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Characterization, dissolution and solubility of the hydroxypyromorphite–hydroxyapatite solid solution [(Pb(x)Ca(1−x))(5)(PO(4))(3)OH] at 25 °C and pH 2–9

BACKGROUND: The interaction between Ca-HAP and Pb(2+) solution can result in the formation of a hydroxyapatite–hydroxypyromorphite solid solution [(Pb(x)Ca(1−x))(5)(PO(4))(3)(OH)], which can greatly affect the transport and distribution of toxic Pb in water, rock and soil. Therefore, it’s necessary...

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Detalles Bibliográficos
Autores principales: Zhu, Yinian, Huang, Bin, Zhu, Zongqiang, Liu, Huili, Huang, Yanhua, Zhao, Xin, Liang, Meina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4858909/
https://www.ncbi.nlm.nih.gov/pubmed/27158243
http://dx.doi.org/10.1186/s12932-016-0034-8
Descripción
Sumario:BACKGROUND: The interaction between Ca-HAP and Pb(2+) solution can result in the formation of a hydroxyapatite–hydroxypyromorphite solid solution [(Pb(x)Ca(1−x))(5)(PO(4))(3)(OH)], which can greatly affect the transport and distribution of toxic Pb in water, rock and soil. Therefore, it’s necessary to know the physicochemical properties of (Pb(x)Ca(1−x))(5)(PO(4))(3)(OH), predominantly its thermodynamic solubility and stability in aqueous solution. Nevertheless, no experiment on the dissolution and related thermodynamic data has been reported. RESULTS: Dissolution of the hydroxypyromorphite–hydroxyapatite solid solution [(Pb(x)Ca(1−x))(5)(PO(4))(3)(OH)] in aqueous solution at 25 °C was experimentally studied. The aqueous concentrations were greatly affected by the Pb/(Pb + Ca) molar ratios (X(Pb)) of the solids. For the solids with high X(Pb) [(Pb(0.89)Ca(0.11))(5)(PO(4))(3)OH], the aqueous Pb(2+) concentrations increased rapidly with time and reached a peak value after 240–720 h dissolution, and then decreased gradually and reached a stable state after 5040 h dissolution. For the solids with low X(Pb) (0.00–0.80), the aqueous Pb(2+) concentrations increased quickly with time and reached a peak value after 1–12 h dissolution, and then decreased gradually and attained a stable state after 720–2160 h dissolution. CONCLUSIONS: The dissolution process of the solids with high X(Pb) (0.89–1.00) was different from that of the solids with low X(Pb) (0.00–0.80). The average K(sp) values were estimated to be 10(−80.77±0.20) (10(−80.57)–10(−80.96)) for hydroxypyromorphite [Pb(5)(PO(4))(3)OH] and 10(−58.38±0.07) (10(−58.31)–10(−58.46)) for calcium hydroxyapatite [Ca(5)(PO(4))(3)OH]. The Gibbs free energies of formation (ΔG(f)(o)) were determined to be −3796.71 and −6314.63 kJ/mol, respectively. The solubility decreased with the increasing Pb/(Pb + Ca) molar ratios (X(Pb)) of (Pb(x)Ca(1‒x))(5)(PO(4))(3)(OH). For the dissolution at 25 °C with an initial pH of 2.00, the experimental data plotted on the Lippmann diagram showed that the solid solution (Pb(x)Ca(1−x))(5)(PO(4))(3)(OH) dissolved stoichiometrically at the early stage of dissolution and moved gradually up to the Lippmann solutus curve and the saturation curve for Pb(5)(PO(4))(3)OH, and then the data points moved along the Lippmann solutus curve from right to left. The Pb-rich (Pb(x)Ca(1−x))(5)(PO(4))(3)(OH) was in equilibrium with the Ca-rich aqueous solution. [Figure: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12932-016-0034-8) contains supplementary material, which is available to authorized users.