scholarly journals Microwave-Assisted Combustion Synthesis of ZnO Nanoparticles

2013 ◽  
Vol 2013 ◽  
pp. 1-4 ◽  
Author(s):  
M. Kooti ◽  
A. Naghdi Sedeh
Keyword(s):  
Electron Microscopy ◽  
Zno Nanoparticles ◽  
Combustion Method ◽  
Zinc Nitrate ◽  
High Yield ◽  
Fast Method ◽  
Simple Method ◽  
X Ray ◽  
Microwave Assisted ◽  
Average Size

A new and simple method was applied for the synthesis of ZnO nanoparticles with an average size of 20 nm. In this microwave-assisted combustion method, glycine as a fuel and zinc nitrate as precursor were used. The final product was obtained very fast with high yield and purity. The synthesized nanoscale ZnO was characterized by X-ray Diffraction (XRD), Energy Dispersive X-ray spectroscopy (EDX), and Fourier transform infrared spectroscopy (FT-IR). The size and morphology of the ZnO nanoparticles have been determined by field emission scanning electron microscopy (FESEM) and transmission electron microscopy (TEM) techniques. This is a simple and fast method for the preparation of ZnO nanoparticles with no need for expensive materials or complicated treatments.

scholarly journals Biosynthesis of ZnO Micro-Nanoflower with Ananas comosus Peel Extract

2021 ◽  
Vol 10 (4) ◽  
pp. 84-87
Author(s):  
Maya Sari ◽  
Yolanda Rati ◽  
Tetty Marta Linda ◽  
Yanuar Hamzah ◽  
Ari Sulistyo Rini
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Physical Properties ◽  
Zno Nanoparticles ◽  
Zinc Nitrate ◽  
Ananas Comosus ◽  
X Ray Diffraction ◽  
X Ray ◽  
Peel Extract ◽  
Scanning Electron

 Abstrak. Dalam rangka mengurangi pemakaian bahan kimia berbahaya, kini telah mulai dikembangkan penggunaan bahan alami pada proses pembentukan nanopartikel. Pada penelitian ini, biosintesis nanopartikel ZnO dilakukan menggunakan ekstrak kulit Ananas comosus sebagai agen capping sekaligus agen pereduksi. Seng nitrat digunakan sebagai prekursor dari ion seng, sedangkan kulit nanas dibuat menjadi ekstrak untuk dimanfaatkan kandungan antioksidannya. Sampel ZnO dipelajari sifat fisisnya dari hasil karakterisasi X-ray diffraction (XRD), scanning electron microscopy (SEM) dan spektroskopi UV-Vis. Berdasarkan pola XRD, nanopartikel ZnO memberikan fasa kristal heksagonal wurtzite dengan ukuran kristal 14 nm. Morfologi SEM masing-masing sampel didapatkan berbentuk bunga atau micro-nanoflower dengan ukuran diameter rata-rata 510 nm dan 560 nm untuk sampel 0,01 M dan 0,025 M. Hasil spektrum absorbansi UV-Vis menunjukkan peningkatan puncak penyerapan cahaya dengan penambahan konsentrasi seng nitrat. Berdasarkan informasi sifat fisis ini, sampel ZnO berpotensi diaplikasikan sebagai material fotokatalis.Abstract. In order to reduce the use of hazardous chemicals, the use of natural ingredients has now been developed in the process of forming nanoparticles. In this study, biosynthesis of ZnO nanoparticles was carried out using Ananas comosus peel extract as capping agent and reducing agent. Zinc nitrate was used as a precursor to zinc ion. The physical properties of ZnO samples were studied from the characterization result of scanning electron microscopy (SEM), UV-Vis spectroscopy, and X-ray diffraction (XRD). The SEM morphology of each different sample was obtained in the form of micro-nanoflower with an average diameter  of 510 nm and 560 nm for 0.01 M and 0.025 M samples, respectively. The UV-Vis absorbance spectrum results showed an increase in the light absorption peak as  zinc nitrate concentration increased. According to the XRD pattern, the ZnO nanoparticles possessed an hexagonal wurtzite crystal phase with a crystal size of 14 nm. Based on this information on physical properties, the ZnO sample has the potential to be applied as a photocatalyst material.

