scholarly journals Comparing study of CuO synthesized by biological and electrochemical methods for biological activity

2019 ◽  
Vol 30 (1) ◽  
pp. 94 ◽  
Author(s):  
Shaimaa Hamed Jaber

In the present work, copper oxide (CuO) nanoparticles have been synthesized by two methods (electro chemical and biological method).The synthesized nanoparticles characterized by x-ray diffraction (XRD), Scanning Electron Microscopy(SEM) and transmission Electron Microscopy(TEM). results show that to copper oxide (CuO) nanoparticle have average size of (11-15)nm of electrochemical method and (6-12 ) nm of biological method by different technique CuO nanoparticles were applied to study the inhibition of bacterial using (staphylococcus and pseudomonas). The antibacterial activity of CuO nanoparticles show a higher inhibition of pseudomonas bacteria when a compared with staphylococcus bacteria.

2011 ◽  
Vol 47 (1) ◽  
pp. 73-78 ◽  
Author(s):  
E. Darezereshki ◽  
F. Bakhtiari

In this study CuO nanoparticles were prepared via direct thermal decomposition method using basic copper sulphates as wet chemically synthesized precursor which was calcined in air at 750?C for 2h. Samples were characterized by thermogravimetric (TG-DSC), X-ray diffraction (XRD), energy dispersive spectroscopy (EDS), infrared spectrum (IR), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The XRD, EDS, and IR results indicated that the synthesized CuO particles were pure. The SEM and TEM results showed that the CuO nanoparticles were of approximate spherical shape, and 170?5 nm in size. Using this method, Cuo nanoparticles could be produced without using organic solvent, expensive raw materials, and complicated equipment.


Nanomaterials ◽  
2019 ◽  
Vol 9 (7) ◽  
pp. 999
Author(s):  
Yi-An Chen ◽  
Kuo-Hsien Chou ◽  
Yi-Yang Kuo ◽  
Cheng-Ye Wu ◽  
Po-Wen Hsiao ◽  
...  

To the best of our knowledge, this report presents, for the first time, the schematic of the possible chemical reaction for a one-pot synthesis of Zn0.5Cd0.5Se alloy quantum dots (QDs) in the presence of low/high oleylamine (OLA) contents. For high OLA contents, high-resolution transmission electron microscopy (HRTEM) results showed that the average size of Zn0.5Cd0.5Se increases significantly from 4 to 9 nm with an increasing OLA content from 4 to 10 mL. First, [Zn(OAc)2]–OLA complex can be formed by a reaction between Zn(OAc)2 and OLA. Then, Fourier transform infrared (FTIR) spectroscopy and X-ray diffraction (XRD) data confirmed that ZnO is formed by thermal decomposition of the [Zn(OAc)2]–OLA complex. The results indicated that ZnO grew on the Zn0.5Cd0.5Se surface, thus increasing the particle size. For low OLA contents, HRTEM images were used to estimate the average sizes of the Zn0.5Cd0.5Se alloy QDs, which were approximately 8, 6, and 4 nm with OLA loadings of 0, 2, and 4 mL, respectively. We found that Zn(OAc)2 and OLA could form a [Zn(OAc)2]–OLA complex, which inhibited the growth of the Zn0.5Cd0.5Se alloy QDs, due to the decreasing reaction between Zn(oleic acid)2 and Se2−, which led to a decrease in particle size.


2014 ◽  
Vol 2014 ◽  
pp. 1-4 ◽  
Author(s):  
Fei Long ◽  
Shuyi Mo ◽  
Yan Zeng ◽  
Shangsen Chi ◽  
Zhengguang Zou

Flower-like Cu2ZnSnS4(CZTS) nanoflakes were synthesized by a facile and fast one-pot solution reaction using copper(II) acetate monohydrate, zinc acetate dihydrate, tin(IV) chloride pentahydrate, and thiourea as starting materials. The as-synthesized samples were characterized by X-ray diffraction (XRD), Raman scattering analysis, field emission scanning electron microscopy (FESEM) equipped with an energy dispersion X-ray spectrometer (EDS), transmission electron microscopy (TEM), and UV-Vis absorption spectra. The XRD patterns shown that the as-synthesized particles were kesterite CZTS and Raman scattering analysis and EDS confirmed that kesterite CZTS was the only phase of product. The results of FESEM and TEM show that the as-synthesized particles were flower-like morphology with the average size of 1~2 μm which are composed of 50 nm thick nanoflakes. UV-Vis absorption spectrum revealed CZTS nanoflakes with a direct band gap of 1.52 eV.


