Synthesis and Characterization of Ceramic Modified with Niobium for Biomedical Applications

2016 ◽  
Vol 869 ◽  
pp. 884-889
Author(s):  
Nadia Sueli Vieira Capanema ◽  
Alexandra A.P. Mansur ◽  
Herman Sander Mansur
Keyword(s):  
Biomedical Applications ◽  
Room Temperature ◽  
Structural Changes ◽  
Calcium Phosphates ◽  
Synthesis And Characterization ◽  
Body Parts ◽  
New Materials ◽  
X Ray Diffraction ◽  
X Ray

The need for obtaining new materials to replace human body parts that were destroyed or damaged led scientists from different areas of research for developing new biomaterials. Thus, the aim of this work was the synthesis and characterization of niobium-modified apatite bioceramics. Calcium phosphates (CaP) were synthesized with niobium partially replacing calcium sites using aqueous precipitation route at room temperature. The bioceramics, with and without Nb incorporation, were characterized by scanning electron microscopy (SEM) coupled with energy dispersive spectroscopy (EDS) and X-ray diffraction (XRD) as prepared and after heat treatments The results indicated that Nb was incorporated in the apatite structure promoting morphological and structural changes in the ceramic properties.

Study and Characterization of Powders Nanocomposites Calcium Phosphate/Silica-Gel (SiO2n) Obtained from Attrition Milling: For Biomedical Applications

2008 ◽  
Vol 396-398 ◽  
pp. 615-618
Author(s):  
Rodrigo Brandão ◽  
Fernando Pupio ◽  
Nelson Heriberto A. Camargo ◽  
E. Gemelli
Keyword(s):  
Calcium Phosphate ◽  
Silica Gel ◽  
Biomedical Applications ◽  
Bone Matrix ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
X Ray ◽  
Attrition Milling ◽  
Bone Calcium

The bioceramics nanostructured have made important characteristics in biomedical applications, especially the calcium phosphate ceramics. The aim of this work is synthesis and characterization of calcium phosphate and nanocomposites powders, the method of dissolution of CaO in liquid medium, precipitation and formation of bone calcium phosphate matrix, and nanocomposites by adding the solution of phosphoric acid (H3PO4). The nanocomposites powders were synthesized using as strengthening silica gel nanometer (20nm) at concentrations of 1%, 2%, 3% and 5% by volume and subjected to heat treatment to 900°C for 2 hours, seeking obtained HA (Hydroxyapatite). Later the bone matrix of calcium phosphate and nanocomposites powders were subjected from process attrition milling for 2 hours, by way of comparison. The studies characterizations were conducted through the technique of X-ray diffraction, scanning electron microscopy (SEM) and dilatometric test.

Solvothermal Synthesis and Characterization of Lithium Tantalate Nanoparticles

2014 ◽  
Vol 602-603 ◽  
pp. 19-22 ◽  
Author(s):  
Lin Qiang Gao ◽  
Hai Yan Chen ◽  
Zhen Wang ◽  
Xin Zou
Keyword(s):  
Electron Microscopy ◽  
Solvothermal Synthesis ◽  
Room Temperature ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Particle Size And Morphology ◽  
Size And Morphology

Nanoscale LiTaO3 powders with perovskite structure were synthesized using the solvothermal technique with glycol as solvent at 240°C for 12h. The powders were characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM) and transmission electron microscopy (TEM). XRD was used to elucidate room temperature structures using Rietveld refinement. The powders were pure single pervoskite phase with high crystallinity. FESEM and TEM were used to determine particle size and morphology. The average LiTaO3 grain size was estimated to be < 200nm, and TEM images indicated that LiTaO3 particles had a brick-like morphology. In addition, the effect of the temperature on the LiTaO3 power characterisitics was also detailed studied.

Synthesis and Characterization of Super Paramagnetic Iron Oxide Nanoparticles

2020 ◽  
Vol 10 (2) ◽  
pp. 123-126
Author(s):  
Debasish Aich ◽  
Pijus Kanti Samanta ◽  
Satyajit Saha ◽  
Tapanendu Kamilya
Keyword(s):  
Iron Oxide ◽  
Room Temperature ◽  
Synthesis And Characterization ◽  
Oxide Nanoparticles ◽  
Fe2o3 Nanoparticles ◽  
X Ray Diffraction ◽  
X Ray ◽  
Paramagnetic Behavior ◽  
Diffraction Peaks

Background: Iron oxide (γ-Fe2O3) nanoparticles have been prepared by a simplified coprecipitation method. Methods: X-ray diffraction peaks of the prepared nanoparticles match well with the characteristic peaks of crystalline g-Fe2O3 as per JCPDS data (JCPDS Card No. 39-1346) and absorption peak at 369 nm along with band gap 2.10 eV suggesting the formation of (γ-Fe2O3) nanoparticles. Results: The γ-Fe2O3 nanoparticles are spherical in nature with a diameter around ~10 nm. Conclusion: The crystalline g-Fe2O3 nanoparticles exhibit excellent super-paramagnetic behavior not only at room temperature (300K) but also at a temperature as low as 100K.