Simplistic Synthesis and Enhanced Photocatalytic Performance of Spherical ZnO Nanoparticles Prepared from Arabinose Solution

2019 ◽  
Vol 74 (10) ◽  
pp. 937-944 ◽  
Author(s):  
Babiker Y. Abdulkhair ◽  
Mutaz E. Salih ◽  
Nuha Y. Elamin ◽  
A. MA. Fatima ◽  
A. Modwi
Keyword(s):  
Zno Nanoparticles ◽  
Photocatalytic Performance ◽  
Hexagonal Wurtzite Structure ◽  
Zinc Nitrate ◽  
Wurtzite Structure ◽  
Sugar Solution ◽  
X Ray Diffraction ◽  
Pollutant Degradation ◽  
X Ray ◽  
Good Crystallinity

AbstractStrenuous efforts have been employed to prepare zinc oxide (ZnO) with eco-friendly methods; however, few studies have reported the fabrication of ZnO using a sustainable procedure. In this study, spherical ZnO nanoparticles were successfully fabricated for photocatalysis applications using a simple and eco-friendly method using an arabinose sugar solution. The ZnO nanoparticles with a wurtzite structure were obtained by combining zinc nitrate and arabinose in water, followed by heating, evaporation, and calcinations at different annealing temperatures. The annealed ZnO photocatalysts were characterised via X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray (EDX), Fourier transform infrared spectroscopy (FTIR), and thermogravimetric analysis (TGA). The findings revealed a hexagonal wurtzite structure and good crystallinity with crystallite size increasing from 18 to 31 nm by means of an increase in the annealing temperature. The photocatalytic performance was examined to determine the degradation of mix dye waste. The spherical ZnO nanoparticles showed mix pollutant degradation of 84 % in 25 min at 400 °C.

scholarly journals Y3+ substituted Sr-hexaferrites: sol-gel synthesis, structural, magnetic and electrical characterization

Cerâmica ◽  
2019 ◽  
Vol 65 (374) ◽  
pp. 274-281 ◽  
Author(s):  
S. S. Satpute ◽  
S. R. Wadgane ◽  
S. R. Kadam ◽  
D. R. Mane ◽  
R. H. Kadam
Keyword(s):  
Electron Microscopy ◽  
Sol Gel ◽  
Electrical Characterization ◽  
Combustion Method ◽  
Hexagonal Structure ◽  
Strontium Hexaferrite ◽  
X Ray Diffraction ◽  
X Ray ◽  
Morphological Studies ◽  
Auto Combustion

Abstract Y3+ substituted strontium hexaferrites having chemical composition SrYxFe12-xO19 (x= 0.0, 0.5, 1.0, 1.5) were successfully synthesized by sol-gel auto-combustion method. The structural and morphological studies of prepared samples were investigated by using X-ray diffraction technique, energy dispersive X-ray spectroscopy, field emission scanning electron microscopy (FE-SEM) and high-resolution transmission electron microscopy. The X-ray diffraction pattern confirmed the single-phase hexagonal structure of yttrium substituted strontium ferrite and the lattice parameters a and c increased with the substitution of Y3+ ions. The crystallite size also varied with x content from 60 to 80 nm. The morphology was studied by FE-SEM, and the grain size of nanoparticles ranged from 44 to 130 nm. The magnetic properties were investigated by using vibrating sample magnetometer. The value of saturation magnetization decreased from 49.60 to 35.40 emu/g. The dielectric constant decreased non-linearly whereas the electrical dc resistivity increased with the yttrium concentration in strontium hexaferrite.

scholarly journals Efficient Removal of Levofloxacin by Activated Persulfate with Magnetic CuFe2O4/MMT-k10 Nanocomposite: Characterization, Response Surface Methodology, and Degradation Mechanism

Water ◽  
2020 ◽  
Vol 12 (12) ◽  
pp. 3583
Author(s):  
Junying Yang ◽  
Minye Huang ◽  
Shengsen Wang ◽  
Xiaoyun Mao ◽  
Yueming Hu ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Response Surface Methodology ◽  
Response Surface ◽  
Photoelectron Spectroscopy ◽  
Degradation Mechanism ◽  
Sol Gel ◽  
Combustion Method ◽  
Copper Ferrite ◽  
X Ray ◽  
Rsm Model

