scholarly journals Antibacterial Shoe Insole-Coated CuO-ZnO Nanocomposite Synthesized by the Sol-Gel Technique

2020 ◽  
Vol 2020 ◽  
pp. 1-13
Author(s):  
Nguyen Lam Uyen Vo ◽  
Thi Thuy Van Nguyen ◽  
Tri Nguyen ◽  
Phung Anh Nguyen ◽  
Van Minh Nguyen ◽  
...  

In this study, CuO-ZnO composite was synthesized via the sol-gel method using oxalic acid to form the medium complex and its applications in antibacterial have been conducted with B. cereus, E. coli, S. aureus, Salmonella, and P. aeruginosa. Then, nanopowder of CuO-ZnO was coated on shoe insoles and their antibacterial effect with S. aureus was tested. The nanocomposite products were characterized by XRD, XPS, SEM, TEM, and UV-Vis. The results showed that the CuO-ZnO composite has the average particle size in a range of 20-50 nm, the point of zero charge of 7.8, and the bandgap of 1.7 eV. XPS result shows the composite structure with Cu2+ in the product. The minimum inhibitory concentration (MIC) of CuO-ZnO nanocomposite was 0.313 mg·mL-1 for S. aureus and Samonella, 0.625 mg·mL-1 for E. coli, and 5 mg·mL-1 for B. cereus and P. aeruginosa. The shoe insoles coated with 0.35 wt.% of CuO-ZnO nanocomposite also had high antibacterial activity against S. aureus, and this antibacterial nanocomposite was implanted durably on the surface of the shoe insoles.

1998 ◽  
Vol 519 ◽  
Author(s):  
Francisco Del Monte ◽  
Yuhuan Xu ◽  
John D. Mackenzie ◽  
B. Claflin ◽  
G. Lucovsky

AbstractSemiconductor PbS quantum dot-doped Ormocers were successfully prepared by the sol-gel technique. Ormocers preparation was based on the use of trifunctional silane precursors at the solution stage. Formation of PbS particles took place in the pores of the Ormocers through lead precursor reaction with H2S gas. It was observed that temperature was an important factor in the reaction leading to the first appearance of PbS particles. The dot size of PbS was controlled through chemical interaction with the non-hydrolyzed groups of the trifunctional silane precursors. These groups prevent uncontrolled nucleation and aggregation processes during the particle formation and growth. The control of particle size was studied at different conditions for nucleation and aggregation. Determination of the average particle size was done by XR-Diffraction. Optical absorption spectra were also measured at the UV-VIS wavelength range. Absorption edge blue shifts show the quantum confinement effect in these materials.


2016 ◽  
Vol 15 (05n06) ◽  
pp. 1660002 ◽  
Author(s):  
V. Kavitha ◽  
P. S. Ramesh ◽  
D. Geetha

Copper doped Titanium dioxide TiO2 nanoparticles were synthesized by sol–gel method using titanium tetraisopropoxide and copper sulfate as precursors. The synthesized nanoparticles were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), Scanning electron microscopy (SEM), UV-Visible spectroscopy (UV-Vis), Photoluminesce spectroscopy (PL) and atomic force microscopy (AFM). XRD analysis confirms the formation of anatase titanium dioxide and average particle size was 35[Formula: see text]nm. Cu– TiO2 exhibits a shift in the absorption edge toward visible spectrum. The rate of recombination and transfer behavior of the photoexcited electron–hole pairs in the semiconductors was recorded by photoluminescence. From SEM spherical shaped nanoparticles was observed. Comparing with pure TiO2 nanoparticles, Cu doped TiO2 photocatalyst exhibited enhanced photocatalytic activity under natural sunlight irradiation in the decomposition of rhodamine B aqueous solution. The maximum 97% of degradation efficiency of Rhodamine B was observed at 0.6% Cu–TiO2 within 180[Formula: see text]min. The photocatalytic efficiency of Rhodamine B of Cu doped TiO2 nanoparticle was higher than the pure TiO2, which could be attributed to the small crystallinity intense light absorption in Sunlight and narrow bandgap energy of Copper.


2021 ◽  
Author(s):  
Mahesh Gaidhane ◽  
Deepak Taikar ◽  
Pravin Gaidhane ◽  
Kalpana Nagde

Abstract Nanocrystalline α-Fe2O3 is synthesized by sol-gel technique. The prepared nanomaterial was characterized by X-ray diffraction (XRD), SEM, TEM, Fourier Transform Infrared (FTIR) spectroscopy, Vibrating Sample Magnetometry (VSM) and photoluminescence (PL) techniques. X-ray powder diffraction analysis confirmed the formation of α-Fe2O3. Electron microscopy showed spherical morphologies with an average particle size of 30-40 nm. The magnetic property of the prepared material was studied by VSM at room temperature. VSM study shows superparamagnetic nature of the synthesized nanoparticles. Photoluminescence (PL) emission spectra show intense broad emission band centered at 570 nm with 393 nm excitation indicating its usefulness for w-LED application. The CIE-chromaticity color coordinates of prepared material were calculated. The photocatalytic activity of the α-Fe2O3 nanoparticles was analyzed and the nanopowder exhibited good photocatalytic activity for the removal AO7 from its aqueous solution.


