Synthesis of Nanocrystalline Hydroxyapatite by Natural Biopolymers Based Sol-Gel Technique

2013 ◽  
Vol 747 ◽  
pp. 83-86
Author(s):  
Jutharatana Klinkaewnarong ◽  
Ekaphan Swatsitang
Keyword(s):  
Particle Size ◽  
Sol Gel ◽  
Hexagonal Structure ◽  
Line Broadening ◽  
X Ray Diffraction ◽  
X Ray ◽  
Amorphophallus Konjac ◽  
Selected Area Electron Diffraction ◽  
Nanocrystalline Hydroxyapatite ◽  
Gel Technique

Nanocrystalline hydroxyapatite (HAp) powders were successfully synthesized by natural biopolymers based sol-gel technique. The biopolymers were extracted from the leaves of Yanang (Tiliacora triandra), Krueo Ma Noy (Cissampelos pareira) and Konjac (Amorphophallus konjac). To obtain HAp powders, the prepared precursors were calcined in air at 600, 700, and 800 °C for 2 h. The phase composition of the calcined samples was studied by X-ray diffraction (XRD) technique. The XRD results confirmed the formation of HAp phase with a small trace of β-tricalcium phosphate (β-TCP). The crystalline sizes of the samples were found to be 20-50 nm as evaluated by the XRD line broadening method. TEM investigation revealed that the synthesized HAp samples consisted of nanoparticles with a particle size in the range of 50-100 nm in diameter. The corresponding selected area electron diffraction (SAED) analysis further confirmed the formation of hexagonal structure of HAp.

ENHANCED MAGNETIZATION IN COBALT SUBSTITUTED Ni–Zn NANOFERRITES

2011 ◽  
Vol 10 (04n05) ◽  
pp. 571-576 ◽  
Author(s):  
M. CHAITANYA VARMA ◽  
A. MAHESH KUMAR ◽  
K. H. RAO
Keyword(s):  
Particle Size ◽  
Room Temperature ◽  
Sol Gel ◽  
Chelating Agent ◽  
Lattice Parameter ◽  
Line Broadening ◽  
X Ray Diffraction ◽  
Chemical Methods ◽  
X Ray ◽  
Nickel Zinc

Cobalt substituted nickel zinc ferrite nanoparticles ( Ni 0.65–x Co x Zn 0.35 Fe 2.0 O 4) X varying from 0.0 to 0.65 in steps of 0.15 have been produced using sol–gel method, with PVA as chelating agent. The phase formation of the sintered ferrite was confirmed by X-ray diffraction studies. The lattice parameter a(A°) has been calculated using Nelson–Riley method. The crystallite size has been estimated by the Williamson–Hall method using the full width at half-maximum (FWHM) of the line broadening of all the peaks. Mössbauer spectroscopy (MS) of the samples showed the clear presence of two sextets and distribution of iron over the two sites has been given. Increase in saturation magnetization with cobalt concentration with a slight decrease for x = 0.15 has been observed with the vibrating sample magnetometry study. The observed value of magnetization for Ni0.65Zn0.35Fe2O4 with a particle size of 43.5 nm has been 71 emu/gm at room temperature, which is higher than that reported for samples prepared using chemical methods of the same composition. The results have been explained on the basis of the particle size and cation distribution among various sites.

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 Effect of the suspension of Ag-incorporated TiO2 nanoparticles (Ag-TiO2 NPs) on certain growth, physiology and phytotoxicity parameters in spinach seedlings

PLoS ONE ◽  
2020 ◽  
Vol 15 (12) ◽  
pp. e0244511
Author(s):  
Fernando Gordillo-Delgado ◽  
Jakeline Zuluaga-Acosta ◽  
Gonzalo Restrepo-Guerrero
Keyword(s):  
Particle Size ◽  
Titanium Dioxide Nanoparticles ◽  
Germination Rate ◽  
Sol Gel ◽  
Control Group ◽  
Human Consumption ◽  
X Ray Diffraction ◽  
X Ray ◽  
Growth Physiology ◽  
Powder Samples

