Rapid Synthesis and Characterization of Maghemite Nanoparticles

2008 ◽  
Vol 8 (2) ◽  
pp. 861-866 ◽  
Author(s):  
Bilsen Tural ◽  
Macit Özenbaş ◽  
Selçuk Atalay ◽  
Mürvet Volkan

Fe2O3–SiO2 nanocomposites were prepared by a sol–gel method using various evaporation surface to volume (S/V) ratios ranging from 0.03 to 0.2. The Fe2O3–SiO2 sols were gelated at various temperatures ranging from 50 °C to 70 °C, and subsequently they were calcined in air at 400 °C for 4 hours. The structure and the magnetic properties of the prepared Fe2O3–SiO2 nanocomposites were characterized using X-ray diffraction (XRD), transmission electron microscopy (TEM), differential thermal analysis (DTA), and vibrating sample magnetometer (VSM) measurements. The gelation temperature of the Fe2O3–SiO2 sols influenced strongly the particle size and crystallinity of the maghemite nanoparticles. It was observed that the particle size of maghemite nanoparticles increased with the increasing of the gelation temperature of the sols, which may be due to the agglomeration of the maghemite particles at elevated temperatures inside the microporosity of the silica matrix during the gelation process, and the subsequent calcination of these gels at 400 °C resulted in the formation of large size iron oxide particles. Magnetization studies at temperatures of 10, 195, and 300 K showed superparamagnetic behavior for all the nanocomposites prepared using the evaporation surface to volume ratio (S/V) of 0.1, 0.2, 0.09, and 0.08. The saturation magnetization, Ms, values measured at 10K were 5.5, 8.5, and 9.5 emu/g, for the samples gelated at 50, 60, and 70 °C, respectively. At the gelation temperature of 70 °C, γ-Fe2O3 crystalline superparamagnetic nanoparticles with the particle size of 9±2 nm were formed in 12 hours for the samples prepared at the S/V ratio of 0.2.

2002 ◽  
Vol 57 (3-4) ◽  
pp. 154-158 ◽  
Author(s):  
C. Cannas ◽  
G. Concas ◽  
F. Congiu ◽  
A. Musinu ◽  
G. Piccaluga ◽  
...  

A series of Fe2O3-SiO2 nanocomposites (25 weight % of Fe2O3) has been prepared using a sol-gel method. Samples showing different features were obtained by varying the evaporation conditions acting on the surface / volume ratio of the starting sol. The samples were investigated using Mössbauer spectroscopy at low temperature. The Fe2O3 nanoparticles have been identified as maghemite ( γ-Fe2O3) particles. The samples show a superparamagnetic behavior with a blocking temperature that depends on the average particle size.


2013 ◽  
Vol 2013 ◽  
pp. 1-6 ◽  
Author(s):  
B. C. Ang ◽  
I. I. Yaacob ◽  
Irwan Nurdin

Superparamagnetic maghemite nanoparticles were synthesized using Massart’s procedure. Nanocomposites that consist of the synthesized maghemite nanoparticles and silica were produced by dispersing the as-synthesized maghemite nanoparticles into the silica xerogel prepared by sol-gel technique. The system was then heated for 3 days at 140°C. The structure, morphology, and texture of the system were analysed by FESEM and TEM. The result from FESEM showed that the silica gel forms a network structure, which contained numerous pores, with an average pore size of 15 nm. EDX line profile analysis was carried out, and the result indicated that the embedded particles were iron oxide. EELS showed the presence of Fe-L2signal, which confirmed the presence of iron oxide particles within the silica matrix. The average diameters were 5.0 nm for as-synthesized maghemite nanoparticles and 4.4 nm for the embedded maghemite nanoparticles in silica xerogel matrix. The embedded maghemite nanoparticles in nanocomposite also showed a narrower distribution compared to as-synthesized particles. The magnetization values at 10 kOe applied field,Ms10 kOe, were 9.53 emu/g and 1.79 emu/g for as-synthesized and embedded nanoparticles, respectively. A reduction in average crystallite size was observed for the dispersed maghemite particles after formation of the nanocomposite indicating a slight dissolution of maghemite nanoparticles in silica gel.


