scholarly journals CHARACTERIZATION OF NANOHYDROXYAPATITE FROM TUNA’S Thunnus sp BONE AS BIOMATERIALS SUBSTANCE

2018 ◽  
Vol 9 (2) ◽  
pp. 619-629
Author(s):  
Aditya Bayu Hanura ◽  
Wini Trilaksani ◽  
Pipih Suptijah
Keyword(s):  
Temperature Variation ◽  
Sintering Temperature ◽  
Statistic Analysis ◽  
Metal Analysis ◽  
X Ray ◽  
Hexagonal Shape ◽  
Particle Size Analyzer ◽  
Degree Level ◽  
Test Level

Tuna Thunnus sp is a high-value fisheries products. The abundance of waste from tuna’s processing industry has not been used optimally. The objective of this study was to produce and characterize nanohidroxyapatite (Ca5(PO4)3((OH)0.8F0.2) of tuna’s Thunnus sp bone waste using high temperature sintering of 400-800OC continuing by nanomilling method. The results of the characterization showed that the sintering temperature of 800OC was the best treatment yielding of hidroxyapatite 57.73%, 89.27% white degree level. The result of statistic analysis showed that the sintering temperature variation gave a significant effect on the white degree at the test level (p <0.05). Proximate result after sintering showed moisture content of 0.15%, 99.83% ash, 0.05% fat, 0.73% protein and 0% crude fiber. Results of heavy metal analysis showed the content of lead (Pb) and mercury (Hg) was negative, and cadmium (Cd) 0.018 ppm. The mineral test consist of calcium, phosphor, kalium, magnesium, iron, zinc, manganese, and sodium with the dominant elements were 49.76% calcium and 9.02% phosphor. The result of statistic analysis showed that the sintering temperature variation gave significant effect to the three main minerals at the test level (p<0.05). The Particle Size Analyzer test showed that nanohidroxyapatite particles was measured at 800-900 nm. The X-Ray Diffractometer analysis showed the results of sample identification contains hydroxyapatite and fluorian, with syn 100.00%. The hidroxyapatite was a compound complex and crystals formed has a hexagonal shape with a percentage of 82.9% crystallinity. Keywords : bone, nanohidroxyapatite, particles, sintering, tuna

Effect of Process on the Dielectric Properties of BaTiO3-Based X9R Ceramics

2014 ◽  
Vol 906 ◽  
pp. 18-24 ◽  
Author(s):  
Bao Lin Zhang ◽  
Bin Bin Zhang ◽  
Ning Ning Wang ◽  
Jing Ming Fei
Keyword(s):  
Particle Size ◽  
Dielectric Properties ◽  
Milling Time ◽  
Sintering Temperature ◽  
Sintering Process ◽  
X Ray Diffraction ◽  
Sintered Ceramic ◽  
X Ray ◽  
Particle Size Analyzer

The effect of milling time and sintering process on the dielectric properties of BaTiO3-based X9R ceramics was investigated. The characterization of the raw powders and the sintered ceramic was carried out by X-ray diffraction and scanning electron microscopy. The particle size distribution of the mixed powders was examined by Laser Particle Size Analyzer. The results shown that with the milling time extended, the Cruie Peak was depressed, or even disappeared. Moreover, with the rise of sintering temperature, the dielectric constant of the ceramics increased and the dielectric loss decreased gradually. Eventually, by milling for 11h and sintering at 1090°Cfor 2h, good dielectric properties were obtained, which were ε25°C≥ 2526, εr/εr25°C≤± 12% (–55~200°C), tanδ≤1.12% (25°C).

scholarly journals Synthesis of Silver Nanoparticles Using Muntingia Calabura L. Leaf Extract as Bioreductor and Applied as Glucose Nanosensor

2018 ◽  
Vol 34 (6) ◽  
pp. 3088-3094 ◽  
Author(s):  
Abdul Wahid Wahab ◽  
Abdul Karim ◽  
Nursiah La Nafie ◽  
Nurafni Nurafni ◽  
I. Wayan Sutapa
Keyword(s):  
Particle Size ◽  
Silver Nanoparticles ◽  
Reduction Method ◽  
Measurement Range ◽  
Structure Characterization ◽  
X Ray Diffraction ◽  
X Ray ◽  
Particle Size Analyzer ◽  
Muntingia Calabura

