简介概要

Synthesis and characterization of cadmium-calcium hydroxyapatite solid solutions

来源期刊:International Journal of Minerals Metallurgy and Materials2014年第6期

论文作者:Xin Zhao Yi-nian Zhu Liu-qin Dai

文章页码:604 - 608

摘    要: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.

详情信息展示

Synthesis and characterization of cadmium-calcium hydroxyapatite solid solutions

Xin Zhao1,Yi-nian Zhu2,Liu-qin Dai2

1. College of Light Industry and Food Engineering, Guangxi University2. College of Environmental Science and Engineering, Guilin University of Technology

摘 要: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.

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