Design and fabrication of a superhydrophobic glass surface with micro-network of nanopillars

The wetting property of a superhydrophobic glass surface with a micro-network of nanopillars fabricated from colloidal lithography and plasma etching is investigated in this paper. The micro-network distribution of nanospheres can be modulated by diluting the nanosphere concentration and controlling the spin rate. The micro-network of nanospheres spun on the glass surface serves as a mask for nanopillars during the plasma etching process. After the fabrication, the nano-structured surface is treated with fluoroalkylsilane self-assembled monolayers to obtain superhydrophobicity. Among several spin rates, the minimum colloidal network area density from a 100 nm polystyrene nanosphere solution diluted to 0.026% was found at a spin rate of 4000 rpm. The sample with the lowest network area density shows a good quality of superhydrophobicity, having the highest water contact angle and the lowest sliding angle among samples with other network area densities. In particular, samples with a micro-network of pillars also showed mechanical robustness against finger rubbing. To assess the superhydrophobic behavior in-depth, a size-dependent contact angle equation is proposed for use with a high contact angle (>135°) and with a Bo (Bond number) ? 1. Furmidge's sliding angle equation is also modified; it is derived considering a static contact angle to simplify the prediction of the sliding angle. The contact and sliding angle measurements from samples with a micro-network of nanopillars show good agreement with the proposed equations.     

电容去离子用功能化电极吸附材料的设计与构建

电容去离子(CDI)是近年来新兴的一种脱盐技术,由于其具有节能环保、实用性强等优势而倍受青睐。作为该技术核心的电极吸附材料,应具有高比表面积、良好导电性、亲水性、适宜孔隙结构、优异的稳定性等特点。这将有效保障该CDI器件不仅具有高CDI脱盐效率,而且拥有更强的循环稳定性。本文结合我们前期研究工作,针对吸附电极的制备、结构与性能构效关系的差异,综述了近年来多种功能化电极材料在CDI技术应用中的最新进展。     

A facile method for fabrication of superhydrophobic coating on aluminum alloy

A superhydrophobic coating applied in corrosion protection was successfully fabricated on the surface of aluminum alloy by chemical etching and surface modification. The water contact angle on the surface was measured to be 161.2° ± 1.7° with sliding angle smaller than 8°, and the superhydrophobic coating showed a long service life. The surface structure and composition were then characterized by means of SEM and XPS. The electrochemical measurements showed that the superhydrophobic coating significantly improved the corrosion resistance of aluminum alloy. The superhydrophobic phenomenon of the prepared surface was analyzed with Cassie theory, and it was found that only about 6% of the water surface is in contact with the metal substrate and 94% is in contact with the air cushion. Copyright © 2011 John Wiley & Sons, Ltd.     

Facile fabrication of a superhydrophobic fabric with mechanical stability and easy-repairability

The poor mechanical stability of superhydrophobic fabrics severely hindered their use in practical applications. Herein, to address this problem, we fabricated a superhydrophobic fabric with both mechanical stability and easy-repairability by a simple method. The mechanical durability of the obtained superhydrophobic fabric was evaluated by finger touching and abrasion with sandpaper. The results show that rough surface textures of the fabric were retained, and the fabric surface still exhibited superhydrophobicity after tests. More importantly, when the fabric lost its superhydrophobicity after a long-time abrasion, it can be easily rendered with superhydrophobicity once more by a regeneration process.     

Facile fabrication of a superhydrophobic surface from natural Eucommia rubber

In this study, we introduce a fabrication method for a superhydrophobic surface made from natural Eucommia rubber. Based on the Eucommia rubber extract solution, we prepared a type of superhydrophobic material using the simple phase separation method and the addition of a low‐surface‐energy substance method, thus developing a new approach for the application of natural Eucommia rubber. The experimental results showed that a superhydrophobic film could be obtained by both the addition of acetone and induction by water vapor. Additionally, the film exhibited properties closely related to the crystalline Eucommia rubber spherical particles with a hierarchical structure. The addition of hydrophobic silica also increased the hydrophobic property of the Eucommia rubber film. When the content of the silica was 4% (wt%), the contact angle of the composite film reached 160.7°, which could be attributed to the properties of the nano‐silica and the micro‐nano structure of the composites. Copyright © 2017 John Wiley & Sons, Ltd.     

Facile transformation of hydrophilic cellulose into superhydrophobic cellulose

Superhydrophobic cellulose-based materials coupled with transparent, stable and nanoscale polymethylsiloxane coating have been successfully achieved by a simple process via chemical vapor deposition, followed by hydrolyzation and polymerization.     

