含氟硅丙烯酸酯乳液超疏水膜中疏水基团的梯度分布与表面微观结构研究

利用含氟疏水基团的梯度分布,结合草莓形纳米SiO2粒子提供的双重粗糙表面,制备了具有类"荷叶效应"的超疏水涂膜,水接触角达(174.2±2)°,滞后角几乎接近0°.通过原子力显微镜、扫描电镜和水接触角的测试对膜表面形貌及疏水性能进行了表征;探讨了其表面微观结构与表面疏水性能的关系.草莓形复合粒子在膜表面的无规则排列赋予涂膜表面不同等级的粗糙度,使水滴与涂膜表面接触时能够形成高的空气捕捉率,这种微观结构与疏水基团的梯度分布相结合,赋予了含氟硅丙烯酸酯乳液涂膜表面超疏水性能.     

Fabrication of hydrophobic surfaces by coupling of Langmuir-Blodgett deposition and a self-assembled monolayer

A novel method coupling the Langmuir-Blodgett (LB) deposition of silica particles and the formation of a self-assembled monolayer (SAM) of alkylsilane is proposed for fabricating hydrophobic surfaces. The LB deposition and the SAM are supposed to confer the substrate surface roughness and low surface energy, respectively. By controlling the hydrophobic-hydrophilic balance of the silica particle surface through the adsorption of surfactant molecules, deposition of monolayers consisting of hexagonally close-packed arrays of particles on a glass substrate can then be successfully conducted in a Langmuir trough. LB particulate films with a particle layer number up to 5 were thereby prepared. A sintered and hydrophobically finished particulate film with roughness factor of 1.9 was finally fabricated by sintering and surface silanization. Effects of particle size and particle layer number on the wetting behavior of the particulate films were systematically studied by measuring static and dynamic water contact angles. The experimental results revealed that a static contact angle of about 130 degrees resulted from the particulate films regardless of the particle size and particle layer number. This is consistent with the predictions of both the Wenzel model and the Cassie and Baxter model in that roughness of a hydrophobic surface can increase its hydrophobicity and a switching of the dominant mode from Wenzel's to Cassie and Baxter's. In general, an advancing contact angle of about 150 degrees , a receding contact angle of about 110 degrees , and a contact angle hysteresis of about 40 degrees were exhibited by the particulate films fabricated.     

Biomimetic superhydrophobic and highly oleophobic cotton textiles

We report a biomimetic procedure to prepare superhydrophobic cotton textiles. By in situ introducing silica particles to cotton fibers to generate a dual-size surface roughness, followed by hydrophobization with polydimethylsiloxane (PDMS), normally hydrophilic cotton has been easily turned superhydrophobic, which exhibits a static water contact angle of 155 degrees for a 10 microL droplet. The roll-off angle of water droplets depends on the droplet volume, ranging from 7 degrees for a droplet of 50 microL to 20 degrees for a 7 microL droplet. When a perfluoroalkyl chain is introduced to the silica particle surface, the superhydrophobic textile also becomes highly oleophobic, as demonstrated by a static contact angle of 140 degrees and a roll-off angle of 24 degrees for a 15 microL sunflower oil droplet.     

Facile method to fabricate raspberry-like particulate films for superhydrophobic surfaces

A facile method using layer-by-layer assembly of silica particles is proposed to prepare raspberry-like particulate films for the fabrication of superhydrophobic surfaces. Silica particles 0.5 microm in diameter were used to prepare a surface with a microscale roughness. Nanosized silica particles were then assembled on the particulate film to construct a finer structure on top of the coarse one. After surface modification with dodecyltrichlorosilane, the advancing and receding contact angles of water on the dual-sized structured surface were 169 and 165 degrees , respectively. The scale ratio of the micro/nano surface structure and the regularity of the particulate films on the superhydrophobic surface performance are discussed.     

Superhydrophobic perpendicular nanopin film by the bottom-up process

We first fabricated the superhydrophobic film with a water contact angle of 178 degrees based on a perpendicular nanopin fractal structure by a bottom-up process. Until now, only materials with an original water contact angle larger than 90 degrees , which is classified as hydrophobicity, could be used to fabricate the superhydrophobic film (>170 degrees ) according to the possible fractal structure by a top-down process. Now, in this work, a water contact angle of about 178 degrees can be achieved using a lauric acid-coated film with an original contact angle of 75 degrees , which is classified as hydrophilicity, based on an ideal fractal structure for the superhydrophobic surface which is fabricated by the nanosize pin with 6.5 nm diameter.     

