scholarly journals Hydroxyapatite Extracted from Waste Fish Bones and Scales via Calcination Method

2015 ◽  
Vol 773-774 ◽  
pp. 287-290 ◽  
Author(s):  
N. Mustafa ◽  
Mohd Halim Irwan Ibrahim ◽  
Rosli Asmawi ◽  
Azriszul Mohd Amin
Keyword(s):  
Chemical Reaction ◽  
Fish Bone ◽  
Powder Size ◽  
X Ray Diffraction ◽  
Calcination Process ◽  
X Ray ◽  
Calcination Temperatures ◽  
Hydroxyapatite Powder ◽  
Before And After ◽  
Calcination Method

A hydroxyapatite is known as one of vital materials and common use in biomedical field and concentrated in clinical area. In relation to the above, the development of hydroxyapatite powder becomes an attractive research lines due to simplify in produce it. Thus in this paper the researcher stress out about Hydroxyapatite powder gained from the natural sources or so called as the waste of Tilapia bone and scales. The raw bones of and scale were undergo to crushing process to form in powder size (0.2 mm) then analysed by X-ray Diffraction (XRD) to identified the mineralogy of raw bone. Moreover the powder of fish bone and scales also go through to Scanning Electron Microscope (SEM) machine to analyse the microstructure of the powder while EDS act as device to determine the chemical composition of the sample powder. Sample powder then forward calcination process at selected temperature range to as a cheaper method in obtained hydroxyapatite raw sources. The range of calcination temperatures are between 800°C to 1000 °C. The sample preparation were analysed in both condition before and after calcination process by using XRD, SEM and EDS. The HAP crystalline composition of tilapia bones for raw powder and at 800 °C are similar with HAP pattern (JDS 00-009-0432) and the chemical reaction is Ca5(PO4)3(OH) then at temperature 900 and 1000 similar to HAP pattern (JDS 00-055-0592) with chemical reaction equal to Ca10(PO4)6(OH)2.

Biocompatible Hydroxyapatite Derive from Selayang Fish Bone via Mechanochemical Treatment

2020 ◽  
Vol 307 ◽  
pp. 339-344
Author(s):  
Ishak Qayyum Afiqah ◽  
Nik Aziz Nik Ali ◽  
Abd Majid Siti Nurhaziqah ◽  
Hasiah Salleh
Keyword(s):  
Room Temperature ◽  
Fish Bone ◽  
X Ray Diffraction ◽  
Synthetic Process ◽  
Calcination Process ◽  
Natural Sources ◽  
X Ray ◽  
Fish Bones ◽  
Phosphate Mineral

Age of monstrous amount of underutilized marine processing byproducts has been perceived as waste and many effort were given to utilize these materials in various application. With an incredible number of study on these byproducts, some compound were identified and apply for human utilization. Hydroxyapatite (HAp) is the main inorganic calcium phosphate mineral with excellent osteoconductivity, good bioactivity and biocompatibility. The production of HAp powder from synthetic process involves many chemicals with complicated procedures. Due to this matter, the raw HAp powder was extracted from natural sources selayang fish bones. Extortion process started with boiling fish bones to eliminate adherent fish meats. After calcination process fish bone were dried in room temperature before crushed by using grinder to obtain the powder. Next, the powder undergo calcination process at 900°C for 5 hours. The characterization of raw HAp was done via X-ray Diffraction, Fourier Transform Infrared Spectometer, Scanning Electron Microscopy, and Thermogravimetric analysis.

