Arun K. Kota

Hygro-responsive membranes for effective oil-water separation.

There is a critical need for new energy-efficient solutions to separate oil-water mixtures, especially those stabilized by surfactants. Traditional membrane-based separation technologies are energy-intensive and limited, either by fouling or by the inability of a single membrane to separate all types of oil-water mixtures. Here we report membranes with hygro-responsive surfaces, which are both superhydrophilic and superoleophobic, in air and under water. Our membranes can separate, for the first time, a range of different oil-water mixtures in a single-unit operation, with >99.9% separation efficiency, by using the difference in capillary forces acting on the two phases. Our separation methodology is solely gravity-driven and consequently is expected to be highly energy-efficient. We anticipate that our separation methodology will have numerous applications, including the clean-up of oil spills, wastewater treatment, fuel purification and the separation of commercially relevant emulsions.

On‐Demand Separation of Oil‐Water Mixtures

In this work, the first-ever membrane-based single unit operation that enables gravity driven, on-demand separation of various oil-water mixtures is developed. Using this methodology, the on-demand separation of free oil and water, oil-in-water emulsions, and water-in-oil emulsions is demonstrated, with ≥99.9% separation efficiency. A scaled-up apparatus to separate larger quantities (several liters) of oil-water emulsions is also developed.

Superomniphobic Surfaces for Effective Chemical Shielding

Superomniphobic surfaces display contact angles >150° and low contact angle hysteresis with essentially all contacting liquids. In this work, we report surfaces that display superomniphobicity with a range of different non-Newtonian liquids, in addition to superomniphobicity with a wide range of Newtonian liquids. Our surfaces possess hierarchical scales of re-entrant texture that significantly reduce the solid-liquid contact area. Virtually all liquids including concentrated organic and inorganic acids, bases, and solvents, as well as viscoelastic polymer solutions, can easily roll off and bounce on our surfaces. Consequently, they serve as effective chemical shields against virtually all liquids--organic or inorganic, polar or nonpolar, Newtonian or non-Newtonian.

Hierarchically structured superoleophobic surfaces with ultralow contact angle hysteresis

Hierarchically structured, superoleophobic surfaces are demonstrated that display one of the lowest contact angle hysteresis values ever reported - even with extremely low-surface-tension liquids such as n-heptane. Consequently, these surfaces allow, for the first time, even ≈2 μL n-heptane droplets to bounce and roll-off at tilt angles. ≤ 2°.

Patterned Superomniphobic–Superomniphilic Surfaces: Templates for Site‐Selective Self‐Assembly

hasexplainedhowre-entrantsurface texture, in conjunction with surface chemistry androughness, can be used to design superomniphobic surfaces.In this work, we report a simple, fast, and practical method-ology to develop patterned superomniphobic–superomni-philic surfaces that exhibit stark contrast in wettability witha wide range of polar and nonpolar liquids. Using thesesurfaces, we demonstrate the site-selective self-assembly ofheptane upon dipping and spraying on textured surfaces, site-selective condensation and boiling with low-surface-tensionliquids, and site-selective self-assembly of both polymers andmicroparticles.When a liquid comes in contact with a textured surface, itadopts either the fully wetted Wenzel

Superhydrophobic Coatings with Edible Materials.

We used FDA-approved, edible materials to fabricate superhydrophobic coatings in a simple, low cost, scalable, single step process. Our coatings display high contact angles and low roll off angles for a variety of liquid products consumed daily and facilitate easy removal of liquids from food containers with virtually no residue. Even at high concentrations, our coatings are nontoxic, as shown using toxicity tests.

