Abstract
The hydrolysis of dicalcium phosphates (CaHPO4·2H2O ; DCPD and CaHPO4 DCPA) to apatite in the presence of CaCO3, which was convenient for the preparation of carbonate-containing apatite (CO3AP), was studied on the reaction process and properties of reaction products.
CaCO3 functioned as a pH compensator to realize pH conditions for the hydrolysis. CO3Ap formed according to the succesive reaction DCPD→Ca8H2 (PO4) 6·H2O→CO3Ap or the simple reaction DCPA→CO3Ap. DCPD tended to form nonstoichiometric CO3Ap containing CO32- locating at the both PO4 and OH sites of the apatite structure, whereas DCPA nearly stoichiometric CO3Ap containing CO32- locating preferentially at the PO4 site. CO3Ap showed various characteristic thermal changes, e. g., additional formation of apatitic OH, formation and trap of CO2 in the apatite structure, shift of CO32- from the PO4 site to the OH site, and finally the formation of hydroxyapatite containing no CO32- and CO2.