fabrication-superhydrophobic-metal-surfaces-for-anti-icing

Fabrication of Superhydrophobic Metal Surfaces for Anti-Icing Applications

Several ways to produce superhydrophobic metal surfaces are presented in this work. Aluminum was chosen as the metal substrate due to its wide use in ...

University of Granada

Contact angle variability, leading to errors in interpretation, arises from various sources. Contact angle hysteresis (history-dependent wetting) and contact angle multiplicity (corrugation of three-phase contact line) are irrespectively the most frequent causes of this uncertainty. Secondary effects also derived from the distribution of chemical defects on solid surfaces, and so due to the existence of boundaries, are the known "stick/jump-slip" phenomena. Currently, the underlying mechanisms in contact angle hysteresis and their connection to "stick/jump-slip" effects and the prediction of thermodynamic contact angle are not fully understood. In this study, axial models of smooth heterogeneous surface were chosen in order to mitigate contact angle multiplicity. For each axial pattern, advancing, receding and equilibrium contact angles were predicted from the local minima location of the system free energy. A heuristic model, based on the local Young equation for spherical drops on patch-wise axial patterns, was fruitfully tested from the results of free-energy minimization. Despite the very simplistic surface model chosen in this study, it allowed clarifying concepts usually misleading in wetting phenomena.

Wetting on axially-patterned heterogeneous surfaces.

The global mechanical equilibrium condition of a liquid on a rough and chemically heterogeneous surface was derived for three-dimensional situations from a statistical outlook of dispensation of many drops and the assumption of local mechanical equilibrium. Unlike the conventional thermodynamic derivations from variational methods, the current proof is based on vector algebra rather than differential geometry. The mechanics-based derivation becomes less intricate although the minimum energy condition is not established. An effective contact angle is computed from the directional sampling of three-phase lines after local drop dispensations. The final expression is a combined mechanical version of the Wenzel and Cassie equations.

Mechanical derivation of the Wenzel and Cassie equations using a statistical interpretation of drop dispensation.

It is well-established that the equilibrium contact angle in a thermodynamic framework is an "unattainable" contact angle. Instead, the most-stable contact angle obtained from mechanical stimuli of the system is indeed experimentally accessible. Monitoring the susceptibility of a sessile drop to a mechanical stimulus enables to identify the most stable drop configuration within the practical range of contact angle hysteresis. Two different stimuli may be used with sessile drops: mechanical vibration and tilting. The most stable drop against vibration should reveal the changeless contact angle but against the gravity force, it should reveal the highest resistance to slide down. After the corresponding mechanical stimulus, once the excited drop configuration is examined, the focus will be on the contact angle of the initial drop configuration. This methodology needs to map significantly the static drop configurations with different stable contact angles. The most-stable contact angle, together with the advancing and receding contact angles, completes the description of physically realizable configurations of a solid-liquid system. Since the most-stable contact angle is energetically significant, it may be used in the Wenzel, Cassie or Cassie-Baxter equations accordingly or for the surface energy evaluation. 

Equilibrium contact angle or the most-stable contact angle?

The interfacial activity of 3.5 nm homogeneous (HPs) and amphiphilic Janus gold nanoparticles (JPs) was characterized by pendant drop tensiometry for water/air and water/decane interfaces. This technique requires a smaller quantity of nanoparticles than the traditional Langmuir balance technique. The direct deposition at the interface of the nanoparticles dispersed in a spreading solvent also requires smaller quantities of sample than does adsorption from the bulk. From the growing and shrinking of the pendant drops, the interfacial activity of the nanoparticles can be evaluated and compared within a wide range of area per particle. In this work, the JPs exhibited a higher interfacial activity than did the HPs in all cases. A hard disk model fits the piecewise compression isotherm of the HPs, yet this model underestimates the interactions between the JPs adsorbed at the interface. 

Comparison of the interfacial activity between homogeneous and Janus gold nanoparticles by pendant drop tensiometry.

