scholarly journals Synthesis and Characterizations of Hydroxyapatite using Precursor Extracted from Chicken Egg Shell Waste

2021 ◽  
Vol 12 (4) ◽  
pp. 5663-5671
Keyword(s):  
Fourier Transforms ◽  
Research Work ◽  
Ceramic Materials ◽  
Xrd Analysis ◽  
Chemical Precipitation ◽  
Precipitation Method ◽  
Oh Groups ◽  
X Ray ◽  
Egg Shell ◽  
Eggshell Waste

Hydroxyapatite (HAP) is considered to be one of the most important members of bio-ceramic materials. HAP is widely investigated for the development of biomaterials because of having remarkable chemical similarity to the mineral component, which comprises the bone and hard tissues. The focus of research is to make the whole process eco-friendly, economical, and minimal waste generating. HAP is one of the biomaterials that can be synthesized using naturally occurring wastes such as chicken eggshells, fish scales, etc. The purpose of this research work is to synthesize HAP from Eggshell waste (ESW). The method of preparation used in the current study is the Conventional chemical precipitation method followed by calcination at diverse temperatures. Characterizations of the Eggshell waste extracted from natural HAP powder were carried out using Fourier transforms infrared spectroscopy (FTIR), X-Ray Diffraction Analysis (XRD), energy dispersive X-ray (EDX) spectroscopy, and scanning electron microscopy (SEM). XRD analysis showed the formation of HAP and gave a characteristic apatite peak at 31.8 to 32.5 for 2θ values. The peaks of FTIR spectrum displays carbonate (CO32-), phosphate (PO43-), and hydroxyl (OH-) groups in the powder sample, which confirms the synthesis of that HAP. EDX validates the elemental composition of HAP by giving the Ca/P ratio, which comes out to be 1.64 for the uncalcined HAP powder. This obtained HAP is the nearest to the pure HAP, which has a Calcium to Phosphate ratio of 1.67. The HAP derived from ESW was synthesized and validated from the results.

Manufacturing of High Toughness Hydroxyapatite Produced by Wet Chemical Method

2011 ◽  
Vol 110-116 ◽  
pp. 1289-1295
Author(s):  
Ranna Tolouei ◽  
Singh Ramesh ◽  
Chou Yong Tan ◽  
Meenaloshini Satgunam ◽  
Mahdi Amiriyan
Keyword(s):  
Mechanical Properties ◽  
Fracture Toughness ◽  
Ceramic Materials ◽  
Xrd Analysis ◽  
Chemical Precipitation ◽  
Holding Time ◽  
Precipitation Method ◽  
Tissue Replacement ◽  
Wet Chemical ◽  
Heating Profile

Hydroxyapatite (HA) is among the leading ceramic materials for hard tissue replacement implants. Despite the excellent bioactivity of HA, low toughness has limited the application of these materials to non-load bearing areas. The sinterability of nanocrystalline hydroxyapatite (HA) powder via new heating profile for conventional pressureless sintering was studied. The starting nanocrystalline HA powder was synthesized by wet chemical precipitation method. After uniaxial pressing followed by isostatic pressing, HA powder compacts are sintered over the temperature range of 1000°C to 1300°C. Different holding time of 1 minute and 120 minutes was applied as a heating profile of HA samples. The results revealed that new heating profile was effective in producing a HA body with high density of 98% when sintered at 1200°C. Subsequently, mechanical properties such as fracture toughness and hardness, of HA compacts increased with decrease in grain size. HA showed the highest hardness of 9.51 GPa and fracture toughness of 1.41 MPa.m1/2 when sintered at 1100 °C. XRD analysis indicated that decomposition of HA phase during sintering at high temperatures do not occur. Short holding time leads to finer microstructure of HA and subsequently better mechanical properties.

