Abstract:
In this study, coatings of hydroxyapatite (HAp) prepared by thermal spraying
technique are investigated for biological response. Spraying was done on two
geometrically different Ti-6Al-4V alloy substrates under atmospheric conditions.
Subsequent immersion experiments, mimicking physiological environment, were
carried out using simulated body fluids (SBF).
Non-destructive techniques utilizing conventional and high-energy synchrotron
diffractometry were employed for depth–resolved investigations of phase
composition, crystallinity and residual stresses within the coating for both substrate
geometries. Microscopy techniques were used to examine surface morphology and
microstructure.
In both substrate geometries and for all immersion periods, HAp is the predominant
phase with tetra-calcium phosphate (TTCP) and tri-calcium phosphate (TCP) the two
main thermal products. The coating deposited on cylindrical rod substrate show a
higher volume fraction of HAp at the near-surface region for the as-sprayed condition
and samples immersed for 7 and 28 days. Further immersion shows the former
decreasing gradually while the latter saturates after 28 days. Thermal products TTCP
and TCP, for the coating deposited on the flat geometry substrate decreased with
immersion, while those deposited on the cylindrical rod remains roughly the same
before increasing slightly. Through-thickness behavior shows the as-sprayed HAp
increasing almost linearly with depth, reaching a maximum around the coating
midpoint before decreasing with further depth. Immersion in SBF does not alter the
general trend across the coating however it increased the volume fraction of HAp
within the first half of the coating with the biggest change occurring between 7 and
28-days of immersion. The variation of HAp with depth and immersion at the three
lateral positions shows agreement within error bars indicating the coating to be
homogenous. The trend is observed for coating deposited on cylindrical substrate
geometry.
Both substrate geometries show high near-surface region crystallinity with an index
of ~90%. The interface region is less crystalline with a degree of crystallinity index of
67% and 56% for the flat and cylindrical substrates, respectively. Immersion in SBF
does not alter the general through-thickness trend however it increased the degree of
crystallinity at both ends.
Residual stresses for the coating deposited on both substrate geometries are tensile
and small, not exceeding 42 MPa and 65 MPa, respectively. The stresses are mainly
confined in the near-surface region with the interior region showing neglible stresses,
<10 MPa. Immersion in SBF relaxes the stress with the interior to almost zero. In the
as-sprayed condition, the magnitudes of the average normal stresses 11 and 22 are
36.1 ± 2.9 MPa and 36.2 3.0 MPa, respectively; the stresses increase by ~10%
and ~13% to 39.6 ± 2.6 MPa and 41.0 ± 2.6 MPa respectively upon immersion. With
further immersion i.e. after 28 days, they relax and stabilize around 25.6 ± 2.8 MPa
and 28.4 ± 2.8 MPa. Coatings deposited on cylindrical rod show similar trend with 11
and 22 increasing from 57.7 ± 3.2 MPa to 37.2 ± 3.1 MPa to 63.4 2.6 MPa and
41.9 3.5 MPa, respectively and subsequently decreasing 51.0 3.5 MPa and 39.3
3.3 MPa, respectively.
Microscopy analysis of the coating show typical plasma sprayed coating morphology
with glassy smooth regions, pancake splats, cracks as well as partial molten particles
across coating surface. Immersion in SBF resulted in dissolution of ions from the
coating hence increasing the surface roughness. Further immersion led to the
formation of a precipitate layer which grew in thickness with immersion period. The
precipitate extended deeper into the coating through a 3-D network of channels.
Overall, the first 7 days of immersion are crucial with SBF-induced changes of the
above-mentioned occurring during this period and the near-surface region being the
most affected. Substrate geometry seems to have an effect on the crystallinity, phase
composition, residual stress as well as their dissolution.