Synthesis and Characterization of a Cubic Iron Hydroxy Boracite

2011 ◽  
Vol 66 (2) ◽  
pp. 107-114 ◽  
Author(s):  
Stephanie C. Neumair ◽  
Johanna S. Knyrim ◽  
Oliver Oeckler ◽  
Reinhard Kaindl ◽  
Hubert Huppertz
Keyword(s):  
Crystal Structure ◽  
High Pressure ◽  
High Temperature ◽  
Single Crystals ◽  
Room Temperature ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
X Ray ◽  
High Pressure High Temperature

The cubic iron hydroxy boracite Fe3B7O13OH・1.5H2O was synthesized from Fe2O3 and B2O3 under high-pressure/high-temperature conditions of 3 GPa and 960 °C in a modified Walker-type multianvil apparatus. The crystal structure was determined at room temperature by X-ray diffraction on single crystals. It crystallizes in the cubic space group F4̄3c (Z = 8) with the parameters a = 1222.4(2) pm, V = 1.826(4) nm3, R1 = 0.0362, and wR2 = 0.0726 (all data). The B-O network is similar to that of other cubic boracites.

scholarly journals Synthesis and Characterization of SPIONs for Biomedical applications

2014 ◽  
Vol 70 (a1) ◽  
pp. C743-C743
Author(s):  
Tatiane Britos ◽  
Li Min ◽  
Lilia De Souza Li ◽  
Paula Haddad
Keyword(s):  
Biomedical Applications ◽  
Superparamagnetic Iron Oxide ◽  
Cell Types ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
X Ray ◽  
Mercaptosuccinic Acid ◽  
Transmission Electron ◽  
Oxidized Iron

This work reports the synthesis and characterization of superparamagnetic iron oxide nanoparticles (SPIONs), with great potential for biomedical applications. SPIONs were prepared through a decomposition of Fe(acac)3 in the presence of 1,2 hexadecanodiol (reducing agent), oleic acid and oleylamine (ligands) in a hot organic solvent. The mercaptosuccinic acid (MSA) and 2,3- dimercaptosuccinic acid (DMSA) were exchanged onto the nanocrystal surface making the particles stable in water. The thiolated nanoparticles (SH-NPs) were characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), transmission electron microscopy (TEM), and vibrating sample magnetometry (VSM). The as-prepared sample presented an amorphous partially oxidized iron structure. The results showed that the SH-NPs have a mean diameter of 6 nm and display superparamagnetic behavior at room temperature. Preliminary tests of incorporation of these systems were evaluated in Hela cells and stem cells. The results showed that the thiolated nanoparticles have no toxic effects for both cell types with good incorporation after 6 hours of transfection. Magnetic resonance image (MRI) were also carried and showed that the MNPs increase the contrast in systems investigated. Acknowledgements: FAPESP (2011/10125-0), CNPq, CAPES, UNICAMP

Synthesis and Characterization of LiMn2O4 Nanoparticles Using Citric Acid as Chelating Agent

2009 ◽  
Vol 67 ◽  
pp. 227-232 ◽  
Author(s):  
Gurpreet Singh ◽  
Amrish Panwar ◽  
Anjan Sil ◽  
Sudipto Ghosh
Keyword(s):  
Citric Acid ◽  
Room Temperature ◽  
Sol Gel ◽  
Chelating Agent ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Powder Particles

Nanocrystalline LiMn2O4 powder was synthesized by sol-gel method using citric acid as a chelating agent. The powders were characterized by X-ray diffraction (XRD), Field emission scanning electron microscopy (FESEM), Differential scanning calorimetry (DSC), Differential thermal analysis (DTA), Impedance spectroscopy (IS) and Electrochemical measurements. The powder particles having slight agglomeration characteristics were found to have prismatic morphology and a wider size distribution from 50 nm to 200 nm, which provides good packing density of the material. The electrical conductivity of the powder at room temperature is in the order of ~10-5 S/cm. The structural stability of LiMn2O4 cubic spinel over the temperature range of battery operation was assessed. Electrochemical performance of the material shows a discharge capacity of ~130 mAh/gm.

