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Hydrolysis of tetracalcium phosphate in H3PO4 and KH2PO4
Authors:S Matsuya  S Takagi  L C Chow
Affiliation:(1) Department of Dental Materials Engineering, Faculty of Dentistry, Kyushu University, 812 Fukuoka, Japan;(2) Paffenbarger Research Center, American Dental Association Health Foundation, National Institute of Standards and Technology, 20899 Gaithersburg, MD, USA
Abstract:The activity product of tetracalcium phosphate (TTCP, Ca4(PO4)2O), was determined at 37°C, and the hydrolysis of TTCP was investigated in 0.01–0.1 mol l–1 H3PO4 and KH2PO4 solutions by means of calcium and phosphorus analyses, X-ray diffraction and infrared analysis. The activity product, defined as K sp=(Ca2+)4 (PO 4 3– )2 (OH)2, was 37.36 as pK sp, which was smaller than that previously reported (42.4). TTCP easily hydrolysed to form calcium-deficient apatite (Ca-def OHAp, Ca5–x (HPO4) x (PO4)3–x (OH)1–x ), or dicalcium phosphate dihydrate (DCPD, CaHPO42H2O), depending on the initial phosphate concentration. With 0.1 mol l–1 H3PO4, TTCP hydrolysed to form DCPD within several minutes. In 0.025 mol l–1 H3PO4 and 0.1 mol l–1 KH2PO4, TTCP hydrolysed to form Ca-def OHAp through DCPD. In the latter solution, a small amount of octacalcium phosphate (OCP, Ca8(H2PO4)2(PO4)45H2O), was detected as an intermediate product. In 0.025 mol l–1 KH2PO4, TTCP hydrolysed directly to form Ca-def OHAp. In 0.01 mol l–1 H3PO4, hydrolysis of TTCP was not completed, although Ca-def OHAp was only a product. Thus the final product and the degree of hydrolysis depended on the pH and the overall Ca/P ratio in the reaction system. The rate of Ca-def OHAp formation seemed to be controlled by the dissolution rate of TTCP rather than the crystallization rate of the OHAp.
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