Xin Zhao, Yi-nian Zhu, and Liu-qin Dai, Synthesis and characterization of cadmium-calcium hydroxyapatite solid solutions, Int. J. Miner. Metall. Mater., 21(2014), No. 6, pp. 604-608. https://doi.org/10.1007/s12613-014-0948-z
Cite this article as:
Xin Zhao, Yi-nian Zhu, and Liu-qin Dai, Synthesis and characterization of cadmium-calcium hydroxyapatite solid solutions, Int. J. Miner. Metall. Mater., 21(2014), No. 6, pp. 604-608. https://doi.org/10.1007/s12613-014-0948-z
Xin Zhao, Yi-nian Zhu, and Liu-qin Dai, Synthesis and characterization of cadmium-calcium hydroxyapatite solid solutions, Int. J. Miner. Metall. Mater., 21(2014), No. 6, pp. 604-608. https://doi.org/10.1007/s12613-014-0948-z
Citation:
Xin Zhao, Yi-nian Zhu, and Liu-qin Dai, Synthesis and characterization of cadmium-calcium hydroxyapatite solid solutions, Int. J. Miner. Metall. Mater., 21(2014), No. 6, pp. 604-608. https://doi.org/10.1007/s12613-014-0948-z
A series of cadmium-calcium hydroxyapatite solid solutions was prepared by an aqueous precipitation method. By various means, the characterizations confirmed the formation of continuous solid solutions over all ranges of Cd/(Cd+Ca) atomic ratio. In the results, both lattice parameters a and c display slight deviations from Vegard’s rule when the Cd/(Cd+Ca) atomic ratio is greater than 0.6. The particles change from smaller acicular to larger hexagonal columnar crystals as the Cd/(Cd+Ca) atomic ratio increases from 0–0.60 to 0.60–1.00. The area of the phosphate peak for symmetric P-O stretching decreases with the increase in Cd/(Cd+Ca) atomic ratio, and the peak disappears when the Cd/(Cd+Ca) atomic ratio is greater than 0.6; the two phosphate peaks of P-O stretching gradually merge together for the Cd/(Cd+Ca) atomic ratio near 0.60. These variations can be explained by a slight tendency of larger Cd ions to occupy M(2) sites and smaller Ca ions to prefer M(1) sites in the structure.
A series of cadmium-calcium hydroxyapatite solid solutions was prepared by an aqueous precipitation method. By various means, the characterizations confirmed the formation of continuous solid solutions over all ranges of Cd/(Cd+Ca) atomic ratio. In the results, both lattice parameters a and c display slight deviations from Vegard’s rule when the Cd/(Cd+Ca) atomic ratio is greater than 0.6. The particles change from smaller acicular to larger hexagonal columnar crystals as the Cd/(Cd+Ca) atomic ratio increases from 0–0.60 to 0.60–1.00. The area of the phosphate peak for symmetric P-O stretching decreases with the increase in Cd/(Cd+Ca) atomic ratio, and the peak disappears when the Cd/(Cd+Ca) atomic ratio is greater than 0.6; the two phosphate peaks of P-O stretching gradually merge together for the Cd/(Cd+Ca) atomic ratio near 0.60. These variations can be explained by a slight tendency of larger Cd ions to occupy M(2) sites and smaller Ca ions to prefer M(1) sites in the structure.