scholarly journals Preparation, characterization and analysis of zinc oxide nano-particles using a sol-gel technique as an inhibitor for bacteria

2020 ◽  
Vol 11 (1) ◽  
pp. 747-754
Author(s):  
Saja S. Al-Taweel ◽  
Rana S. Al-Taweel ◽  
Hasan M. Luaibi

In this work, zinc oxide nanoparticles (ZnO - NPs) were prepared using a sol-gel methodology and tested for their antibacterial activity against each of the following pathogenic species: Escherichia coli, Klebsiella pneumonia, and Staphylococcus aureus by well diffusion assay. The sample prepared was characterized by different techniques: Atomic Force Microscope AFM; Fourier Transform Infrared FT-IR; Scanning Electron Microscope SEM and X-Ray Diffraction Spectroscopy XRD. The XRD result showed that ZnO - NPs presence in wurtzite the structure of ZnO. The AFM and SEM of the surface analysis indicate that the most ZnO – NPs appear approximately in a spherical shape with some agglomeration. The average particle size for  ZnO - NPs is nearly 37 nm. Volumes 25µl, 50µl, 75µl, 100µl, 125µl, and 150µl of 10 mg\ ml concentration of  ZnO - NPs were used, the antimicrobial activity results showed that ability for  ZnO - NPs to inhibit the growth of S.aureus increased as the solution volume increased, while the growing of (K. pneumonia) and (E. coli) was inhibited only with the volume 75µl where the inhibition zones diameters were 15mm and 10mm respectively.

2021 ◽  
Vol 17 (9) ◽  
pp. 1824-1829
Author(s):  
Junlin Li ◽  
Xiangfei Li ◽  
Dong Liang ◽  
Xiaojuan Zhang ◽  
Qing Lin ◽  
...  

This study exploits the potential of zinc oxide nanoparticles (ZnO-NPs) with diverse morphologies as catalysts and antibacterial agent. Spherical ZnO-NPs, rod-shaped ZnO-NPs and flower-shaped ZnO-NPs were prepared by microemulsion method, solvent heat method and hydrothermal method, respectively. The structural characterizations of samples were investigated by X-ray diffraction (XRD) and scanning electron microscopy (SEM) techniques. XRD results revealed the formation of spherical ZnO-NPs, rod-shaped ZnO-NPs and flower-shaped ZnO-NPs were all wurtzite crystal structure. SEM results showed that spherical ZnO-NPs had an average particle size of 30–40 nm, rod-shaped ZnO-NPs were about 500 nm long and 100 nm wide with obvious hexagonal crystals. Flower-shaped ZnO-NPs had a three-dimensional appearance with obvious petals. Results of electrochemical HER (Hydrogen evolution reaction) experiments revealed that spherical ZnO-NPs exhibited the highest electrocatalytic activity at the lowest potential voltage due to their largest specific surface area. The antibacterial property of ZnO-NPs samples were studied by the optical density method and disc diffusion method. All samples had antibacterial effects against E. coli. and flower-shaped ZnO-NPs showed the best antibacterial activity due to the largest surface area in comparison with spherical ZnO-NPs and rod-shaped ZnO-NPs, which promised the maximum Zn2+ release as bactericide mechanism that registered in the case of different ZnO-NPs morphologies.


2008 ◽  
Vol 8 (3) ◽  
pp. 1199-1202 ◽  
Author(s):  
Li Qing Yue ◽  
Fu Jun Zhang ◽  
Jin Zhao Huang ◽  
Li Wei Wang

The sol–gel method was used to obtain a kind of white-light emitting ZnS:Mn2+ nanoparticles capped by methacrylic acid with an average particle size of ∼7nm. The photoluminescence spectra, X-ray diffraction spectra, Fourier transform infrared reflection spectra and ultraviolet absorption spectra were used to measure their optical properties and crystal structures. The ZnS:Mn2+ nanoparticles with 0.58 wt% Mn2+ concentration emitted white light when excited by 380 nm. The PL spectrum exhibits two emission peaks under irradiation: one at 480 nm generated from the ZnS matrix, and one at 590 nm emitted by the doped Mn2+ ions. The nanoparticles will only emit white light with the optimum Mn2+ concentration (0.58 wt%). X-ray diffraction demonstrates the synthesized ZnS:Mn2+ nanoparticles have zinc blend crystal structure, and the infrared patterns of the capped ZnS:Mn2+ nanoparticles and methacrylic acid are comparable, indicating that the methacrylic polymer has capped or modified ZnS:Mn2+ nanoparticles.


