Effects of Aging and Temperature on the Oriental Growth of Hydroxyapatite

2011 ◽  
Vol 308-310 ◽  
pp. 2180-2186
Author(s):  
Hui Yang ◽  
Fei Fei Huang ◽  
Ke Wei Xu

In order to find a simple way to prepare oriental HA, only by controlling the preparation conditions, a co-precipitation method was used to prepare an oriented HA. The influences of temperature and aging on its directional growth were investigated kinetically and thermodynamically. The chemical composition was characterized by X-Ray diffraction and Fourier transform infrared. The morphologies were observed by scanning electron microscopy (SEM). The oriented parameters of HA (c/a) were calculated by Scherrer equation. The results show that the temperature rise in the process of synthesis, aging or calcining inhibited the growth of HA crystal in the direction of c-axis. Aging for 24 h benefited the growth along c-axis, whereas aging for 36 h was in favor of the decreasing of the c/a value. The supernatant-replacement during aging exerted the same effect on the growth with the rising of temperature. The SEM analysis result shows that the morphology of the produced HA particles looked like a uniform needle shape and had a good dispersion.

2013 ◽  
Vol 838-841 ◽  
pp. 2306-2309
Author(s):  
Guang Hua Wang ◽  
Kun Chen ◽  
Wen Bing Li ◽  
Dong Wan ◽  
Qin Hu ◽  
...  

Magnetic modified organobentonite (Fe3O4/CTAB–Bent) was synthesized by chemical co-precipitation method in which CTAB–Bent was firstly achieved via ion–exchange.The composite materials have been characterized by powder X–ray diffraction (XRD), Fourier transform infrared spectroscopy (FT–IR) and Scanning electron microscopy (SEM) . The results revealed that basal spacing of bentonite was increased through organic modification and the Fe3O4 particles synthesized which covering the surfaces of bentonite .Compared with natural bentonite, the adsorption capacity of Fe3O4/CTAB–Bent for Orange II was greatly enhanced and can be easily separated from the reaction medium by an external magnetic field after the treatment.


2019 ◽  
Vol 969 ◽  
pp. 169-174
Author(s):  
R. Sivanand ◽  
S. Chellammal ◽  
S. Manivannan

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.


2016 ◽  
Vol 16 (4) ◽  
pp. 3534-3541
Author(s):  
Yanqiu Zhang ◽  
Baojiu Chen ◽  
Xiangping Li ◽  
Jiashi Sun ◽  
Jinsu Zhang ◽  
...  

Nanosized Gd6WO12 phosphors containing various Er3+ concentrations and fixed Yb3+ concentration were synthesized by a co-precipitation method. The crystal structure and microscopic morphology of the obtained nanophosphors were characterized by means of X-ray diffraction (XRD) and field emission scanning electron microscopy (FE-SEM). Two-photon processes for both the green and red upconversion (UC) emissions were confirmed by analyzing the dependence of UC intensities on 980 nm laser working current. UC emission intensity changing with temperature displays different trends for the samples with different Er3+ concentrations. The experimental results indicated that thermal quenching behavior of UC luminescence could not be simply explained by crossover mechanism. The enhancement for green UC emission in the sample with higher Er3+ concentration was discussed. Finally, the Er3+ concentration dependence of UC luminescence was experimentally observed, and its mechanisms were analyzed.


2015 ◽  
Vol 816 ◽  
pp. 676-681 ◽  
Author(s):  
Xiao Long Qu ◽  
Zheng Fu Zhang ◽  
Jin Cheng ◽  
Xiao Yan Wang

The spherical Ni0.5Co0.2Mn0.3(OH)2 powders were prepared by ammonia-hydroxide co-precipitation method. The influence of different synthesizing factors on the precursors characteristic were investigated. The product prepared with optimized condition has tap density of D≥1.7g·cm-3, and middle particle size D50≈3.6μm. The X-ray diffraction (XRD) results showed that the precursor can be indexed by a hexagonal β-Ni (OH)2 structure. The scanning electron microscope (SEM) results showed that the powders had quasi-spherical pattern and homogeneous particle size distribution.


2009 ◽  
Vol 23 (06n07) ◽  
pp. 1449-1454 ◽  
Author(s):  
HONGFEI LIU ◽  
ZHIPING ZHANG ◽  
XIAONONG CHENG ◽  
JUAN YANG

In this work, a series of ZrO 2/ ZrW 2 O 8 ceramic composites with different amounts of ZrW 2 O 8 were successfully prepared by calcining the precursors synthesized using co-precipitation route at 1150°C for 3 h. The X-ray diffraction (XRD) data confirmed that the composites only consisted of α- ZrW 2 O 8 phase and m - ZrO 2 phase. The scanning electron microscopy (SEM) analysis of the synthesized ZrO 2/ ZrW 2 O 8 composites showed that the specimens had good mixed-uniformities. In addition, the thermal expansion coefficients of the composites decreased with increased amounts of negative thermal expansion ZrW 2 O 8, specimen with 26wt% ZrW 2 O 8 shows almost zero thermal expansion and its average thermal expansion coefficient is -0.5897×10-6K-1 in the temperature range from 30°C to 600°C.


