scholarly journals Synthesis of bioactive materials for implants in the system Ca3(PO4)2-Ca2GeO4

2018 ◽  
Vol 226 ◽  
pp. 03011
Author(s):  
Elizaveta A. Mukhanova ◽  
Vyacheslav G. Vetokhin ◽  
Alexander A. Rybalkin

Various modifications of Ge-substituted calcium phosphates were obtained using solid-phase synthesis, co-precipitation in solution, and combustion synthesis. Structural changes in the synthesis process are established using X-ray diffraction. The biological activity of the obtained samples in model fluids was estimated. It has been found that the synthesis method can lead to various structural modifications of calcium phosphate, which is a significant refinement to the phase diagram of the Ca3(PO4)2- Ca2GeO4 system described in the literature.

Catalysts ◽  
2020 ◽  
Vol 10 (6) ◽  
pp. 640
Author(s):  
Hideaki Sasaki ◽  
Keisuke Sakamoto ◽  
Masami Mori ◽  
Tatsuaki Sakamoto

CeO2-based solid solutions in which Pd partially substitutes for Ce attract considerable attention, owing to their high catalytic performances. In this study, the solid solution (Ce1−xPdxO2−δ) with a high Pd content (x ~ 0.2) was synthesized through co-precipitation under oxidative conditions using molten nitrate, and its structure and thermal decomposition were examined. The characteristics of the solid solution, such as the change in a lattice constant, inhibition of sintering, and ionic states, were examined using X-ray diffraction (XRD), scanning electron microscopy–energy-dispersive X-ray spectroscopy (SEM−EDS), transmission electron microscopy (TEM)−EDS, and X-ray photoelectron spectroscopy (XPS). The synthesis method proposed in this study appears suitable for the easy preparation of CeO2 solid solutions with a high Pd content.


2006 ◽  
Vol 70 (3) ◽  
pp. 319-328 ◽  
Author(s):  
M. Zema ◽  
S.C. Tarantino ◽  
A. Giorgiani

AbstractStructural modifications as a function of the degree of order (Q) in FeTa2O6 ferrotapiolite have been characterized by means of single-crystal X-ray diffraction (SC-XRD). A total of 26 datasets covering the range of Q between 0.154 and 1 have been obtained by thermal treatments followed by quenching of natural tapiolite crystals. Ordering of Fe2+ at the A sites and of Ta5+ at the B sites causes a linear increase in the a/c lattice constants ratio, as a consequence of a linear decrease of the c dimension and only slight modifications of the a parameter. Calibration of a/c vs. Q represents a very useful tool for a rapid determination of the degree of order of tapiolite samples. Polyhedral volumes of the two octahedral sites vary linearly with Q as a consequence of the different ionic radii of the two species. Both the sites remain almost regular at all Q values but the B site shows an increasing off-centre displacement of the cation with increasing Q. Observed structure factors of supercell reflections, characterized by l ≠ 3n, increase linearly as a function of Q, thus representing a further tool for a quick evaluation of the degree of order.


2018 ◽  
Vol 281 ◽  
pp. 40-45
Author(s):  
Jie Guang Song ◽  
Lin Chen ◽  
Cai Liang Pang ◽  
Jia Zhang ◽  
Xian Zhong Wang ◽  
...  

YAG materials has a number of unique properties, the application is very extensive. In this paper, the superfine YAG powder materials were prepared by co-precipitation method and hydrothermal precipitation method. The influence of synthesis process on the morphology of the powder was investigated. The results showed that the precursor powder prepared via the co-precipitation method is mainly from amorphous to crystalline transition with the increasing calcination temperature, the precursor agglomeration is more serious, In the process of increasing the calcination temperature, the dispersibility of the roasted powder is greatly improved, which is favorable for the growth of the crystal grains, so that the particle size of the powder is gradually increased, the YAG precursor prepared by the co-precipitation method is transformed into YAG crystals, the phase transition occurs mainly between 900 and 1100°C. When the molar ratio of salt to alkali is Y3+: OH-=1: 8 via the hydrothermal reaction, the YAG particles with homogeneous morphology can be obtained. When the molar ratio of salt and alkali is increased continuously, the morphology of YAG particles is not obviously changed. The co-precipitation method is easy to control the particle size, the hydrothermal method is easy to control the particle morphology.


