Synthesis and Characterization of Zinc Doped Hydroxyapatite for Bone Substitute Applications

2014 ◽  
Vol 660 ◽  
pp. 942-946
Author(s):  
Mohamad Firdaus Abdul Wahid ◽  
C.M. Mardziah ◽  
Koay Mei Hyie ◽  
N.R. Nik Roselina
Keyword(s):  
Crystal Size ◽  
Diffraction Method ◽  
Lattice Parameters ◽  
Phase Changes ◽  
Precipitation Method ◽  
Zinc Ions ◽  
Crystal Shape ◽  
X Ray Diffraction ◽  
X Ray

Hydroxyapatite was prepared by using precipitation method. The substitution of zinc ions in hydroxyapatite structure was studied by several characterization techniques. Several concentration of zinc ions were substituted into hydroxyapatite. Characterization technique such as X-ray diffraction method was used to study the phase changes and the lattice parameters with the addition of zinc. Field emission scanning electron microscopy was used to examine the influence of zinc on the crystal size and the morphology of the as-synthesized powders. Based on X-ray diffraction result, the addition of zinc affects the lattice parameters and phase. The result showed that zinc ions were substituted in the structure. As zinc substitution increased, the lattice parameters a and c decreased. The crystal shape of hydroxyapatite without zinc ions was regular shapes while hydroxyapatite with zinc ions was irregular and also tends to agglomerates with single particle was calculated about 28 - 34 nm .

scholarly journals Synthesis and characterization of apatite silicated powders with wet precipitation method

2021 ◽  
Vol 234 ◽  
pp. 00106
Author(s):  
Houda Labjar ◽  
Hassan Chaair
Keyword(s):  
Electron Microscopy ◽  
Heat Treatment ◽  
Analytical Techniques ◽  
Precipitation Method ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
X Ray ◽  
Wet Precipitation ◽  
Scanning Electron

The synthesis of apatite silicated Ca10(PO4)6-x(SiO4)x(OH)2-x (SiHA) with 0≤x≤2 was investigated using a wet precipitation method followed by heat treatment using calcium carbonate CaCO3 and phosphoric acid H3PO4 and silicon tetraacetate SiC8H20O4 (TEOS) in medium of water ethanol, with three different silicate concentrations. After drying, the samples are ground and then characterized by different analytical techniques like X-ray Diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR) and Scanning electron Microscopy (SEM) and chemical analysis.

scholarly journals Magnetically Oriented Powder Crystal to Indexing and Structure Determination

2014 ◽  
Vol 70 (a1) ◽  
pp. C1560-C1560
Author(s):  
Fumiko Kimura ◽  
Wataru Oshima ◽  
Hiroko Matsumoto ◽  
Hidehiro Uekusa ◽  
Kazuaki Aburaya ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Single Crystal ◽  
Crystal Lattice ◽  
Powder Diffraction ◽  
Diffraction Method ◽  
Lattice Parameters ◽  
X Ray Diffraction ◽  
X Ray ◽  
Crystal Lattice Parameters

In pharmaceutical sciences, the crystal structure is of primary importance because it influences drug efficacy. Due to difficulties of growing a large single crystal suitable for the single crystal X-ray diffraction analysis, powder diffraction method is widely used. In powder method, two-dimensional diffraction information is projected onto one dimension, which impairs the accuracy of the resulting crystal structure. To overcome this problem, we recently proposed a novel method of fabricating a magnetically oriented microcrystal array (MOMA), a composite in which microcrystals are aligned three-dimensionally in a polymer matrix. The X-ray diffraction of the MOMA is equivalent to that of the corresponding large single crystal, enabling the determination of the crystal lattice parameters and crystal structure of the embedded microcrytals.[1-3] Because we make use of the diamagnetic anisotropy of crystal, those crystals that exhibit small magnetic anisotropy do not take sufficient three-dimensional alignment. However, even for these crystals that only align uniaxially, the determination of the crystal lattice parameters can be easily made compared with the determination by powder diffraction pattern. Once these parameters are determined, crystal structure can be determined by X-ray powder diffraction method. In this paper, we demonstrate possibility of the MOMA method to assist the structure analysis through X-ray powder and single crystal diffraction methods. We applied the MOMA method to various microcrystalline powders including L-alanine, 1,3,5-triphenyl benzene, and cellobiose. The obtained MOMAs exhibited well-resolved diffraction spots, and we succeeded in determination of the crystal lattice parameters and crystal structure analysis.

