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Integrated ultrasound-assisted magnetic solid-phase extraction for efficient determination and pre-concentration of polycyclic aromatic hydrocarbons from high-consumption soft drinks and non-alcoholic beers in Iran.
Azari, Ali; Abtahi, Mehrnoosh; Saeedi, Reza; Yari, Ahmad Reza; Vaziri, Mohammad Hossein; Mohammadi, Gholamabbas.
Affiliation
  • Azari A; Workplace Health Promotion Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Abtahi M; Sirjan School of Medical Sciences, Sirjan, Iran.
  • Saeedi R; Workplace Health Promotion Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Yari AR; Department of Environmental Health Engineering, School of Public Health and Safety, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Vaziri MH; Workplace Health Promotion Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Mohammadi G; Department of Health, Safety, and Environment (HSE), School of Public Health and Safety, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
J Sep Sci ; 45(16): 3139-3149, 2022 Aug.
Article in En | MEDLINE | ID: mdl-35789060
ABSTRACT
In the present research, an ultrasound-assisted magnetic solid-phase extraction coupled with a gas chromatography-mass spectrometry hybrid system was developed for the extraction/determination of trace amounts of polycyclic aromatic hydrocarbons in high-consumption soft drinks and non-alcoholic beers in Iran using magnetite graphene oxide adsorbent. The magnetite graphene oxide was characterized by scanning electron microscope, transmission electron microscopy, Fourier-transform infrared spectroscopy, X-ray diffraction, and vibrating-sample magnetometer techniques. The highest extraction recovery (73.05%-95.56%) and enrichment factor (90.65-106.38) were obtained at adsorbent mass 10 mg, adsorption time 30 min, salt addition sodium chloride 10% w/v, desorption time 20 min, eluent type hexane acetone (11, v/v), and desorption solvent volumes 200 µl. Under optimum conditions, the linearity range for polycyclic aromatic hydrocarbons determination was 0.2-200 ng/ml with a coefficient of determination > 0.993, the limit of detection = 0.09-0.21 ng/ml, the limit of quantitation = 0.3-0.7 ng/ml, and relative standard deviation < 8.1%, respectively. Relative recoveries in spiked real samples ranged from 94.67 to 109.45% with a standard deviation < 6.05%. The proposed method is effective, sensitive, and reusable and it is promising for the analysis of polycyclic aromatic hydrocarbons residues in environmental samples.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polycyclic Aromatic Hydrocarbons Country/Region as subject: Asia Language: En Journal: J Sep Sci Year: 2022 Document type: Article Affiliation country: Iran

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polycyclic Aromatic Hydrocarbons Country/Region as subject: Asia Language: En Journal: J Sep Sci Year: 2022 Document type: Article Affiliation country: Iran