Synthesis and Characterization of Nickel Manganite Ceramics by Polymeric Precursors Method

2016 ◽  
Vol 881 ◽  
pp. 123-127 ◽  
Author(s):  
A.C.B. de Oliveira ◽  
D.M.S. Ribeiro ◽  
C.G.P. Moraes ◽  
R.S. Silva ◽  
Nilson Santos Ferreira ◽  
...  
Keyword(s):  
Room Temperature ◽  
Sintering Temperature ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
Temperature Dependent ◽  
Precursor Method ◽  
Spinel Type ◽  
X Ray ◽  
Lower Resistivity

This work presents the synthesis and characterization of NTC ceramic (Negative coefficient Temperature) based on nickel manganite (NiMn2O4) produced by the polymeric precursor method. NiMn2O4 were sintered at 900-1200 °C during 3h to produce the ceramics samples. The effect of sintering temperature on microstructure and electric properties of the NiMn2O4 ceramics was studied by X-ray diffraction (XRD), scanning electron microscopy (SEM) and temperature dependent resistance R(T) measurements. The XRD measurement indicated formation of cubic spinel-type structure of NiMn2O4. The crystallite size (as confirmed by XRD) and the particle size (as confirmed by SEM) increased as the sintering temperature increased from around 18nm (900 °C) to 100nm (1200 °C). All samples showed NTC behavior and, among the studied ceramics, that one sintered at 1200 °C showed lower resistivity value (~103Ω.cm) at room temperature.

Synthesis and Characterization of BNKT/ZnO Ferroelectric Lead-Free Nanocomposites

2014 ◽  
Vol 979 ◽  
pp. 232-235 ◽  
Author(s):  
C. Wichasilp ◽  
S. Introng ◽  
W. Maithong ◽  
N. Kruea-In ◽  
C. Kruea-In
Keyword(s):  
Room Temperature ◽  
Crystallization Behavior ◽  
Ferroelectric Properties ◽  
Measurement Data ◽  
Dielectric Measurement ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
Solid State Reaction Technique ◽  
X Ray

In this research, the effects of ZnO nanoparticles additive on crystallization behavior, dielectric and ferroelectric properties of Bi0.5(Na0.81,K0.19)0.5TiO3 ceramics were investigated. The samples were synthesized by solid state reaction technique, where powders were calcined at 850 °C for 4 h and ceramics were sintered at 1100-1150 °C for 4 h. Phase formation was determined by X-ray diffraction technique (XRD). The X-ray diffraction analysis of the ceramics suggests that all samples exhibited a perovskite structure. The dielectric properties under room temperature and various temperatures were also determined. Dielectric measurement data showed that the additive influenced dielectric constant and dielectric loss. Furthermore, the hysteresis loop behaviors slightly changed with increasing the nanoparticles contents.

Solvothermal Synthesis and Characterization of Zn(NH3)CO3 Single Crystal

2004 ◽  
Vol 817 ◽  
Author(s):  
Fushan Wen ◽  
Jiesheng Chen ◽  
Jin Hyeok Kim ◽  
Taeun Kim ◽  
Wenlian Li
Keyword(s):  
Solvothermal Synthesis ◽  
Room Temperature ◽  
Raw Materials ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
Photoluminescent Property ◽  
X Ray ◽  
3 Dimensional ◽  
Zinc Carbonate

AbstractA new 3-dimensional zinc carbonate Zn(NH3)CO3 has been synthesized from a glycol system with urea and zinc acetate as raw materials. The crystal structure and photoluminescent properties have been investigated using X-ray diffraction, smart CCD and FL. The compound had an orthorhombic system with space group of Pna21 with M = 142.41, a = 9.1449(18) Å, b = 7.5963(15) Å, c = 5.4982(11) Å, V = 381.95(13) Å3, Z = 4, R = 0.0285 and RW = 0.0745. The NH3 and CO32- were connected through the Zn-N bond and Zn-O bond in the symmetric unit. Photoluminescent property was observed in the compound at room temperature and the exited and emission peaks were located at about 350 nm and 426 nm, respectively.

Synthesis and Characterization of Missile-Like ZnO

2011 ◽  
Vol 236-238 ◽  
pp. 2183-2186
Author(s):  
Yan Li ◽  
Yun Ling Zou ◽  
Yan Yan Hou
Keyword(s):  
Room Temperature ◽  
Green Emission ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
Absolute Alcohol ◽  
X Ray ◽  
Room Temperature Photoluminescence ◽  
Zno Crystal ◽  
Hexagonal Pyramid

A novel missile-like ZnO structure has been synthesized solvo-thermally in absolute alcohol using Zn(NO3)2·6H2O and NaOH as starting materials, and characterized by Scanning Electron Microscopy, powder X-ray diffraction and room temperature photoluminescence. The missile-like ZnO crystal, with a wurtzite structure and a blue-green emission at 459 nm, is made up of two symmetrical rocket-like crystals possessing a prismatic base and a hexagonal pyramid linking with each other along plane (0001(_)).

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