In this work, the effect of the inoculation of silver-incorporated titanium dioxide nanoparticles (Ag-TiO2 NPs) in spinach seeds was evaluated on certain growth, physiology and phytotoxicity parameters of the plants. This is an important crop for human consumption with high nutritional value due to their low calorie and fat content, providing various vitamins and minerals, especially iron. These NPs were obtained by means of the sol-gel method and heat treatment; the resulting powder material was characterized using X-ray diffraction and scanning electron microscopy and the influence of these NPs on plants was measured by estimating the germination rate, monitoring morphological parameters and evaluating phytotoxicity. The photosynthetic activity of the spinach plants was estimated through the quantification of the Ratio of Oxygen Evolution (ROE) by the photoacoustic technique. Samples of TiO2 powder with particle size between 9 and 43 nm were used to quantify the germination rate, which served to determine a narrower size range between 7 and 26 nm in the experiments with Ag-TiO2 NPs; the presence of Ag in TiO2 powder samples was confirmed by energy-dispersive X-ray spectroscopy. The analysis of variance showed that the dependent variable (plant growth) could be affected by the evaluated factors (concentration and size) with significant differences. The statistical trend indicated that the application of the Ag-TiO2 NPs suspension of lowest concentration and smallest particle size could be a promoting agent of the growth and development of these plants. The inoculation with NPs of 8.3 nm size and lowest concentration was related to the highest average ROE value, 24.6 ± 0.2%, while the control group was 20.2 ± 0.2%. The positive effect of the Ag-TiO2 NPs treatment could be associated to the generation of reactive oxygen species, antimicrobial activity, increased biochemical attributes, enzymatic activity or improvements in water absorption.

scholarly journals Calcination Effect on Structural Trasformation of Barium Titanite Ferroelectric Ceramic by Sol-Gel Method

2019 ◽  
Vol 9 (1) ◽  
pp. 5893-5896
Keyword(s):  
Glacial Acetic Acid ◽  
Sol Gel ◽  
Ferroelectric Ceramic ◽  
Tetrabutyl Titanate ◽  
Chemical Modifier ◽  
Barium Acetate ◽  
X Ray Diffraction ◽  
X Ray ◽  
Gel Technique ◽  
Scanning Electron

High purity barium titanate BaTiO3 was successfully synthesized by using the sol-gel technique. Barium acetate Ba(CH3COO)2 and tetrabutyl titanate, Ti(C4H9O)4 was dissolved moderately in the solvent of glacial acetic acid and ethanol was added as the chemical modifier. The synthesized BaTiO3 nanoparticle was calcined at the temperature range of 700 ºC to 1100 ºC. The powders were further characterized by X-ray diffraction and scanning electron microscopy (SEM). Fined BaTiO3 powders result indicates the phase of tetragonal structures and high crystallites of BaTiO3. It was observed that the crystallinity and particle size of BaTiO3 is greatly influenced by the calcination temperature.

scholarly journals Synthesis Photocatalytic and Antibacterial Activities of Nickle Doped Tio2 Nanoparticles

2018 ◽  
Vol 34 (6) ◽  
pp. 3140-3144
Author(s):  
Ritu Vershney ◽  
Komal Chelaramani ◽  
Arpan Bhardwaj ◽  
Nayma Siddiqui ◽  
Suresh Kumar Verma
Keyword(s):  
Photocatalytic Degradation ◽  
Tio2 Nanoparticles ◽  
Sol Gel ◽  
Antibacterial Activities ◽  
X Ray Diffraction ◽  
Zone Of Inhibition ◽  
Time Duration ◽  
X Ray ◽  
Gel Technique ◽  
Doped Titania

The synthesis of Ni doped titania (TiO2) nanoparticles were achieved via simple novel sol gel technique, in which Titanium-n-butoxide and NiCl2 were taken as precursors. Effect of different wt% of dopant in TiO2 was studied on photocatalytic degradation of Aniline blue and Toluidine Blue. The study suggested the increased photocatalytic degradation with increased time duration. The synthesized samples were analyzed by surface electron microscopy (SEM) and X-ray diffraction studies. The antibacterial activity was investigated against Gram-positive Staphylococcus aureus bacteriae. Studies revealed that on increasing the dopant concentration, the diameter of zone of inhibition also increased upto 1.5 wt%.