超疏水油水分离材料研究进展

近年来,石油泄漏和有机污染物排放对环境和生态系统造成了严重甚至不可挽回的损害,油水分离已成为一个全球性的挑战,如何处理油水混合物并将其有效分离已成为目前亟待解决的问题.许多仿生超疏水材料已被用于选择性油水分离研究,显示出诱人的应用前景.本文作者简要介绍了自然界超疏水现象以及固体表面浸润性理论,分析了材料的疏水亲油原理,重点介绍了近年来超疏水油水分离材料的研究应用进展,并对本领域的研究趋势进行了展望.     

Application of laser micro- and nanotexturing for the fabrication of superhydrophobic corrosion-resistant coatings on aluminum

A new efficient method for the fabrication of corrosion-resistant composite superhydrophobic coatings on aluminum and its alloys is presented. The laser micro- and nanotexturing of the surface combined with the deposition of a hydrophobic agent makes it possible to obtain superhydrophobic coatings with unique properties on aluminum materials. The complex studies by electrochemical methods and wettability analysis showed that the proposed type of coatings is characterized by very high resistance to corrosion, including pitting resistance, and by the durability of the superhydrophobic state upon prolonged contact with aqueous chloride-containing media.     

Fabrication of superhydrophobic cellulose-based materials through a solution-immersion process

An industrial waterproof reagent [(potassium methyl siliconate) (PMS)] was used for fabricating a superhydrophobic surface on a cellulose-based material (cotton fabric or paper) through a solution-immersion method. This method involves a hydrogen bond assembly and a polycondensation process. The silanol, which was formed by a reaction of PMS aqueous solution with CO 2, was assembled on the cellulose molecule surface via hydrogen bond interactions. The polymethylsilsesquioxane coatings were prepared by a polycondensation reaction of the hydroxyl between cellulose and silanol. The superhydrophobic cellulose materials were characterized by FTIR spectroscopy, thermogravimetry, and surface analysis (XPS, FESEM, AFM, and contact angle measurements). Analytical characterization revealed that nanoscale roughness protuberances uniformly covered the surface, thus transforming the cellulose from superhydrophilic to superhydrophobic with a water contact angle of 157 degrees . The superhydrophobic coatings were satisfactory with regard to both chemical and mechanical durability, and because of the transparency of the coatings the native cotton fabric displayed no changes with regard to either morphology or color. The easy availability of the materials and simplicity of this method render it convenient for mass production.     

Facile fabrication of colored superhydrophobic coatings by spraying a pigment nanoparticle suspension

Superhydrophobic coatings were prepared by spraying a pigment nanoparticle suspension. By changing the type of pigment nanoparticles, the colors of the coating could be controlled. The particle size of the pigments, which determines the surface structure of the coatings, played an important role in exhibiting superhydrophobicity. The spray-coating process is applicable to a variety of materials (e.g., copper, glass, paper, coiled wire, and tied thread), and the superhydrophobicity was repairable.     

Facial fabrication of superhydrophobic cellulose film with hierarchical morphologies

Hierarchical CuO spheres were firstly grown on the surface of cellulose film, and then stearic acid (STA) was utilized to decrease surface energy. The cupric ions fixed on the cellulose film transferred to one side and reacted with STA forming cupric stearates. The cupric stearates then self-assembled into nanobelts/nanoribbons and spread over the film, which induces to form hierarchical morphologies. Both sides of CuO modified film are black and superhydrophilic in air; after modification with STA, the film becomes superhydrophobic for both sides, whereas one side is blue and the other side is black showing different morphologies. Water contact angles (WCAs) of the superhydrophobic film for both black and blue sides are 153.9 ± 0.6° and 153.5 ± 0.8°, respectively. Sliding angles (SAs) for both sides are lower than 9.5°, indicating non-sticking superhydrophobic state. More importantly, the superhydrophobic cellulose–CuO–STA film is still superhydrophobic under hydrodynamic impact or pH of 3–11.     

Simple fabrication of superhydrophobic PLA with honeycomb-like structures for high-efficiency oil-water separation

Polylactic acid(PLA) is one of the most suitable candidates for environmental pollution treatment because of its biodegradability which will not cause secondary pollution to the environment after application.However,there is still a lack of a green and facile way to prepare PLA oil-water separation materials.In this work,a water-assisted thermally induced phase separation method for the preparation of superhydrophobic PLA oil-water separation material with honeycomb-like structures is reported.The PLA material shows great ability in application and could adsorb 27.3 times oil to its own weight.In addition,it could also be applicated as a filter with excellent efficiency(50.9 m^3 m^-2 h^-1).     