2019 ◽  
Vol 288 ◽  
pp. 140-147 ◽  
Author(s):  
Andrey V. Nomoev ◽  
Erzhena C. Khartaeva ◽  
Natalia V. Yumozhapova ◽  
Tumen G. Darmaev ◽  
S.P. Bardakhanov ◽  
...  

The copper nanoparticles were obtained by evaporating the metal by the relativistic electron beam. The average size of synthesized particles was about 120 nm. They were characterized by X-ray diffraction, transmission electron microscopy. The results of the X-ray diffraction showed high content of the pure copper for closed setup with an inert gas. Transmission electron microscopy cleared some particles to have an icosahedral structure. These nanoparticles were obtained when the target was exposed by the beam with the highest current strength used in the experiment and the highest cooling of the copper vapor. The process of copper nanoparticle formation by the molecular dynamic method using EAM – potentials (potentials in the Embedded Atom Method form) was studied.


2011 ◽  
Vol 52-54 ◽  
pp. 1884-1889 ◽  
Author(s):  
Dariush Jafar Khadem ◽  
Zahira Yaakob ◽  
Samaneh Shahgaldi ◽  
Wan Ramli Wan Daud ◽  
Edy Herianto Majlan

Metal and Metal oxide nanofibers have different potential to play an essential role in a series of application, among them copper and copper oxide nanostructures is a promising semiconductor material with potential applications in many field. In this paper, electrospinning method via sol-gel was used to fabricate copper and copper oxide nanofibers. Synthesize of copper and copper oxide nanofibers and also effect of calcinations temperature on morphology investigated by thermal gravimetric analysis, scanning electron microscopy (SEM), Transmission electron microscopy, x-ray diffraction(XRD), Fourier transform infrared spectroscopy (FTIR) and Brunauer Emmett and Teller (BET).


Author(s):  
С.С. Подсухина ◽  
А.В. Козинкин ◽  
В.Г. Власенко ◽  
Г.Ю. Юрков ◽  
О.В. Попков

The composition, electronic and atomic structure of palladium nanoparticles stabilized in high pressure polyethylene (with palladium concentrations of 10 and 20 mass%) were studied by transmission electron microscopy, X-ray diffraction, and X-ray absorption spectroscopy. It was found that nanoparticles consist of metal (Pd) and oxide (Pd2O3) components, and their average size and coordination numbers for first Pd coordination sphere decrease(from 7 to 6 nm and from 7 to 5.7, respectively) with a decrease in metal concentration.


2014 ◽  
Vol 2014 ◽  
pp. 1-5 ◽  
Author(s):  
Nittaya Tamaekong ◽  
Chaikarn Liewhiran ◽  
Sukon Phanichphant

Copper oxide (CuO) nanoparticles were successfully synthesized by a thermal method. The CuO nanoparticles were further characterized by thermogravimetric analysis (TGA), differential thermal analysis (DTA), X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray spectrometry (EDS), and high resolution transmission electron microscopy (HRTEM), respectively. The specific surface area (SSABET) of CuO nanoparticles was determined by nitrogen adsorption. TheSSABETwas found to be 99.67 m2/g (dBETof 9.5 nm). The average diameter of the spherical CuO nanoparticles was approximately 6–9 nm.