The Influences of Addition of MgCO3 on the Properties of the Magnesia Prepared Using Magnesite

2018 ◽  
Vol 281 ◽  
pp. 230-235
Author(s):  
Wang Nian Zhang ◽  
Li Wang ◽  
Ni Deng
Keyword(s):  
Grain Size ◽  
Bulk Density ◽  
Raw Materials ◽  
Apparent Porosity ◽  
X Ray Diffraction ◽  
Linear Change ◽  
Change Rate ◽  
X Ray ◽  
Before And After ◽  
Calcination Method

Micropowder MgCO3 was added into magnesite as raw materials to prepare magnesia using a two-step calcination method. The sample magnesite was characterized use X-ray diffraction (XRD) and scanning electron microscopy (SEM). Experimental results showed that the sample insulated at 1600° C for 3 hours before and after sintering presented a linear change rate of 15.6 % in the case of without adding micropowder MgCO3, the prepared magnesia had a bulk density of 2.31 g/cm3 and apparent porosity of 32.8 %, while MgO grain size was 3.11 μm. In the case of adding 8 % micropowder MgCO3, the sample magnesite before and after sintering showed a linear change rate of 17.9 %. The bulk density, apparent porosity of prepared magnesia were 2.46 g/cm3 and 28.1 % respectively, while the grain size of MgO was 5.15 mm.

scholarly journals Potential Peat Clay for Minerals Source Utilized as Adsorbent and Catalyst

2019 ◽  
Vol 280 ◽  
pp. 04003
Author(s):  
Agus Mirwan ◽  
Meilana Dharma Putra ◽  
Riani Ayu Lestari
Keyword(s):  
Xrd Analysis ◽  
Sem Analysis ◽  
X Ray Diffraction ◽  
Huge Amount ◽  
Calcination Process ◽  
X Ray ◽  
Potential Source ◽  
Before And After ◽  
Flake Structure

The existence of peat clay is scattered in many parts of the world with the huge amount. The high compound of minerals in the peat clay can be potentially used as adsorbent and catalyst. This research aims to study the composition of peat clay and functional group of the compound in the peat clay. The characterization of x-ray fluorescence (XRF), fourier transform infrared spectroscopy (FTIR), x-ray diffraction (XRD), and scanning electron microscope-energy dispersive x-ray (SEM- EDX) were assigned to compare the sample before and after calcination process at 700 oC 120 min. FTIR analysis showed the presence of quartz, kaolinite, hematite, illite in peat clay. The results of XRF analysis showed that chemical composition of peat clay was dominantly in the form of silica oxide (18%), aluminum oxide (7%), and iron oxide (15%). The amount of compounds was observed to increase to be 32%, 18% and 11%, respectively after calcinations. XRD analysis confirmed the presence of this mineral in the peat clay. SEM analysis showed flake structure of peat clay with EDX which indicated composition of the dominant element namely the presence of Al, Si, and Fe before and after calcination. This high amount of minerals in peat clay led to potential source to be utilized as adsorbent for removing the pollutant or as and catalyst for chemical process.

Synthesis of Gadolinium Doped Ceria Ceramic Powder by Polymeric Precursor Method (Pechini)

2014 ◽  
Vol 798-799 ◽  
pp. 182-188 ◽  
Author(s):  
Jesús Mauricio González Martínez ◽  
Rodrigo Arabey Muñoz Meneses ◽  
Cosme Roberto Moreira da Silva
Keyword(s):  
Ceramic Powder ◽  
Doped Ceria ◽  
Polymeric Precursor ◽  
X Ray Diffraction ◽  
Precursor Method ◽  
Calcination Process ◽  
X Ray ◽  
Before And After ◽  
Fluorite Type ◽  
Gadolinium Doped Ceria

The synthesis by polymeric precursors method (Pechini) was used to acquire gadolinium doped ceria forming Ce0,8Gd0,2O1,9 system, reaching high stoichiometric control features and nanosized particles to form dense solid electrolyte of high ionic conductivity. The synthesis was performed with cerium and gadolinium nitrates hexahydrates, citric acid and ethylene glycol. After the pre-calcination at 250°C/18h a resin was obtained like an expanded foam (puff). According to the iterature, this fact indicates that there is a reduction of agglomerates amount in a ceramic powder. A thermogravimetry-differential thermal analysis evaluated the thermal behavior of the resin. Infrared spectroscopy determined the organic matter and nitrates presence, before and after the calcination process. The X-ray diffraction identified the fluorite-type structure and was determined the crystallite size by the Scherrer equation in 22 and 46 nm for the powder calcined respectively at 600 and 800°C. The scanning electron microscopy evaluated the agglomeration degree and the morphology of the powders.

