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« Previous AbstractInfluence of polyelectrolyte architecture on the electrokinetics and dewaterability of industrial membrane bioreactor activated sludge    Next AbstractModification of a steel fiber with a graphene based bucky gel for headspace solid-phase microextraction of volatile aromatic hydrocarbons prior to their quantification by GC »

J Sep Sci


Title:Enhanced headspace single drop microextraction method using deep eutectic solvent based magnetic bucky gels: Application to the determination of volatile aromatic hydrocarbons in water and urine samples
Author(s):Yousefi SM; Shemirani F; Ghorbanian SA;
Address:"Department of Analytical Chemistry, Faculty of Chemistry, University College of Science, University of Tehran, Tehran, Iran. Faculty of Chemical Engineering, School of Engineering, University of Tehran, Tehran, Iran"
Journal Title:J Sep Sci
Year:2018
Volume:20171227
Issue:4
Page Number:966 - 974
DOI: 10.1002/jssc.201700807
ISSN/ISBN:1615-9314 (Electronic) 1615-9306 (Linking)
Abstract:"A facile headspace single drop microextraction method was developed using deep eutectic solvent-based magnetic bucky gel as the extraction solvent for the first time. The hydrophobic magnetic bucky gel was formed by combining choline chloride/chlorophenol deep eutectic solvent and magnetic multiwalled carbon nanotube nanocomposite. Magnetic susceptibility, high viscosity, high sorbing ability, and tunable extractability of organic analytes are the desirable advantages of the prepared gel. Using a rod magnet as a suspensor in combination with the magnetic susceptibility of the prepared gel resulted in a highly stable droplet. This stable droplet eliminated the possibility of drop dislodgement. The prepared droplet made it possible to complete the extraction process in high temperatures and elevated agitation rates. Furthermore, using larger micro-droplet volumes without any operational problems became possible. These facts resulted in shorter sample preparation time, higher sensitivity of the method, and lower detection limits. Under the optimized conditions, an enrichment factor of 520-587, limit of detection of 0.05-0.90 ng/mL, and linearity range of 0.2-2000 ng/mL (coefficient of determination = 0.9982-0.9995) were obtained. Relative standard deviations were < 10%. This method was successfully coupled with gas chromatography and used for the determination of benzene, toluene, ethylbenzene, and xylene isomers as harmful volatile organic compounds in water and urine samples"
Keywords:"Gels/chemistry Healthy Volunteers Humans Hydrocarbons, Aromatic/*analysis *Liquid Phase Microextraction Magnetic Fields Particle Size Solvents/chemistry Volatile Organic Compounds/*analysis Water Pollutants, Chemical/*analysis deep eutectic solvents gas c;"
Notes:"MedlineYousefi, Seyedeh Mahboobeh Shemirani, Farzaneh Ghorbanian, Sohrab Ali eng Germany 2017/12/02 J Sep Sci. 2018 Feb; 41(4):966-974. doi: 10.1002/jssc.201700807. Epub 2017 Dec 27"

 
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