2017 ◽  
Vol 17 (01n02) ◽  
pp. 1760012
Author(s):  
S. Gowreesan ◽  
A. Ruban Kumar

The scope of the present work is in enhancing the particle size, and dielectric properties of Mg-substituted Cobalt ferrites nanoparticles prepared by sol–gel auto combustion method. The different ratios of Mg-substituted Co Ferrites (Co[Formula: see text]MgxFe2O4([Formula: see text], 0.05, 0.10, 0.15, 0.20 and 0.30)) are calcinated at 850[Formula: see text]C. The synthesized nanoparticles were characterized by powder XRD, FTIR, FE-SEM, EDX techniques and dielectric behavior. The structural parameters were confirmed from powder XRD and the average particle size is obtained from 39 to 67 nm due to the substitution of Mg[Formula: see text] which was calculated by Debye Scherrer’s formula. FE-SEM showed the surface morphology of the different ratio of the sample. The dielectric loss has measured the frequency range of 50[Formula: see text]Hz–5[Formula: see text]MHz. From electrical modulus, conductivity relaxation and thermal activation of charge carriers has been discussed.


2006 ◽  
Vol 510-511 ◽  
pp. 786-789 ◽  
Author(s):  
Dong Sik Bae ◽  
Byung Ik Kim ◽  
Kyong Sop Han

ZnO-TiO2 nanoparticles were synthesized by a reverse micelle and sol-gel process. The average particle size of the colloid was below 30 nm and well dispersed in the solution. ZnOTiO2 composite membranes were fabricated by using the dip-coating method on a porous alumina support. ZnO-TiO2 composite membranes showed a crack-free microstructure and narrow particle size distribution even after the heat treatment up to 600°C. The average particle size of the membrane was 30-40nm, and the pore size of ZnO-TiO2 composite membrane was below 10 nm.


2018 ◽  
Vol 762 ◽  
pp. 408-412
Author(s):  
Raivis Eglītis ◽  
Gundars Mežinskis

In this work two different hydrosols were used to impregnate a commercially available cotton fabric with anatase nanoparticles to give it photocatalytic activity. To increase the activity, different pre-treatment methods were applied. The nanoparticle size was determined using dynamic light scattering and x-ray diffraction and the fabrics were examined using scanning electron microscopy. Photocatalytic activity was measured using the degradation of methyl-orange while irradiating the samples with UV light. The synthesis method allowed to produce anatase with an average particle size of 32 to 37 nm depending on the synthesis method used.


2019 ◽  
Vol 2019 ◽  
pp. 1-7 ◽  
Author(s):  
George Fedorenko ◽  
Ludmila Oleksenko ◽  
Nelly Maksymovych

Nanosized tin dioxide with an average particle size of 5.3 nm was synthesized by a sol-gel method and characterized by IR spectroscopy, TEM, X-ray, and electron diffraction. The obtained SnO2 can be used as initial material for creation of gas-sensitive layers of adsorption semiconductor sensors. Addition of palladium into the initial nanomaterial allows to improve response to hydrogen of such sensors in comparison with sensors based on undoped SnO2 and provides fast response and recovery time, a wide measuring range of hydrogen content in air ambient, and good repeatability of the sensor signal. Such promising properties could make useful the sensors based on these nanomaterials for devices intended to determine hydrogen in air.


2016 ◽  
Vol 709 ◽  
pp. 66-69
Author(s):  
Jeyashelly Andas ◽  
Rahmah Atikah Rosdi ◽  
Nur Izzati Mohd Anuar

A series of Fe-Co nanoparticles were synthesized via sol-gel route at acidic, neutral and basic condition using rice husk as the silica source. The synthesized nanomaterials were designated as Fe-Co3, Fe-Co7 and Fe-Co9 and characterized by Fourier Transform Infrared (FTIR), Transmission Electron Microscope (TEM) and particle size analyzer. The great effect of pH was clearly evidenced from the shifting in the siloxane bond in the FTIR spectrum. TEM investigation confirmed the existence of discrete and almost sphere like nanoparticles. The particle size decreased with an increase in the pH, registering the smallest average particle size at pH 9. In brief, this study promises a fast, rapid and promising method for the conversion of silica rice husk into nanoscale bimetallic materials.


2011 ◽  
Vol 266 ◽  
pp. 76-79
Author(s):  
Yu Wang ◽  
Xiao Lin Jia ◽  
Lin Dong ◽  
Shao Kang Guan

SnO2 nanoparticles were prepared via a sol-gel method by heating the mixture of hydrous SnO2 nanoparticles and SiO2 nanospheres at 600 °C. The average particle size of the obtained SnO2 nanoparticles is 3.3 nm, smaller than that of the SnO2 nanoparticles (~ 6.4 nm) prepared by calcining the pure hydrous SnO2 at 600 °C. The SiO2 nanospheres play an important role in restricting SnO2 nanocrystal growth. The ~3.3 nm-sized SnO2 nanoparticles exhibited high sensitivity for ethanol as well as quick response and recovery time. The concentration detection limit can be as low as 5 ppm at room temperature.


2010 ◽  
Vol 152-153 ◽  
pp. 81-85
Author(s):  
Xiong Wang ◽  
Yin Lin ◽  
Jin Guo Jiang

The homogeneous multiferroic BiFeO3 nanoparticles with average particle size of 85 nm have been successfully synthesized by a simple sol-gel route. The prepared sample was characterized by a variety of techniques, such as X-ray diffractometry, thermogravimetric analysis and differential thermal analysis, differential scanning calorimeter analysis, scanning electron microscopy, transmission electron microscopy and X-ray photoelectron spectroscopy. The obtained results shows that rapid sintering and subsequently quenching to room temperature are the two vital important factors for the preparation of pure BiFeO3. The magnetic phase transition (TN = 369 °C) and the ferroelectric phase transition (TC = 824.5 °C) were determined, revealing the antiferromagnetic and ferroelectric nature of the as-prepared BiFeO3 nanoparticles. The optical properties of the nanopowders were investigated. The strong band-gap absorption at 486 nm (2.55 eV) of the BiFeO3 nanoparticles may bring some novel applications.


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