Silver nanoparticles have been synthesized by reduction method using extract of Muntingia calabura L. leaf a bioreductor. The process of silver nanoparticles formation was monitored by UV-Vis method. The results showed that the absorbance values increased according to the increase of reaction time. Maximum absorption of silver nanoparticle was obtained at a wavelength of 41-421 nm. The size of silver nanoparticles was determined using a PSA (Particle Size Analyzer) with a particle size distribution of 97.04 nm. The functional groups compound that contribute in the synthesis was analyzed using Fourier Transform Infrared Spectroscopy (FTIR). Morphology of the silver nanoparticles was observed by an Scanning Electron Microscope instrument and the structure characterization of the compounds were analyzed using X-Ray Diffraction. The glucose nanosensor based on silver nanoparticles have the measurement range of 1 mM - 4 mM with the regretion (R2) is 0,9516, the detection limit of sensor is 3,2595 mM, the sensitivity of sensor is 2,0794 A. mM-1. mM-2.

Preparation and Characterization of Monodisperse Ceria Microspheres

2010 ◽  
Vol 434-435 ◽  
pp. 850-852
Author(s):  
Qi Wang ◽  
Bo Yin ◽  
Zhen Wang ◽  
Gen Li Shen ◽  
Yun Fa Chen
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Particle Size ◽  
Electron Microscope ◽  
Crystalline Form ◽  
X Ray ◽  
Transmission Electron ◽  
Particle Size Analyzer ◽  
Scanning Electron

In present work, ceria microspheres were synthesized by template hydrothermal method. Crystalline form of the as-synthesized ceria microspheres was defined by X-ray powder diffraction (XRD) and high resolution transmission electron microscopy (HRTEM). Dispersibility of ceria microspheres was comprehensively characterized using scanning electron microscope (SEM) observation and laser particle size analyzer. Furthermore, the ultraviolet light absorption performances of ceria microspheres with several different sizes were compared by ultraviolet visible spectrophotometer. The results showed that ceria microspheres presented excellent UV absorbent property and the size influence was remarkable.

SYNTHESIS AND CHARACTERIZATION OF HIGH-Tc SUPERCONDUCTORS IN THE Tl–Ca–Ba–Cu–O SYSTEM

1989 ◽  
Vol 03 (05) ◽  
pp. 733-741
Author(s):  
NAROTTAM P. BANSAL ◽  
D. E. FARRELL
Keyword(s):  
Sintering Temperature ◽  
Resistive Transition ◽  
X Ray Diffraction ◽  
High Tc Superconductors ◽  
High Tc ◽  
X Ray ◽  
Resistivity Measurements ◽  
Temperature Time ◽  
Dominant Phase

In an effort to synthesize the high-T c superconducting phase in the thallium system, two nominal compositions, Tl 2 Ca 2 Ba 2 Cu 3 O 10 and Tl 1 Ca 3 Ba 1 Cu 3 O 8.5, have been investigated for superconductivity as a function of the sintering temperature, time, atmosphere, and quench rate. Samples have been characterized by electrical resistivity measurements, X-ray diffraction, and scanning electron microscopy. Samples of starting composition Tl 2 Ca 2 Ba 2 Cu 3 O 10 fired in air at 860–900°C and rapidly quenched showed T c (R = 0) of 96–107 K. In contrast, specimens of starting composition Tl 1 Ca 0 Ba 1 Cu 3 O 8.5 when baked at 900°C and slow cooled in oxygen were superconducting at ≥ 116 K and consisted of Tl 2 Ca 2 Ba 2 Cu 3 O 10+x as the dominant phase. Our results also show that, in contrast to the case of YBa 2 Cu 3 O 7−x, doping with a small concentration of fluorine sharpens the resistive transition and produces large T c increase in thallium-based superconductors.

scholarly journals Synthesis and Characterization of CdS Slim Film Grown by CBD Method

2020 ◽  
Vol 5 (7) ◽  
pp. 170-172
Author(s):  
Vhadgal Gorakh Anna
Keyword(s):  
Living Arrangements ◽  
Uv Spectroscopy ◽  
X Ray Diffraction ◽  
Cadmium Sulfate ◽  
Morphological Attributes ◽  
X Ray ◽  
Hexagonal Shape ◽  
Cbd Method ◽  
The Ideal

