Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractA new high-speed hollow fiber based liquid phase microextraction method using volatile organic solvent for determination of aromatic amines in environmental water samples prior to high-performance liquid chromatography    Next AbstractAssessment of odorous VOCs released from a main MSW landfill site in Istanbul-Turkey via a modelling approach »

J Chromatogr A


Title:Highly porous nanostructured copper foam fiber impregnated with an organic solvent for headspace liquid-phase microextraction
Author(s):Saraji M; Ghani M; Rezaei B; Mokhtarianpour M;
Address:"Department of Chemistry, Isfahan University of Technology, Isfahan 84156-83111, Iran. Electronic address: saraji@cc.iut.ac.ir. Department of Chemistry, Isfahan University of Technology, Isfahan 84156-83111, Iran"
Journal Title:J Chromatogr A
Year:2016
Volume:20160924
Issue:
Page Number:25 - 34
DOI: 10.1016/j.chroma.2016.09.058
ISSN/ISBN:1873-3778 (Electronic) 0021-9673 (Linking)
Abstract:"A new headspace liquid-phase microextraction technique based on using a copper foam nanostructure substrate followed by gas chromatography-flame ionization detection was developed for the determination of volatile organic compounds in water and wastewater samples. The copper foam with highly porous nanostructured walls was fabricated on the surface of a copper wire by a rapid and facile electrochemical process and used as the extractant solvent holder. Propyl benzoate was immobilized in the pores of the copper foam coating and used for the microextraction of benzene, toluene, ethylbenzene and xylenes. The experimental parameters such as the type of organic solvent, desorption temperature, desorption time, salt concentration, sample temperature, equilibrium time and extraction time, were investigated and optimized. Under the optimum conditions, the method detection limit was between 0.06 and 0.25mugL(-1). The relative standard deviation of the method for the analytes at 4-8mugL(-1) concentration level ranged from 7.9 to 11%. The fiber-to-fiber reproducibility for three fibers prepared under the same condition was 9.3-12%. The enrichment factor was in the range of 615-744. Different water samples were analyzed for the evaluation of the method in real sample analysis. Relative recoveries for spiked tap, river and wastewater samples were in the range of 85-94%. Finally, the extraction efficiency of the method was compared with those of headspace single drop microextraction and headspace SPME with the commercial fibers"
Keywords:"Benzene Derivatives/*isolation & purification Benzoates/*chemistry Chromatography, Gas/methods Copper/*chemistry Flame Ionization Fresh Water/chemistry Limit of Detection Liquid Phase Microextraction/methods Nanostructures Porosity Reproducibility of Resu;"
Notes:"MedlineSaraji, Mohammad Ghani, Milad Rezaei, Behzad Mokhtarianpour, Maryam eng Netherlands 2016/10/01 J Chromatogr A. 2016 Oct 21; 1469:25-34. doi: 10.1016/j.chroma.2016.09.058. Epub 2016 Sep 24"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 24-11-2024