

Direct mass spectrometric analysis of naphthenic acids and polycyclic aromatic hydrocarbons in waters impacted by diluted bitumen and conventional crude oil

期刊

SCIENCE OF THE TOTAL ENVIRONMENT
卷 765, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.scitotenv.2020.144206

关键词

Oil spill; Direct analysis; On-line membrane sampling; Condensed-phase membrane introduction mass spectrometry; Chemometrics; Contaminants

资金

  1. Natural Science and Engineering Research Council (NSERC) of Canada Discovery Grant Program [RGPIN-2016-06454, RGPIN-2016-05380]
  2. Government of Canada's Program for Energy Research and Development (PERD)

向作者/读者索取更多资源

This study investigated the effects of crude oil spills on the hydrosphere, comparing the concentrations of petroleum-derived compounds in natural and constructed waters. Different types of oil were found to have varying impacts on water contamination. A novel mass spectrometry technique was used to concurrently analyze trace NAs and PAHs in water samples, providing a new method for rapid monitoring of contamination processes.
Crude oil spills have well-documented, deleterious impacts on the hydrosphere. In addition to macroscopic effects on wildlife and waterscapes, several classes of petroleum derived compounds, such as naphthenic acids (NAs) and polycyclic aromatic hydrocarbons (PAHs), may be released into the water and present aquatic contamination hazards. The concentrations of these contaminants may be affected by both oil type and water chemistry. We characterize the concentrations of NAs and PAHs in natural and constructed waters, spanning a range of pH and salinity, and directly compare the influence of diluted bitumen (DB) and conventional crude (CC) oil, using condensed-phase membrane introduction mass spectrometry (CP-MIMS) as a direct sampling, on-line technique. The concentration and isomer class profiles of classical NAs in the aqueous phase were assessed using electrospray ionization in negative-ion mode as [M-H](-) whereas PAH concentrations were monitored using liquid electron ionization (LEI) in positive-ion mode as [M+]. NA concentrations (0.03-25 ppm) were highly pH-dependent, and an order of magnitude greater in water samples contaminated with DB than CC. Conversely, concentrations of naphthalene (10-130 ppb) and alkyl-naphthalenes (10-90 ppb) were three to four-fold higher in water samples exposed to CC. We demonstrate that naturally occurring dissolved organic matter does not bias results from the membrane sampling approach employed, and that DB and CC contaminated waters can be differentiated using principal component analysis of the NA isomer class distribution in both constructed and natural waters. Finally, we describe the first demonstration of the concurrent analysis of trace NAs and PAHs in the same water sample by controlling perm-selectivity at the membrane and the ionization mode of the mass spectrometer. The techniques employed here for trace analysis of petroleum derived compounds in water can be applied to rapid screening and real-time monitoring of contamination and remediation processes. (C) 2020 Elsevier B.V. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据