Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/46756
Title: A novel paraoxon imprinted electrochemical sensor based on MoS(2)NPs@MWCNTs and its application to tap water samples
Authors: Bolukbasi, Omer Saltuk
Yola, Bahar Bankoglu
Boyacioglu, Havva
Yola, Mehmet Lutfi
Keywords: Paraoxon
Paraoxon
Molecularly imprinting
Molecularly imprinting
Voltammetry
Voltammetry
Nanocomposite
Nanocomposite
Food safety
Food safety
Carbon Nanotubes
Carbon Nanotubes
Glassy-Carbon
Glassy-Carbon
Organophosphate Pesticides
Organophosphate Pesticides
Graphene Analog
Graphene Analog
Mos2
Mos2
Electrode
Electrode
Nanocomposite
Nanocomposite
Nanoparticles
Nanoparticles
Metabolites
Metabolites
Composites
Composites
Publisher: Pergamon-Elsevier Science Ltd
Abstract: Organophosphorus pesticides are widely utilized in agricultural fertility. However, their long-term accumulations result in serious damage to human health and ecological balance. Paraoxon (PAR) can block acetylcholinesterase in the human body, resulting in death. Thus, in this study, a molecularly imprinted electrochemical PAR sensor based on multiwalled carbon nanotubes (MWCNTs)/molybdenum disulfide nanoparticles (MoS(2)NPs) nanocomposite (MoS(2)NPs@MWCNTs) was proposed for selective tap water determination. A hydrothermal fabrication approach was firstly implemented to prepare MoS(2)NPs@MWCNTs nanocomposite. Afterwards, the formation of PAR imprinted electrochemical electrode was performed on nanocomposite modified glassy carbon electrode (GCE) in presence of PAR as template and pyrrole (Py) as a monomer by cyclic voltammetry (CV) technique. Just after determining the physicochemical features of as-fabricated nanostructures by scanning electron microscopy (SEM), transmission electron microscopy (TEM), x-ray diffraction (XRD), Raman spectros-copy, and atomic force microscopy (AFM), the electrochemical behavior of the fabricated sensors was deter-mined through CV, differential pulse voltammetry (DPV), and electrochemical impedance spectroscopy (EIS). The suggested imprinted electrode provided the acceptable limit of quantification (LOQ) and limit of detection (LOD) values of 1.0 x 10(-11) M, and 2.0 x 10(-12) M, respectively. As a consequence, the proposed PAR imprinted electrochemical sensor can be offered for the determining safe tap water and its utility.
Organophosphorus pesticides are widely utilized in agricultural fertility. However, their long-term accumulations result in serious damage to human health and ecological balance. Paraoxon (PAR) can block acetylcholinesterase in the human body, resulting in death. Thus, in this study, a molecularly imprinted electrochemical PAR sensor based on multiwalled carbon nanotubes (MWCNTs)/molybdenum disulfide nanoparticles (MoS(2)NPs) nanocomposite (MoS(2)NPs@MWCNTs) was proposed for selective tap water determination. A hydrothermal fabrication approach was firstly implemented to prepare MoS(2)NPs@MWCNTs nanocomposite. Afterwards, the formation of PAR imprinted electrochemical electrode was performed on nanocomposite modified glassy carbon electrode (GCE) in presence of PAR as template and pyrrole (Py) as a monomer by cyclic voltammetry (CV) technique. Just after determining the physicochemical features of as-fabricated nanostructures by scanning electron microscopy (SEM), transmission electron microscopy (TEM), x-ray diffraction (XRD), Raman spectros-copy, and atomic force microscopy (AFM), the electrochemical behavior of the fabricated sensors was deter-mined through CV, differential pulse voltammetry (DPV), and electrochemical impedance spectroscopy (EIS). The suggested imprinted electrode provided the acceptable limit of quantification (LOQ) and limit of detection (LOD) values of 1.0 x 10(-11) M, and 2.0 x 10(-12) M, respectively. As a consequence, the proposed PAR imprinted electrochemical sensor can be offered for the determining safe tap water and its utility.
URI: https://doi.org/10.1016/j.fct.2022.112994
https://hdl.handle.net/11499/46756
ISSN: 0278-6915
1873-6351
Appears in Collections:Mühendislik Fakültesi Koleksiyonu
PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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