کلیدواژهها
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electrophoretic deposition (EPD), electrochemical potential difference, hydroxyapatite (HA) nanoparticles, in-situ kinetics, f
factor
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چکیده
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Suspensions ofHAnanoparticles were prepared in different alcohols using triethanolamine (TEA) as
dispersant. Optimum concentration of TEA increased with molecular weight of alcohol: 0.67, 0.67
and 8ml L−1, respectively, in methanolic, ethanolic and butanolic suspensions. Current density
increased during EPD from TEA containing methanolic and ethanolic suspensions due to desorption
ofH+TEA ions from depositedHAnanoparticles under the influence of applied electric field. Particles
were detached from deposits into the suspensions at the interface after switching off the voltage due to
the generation of an electrochemical potential difference there. The rate of detachment decreased
continuously in all methanolic suspensions and ethanolic suspensions with 4ml L−1TEA due to
the continuous reduction in the electrochemical potential difference at the interface caused by the
effective diffusion of high concentration of free TEA andH+TEA species present in the liquid phase of
deposits into the suspension. However, the rate of detachment remained constant in ethanolic
suspensions with TEA<4ml L−1 and in all butanolic suspensions. The mass flow of TEA and
H+TEA species from deposit into the suspensions is negligible in these suspensions so that the
electrochemical potential difference and so detachment rate remain constant.
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