4.3 Article

Graphene oxide reinforced polyamide nanocomposite coated on paper as a novel layered sorbent for microextraction by packed sorbent

Journal

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/03067319.2018.1535061

Keywords

Microextraction by packed sorbent; graphene oxide/polyamide/cellulose paper; central composite design; organophosphorous pesticides; gas chromatography

Funding

  1. Research Council of Azarbaijan Shahid Madani University

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In this work, a novel layered sorbent for microextraction by packed sorbent (MEPS) was introduced, which has been prepared by coating graphene oxide/polyamide (GO/PA) nanocomposite (NC) onto cellulose paper through solvent exchange method. Scanning electron microscopy (SEM) was applied to investigate the surface characteristic and morphology of PA and GO/PA NC coated on cellulose paper. The prepared MEPS device was used for extraction of organophosphorous pesticides (OPPs) including chlorpyrifos, fenthion, fenithrothion, ethion, edifenphos and phosalone in environmental aqueous samples followed by detection using gas chromatography-flame ionisation detector (GC-FID). Important parameters affecting the MEPS method including pH of sample solution, extraction draw-discard cycles, sorbent layers, desorption solvent volume and desorption draw-eject number were studied and optimised using central composite design (CCD). Based on the method validation, limits of detection (LODs) were in the range of 0.2-1 mu g L-1. The calibration graphs for chlorpyrifos, fenthion and edifenphos are linear in the concentration range of 1 to 500 mu g L-1; for ethion and phosalone are linear in the range of 1-1000 mu g L-1 and for fenithrothion is linear in the range of 3-1000 mu g L-1. The method precision (RSD %) with six replicates determinations was in the range of 3 to 9.4 % and 3.9 to 11.9% for distilled water and spiked river water sample, respectively, at the concentration level of 300 mu g L-1 . The developed method was applied successfully to determine OPP compounds in river, dam and tap water samples; accordingly, the relative recoveries (RR%) were obtained in the range of 77.8 to 113.3%.

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