Synthesis and characterization of calcium hydroxyapatite (Hap) and Ti(IV)-substituted Hap particles by forced hydrolysis of Ca(OH)2-Na4P2O7 solution

JOURNAL OF THE CERAMIC SOCIETY OF JAPAN(2016)

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摘要
The productions of calcium hydroxyapatite (Hap) and Ti(IV)-doped Hap (TiHap) particles were examined by forced hydrolysis reaction of Ca(OH)(2)-pyrophosphate (pp: P2O74-) and Ca(OH)(2)-pp-TiCl4 mixed solutions under 100 and 140 degrees C, respectively, and precipitated particles were characterized by various physicochemical techniques. The degree of hydrolysis of pp ions was remarkably improved and the yields of the precipitates by using the pp ions was increased rather than the tpp one. No particles were produced at higher concentration of pp ions. On the other hand, ellipsoidal aggregated and rod-like particles were produced at other concentration domains. The Hap particles produced were ellipsoidal secondary particles with ca. 210-240nm in the particle length which were composed by aggregation of small primary single crystal particles with ca. 20-50nm in length. The TiHap particles facilitated at atomic ratio of Ti/(Ca+ Ti) [X-Ti] <= 0.20 were ellipsoidal secondary particles with ca. 240-380nm in length composing by aggregation of small primary particles with ca. 30-100nm in length, while they were changed to very fine particles with ca. 5-10nm in diameter along with small amounts of large rod-like particles at X-Ti = 0.3. The highly crystallized pure TiHap particles were produced at X-Ti <= 0.15, while the Hap structure was almost disappear at X-Ti = 0.2. All the TiHap particles produced at X-Ti <= 0.2 were phosphorus deficient. The diffuse reflectance UV spectra of TiHap particles revealed that these particles have a UV absorption property, especially fabricated at X-Ti = 0.05. The highly crystallized TiHap particles (0.05 <= X-Ti <= 0.15) had also large specific surface area. (C)2016 The Ceramic Society of Japan. All rights reserved.
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关键词
Calcium hydroxyapatite,Ti(IV)-substituted calcium hydroxyapatite (TiHap) particles,Forced hydrolysis of pyrophosphate
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