Crystallization fouling in heat exchangers, subsurface
energy production,
and membrane technology remains a challenge. The reactive crystallization
process is governed by whether growth or nucleation dominates the
precipitation process. However, there is little direct experimental
evidence on the fundamentals of nucleation and growth on surfaces
over a wide range of supersaturations. We investigated the crystallization
fouling of BaSO4 at 10 different supersaturations (saturation
ratios from 6.6 to 457.1). We show that deposition behavior changes
from a growth-dominated regime to a nucleation-dominated regime as
the supersaturation increases; these changes in the dominant regime
affect the resilience of the surface deposits. At low supersaturations,
crystals have a secondary order, which increases their surface resilience.
At high supersaturations, where nucleation processes dominate, crystals
aggregate on the surface with no discernible secondary structure.
At a saturation ratio of 457, nucleation processes are accelerated,
causing previously aggregated crystals to become isolated. Due to
increased isolation, the crystal resilience decreases, and the crystals
become more vulnerable to detaching from the surface. To characterize
surface deposition, we introduced the sticking factor as a measure
of the stickability. We present an analysis of the stickability of
BaSO4, CaCO3, and CaSO4, based on
published data, and observe mean sticking factors of 1.15%, 0.80%,
and 0.11%, respectively.