November 23, 2024

Mahboube Shirani

Academic rank: Associate professor
Address: Jiroft, km 8 Bandar Abbas Road, University Of Jiroft
Education: PhD. in Analytical Chemistry
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Faculty:

Research

Title
Reduced graphene oxide decorated NiCo2(OH)6 nanoflowers for vortexed assisted dispersive μ-solid-phase extraction of organophosphorus pesticides in baby food cereal, rice and wheat flour
Type Article
Keywords
Reduced graphene oxide NiCo2(OH)6 nanoflowers Vortexed assisted Dispersive μ-solid-phase organophosphorus pesticides Baby food cereal Rice flour Wheat flour
Researchers Mahboube Shirani, Mahboobe Amiranipoor, Ozgur Ozalp, Mandegar Ghaffari, Mustafa Soylak

Abstract

Food safety is an important issue to protect humane health and improve the life quality. Hence, analysis of the possible contaminants in food samples is essential. A rapid and efficient vortexed-assisted dispersive μ-solidphase extraction coupled with gas chromatography-mass spectrometry was proposed for simultaneous separation/ preconcentration and determination of five commonly used organophosphorus pesticides. Reduced graphene oxide decorated NiCo2(OH)6 nanoflowers as a novel nanostructure was synthetized and introduced for separation of the target pesticides from the wheat flour, rice flour, and baby food cereal samples. The characterization of the nanoflowers was accomplished by SEM-EDX, XRD, and FT-IR techniques. The main factors including pH, the amount of nanoflower, the volume of sample solution, salt concentration (ionic strength), desorption conditions (i.e. desorption solvent type and volume, and desorption time) on the pesticides extraction efficiencies were inquired using matrixed match method. Applying the optimum conditions, the linearity of 0.100–500.000 μg kg􀀀 1, LODs and LOQs in the range of 0.03–0.04 μg kg􀀀 1 and 0.1 μg kg􀀀 1 for the studied food samples were obtained. The repeatability (intra–day precision (n = 5)) of ≤ 2.0 % and reproducibility (inter–day precision, days = 5, n = 3) of ≤3.1 % and were appraise at three concentration levels (10, 50 and 100 μg kg􀀀 1 of each analyte). High relative recoveries of 90.0–99.3 % ascertained high potential of the presented method for complex matrix analysis