Nanomaterials ◽  
2020 ◽  
Vol 10 (7) ◽  
pp. 1288 ◽  
Author(s):  
Alexander Omelyanchik ◽  
María Salvador ◽  
Franco D’Orazio ◽  
Valentina Mameli ◽  
Carla Cannas ◽  
...  

The effect of the annealing temperature Tann on the magnetic properties of cobalt ferrite nanoparticles embedded in an amorphous silica matrix (CoFe2O4/SiO2), synthesized by a sol-gel auto-combustion method, was investigated by magnetization and AC susceptibility measurements. For samples with 15% w/w nanoparticle concentration, the particle size increases from ~2.5 to ~7 nm, increasing Tann from 700 to 900 °C. The effective magnetic anisotropy constant (Keff) increases with decreasing Tann, due to the increase in the surface contribution. For a 5% w/w sample annealed at 900 °C, Keff is much larger (1.7 × 106 J/m3) than that of the 15% w/w sample (7.5 × 105 J/m3) annealed at 700 °C and showing comparable particle size. This indicates that the effect of the annealing temperature on the anisotropy is not only the control of the particle size but also on the core structure (i.e., cation distribution between the two spinel sublattices and degree of spin canting), strongly affecting the magnetocrystalline anisotropy. The results provide evidence that the magnetic anisotropy comes from a complex balance between core and surface contributions that can be controlled by thermal treatments.


Nanomaterials ◽  
2021 ◽  
Vol 11 (10) ◽  
pp. 2680
Author(s):  
Alizé V. Gaumet ◽  
Francesco Caddeo ◽  
Danilo Loche ◽  
Anna Corrias ◽  
Maria F. Casula ◽  
...  

CuFe2O4 is an example of ferrites whose physico-chemical properties can vary greatly at the nanoscale. Here, sol-gel techniques are used to produce CuFe2O4-SiO2 nanocomposites where copper ferrite nanocrystals are grown within a porous dielectric silica matrix. Nanocomposites in the form of both xerogels and aerogels with variable loadings of copper ferrite (5 wt%, 10 wt% and 15 wt%) were synthesized. Transmission electron microscopy and X-ray diffraction investigations showed the occurrence of CuFe2O4 nanoparticles with average crystal size ranging from a few nanometers up to around 9 nm, homogeneously distributed within the porous silica matrix, after thermal treatment of the samples at 900 °C. Evidence of some impurities of CuO and -Fe2O3 was found in the aerogel samples with 10 wt% and 15 wt% loading. DC magnetometry was used to investigate the magnetic properties of these nanocomposites, as a function of the loading of copper ferrite and of the porosity characteristics. All the nanocomposites show a blocking temperature lower than RT and soft magnetic features at low temperature. The observed magnetic parameters are interpreted taking into account the occurrence of size and interaction effects in an ensemble of superparamagnetic nanoparticles distributed in a matrix. These results highlight how aerogel and xerogel matrices give rise to nanocomposites with different magnetic features and how the spatial distribution of the nanophase in the matrices modifies the final magnetic properties with respect to the case of conventional unsupported nanoparticles.


2010 ◽  
Vol 653 ◽  
pp. 23-30 ◽  
Author(s):  
Karuna Kar Nanda

Understanding of the melting temperature of nanostructures is beneficial to exploit phase transitions and their applications at elevated temperatures. The melting temperature of nanostructured materials depends on particle size, shape and dimensionality and has been well established both experimentally and theoretically. The large surface-to-volume ratio is the key for the low melting temperature of nanostructured materials. The melting temperature of almost free nanoparticles decreases with decreasing size although there are anomalies for some cases. Superheating has been reported for some embedded nanoparticles. Local maxima and minima in the melting temperature have been reported for particles with fewer atoms. Another quantity that is influenced by large surface-to-volume ratio and related to the thermal stability, is the vapour pressure. The vapour pressure of nanoparticles is shown to be enhanced for smaller particles. In this article, we have discussed the anomaly in thermal stability of nanostructured materials.


