Papers by Keyword: Dicalcium Phosphate Dihydrate

Abstract: Porous β-tricalcium phosphate (β-TCP) foam granular cements was obtained by exposing different range size of β-TCP foam granular (300-600 μm and 600-1000 μm) with 1.4 mol/L of saturated acidic calcium phosphate solution at various setting reaction times. It was found that large amount of dicalcium phosphate dihydrate (DCPD) was formed in the set specimens after exposing small size of β-TCP foam granular with saturated acidic calcium phosphate solution. Morphological observation shows that the bridging of DCPD platelet-like crystals between β-TCP foam granular surfaces were detected as early as 10 mins after exposing 300-600 μm of β-TCP foam granules with saturated acidic calcium phosphate solution. In fact, the amount of DCPD formed in the specimens obtained from small size of β-TCP foam granules is higher than large sized foam granules. These results demonstrated that small size of β-TCP foam granules induced fast setting reaction of β-TCP foam granules to produce porous β-TCP foam granular cements.

Abstract: Regulation of DCPD formation on β-TCP granules was achieved by exposing β-TCP granular with different concentration of acidic calcium phosphate solution. It was found that a higher amount of DCPD was formed when exposed β-TCP granular with the higher concentration of acidic calcium phosphate solution. Morphological observation shows that the surface of β-TCP granular was fully coated with DCPD crystals after exposed with the higher concentration of acidic calcium phosphate solution. These results demonstrated that the DCPD formation on the β-TCP granular surface could be regulated by varying the concentration of acidic calcium phosphate solution.

Abstract: Calcium phosphate cement has been widely used as a bone substitute because of its chemical similarity to natural bone. In this study, calcium phosphate cement was prepared using dicalcium phosphate dihydrate (CaHPO₄.2H₂O) and calcium carbonate (CaCO₃) as starting raw materials. The cement pastes were mixed and the chemistry adjusted with two different aqueous solutions of sodium hydroxide (NaOH) and disodium hydrogen phosphate (Na₂HPO₄). Concentrations of the solution were varied in the range 0.5 to 5.0 mol/L with the ratio of solid/liquid = 2 g/ml. The cement paste was then poured into a silicone mold having a diameter of 10 mm and a height 15 mm. Setting times for the cement were measured using a Vicat apparatus. XRD, FT-IR, and SEM techniques were used to characterize properties and microstructure of the cement. From the experimental results, it is clear that different concentrations of Na₂HPO₄ and NaOH have affected the setting times of the cement. The relationship between concentration of NaOH and Na₂HPO₄ and setting time, including final properties of the cement, is discussed.

Abstract: In situ monitoring of structural changes, taking place upon calcium phosphate bone cements hardening process was carried out by means of the Energy Dispersive X-Ray Diffraction method. Two different cement systems were studied, one of them based on the octacalcium phosphate and another - on the dicalcium phosphate dehydrate. Both systems contained natural biopolymer chitosan and were soaked in Simulated Body Fluid. The obtained experimental results evidence that during the hardening of the cement containing octacalcium phosphate its partial transformation into hydroxyapatite takes place, whereas no significant changes were detected during the hardening process of cement containing the dicalcium phosphate dehydrate.

Abstract: This study reports a novel method for the preparation of several biologically important calcium phosphate (Ca-P) phases such as hydroxyapatite (HA), dicalcium phosphate dihydrate (DCPD) and dicalcium phosphate anhydrous (DCPA). X-ray diffraction (XRD) results showed that phase pure DCPD, DCPA and HA nano-crystals could be produced in the Ca2+/PO4 3- solutions with the presence of EDTA at 120 oC, 180 oC and 210 oC, respectively. Transmission electron microscope (TEM) micrographs revealed that all the Ca-P precipitates were needle-like or rod-like. Most of the precipitates ranged from 100 ~ 200 nm in length. Selected area electron diffraction confirmed that the longitude direction of the rod-like HA precipitates were along c-axis and the flat surface was (110). Thermal gravimetric analysis of the DCPD precipitates revealed that phase transformations of DCPD to DCPA and DCPA to HA occurred at 139 oC and 195 oC, respectively, which resulted in the different Ca-P phases during hydrothermal synthesis at different temperature ranges.

Abstract: The progression of the setting reaction of a tetracalcium phosphate (TTCP) –dicalcium phosphate dihydrate (DCPD) rapid setting cement was investigated as a function of time. Compressive strength and extent of conversion to hydroxyapatite (HA) were obtained at different incubation times. The results indicated a rapid development of both strength and HA conversion in the early stages of the reaction, which slowed down after 4 h, presumably as a result of HA formation on the surface of the reactants. This hypothesis was supported by scanning electron microscopy examination of cement fracture surfaces.