Skip to main navigation Skip to search Skip to main content

Fabrication and characterization of hydroxycarbonate apatite with mesoporous structure

  • Harbin Institute of Technology

Research output: Contribution to journalArticlepeer-review

Abstract

Mesoporous hydroxycarbonate apatite (MHCAp) was converted directly from calcium carbonate particles by treatment with a phosphate buffer solution (PBS). After soaking in PBS, the calcium ions are released from CaCO3 particles and react with phosphate ions to form hydroxycarbonate apatite nanoparticles. The aggregation of the nanoparticles not only produces apatite plates, but also forms mesopores within the plates. The phases of CaCO3 play an important role in the conversion rate because of the different solubility products. If the main phase is vaterite, CaCO3 particles are converted completely to MHCAp after soaking in PBS for 24 h. However, if the main phase is calcite, the percentage of the unreacted CaCO3 particles is ∼19.7%. In addition, the conversion percentages of MHCAp increase with prolonging immersion time in PBS and increasing temperatures. The most of pore sizes of MHCAp are distributed around 4.1 ± 0.3 nm, which are not affected by the experimental conditions such as the phases of calcium carbonate, immersion time (6-24 h) and temperatures (25-50 °C). Simulated body fluid (SBF) immersion tests reveal that MHCAp exhibits a superior in vitro bone-forming bioactivity. It is hypothesized that the conversion mechanism of CaCO3 to MHCAp may be rationalized in terms of a dissolution-precipitation process.

Original languageEnglish
Pages (from-to)480-488
Number of pages9
JournalMicroporous and Mesoporous Materials
Volume118
Issue number1-3
DOIs
StatePublished - 1 Feb 2009

Keywords

  • Calcium carbonate
  • Dissolution-precipitation reaction
  • Hydroxycarbonate apatite
  • Mesopore

Fingerprint

Dive into the research topics of 'Fabrication and characterization of hydroxycarbonate apatite with mesoporous structure'. Together they form a unique fingerprint.

Cite this