In this study, a magnetic copper ferrite/montmorillonite-k10 nanocomposite (CuFe2O4/MMT-k10) was successfully fabricated by a simple sol-gel combustion method and was characterised by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), the Brunner–Emmett–Teller (BET) method, vibrating sample magnetometer (VSM), and X-ray photoelectron spectroscopy (XPS). For levofloxacin (LVF) degradation, CuFe2O4/MMT-k10 was utilized to activate persulfate (PS). Due to the relative high adsorption capacity of CuFe2O4/MMT-k10, the adsorption feature was considered an enhancement of LVF degradation. In addition, the response surface methodology (RSM) model was established with the parameters of pH, temperature, PS dosage, and CuFe2O4/MMT-k10 dosage as the independent variables to obtain the optimal response for LVF degradation. In cycle experiments, we identified the good stability and reusability of CuFe2O4/MMT-k10. We proposed a potential mechanism of CuFe2O4/MMT-k10 activating PS through free radical quenching tests and XPS analysis. These results reveal that CuFe2O4/MMT-k10 nanocomposite could activate the persulfate, which is an efficient technique for LVF degradation in water.

scholarly journals Crystallite Size Evaluation of ZnO Nanoparticles via Transmission Electron Microscopy and X-ray Powder Diffraction

2016 ◽  
Vol 22 (S3) ◽  
pp. 1610-1611
Author(s):  
Jonathan E. Cowen ◽  
Ashley E. Harris ◽  
Cecelia C. Pena ◽  
Stephen C. Bryant ◽  
Allison J. Christy ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Crystallite Size ◽  
Powder Diffraction ◽  
Zno Nanoparticles ◽  
X Ray ◽  
Transmission Electron ◽  
Size Evaluation

Microwave-Assisted Hydrothermal Synthesis of ZnFe2O4/TiO2 Composite and Photocatalytic Properties

2018 ◽  
Vol 788 ◽  
pp. 102-107
Author(s):  
Pavels Rodionovs ◽  
Jānis Grabis ◽  
Aija Krūmiņa
Keyword(s):  
Photocatalytic Activity ◽  
Photon Absorption ◽  
Light Sources ◽  
Mass Loading ◽  
Spherical Nanoparticles ◽  
X Ray Diffraction ◽  
X Ray ◽  
Microwave Assisted ◽  
Average Size ◽  
Prepared Nanostructures

In order to improve TiO2 photocatalytic activity ZnFe2O4/TiO2 nanocomposites with different ZnFe2O4 mass loading were produced. Obtained ZnFe2O4 nanoparticles were coupled with TiO2 via microwave-assisted hydrothermal method in order to improve photon absorption in a range of visible light. Prepared nanostructures were characterized with scanning electron microscopy and X-ray diffraction. Photocatalytic activity of prepared samples was investigated by degradation of methylene blue under different light sources – LED, Hg and Osram Vitalux lamps. ZnFe2O4 consists of spherical nanoparticles with average size of 15 nm. TiO2 spherical nanoparticles size is in a range of 30÷45 nm. The results show that doping TiO2 with ZnFe2O4 nanoparticles increases photocatalytic activity. Photocatalytic activity increases as mass loading of ZnFe2O4 decreases.

scholarly journals Green Synthesis and Catalytic Activity of Silver Nanoparticles Based on Piper chaba Stem Extracts

Nanomaterials ◽  
2020 ◽  
Vol 10 (9) ◽  
pp. 1777 ◽  
Author(s):  
Md. Mahiuddin ◽  
Prianka Saha ◽  
Bungo Ochiai
Keyword(s):  
Electron Microscopy ◽  
Silver Nanoparticles ◽  
Green Synthesis ◽  
Ftir Spectroscopy ◽  
Visual Observation ◽  
Face Centered Cubic ◽  
X Ray ◽  
Vis Spectroscopy ◽  
Face Centered ◽  
Average Size

A green synthesis of silver nanoparticles (AgNPs) was conducted using the stem extract of Piper chaba, which is a plant abundantly growing in South and Southeast Asia. The synthesis was carried out at different reaction conditions, i.e., reaction temperature, concentrations of the extract and silver nitrate, reaction time, and pH. The synthesized AgNPs were characterized by visual observation, ultraviolet–visible (UV-vis) spectroscopy, dynamic light scattering (DLS), scanning electron microscopy (SEM), transmission electron microscopy (TEM), x-ray diffraction (XRD), energy dispersive x-ray (EDX), and Fourier transform infrared (FTIR) spectroscopy. The characterization results revealed that AgNPs were uniformly dispersed and exhibited a moderate size distribution. They were mostly spherical crystals with face-centered cubic structures and an average size of 19 nm. The FTIR spectroscopy and DLS analysis indicated that the phytochemicals capping the surface of AgNPs stabilize the dispersion through anionic repulsion. The synthesized AgNPs effectively catalyzed the reduction of 4-nitrophenol (4-NP) and degradation of methylene blue (MB) in the presence of sodium borohydride.

