scholarly journals Wet synthesis of carbonated hydroxyapatite

Author(s):  
I. E. Glazov ◽  
V. K. Krut’ko ◽  
O. N. Musskaya ◽  
A. I. Kulak

Carbonated hydroxyapatite of predominant B-type of substitution has been synthesized at various temperatures, carbonate concentrations and time of immersion in mother solution. Carbonated hydroxyapatite synthesized at 80 °C contains the largest amount (up to 9 wt.%) of calcite impurity and has a low specific surface area (40 m2/g). Lowering the synthesis temperature to 20 °C leads to a slight decrease in the content of calcite impurity (up to 5–7 wt.%) and an increase in the specific surface up to 125 m2/g. The introduction of the maturation stage for carbonated hydroxyapatite precipitated at 20 °C for 4 days suppresses the calcite impurity formation and leads to the increase in the specific surface up to 155 m2/g.

2016 ◽  
Vol 721 ◽  
pp. 172-176 ◽  
Author(s):  
Jana Vecstaudza ◽  
Janis Locs

Amorphous and low crystalline calcium phosphates are prospective candidates for bone implant manufacturing. Amorphous calcium phosphate (ACP) preparation technologies could be improved in terms of specific surface area (SSA) of obtained products. Current study is dedicated to the effect of synthesis temperature and Ca and P molar ratios (Ca/P) on SSA of ACP. Higher SSA can improve bioactivity of biomaterials. ACP was characterized by XRD, FT-IR, SEM and BET N2 adsorption techniques. Spherical nanoparticles (<45 nm in size) were obtained independently of initial Ca/P ratio and synthesis temperature. For the first time comparison of SSA was shown for ACP obtained at different temperatures (0 °C and 20 °C) and Ca/P molar ratios (1.5, 1.67 and 2.2).


2012 ◽  
Vol 427 ◽  
pp. 123-127
Author(s):  
Yuan Hui Ma ◽  
Lei Zhang ◽  
Cheng Chun Tang

The nanoporous metal-organic frameworks were synthesized under solvothermal conditions using organic solvent dimethylformamide. The samples were characterized by XRD, SEM, TGA, FT-IR and specific surface area for their properties difference. When the reaction temperature rises, the particle size becomes larger. All TGA curves are the basically same, the framework structure begins to be destroyed from 500°C up to around 600°C. The metal-organic frameworks accepted at reaction temperature 190°C have larger specific surface area and better structure stability.


2008 ◽  
Vol 20 (19) ◽  
pp. 5942-5944 ◽  
Author(s):  
S. Padilla ◽  
I. Izquierdo-Barba ◽  
M. Vallet-Regí

2017 ◽  
Vol 36 (1-2) ◽  
pp. 247-269 ◽  
Author(s):  
Armin Taheri ◽  
Ensieh Ganji Babakhani ◽  
Jafar Towfighi

In this study hydrothermal method was used to synthesize MIL-53(Al) (MIL stands for Materials Institute of Lavoisier). Plackett–Burman (P–B) as an experimental design method was applied to investigate the effect of synthesis and activation conditions on specific surface area, relative crystallinity, and production yield of MIL-53(Al) synthesis. Some parameters such as ligand-to-metal molar ratio, synthesis time, synthesis temperature, calcination temperature, and calcination time were selected as the variables. The Brunauer–Emmett–Teller (BET) technique was used in order to estimate the specific surface area of samples while the relative crystallinity of the samples was estimated by comparing their X-Ray Diffraction (XRD) pattern. The morphology of the samples was investigated by field emission scanning electron microscopy. The yield of final products was determined based on organic ligands. The results revealed the significant effect of synthesis temperature on BET surface area, particle size, yield, and crystallinity. The calcination temperature has significant positive effect on BET and crystallinity. Also, the negative significant effect of molar ratio on yield was concluded from the results. However, negligible effect of synthesis and calcination time on the properties of prepared materials were observed. Furthermore, separation capability of a selected sample for carbon dioxide (CO2) and methane (CH4) was measured. Pure gas adsorption data were successfully fitted to Langmuir, Sips, and Toth models. The selected sample provided high adsorption capacity for both gases. The binary adsorption of gases was also investigated based on extended Langmuir equations and the ideal adsorbed solution theory (IAST) models. Comparing the experimental and models data indicated good agreement between the IAST model and experiments. Finally, high CO2/CH4 selectivity of 7.6 was obtained experimentally for the CO2/CH4 molar ratio of 0.2/0.8.


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