Controlling the breakup of toroidal liquid films on solid surfaces.
Ontology highlight
ABSTRACT:
SUBMITTER: Edwards AMJ
PROVIDER: S-EPMC8046813 | biostudies-literature |
REPOSITORIES: biostudies-literature
Similar Datasets
Project description:Although the anisotropy of the solid-liquid interfacial free energy for most alloy systems is very small, it plays a crucial role in the growth rate, morphology and crystallographic growth direction of dendrites. Previous work posited a dendrite orientation transition via compositional additions. In this work we examine experimentally the change in dendrite growth behaviour in the Al-Sm (Samarium) system as a function of solute concentration and study its interfacial properties using molecular dynamics simulations. We observe a dendrite growth direction which changes from [Formula: see text] to [Formula: see text] as Sm content increases. The observed change in dendrite orientation is consistent with the simulation results for the variation of the interfacial free energy anisotropy and thus provides definitive confirmation of a conjecture in previous works. In addition, our results provide physical insight into the atomic structural origin of the concentration dependent anisotropy, and deepen our fundamental understanding of solid-liquid interfaces in binary alloys.
| S-EPMC7002690 | biostudies-literature
Project description:Deposition of liquid droplets on solid surfaces is of great importance to many fundamental scientific principles and technological applications, such as spraying, coating, and printing. For example, during the process of pesticide spraying, more than 50% of agrochemicals are lost because of the undesired bouncing and splashing behaviors on hydrophobic or superhydrophobic leaves. We show that this kind of splashing on superhydrophobic surfaces can be greatly inhibited by adding a small amount of a vesicular surfactant, Aerosol OT. Rather than reducing splashing by increasing the viscosity via polymer additives, the vesicular surfactant confines the motion of liquid with the help of wettability transition and thus inhibits the splash. Significantly, the vesicular surfactant exhibits a distinguished ability to alter the surface wettability during the first inertial spreading stage of ~2 ms because of its dense aggregates at the air/water interface. A comprehensive model proposed by this idea could help in understanding the complex interfacial interactions at the solid/liquid/air interface.
| S-EPMC5332151 | biostudies-literature
Project description:In industrial applications involving spray-cooling, combustion, and so on, prediction of the maximum spreading diameter of a droplet impinging on a solid surface permits a quantitative estimation of heat removal and energy consumption. However, although there are many experimental studies regarding droplet impingement behaviour, theoretical models have an applicability limit for predicting the maximum spreading diameter. In the present study, we have developed an analytical model for droplet impingement based on energy conservation that considers adhesion energy in both horizontal and vertical directions at the contact line. The theory is validated by our experiment and existing experimental data possessing a wide range of Weber numbers. We demonstrate that our model can predict β m (i.e., the maximum spreading diameter normalised in terms of initial droplet diameter) for various Newtonian liquids ranging from micro- to millimetre-sized droplets on different solid surfaces and can determine the transition between capillary and viscous regimes. Furthermore, theoretical relations for scaling laws observed by many researchers are derived.
| S-EPMC5443818 | biostudies-literature
Project description:Wetting of solid surfaces occurs when the intervening air film between a water droplet and a solid surface ruptures. Although this rupturing phenomenon is well known, the underlying mechanism has not yet been well understood. In this work, the rupture of intervening air films is systematically studied by measuring the spatiotemporal thickness profiles of the air films between droplets of deionized water and flat solid surfaces using a synchronized triwavelength reflection interferometry microscope. It has been shown that the critical rupture thickness of the air film (h c) depends on the surface hydrophobicity of solid surfaces. The h c value was increased from 50 nm on a hydrophobic surface having an equilibrium water contact angle (?w) of 96° to 1.42 ?m on a hydrophilic surface having a ?w of 25°. In addition, an increase in the critical rupture thickness with decreasing surface hydrophobicity was found to be applicable not only to chemically treated quartz surfaces but also to a variety of natural mineral surfaces. By determining the pressure within the air films, we have shown that a strong attractive force is present between water droplets and hydrophilic surfaces, thereby accelerating the draining of air films. The measured forces might be of electrostatic origin, and the forces become less attractive with increasing hydrophobicity of solid surfaces. The present result provides a fundamental insight into the rupture of air films from the perspective of surface forces.