Characterisation of undoped Zns and fecl3 doped Zns nanoparticles are synthesized by chemical precipitation method

2020 ◽  
Vol 3 (2) ◽  
Author(s):  
Aarthe K G ◽  
Kiruthika P
Keyword(s):  
Xrd Analysis ◽  
Chemical Precipitation ◽  
Zinc Sulphide ◽  
Chemical Precipitation Method ◽  
Precipitation Method ◽  
Flat Panel Displays ◽  
X Ray Diffraction ◽  
Nano Structure ◽  
X Ray ◽  
Vibrational Bands

Nanoparticles of Ferric chloride (FeCl3) doped Zinc Sulphide (ZnS) and Undoped Zinc Sulphide (ZnS) had been synthesized successfully by simple chemical precipitation method. Particlesizes have been calculated from X-ray diffraction (XRD) analysis which confirms the nano structure of the samples. The Molecular structure of the compound was determined by theFourier transform infrared spectroscopy (FTIR) analysis and the different vibrational bands confirmed the functional groups present in the sample. The bandwidth of the absorbance isexamined by using (UV)-Visible Spectroscopy. The Morphological structures have been confirmed by using Scanning Electron Microscope (SEM). Energy Dispersive analysis of X-ray (EDAX) shows the composition of elements present in the nanoparticles. The applications of ZnS were used in the field such as Field Emitting Diodes (FET), sensors (gas sensors, biosensors), Flat panel displays, Electroluminescence.

Synthesis and photocatalytic properties of magnetic separable and recyclable p-n heterojunction CoFe2O4/Bi12O17Cl2 photocatalyst

CrystEngComm ◽  
2021 ◽  
Author(s):  
Kexin Fang ◽  
Lei Shi ◽  
Lishuang Cui ◽  
Chunwei Shi ◽  
Weiwei Si
Keyword(s):  
Chemical Precipitation ◽  
Photocatalytic Properties ◽  
Chemical Precipitation Method ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
High Crystallinity

A series of CoFe2O4/Bi12O17Cl2 (CFO/Bi12O17Cl2) nanocomposites have been prepared by chemical precipitation method. The result of X-ray diffraction showed that CFO/Bi12O17Cl2 composites had high crystallinity. It was found that CoFe2O4...

Monodisperse Fe3O4/Fe Core/Shell Nanoparticles with Enhanced Magnetic Property

2011 ◽  
Vol 306-307 ◽  
pp. 410-415
Author(s):  
Li Sun ◽  
Fu Tian Liu ◽  
Qi Hui Jiang ◽  
Xiu Xiu Chen ◽  
Ping Yang
Keyword(s):  
Average Diameter ◽  
Chemical Precipitation ◽  
Precipitation Method ◽  
Core Shell ◽  
X Ray Diffraction ◽  
Shell Nanoparticles ◽  
X Ray ◽  
Transmission Electron ◽  
Shell Particles ◽  
Core Shell Nanoparticles

Core/shell type nanoparticles with an average diameter of 20nm were synthesized by chemical precipitation method. Firstly, Monodisperse Fe3O4 nanoparticles were synthesized by solvethermal method. FeSO4ž7H2O and NaBH4 were respectively dissolved in distilled water, then moderated Fe3O4 particles and surfactant(PVP) were ultrasonic dispersed into the FeSO4ž7H2O solution. The resulting solution was stirred 2 h at room temperature. Fe could be deposited on the surface of monodispersed Fe3O4 nanoparticles to form core-shell particles. The particles were characterized by using various experimental techniques, such as transmission electron microscopy (TEM), X-ray diffraction (XRD), AGM and DTA. The results suggest that the saturation magnetization of the nanocomposites is 100 emu/g. The composition of the samples show monodisperse and the sides of the core/shell nanoparticles are 20-30nm. It is noted that the formation of Fe3O4/Fe nanocomposites magnetite nanoparticles possess superparamagnetic property.

scholarly journals STUDY OF ANTIMICROBIAL ACTIVITY OF SILVER-DOPED HYDROXYAPATITE

2019 ◽  
pp. 243-245
Author(s):  
HIBU WAHID ◽  
ANJUVAN SINGH
Keyword(s):  
Escherichia Coli ◽  
Antimicrobial Activity ◽  
Fourier Transform ◽  
Infrared Spectroscopy ◽  
Fourier Transform Infrared Spectroscopy ◽  
Xrd Analysis ◽  
Chemical Precipitation ◽  
Silver Concentration ◽  
Precipitation Method ◽  
Zone Of Inhibition