Hydrophobicity modification of woven cotton fabric by hydrophobic fumed silica coating

Water repellency of woven cotton fabric was achieved by coating with the aqueous dispersion containing organosilane agent (HDTMS) and fumed silica. The coating agents were applied using padding method and then followed by batching the coated fabric at the ambient temperature for 24 h to allow the condensation reaction between HDTMS silanol group and fumed silica silanol group, rendering silica particles hydrophobic. An ultrasonicator was employed to prepare the homogenous coating dispersion. The water repellency evaluated by water contact angle determination which showed the contact angle over 110° was obtained with low amount of applied HDTMS of 1 wt%. The effect of fumed silica addition on an increase in fiber surface roughness geometry showed the influential result in improving the water contact angle. From durability to washing test, the hydrophobic coatings evidenced from SEM and ATR/FTIR remained adhering to fiber surface, indicating the durability. After washing, the coating on the fabric with fumed silica addition appeared to be scatter particles which made a contribution to the higher contact angle value when compared to sheet-like layer coating in case of HDTMS coating alone.     

微结构与表面修饰对二氧化硅多孔薄膜疏水性能的影响

通过引入聚乙二醇(PEG)改性传统二氧化硅(SiO2)溶胶,得到了粒径分布较宽且粒径可控的溶胶。比较了六甲基二硅氮烷(HMDS)溶胶内修饰和薄膜表面修饰以及溶胶粒径对SiO2薄膜疏水性能的影响。采用动态光散射粒度仪定量测试了二氧化硅溶胶老化过程中粒度的变化,用原子力显微镜、接触角测试仪、红外光谱仪、紫外-可见-近红外分光光度计分别对薄膜的表面形貌、表观静态接触角、薄膜成分及透光率等进行了测量。结果表明:PEG的添加可有效增大溶胶粒度从而增大薄膜的粗糙度,提高薄膜的疏水性。表面修饰效果受修饰方式和SiO2粒径影响,粒径较小时有利于溶胶内修饰,粒径较大时有利于对薄膜修饰。经过表面修饰剂(HMDS)的气氛处理得到了接触角为152°的超疏水薄膜,而且相比溶胶内修饰可以减小薄膜透光率的损失。     

Investigating the interface of superhydrophobic surfaces in contact with water

Neutron reflectivity (NR) is used to probe the solid, liquid, vapor interface of a porous superhydrophobic (SH) surface submerged in water. A low-temperature, low-pressure technique was used to prepare a rough, highly porous organosilica aerogel-like film. UV/ozone treatments were used to control the surface coverage of hydrophobic organic ligands on the silica framework, allowing the contact angle with water to be continuously varied over the range of 160 degrees (superhydrophobic) to <10 degrees (hydrophilic). NR shows that the superhydrophobic nature of the surface prevents infiltration of water into the porous film. Atomic force microscopy and density functional theory simulations are used in combination to interpret the NR results and help establish the location, width, and nature of the SH film-water interface.     

Contact angle determination of nanoparticles: film balance and scanning angle reflectometry studies

St?ber silica nanoparticles of diameter about 45, 60 and 100 nm and different hydrophobicity are used to produce monolayers at a water-air interface. Both the surface pressure-area isotherms and the reflectivity angle of incidence curves of the layers have been measured in a Wilhelmy film balance. The contact angle of the as-prepared particles have been determined from the isotherms by two different evaluation methods, and compared to those obtained from in situ scanning angle reflectometry (SAR) measurements. SAR is proved to be an effective tool for the estimation of contact angles on nanoparticles of different wettability, using a modified version of the previously published gradient layer model (E. Hild, T. Seszták, D. V?lgyes and Z. Hórv?lgyi, Prog. Colloid Polym. Sci., 2004, 125, 61, ref. 1) for evaluation. The results are in fairly good agreement with those determined from the non-dissipative part of the isotherms of the as prepared particles, assuming a weakly cohesive film model (S. Bordács, A. Agod and Z. Hórv?lgyi, Langmuir, 2006, 22, 6944, ref. 2). It seems that the traditional way to calculate the contact angle from the film balance experiments (J.H. Clint and N. Quirke, Colloids Surf., A, 1993, 78, 277, ref. 3) results in unreasonably high contact angles for the investigated systems and the homogeneous layer optical model gives unrealistic film thickness values in the case of hydrophobic particles.     