2021 ◽  
Vol 39 (1B) ◽  
pp. 197-202
Author(s):  
Ghufran S. Jaber ◽  
Khawla S. Khashan ◽  
Maha J. Abbas

The effects of varying laser pulse numbers on the fabricated of ZnONPs by pulsed laser ablation in deionized water of Zn-metal are investigated. The Nd: YAG laser at energy 600mJ prepared three samples by change the laser pulse number (100, 150, and 200). The results were collected and examined using an electron scanning microscope, XRD – diffraction, and transmission electron microscope. The result revealed the colloidal spherical shape and the homogeneous composition of the ZnO NPs. The nanoparticles resulted in different concentrations and sized distributions by changing the pulse number of a laser. The average particle size and the mass concentration of particle size increase with an increasing number of laser pulses by fixed the laser energy.


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.


2014 ◽  
Vol 2014 ◽  
pp. 1-7 ◽  
Author(s):  
Malathi Sampath ◽  
Ramya Vijayan ◽  
Ezhilarasu Tamilarasu ◽  
Abiraman Tamilselvan ◽  
Balasubramanian Sengottuvelan

Novel jasmine bud-shaped copper nanoparticles were synthesized by a green chemical reduction method using polyvinylpyrrolidone (PVP) as a capping agent, L-ascorbic acid (AA) as a reducing agent as well as antioxidant agent, isonicotinic acid hydrazide (INH) as a reducing agent, and water as a solvent at 60–70°C (pH-7) in the presence of air. The UV-Vis absorption maximum obtained is 573 nm. The crystal lattice (fcc) structure of Cu Nps was confirmed by X-ray diffraction (XRD). The novel jasmine bud shape was visualized in a transmission electron microscope (TEM). The height of single copper nanobud was 6.41 nm as measured by atomic force microscope (AFM). The average particle size 6.95 nm is obtained by XRD results. Antibacterial activity of the Cu nanobuds was evaluated by testing against Gram-negative (Escherichia coli) and Gram-positive (Staphylococcus aureus) bacteria.


2011 ◽  
Vol 412 ◽  
pp. 271-274
Author(s):  
Ying Li ◽  
Qiang Xu ◽  
Ling Dai

In order to prepare ultrafine La3NbO7 powder, a potential material for thermal barrier coatings, the calcination process of La3NbO7 was studied in this paper.The precursor of La3NbO7 was synthesized by using a citric acid complex method. A calcination process had been systematically investigated. The reaction temperature was determined by differential scanning calorimetry (DSC). The phase composition of powders was characterized by X-ray diffraction (XRD), and the morphology was obtained by scanning electron microscope (SEM). The results revealed that the single-phase La3NbO7 powder could be successfully prepared while the calcination temperature exceeded 800°C and a better morphology could be maintained at 800°C for 4 hours. Considering all above, an optimum calcination scheme was adopted at 800°C for 4 hours. The as-prepared La3NbO7 powders had a grain size of about 50nm and an average particle size of about 300nm.