Objective: Hydroxyapatite (Hap) is an important material used for implants because of its structural similarity with calcium phosphate of the teeth and bones. Hap is mostly used in the situations where load-bearing implants are needed, such as in dental and orthopedic applications. Dental plaque is caused due to the bacteria which induces secondary caries through microleakage between the restoration and the tooth structure. Methods: An attempt has been made to provide materials with antibacterial activity by incorporating an antibacterial agent into the chemical mixture (Hap). This study delineates the process of synthesizing silver-doped Hap (Ca10Agx(PO4)6(OH)2) by wet chemical precipitation method and by varying the silver concentration (0.3%–0.5%). The synthesized silver-doped Hap was further characterized using Fourier transform infrared spectroscopy and X-ray diffraction (XRD) analysis. The antimicrobial activities were tested against Gram-negative bacteria Escherichia coli. Results: The maximum zone of inhibition against Escherichia coli was observed when equal concentration of Hydroxyapatite and Silver were mixed together i.e XAg=0.5% Zone of inhibition helps to determine the antimicrobial activity of silver-doped Hap. An increase in the zone of inhibition indicates the least growth of microorganisms which was observed at a silver concentration XAg=0.5%. Conclusions: Silver-doped Hap was synthesized successfully using the chemical precipitation method and was characterized using Fourier transform infrared spectroscopy and XRD analysis. It can be concluded that silver-doped Hap can be an excellent substitute material used as dental implant device.

scholarly journals Crystal Chemistry and Luminescence Properties of Eu-Doped Polycrystalline Hydroxyapatite Synthesized by Chemical Precipitation at Room Temperature

Crystals ◽  
2020 ◽  
Vol 10 (4) ◽  
pp. 250 ◽  
Author(s):  
Francesco Baldassarre ◽  
Angela Altomare ◽  
Nicola Corriero ◽  
Ernesto Mesto ◽  
Maria Lacalamita ◽  
...  
Keyword(s):  
Fourier Transform ◽  
High Temperature ◽  
Inductively Coupled Plasma ◽  
Room Temperature ◽  
Annealing Temperature ◽  
Chemical Precipitation ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Inductively Coupled

Europium-doped hydroxyapatite Ca10(PO4)6(OH)2 (3% mol) powders were synthesized by an optimized chemical precipitation method at 25 °C, followed by drying at 120 °C and calcination at 450 °C and 900 °C. The obtained nanosized crystallite samples were investigated by means of a combination of inductively coupled plasma (ICP) spectroscopy, powder X-ray diffraction (PXRD), Fourier Transform Infrared (FTIR), Raman and photoluminescence (PL) spectroscopies. The Rietveld refinement in the hexagonal P63/m space group showed europium ordered at the Ca2 site at high temperature (900 °C), and at the Ca1 site for lower temperatures (120 °C and 450 °C). FTIR and Raman spectra showed slight band shifts and minor modifications of the (PO4) bands with increasing annealing temperature. PL spectra and decay curves revealed significant luminescence emission for the phase obtained at 900 °C and highlighted the migration of Eu from the Ca1 to Ca2 site as a result of increasing calcinating temperature.

Synthesis, Structural Analysis of Cadmium Sulphide Nanocrystallites

2019 ◽  
Vol 969 ◽  
pp. 169-174
Author(s):  
R. Sivanand ◽  
S. Chellammal ◽  
S. Manivannan
Keyword(s):  
Size Variation ◽  
Cadmium Sulphide ◽  
Xrd Analysis ◽  
Sem Analysis ◽  
Precipitation Method ◽  
Capping Agent ◽  
Energy Dispersive Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Scanning Electron

In this paper, the effect of size variation of cadmium sulphide nanocrystallites which have been prepared by precipitation method is analyzed. These prepared samples were studied using X-ray diffraction (XRD), Scanning electron microscopy (SEM), and Energy dispersive analysis of spectroscopy (EDAX) techniques. SEM analysis represents the morphological nature of prepared samples and EDAX indicates the confirmation of elements present in the sample. XRD analysis determines the size of the samples and identifies the structure using miller indices (h k l values) of the nanocrystallies matches with JCPDS. From the XRD analysis, the size variation which depends on dopant, capping agent are discussed and corresponding results are reported in this paper.

Preparation of Amorphous Calcium Phosphate/Triclcium Silicate Composite Powders

2009 ◽  
Vol 79-82 ◽  
pp. 1643-1646 ◽  
Author(s):  
Qing Lin ◽  
Yan Bao Li ◽  
Xiang Hui Lan ◽  
Chun Hua Lu ◽  
Zhong Zi Xu
Keyword(s):  
Calcium Phosphate ◽  
Shell Structure ◽  
Amorphous Calcium Phosphate ◽  
Chemical Precipitation ◽  
Precipitation Method ◽  
Core Shell ◽  
X Ray Diffraction ◽  
Composite Powders ◽  
X Ray ◽  
Core Shell Structure