A New Method in Producing Ni Deposited Hydroxyapatite Composite by Modification of Electroless Deposition Technique

2014 ◽  
Vol 699 ◽  
pp. 99-104
Author(s):  
M.A. Sri Asliza ◽  
K. Mohd Zaheruddin ◽  
Azmi Rahmat ◽  
Shamsul Baharin Jamaludin ◽  
Rafezi Ahmad Khairel
Keyword(s):  
Electroless Deposition ◽  
Deposition Technique ◽  
X Ray Diffraction ◽  
Tetracalcium Phosphate ◽  
X Ray ◽  
Hydroxyapatite Powder ◽  
Hydroxyapatite Composite ◽  
Before And After ◽  
Surface Morphologies ◽  
Scanning Electron

Ni deposited Hydroxyapatite powder was prepared by electroless deposition technique without sensitization and activation treatments. The composition and phase of deposition were studied. The surface morphologies and composition of initial pure HA powder, as received Ni deposited HA powder and compacted Ni deposited HA powder after sintering were characterized by scanning electron microscopy (SEM) and energy dispersive spectroscopy (EDS) respectively. The phases in the powder before and after sintering were investigated by x-ray diffraction (XRD). From the experiment, with the increase of reduction agent, the plating time becomes shorter and optimal concentration of reduction agent and powder ratio is 3:1. The result shows that Ni succesfully deposited on HA powder and confirmed by EDX result. The Ni grain size distribution of 75nm to 250nm can be clearly observed on the HA surface from the micrograph after sintering. Decomposition of hydroxyapatite into α-TCP (α tricalcium phosphate) and TTCP (tetracalcium phosphate) did not occur in nickel deposited HA before and after sintering. On the other hand, a sharp Ni peak were detected

Evaluation of Freezing Methods by Low Temperature X-Ray Diffraction

1977 ◽  
Vol 35 ◽  
pp. 330-333
Author(s):  
T. Gulik-Krzywicki ◽  
M.J. Costello
Keyword(s):  
Biological Materials ◽  
Molecular Organization ◽  
X Ray Diffraction ◽  
Glass Capillary ◽  
X Ray ◽  
Rate Dependent ◽  
Before And After ◽  
Freeze Etching ◽  
Diffraction Patterns ◽  
Set Up

Freeze-etching electron microscopy is currently one of the best methods for studying molecular organization of biological materials. Its application, however, is still limited by our imprecise knowledge about the perturbations of the original organization which may occur during quenching and fracturing of the samples and during the replication of fractured surfaces. Although it is well known that the preservation of the molecular organization of biological materials is critically dependent on the rate of freezing of the samples, little information is presently available concerning the nature and the extent of freezing-rate dependent perturbations of the original organizations. In order to obtain this information, we have developed a method based on the comparison of x-ray diffraction patterns of samples before and after freezing, prior to fracturing and replication.Our experimental set-up is shown in Fig. 1. The sample to be quenched is placed on its holder which is then mounted on a small metal holder (O) fixed on a glass capillary (p), whose position is controlled by a micromanipulator.

