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Liquids

Liquids is an international, peer-reviewed, open access journal on all aspects of liquid material research published quarterly online by MDPI.

All Articles (140)

Droplets sliding down a partially wetted surface are a ubiquitous phenomenon in nature and everyday life. Despite its apparent simplicity, it hinders complex intricacies for theoretical and numerical descriptions matching the experimental observations, even for the simplest case of a drop sliding down a homogeneous surface. A key aspect to be considered is the distribution of contact angles along the droplet perimeter, which can be challenging to include in the theoretical/numerical analysis. The scenario can become more complex when considering geometrically or chemically patterned surfaces or complex fluids. Indeed, these aspects can provide strategies to passively control the droplet motion in terms of velocity or direction. This review gathers the state of the art of experimental, numerical, and theoretical research about droplets made of Newtonian and non-Newtonian fluids sliding down homogeneous, chemically heterogeneous, or geometrically patterned surfaces.

31 October 2025

Onset of sliding. (a) Advancing (θA) and receding (θR) contact angles defined from the shape of a drop lying on a surface inclined by the sliding angle, as, the smallest inclination angle necessary to observe sliding. (b) Planar view of a liquid drop having a parallel-sided contact line. The dashed line represents the same contact line after a displacement of the drop equal to dx. (c) Time evolution of the lateral adhesion force experienced by a drop of ionic liquid (volume~1.5 μL) on a fluorinated silicon wafer [32]. Reprinted with permission from Ref. [32]. 2017 Springer Nature.

The rheological properties of aqueous solutions of wormlike micelles (WLMs) of cationic surfactant erucyl bis(hydroxyethyl)methylammonium chloride (EHAC) in the presence of hydrotropic salt sodium salicylate (NaSal) and inorganic salt sodium chloride (NaCl) have been studied. The conditions for maximum zero-shear viscosity at fixed surfactant concentration were investigated. It has been shown that charged WLMs in the presence of NaSal have higher viscosities than well-screened micelles in the presence of NaCl. This is because the adsorption of hydrophobic salicylate ions onto the micelles increases their length more significantly than the presence of a large amount of sodium ions in the solution. It was discovered that the effect of temperature on the rheological properties depends on both the type of salt used and the salt/surfactant molar ratio. An unusual increase in zero-shear viscosity and elastic modulus was observed at a NaSal concentration that corresponds to the maximum zero-shear viscosity when the WLMs are linear, charged, and “unbreakable”. These results expand the possibilities of using hydrotropic salts to create stable, highly viscous systems in various fields, and opening up new horizons for applications in oil production, cosmetics, and household chemicals.

26 October 2025

(a) Zero-shear viscosity as a function of NaSal/EHAC molar ratio at two different EHAC concentrations: 13 mM (circles) and 18 mM (squares) at 25 °C. (b) Frequency dependences of storage G′ (filled symbols) and loss G″ (open symbols) moduli for 13 mM aqueous solutions of EHAC at increasing molar ratios of NaSal/EHAC: 0.4 (triangles), 0.5 (circles), and 0.6 (squares) at 25 °C.

Liquids like water are not expected to produce a thermal change under shear strain or flow (away from extreme conditions). In this study, we reveal experimental conditions for which the conventional athermal hydrodynamic assumption is no longer valid. We highlight the establishment of non-equilibrium hot and cold thermal states occurring when a mesoscopic confined liquid is set in motion. Two stress situations are considered: low-frequency shear stress at large strain amplitude and microfluidic transport (pressure gradient). Two liquids are tested: water and glycerol at room temperature. In confined conditions (submillimeter scale), these liquids exhibit stress-induced thermal waves. We interpret the emergence of non-equilibrium temperatures as a consequence of the solicitation of the mesoscopic liquid elasticity. In analogy with elastic deformation, the mesoscopic volume decreases or increases slightly, which leads to a change in temperature (thermo-mechanical energy conversion). The energy acquired or released is converted to heat or cold, respectively. To account for these non-equilibrium temperatures, the mesoscopic flow is no longer considered as a complete dissipative process but as a way of propagating shear and thus compressive waves. This conclusion is consistent with recent theoretical developments showing that liquids propagate shear elastic waves at small scales.

9 October 2025

Mechanical response of a water layer of 125 µm confined between high-energy surfaces (alumina) subjected to a low-frequency oscillatory shear strain of 1 rad/s versus increasing shear amplitude (from γ = 1% to 7500%). Measurements carried out at room temperature. The central figure superposes raw waves (blue wave for the shear strain γ and red for the torque Γ(γ)), the shear elastic modulus G′ (■) and the viscous modulus G″ (•), calculated by the rheometer software using the assumption of a sinus stress wave response. The two light-blue dotted squares detail the waves illustrated in inserts (a,b). The white dotted arrow indicates the entrance in the non-linear regime assimilated to a viscous-like behavior according to the viscoelasticity theory. The satellite figures are described as follows. (a) At low shear strain amplitude (2–4%), stress and strain waves are in-phase, indicating an instantaneous (elastic) response (indicated in Figure 1 by the left blue dotted square). (b) At large shear strain amplitude (c), the shear stress signal is a distorted wave leading by a π/2 advance of phase with respect to the imposed strain wave. (c) Stress relaxation: the vertical dotted line corresponds to the moment at which the strain stops (detail of the blue circle in (b)). The shear wave is relaxed within 0.2 s after the mechanical stop.

This study investigates the formation of hydroxyl radicals (OH radicals) in cavitation bubble plasma-treated water (CBPTW) using a chemical probe method. CBPTW samples were prepared with different electrode materials (W, Fe, Cu, and Ag), and the chemical scavenger was added two minutes after the completion of cavitation and plasma treatments. The concentrations of metal ions and hydrogen peroxide (H2O2) generated in the CBPTW were also measured over time. This study reveals a novel mechanism whereby metal nanoparticles and ions released from electrodes catalyze the continuous generation of hydroxyl radicals in CBPTW, which has not been fully addressed in previous studies. The results suggest a continuous generation of OH radicals in CBPTW prepared with W, Fe, and Cu electrodes, with the amount of OH radicals produced in the order Cu > Fe > W. The study reveals a correlation between OH radical production and electrode wear, suggesting that the continuous generation of OH radicals in CBPTW results from the catalytic decomposition of H2O2 by metal nanoparticles or ions released from the electrodes. It should be noted that cavitation bubble plasma (CBP) is fundamentally different from sonochemistry. While sonochemistry utilizes ultrasound-induced cavitation to generate radicals, CBP relies on plasma discharge generated inside cavitation bubbles. No ultrasound was applied in this study; therefore, all observed radical formation is attributable exclusively to plasma processes rather than sonochemical effects. However, the precise mechanism of continuous OH radical formation in CBPTW remains unclear and requires further investigation. These findings provide new insights into the role of electrode materials in continuous OH radical generation in cavitation bubble plasma treated water, offering potential applications in water purification and sterilization technologies.

1 October 2025

Schematic diagram of CBP apparatus for preparation of CBPTW.

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Liquids - ISSN 2673-8015Creative Common CC BY license