Dynamic Water Contact Angle Research Articles

Wetting behavior of high energy electron irradiated porous superhydrophobic silica films

The nature of adhesive forces between water and hydrophobic materials has been a subject of great interest. The influence of high energy electron irradiation (7MeV) on wetting behavior of superhydrophobic silica films has been investigated. The results of surface morphological study suggest that the porous morphology of pristine (non-irradiated) silica film was changed to compact morphology after electron irradiation (of energy 7MeV). The experiments showed that a gradual decrease in static water contact angle (SWCA); whereas an abrupt increase in water sliding angle (WSA) of irradiated silica film. The water droplets easily roll off on the pristine silica films, whereas the water droplet does not slide on the irradiated silica film surface even when the surface is tilted vertically or turned upside down. We characterized the pristine and irradiated silica films by Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), atomic force microscopy (AFM), and static and dynamic water contact angle measurements.

Chemical modification of chloromethylated polysulfones via click reactions

AbstractA new approach to the modification of azidomethyl polyethersulfones using click reactions with acetylenic derivatives in the presence of CuBr as catalyst is presented. An azidomethyl polyethersulfone was prepared by the reaction of chloromethylated polysulfone with sodium azide in dimethylformamide. By the Cu(I)‐catalysed Huisgen 1,3‐dipolar cycloaddition reaction of the azidomethyl polyethersulfone to acetylenic derivatives, new polyethersulfones containing 1,2,3‐triazole rings were obtained. The structures of the polymers were confirmed using attenuated total reflectance Fourier transform infrared and NMR spectroscopy. The polymers were characterized using dynamic mechanical analysis, thermogravimetric analysis, stress‐strain and water contact angle measurements and solubility tests. The polymers bearing 1,2,3‐triazole rings having OH or COOH as substituents exhibited static contact angles smaller than that of the parent polyethersulfone. Copyright © 2010 Society of Chemical Industry

Contribution Toward Comprehension of Contact Angle Values on Single Polydimethylsiloxane and Poly(ethylene oxide) Polymer Networks

The large application ranges of polydimethylsiloxane (PDMS) and poly(ethylene oxide) (PEO) based materials justify the importance of controlling polymer surface properties including morphology and wettability behavior. However, it appears that the reported contact angle values of PDMS surfaces show significant scattering which cannot always be interpreted in terms of sole chemical data. In addition, few values are reported concerning pure PEO surfaces, since the polymer generally swells in the presence of water. Thus, in order to correlate surface properties with sample preparation, several single PDMS and PEO polymer networks were synthesized with varying cross-linkers and different cross-linking densities. First, the sample surface topography was systematically analyzed by atomic force microscopy (AFM). It was proven that the removal process of the polymer film from the mold plays a significant role in surface topography according to the vitreous or rubbery state of the given polymer network at room temperature irrespective of mold surface treatment. AFM-scale smooth surfaces can be obtained for all the samples by removing them systematically from the mold at a temperature below the α-relaxation temperature. Dynamic water contact angles were then measured and the values analyzed as a function of cross-linker nature and cross-linking density.

Water repellent porous silica films by sol–gel dip coating method

The wetting of solid surfaces by water droplets is ubiquitous in our daily lives as well as in industrial processes. In the present research work, water repellent porous silica films are prepared on glass substrate at room temperature by sol-gel process. The coating sol was prepared by keeping the molar ratio of methyltriethoxysilane (MTES), methanol (MeOH), water (H(2)O) constant at 1:12.90:4.74, respectively, with 2M NH(4)OH throughout the experiments and the molar ratio (M) of MTES/Ph-TMS was varied from 0 to 0.22. A simple dip coating technique is adopted to coat silica films on the glass substrates. The static water contact angle as high as 164° and water sliding angle as low as 4° was obtained for silica film prepared from M=0.22. The surface morphological studies of the prepared silica film showed the porous structure with pore sizes typically ranging from 200nm to 1.3μm. The superhydrophobic silica films prepared from M=0.22 retained their superhydrophobicity up to a temperature of 285°C and above this temperature the films became superhydrophilic. The porous and water repellent silica films are prepared by proper alteration of the Ph-TMS in the coating solution. The prepared silica films were characterized by surface profilometer, scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier Transform Infrared (FT-IR) spectroscopy, humidity tests, chemical aging tests, static and dynamic water contact angle measurements.

