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Adair Gallo Jr.

Publications and source records attributed to Adair Gallo Jr..

6 recordsLinked to original sources

Superhydrophobic Sand Mulch Shifts Soil Evaporation from Temperature-Controlled to Diffusion-Limited Regimes

In hot arid and semi-arid regions, substantial irrigation water is lost through surface evaporation under intense solar irradiation and high temperatures, limiting freshwater sustainability and crop productivity. Superhydrophobic Sand (SHS) mulch, a plastic-free, bio-inspired technology, has been proposed as a dry diffusion barrier to suppress evaporative losses. Here, we combine controlled column experiments with heat and mass transfer modeling to quantify how SHS thickness and soil properties govern evaporation under fixed irradiation. Relative to unmulched controls, a 5 mm SHS layer reduced evaporative flux by 65$\%$ in fine sand and 63$\%$ in coarse sand, while a 10 mm layer reduced flux by 83$\%$ and 70$\%$, respectively. Notably, soil-type trends reversed after mulching: although unmulched fine sand exhibited 37.5$\%$ higher evaporation than coarse sand, application of a 10 mm SHS layer reduced fine-sand evaporation to 40$\%$ below that of coarse sand. To explain this counterintuitive behavior, we developed a coupled heat and vapor transport model incorporating soil thermophysical properties and diffusion through the porous mulch layer. The model accurately predicted steady-state temperature profiles and evaporation rates for both mulched and unmulched systems. Our results show that SHS mulch shifts evaporation from a surface-temperature-controlled regime to a diffusion-limited regime governed by mulch thickness and soil thermal conductivity. This mechanistic understanding clarifies the performance of SHS and supports its potential to enhance irrigation efficiency in arid agricultural and landscaping applications.

physics.geo-ph

On the Formation of Hydrogen Peroxide in Water Microdroplets

Recent reports on the formation of hydrogen peroxide (H$_2$O$_2$) in water microdroplets produced via pneumatic spraying or capillary condensation have garnered significant attention. How covalent bonds in water could break under such conditions challenges our textbook understanding of physical chemistry and the water substance. While there is no definitive answer, it has been speculated that ultrahigh electric fields at the air-water interface are responsible for this chemical transformation. Here, we resolve this mystery via a comprehensive experimental investigation of H$_2$O$_2$ formation in (i) water microdroplets sprayed over a range of liquid flow-rates, the (shearing) air flow rates, and the air composition (ii) water microdroplets condensed on hydrophobic substrates formed via hot water or humidifier under controlled air composition. Specifically, we assessed the contributions of the evaporative concentration and shock waves in sprays and the effects of trace O$_3$(g) on the H$_2$O$_2$ formation. Glovebox experiments revealed that the H$_2$O$_2$ formation in water microdroplets was most sensitive to the air-borne ozone (O$_3$) concentration. In the absence of O$_3$(g), we could not detect H$_2$O$_2$(aq) in sprays or condensates (detection limit: 250 nM. In contrast, microdroplets exposed to atmospherically relevant O$_3$(g) concentration (10-100 ppb) formed 2-30 $μ$M H$_2$O$_2$(aq); increasing the gas-liquid surface area, mixing, and contact duration increased H$_2$O$_2$(aq) concentration. Thus, the mystery is resolved - the water surface facilitates the O$_3$(g) mass transfer, which is followed by the chemical transformation of O$_3$(aq) into H$_2$O$_2$(aq). These findings should also help us understand the implications of this chemistry in natural and applied contexts.

cond-mat.soft

The air-water interface of condensed water microdroplets does not produce H$_2$O$_2$

Recent reports on the production of hydrogen peroxide (H$_2$O$_2$) on the surface of condensed water microdroplets without the addition of catalysts or additives have sparked significant interest. The underlying mechanism is speculated to be ultrahigh electric fields at the air-water interface; smaller droplets present higher interfacial area and produce higher (detectable) H$_2$O$_2$ yields. Herein, we present an alternative explanation for these experimental observations. We compare H$_2$O$_2$ production in water microdroplets condensed from vapor produced via (i) heating water to 50-70 °C and (ii) ultrasonic humidification (as exploited in the original report). Water microdroplets condensed after heating do not show any enhancement in the H$_2$O$_2$ level in comparison to the bulk water, regardless of droplet size or the substrate wettability. In contrast, those condensed after ultrasonic humidification produce significantly higher H$_2$O$_2$ quantities. We conclude that the ultrasonication of water contributes to the H$_2$O$_2$ production, not droplet interfacial effects.

cond-mat.soft

Superhydrophobic sand mulches increase agricultural productivity in arid regions

Excessive evaporative loss of water from the topsoil in arid-land agriculture is compensated via irrigation, which exploits massive freshwater resources. The cumulative effects of decades of unsustainable freshwater consumption in many arid regions are now threatening food-water security. While plastic mulches can reduce evaporation from the topsoil, their cost and non-biodegradability limit their utility. In response, we report on superhydrophobic sand (SHS), a bio-inspired enhancement of common sand with a nanoscale wax coating. When SHS was applied as a 5 mm-thick mulch over the soil, evaporation dramatically reduced and crop yields increased. Multi-year field trials of SHS application with tomato (Solanum lycopersicum), barley (Hordeum vulgare), and wheat (Triticum aestivum) under normal irrigation enhanced yields by 17%-73%. Under brackish water irrigation (5500 ppm NaCl), SHS mulching produced 53%-208% higher fruit yield and grain gains for tomato and barley. Thus, SHS could benefit agriculture and city-greening in arid regions.

physics.app-ph

A General Framework for Liquid Marbles

Liquid marbles refer to liquid droplets that are covered with a layer of non-wetting particles. They are observed in nature and have practical significance. However, a generalized framework for analyzing liquid marbles as they inflate or deflate is unavailable. The present study fills this gap by developing an analytical framework based on liquid-particle and particle-particle interactions. We demonstrate that the potential final states of evaporating liquid marbles are characterized by one of the following: (I) constant surface area, (II) particle ejection, or (III) multilayering. Based on these insights, a single-parameter evaporation model for liquid marbles is developed. Model predictions are in excellent agreement with experimental evaporation data for water liquid marbles of particle sizes ranging from 7 nanometers to 300 micrometers (over four orders of magnitude) and chemical compositions ranging from hydrophilic to superhydrophobic. These findings lay the groundwork for the rational design of liquid marble applications.

cond-mat.mtrl-sci

The Chemical Reactions in Electrosprays of Water Do Not Always Correspond to Those at the Pristine Air-Water Interface

The recent application of electrosprays to characterize the air-water interface, along with the reports on dramatically accelerated chemical reactions in aqueous electrosprays, have sparked a broad interest. Herein, we report on complementary laboratory and in silico experiments tracking the oligomerization of isoprene, an important biogenic gas, in electrosprays and isoprene-water emulsions to differentiate the contributions of interfacial effects from those of high voltages leading to charge-separation and concentration of reactants in the electrosprays. To this end, we employed electrospray ionization mass spectrometry, proton nuclear magnetic resonance, and quantum mechanical simulations. We found that the oligomerization of isoprene in aqueous electrosprays involved minimally hydrated and highly reactive hydronium ions. Those conditions, however, are non-existent at pristine air-water interfaces and oil-water emulsions under normal temperature and pressure. Thus, electrosprays should be complemented with surface-specific platforms and theoretical methods to reliably investigate chemistries at the pristine air-water interface.

physics.chem-ph