Substance shower testimony strategy have been utilized to store Cadmium sulfide dainty film. The affect of the appropriate response temperature and PH is explored on this work. The introduction of CdS dainty film Cadmium Sulfate, Anomia, Thiourea and Double refined water is utilized as wellspring of material . Examining Electron microscopy (SEM ) is utilized for morphological attributes of CdS slender film. UV spectroscopy have been utilized for optical living arrangements of the CdS slender film .The band hole of CdS dainty film by methods for UV spectroscopy changed into 2.42 eV . The X-R diffraction investigation is affirmed that the CdS meager film were polycrystline with hexagonal shape the ideal direction of CdS slender film had been(002) and crystalline size 50nM .It changed into chose from the broadenings of corrousponding X-Ray diffraction tops by means of the utilization of Debye scherrer recipe.

Preparation and Characterization of the Ceramsites with Microscale Pores from Iron Tailing and Fly Ash

2020 ◽  
Vol 12 ◽  
Author(s):  
Zeyang Xue ◽  
Zi Wang ◽  
Chunhu Yu ◽  
Yajing Mao ◽  
Lizhai Pei
Keyword(s):  
Fly Ash ◽  
Mechanical Performance ◽  
Sintering Temperature ◽  
X Ray Diffraction ◽  
X Ray ◽  
Sintering Time ◽  
Duration Time ◽  
Important Significance ◽  
Scanning Electron

Background: Iron tailing causes great environmental and social problems which contaminate water, air and soil. Therefore, it is of important significance to prepare iron tailing ceramsites with microscale pores which can recycle the deposited iron tailing. Objective: The aim of the research is to obtain iron tailing ceramsites with microscale pores and good mechanical performance. Methods: The iron tailing ceramsites have been characterized via scanning electron microscopy (SEM) and X-ray diffraction (XRD). Influence of the content of iron tailing, temperature and duration time on the mechanical performance of the obtained ceramsites was performed and the optimal sintering parameter was determined. The bulk density, apparent density and cylinder compressive strength of the obtained ceramsites increase obviously as improving the iron tailing content, temperature and sintering time. Results: Duration time and sintering temperature play important roles in the formation and size of the pores of the ceramsites. The optimal iron tailing content and sintering parameter are 70wt.%, 1100 ℃ for 40 min. The iron tailing ceramsites mainly consist of orthorhombic CaAl2Si2O8, monoclinic CaSiO3, hexagonal Ca7Si2P2O16, triclinic MgSiO3, triclinic Al2SiO5 and triclinic Ca2Fe2O5 phases. Iron tailing ceramsites from 1100 ℃ for 40 min are composed of irregular particles with several hundreds of micrometers improving the density and strength of the ceramsites. Conclusion: Iron tailing ceramsites containing microscale pores were prepared using iron tailing and fly ash, and exhibit excellent potential for the application in the field of construction.

scholarly journals Characterization of CaTi0.9Fe0.1O3/La0.98Mg0.02NbO4 composite

Open Physics ◽  
2013 ◽  
Vol 11 (2) ◽  
Author(s):  
Aleksandra Mielewczyk-Gryn ◽  
Tomasz Lendze ◽  
Katarzyna Gdula-Kasica ◽  
Piotr Jasinski ◽  
Andrzej Krupa ◽  
...  
Keyword(s):  
Sintering Temperature ◽  
Perovskite Phase ◽  
Pyrochlore Phase ◽  
Diffraction Method ◽  
Total Conductivity ◽  
X Ray Diffraction ◽  
X Ray ◽  
Temperature Interaction ◽  
Composite Samples

AbstractA composite of CaTi0.9Fe0.1O3 and electrolyte material, i.e. magnesium doped La0.98Mg0.02NbO4 was prepared and studied. The phase content and the sample microstructure was examined by an X-ray diffraction method and scanning electron microscopy. EDS measurements were done both for composite samples and the diffusion couple. The electrical properties were studied by four terminal DC method. The high-temperature interaction between the two components of the composite has been observed. It has been suggested that lanthanum diffused into the perovskite phase and substituted for calcium whereas calcium and niobium formed the Ca2Nb2O7 pyrochlore phase. At 1500°C very large crystallites of the pyrochlore were observed. Regardless of strong interaction between the composite components, its total conductivity was weakly dependent on the sintering temperature.