2005 ◽  
Vol 480-481 ◽  
pp. 13-20 ◽  
Author(s):  
Khalil Arshak ◽  
Olga Korostynska ◽  
John Henry

This paper reports on the gamma radiation-induced changes in thin oxide films deposited by thermal vacuum technique. Structures of various oxides thin films, such as In2O3, SiO and TeO2 and their mixtures in different proportions were studied. The influence of gamma radiation on In2O3/SiO films has resulted in significant changes in the microstructure of this film. Some kind of agglomerations with variable sizes in the range 0.5-3 µm has occurred. After a dose of 8160 µSv an evidence of partial crystallisation was observed with X-ray diffraction. Structural changes in TeO2 thin film were explored by means of Raman spectroscopy. After they have been exposed to g- radiation, a strong peak appeared at 448.83 cm-1, indicating further transformation to g-TeO2 modification.


2011 ◽  
Vol 236-238 ◽  
pp. 2076-2079
Author(s):  
Yan Rong Sun ◽  
Tao Fan ◽  
Yong Huang ◽  
Li Guo Ma ◽  
Feng Liu

The introduction of biomineralization was coupled with the co-precipitation synthesis process of nano-hydroxyapatite with the addition of chondroitin sulfate as a template agent. The effect of a variety of processing conditions on the properties of final hydroxyapatite (HA) product was investigated by orthogonal design. The ratio of calcium to phosphorus was detected by chemical analysis, the phase composition was evaluated by X-ray diffraction (XRD), and the powder morphology was characterized by transmission electron microscope (TEM). The process scheme, moreover, was optimized by the analysis of four aspects which may have different extent of influence on product properties. It can be concluded from the results that product properties can be affected remarkably by the content of chondroitin sulfate and the pH value of reactant, less remarkably by the reaction temperature and slightly by the reaction time.


2013 ◽  
Vol 634-638 ◽  
pp. 2909-2915 ◽  
Author(s):  
Fang Jie Cheng ◽  
Jun Xiang Yang ◽  
Hai Wei Zhao ◽  
Guan Xing Zhang ◽  
Jun Lan Huang ◽  
...  

The melting curves of high cesium content KF-CsF-AlF3 flux samples prepared by the wetting synthesis method were measured by differential scanning calorimetry (DSC), and the effect of the flux compositions on the melting characteristics was analyzed and summarized. Existing phases of every representation sample was identified by X-ray diffraction (XRD), meanwhile, the morphology and chemical elements of the typical flux samples were analyzed by scanning electron microscope (SEM) and energy spectrum analysis (EDS), respectively. The results indicated that solid phase decomposition first occurred in the common phase Cs2AlF5 for all the flux samples at 420°C; one of the decomposition products, Cs3AlF6 take the eutectic reaction with the Cs2KAlF6 at about 450°C; the flux samples containing phase CsAl2F7 or Cs2KAl3F12 have the e5 and e1 eutectic reaction at 471°C and 525°C, respectively, and their liquidus increased correspondingly. The liquidus for regionⅠflux samples is about 450°C and with a narrow melting range, which would make them good substrates for aluminum alloy middle temperature brazing.


2015 ◽  
Vol 659 ◽  
pp. 604-608 ◽  
Author(s):  
Jiruntanin Kanoksinwuttipong ◽  
Wisanu Pecharapa ◽  
Russameeruk Noonuruk ◽  
Wicharn Techitdheera

Indium oxide:tin nanoparticles were synthesized by co-precipitation method using InCl3 and SnCl4·5H2O as starting precursor with different molar ratios of Sn:In. The crystalline structure, optical properties, chemical bonding and morphologies of all samples were characterized by X-ray diffraction (XRD), UV–vis spectrometer, Raman spectroscopy and field emission scanning electron microscope, respectively. The XRD results show that the crystallinity of as-synthesized powders was initially amorphous phase. After calcination at 400 °C for 2 h, a single phase ITO powder with 10% (mol%) SnO2 was obtained. The particle size of each sample is approximately 20-25 nm. The color of indium oxide:tin nanopowders after heat treatment changed from white to yellow due to the substitution of oxygen vacancies in the sample. After calcination, the intensity of Raman peak significantly decreased with increasing amount of Sn loading. This phenomenon indicates that ion substitution may occur during the synthesis process. Moreover, it is noticed that the optical absorbance of obviously changed with increasing Sn loading.