Direct catalytic route to superhydrophobic polyethylene films

Polyethylene films grow on a flat silica surface modified by the bis(imino)pyridyl iron(II) catalyst during ethylene polymerization in toluene solvent. The resulting films show superhydrophobic properties. Advancing water contact angle as high as 169 degrees and sliding angles as low as 2 degrees are obtained on these films. SEM images reveal special surface structures of these films containing micrometer-sized islands, submicrometer particles on the islands, and stress nanofibers between the islands, which render superhydrophobicity to the polyethylene surfaces. After the submicrometer particles and stress nanofibers are removed by annealing, the superhydrophobic properties of the polymer films disappear.     

Surface modification of glass plates and silica particles by phospholipid adsorption

The effect of phospholipid adsorption on the hydrophobicity of glass plates and on the surface charge of silica particles using contact angle and electrophoretic mobility measurements, respectively, was investigated. Deposition of successive statistical monolayers of dipalmitoylphosphatidylcholine (DPPC) on the glass surface showed zig-zag changes of water contact angle, especially on the first few monolayers. This behavior is qualitatively coherent with the oscillations observed in zeta potential values for increasing DPPC concentration. The results indicate that the phospholipid is adsorbed vertically on the plates, exposing alternately its polar head and non-polar hydrocarbon chains in successive layers. On the other hand, experiments conducted on glass plates prior hydrophobized by contact with n-tetradecane suggest that DPPC molecules may to some extent dissolve in the relatively thick n-alkane film and then expose their polar heads over the film surface thus producing polar electron-donor interactions. The effect of both DPPC and dioleoylphosphatidylcholine (DOPC) on the electrokinetic potential of silica spheres confirms adsorption of the phospholipids, leading to a decrease in the (originally negative) zeta potential of silica and even reversal of its sign to positive at acidic pH. Hydrophobic interactions between phospholipid molecules in the medium and those already adsorbed may explain the overcharging. The adsorption of neutral phospholipids may reduce the zeta potential as a consequence of the shift of the electrokinetic or slip plane. The effect is more evident in the case of DOPC, suggesting a less efficient packing of this phospholipid because of the presence of double bonds in its molecule, which in fact is well known.     

Highly transparent superhydrophobic thin film with low refractive index prepared by one-step coating of modified silica nanoparticles

An easy and effective method to prepare superhydrophobic thin film has been developed. The film with optically transparent and low refractive index was composed by one-step coating with modified silica nanoparticles. The silica nanoparticles were prepared by sol–gel process of hydrolysis and condensation of alkoxysilane compounds and then surface modification silica nanoparticles, 50 ± 10 nm, were accomplished using methoxytrimethylsilane (MOTMS). Water contact angle of film increased with the weight of MOTMS of silica sol. When the weight of MOTMS was optimized, the water contact angle and sliding angle of film were 152.8° and less than 10°, respectively. The transmittance of film was also increased as compared to the un-coated microscope glass slide, from 91 to 93.5 %. The refractive index of the film was approximately 1.09 as measured by ellipsometer. The superhydrphobic thin film was also successfully made by using spray coating and the water contact angle of this film was more than 160°. Surface morphology of difference coating methods, dip and spray, were studied. Our result suggests that the film can be applied for superhydrophobicity and optical applications.     

Nanoporosity-driven superhydrophilicity: a means to create multifunctional antifogging coatings

Multifunctional nanoporous thin films have been fabricated from layer-by-layer assembled silica nanoparticles and a polycation. The resultant multilayer films were found to exhibit both antifogging and antireflection properties. The antifogging properties are a direct result of the development of superhydrophilic wetting characteristics (water droplet contact angle <5 degrees within 0.5 s or less). The nearly instantaneous sheetlike wetting promoted by the superhydrophilic multilayer prevents light scattering water droplets from forming on a surface. The low refractive index of the multilayer film (as low as 1.22) resulting from the presence of nanopores was found to impart excellent antireflection properties. Glass slides coated on both sides with a nanoporous multilayer film exhibited transmission levels as high as 99.8%. Stable superhydrophilic wetting characteristics were obtained only after a critical number of bilayers were deposited onto a surface. The assembly conditions (solution pH and nanoparticle concentration), as well as the choice of nanoparticle size, were found to strongly influence film properties. It is suggested that the superhydrophilic behavior is driven by the rapid infiltration of water into a 3D nanoporous network created under specific assembly conditions.     

