Mineral scaling is a major constraint
that limits the performance
of membrane distillation (MD) for hypersaline wastewater treatment.
Although the use of antiscalants is a common industrial practice to
mitigate mineral scaling, the effectiveness and underlying mechanisms
of antiscalants in inhibiting different mineral scaling types have
not been systematically investigated. Herein, we perform a comparative
investigation to elucidate the efficiencies of antiscalant candidates
with varied functional groups for mitigating gypsum scaling and silica
scaling in MD desalination. We show that antiscalants with Ca(II)-complexing
moieties (e.g., carboxyl group) are the most effective to inhibit
gypsum scaling formed via crystallization, whereas amino-enriched
antiscalants possess the best performance to mitigate silica scaling
created by polymerization. A set of microscopic and spectroscopic
analyses reveal distinct mechanisms of antiscalants required for those
two common types of scaling. The mitigating effect of antiscalants
on gypsum scaling is attributed to the stabilization of scale precursors
and nascent CaSO4 nuclei, which hinders phase transformation
of amorphous CaSO4 toward crystalline gypsum. In contrast,
antiscalants facilitate the polymerization of silicic acid, immobilizing
active silica precursors and retarding the gelation of silica scale
layer on the membrane surface. Our study, for the first time, demonstrates
that antiscalants with different functionalities are required for
the mitigation of gypsum scaling and silica scaling, providing mechanistic
insights on the molecular design of antiscalants tailored to MD applications
for the treatment of wastewaters containing different scaling types.
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