2006 ◽  
Vol 916 ◽  
Author(s):  
Alp Manavbasi ◽  
Jeffrey C LaCombe

AbstractTwo new blue emitting phosphors, SrZnO2:Pb2+ and Ce3+ were synthesized by adipic acid and sucrose templated sol-gel routes, respectively. The resulting phosphor particles were fine, nanocrystalline and pure. The optimum activator concentrations were found to be 1 mol% Pb2+ and 12 mol% Ce3+. Two excitation bands centered at 283 and 317 nm, plus a weak shoulder at 275 nm were observed for Pb2+ doped samples, however only one broad excitation band with a maximum at 294 nm was observed for Ce3+ doped samples fired at 1000 °C for 2h. The emission spectra of SrZnO2:Pb2+ showed a very broad band extending from 374 to 615 nm with a maximum at ~455 nm which was ascribed to the 3P1 ¡æ 1S0 transition on the Pb2+ ions allowed by the strong spin-orbit (SO) coupling. Similarly, SrZnO2:Ce3+ showed a broad emission band extending from 374 to 609 nm and centered at 467 nm. This broad emission was attributed to the 5d1 ¡æ 4f1 transition of Ce3+ ions. The lower level 2F5/2 of the 4f1 is populated but the level 2F7/2 is almost empty at room temperature where all measurements were taken. The luminescence properties of Ce3+, K+ co-doped SrZnO2 revealed that the characteristic band locations remained the same and the ratio of emission to excitation intensities were constant. X-ray diffraction patterns showed that the SrZnO2 phase started to form at 900 °C (after 2 hrs), and the single-phase SrZnO2 obtained at 1000 °C. SEM micrographs of both phosphors have a rounded and filled morphology for individual particles with an approximate diameter of 50-250 nm. Dynamic light scattering studies revealed that average particle size is around 1 ¥ìm for both phosphors.


2006 ◽  
Vol 45 ◽  
pp. 1803-1808 ◽  
Author(s):  
I.C. Cosentino ◽  
E.N.S. Muccillo ◽  
F.M. Vichi ◽  
R. Muccillo

Ceramic ZrTiO4 powders were prepared by a sol-gel method using zirconium oxychloride and titanium tetraisopropoxide. In situ high temperature X-ray diffraction results show that crystallization of the amorphous gel starts at 400°C. Single-phase ZrTiO4 nanoparticles of 46 nm average particle size, determined by nitrogen adsorption analysis, were obtained after heat treatment at 450°C for 1 h. After pressing these sinteractive powders, pellets with controlled pore size distribution were obtained by sintering at temperatures as low as 400°C. The analysis of pores by mercury porosimetry gives an average porosity of 45%. The electrical resistivity, determined by impedance spectroscopy measurements at 24°C under different humidity environments, shows the ability of these pellets to adsorb water vapor in the porous surfaces.


2015 ◽  
Vol 719-720 ◽  
pp. 132-136 ◽  
Author(s):  
Ghazaleh Allaedini ◽  
Siti Masrinda Tasirin ◽  
Meor Zainal Meor Talib ◽  
Payam Aminayi ◽  
Ifa Puspasari

This study presents comparisons between the morphologies and photoluminescence properties of tin oxide (SnO2) nanoparticles prepared by two methods, namely the sol gel and the co-precipitation methods. The characteristics of the particles were analyzed using X-ray diffraction (XRD), fourier transform infrared spectroscopy (FTIR), and scanning electron microscopy (SEM). The particles prepared using the sol-gel method have a finer particle size and more spherical shape. However, no significant difference was observed in terms of morphology and homogeneity in the samples produced by either the co-precipitation or sol-gel methods. In contrast, the photoluminescence study shows that the emission peak for powder prepared using the sol-gel method was higher than that of the co-precipitation method.


2014 ◽  
Vol 2014 ◽  
pp. 1-10 ◽  
Author(s):  
Fernanda Malaquias Barboza ◽  
Willian Moreira Machado ◽  
Luiz Renato Olchanheski Junior ◽  
Josiane Padilha de Paula ◽  
Sônia Faria Zawadzki ◽  
...  

Microparticles of poly(ε-caprolactone) (PCL) and poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) containing manidipine dihydrochloride (MAN) were successfully prepared by the simple emulsion/solvent evaporation method. All formulations showed loading efficiency rates greater than 80% and average particle size less than 8 μm. Formulations had spherical shape with smooth and porous surface for PCL and PHBV, respectively. According to Fourier-transform infrared spectroscopy, initial components were not chemically modified during microencapsulation. X-ray diffraction patterns and differential scanning calorimetry demonstrated that this process led to drug amorphization.In vitrodissolution studies showed that all microparticles prolonged MAN release, mainly which one obtained using PCL that contained 5% of drug loaded (PCL-M5). Animal studies demonstrated that formulationPCL-M5was able to keep the variation of mean arterial pressure after phenylephrine administration up to 24 hours. These data confirmed the sustained antihypertensive effect of the investigated microparticles. Results provided an experimental basis for using formulationPCL-M5as a feasible carrier for oral controlled release of MAN intended for treating high blood pressure.


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