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Mechanochemical Synthesis of SiO 4 4– ‐Substituted Hydroxyapatite, Part II – Reaction Mechanism, Structure, and Substitution Limit
Author(s) -
Bulitalya V.,
Chaikina Marina V.,
Andreev Andrey S.,
Lapina Olga B.,
Ishchenko Arcady V.,
Prosanov Igor Yu.,
Gerasimov Konstantin B.,
Solovyov Leonid A.
Publication year - 2014
Publication title -
european journal of inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 1434-1948
DOI - 10.1002/ejic.201402246
Subject(s) - chemistry , silicate , apatite , hydroxyapatites , nanocrystalline material , silicon , orthosilicate , calcium silicate , carbonate , mineralogy , inorganic chemistry , chemical engineering , crystallography , nuclear chemistry , calcium , organic chemistry , engineering , tetraethyl orthosilicate
For the first time, silicate‐substituted hydroxyapatites have been prepared from mixtures containing different amounts of silicon (0.2–2 mol per mol of apatite unit cell) by dry mechanochemical synthesis at room temperature in a planetary ball mill. The XRD, FTIR, TEM, and NMR spectroscopic data show that the product of the mechanochemical synthesis is a single‐phase nanocrystalline apatite containing different amounts of carbonate and silicate ions and adsorbed water. In the annealed samples, three silicon concentration subranges can be distinguished, each of which is characterized by specific evolution of the lattice parameters. The formation mechanism of the silicate‐substituted hydroxyapatite obtainable by this method is discussed. The studies indicate that the silicon substitution limit in the silicate‐substituted lattice achievable by the dry mechanochemical synthesis followed by heat treatment is 1.2 mol per mol of apatite unit cell.