Quantitative characterization of the formation of an interpenetrating phase composite in polystyrene from the percolation of multiwalled carbon nanotubes

For the first time, an interpenetrating phase polymer nanocomposite formed by the percolation of multiwalled carbon nanotubes (MWCNTs) in polystyrene (PS) has been quantitatively characterized through electrical conductivity measurements and melt rheology. Both sets of measurements, in conjunction with scanning electron microscopy (SEM) images, indicate the presence of a continuous phase of percolated MWCNTs appearing at particle concentrations exceeding 2 vol% MWCNTs in PS. To quantify the amount of this continuous phase present in the PS/MWCNT composite, electrical conductivity data at various MWCNT concentrations, β, are correlated with a proposed degree of percolation, , developed using a conventional power-law formula with and without a percolation threshold. To quantify the properties of the interpenetrating phase polymer nanocomposite, the PS/MWCNT composite is treated as a combination of two phases: a continuous phase consisting of a pseudo-solid-like network of percolated MWCNTs, and a continuous PS phase reinforced by non-interacting MWCNTs. The proposed degree of percolation is used to quantify the distribution of MWCNTs among the phases, and is then used in a rule-of-mixtures formulation for the storage modulus, , and the loss modulus, , to quantify the properties of the continuous phase consisting of percolated MWCNTs and the continuous PS phase reinforced by non-interacting MWCNTs from the experimental melt rheology data. The properties of the continuous phase of percolated MWCNTs are indicative of a scaffold-like microstructure exhibiting an elastic behavior with a complex modulus of 360 kPa at lower frequencies and viscoplastic behavior with a complex viscosity of 6 kPa s rad−1 at higher frequencies, most likely due to a stick–slip friction mechanism at the interface of the percolated MWCNTs. Additional evidence of this microstructure was obtained via scanning electron microscopy. This research has important implications in providing a new methodology based on the electrical and rheological properties of the polymer nanocomposite for quantifying the continuous phase formed by the percolation of new functionalized nanostructures being developed for: (a) controlling the percolation of the nanostructures through self-assembly, (b) enhancing their interaction with the continuous reinforced polymer phase, (c) enhancing the cohesion between nanostructures.

Metamorphic Superomniphobic Surfaces

Superomniphobic surfaces are extremely repellent to virtually all liquids. By combining superomniphobicity and shape memory effect, metamorphic superomniphobic (MorphS) surfaces that transform their morphology in response to heat are developed. Utilizing the MorphS surfaces, the distinctly different wetting transitions of liquids with different surface tensions are demonstrated and the underlying physics is elucidated. Both ex situ and in situ wetting transitions on the MorphS surfaces are solely due to transformations in morphology of the surface texture. It is envisioned that the robust MorphS surfaces with reversible wetting transition will have a wide range of applications including rewritable liquid patterns, controlled drug release systems, lab-on-a-chip devices, and biosensors.

Free-Standing, Flexible, Superomniphobic Films

Fabrication of most superomniphobic surfaces requires complex process conditions or specialized and expensive equipment or skilled personnel. In order to circumvent these issues and make them end-user-friendly, we developed the free-standing, flexible, superomniphobic films. These films can be stored and delivered to the end-users, who can readily attach them to virtually any surface (even irregular shapes) and impart superomniphobicity. The hierarchical structure, the re-entrant texture, and the low solid surface energy render our films superomniphobic for a wide variety of liquids. We demonstrate that our free-standing, flexible, superomniphobic films have applications in enhanced chemical resistance and enhanced weight bearing.

Amphiphilic Colloidal Surfactants Based on Electrohydrodynamic Co-jetting

A novel synthetic route for the preparation of amphiphilic Janus particles based on electrohydrodynamic cojetting has been developed. In this approach, selective encapsulation of hydrophobic fluorodecyl-polyhedral oligomeric silsesquioxane (F-POSS) in one compartment and a poly(vinyl alcohol) in the second compartment results in colloidal particles with surfactant-like properties including the self-organization at oil-water and air-water interfaces. Successful localization of the respective polymers in different compartments of the same particle is confirmed by a combination of fluorescence microscopy, vibrational spectroscopy, and ζ-potential measurements. We believe that this straightforward synthetic approach may lead to a diverse class of surface-active colloids that will have significant relevance ranging from basic scientific studies to immediate applications in areas, such as pharmaceutical sciences or cosmetics.