Design and fabrication of highly hydrophilic magnetic material by anchoring l-cysteine onto chitosan for efficient enrichment of glycopeptides

Hydrophilic interaction liquid chromatography(HILIC) has been recognized as an effective strategy for glycopeptide enrichment. Hydrophilic materials pave the way to solve the limit of low enrichment capacity and poor selectivity. The present study is the first attempt to combine chitosan(CS) and L-cysteine(L-Cys) to design a novel hydrophilic material focusing on glycopeptide enrichment. CS containing a large number of hydrophilic amino and hydroxyl groups has unique chemical properties, which m...     

Design parameters for a robust superhydrophobic electrospun nonwoven mat

Electrospun nonwoven mats exhibiting extreme hydrophobicity have recently attracted much attention for their use in a wide range of applications. These materials are highly heterogeneous and irregular in structure, and accordingly, the design parameters of such materials need to be carefully chosen for obtaining higher apparent contact angles along with the robust composite solid-liquid-vapor interface. Here, we present two dimensionless design parameters, namely, the spacing ratio and pressure difference across the liquid-vapor interface, for enhancing the stability of the Cassie regime. These design parameters are essentially dependent upon the structural characteristics of the electrospun mat and equilibrium contact angle of the liquid. Interestingly, the stability of the composite interface is a trade-off between these dimensionless parameters. Moreover, the pressure difference across the interface can significantly increase by reducing the fiber diameter to nanoscale. The stability of the Cassie state in an electrospun nonwoven mat consisting of lower fiber volume fractions at the nanostructural scale can restore superhydrophobicity even after the impact of a rainfall.     

Fabrication and superhydrophobic behavior of fluorinated microspheres

We describe the preparation of fluorinated microspheres by precipitation polymerization and their use to fabricate superhydrophobic surfaces. For that purpose, two different approaches have been employed. In the first approach, a fluorinated monomer (either 4-fluorostyrene or 2,3,4,5,6-pentafluorostyrene) was added to the initial mixture of monomers constituted by styrene (S) and divinylbenzene (DVB). The second approach is based on the encapsulation of a block copolymer, polystyrene-b-poly(2,3,4,5,6-pentafluorostyrene), during the polymerization of the monomers (S and DVB), thus enabling the formation of particles with perfluorinated chains instead of single functional groups at the interface. Both approaches led to narrow polydisperse particles with fluoro-functional groups at the interface as demonstrated by scanning electron microscopy (SEM), infrared (IR) spectroscopy, and X-ray photoelectron spectroscopy (XPS). Surface array of particles obtained by simple solvent casting presented superhydrophobic behavior with contact angles of water droplets of ca. 160-165°.     

Responsive colloidal systems: reversible aggregation and fabrication of superhydrophobic surfaces

We report on a method of fabricating stimuli-responsive core-shell nanoparticles using block copolymers covalently bound to a silica nanoparticle surface. We used the "grafting to" approach to graft amphiphilic block copolymer brushes of poly(styrene-b-2-vinylpyridine-b-ethylene oxide) and poly(styrene-b-4-vinylpyridine) onto silica nanoparticles with two different diameters: colloidal silica 200 nm in diameter and fumed silica 15 nm in diameter. We used the pH-responsive properties of the grafted brush to regulate the interactions between the particles, and between the particles and their environment. We show that this behavior can be applied for a reversible formation of particle aggregates, and can be used to tune and stabilize the secondary aggregates of particles of the appropriate size and morphology in an aqueous environment. The suspensions of the particles form a textured hydrophilic coating on various substrates upon casting and the evaporation of water. Heating above the polymer's glass transition temperature or treatment in acidic water result in back and forth switching between superhydrophobic and hydrophilic surfaces, respectively.     

Simultaneous fabrication of superhydrophobic and superhydrophilic polyimide surfaces with low hysteresis

Polyimide is of great interest in the field of MEMS and microtechnology. It is often used for its chemical, thermal, mechanical, and optical properties. In this paper, an original study is performed on controlled variation of polyimide film wettability. A two-step microtexturing method is developed to transform hydrophilic polyimide surfaces into a superhydrophobic surface with low magnitude of hysteresis (Δθ ≈ 0° and contact angle θ ≈ 158°). This method is based on the conception of a new kind of fakir surface with triangular cross-section micropillars, the use of a two-scale roughening, and a C(4)F(8) coating. We demonstrate that the absence of hysteresis is related to a combination of two scales of structuring and the pillar shape. The technology that has been developed results in the simultaneous fabrication of adjacent superhydrophobic and superhydrophilic small areas, which allows an effect of self-positioning of water droplets when deposited on such a checkerboard-like surface.