scholarly journals Application of Partial Least-Squares Calibration to Phosphorimetric Data for Determination of Polycyclic Aromatic Hydrocarbons in Spiked Environmental Samples

2000 ◽  
Vol 83 (2) ◽  
pp. 391-398
Author(s):  
A Segura Carretero ◽  
M Martinez Galera ◽  
C Cruces Blanco ◽  
M D Gil García ◽  
A Fernández Gutiérrez ◽  
...  

Abstract A partial least-squares calibration method is proposed, for the first time, for phosphorescence signals. The proposed method is based on the determination of phenanthrene, fluoranthene, and benz[a]anthracene by room temperature phosphorimetry, using microemulsion solutions. The emission and first-derivative emission spectra of the ternary mixtures were tested to perform the calibration matrix. Improved recoveries were found for the prior differentiation step in the analysis of ternary mixtures of these polycyclic aromatic hydrocarbons in road dust samples. The proposed method yielded recoveries ranging from 93.2 to 115.3%, with relative standard deviations of < 6.8%.

2010 ◽  
Vol 2010 ◽  
pp. 1-8 ◽  
Author(s):  
Amal Al-Rashdan ◽  
Murad I. H. Helaleh ◽  
A. Nisar ◽  
A. Ibtisam ◽  
Zainab Al-Ballam

Concentration of 16 polycyclic aromatic hydrocarbons (PAHs) in eighteen baked bread samples using gas oven toasting were evaluated in this study. Samples were classified into the following categories: (1) bread baked from white wheat flour, (2) bread baked from brown wheat flour, and (3) sandwich bread baked from white wheat flour. Analysis was performed by GC-MS after Soxhlet extraction of the sample and clean up of the extract. The levels of B[a]P was not detected in ten of eighteen samples. In the rest of the samples, B[a]P are varied from 2.83 to 16.54 g/kg. B[a]A, CHR, B[b]FA, B[k] FA, IP, DB[a,h]A, and B[ghi]P concentrations were found to be less than 10.0 g/kg. However, B[a]P are not detected in original white and brown wheat flour. The total PAHs were varied in the range 1.06–44.24 g/kg and 3.08–278.66 g/kg for H-PAH and L-PAH, respectively. Reproducibility and repeatability of the proposed method was calculated and presented in terms of recovery and relative standard deviations (RSD, %). Recoveries were varied from 72.46% to 99.06% with RSD ± 0.28–15.01% and from 82.39% to 95.01% with RSD ±1.91–13.01% for repeatability and reproducibility, respectively. Different commercialized samples of toasted bread were collected and analyzed.


1986 ◽  
Vol 69 (1) ◽  
pp. 110-114
Author(s):  
John T Coates ◽  
Alan W Elzerman ◽  
A Wayne Garrison

Abstract A procedure has been developed for analysis of plant material for polycyclic aromatic hydrocarbons (PAHs). Sonication is used to extract the PAHs from homogenized plant material into acetonitrile and then the PAHs are partitioned into pentane. The pentane extract is fractionated on a micro silicic acid column and is analyzed by capillary gas chromatography with flame ionization detection. Overall method recoveries for 16 PAHs spiked into hybrid grain sorghum ranged from 45 to 90%, with relative standard deviations ranging from 3 to 38% and averaging 17%. This method can be used to measure PAHs in hybrid grain sorghum, fescue grass, and similar plants at the 25 μ/kg level. The procedure was applied to a preliminary study of PAH uptake by sorghum and fescue irrigated with secondary treated municipal wastewater spiked with 5 PAHs. Accumulation of fluoranthene and pyrene by fescue and hybrid grain sorghum from the PAH-contaminated irrigation water was apparent.


