The leucite particles in dental porcelains are often partially encircled by
microcracks that are the result of the thermal expansion mismatch between
leucite and the surrounding glass matrix. Although the magnitude of the str
ess at the particle-matrix interface is independent of the particle size (S
elsing, 1961), Davidge and Green (1968) showed experimentally that there is
a critical particle size below which microcracking is absent. The critical
particle size is explained by a Griffith-type energy balance criterion: Be
low the critical size, the stress magnitude may be sufficient to cause crac
king, but there is insufficient strain energy for the creation of the new s
urfaces of the microcrack. The purpose of the present study was to determin
e whether the mean leucite particle size of a dental porcelain influences t
he degree of microcracking in the porcelain. Microcrack density, leucite pa
rticle surface area per unit volume, and leucite mean volume-surface diamet
er, D-3,D-2, were determined by quantitative stereology on 10 specimens eac
h of 6 dental porcelains and Component No. 1 of the Weinstein et al. patent
(US Patent 3,052,982, 1962). The fraction of leucite particles with microc
racks around them, f(mc) was estimated for each porcelain from the microcra
ck density and the leucite surface area. Using the equations of Selsing (19
61) and Davidge and Green (1968), we calculated the critical particle diame
ter, D-c for leucite to be 4 mum. The porcelains were partitioned according
to whether their mean leucite particle diameters, D-3,D-2, fell above or b
elow DO and their values of f(mc) were analyzed by a permutation test with
random re-sampling. The porcelains with mean leucite particle diameters bel
ow Dc had a significantly lower fraction of cracked particles compared with
the porcelains with mean leucite particle diameters above D-c (p < 0.05).
This study provides evidence that microcracking in dental porcelain can be
minimized by a reduction of the mean leucite particle diameter to less than
4 Vim.