The amorphous calcium phosphate (ACP)/tricalcium silicate (Ca3SiO5, C3S) composite powders were synthesized in this paper. The exothermal behavior of C3S determined by isothermal conduction calorimetry indicated that the ACP could be synthesis by chemical precipitation method during the induction period (stage II) of C3S. The composite powders were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDS). The results indicated that nanosized ACP particles deposited on the surface of C3S particles to form core-shell structure at pH=10.5, and the nCa/nP of ACP could be controlled between 1.0 and 1.5. The core-shell structure is stable after sintered at 500 oC for 3 h to remove the β-cyclodextrin (β-CD). As compared with the irregular C3S particles (1~5 μm), the composite powders particles are spherical with a diameter of 40~150 μm. Therefore, to obtain the smaller size of composite powders, it is expected to avoid the aggregate of C3S particles in the aqueous solution by addition of dispersant. As compared with C3S, the composite powders may contribute better injectability, strength and biocompatibility.

Effects of Different Content of TiO2 on Crystallization Behavior and Properties of Li2O-ZnO-SiO2 Glass-Ceramics

2014 ◽  
Vol 1035 ◽  
pp. 263-267
Author(s):  
Xiu Quan Zhao ◽  
Zheng Cao ◽  
Yu Teng Wu ◽  
Hong Jiang ◽  
Chang Jiu Li ◽  
...  
Keyword(s):  
Crystallization Behavior ◽  
Glass Ceramics ◽  
Ceramic Materials ◽  
Xrd Analysis ◽  
Spherical Particles ◽  
X Ray Diffraction ◽  
X Ray ◽  
Glass Ceramic Materials ◽  
Average Coefficient ◽  
Different Content

Glass-ceramic materials of the Li2O-ZnO-SiO2 system, with various amounts of TiO2 added, have been prepared. The appropriate heat treatment temperatures were selected according to the information provided by the differential thermal analysis (DTA). X-ray diffraction (XRD) analysis demonstrated that in the LZS glass-ceramics system, the main phases are Li2ZnSiO4, cristobalite, tridymite and quartz. The scanning electron microscopy (SEM) revealed that crystals appear as lamellar and spherical particles in the glass-ceramics samples. In addition, the average coefficient of the thermal expansion (CTE) values first decreased, then increased and finally tended to flatten. When the content of TiO2 increased to 6%, the CTE value decreased to 9.15×10-6/K, reached the lowest value. When the content of TiO2 increased to 10%, the CTE value reached highest value 13.90×10-6/K.

Influence of Zinc Substitution on Hydroxyapatite Structure Prepared by Chemical Precipitation Method

2018 ◽  
Vol 879 ◽  
pp. 3-7 ◽  
Author(s):  
Nisakorn Nuamsrinuan ◽  
Patcharin Naemchanthara ◽  
Pichet Limsuwan ◽  
Kittisakchai Naemchanthara
Keyword(s):  
Heat Treatment ◽  
Fourier Transforms ◽  
Chemical Precipitation ◽  
Zinc Nitrate ◽  
Treatment Temperature ◽  
Chemical Precipitation Method ◽  
Precipitation Method ◽  
Phosphate Phase ◽  
Chicken Eggshell ◽  
Hydroxyapatite Phase

The zinc (Zn) substituted hydroxyapatite were synthesized using a chemical precipitation method. The chemical precursors were prepared from di-ammonium hydrogen orthophosphate, calcium oxide (CaO) derived from chicken eggshell and zinc nitrate (Zn(NO3)2). The Zn(NO3)2contents in the prepared samples were varied from 1 to 25 %wt of CaO. The Zn substituted hydroxyapatite were heated at the various temperatures from 200 to 1300 °C in the furnace with an incremental temperature of 100 °C. The crystal structure, function group and morphology of sample were analyzed by X-ray diffraction (XRD), Fourier transforms infrared spectroscopy (FTIR) and field emission scanning electron microscopy (FESEM), respectively. The results show that the hydroxyapatite doped Zn was a hydroxyapatite phase as well as pure hydroxyapatite. The crystalline size of sample decreased with increasing the Zn content. And, the crystallinity of hydroxyapatite phase was increased following by increasing heat treatment temperature. However, the amount of Zn has the effect on phase transformation of hydroxyapatite phase after heat treatment. Zn concentration accelerates hydroxyapatite transforms to β-tricalcium phosphate phase.

Sign in / Sign up

Export Citation Format

Share Document