1986 ◽  
Vol 69 (3) ◽  
pp. 462-466 ◽  
Author(s):  
Charles J Musial ◽  
John F Uthe

Abstract A simple, rapid, easily automated method is described for the determination of polycyclic aromatic hydrocarbons (PAHs) in shellfish such as American lobster (Homarus americanus) and blue mussel (Mytilus edulis). PAHs are extracted from small amounts (1-8 g) of tissue by saponification in IN ethanolic potassium hydroxide followed by partitioning into 2,2,4-trimethylpentane. This solution is evaporated just to dryness by rotary evaporation and the residue is dissolved in cyclohexane- dichloromethane (1 + 1) for gel permeation chromatography (GPC) on Bio-Beads SX-3. The GPC procedure is ideal as a screening method in the range 25-18 000 ng PAHs/g tissue. If individual PAH measurements are required, the appropriate GPC fraction is collected and PAHs are separated by reverse phase liquid chromatography (LC) with fiuorometric detection. Individual PAHs at concentrations as low as 0.25-10 ng/g can be determined. Recoveries of added fluoranthene, pyrene, benz[a]anthracene, chrysene, benzo[e]pyrene, benzo[A]fluoranthene, benzo[b]fluoranthene, benzo[α]pyrene, dibenz[a,h]anthracene, benzo[ghi]perylene, and indeno[l,2,3-cd]pyrene were quantitative, with relative standard deviations ranging from 0.0 to 16.9%.


2015 ◽  
Vol 2015 ◽  
pp. 1-7 ◽  
Author(s):  
Mona Khorshid ◽  
Eglal R. Souaya ◽  
Ahmed H. Hamzawy ◽  
Moustapha N. Mohammed

A gas chromatography equipped with mass spectrometer (GCMS) method was developed and validated for determination of 16 polycyclic aromatic hydrocarbons (PAHs) in fish using modified quick, easy, cheap, effective, rugged, and safe (QuEChERS) method for extraction and solid phase extraction for sample cleanup to remove most of the coextract combined with GCMS for determination of low concentration of selected group of PAHs in homogenized fish samples. PAHs were separated on a GCMS with HP-5ms Ultra Inert GC Column (30 m, 0.25 mm, and 0.25 µm). Mean recovery ranged from 56 to 115%. The extraction efficiency was consistent over the entire range where indeno(1,2,3-cd)pyrene and benzo(g,h,i)perylene showed recovery (65, 69%), respectively, at 2 µg/kg. No significant dispersion of results was observed for the other remaining PAHs and recovery did not differ substantially, and at the lowest and the highest concentrations mean recovery and RSD% showed that most of PAHs were between 70% and 120% with RSD less than 10%. The measurement uncertainty is expressed as expanded uncertainty and in terms of relative standard deviation (at 95% confidence level) is±12%. This method is suitable for laboratories engaged daily in routine analysis of a large number of samples.


2018 ◽  
Vol 56 (3) ◽  
pp. 324
Author(s):  
Duong Thi Hanh ◽  
Ha Thu Trinh ◽  
Phan Quang Thang ◽  
Nguyen Trung Dung ◽  
Nguyen Tran Dien

The aim of this study is to develop the quick ultrasonication extraction procedure for determination of 16 typical polycyclic aromatic hydrocarbons (PAHs) in air particles. The  determination and quantification of PAHs in air particles samples were performed using gas chromatography coupled to mass spectrometry (GC-MS) with the aid of deuterated PAH internal standards. 1ug mixture of PAHs was spiked to a quarter of quartz fiber filter and extracted with four different solvents/solvent mixtures (methanol:dichloromethane, acetone:dichloromethane; acetone:hexane; dichloromethane). Ultrasonication extraction was carried out in dark at uncontrolled and controlled ultrasonication temperature (25-28oC). The unique extraction time (20 minutes) was applied for all experiments. The results showed that high recovery rate of PAHs (82-108%) were obtained with dichloromethane (as extraction solvent) in dark at ultrasonication temperature of 25 to 28oC, while generally low recovery rate of PAHs, especially naphthalene (57%) were obtained with methanol:dichloromethane (1:1). The ultrasonication extraction method with dichloromethane showed good reproductively and repeatability with relative standard deviation of 16 PAHs below 6,14%, confirming that samples analyses were precise.  Analytical results of PAHs in air particles collected in Hanoi using the developed ultrasonication extraction procedure showed that 15 out of 16 PAHs were detected, in which high molecular weight (MW) PAHs (>5 rings) were abundance compared to low molecular weight PAHs (< 3 rings). This developed ultrasonication extraction method is quick, easy and sufficient for determination of PAHs in air particle


Sign in / Sign up

Export Citation Format

Share Document