scholarly journals Formation of ZnO/Zn0.5Cd0.5Se Alloy Quantum Dots in the Presence of High Oleylamine Contents

Nanomaterials ◽  
2019 ◽  
Vol 9 (7) ◽  
pp. 999
Author(s):  
Yi-An Chen ◽  
Kuo-Hsien Chou ◽  
Yi-Yang Kuo ◽  
Cheng-Ye Wu ◽  
Po-Wen Hsiao ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Quantum Dots ◽  
Particle Size ◽  
X Ray Diffraction ◽  
One Pot ◽  
X Ray ◽  
Transmission Electron ◽  
Average Size ◽  
Alloy Quantum Dots ◽  
First Time

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.

scholarly journals Layer-by-Layer Self-Assembled Ferrite Multilayer Nanofilms for Microwave Absorption

2015 ◽  
Vol 2015 ◽  
pp. 1-8 ◽  
Author(s):  
Jiwoong Heo ◽  
Daheui Choi ◽  
Jinkee Hong
Keyword(s):  
Electron Microscopy ◽  
Self Assembly ◽  
Precursor Solution ◽  
Ferrite Nanoparticles ◽  
Energy Dispersive ◽  
Layer By Layer ◽  
X Ray Diffraction ◽  
Simple Method ◽  
X Ray ◽  
Scanning Electron

We demonstrate a simple method for fabricating multilayer thin films containing ferrite (Co0.5Zn0.5Fe2O4) nanoparticles, using layer-by-layer (LbL) self-assembly. These films have microwave absorbing properties for possible radar absorbing and stealth applications. To demonstrate incorporation of inorganic ferrite nanoparticles into an electrostatic-interaction-based LbL self-assembly, we fabricated two types of films: (1) a blended three-component LbL film consisting of a sequential poly(acrylic acid)/oleic acid-ferrite blend layer and a poly(allylamine hydrochloride) layer and (2) a tetralayer LbL film consisting of sequential poly(diallyldimethylammonium chloride), poly(sodium-4-sulfonate), bPEI-ferrite, and poly(sodium-4-sulfonate) layers. We compared surface morphologies, thicknesses, and packing density of the two types of ferrite multilayer film. Ferrite nanoparticles (Co0.5Zn0.5Fe2O4) were prepared via a coprecipitation method from an aqueous precursor solution. The structure and composition of the ferrite nanoparticles were characterized by X-ray diffraction, energy dispersive X-ray spectroscopy, transmission electron microscopy, and scanning electron microscopy. X-ray diffraction patterns of ferrite nanoparticles indicated a cubic spinel structure, and energy dispersive X-ray spectroscopy revealed their composition. Thickness growth and surface morphology were measured using a profilometer, atomic force microscope, and scanning electron microscope.

A Simple Method for Controlling the Morphology of CuO Nanostructures by Droplet

2012 ◽  
Vol 535-537 ◽  
pp. 280-283 ◽  
Author(s):  
Hao Ran An ◽  
Feng Shi Cai ◽  
Xue Wei Wang ◽  
Zhi Hao Yuan
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Optical Microscope ◽  
Growth Mechanisms ◽  
X Ray Diffraction ◽  
Simple Method ◽  
Hydrophobic Substrate ◽  
X Ray ◽  
Shape Selective ◽  
Scanning Electron

Different morphology CuO nanostructures, including platelets, flower-like were simply synthesized at 350 °C controlled by droplet on hydrophobic substrate. This is a simple method which does not require any template, catalyst, or surfactant but can control the morphology of CuO from platelets to flowerlike. The morphologies are strongly dependent on the volume of droplet. Scanning electron microscopy (SEM), Optical microscope and X-ray diffraction (XRD) were used to observe the morphology, crystallinity, and chemical composition of the CuO structures. Growth mechanisms for shape selective CuO synthesis were proposed based on these results.

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