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Quantitative analysis of fuel-related hydrocarbons in surface water and wastewater samples by solid-phase microextraction

Journal Article · · Analytical Chemistry (Washington)
DOI:https://doi.org/10.1021/ac950862w· OSTI ID:223624
; ;  [1]
  1. Univ. of North Dakota, Grand Forks, ND (United States)

Solid-phase microextraction (SPME) parameters were examined on water contaminated with hydrocarbons including benzene and alkylbenzenes, n-alkanes, and polycyclic aromatic hydrocarbons (PAHs). Absorption equilibration times ranged from several minutes for low molecular weight compounds such as benzene to 5 h for high molecular weight compounds such as benzo[a]pyrene. Under equilibrium conditions, SPME analysis with GC/FID was linear over 3-6 orders of magnitude, with linear correlation coefficients (r{sup 2}) greater than 0.96. Experimentally determined FID detection limits ranged from nearly 30 ppt (w/w hydrocarbon/sample water) for high molecular weight PAHs (e. g., MW > 202) to nearly 1 ppb for low molecular weight aromatic hydrocarbons. Experimental distribution constants (K) were different with 100- and 7-{mu}m poly(dimethylsiloxane) fibers, and poor correlations with previously published values suggest that K depends on the fiber coating thickness and the sorbent preparation method. SPME analysis gave good quantitative performance with surface waters having high suspended sediment contents, as well as with coal gasification wastewater which contained matrix organics at 10{sup 6} -fold higher concentrations than the target aromatic hydrocarbons. Good agreement was obtained between a 45-min SPME and methylene chloride extraction for the determination of PAH concentrations in creosote-contaminated water. 17 refs., 5 figs., 6 tabs.

OSTI ID:
223624
Journal Information:
Analytical Chemistry (Washington), Journal Name: Analytical Chemistry (Washington) Journal Issue: 1 Vol. 68; ISSN ANCHAM; ISSN 0003-2700
Country of Publication:
United States
Language:
English

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