Solubility of Mn in ZnO Nanocrystallites using Wet Chemical Synthesis

2019 ◽  
Vol 2 (1) ◽  
pp. 53-61
Author(s):  
Esau Abekah Armah ◽  
Francis Kofi Ampong ◽  
Martin Egblewogbe ◽  
Hubert Azoda Koffi ◽  
Francis Boakye ◽  
...  

There is a substantial amount of literature dealing with many aspects of synthesis and characterization of pure and doped binary compounds including Mn-doped ZnO which has been widely studied due to its superb properties as a dilute magnetic semiconductor (DMS). Aspects concerning doping limits for these compounds is an important stage in the search for new materials. Samples of Zn1-xMnxO nanocrystal were synthesized at temperatures of 180 °C and 200 °C using wet or liquid phase synthesis method. Dopant concentrations x=0.5, 1, 1.5, 2, 2.5, 5, 10, 20, 30, 40 and 50 per cent were studied. Powder x-ray diffraction (PXRD) patterns of the samples were analyzed with a view to determining the onset of secondary phases and hence the solubility limit of the dopant. The solubility limit for Mn in ZnO samples synthesized at temperature of 200 °C is realized at x <20%. For samples synthesized at temperature of 180 °C, the solubility limit is x <0.5%.

2020 ◽  
Vol 4 (11) ◽  
Author(s):  
Fabian L. M. Bernal ◽  
Bruno Gonano ◽  
Fredrik Lundvall ◽  
David S. Wragg ◽  
Helmer Fjellvåg ◽  
...  

2020 ◽  
Vol 43 (1) ◽  
pp. 26-42 ◽  
Author(s):  
Zahra Hajian Karahroudi ◽  
Kambiz Hedayati ◽  
Mojtaba Goodarzi

AbstractThis study presents a preparation of SrFe12O19– SrTiO3 nanocomposite synthesis via the green auto-combustion method. At first, SrFe12O19 nanoparticles were synthesized as a core and then, SrTiO3 nanoparticles were prepared as a shell for it to manufacture SrFe12O19–SrTiO3 nanocomposite. A novel sol-gel auto-combustion green synthesis method has been used with lemon juice as a capping agent. The prepared SrFe12O19–SrTiO3 nanocomposites were characterized by using several techniques to characterize their structural, morphological and magnetic properties. The crystal structures of the nanocomposite were investigated via X-ray diffraction (XRD). The morphology of SrFe12O19– SrTiO3 nanocomposite was studied by using a scanning electron microscope (SEM). The elemental composition of the materials was analyzed by an energy-dispersive X-ray (EDX). Magnetic properties and hysteresis loop of nanopowder were characterized via vibrating sample magnetometer (VSM) in the room temperature. Fourier transform infrared spectroscopy (FTIR) spectra of the samples showed the molecular bands of nanoparticles. Also, the photocatalytic behavior of nanocomposites has been checked by the degradation of azo dyes under irradiation of ultraviolet light.


2014 ◽  
Vol 625 ◽  
pp. 661-664
Author(s):  
Chen Chuang Lok ◽  
Yin Fong Yeong

In the present work, ZIF-8/6FDA-durene mixed matrix membranes (MMMs) were synthesized and characterized. ZIF-8 nanocrystals, which were used as the inorganic filler, were synthesized using rapid room-temperature synthesis method whereas 6FDA-durene polyimide was synthesized by polycondensation method followed by chemical imidization. Pure and 6FDA-durene membranes loaded with 5 wt%, 10 wt% and 15 wt% of ZIF-8 were fabricated. The structural properties and morphology of the resultant membranes were characterized by using X-ray Diffraction (XRD) and Field emission scanning electron microscope (FESEM) . The EDX images showed that ZIF-8 particles agglomerated in the polymer matrix. However, no phase separation was observed for all resultant MMMs.


