COMPARISON OF ASE AND SFE WITH SOXHLET, SONICATION, AND METHANOLIC SAPONIFICATION EXTRACTIONS FOR THE DETERMINATION OF ORGANIC MICROPOLLUTANTS IN MARINE PARTICULATE MATTER
Op. Heemken et al., COMPARISON OF ASE AND SFE WITH SOXHLET, SONICATION, AND METHANOLIC SAPONIFICATION EXTRACTIONS FOR THE DETERMINATION OF ORGANIC MICROPOLLUTANTS IN MARINE PARTICULATE MATTER, Analytical chemistry, 69(11), 1997, pp. 2171-2180
The methods of accelerated solvent extraction (ASE) and supercritical
fluid extraction (SFE) of polycyclic aromatic hydrocarbons (PAHs), ali
phatic hydrocarbons, and chlorinated hydrocarbons from marine samples
were investigated, The results of extractions of a certified sediment
and four samples of suspended particulate matter (SPM) were compared t
o classical Soxhlet (SOX), ultrasonication (USE), and methanolic sapon
ification extraction (MSE) methods, The recovery data, including preci
sion and systematic deviations of each method, were evaluated statisti
cally, It was found that recoveries and precision of ASE and SFE compa
red well with the other methods investigated, Using SFE, the average r
ecoveries of PAHs in three different samples ranged from 96 to 105%, f
or ASE the recoveries were in the range of 97-108% compared to the ref
erence methods, Compared to the certified values of sediment HS-6, the
average recoveries of SFE and ASE were 87 and 88%, most compounds bei
ng within the limits of confidence, Also, for alkanes the average reco
veries by SFE and ASE were equal to the results obtained by SOX, USE,
and MSE, In the case of SFE, the recoveries were in the range 93-115%,
and ASE achieved recoveries of 94-107% as compared to the other metho
ds, For ASE and SFE, the influence of water on the extraction efficien
cy was examined, While the natural water content of the SPM sample (56
wt %) led to insufficient recoveries in ASE and SFE, quantitative ext
ractions were achieved in SFE after addition of anhydrous sodium sulfa
te to the sample, Finally, ASE was applied to SPM-loaded filter candle
s whereby a mixture of n-hexane/acetone as extraction solvent allowed
the simultaneous determination of PAHs, alkanes, and chlorinated hydro
carbons.