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Exploring the water capture efficiency of covalently attached liquid-like surfaces

材料科学 接触角 露水 冷凝 聚二甲基硅氧烷 化学工程 过冷 复合材料 化学 有机化学 热力学 物理 工程类 沸腾
作者
Anthony Katselas,Isaac J. Gresham,Andrew Nelson,Chiara Neto
出处
期刊:Journal of Chemical Physics [American Institute of Physics]
卷期号:158 (21) 被引量:4
标识
DOI:10.1063/5.0146847
摘要

The capture of moisture from the atmosphere through condensation has the potential to provide a sustainable source of water. Here, we investigate the condensation of humid air at low subcooling condition (11 °C), similar to conditions for natural dew capture, and explore how water contact angle and contact angle hysteresis affect the rates of water capture. We compare water collection on three families of surfaces: (i) hydrophilic (polyethylene oxide, MPEO) and hydrophobic (polydimethylsiloxane, PDMS) molecularly thin coatings grafted on smooth silicon wafers, which produce slippery covalently attached liquid surfaces (SCALSs), with low contact angle hysteresis (CAH = 6°); (ii) the same coatings grafted on rougher glass, with high CAH (20°-25°); (iii) hydrophilic polymer surfaces [poly(N-vinylpyrrolidone), PNVP] with high CAH (30°). Upon exposure to water, the MPEO SCALS swell, which likely further increases their droplet shedding ability. MPEO and PDMS coatings collect similar volume of water (around 5 l m-2 day-1), both when they are SCALS and non-slippery. Both MPEO and PDMS layers collect about 20% more water than PNVP surfaces. We present a basic model showing that, under low heat flux conditions, on all MPEO and PDMS layers, the droplets are so small (600-2000 µm) that there is no/low heat conduction resistance across the droplets, irrespective of the exact value of contact angle and CAH. As the time to first droplet departure is much faster on MPEO SCALS (28 min) than on PDMS SCALS (90 min), slippery hydrophilic surfaces are preferable in dew collection applications where the collection time frame is limited.

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