2017 ◽  
Vol 8 ◽  
pp. 1257-1265 ◽  
Author(s):  
Urszula Klekotka ◽  
Magdalena Rogowska ◽  
Dariusz Satuła ◽  
Beata Kalska-Szostko

Ferrite nanoparticles with nominal composition Me0.5Fe2.5O4 (Me = Co, Fe, Ni or Mn) have been successfully prepared by the wet chemical method. The obtained particles have a mean diameter of 11–16 ± 2 nm and were modified to improve their magnetic properties and chemical activity. The surface of the pristine nanoparticles was functionalized afterwards with –COOH and –NH2 groups to obtain a bioactive layer. To achieve our goal, two different modification approaches were realized. In the first one, glutaraldehyde was attached to the nanoparticles as a linker. In the second one, direct bonding of such nanoparticles with a bioparticle was studied. In subsequent steps, the nanoparticles were immobilized with enzymes such as albumin, glucose oxidase, lipase and trypsin as a test bioparticles. The characterization of the nanoparticles was acheived by transmission electron microscopy, X-ray diffraction, energy dispersive X-ray and Mössbauer spectroscopy. The effect of the obtained biocomposites was monitored by Fourier transform infrared spectroscopy. The obtained results show that in some cases the use of glutaraldehyde was crucial (albumin).


2013 ◽  
Vol 873 ◽  
pp. 152-157
Author(s):  
Long Long Chen ◽  
Jun Ming Li ◽  
Xiao Min Gong ◽  
Jian Li

Using a chemically induced transition in an FeCl2 solution, γ-Fe2O3 nanoparticles can be prepared from an amorphous precursor composed of FeOOH and Mg (OH)2. Surface modification by adding ZnCl2 during liquid-phase synthesis was attempted. The magnetization, morphology, crystal structure, and chemical species of as-prepared samples were characterized by vibrating sample magnetometer (VSM), transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray energy-dispersive spectroscopy (EDX), and X-ray photoelectron spectroscopy (XPS). The experimental results showed that the surface of the γ-Fe2O3 nanoparticles can be modified by adding ZnCl2 to form composite nanoparticles with a γ-Fe2O3/ZnFe2O4 ferrite core coated with Zn (OH)2 and absorbed FeCl36H2O; this modification can be enhanced by additional NaOH.


1998 ◽  
Vol 13 (9) ◽  
pp. 2580-2587 ◽  
Author(s):  
K. H. Ryu ◽  
J-M. Yang

The characteristics of nanosized silicon nitride powders with doped Y2O3 and Al2O3 fabricated by a plasma-reacted chemical process were investigated. The chemical compositions of the powders were analyzed by wet chemical analysis. The morphology and the size distribution were determined by transmission electron microscopy (TEM). TEM with energy dispersive spectroscopy (EDS) was used to verify the existence of sintering additives in each individual particle. The crystal structure of the powders was identified by the selected area diffraction pattern (SADP). X-ray diffraction (XRD) technique was used for phase analysis and the measurement of degree of crystallinity. The characteristics of chemical bonding was analyzed by using Fourier transform infrared spectroscopy (FTIR).


2012 ◽  
Vol 629 ◽  
pp. 279-283 ◽  
Author(s):  
Rameshwar Rao ◽  
C. Shilpa Chakra ◽  
K. Venkateswara Rao

Nanobiotechnology emerged as integration of nanotechnology and biotechnology for developing bioactive, biosynthetic and eco -friendly technology for synthesis of nanomaterials. Nanostructures have great demand in areas such as chemistry, catalysis, electronics, energy, and medical applications. Metallic nano-particles are normally synthesized by wet chemical synthesis techniques using the toxic and inflammable chemicals. Present research work on preparation of silver nano-particles by green nano synthesis method and has advantages over conventional methods involving chemical agents which can cause environmental toxicity. The synthesis technique is a cost effective and environment friendly technique for green nano synthesis of silver nano-particles from varying concentrations of AgNO3 solution and extract of Carica papaya fruit of different concentrations which acts as reducing and capping agent. Characterizations has been done using UV–Vis absorption spectroscopy, XRD, particle size analyser and SEM with EDX. Antimicrobial activity was done using Escherichia coli and Pseudomonas.


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