RESUMEN
Membrane distillation (MD) is an important technique for brine desalination and wastewater treatment that may utilize waste or solar heat. To increase the distillation rate and minimize membrane wetting and fouling, we deposit a layer of polysiloxane nanofilaments on microporous membranes. In this way, composite membranes with multiscale pore sizes are created. The performance of these membranes in the air gap and direct contact membrane distillation was investigated in the presence of salt solutions, solutions containing bovine serum albumin, and solutions containing the surfactant sodium dodecyl sulfate. In comparison to conventional hydrophobic membranes, our multiscale porous membranes exhibit superior fouling resistance while attaining a higher distillation flux without using fluorinated compounds. This study demonstrates a viable method for optimizing MD processes for wastewater and saltwater treatment.
RESUMEN
Membrane distillation (MD) is an emerging desalination technology that exploits phase change to separate water vapor from saline based on low-grade energy. As MD membranes come into contact with saline for days or weeks during desalination, membrane pores have to be sufficiently small (typically <0.2 µm) to avoid saline wetting into the membrane. However, in order to achieve high distillation flux, the pore size should be large enough to maximize transmembrane vapor transfer. These conflicting requirements of pore geometry pose a challenge to membrane design and currently hinder broader applications of MD. To address this fundamental challenge, we developed a super liquid-repellent membrane with hierarchical porous structures by coating a polysiloxane nanofilament network on a commercial micro-porous polyethersulfone membrane matrix. The fluorine-free nanofilament coating effectively prevents membrane wetting under high hydrostatic pressure (>11.5 bar) without compromising vapor transport. With large inner micro-porous structures, the nanofilament-coated membrane improves the distillation flux by up to 60% over the widely used commercially available membranes, while showing excellent salt rejection and operating stability. Our approach will allow the fabrication of high-performance composite membranes with multi-scale porous structures that have wide-ranging applications beyond desalination, such as in cleaning wastewater.
RESUMEN
Superhydrophobicity has only recently become a requirement in membrane fabrication and modification. Superhydrophobic membranes have shown improved flux performance and scaling resistance in long-term membrane distillation (MD) operations compared to simply hydrophobic membranes. Here, we introduce plasma micro- and nanotexturing followed by plasma deposition as a novel, dry, and green method for superhydrophobic membrane fabrication. Using plasma micro- and nanotexturing, commercial membranes, both hydrophobic and hydrophilic, are transformed to superhydrophobic featuring water static contact angles (WSCA) greater than 150° and contact angle hysteresis lower than 10°. To this direction, hydrophobic polytetrafluoroethylene (PTFE) and hydrophilic cellulose acetate (CA) membranes are transformed to superhydrophobic. The superhydrophobic PTFE membranes showed enhanced water flux in standard air gap membrane distillation and more stable performance compared to the commercial ones for at least 48 h continuous operation, with salt rejection >99.99%. Additionally, their performance and high salt rejection remained stable, when low surface tension solutions containing sodium dodecyl sulfate (SDS) and NaCl (down to 35 mN/m) were used, showcasing their antiwetting properties. The improved performance is attributed to superhydrophobicity and increased pore size after plasma micro- and nanotexturing. More importantly, CA membranes, which are initially unsuitable for MD due to their hydrophilic nature (WSCA ≈ 40°), showed excellent performance with stable flux and salt rejection >99.2% again for at least 48 h, demonstrating the effectiveness of the proposed method for wetting control in membranes regardless of their initial wetting properties.