Structure Characterization of Sintered CaO-Al2O3-SiO2 Glass-Ceramic Reinforced with Spodumene

2013 ◽  
Vol 834-836 ◽  
pp. 309-314
Author(s):  
Zi Fan Xiao ◽  
Jin Shu Cheng ◽  
Jun Xie
Keyword(s):  
Glass Ceramic ◽  
Energy Dispersive Spectrometry ◽  
Crystal Size ◽  
Bending Strength ◽  
Glass Ceramics ◽  
Structure Characterization ◽  
X Ray Diffraction ◽  
Crystalline Phases ◽  
X Ray

A glass-ceramic belonging to the CaO-Al2O3-SiO2(CAS) system with different composition of spodumene and doping the Li2O with amount between 0~2.5 % (mass fraction) were prepared by onestage heat treatment, under sintering and crystallization temperature at 1120 °C for two hours. In this paper, differential thermal analysis, X-ray diffraction, scanning electron microscopy, energy dispersive spectrometry and bending strength test were employed to investigate the microstructure and properties of all samples. β-wollastonite crystals were identified as the major crystalline phases, and increasing Li2O was found to be benefit for the crystallization and tiny crystalline phases remelting, resulting in the content of major crystalline phases increased first and then decreased with increasing the expense of spodumene. Meanwhile, the crystal size can be positively related with the content of Li2O. The preferable admixed dosage of spodumene can be obtained, besides the strength of glass-ceramics can be more than 90 MPa.

Polymorphic transformations and thermal expansion of some modifications in Ag1.5Cu0.5Se and Ag0.4Cu1.6Se

2019 ◽  
Vol 33 (23) ◽  
pp. 1950271 ◽  
Author(s):  
Y. I. Aliyev ◽  
Y. G. Asadov ◽  
A. O. Dashdemirov ◽  
R. D. Aliyeva ◽  
T. G. Naghiyev ◽  
...  
Keyword(s):  
Thermal Expansion ◽  
High Temperature ◽  
Temperature Dependence ◽  
Single Crystals ◽  
Diffraction Method ◽  
Lattice Parameters ◽  
X Ray Diffraction ◽  
Polymorphic Transformations ◽  
X Ray

The Ag[Formula: see text]Cu[Formula: see text]Se and Ag[Formula: see text]Cu[Formula: see text]Se compounds have been synthesized and grown as single crystals. High-temperature X-ray diffraction method was used to study polymorphic transformations. It is shown that the Ag[Formula: see text]Cu[Formula: see text]Se crystals of high-temperature FCC modification are decomposed into Ag2Se and AgCuSe when the temperature decreases below T = 488 K and Ag[Formula: see text]Cu[Formula: see text]Se is decomposed into Cu2Se and AgCuSe when the temperature decreases below T = 540 K. Transformations in both compounds are reversible. Crystalline parameters are obtained and the temperature dependence of the lattice parameters for each phase is built.

Studied on Structural Characterization of Lanthanum Doped Barium Titanium Ceramics

2015 ◽  
Vol 819 ◽  
pp. 198-203
Author(s):  
Nur Farahin Abdul Hamid ◽  
Rozana Aina Maulat Osman ◽  
Mohd Sobri Idris ◽  
Tze Qing Tan
Keyword(s):  
Crystal Structure ◽  
Lattice Parameter ◽  
Phase Changes ◽  
X Ray Diffraction ◽  
X Ray ◽  
Tetragonal Crystal ◽  
Tetragonal Crystal Structure ◽  
La Doped ◽  
Conventional Solid State Synthesis

La-doped barium titanate (BaTiO3) was prepared using conventional solid state synthesis route. All peaks for sample x=0 are approaching the phase pure of BaTiO3 structure with tetragonal crystal structure (P4mm). Sintering of pressed powder are performed at 1300oC, 1400oC and 1450oC for overnight for pure BaTiO3 and 1350oC for 3 days for BaTiO3 doped lanthanum with intermittent grinding. Phase transition was studied by different x composition. The changes in the crystal structure of the composition x=0.1 and 0.2 were detected by using X-ray diffraction (XRD). The phase changes between tetragonal-cubic and cubic-tetragonal depending on the temperature. Rietveld Refinement analysis is carried out to determine the lattice parameter and unit cell for BaTiO3.

scholarly journals Growth and Characterization of Pure and Doped L-Alanine Tartrate Single Crystals

2013 ◽  
Vol 2013 ◽  
pp. 1-5 ◽  
Author(s):  
K. Rajesh ◽  
B. Milton Boaz ◽  
P. Praveen Kumar
Keyword(s):  
Single Crystals ◽  
Vickers Microhardness ◽  
Diffraction Method ◽  
Dielectric Studies ◽  
X Ray Diffraction ◽  
X Ray ◽  
Cell Parameters ◽  
Ft Ir ◽  
Ft Ir Spectroscopy

Single crystals of pure and Lanthanum doped L-Alanine Tartrate were grown by slow evaporation method. The cell parameters were determined using single crystal X-ray diffraction method. To improve the physical properties of the LAT crystal, Lanthanum dopant was added by 2 mol%. ICP studies confirm the presence of Lanthanum in the grown LAT crystal. Transparency range of the crystal was determined using UV-VIS-NIR spectrophotometer. The functional groups of pure and doped LAT crystals were analyzed by FT-IR spectroscopy. Using Vickers microhardness tester, mechanical strength of the material was found. Dielectric studies of pure and doped LAT single crystals were carried out. The doped LAT crystal is found to have efficiency higher than that of pure LAT crystal.

