Superdurable Full-Life Superhydrophobic Composite Block.

Superhydrophobic materials are attractive for industrial development but plagued by poor mechanical stability. Herein, a superdurable full-life superhydrophobic composite block is designed and fabricated by embedding near-zero contractive superhydrophobic silica aerogel into a rigid iron-nickel foam structured similarly to a regular dodecahedron. The synergistic protection afforded by these materials ensures superrobust mechanical stability for the composite block, which features a high compressive strength of up to ≈7.4 MPa, and ultralow Taber abrasion of down to ≈0.567 mm after withstanding 50 000 cycles, and highly efficient water harvesting capability of up to ≈3114.3 mg min-1 cm-2 at a supercooling degree of 40 K. This robust material system provides a novel strategy to design superhydrophobic materials capable of withstanding extreme conditions, including high temperature, humidity, pressure, and abrasion.

Incorporation of Th4+ and Sr2+ into Rhabdophane/Monazite by Wet Chemistry: Structure and Phase Stability.

Rhabdophane is an important permeable reactive barrier to enrich radionuclides from groundwater and has been envisaged to host radionuclides in the backend of the nuclear fuel cycle. However, understanding of how An4+ and Sr2+ precipitate into rhabdophane by wet chemistry has not been resolved. In this work, Th4+ and Sr2+ incorporation in the rhabdophane/monazite structure as La1-2xSrxThxPO4·nH2O solid solutions is successfully achieved in the acid solution at 90 °C. Some specific issues such as lattice occupation of Th4+ and Sr2+, precipitation reaction kinetics, and crystal growth affected by starting stoichiometry are discussed in detail, along with investigating the chemical stability of La1-2xSrxThxPO4·nH2O precipitations and associated La1-2xSrxThxPO4 monazite. The results reveal that the excess of Sr2+ appears to be a prevailing factor with a suggested initial Sr: Th ≥ 2 to obtain the stability domain of La1-2xSrxThxPO4·nH2O (x = 0∼ 0.1). A rapid ion removal associated with a nucleation process has been observed within 8 h, and Th4+ can be removed more than 98% after 24 h in 0.01 mol/L solutions. From structural energetics based on density functional theory, the lattice occupation of Th4+ and Sr2+ is energetically favorable in nonhydrated lattice sites of [LaO8], although two-thirds of lattice sites are associated with [LaO8·H2O] hydrated sites. Intriguingly, the crystal transformation from rhabdophane to monazite associated with the transformation from [SrO8] to [SrO9] polyhedra can greatly improve the leaching stability of Sr2+.

Large-Scale Fabrication of Wettability-Controllable Coatings for Optimizing Condensate Transfer Ability.

Systematic regulation of hydrophilic regions plays a key role in optimizing the heterogeneous hydrophilic-hydrophobic surface for promoting condensate transfer ability (CTA) under subcooling or high-humidity conditions. In this work, we develop an operable method to fabricate wettability-controllable coatings by regulating the mass ratio of superamphiphobic and superamphiphilic powder (MRP). By investigating the synergic relationship between CTA and MRP, we display an interesting competition between condensation and detachment of condensates. The initial dewing rate associated with reflecting phase change heat transfer capacity could be continuously strengthened by promoting MRP, while the detachment capacity with respect to improving the long-term condensing rate can be limited by the excessive superamphiphilic microregions. Based on this, we have optimized the threshold of MRP for promoting the condensation heat transfer ability and the water harvesting efficiency with the values of 10:0-8:2 and 10:0-4:6, respectively. This work provides important guidance in designing and optimizing heterogeneous hydrophilic-hydrophobic surfaces for multiple industrial applications including heat management, water harvesting, and desalination.

Design of Continuous Transport of the Droplet by the Contact-Boiling Regime.

Joule-heat-driven directional transport of liquid droplets has comprehensive engineering applications in various water and thermal management, cooling systems, and self-cleaning. Generally, the driving force for the transport of liquid droplets was always observed at an extremely high Leidenfrost temperature, which limits the potential application between liquid boiling and Leidenfrost points. In this work, we design a new strategy to directionally drive the transport of droplets by blockading the vapor cushion at a temperature much lower than the Leidenfrost point. On the surface of the microhole arrays, we observed the continuous rebound behavior of ethanol droplets at Ts = 110 °C. Employing the thermal multiphase lattice Boltzmann model, the continuous rebound behavior was reproduced, verifying that the driving force was provided by the blockaded vapor pressure in microholes. By cooperating with the Laplace pressure difference, we directionally transport ethanol and water droplets on the horizontal asymmetrical concentric microridge surface. The horizontal velocity of water is 11.25 cm/s at Ts = 180 °C, similar to the traditional ratchets at the Leidenfrost point. The design of microtextures enriches the fundamental understanding of how to drive droplets at far below the Leidenfrost point and pushes the application in nongravity-driven self-cleaning and cooling systems.