Comparing d-SPE Sorbents of the QuEChERS Extraction Method and EMR-Lipid for the Determination of Polycyclic Aromatic Hydrocarbons (PAH4) in Food of Animal and Plant Origin

2017 ◽  
Vol 10 (7) ◽  
pp. 2111-2124 ◽  
Author(s):  
Michael Urban ◽  
Céline Lesueur
2021 ◽  
Vol 9 ◽  
Author(s):  
Caroline Scaramboni ◽  
Jordan Brizi Neris ◽  
Rita de Kássia Silva do Nascimento ◽  
Natasha Leandra Chiaranda da Rosa ◽  
Jonatas Schadeck Carvalho ◽  
...  

This work describes the optimization of an extraction method for the determination of polycyclic aromatic hydrocarbons (PAHs) and their nitro- and oxy-PAH derivatives in atmospheric particulate matter (PM) samples, and demonstrates that this method is also effective for the determination of levoglucosan. The optimization of the extraction solvents was performed using a three-component mixture design with the solvents dichloromethane, methanol, and acetonitrile. The number of extractions, volume of solvent, and duration of extraction in an ultrasonic bath were optimized using a full factorial design followed by a central composite design. The analyses were performed by gas chromatography coupled with mass spectrometry. The optimized conditions of the method were three extractions using 4.0 ml of acetonitrile, with ultrasonication for 34 min. The proposed method presented good linearity (r > 0.990) and acceptable precision for low (100 ng ml−1, RSD: 1–16%), medium (300 ng ml−1, RSD: 1–19%), and high (500 ng ml−1, RSD: 2–16%) concentrations of PAHs. The limits of quantification for different PAHs ranged from 10 to 50 ng ml−1, which were suitable for atmospheric PM. Assessment of the method using sample matrix spiking/recovery assays, as well as use of a reference method, showed good recoveries for levoglucosan and for most of the PAHs and their derivatives, except for the most volatile compounds, which were lost during the evaporation of the solvent. The results for PM samples extracted by the optimized method and the reference method were in good agreement. The proposed method required 97% less solvent than the reference method, shortened the analysis time by 85%, and proved to be accurate and precise for the determination of at least 27 PAHs and their derivatives present in PM samples collected with a low-volume sampler.


2015 ◽  
Vol 48 ◽  
pp. 67-80
Author(s):  
Muhammad Nuraddeen Bui

This study shows the sensitivity of using silicone rubber passive sampler(SR-PS) andgas chromatography with mass spectrometer (GC-MS) detection for monitoring and identification of polycyclic aromatic hydrocarbons in surface water systems. The analysis was performed for eighteen PAHs compounds after pre-concentration using Soxhlet extraction method. By comparison, a total of 13 PAHs were detected in the spot water samples, of which none was quantifiable. The freely dissolved PAH concentrations were found to range from 0.17 ng/L to 0.76 ng/L at Ugieriver. The use of fluorine d10 as Performance reference compound(PRC) gives a sampling rates of 8.14 (L/day) for silicone rubber passive samplers. Analysis of PAHs concentrations suggest the contaminants are mainly from pyrolytic sources. Overall it can be concluded that SR-PS are viable alternatives in the environmental monitoring of PAHs.


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


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