Fabrication of Porous LSCF-SDC Carbonates Composite Cathode for Solid Oxide Fuel Cell (SOFC) Applications

2011 ◽  
Vol 471-472 ◽  
pp. 179-184 ◽  
Author(s):  
Raharjo Jarot ◽  
Andanastuti Muchtar ◽  
Wan Ramli Wan Daud ◽  
Norhamidi Muhamad ◽  
Edy Herianto Majlan
Keyword(s):  
Thermal Expansion ◽  
Sol Gel ◽  
Composite Cathode ◽  
X Ray Diffraction ◽  
X Ray ◽  
Structure Morphology ◽  
Composite Cathodes ◽  
Gel Technique ◽  
Optimum Porosity ◽  
Cold Pressed

Composite cathodes made of perovskite La0.6Sr0.4Co0.2Fe0.8O3 (LSCF) and SDC carbonates (SDC-(Li/Na)2CO3) were investigated in relation to their structure, morphology, thermal expansion coefficient and porosity. As a first step, the LSCF powder was prepared by sol-gel technique. This was followed by the preparation of the LSCF-SDC carbonates composite cathode by mixing the LSCF with SDC-(Li/Na)2CO3 electrolyte via solid state reaction in various compositions, i.e. 30, 40 and 50 wt.%, namely 70LSCF-30SDC7030, 60LSCF-40SDC7030 and 50LSCF-50SDC7030, respectively. The powder mixtures were then calcined at 680oC. The resultant powder was fine with surface area of about 3.39-7.42 m2/g and particle size of 0.56-0.66µm. The powder consists of two distinct phases, i.e. LSCF and SDC-(Li/Na)2CO3 as confirmed with x-ray diffraction. The microstructures were observed under scanning electron microscopy (SEM). Increasing the amount of the SDC-(Li/Na)2CO3 electrolyte in the composite cathode was found to bring the thermal expansion of the cathode closer to that of the electrolyte. The cathode pellets were later compacted at different pressures (27, 32 and 37 MPa) and sintered at 600oC. The optimum porosity (20.99-24.98%) was achieved for samples with SDC-(Li/Na)2CO3 content of 30-50% sintered at 600oC and cold pressed at 37 MPa.

scholarly journals Sol-Gel Template Synthesis and Characterization of Lu2O3:Eu3+ Nanowire Arrays

Micromachines ◽  
2018 ◽  
Vol 9 (11) ◽  
pp. 601
Author(s):  
Yahua Hu ◽  
Mu Gu ◽  
Xiaolin Liu ◽  
Juannan Zhang ◽  
Shiming Huang ◽  
...  
Keyword(s):  
Sol Gel ◽  
Nanowire Arrays ◽  
X Ray Diffraction ◽  
Aao Template ◽  
X Ray ◽  
Selected Area Electron Diffraction ◽  
Sol Gel Process ◽  
Optical Luminescence ◽  
Uniform Diameter

Uniform Lu2O3:Eu3+ nanowire arrays were successfully prepared by the sol-gel process using anodic aluminum oxide (AAO) templates. The as-synthesized nanowires are homogeneous, highly ordered, and dense and have a uniform diameter of ~300 nm defined by the AAO templates. The X-ray diffraction and selected area electron diffraction results show that the Lu2O3:Eu3+ nanowires have a polycrystalline cubic structure, and the crystallite size of the Lu2O3:Eu3+ nanowires is confined by the AAO template. The nanowires within the AAO template showed good photoluminescence and X-ray-excited optical luminescence performances for Lu2O3:Eu3+. The emission peaks were attributed to the 5D0 → 7FJ transitions of Eu3+ (J = 0, 1, 2, 3).