SYNTHESIS AND CHARACTERIZATION OF La2Ca3Cu4Oy

1999 ◽  
Vol 13 (12n13) ◽  
pp. 451-453
Author(s):  
K. JEYABALAN ◽  
L. K. KALIYAPERUMAL
Keyword(s):  
Diffraction Analysis ◽  
Lattice Parameters ◽  
Synthesis And Characterization ◽  
Orthorhombic Structure ◽  
X Ray Diffraction ◽  
X Ray

Synthesis and characterization of La 2 Ca 3 Cu 4 O y compound is reported here. The powder X-ray diffraction analysis shows that the system belongs to an orthorhombic structure and the lattice parameters are a = 3.814(4)Å, b = 3.930(5)Å and c = 34.772(3)Å.

Size Controllable Synthesis and Characterization of CuO Nanostructure

2018 ◽  
Vol 915 ◽  
pp. 98-103 ◽  
Author(s):  
Duygu Candemir ◽  
Filiz Boran
Keyword(s):  
Freeze Drying ◽  
Chemical Precipitation ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Peg 4000 ◽  
Structure Morphology ◽  
Cuo Nanostructure

In this study, copper oxide (CuO) nanostructures were successfully prepared by adding EG (ethylene glycol) and PEG (4000, 8000) (polyethylene glycol) via an in-situ chemical precipitation method. EG and PEG (4000, 8000) were effective for changing the particular size of CuO and we examined the effects of drying type such as freeze drying, muffle and horizontal furnace on the size of CuO nanostructure. The structure, morphology and elemental analysis of CuO nanostructure were analyzed by field-emission scanning electron microscopy (FE-SEM), X-ray diffraction (XRD) and energy dispersive X-ray spectroscopy (EDS). Also, the CuO nanostructures showed excellent electrical conductivity by the changing of PEG’s molecular weight and drying processes.

scholarly journals STRUCTURE CHARACTERIZATION OF CALCIUM DEFICIENT ELEMENT-SUBSTITUTED HYDROXYAPATITE WITH CONSTANT DOPANT RATIO OF DIFFERENT ELEMENTS

2020 ◽  
Vol 51 (5) ◽  
pp. 1420-1427
Author(s):  
Al-Sabbagh & et al.
Keyword(s):  
Single Phase ◽  
Atomic Radius ◽  
Calcium Hydroxyapatite ◽  
Structure Characterization ◽  
Precipitation Method ◽  
Vibration Modes ◽  
X Ray Diffraction ◽  
X Ray ◽  
Oxygen Groups

The element-substituted calcium Deficient hydroxyapatite samples were synthesized using liquid-phase precipitation method. Different element ions (Mg+2, Zn+2, and Cu+2) were added at constant ratio (5% wt.). The phase composition of the element-substituted calcium hydroxyapatite samples was investigated by using X-ray diffraction. A comparison with known characteristics of the synthetic ion-substituted forms of hydroxyapatite was conducted. It was determined, that the investigated materials are single-phase solid solutions of the element-substituted hydroxyapatite. By the methods of IR spectroscopy and Raman scattering (RS) it was discovered the dependence of incorporation of the carbonate anion that occupies a positions of phosphorus-oxygen groups in the hydroxyapatite structure as a result of embedding element ions (Zn+2, Cu+2, Mg+2) in the crystal lattice. Besides, It was determined, that the ratio of the intensities for the C03 group mode to the P04 groups mode depended on the nature of the element atom, which replace the calcium in the lattice of HAP, and reduced by substituting the calcium atoms by the atoms of Zn, Cu, and Mg from 0.15 to 0.06. Modeling of the vibration modes of Raman spectroscopy showed that incorporation of carbon atoms to the hydroxyapatite structure correlate with the Zn, Cu and Mg atomic radius, charge, and activity   

scholarly journals Kandungan Mineral dan Struktur Kristal Batu Sekis

2020 ◽  
Vol 4 (1) ◽  
pp. 24-30
Author(s):  
Muhamad Ragil Setiawan ◽  
Rahmat Nawi Siregar
Keyword(s):  
Crystal Structure ◽  
Data Processing ◽  
Mineral Content ◽  
Diffraction Method ◽  
Lattice Parameters ◽  
X Ray Diffraction ◽  
Rock Crystal ◽  
X Ray ◽  
Two Samples ◽  
Processing Information

This study aims to determine the mineral content and crystal structure of schist rocks in South Lampung. The method used in this research is the X-ray diffraction method to see the lattice parameters and the crystal structure of the schist rocks. Based on data processing, information was obtained that two main minerals were found, namely quartz and albite minerals. In conclusion, the Albit minerals found in the two samples of rock crystal schists in South Lampung have the same crystal structure and lattice parameters, while the quartz minerals from the two samples have different crystal structures and lattice parameters. Keywords: Lampung, Schis, XRD, Crystal Structure

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