UVO-tunable superhydrophobic to superhydrophilic wetting transition on biomimetic nanostructured surfaces

A novel strategy for a tunable sigmoidal wetting transition from superhydrophobicity to superhydrophilicity on a continuous nanostructured hybrid film via gradient UV-ozone (UVO) exposure is presented. Along a single wetting gradient surface (40 mm), we could visualize the superhydrophobic (thetaH2O > 165 degrees and low contact angle hysteresis) transition (165 degrees > thetaH2O > 10 degrees ) and superhydrophilic (thetaH2O < 10 degrees within 1 s) regions simply through the optical images of water droplets on the surface. The film is prepared through layer-by-layer assembly of negatively charged silica nanoparticles (11 nm) and positively charged poly(allylamine hydrochloride) with an initial deposition in a fractal manner. The extraordinary wetting transition on chemically modified nanoparticle layered surfaces with submicrometer- to micrometer-scale pores represents a competition between the chemical wettability and hierarchical roughness of surfaces as often occurs in nature (e.g., lotus leaves, insect wings, etc).     

Surface hydration and its effect on fluorinated SAM formation on SiO2 surfaces

Substrate hydration is demonstrated to be crucial to film quality during self-assembled (SA) film deposition of tridecafluoro-1,1,2,2,-tetrahydrooctyltrichlorosilane (FOTS) from the vapor phase. The surface hydration was studied by thermogravimetric analysis, and a model was developed to predict the conditions necessary to desorb all of the water adsorbed on a fused silica surface without significantly altering the concentration of the surface hydroxyl groups. The nature of the SA film was investigated as a function of the degree of rehydration of the dehydrated silica surface. The wettability and microstructure of the SA films were examined by water contact angle, ellipsometry, X-ray photoelectron spectroscopy, and atomic force microscopy. There is an optimum degree of substrate hydration, on the order of 1-1.2 monolayers of adsorbed water, required to produce a dense, durable and uniform FOTS film with high water repellency and a smooth surface.     

Superhydrophobic polyimide films with a hierarchical topography: combined replica molding and layer-by-layer assembly

Artificial superhydrophobic surfaces with a hierarchical topography were fabricated by using layer-by-layer assembly of polyelectrolytes and silica nanoparticles on microsphere-patterned polyimide precursor substrates followed with thermal and fluoroalkylsilane treatment. In this special hierarchical topography, micrometer-scale structures were provided by replica molding of polyamic acid using two-dimensional arrays of polystyrene latex spheres as templates, and nanosized silica particles were then assembled on these microspheres to construct finer structures at the nanoscale. Heat treatment was conducted to induce chemical cross-linking between polyelectrolytes and simultaneously convert polyamic acid to polyimide. After surface modification with fluoroalkylsilane, the as-prepared highly hydrophilic surface was endowed with superhydrophobicity due to the bioinspired combination of low surface energy materials and hierarchical surface structures. A superhydrophobic surface with a static water contact angle of 160 degrees and sliding angle of less than 10 degrees was obtained. Notably, the polyimide microspheres were integrated with the substrate and were mechanically stable. In addition, the chemical and mechanical stability of the polyelectrolyte/silica nanoparticle multilayers could be increased by heat-induced cross-linking between polyelectrolytes to form nylon-like films, as well as the formation of interfacial chemical bonds.     

Wetting and absorption of water drops on Nafion films

Water drops on Nafion films caused the surface to switch from being hydrophobic to being hydrophilic. Contact angle hysteresis of >70 degrees between advancing and receding values were obtained by the Wilhelmy plate technique. Sessile drop measurements were consistent with the advancing contact angle; the sessile drop contact angle was 108 degrees . Water drop adhesion, as measured by the detachment angle on an inclined plane, showed much stronger water adhesion on Nafion than Teflon. Sessile water and methanol drops caused dry Nafion films to deflect. The flexure went through a maximum with time. Flexure increased with contact area of the drop, but was insensitive to the film thickness. Methanol drops spread more on Nafion and caused larger film flexure than water. The results suggest that the Nafion surface was initially hydrophobic but water and methanol drops caused hydrophilic sulfonic acid domains to be drawn to the Nafion surface. Local swelling of the film beneath the water drop caused the film to buckle. The maximum flexure is suggested to result from motion of a water swelling front through the Nafion film.     

Fabrication of superhydrophobic silica film by removing polystyrene spheres

A superhydrophobic silica film has been fabricated by a facile method, which combines the co-sedimentation of dual-sized polystyrene (PS) spheres and the infiltration of a silica sol. The scanning electron microscopy (SEM) observations indicate that the as-prepared silica surface has a hierarchical micro/nano-structure. The micrometer-sized hollow silica particle with nanometer-sized holes on its surface was created by removing the organic polymer at high temperature. After chemically modified by a layer of dodecafluoroheptyl-methyl-dimethoxysilane (DFMS), the silica film has a water contact angle up to 156.4°, showing excellent superhydrophobic property. The present method may enhance widespread application of superhydrophobic film because of its simplicity and cheapness.     