Preparation of LaFeO3 particles by sol-gel technology

1998 ◽  
Vol 13 (2) ◽  
pp. 451-456 ◽  
Author(s):  
C. Vázquez-Vázquez ◽  
P. Kögerler ◽  
M. A. López-Quintela ◽  
R. D. Sánchez ◽  
J. Rivas
Keyword(s):  
Particle Size ◽  
Magnetic Properties ◽  
Infrared Spectroscopy ◽  
Sol Gel ◽  
Diffraction Peak ◽  
Gel Formation ◽  
X Ray Diffraction ◽  
X Ray ◽  
Ferromagnetic Component ◽  
Peak Broadening

The study of submicroscopic particles in already known systems has resulted in a renewed interest due to the large differences found in their properties when the particle size is reduced, and because of possible new technological applications. In this work we report the preparation of LaFeO3 particles by the sol-gel route, starting from a solution of the corresponding metallic nitrates and using urea as gelificant agent. Gels were decomposed at 200 °C and calcined 3 h at several temperatures, T, in the range 250–1000 °C. The samples were structurally characterized by x-ray diffraction (XRD) showing that the orthoferrite crystallizes at T as low as 315 °C. From the x-ray diffraction peak broadening, the particle size was determined. The size increases from 60 to 300 nm as the calcination T increases. Infrared spectroscopy was used to characterize gels and calcined samples. From these studies a mechanism for the gel formation is proposed. Study of the magnetic properties of LaFeO3 particles shows the presence of a ferromagnetic component which diminishes as the calcination temperature increases, vanishing at T = 1000 °C.

Thick PLZT Films Grown by Sol-gel for Optical Device Applications

1998 ◽  
Vol 541 ◽  
Author(s):  
M. Linnik ◽  
O. Wilson ◽  
A. Christou
Keyword(s):  
Electron Microscopy ◽  
Sol Gel ◽  
Phase Modulator ◽  
X Ray Diffraction ◽  
X Ray ◽  
Device Applications ◽  
Gel Technique ◽  
Scanning Electron

AbstractThe preparation and characterization of thick PLZT films for spatial phase modulator applications are reported. Films were fabricated on LSCO/LAO substrates by a sol-gel technique using multiple heat-treatment parameters. The crystal quality of PLZT 9/65/35 films was investigated by X-ray diffraction and scanning electron microscopy.

Synthesis and Characterization of CeO2 Doped ZrO2 Ceramics by a Simple Sol-Gel Route

2017 ◽  
Vol 907 ◽  
pp. 56-60
Author(s):  
Ummuhanı Hilal Özer ◽  
Kerim Emre Öksüz ◽  
Ali Özer
Keyword(s):  
Tetragonal Phase ◽  
Sol Gel ◽  
Lattice Parameter ◽  
X Ray Diffraction ◽  
Ceramic Powders ◽  
Zirconia Ceramics ◽  
Simple Method ◽  
X Ray ◽  
Gel Technique

It is well known that sol-gel technique is a simple method to produce nano sized ceramic powders. In this study, cerium oxide doped zirconia samples, with 10 mol%-12mol% and14mol% CeO2, were synthesized by sol-gel technique and characterized. The surface morphology, elemental composition, microstructure, and phase analysis, of the sintered CeO2 doped ZrO2 ceramics were characterized by field emission scanning electron microscopy (FE-SEM), energy dispersive X-ray (EDS) analysis, and X-ray diffraction (XRD) respectively. X-ray diffraction for samples sintered at 1550 °C for 4h revealed that the zirconia ceramics have a tetragonal phase structure. The addition of CeO2 can raise the content of the tetragonal phase, but the minor monoclinic phase exists even at the CeO2 content of 10 mol%. The effect of dopant concentration on the lattice parameter, average primary crystallite size and micro-strain was studied. Relative densities for CeO2 doped ZrO2 bulk ceramics varied between 95% and 99 %, depending on the CeO2 addition.

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