Dioctyl sulfosuccinate analysis in near-shore Gulf of Mexico water by direct-injection liquid chromatography-tandem mass spectrometry

被引:24
|
作者
Mathew, Johnson [1 ]
Schroeder, David L. [2 ]
Zintek, Lawrence B. [2 ]
Schupp, Caitlin R. [2 ]
Kosempa, Michael G. [2 ]
Zachary, Adam M. [2 ]
Schupp, George C. [2 ]
Wesolowski, Dennis J. [2 ]
机构
[1] US EPA, Houston Reg Lab, Houston, TX 77099 USA
[2] US EPA, Chicago Reg Lab, Chicago, IL 60605 USA
关键词
Dioctyl sulfosuccinate; Dispersant; Aggregate; Deuterated surrogate; Corexit EC9500A; Oil spill; GAS-PHASE;
D O I
10.1016/j.chroma.2012.01.088
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Dioctyl sulfosuccinate (DOSS) was a major component of the dispersants most used in the 2010 Deepwater Horizon Oil Spill incident response. This analytical method quantifies salt water DOSS concentrations to a reporting limit of 20 mu g/L, which was below the United States Environmental Protection Agency's (U.S. EPA) 40 mu/L DOSS Aquatic Life Benchmark. DOSS in Gulf of Mexico water samples were analyzed by direct-injection reversed-phase liquid chromatography-tandem mass spectrometry (LC-MS/MS). Sample preparation with 50% acetonitrile (ACN) enabled quantitative transfer of DOSS and increased DOSS response 20-fold by reducing aggregation. This increased sensitivity enabled the detection of a confirmatory transition over the calibration range of 10-200 mu g/L. U.S. EPA Region 5 and Region 6 laboratories analyzed hundreds of near-shore surface Gulf of Mexico water samples, none contained more than the 20 ppb reporting limit. The matrix spike DOSS/deuterated surrogate (DOSS-D34) correlation of determination varied with mobile phase modifier (ammonium formate R-2 = 0.95 and formic acid R-2 = 0.27). Using ammonium formate. DOSS-D34 accurately measured DOSS matrix effect. The near-shore sodium concentrations varied more than 10,000-fold, but were not strongly correlated with DOSS recovery. DOSS detection by LC-MS/MS enabled rapid analysis which was valuable in guiding incident response. Published by Elsevier B.V.
引用
收藏
页码:46 / 51
页数:6
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