A New Polyethylene Corrosion Protecting Coating with Ion Selectivity

2011 ◽  
Vol 314-316 ◽  
pp. 273-278
Author(s):  
Yu Hua Dong ◽  
Ke Ren ◽  
Qiong Zhou
Keyword(s):  
Ion Selectivity ◽  
Nano Particles ◽  
Ammonium Bromide ◽  
Linear Low Density Polyethylene ◽  
X Ray Diffraction ◽  
Sulfosalicylic Acid ◽  
X Ray ◽  
Chemically Modified ◽  
Before And After ◽  
Industrial Standards

Linear low density polyethylene (LLDPE) was chemically modified with grafting maleic anhydride (MAH) monomer on its backbone by melting blending. Nano-particles SiO2 was modified by cationic surfactant hexadecyl trimethyl ammonium bromide (CTAB) and anionic surfactant sulfosalicylic acid (SSA) and added to PE coating respectively. Measurement of membrane potential showed that the coating containing modified SiO2 nano-particles had characteristic of ion selectivity. The properties of the different coatings were investigated according to relative industrial standards. Experimental results indicated that PE coating with ion selectivity had better performances, such as adhesion strength, cathodic disbonding and anti-corrosion, than those of coating without ion selectivity. Crystal structure of the coatings before and after alkali corrosion was characterized by Fourier transform infrared spectra (FTIR) and X-ray diffraction (XRD). Structure of the coating without ion selectivity was damaged by NaOH alkali solution, causing mechanical properties being decreased. And the structure of the ion selective coatings was not affected.

Sedimentary Clays as Geopolymer Precursor

2018 ◽  
Vol 39 ◽  
pp. 97-111
Author(s):  
F. Mostefa ◽  
Nasr Eddine Bouhamou ◽  
H.A. Mesbah ◽  
Salima Aggoun ◽  
D. Mekhatria
Keyword(s):  
Sodium Hydroxide ◽  
Mineralogical Composition ◽  
Cementitious Materials ◽  
Raw Material ◽  
X Ray Diffraction ◽  
Calcination Time ◽  
Calorimetric Analysis ◽  
X Ray ◽  
Before And After ◽  
Mechanical Performances

This work aims to study the feasibility of making a geopolymer cement based on dredged sediments, from the Fergoug dam (Algeria) and to evaluate their construction potential particularly interesting in the field of special cementitious materials. These sediments due to their mineralogical composition as aluminosilicates; are materials that can be used after heat treatment. Sedimentary clays were characterized before and after calcination by X-ray diffraction, ATG / ATD, spectroscopy (FTIR) and XRF analysis. The calcination was carried out on the raw material sieved at 80 μm for a temperature of 750 ° C, for 3.4 and 5 hours. The reactivity of the calcined products was measured using isothermal calorimetric analysis (DSC) on pastes prepared by mixing an alkaline solution of sodium hydroxide (NaOH) 8 M in an amount allowing to have a Na / Al ratio close to 1 (1: 1). Also, cubic mortar samples were prepared with a ratio L / S: 0.8, sealed and cured for 24 hours at 60 ° C and then at room temperature until the day they were submited to mechanical testing. to check the extent of geopolymerization. The results obtained allowed to optimize the calcination time of 5 hours for a better reactivity of these sediments, and a concentration of 8M of sodium hydroxide and more suitable to have the best mechanical performances.

Aging of iron manganite negative temperature coefficient thermistors

1998 ◽  
Vol 13 (5) ◽  
pp. 1238-1242 ◽  
Author(s):  
T. Battault ◽  
R. Legros ◽  
A. Rousset
Keyword(s):  
Temperature Coefficient ◽  
Spinel Structure ◽  
Negative Temperature Coefficient ◽  
Negative Temperature ◽  
X Ray Diffraction ◽  
X Ray ◽  
Octahedral Sites ◽  
Before And After ◽  
Structural Equilibrium ◽  
Electrical Data

“Aging,” defined as the drift of resistance with temperature after 1000 h, was investigated for iron manganite temperature coefficient thermistors. For these devices, aging is relatively large, about 10%. The cationic distributions before and after aging were determined by Mössbauer spectroscopy. These distributions explain all the x-ray diffraction and correlated electrical data. The origin of the aging observed on iron manganites thermistors has been identified. It is due to the migration of Fe3+ ions from tetrahedral to octahedral sites of the spinel structure in order to reach a structural equilibrium.

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