Flotation de-inking studies using model hydrophobic particles and non-ionic dispersants

A series of non-ionic alcohol ethoxylated surfactants (with HLB within the range of 11.1–12.5) were used as dispersants during flotation of mondisperse hydrophobised silica particles (representing ink particles) in de-inking formulations. Laboratory scale flotation experiments, contact angle, dynamic surface tension and thin film drainage experiments were carried out. The reduction in dynamic surface tension at the air/solution interface (which is dependent on the adsorption kinetics) followed the order C₁₀E₆>C₁₂E₈≈C₁₂E₆>C₁₄E₆ and these values were lower than sodium oleate, which is commonly used in de-inking systems. In addition the non-ionics adsorbed on the hydrophobised silica particles reducing the contact angle. These results indicated that the non-ionic surfactant with the highest CMC (C₁₀E₆) gave (a) the highest rate of adsorption at the air/solution interface (b) the froth with the greatest water content and higher froth volume (c) the lowest reduction in contact angle and (d) the highest flotation efficiency at concentrations above the CMC. It was also observed that flotation occurred, in spite of the fact that thin-film measurements indicated that the adsorption of non-ionic at the air/solution and silica/solution interfaces reduced the hydrophobicity of the particles, as indicated by an increase in stability of the aqueous thin film between the particle and air-bubble. This result suggests that the bubble-ink particle captures mechanism (occurring through rupture of the thin aqueous film separating the interfaces) is not the only mechanism controlling the flotation efficiency and that other parameters (such as the kinetics of surfactant adsorption, foaming characteristics, and bubble size) need to be taken into account. The kinetics is important with respect to the rate of adsorption of surfactant to both interfaces. Under equilibrium conditions, this may give rise to repulsive steric forces between the air-bubble and the particles (stable aqueous thin-films). However, a lower amount of surfactant adsorbed at a freshly formed air bubble or inkparticle (caused by slow adsorption rates) will produce a lower steric repulsive force allowing effective collection of particles by the bubble. Also, it was suggested that the influence of alcohol ethoxylates on bubble-size could effect the particle capture rate and mechanical entrainment of particles in an excessively buoyant froth, which will also play an important role in the flotation recovery.     

Hydrophobization of glass surface by adsorption of poly(dimethylsiloxane)

Silica or glass particles are introduced in a poly(dimethylsiloxane) (PDMS) matrix for various applications. A particular feature of these systems is that PDMS adsorbs on the surface of the dispersed particles, thus rendering them more hydrophobic with time. The mechanism of this process of in situ hydrophobization is still poorly understood. The major aims of the present study are (1) to quantify the rate of surface hydrophobization by PDMS and, on this basis, to discuss the mechanism of the process; (2) to compare the contact angles of surfaces that are hydrophobized by different procedures and are placed in contact with different fluid interfaces-PDMS-water, hexadecane-water, and air-water; and (3) to check how the type of surfactant affects the contact angles, viz., the effective hydrophobicity of the surface. We present experimental results for the kinetics of hydrophobization of glass surfaces, which are characterized by measuring the three-phase contact angle of glass-surfactant solution-PDMS. The data reveal two consecutive stages in the hydrophobization process: The first stage is relatively fast and the contact angle increases from 0 degrees to about 90 degrees within several minutes. This stage is explained with the physical adsorption of the PDMS chains, as a result of hydrogen-bond formation with the surface silanol groups. The second stage is much slower and hours or days are required at room temperature to reach the final contact angle (typically, 150-160 degrees). This stage is explained as grafting of the PDMS molecules on the surface by chemical reaction with the surface silanol groups. If the glass surface had been pretreated by hexamethyldisilazane (HMDS), so that CH(3) groups had blocked most of the surface silanol groups, the first stage in the hydrophobization process is almost missing-the contact angle slowly changes at room temperature from about 90 degrees up to 120 degrees. The experiments aimed to compare several hydrophobization procedures showed that PDMS ensures larger contact angle (more hydrophobic surface) than grafted alkyl chains. The contact angles at the PDMS-water and hexadecane-water interfaces were found to be very similar to each other, and much larger than that at the air-water interface. Interestingly, we found that the ionic surfactants practically do not affect the contact angle of PDMS-hydrophobized surface, whereas the nonionic surfactants reduce this angle. Similar trends are expected with silica surfaces, as well.