TY - JOUR
T1 - Formation of hydroxyapatite on CaSiO3 powders in simulated body fluid
AU - Siriphannon, Punnama
AU - Kameshima, Yoshikazu
AU - Yasumori, Atsuo
AU - Okada, Kiyoshi
AU - Hayashi, Shigeo
N1 - Funding Information:
A part of this work was financially supported by the Japan Society for the Promotion of Science (Project: Preparation of Advanced Inorganic Materials by Soft, Solution Processing). We are also grateful to Dr. K.J.D. MacKenzie for critical reading and editing of the manuscript.
PY - 2002/4
Y1 - 2002/4
N2 - CaSiO3 powders were prepared from ethanol solutions of Ca(NO3)2·4H2O and Si(OC2H5)4 using NaOH as a precipitant. The resultant powders were heated at three different temperature regimes, (1) 500°C, (2) 500 and 1000°C and (3) 500 and 1400°C, to obtain the amorphous phase (amorphous-CS), low temperature phase (β-CS), and high temperature phase (α-CS) of CaSiO3, respectively. The different amorphous and crystalline phases exhibited different microtextures and specific surface areas of the powders. The rough, porous particles of amorphous-CS and β-CS have higher specific surface areas than the smooth, dense particles of α-CS. These CaSiO3 powders were soaked in a simulated body fluid (SBF) at 36.5°C for 2 h to 30 days. Formation of hydroxyapatite (HAp) was observed on the surfaces of all samples, but the formation behavior and microstructures were different, resulting the differences in microstructure and crystal structure of the starting powders as well as particle size and specific surface area. The HAp formed on the amorphous-CS was a loose porous layer consisting of uniformly-sized tiny ball-like agglomerated particles, while that formed on the β-CS and α-CS was a dense layer consisting of larger ball-like agglomerated particles.
AB - CaSiO3 powders were prepared from ethanol solutions of Ca(NO3)2·4H2O and Si(OC2H5)4 using NaOH as a precipitant. The resultant powders were heated at three different temperature regimes, (1) 500°C, (2) 500 and 1000°C and (3) 500 and 1400°C, to obtain the amorphous phase (amorphous-CS), low temperature phase (β-CS), and high temperature phase (α-CS) of CaSiO3, respectively. The different amorphous and crystalline phases exhibited different microtextures and specific surface areas of the powders. The rough, porous particles of amorphous-CS and β-CS have higher specific surface areas than the smooth, dense particles of α-CS. These CaSiO3 powders were soaked in a simulated body fluid (SBF) at 36.5°C for 2 h to 30 days. Formation of hydroxyapatite (HAp) was observed on the surfaces of all samples, but the formation behavior and microstructures were different, resulting the differences in microstructure and crystal structure of the starting powders as well as particle size and specific surface area. The HAp formed on the amorphous-CS was a loose porous layer consisting of uniformly-sized tiny ball-like agglomerated particles, while that formed on the β-CS and α-CS was a dense layer consisting of larger ball-like agglomerated particles.
KW - Apatite
KW - Bioactive materials
KW - CaSiO powders
KW - Simulated body fluid (SBF)
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U2 - 10.1016/S0955-2219(01)00301-6
DO - 10.1016/S0955-2219(01)00301-6
M3 - Article
AN - SCOPUS:0036532871
SN - 0955-2219
VL - 22
SP - 511
EP - 520
JO - Journal of the European Ceramic Society
JF - Journal of the European Ceramic Society
IS - 4
ER -