1996 ◽  
Vol 465 ◽  
Author(s):  
N. A. Stump ◽  
R. G. Haire ◽  
S. Dai

ABSTRACTSeveral oxidation states of neptunium and plutonium, Pu(III), Pu(IV), Pu(VI), Np(IV), Np(V), and Np(VI), were studied in glasses prepared by a sol-gel technology. The oxidation state of these actinides in the sol-gel product was examined by absorption spectroscopy after solidification, aging, and thermal treatment. The oxidation state of the actinides in the starting solutions was essentially maintained through the solidification process of the silica matrix. However, during densification and removal of residual solvents at elevated temperatures, both actinides converted eventually to their tetra valent states while in the different sol-gel products. This finding is in accord with reports that tetravalent states of plutonium and neptunium are acquired in glass products prepared by dissolution of the actinide in molten glasses. Comparisons between room temperature spectra obtained from neptunium and plutonium in heated sol-gel products and from molten glass products showed subtle differences that can be related to the metal ion's environments.


2010 ◽  
Vol 97-101 ◽  
pp. 2140-2143 ◽  
Author(s):  
Bee Chin Ang ◽  
Iskandar Idris Yaacob

Superparamagnetic maghemite nanoparticles were successfully produced using Massart’s procedure. Nanocomposites consisting of the synthesized maghemite nanoparticles and silica were produced by dispersing the as-synthesized maghemite nanoparticles into the silica xerogel, which was prepared by sol-gel technique. The system was then heated for 3 days at 140oC. A variety of weight ratios of Fe2O3/SiO2 was investigated. The nanocomposites were characterized using TGA, XRD, TEM and AGM. TGA thermogram showed one significant weight loss at around 250oC. It was caused by dehydration and evaporation of solvent from sol-gel process. XRD showed that the dispersed particles were still maghemite. TEM micrographs showed that the maghemite nanoparticles were in spherical shape and they were homogeneously incorporated in the silica matrix. The values of magnetization at 10kOe applied field were in the range of 1.79emu/g to 9.53emu/g depending of the Fe2O3/SiO2 ratio. Reduction of average crystallite size of dispersed maghemite particles was observed after encapsulation process. Increasing weight ratio of Fe2O3/SiO2 caused increase of the average crystallite size of maghemite nanoparticles.


2008 ◽  
Vol 320 (20) ◽  
pp. e725-e729 ◽  
Author(s):  
M. Domínguez ◽  
D. Ortega ◽  
J.S. Garitaonandía ◽  
R. Litrán ◽  
C. Barrera-Solano ◽  
...  

2013 ◽  
Vol 446-447 ◽  
pp. 408-413
Author(s):  
Suchaya Sriudom ◽  
Hataichanoke Niamsup ◽  
Surin Saipanya ◽  
Ruangsri Watanesk ◽  
Surasak Watanesk

Hydroxyapatite (HA) has been widely utilized in the biomedical applications due to its chemical and structural features that are similar to the natural bones. The addition of organic components enhances the flexibility of the HA-based composites which result in increasing its molding ability into any desirable shapes. In this article, preparation of hydroxyapaptite/silk fibroin (HA/SF) composite using sol-gel method is reported. The optimal condition for preparing the HA/SF composites was determined by judging from their crystallite size, crystallinity and particle size distribution, morphology and calcium/phosphorus (Ca/P) ratio investigated with X-ray diffraction analysis, particle size analyzer, scanning electron microscopy and energy dispersive X-ray spectroscopy, respectively. The HA/SF composite was successfully prepared in the binary solvent of ethanol and water at the optimal volume ratio of 4:1. At this solvent condition, the composites had a uniform rod-liked shape, ranging from 30-70 nanometers. The Ca/P ratios of all composites are close to the theoretical value of about 1.67.


Author(s):  
George C. Ruben ◽  
Merrill W. Shafer

Traditionally ceramics have been shaped from powders and densified at temperatures close to their liquid point. New processing methods using various types of sols, gels, and organometallic precursors at low temperature which enable densificatlon at elevated temperatures well below their liquidus, hold the promise of producing ceramics and glasses of controlled and reproducible properties that are highly reliable for electronic, structural, space or medical applications. Ultrastructure processing of silicon alkoxides in acid medium and mixtures of Ludox HS-40 (120Å spheres from DuPont) and Kasil (38% K2O &62% SiO2) in basic medium have been aimed at producing materials with a range of well defined pore sizes (∼20-400Å) to study physical phenomena and materials behavior in well characterized confined geometries. We have studied Pt/C surface replicas of some of these porous sol-gels prepared at temperatures below their glass transition point.


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