2021 ◽  
Author(s):  
Ruifei Qin ◽  
lina liu

Abstract Multifunctional Fe3O4/Eu(DBM)3phen/PVP ((DBM: dibenzoylmethane, phen: 1,10-phenanthroline, PVP: polyvinyl pyrrolidone) microfibers were constructed by simple electrospinning process. The structure and morphology of the microfibers were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM) images. The diameters of pure PVP microfibers and the microfibers doped only with Fe3O4 nanoparticles (NPs) were uniformly distributed, with an average size of about 360 nm. When 3% Eu(DBM)3phen complex and Fe3O4 NPs were both added to the precursor for electrospinning, the microfibers became very inhomogeneous in diameter. The photoluminescent properties of pure Eu(DBM)3phen complex and composite microfibers were also studied. The characteristic emission peaks of Eu3+ appeared in the composite microfibers. The intensities of emission and excitation spectra gradually decrease with adding more Fe3O4 NPs. The unit mass of the pure europium complex in some composite microfibers gave stronger luminescence than the pure europium complex. The fluorescence lifetime of 5D0 state in the composite microfibers is longer than that of pure europium complex. Additionally, the magnetic properties of Fe3O4 NPs and the composite microfibers were investigated. Fe3O4 NPs and composite microfibers were both superparamagnetic. The saturation magnetization of the composite microfibers was smaller than that of pure Fe3O4 NPs.


2015 ◽  
Vol 2015 ◽  
pp. 1-9 ◽  
Author(s):  
Héctor Guillén-Bonilla ◽  
Lorenzo Gildo-Ortiz ◽  
M. de la L. Olvera-Amador ◽  
Jaime Santoyo-Salazar ◽  
Verónica M. Rodríguez-Betancourtt ◽  
...  

Mesoporous CoSb2O6nanoparticles, synthesized through a nonaqueous method (using cobalt nitrate, antimony trichloride, ethylenediamine, and ethanol as a solvent), were tested to establish their sensitivity to CO and C3H8atmospheres at relatively low temperatures. The precursor material was dried at 200°C and calcined at 600°C. X-ray diffraction and scanning electron microscopy were employed to verify the existence of crystal phases (P42/mnm) and the morphology of this trirutile-type CoSb2O6oxide. Pyramidal and cubic shaped crystals (average size: 41.1 nm), embedded in the material’s surface, were identified. Mesopores (average size: 6.5 nm) on the nanoparticles’ surface were observed by means of transmission electron microscopy. The best sensitivity of the CoSb2O6in a CO atmosphere was at the relatively low temperatures of 250 and 350°C, whereas, in a C3H8atmosphere, the sensitivity increased uniformly with temperature. These results encourage using the CoSb2O6nanoparticles as gas sensors.


2020 ◽  
Vol 10 ◽  
pp. 184798042096169
Author(s):  
Periasamy Anbu ◽  
Subash CB Gopinath ◽  
S Jayanthi

Gold nanoparticles have many applications in the biomedical field, mainly for drug delivery, cancer therapy, and detection of pathogenic microorganisms. In this study, gold nanoparticles synthesized using Platycodon grandiflorum (Balloon flower plant) extracts were evaluated for their antibacterial potential. Gold nanoparticles were synthesized at 20–50°C using different volumes of the leaf extract. Biosynthesis of gold nanoparticles was confirmed by ultraviolet–visible spectral absorption at 545 nm by surface plasmon resonance. The morphology and size of the P. grandiflorum gold nanoparticles were further characterized as spherical in shape with an average size of 15 nm in diameter by scanning electron microscopy and transmission electron microscopy. Energy-dispersive X-ray analysis clearly displayed the presence of gold particles. The structural analysis results with face central cubic crystalline nature and elemental composition, including gold, were confirmed by X-ray diffraction and X-ray photoelectron spectroscopy, respectively. In addition, Fourier transform infrared results identified the functional group in P. grandiflorum that is involved in the reduction of metal ions to gold nanoparticles. The synthesized P. grandiflorum gold nanoparticles exhibited efficient antibacterial activity against Escherichia coli (16 mm) and Bacillus subtilis (11 mm). This report confirms the synthesis of gold nanoparticle from balloon flower plant extracts, which can be used as a reducing and stabilizing agent and demonstrates its antibacterial applications.


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