Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/2565
Title: INVESTIGATIONS ON METAL AG AU METAL OXIDES ZNO CUO NANOPARTICLES INCORPORATED ON CHITOSAN BLENDED REDUCED GRAPHENE OXIDE NANOCOMPOSITES FOR ELECTROCHEMICAL SENSING OF P AMINOPHENOL AND ANTIBACTERIAL AND ANTICANCER APPLICATIONS
Authors: Yuvashree S
Balavijayalakshmi J
Keywords: Physical Sciences
Physics
Physics Applied
Issue Date: 2019
Abstract: Graphene, a thin planar sheet of sp 2 hybridized carbon atoms has created a revolution over the past few decades in materials science and technology since from its invention. Owing to its excellent mixture of physical and chemical properties, it becomes a potential candidate in many interesting research areas such as supercapacitors, batteries, solar cells, nanoelectronics, metal oxides, functional nanocomposites, sensing, catalysis etc. Recently, efforts have been made to develop technologically feasible graphene-based devices. The development of composite materials based on graphene and natural polymers provide an ideal material in the biomedical field. However, the lack of good mechanical and thermal properties limits its applications. This drawback could be overcome by the reduction of graphene oxide into reduced graphene oxide (rGO). The rGO combined with the polymer helps to increase the adsorption of nanocomposites which thereby enhances the properties of the material to suit commercial applications. In addition to these, metal and metal oxide nanoparticles are decorated on the surface of polymer blended reduced graphene oxide that enhances the conductivity of hybrid nanocomposites. This present research is focused on the development of simple hybrid nanocomposites for the electrochemical determination of p-Aminophenol and biological applications. The metal and metal oxides nanoparticles ensembled on chitosan blended reduced graphene oide nanocomposites are synthesized by chemical reduction method. The as synthesized nanocomposites are analyzed through an assortment of characterization to investigate their structural, morphological, and electrocatalytic properties along with their biological applications. The graphene oxide is synthesized by modified Hummer’s method and the chitosan functionalized reduced graphene oxide is synthesized by chemical reduction method. The structural, spectral, morphological and elemental studies of the synthesized nanocomposites are characterized by X-ray powder diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), Scanning Electron Microscopy (SEM) and Energy Dispersive X-Ray Analysis (EDAX). XRD analysis reveals that the small diffraction peak at 10.3 ○ corresponds to the plane of chitosan iand the broadening of the peak at 24 o may be due to the amorphous nature of chitosan. The band at 1640 cm −1 corresponds to the NHCO stretching vibrations of amine groups of chitosan. The surface morphology of rGO/CS nanocomposites reveals that the formation of white patches on the surface of flat wrinkled leaf like structure of rGO. The electro-chemical behaviour for the prepared GO and rGO/CS nanocomposites is investigated using cyclic voltammetry. The rGO/CS nanocomposites exhibits high redox peak current for p-AP compared to GO modified GCE. The various concentrations of (0.002M, 0.004M, 0.006M, 0.008M and 0.01M) zinc nanoparticles embedded on chitosan blened reduced graphene oxide nanocomposites are synthesized by chemical reduction method. The nanocomposites are characterized using XRD, FT-IR, SEM, EDAX, HR-TEM and SAED analysis. The XRD pattern of rGO/CS/ZnO nanocomposites shows the hexagonal wurtzite phase of ZnO and the crystallite size is found to be about 27.3 nm, 33.4 nm and 34.9 nm. The surface morphological analysis reveals that the rod shaped ZnO nanoparticles found to be homogeneously distributed on the surface of rough, thin, wrinkled reduced graphene oxide/chitosan nanosheets. EDAX analysis reveals the presence of carbon, oxygen and zinc without any impurities that further confirms the formation of rGO/CS/ZnO nanocomposites. The electrochemical behaviour of rGO/CS/ZnO nanocomposite towards the detection of p-AP at the modified glassy carbon electrode is studied using cyclic voltammetry. The maximum redox peak current is observed to be 0.06μA for pH 7 of 0.008M of rGO/CS/ZnO nanocomposite with a wide linear range of detection about 10μM to 180μM. This is due to its uniform dispersion of ZnO nanoparticles on the large surface area of rGO/CS, leads to good electron transfer rate between p-AP and rGO/CS/ZnO nanocomposite