Characterization of Well-Dispersed CeO2 Nanoparticles Prepared by a New Method of Reverse Microemulsion

2011 ◽  
Vol 194-196 ◽  
pp. 781-784
Author(s):  
Fa Mei Feng ◽  
Jia Qing Xie ◽  
Li Ke Zou ◽  
Bin Xie
Keyword(s):  
Particle Size ◽  
Fourier Transform ◽  
Ceo2 Nanoparticles ◽  
Size Distributions ◽  
X Ray ◽  
Transmission Electron ◽  
Particle Size Analyzer ◽  
Ft Ir ◽  
Cubic Structure

Well-dispersed CeO2 nanoparticles were successfully prepared in a simple system composed of sodium bis (2-ethylhexyl) sulfosuccinate (AOT)- octane-water (W/O) microemulsion in this paper. The morphology and microstructure of the products were characterized by the laser particle size analyzer, Fourier transform infrared spectroscopy (FT-IR), X-ray diffractometer (XRD), differential scanning calorimeter (DSC) and transmission electron microscope (TEM). It was found that the CeO2nanoparticles obtained from this method have well-proportioned size distributions; the surfactant (AOT) molecule was adsorbed on the surface of CeO2nanoparticles precursor, which is favorable for the dispersion of CeO2nanoparticles; the CeO2nanoparticles calcined was a crystal of the cubic structure. In addition, the mechanism on the formation of the CeO2nanoparticles was also proposed in this paper.

Fabrication and Characterization of In-Doped Zinc Oxide Nanodisks

2007 ◽  
Vol 121-123 ◽  
pp. 127-130
Author(s):  
Juan Liu ◽  
Yue Zhang ◽  
Jun Jie Qi ◽  
Yun Hua Huang ◽  
Xiao Mei Zhang
Keyword(s):  
Room Temperature ◽  
Thermal Evaporation ◽  
Graphite Powder ◽  
X Ray Diffraction ◽  
X Ray ◽  
Uv Emission ◽  
Hexagonal Shape ◽  
Catalyst Morphology ◽  
Fabrication And Characterization

In-doped ZnO nanodisks were successfully fabricated by thermal evaporation Zn, In2O3 and graphite powder mixture without catalyst. Morphology, structures and components of ZnO nanodisks were investigated by SEM, HRTEM, EDS and X-Ray diffraction. ZnO nanodisks have perfect hexagonal shape, with 1~3μm size and 40~100 nm in thickness. The nanodisks are single-crystalline ZnO with wurtzite structure and In content of nanodisks reaches 2.2%. The growth along [0001] is suppressed leading to the formation of ZnO nanodisks. Room temperature photoluminescence spectra of the nanodisks shows that the UV emission peak blueshifts and becomes broader after doping.

scholarly journals Interaction between WC and Inconel 625 under Solid and Liquid State Sintering Conditions

Metals ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 666
Author(s):  
Lorena Emanuelli ◽  
Alberto Molinari ◽  
Massimo Pellizzari
Keyword(s):  
Solid Solutions ◽  
Sintering Temperature ◽  
Inconel 625 ◽  
High Temperature Strength ◽  
X Ray Diffraction ◽  
X Ray ◽  
Hard Metals ◽  
Solid State Sintering ◽  
Sintering Conditions

Cobalt is the most used metal binder in hard metals since its extraordinary wetting, adhesion and mechanical properties. Nevertheless, it has been recognized genotoxic and cancerogenic with higher toxicity in combination with WC. To substitute Co with an alternative binder, the interaction between the binder and WC must be taken into account. In this work, IN625 is considered as a binder alternative due to its desirable combination of high-temperature strength and corrosion/oxidation resistance. A characterization of the interaction between WC and IN625 was carried out by means of Scanning Electron Microscopy (SEM), Energy Dispersive X-Ray Spectroscopy (EDXS) and X-Ray Diffraction (XRD). Depending on the sintering temperatures, different phases were evidenced at the WC–IN625 superalloy interface. From 1250 °C to 1300 °C, where solid-state sintering takes place, (Cr,Mo)23C6, W2C and (Cr,W) solid solutions were detected. At a sintering temperature of 1350 °C, IN625 melts and the formation of additional phases, such as an intermetallic Ni4W phase and (Mo,W) and (Mo,Nb) solid solutions, were observed. The precipitation of NbC and (Mo,Cr)23C6 carbides in IN625 was also detected.

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