| S-EPMC6788057 | biostudies-literature
Project description:Thin ionic liquid (IL) films play an important role in many applications. To obtain a better understanding of the ion distribution within IL mixture films, we sequentially deposited ultrathin layers of two ILs with the same cation but different anions onto Ag(111), and monitored their dynamic behaviour by angle-resolved X-ray photoelectron spectroscopy. Upon depositing [C8 C1 Im][PF6 ] on top of a wetting layer of [C8 C1 Im][Tf2 N] at room temperature (RT), we found a pronounced enrichment of the [Tf2 N]- anions at the IL/vacuum interface, due to a rapid anion exchange at the IL/solid interface. In contrast, at 90?K, the [Tf2 N]- anions remain at the IL/solid interface. Upon heating, we observe a rearrangement of the cations between 140 and 160?K, such that the octyl chains preferentially point towards the vacuum. Above 170?K, the ions start to become mobile, and at 220?K, the anion exchange is completed, with the [Tf2 N]- anions enriched at the IL/vacuum interface in the same way as found for deposition at RT. The temperature range for the anion exchange corresponds well to glass transition temperatures reported in literature. We propose two driving forces to be cooperatively responsible for the replacement/exchange of [Tf2 N]- at the IL/solid interface and its enrichment at the IL/vacuum interface. First, the adsorption energy of [C8 C1 Im][PF6 ] is significantly larger than that of [C8 C1 Im][Tf2 N], and second, the surface tension of [C8 C1 Im][Tf2 N] is lower than that of [C8 C1 Im][PF6 ].
| S-EPMC6282575 | biostudies-literature
Project description:In light of increasing interest in the development of organic-organic multicomponent heterostructures on metals, this molecular-scale study investigates prototypical composite systems of ultrathin porphyrin and ionic liquid (IL) films on metallic supports under well-defined ultrahigh vacuum conditions. By means of angle-resolved X-ray photoelectron spectroscopy, we investigated the adsorption, stability, and thermal exchange of the resulting films after sequential physical vapor deposition of the free-base porphyrin 5,10,15,20-tetraphenylporphyrin, 2H-TPP, and the IL 1-methyl-3-octylimidazolium hexafluorophosphate, [C8C1Im][PF6], on Ag(111) and Au(111). 2H-TPP shows two-dimensional growth of up to two closed molecular layers on Ag(111) and Au(111) and three-dimensional island growth for thicker films. IL films on top of a monolayer of 2H-TPP exhibit Stranski-Krastanov-like growth and are stable up to 385 K. The 2H-TPP layer leads to destabilization of the IL films, compared to the IL in direct contact with the bare metals, by inhibiting the specific adsorption of the ions on the metal surfaces. When the porphyrin is deposited on top of [C8C1Im][PF6] at low temperature, the 2H-TPP molecules adsorb on top of the IL film at first but replace the IL at the IL/metal interfaces upon heating above 240 K. This exchange process is most likely driven by the higher adsorption energy of 2H-TPP on Ag(111) and Au(111) surfaces, as compared to the IL. The behavior observed on Ag(111) and Au(111) is identical. The results are highly relevant for the stability of porphyrin/IL-based thin film catalyst systems and molecular devices, and more generally, stacked organic multilayer architectures.
| S-EPMC6913898 | biostudies-literature
Project description:In underwater adhesion of a topographically patterned surface with a very soft material such as human skin, the elastic deformation can be large enough to achieve solid-on-solid contact not only on top of the hills but also in the valleys of the substrate topography. In this context, we have studied the dynamics of dewetting of a thin liquid film confined between a rigid, periodic micropillar array and a soft, elastic sphere. In our experiments, we observed two very distinct dewetting morphologies. For large ratios of array period to micropillar height and width, the dewetted areas tend to have a diamond-like shape and expand with a rate similar to a flat, unpatterned substrate. When the array period is reduced, the morphology of the dry spot becomes irregular and its expansion rate is significantly reduced. We developed a fully coupled numerical model of the dewetting process that reproduces the key features observed in experiments. Moreover, we performed contact mechanics simulations to characterize the deformation of the elastomer and the shape of the dewetted area in a unit cell of the micropillar array.
