Synergy of slippery surface and pulse flow: An anti-scaling solution for direct contact membrane distillation

Abstract

Recent progress on mitigating scaling on hydrophobic membrane distillation (MD) membrane focuses on the design of superhydrophobic/omniphobic surface and process optimization. However, the rationale for scaling resistance is not yet complete. We attempted in this work to unravel the correlation of scaling resistance based on the synergy of slippery surface (via chem-physical engineering) and pulse flow (process engineering). Superhydrophobic micro-pillared polyvinylidene fluoride (MP-PVDF) and CF4 plasma modified MP-PVDF (CF4-MP-PVDF) were utilized as the model membranes. We proposed rheometry as a simple quantitative measure for the wetting state in a hydrodynamic environment. Results showed that MP-PVDF possessed pinned wetting and prone to scaling (2000 mg/L CaSO4 solution) in both steady and pulse flow. In contrast, the CF4-MP-PVDF showed suspended wetting and excellent scaling resistance (at water recovery of 60%, the CF4-MP-PVDF surface was still clean without any crystals) under pulse flow, but not at steady flow. At steady flow, feed over-pressure changes the suspended wetting to pinned wetting by pushing the water-gas interface into the pillars, thereby resulting in scaling for CF4-MP-PVDF. At pulse flow, rhythmic fluctuation in the water-gas interface for CF4-MP-PVDF led to sustained scaling resistance. For the first time, we experimentally demonstrated a scaling resistance in DCMD via engineering surface wetting state and process. We envision that this rationale would pave the forward-looking strategy for a robust stable MD process in the near future.