2005 ◽  
Vol 284-286 ◽  
pp. 701-704 ◽  
Author(s):  
S.A. Costa ◽  
J. Miguel Oliveira ◽  
Isabel B. Leonor ◽  
Rui L. Reis

In this study, it is shown that it is possible to prepare carboxymethyl-chitosan/Ca-P hybrids using an innovative “auto-catalytic” co-precipitation method, namely by using an acid and an oxidant bath. The X-ray diffraction (XRD) patterns evidenced the formation of crystalline calcium-phosphate precipitates when using an acid bath, while amorphous ones were obtained for those produced in the oxidant bath. The Fourier Transform Infrared spectroscopy (FTIR) and Scanning Electron Microscopy (SEM/EDS) studies revealed that the extent of the polymer precipitation and formation of calcium-phosphates is directly dependent on the pH and composition of the baths. Furthermore, by conducting bioactivity tests in a simulated body fluid (SBF) followed by the SEM/EDS analysis it was possible to detect the formation of an apatite layer with a cauliflower-like morphology on the surface of hybrids prepared by the acid bath, after 7 days of immersion. These results are quite promising because they can allow for the production of bioactive and biodegradable 3D porous scaffolds to be used in bone tissue engineering applications.


Materials ◽  
2021 ◽  
Vol 14 (24) ◽  
pp. 7673
Author(s):  
Ziyang You ◽  
Jing Xu

The usage of nanoscale calcium silicate hydrate (nano C-S-H) proved to have an excellent promotion effect on the early performance of concrete as nano C-S-H with ultra-fine particle size can act as seeding for cement hydration. Therefore, it is of importance to tune the particle size during the synthesis process of nano C-S-H. In this paper, the influence of several variables of the particle size distribution (PSD) of nano C-S-H synthesized by chemical co-precipitation method with the aid of polycarboxylate (PCE) was studied by orthogonal experimental design. In addition, the composition, microstructure, and morphology of the C-S-H/PCE nanocomposites were analyzed by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and Raman spectrum. The results showed that the concentration of reactants had a significant impact on the PSD of C-S-H/PCE nanocomposites, followed by the dosage of dispersant. Ultrasonic treatment was effective in breaking the C-S-H/PCE aggregates with unstable agglomeration structures. The change in synthetic variables had a negligible effect on the composition of the C-S-H/PCE nanocomposites but had a significant influence on the crystallinity and morphology of the composites.


2021 ◽  
Vol 407 ◽  
pp. 161-172
Author(s):  
Mahbboobeh Rezaei ◽  
Ali Shokuhfar ◽  
Nikta Shahcheraghi

In this work, a flower-shaped ZnO/GO/Fe3O4 ternary nanocomposite was synthesized via the co-precipitation method. Two significant goals of the study were boosting the degradation efficiency of ZnO and achieving a fast and simple synthesis approach. The structure, properties, and morphology of the product were characterized, and the effect of the ZnO flower-shaped structure in combination with GO nanosheets and magnetite nanoparticles was investigated on the photocatalytic activity. The structure and quality of the prepared nanocomposite were assessed by X-ray diffraction pattern, UV-visible DRS spectroscopy, Field Emission Scanning Electron Microscopy (FE-SEM). The catalytic activity of the nanocomposite was assessed by spectrophotometric analysis. The developed nanocomposite offered high photodegradation efficiency in Rhodamine B degradation under UV-C light in comparison with pure ZnO. At a specific period, the efficiency of the synthesized sample was about two times greater than that of pristine ZnO particles. Our nanocomposite is anticipated to have practical benefits in wastewater treatment given its good performance, economic savings through reducing the amount of catalyst consumption and saving time, and being a facile and fast synthesis method.


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