X-ray diffraction (XRD) was employed to study dental alloy-ceramic interfac
es. A Au-Pd-In alloy, which requires oxidation before porcelain firing, and
a Au-Pt-Pd-In alloy, which does not require oxidation before porcelain fir
ing, were selected in this study. Alloy specimens were centrifugally cast.
Specimen surfaces were metallographically polished through 0.05 mum Al2O3 s
lurries. A thin layer (<50 <mu>m) of a dental opaque porcelain was fired on
the alloy surfaces with and without initial oxidation. XRD was conducted a
t room temperature on four types of alloy specimens: polished, oxidized, po
rcelain fired after alloy oxidation, and porcelain fired without initial al
loy oxidation. XRD was also performed on fired opaque porcelain without an
alloy substrate. The detection of prominent gold solid solution peaks from
alloy-ceramic specimens indicated that the incident X-ray beam reached the
alloy-ceramic interface. In2O3 and beta -Ga-2 O-3 were identified on the ox
idized Au-Pd-In alloy, while In2O3 and SnO2 were detected on the oxidized A
u-Pt-Pd-In alloy. Preferred orientation was observed for all the oxides for
med on the alloys. Minimum lattice parameter changes (<1%) for the gold sol
id solutions were observed for both alloys before and after oxidation and p
orcelain firing. Leucite (KAlSi2O6), TiO2, ZrO2 and SnO2 were detected on t
he fired opaque porcelain. For both alloys, no additional oxides were ident
ified at the metal-ceramic interfaces beyond those present in the oxidized
alloys and the opaque porcelain. Similar results were obtained from alloy-c
eramic interfaces where there was no prior alloy oxidation. The results ind
icate the critical role of alloy surface oxides in metal-ceramic bonding an
d support the chemical bonding mechanism for porcelain adherence. (C) 2001
Kluwer Academic Publishers.