Abstract

Carbon sheets were attached to magnetite (Fe3O4)nanoparticles. The resulting nanocomposite is shown to be a viable sorbent for use in magnetic dispersive solid-phase microextraction of three organophosphorus pesticides. The sorbent was synthesized via the sol-gel process followed by calcination and was characterized by an X-ray diffractometer, field emission scanning electron microscopy and energy dispersive X-ray spectroscopy, Fourier transform infrared spectroscopy, and Raman spectrometry techniques. The affecting parameters in the adsorption and desorption steps were assessed and optimized via response surface methodology. Following desorption with dichloromethane, the OPPs were quantified by gas chromatography along with ion mobility spectrometry detection. Under optimized conditions, the limits of detection were 1.00, 0.46 and 0.85μgL-1 for fenthion, malathion and chlorpyrifos, respectively. Response is linear in the concentration range of 2-500μgL-1 for fenthion and malathion, and 2-1000μgL-1 for chlorpyrifos with the determination coefficient larger than 0.9969. The intra-day and inter-day precision were from 3 to 9% and 5 to 16%, respectively. The enrichment factor was greater than 142 for all the studied pesticides. The sorbent was used for analyze spiked water and vegetable samples and gave relative recovery higher than 82%. Graphical abstract A flowchart of the synthesis of porous magnetized carbon sheet nanocomposites and the process of the magnetic dispersive solid-phase microextraction (MD-μ-SPE) of three organophosphorus pesticides prior to analysis by gas chromatography-ion mobility spectrometry (GC-IMS).

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.