2014 ◽  
Vol 25 (1) ◽  
pp. 43-46
Author(s):  
Cristina Ileana Covaliu ◽  
Gina Alina Traistaru ◽  
Gigel Paraschiv

Abstract Methane oxidation using different catalysts is an useful process for preventing air pollution. This study presents the methane oxidation by two types of catalysts: Pd-Sn/Al2O3 and spinel mixed oxide, CuFe2O4. The Pd-Sn/Al2O3 was successfully prepared by sol-gel method and CuFe2O4 by co-precipitation method. The catalysts obtained have been characterized structurally, morphologically and texturally by X-ray diffraction (XRD), scanning electron microscopy (SEM) and specific surface area (BET). The catalytic activity tests regarding methane oxidation were also performed.


2013 ◽  
Vol 320 ◽  
pp. 40-43 ◽  
Author(s):  
Shi Xing Liu ◽  
Wei Zhang ◽  
Zheng Fa Hu ◽  
Hao Yi Wu ◽  
Xia Sheng

Ho-doped Yttrium aluminum indium garnet, Y3Al4.5In0.5O12 (YAIG), was synthesized by co-precipitation method. Effects of Ho concentration, reaction mechanism, crystallinity and luminescence properties of the phosphor powders were studied using the X-ray diffraction, thermo-gravimetry Analyzer,scanning electron microscopy and photoluminescence. The performances of samples were analyzed by changing the concentration of Ho3+ and the substitution of indium for aluminum. The results showed that pure cubic garnet phase was formed in the Indium-substituted samples, and the critical distance of the energy transfer was 1.41 nm. Both the excitation and emission intensities increased firstly and then decreased with the increasing of Ho3+ concentration. When the concentration of Ho3+ reached 15%, the photoluminescence property of the sample was best.


2011 ◽  
Vol 675-677 ◽  
pp. 57-60
Author(s):  
Yuan Sun ◽  
Xiu Juan Zhao ◽  
Rui Ming Ren

The olivine-type LiFePO4 powder was prepared by a chemical method using the synthesized FePO4⋅2H2O, LiOH and glucose as raw materials. The synthesized FePO4⋅2H2O powder was obtained by co-precipitation method. FePO4⋅2H2O and LiFePO4 powders were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). The results showed the synthesized FePO4⋅2H2O powder at pH of 2.05 was in a single phase and nearly spherical in shape. Using the synthesized powders to prepared LiFePO4 at 600 °C in vacuum for 2 h was nearly spherical in shape and whose size was in the range of 0.1-0.5μm.


2022 ◽  
Vol 19 ◽  
Author(s):  
Runjhun Tandon ◽  
Shripad Patil ◽  
Nitin Tandon ◽  
Pushpendra Kumar

Abstract: A novel magnetite silica-coated nanoparticle-supported molybdate nanocatalyst has been prepared successfully by a simple co-precipitation method. Prepared nanocatalyst has been characterized by different techniques like Fourier Transmission Infrared Spectroscopy (FT-IR), X-ray diffraction (XRD), Field Emission Scanning Electron Microscope (FE-SEM) and Energy Dispersive X-ray Spectroscopy (EDX). Further, the catalytic activity of the nanocatalyst was explored for N-formylation reactions under solvent-free conditions. Interestingly, the catalyst could be reused for 10 cycles and only 2 mol % of the catalyst was sufficient to catalyze the N-formylation reaction at 700C under solvent-free conditions.


2021 ◽  
Author(s):  
senthil kumar ◽  
C. Arunagiri

Abstract FexZn1-xO (x = 0, 0.05, 0.075, and 0.1 M) nanoparticles based photocatalysts are successfully synthesized by co-precipitation method. The synthesized nanoparticles are characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM) with energy-dispersive X-ray spectroscopy (EDX), and UV–visible double beam spectroscopy (UV–Vis) techniques. The prepared catalysts and its photocatalytic activity was evaluated by methylene blue (MB) and methyl orange (MO) dye under visible light irradiation. The effect of various photocatalyst parameters such as pH, catalyst dosage, and initial dye concentration on the photodegradation was examined in detail.


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