posted on 2006-11-15, 00:00authored byMadhavi Srinivasan, Cristiano Ferraris, Tim White
The capability of three dimensionally ordered macroporous
(3DOM) hydroxyapatite, Ca10(PO4)6(OH)2 (HAp), to capture
cadmium and lead ions from their respective salt solutions
was studied as a function of temperature. Synthesis of
3DOM material was achieved by colloidal crystal templating
of polystyrene spheres (1 μm diameter) using calcium
nitrate (Ca(NO3)2) and orthophosphoric acid (H3PO4) as
precursors. The macroporous product consisted primarily
of HAp (>80% depending on the sintering temperature)
together with amorphous calcium phosphate. The sorption
ability of 3DOM material to Cd/Pb ion was benchmarked
against HAp powder prepared via the same route without
the template. On the basis of quantitative X-ray diffraction
(XRD) and analytical transmission electron microscopy (ATEM)
3DOM HAp demonstrated a higher uptake of cadmium,
viz. x = 0.71 in Ca10-xCdx(PO4)6(OH)2 than nonporous HAp
(x = 0.42). The incorporation of Cd was homogeneous in the
3DOM HAp crystals (as compared to the powder) leading
to a decrease in lattice parameters as Cd2+ has a
smaller ionic radius compared to Ca2+. A preference for
Cd to enter the CaII tunnel site of HAp was consistent with
this being the readily exchangeable site. The lead-bearing solution acted to collapse the macropores through
the rapid crystallization of pyromorphite (Pb10(PO4)6(OH)2)
via a dissolution-precipitation mechanism, possibly promoted
by the amorphous component, that overwhelmed HAp
ion exchange. The rapid crystallochemical incorporation
of Cd and fixation of Pb by 3DOM HAp demonstrates the
potential of thin-walled porous structures for the treatment
of contaminated waters.