Thus, the activation energy for bubble nucleation, Δ F *,
is reduced by a factor ϕ compared to the case of homogeneous
nucleation (Hurwitz and Navon 1994 ): 15 $$ \Updelta F^* =
\frac{{16\pi \sigma _{\rm LB} ^3 }}{{3\left( {\mathop
P\nolimits_{\rm B}^* - P_{\rm L} } \right)^2 }}\phi, $$ where
0 ≤ ϕ ≤ 1 is a geometrical factor depending on
the wetting relationships between the bubble and the crystal, as
measured by the contact angle θ (Fig. 7 ): 16 $$ \phi =
\frac{{\left( {2 - \cos \theta } \right)\left( {1 + \cos \theta }
\right)^2 }}{4} $$ Angle θ is controlled by the relative values of
the surface tensions associated with the bubble–liquid,
bubble–crystal, and liquid–crystal interfaces, σ LB , σ
SB , and σ SL , respectively: 17 $$ \cos
\theta = \frac{{\sigma _{\rm SB} - \sigma _{\rm SL} }}{{\sigma
_{\rm LB} }} $$ Recalling that wetting refers to the tendency of a
liquid to spread over a solid surface (like in the case of a
droplet of liquid on a solid substrate; Eustathopoulos et al.