HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHIC DETERMINATION OF AZAARENES AND THEIR METABOLITES IN GROUNDWATER AFFECTED BY CREOSOTE WOOD PRESERVATIVES

被引:26
作者
ONDRUS, MG
STEINHEIMER, TR
机构
[1] US GEOL SURVEY,WRD,5293 WARD RD,MAIL STOP 407,ARVADA,CO 80002
[2] UNIV WISCONSIN STOUT,DEPT CHEM,MENOMONIE,WI 54751
基金
美国国家科学基金会;
关键词
D O I
10.1093/chromsci/28.6.324
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Polynuclear azaheterocyclic compounds (azaarenes) are nitrogen-containing analogs of polycyclic aromatic hydrocarbons (PAHs). The nitrogen atom in t he ring system causes these compounds to be slightly polar and considerably more water soluble than related PAHs. A method using a solid-surface sorption technique to extract and concentrate azaarenes and their principle metabolites present in groundwater that contains creosote waste is described. Analyte isolation and concentration is accomplished by solid-phase extraction on n-octadecyl cartridges followed by instrumental determination involving high-performance liquid chromatography. Separations and detection are achieved using flexible-walled, wide-bore columns with ultraviolet and fluorescence photometric detectors connected in series. Fluorescence detection alone is insufficient because the fluorescence response produced by two-ring azaarenes is limited. Short wavelength (229 nm) absorbance detection provides improved sensitivity for these compounds and peak ratioing for more definitive identification. In this study, oxygen-containing metabolites of quinoline, isoquinoline, and acridine are detected in groundwater from hazardous waste sites in Pensacola, Florida and St. Louis Park, Minnesota. Concentrations ranging from mg/L to ng/L are measured. The dependence of measured octanol-water partition coefficients on pH is discussed in the context of the isolation chemistry. As a direct bacterial degradation product of acridine with a relatively long environmental persistence, 9-acridinone may serve as a biogenic marker signaling creosote contamination of groundwater. © 1990 Oxford University Press.
引用
收藏
页码:324 / 330
页数:7
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