modified GCE. The various concentrations of (0.002M, 0.004M, 0.006M, 0.008M and 0.01M) copper oxide decorated chitosan blended reduced graphene oxide are synthesized by a facile chemical reduction method. The prepared nanocomposites are characterized by XRD, FT-IR, SEM, EDAX, HR-TEM and SAED analysis. The XRD analysis reveals that the crystallite size of copper oxide nanoparticles is in the iirange from 9.16 nm to 18.5 nm. SEM and HR-TEM analysis reveals that the spherical shaped copper oxide nanoparticles well dispersed on to the chitosan blended rGO nanosheets. Elemental analysis reveals the presence of carbon, oxygen and copper without any impurities. Under optimized conditions, the maximum redox peak current is 0.18μA for pH 5 of 0.008M of rGO/CS/CuO nanocomposite and the linear range of detection about 60μM to 150μM. The incorporation of silver nanoparticles onto the chitosan blened reduced graphene oxide nanocomposites are synthesized by chemical reduction method. The influence of various concentrations of (0.002 M, 0.004 M, 0.006 M, 0.008 M and 0.01 M) of silver nanoparticles on the surface of rGO/CS nanocomposites is investigated using FT-IR, XRD, SEM, HR-TEM and SAED analysis. XRD analysis reveals that the rGO/CS/Ag nanocomposites are well crystallized and the crystallite size is found to be about 23.6 nm. The band formed around 596 cm −1 confirms the formation of Ag nanoparticles on the surface of rGO/CS. The surface morphology analysis reveals that the spherical shaped Ag nanopartices are well dispersed on the surface of rGO/CS sheets. The electrochemical property of prepared rGO/CS/Ag nanocomposites is investigated using cyclic voltammetry. The electrochemical behaviour reveals that the large effective surface area of the prepared nanocomposites allows it to function as an electron transfer medium and enhances the charge transfer rate. The decoration of various concentrations of (0.002 M, 0.004 M, 0.006 M, 0.008 M and 0.01 M) of gold nanoparticles on the surface of rGO/CS/Au nanocomposites synthesized by chemical reduction method and investigated using FT-IR, XRD, SEM, HR-TEM and SAED analysis. The interaction of functional groups between rGO, CS and Au is confirmed using FT-IR analysis. It reveals that the band formed around 586 cm -1 corresponds to the stretching of metallic vibrations. XRD reveals that the nanocomposites are of high crystalline in nature with the crystallite size of about 8.9 nm to 16.5 nm. SEM and HRTEM analysis confirms that the spherical shaped gold nanoparticles are closely anchored onto the surface of rGO/CS nanosheets. EDAX analysis confirms the presence of carbon, oxygen and gold in the prepared nanocomposites. The electrochemical behaviour iiireveals that 0.006M of rGO/CS/Au nanocomposites has shown prominent electrochemical behavior towards the detection of p-aminophenol. The prepared nanocomposites are tested for antibacterial and anticancer activity. The antibacterial activity is done against Gram-positive (B. subtilis and S. aureus) and Gram-negative (E.coli and K. pneumoniae) using disc diffusion technique. The cytotoxicity effect is studied against Human hepatocarcinoma (HepG–2) cell lines. The prepared nanocomposite shows the reduction in cell viability by dose-dependent manner. These results attest an efficacy as a substantial material for the treatment of HepG–2 cancer cell lines. Hence the prepared nanocomposites may be applied in biomedical field. In summary, prepared rGO/CS/ZnO, rGO/CS/CuO, rGO/CS/Ag and rGO/CS/Au show an excellent electrocatalytic activity which acts as a good electrode material and can be applied in environment for the detection of p- Aminophenol. Moreover, the nanocomposites show outstanding bactericidal activity and antiproliferative activity that can be potentially applied in biomedical field.
URI: http://localhost:8080/xmlui/handle/123456789/2565
Appears in Collections:Department of Physics

Files in This Item:
File Description SizeFormat 
01_title (1).pdf59.3 kBAdobe PDFView/Open
02_certificate.pdf143.99 kBAdobe PDFView/Open
03_preliminary pages.pdf344.49 kBAdobe PDFView/Open
04_chapter1.pdf1.69 MBAdobe PDFView/Open
05_chapter2.pdf593.46 kBAdobe PDFView/Open
06_chapter3.pdf881.73 kBAdobe PDFView/Open
07_chapter4.pdf1.06 MBAdobe PDFView/Open
08_chapter5.pdf1.18 MBAdobe PDFView/Open
09_chapter6.pdf1.07 MBAdobe PDFView/Open
10_chapter7.pdf1.42 MBAdobe PDFView/Open
11_chapter8.pdf105.13 kBAdobe PDFView/Open
80_recommendation.pdf164.53 kBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.