Complete understanding of colloidal assembly is still a goal to be reached. In convective assembly deposition, the concentration gradients developed in evaporating drops or reservoirs are usually significant. However, collective diffusion of charge-stabilized particles has been barely explored. The balance between convective and diffusive flows may dictate the particle dynamics inside evaporating colloidal drops. In this work we performed in situ counting of fluorescent particles in the vicinity of the triple line of evaporating sessile drops by using confocal laser scanning microscopy. We used particles of different sizes, with different charge response over the pH scale and we focused on charged and nearly uncharged particles. Two substrates with different receding contact angles were used. Binary colloidal mixtures were used to illustrate simultaneously the accumulation of particles with two different charge states at the triple line. The deposition rate close to the triple line was different depending on the electric state of the particle, regardless of the substrate used. 

In-plane particle counting at contact lines of evaporating colloidal drops: effect of the particle electric charge.

Since de Gennes coined in 1992 the term Janus particle (JP), there has been a continued effort to develop this field. The purpose of this review is to present the most relevant theoretical and experimental results obtained so far on the surface activity of amphiphilic JPs at fluid interfaces. The surface activity of JPs at fluid-fluid interfaces can be experimentally determined using two different methods: the classical Langmuir balance or the pendant drop tensiometry. The second method requires much less amount of sample than the first one, but it has also some experimental limitations. In all cases collected here the JPs exhibited a higher surface or interfacial activity than the corresponding homogeneous particles. This reveals the significant advantage of JPs for the stabilization of emulsions and foams. 

Surface activity of Janus particles adsorbed at fluid-fluid interfaces: Theoretical and experimental aspects.

Surface heterogeneity affects the behavior of nanoparticles at liquid interfaces. To gain a deeper understanding on the details of these phenomena, we have measured the interfacial activity and contact angle at water/decane interfaces for three different types of nanoparticles: homogeneous poly(methyl methacrylate) (PMMA), silica functionalized with a capping ligand containing a methacrylate terminal group, and Ag-based Janus colloids with two capping ligands of different hydrophobicity. The interfacial activity was analyzed by pendant drop tensiometry, and the contact angle was measured directly by freeze-fracture shadow-casting cryo-scanning electron microscopy. The silver Janus nanoparticles presented the highest interfacial activity, compared to the silica nanoparticles and the homogeneous PMMA nanoparticles. Additionally, increasing the bulk concentration of the PMMA and silica nanoparticles up to 100-fold compared to the Janus nanoparticles led to silica particles forming fractal-like structures at the interface, contrary to the PMMA particles that did not show any spontaneous adsorption. 

Interfacial Activity and Contact Angle of Homogeneous, Functionalized, and Janus Nanoparticles at the Water/Decane Interface.

Janus gold nanoparticles (JPs) of ∼4 nm-diameter half functionalized with 1-hexanethiol as a hydrophobic capping ligand exhibit significantly higher interfacial activity, reproducibility and rheological response when the other half is functionalized with 1,2-mercaptopropanediol (JPs-MPD) than with 2-(2-mercaptoethoxy)ethanol (JPs-MEE), both acting as hydrophilic capping ligands. The interfacial pressure measured by pendant drop tensiometry reaches 50 mN m(-1) and 35 mN m(-1) for the JPs-MPD at the water/air and water/decane interface, respectively. At the same area per particle, the JPs-MEE reveal significantly lower interfacial pressure: 15 mN m(-1) and 5 mN m(-1) at the water/air and water/decane interface, respectively. Interfacial dilatational rheology measurements also show an elastic shell behaviour at higher compression states for JPs-MPD while the JPs-MEE present near-zero elasticity. The enhanced interfacial activity of JPs-MPD is explained in terms of chemical and hydration differences between the MPD and MEE ligands, where MPD has a shorter hydrocarbon chain and twice as many hydroxyl terminal groups as MEE. 

A simple strategy to improve the interfacial activity of true Janus gold nanoparticles: a shorter hydrophilic capping ligand.