| S-EPMC7558345 | biostudies-literature
Project description:In this paper, we describe methods for manipulating the morphology of side-chain liquid crystalline block copolymers through variations in the liquid crystalline content. By systematically controlling the covalent attachment of side chain liquid crystals to a block copolymer (BCP) backbone, the morphology of both the liquid crystalline (LC) mesophase and the phase-segregated BCP microstructures can be precisely manipulated. Increases in LC functionalization lead to stronger preferences for the anchoring of the LC mesophase relative to the substrate and the intermaterial dividing surface. By manipulating the strength of these interactions, the arrangement and ordering of the ultrathin film block copolymer nanostructures can be controlled, yielding a range of morphologies that includes perpendicular and parallel cylinders, as well as both perpendicular and parallel lamellae. Additionally, we demonstrate the utilization of selective etching to create a nanoporous liquid crystalline polymer thin film. The unique control over the orientation and order of the self-assembled morphologies with respect to the substrate will allow for the custom design of thin films for specific nanopatterning applications without manipulation of the surface chemistry or the application of external fields.
| S-EPMC2656565 | biostudies-literature
Project description:Thinning and breakup of liquid filaments are central to dripping of leaky faucets, inkjet drop formation, and raindrop fragmentation. As the filament radius decreases, curvature and capillary pressure, both inversely proportional to radius, increase and fluid is expelled with increasing velocity from the neck. As the neck radius vanishes, the governing equations become singular and the filament breaks. In slightly viscous liquids, thinning initially occurs in an inertial regime where inertial and capillary forces balance. By contrast, in highly viscous liquids, initial thinning occurs in a viscous regime where viscous and capillary forces balance. As the filament thins, viscous forces in the former case and inertial forces in the latter become important, and theory shows that the filament approaches breakup in the final inertial-viscous regime where all three forces balance. However, previous simulations and experiments reveal that transition from an initial to the final regime either occurs at a value of filament radius well below that predicted by theory or is not observed. Here, we perform new simulations and experiments, and show that a thinning filament unexpectedly passes through a number of intermediate transient regimes, thereby delaying onset of the inertial-viscous regime. The new findings have practical implications regarding formation of undesirable satellite droplets and also raise the question as to whether similar dynamical transitions arise in other free-surface flows such as coalescence that also exhibit singularities.
| S-EPMC4403208 | biostudies-other
Project description:The preparation of thin composite layers has promising advantages in a variety of applications like transdermal, buccal, or sublingual patches. Within this model study the impact of the matrix material on the film forming properties of ibuprofen-matrix composite films is investigated. As matrix materials polystyrene, methyl cellulose, or hydroxyl-ethyl cellulose were used. The film properties were either varied by the preparation route, i.e., spin coating or drop casting, or via changes in the relative ratio of the ibuprofen and the matrix material. The resulting films were investigated via X-ray diffraction and atomic force microscope experiments. The results show that preferred (100) textures can be induced via spin coating with respect to the glass surface, while the drop casting results in a powder-like behavior. The morphologies of the films are strongly impacted by the ibuprofen amount rather than the preparation method. A comparison of the various matrix materials in terms of their impact on the dissolution properties show a two times faster zero order release from methyl cellulose matrix compared to a polystyrene matrix. The slowest rate was observed within the hydroxyl ethyl cellulose as the active pharmaceutical ingredients (APIs) release is limited by diffusion through a swollen matrix. The investigation reveals that the ibuprofen crystallization and film formation is only little effected by the selected matrix material than that compared to the dissolution. A similar experimental approach using other matrix materials may therefore allow to find an optimized composite layer useful for a defined application.
| S-EPMC4223873 | biostudies-other