Senbo Xiao

Enhancing the Mechanical Durability of Icephobic Surfaces by Introducing Autonomous Self-Healing Function

Ice accretion presents a severe risk for human safety. Although great efforts have been made for developing icephobic surfaces (the surface with an ice adhesion strength below 100 kPa), expanding the lifetime of state-of-the-art icephobic surfaces still remains a critical unsolved issue. Herein, a novel icephobic material is designed by integrating an interpenetrating polymer network (IPN) into an autonomous self-healing elastomer, which is applied in anti-icing for enhancing the mechanical durability. The molecular structure, surface morphology, mechanical properties, and durable icephobicity of the material were studied. The creep behaviors of the new icephobic material, which were absent in most relevant studies on self-healing materials, were also investigated in this work. Significantly, the material showed great potentials for anti-icing applications with an ultralow ice adhesion strength of 6.0 ± 0.9 kPa, outperforming many other icephobic surfaces. The material also exhibited an extraordinary durability, showing a very low long-term ice adhesion strength of ∼12.2 kPa after 50 icing/deicing cycles. Most importantly, the material was able to exhibit a self-healing property from mechanical damages in a sufficiently short time, which shed light on the longevity of icephobic surfaces in practical applications.

Systematic comparison of model polymer nanocomposite mechanics

Polymer nanocomposites render a range of outstanding materials from natural products such as silk, sea shells and bones, to synthesized nanoclay or carbon nanotube reinforced polymer systems. In contrast to the fast expanding interest in this type of material, the fundamental mechanisms of their mixing, phase behavior and reinforcement, especially for higher nanoparticle content as relevant for bio-inorganic composites, are still not fully understood. Although polymer nanocomposites exhibit diverse morphologies, qualitatively their mechanical properties are believed to be governed by a few parameters, namely their internal polymer network topology, nanoparticle volume fraction, particle surface properties and so on. Relating material mechanics to such elementary parameters is the purpose of this work. By taking a coarse-grained molecular modeling approach, we study an range of different polymer nanocomposites. We vary polymer nanoparticle connectivity, surface geometry and volume fraction to systematically study rheological/mechanical properties. Our models cover different materials, and reproduce key characteristics of real nanocomposites, such as phase separation, mechanical reinforcement. The results shed light on establishing elementary structure, property and function relationship of polymer nanocomposites.

Displacement of Nanofluids in Silica Nanopores: Influenced by Wettability of Nanoparticles and Oil Components

The fundamental understanding of fluid transportation in confined nanopores is essential for groundwater remediation, oil exploration, water purification, etc. Here, all-atom models of various oil components and nanoparticles were analyzed using molecular dynamics simulations for investigating their influences on the displacement of fluid flow into silica nanopores. The simulations indicated that heavy and polar oil components, carrying electronegative atoms (–N and –O), were more favorable to adsorb onto silica nanopores than light and apolar molecules. The polar molecules, such as pyridine and asphaltene, preferred to accumulate at the fluid interface, which led to increased viscosity of the oil phase and hindered the spontaneous displacement process. Silica nanoparticles (NPs) in the displacing phase could modulate the fluid–fluid meniscus regardless of hydrophobic or hydrophilic surface modification and slow down the displacement process. Most importantly, the presence of NPs induced the pressure difference in the fluids along the nanopores to govern the fluid flow process, which shed light on resolving the nanoscale water–oil displacement mechanism in sandstone reservoirs. The results provided guidance for designing suitable nanoparticles for targeted applications.

One-Step Fabrication of Bioinspired Lubricant-Regenerable Icephobic Slippery Liquid-Infused Porous Surfaces

Icephobic coating and surfaces are essential for protecting infrastructures such as transmission lines, transportation vehicles, and many others from severe damages of excessive icing. The slippery liquid-infused porous surfaces (SLIPS) are attracting escalating attention because of their low-ice adhesion strength. Despite all of the encouraging laboratory scale results, the SLIPS are still far from being applicable in real environments owing to the key unsolved problem, namely anti-icing durability. Inspired by the functionality of the amphibians’ skin, lubricant regenerability was introduced to conventional SLIPS and realized by a facile and scalable fabrication route. A series of polydimethylsiloxane (PDMS)-based skinlike SLIPS were designed and fabricated by using a one-step method, the solvent evaporation-induced phase separation technique. The obtained skinlike SLIPS were able to regenerate surface lubricant constantly by internal residual stress because of phase separation and survive more than 15 cycles of wiping/regenerating tests. Thanks to the regenerability of the surface lubricant, the new SLIPS demonstrated durable icephobicity, showing a long-term low-ice adhesion strength below 70 kPa, which was only 43% of 160 kPa that for the pristine PDMS (Sylgard 184), even after 15 icing/deicing cycles. This work paves a new and facile way for achieving icephobic durability of SLIPS.