The motion of electrically charged particles under crowding conditions and subjected to evaporation-driven capillary flow might be ruled by collective diffusion. The concentration gradient developed inside an evaporating drop of colloidal suspension may reduce by diffusion the number of particles transported toward the contact line by convection. Unlike self-diffusion coefficient, the cooperative diffusion coefficient of interacting particles becomes more pronounced in crowded environments. In this work, we examined experimentally the role of the collective diffusion of charge-stabilized nanoparticles in colloidal patterning. To decouple the sustained evaporation from the contact line motion, we conducted evaporating menisci experiments with driven receding contact lines at low capillary number. This allowed us to explore convective assembly at fixed and low bulk concentration, which enabled to develop high concentration gradients. At fixed velocity of receding contact line, we explored a variety of substrate-particle systems where the particle-particle electrostatic interaction was changed (via p H) as well as the substrate receding contact angle and the relative humidity. We found that the particle deposition directed by receding contact lines may be controlled by the interplay between evaporative convection and collective diffusion, particularly at low particle concentration. 

Impact of the collective diffusion of charged nanoparticles in the convective/capillary deposition directed by receding contact lines.

Particles adsorbed at liquid interfaces are commonly used to stabilise water-oil Pickering emulsions and water-air foams. The fundamental understanding of the physics of particles adsorbed at water-air and water-oil interfaces is improving significantly due to novel techniques that enable the measurement of the contact angle of individual particles at a given interface. The case of non-aqueous interfaces and emulsions is less studied in the literature. Non-aqueous liquid-liquid interfaces in which water is replaced by other polar solvents have properties similar to those of water-oil interfaces. Nanocomposites of non-aqueous immiscible polymer blends containing inorganic particles at the interface are of great interest industrially and consequently more work has been devoted to them. By contrast, the behaviour of particles adsorbed at oil-oil interfaces in which both oils are immiscible and of low dielectric constant (ε<3) is scarcely studied. Hydrophobic particles are required to stabilise these oil-oil emulsions due to their irreversible adsorption, high interfacial activity and elastic shell behaviour.

Particles adsorbed at various non-aqueous liquid-liquid interfaces.

A successful methodology for obtaining hybrid films which allow thermal triggering and continuous, irreversible, control of their hydrophilicity/hydrophobicity nature was developed. Two types of poly(dimethylsiloxane)-silica (PDMS@SiO) films were prepared for that purpose: A hydrophilic film in which the thermal treatment causes an irreversible gradual increase of hydrophobicity; and a hydrophobic film that turns more hydrophilic upon thermal treatment. The opposite directionality of the change is dictated by the film substrate, on which the same hybrid is deposited. In both cases the thermal treatment induced a phase separation which caused the change in hydrophobicity. The magnitude of change in hydrophilicity/hydrophobicity is continuously controllable in both types of films by either the temperature or heating time. The films were characterized before and after heating by a variety of methods, including contact angle (CA) measurements with the sessile drop and the tilting plate methods, and by X-ray photoelectron spectroscopy (XPS) analysis. A thorough kinetic study was carried out, following the progress of the changes in the wettability property of the surfaces. The kinetics analyses proved that the changes in the wettability in all cases are due to phase separation processes, the directionality of which is determined by the treatment of the substrate on which the films are deposited. By monitoring the change of wettability (ΔCA) at various temperatures, an Arrhenius plot was obtained from which the activation energy and Arrhenius pre-exponential factor for the phase separation were derived, corroborating the proposed mechanism. To the best of our knowledge, this is the first use of phase separation behavior of a hybrid film in order to apply irreversible, thermally controllable change of surface wettability, tailored to proceed in opposite directions, and the first kinetic study of such a process.

Miguel Angel Rodriguez-Valverde

Biocolloid and Fluid Physics Group,
Faculty of Sciences,
Applied Physics Department,
Biocolloid and Fluid Physics Group, Faculty of Sciences, Applied Physics Department

University of Granada

Fabrication of Superhydrophobic Metal Surfaces for Anti-Icing Applications

Miguel Angel Rodriguez-Valverde

.css-o250i3{font-size:18px;font-family:Open Sans,sans-serif;line-height:21.6px;}Biocolloid and Fluid Physics Group,Faculty of Sciences,Applied Physics Department,Biocolloid and Fluid Physics Group, Faculty of Sciences, Applied Physics Department

University of Granada

Fabrication of Superhydrophobic Metal Surfaces for Anti-Icing Applications

Biocolloid and Fluid Physics Group,
Faculty of Sciences,
Applied Physics Department,
Biocolloid and Fluid Physics Group, Faculty of Sciences, Applied Physics Department