Preparation method and pervaparation performance of polyelectrolyte complex/PVA blend membranes for dehydration of isopropanol

Poly(diallyldimethylammonium chloride) (PDDA)/sodium polyacrylate (PAANa) polyelectrolyte complex (PEC) was fabricated by adding PDDA dilute aqueous solution dropwise into PAANa dilute aqueous solution with 0.007 M HCl. PEC/PVA(polyvinyl alcohol) blend liquids and their blend membranes were prepared by two blend methods of (a) PVA-solution/PEC-solution blending commonly used and (b) PVA-solid/PEC-solution blending proposed. Both blend liquids obtained were studied by viscometry and particle size analysis meter. Surface morphologies of PEC/PVA blend membranes cast from blend liquids were characterized by atomic force microscopy (AFM) and field emission scanning electron microscope (FESEM). Dynamic water contact angle and equilibrium swelling degree (ESD) of blend membranes in water–isopropanol feed were measured. Pervaporation (PV) dehydration of blend membranes for water–isopropanol feed was investigated. It was found that the structure and property of blend liquids, the surface property and ESD of blend membranes prepared by (b) are quite different from those prepared by (a). The stability and PV performance of PEC/PVA blend membranes prepared by (b) is much better than that prepared by (a). It is attributed to the preparation methods, which led to the difference in the interaction in blend liquids and the transition of fluid property and finally the change of the compatibility between PEC and PVA in blend membranes.

Amphiphilic Surface Active Triblock Copolymers with Mixed Hydrophobic and Hydrophilic Side Chains for Tuned Marine Fouling-Release Properties

Two series of amphiphilic triblock surface active block copolymers (SABCs) were prepared through chemical modification of two polystyrene-block-poly(ethylene-ran-butylene)-block-polyisoprene ABC triblock copolymer precursors. The methyl ether of poly(ethylene glycol) [M(n) approximately 550 g/mol (PEG550)] and a semifluorinated alcohol (CF(3)(CF(2))(9)(CH(2))(10)OH) [F10H10] were attached at different molar ratios to impart both hydrophobic and hydrophilic groups to the isoprene segment. Coatings on glass slides consisting of a thin layer of the amphiphilic SABC deposited on a thicker layer of an ABA polystyrene-block-poly(ethylene-ran-butylene)-block-polystyrene thermoplastic elastomer were prepared for biofouling assays with algae. Dynamic water contact angle analysis, X-ray photoelectron spectroscopy (XPS) and near-edge X-ray absorption fine structure (NEXAFS) measurements were utilized to characterize the surfaces. Clear differences in surface structure were realized as the composition of attached side chains was varied. In biofouling assays, the settlement (attachment) of zoospores of the green alga Ulva was higher for surfaces incorporating a large proportion of the hydrophobic F10H10 side chains, while surfaces with a large proportion of the PEG550 side chains inhibited settlement. The trend in attachment strength of sporelings (young plants) of Ulva did not show such an obvious pattern. However, amphiphilic SABCs incorporating a mixture of PEG550 and F10H10 side chains performed the best. The number of cells of the diatom Navicula attached after exposure to flow decreased as the content of PEG550 to F10H10 side chains increased.

Orthogonal, Three-Component, Alkanethiol-Based Surface-Chemical Gradients on Gold

An orthogonal surface-chemical gradient composed of self-assembled monolayers on gold has been prepared by successive, controlled immersions in orthogonal directions into dilute solutions of dodecanethiol and perfluorododecanethiol. The resulting two-component orthogonal gradient in surface coverage was backfilled with 11-mercaptoundecanol, leading to a two-directional, three-component surface-chemical gradient. Water and hexadecane show distinctly different wetting behaviors on the gradient surface because of the differences in the hydrophobic and oleophobic natures of the three different constituents. These results are correlated with the chemical composition maps of the surface obtained by X-ray photoelectron spectroscopy. The homogeneity and the ordering of the self-assembled monolayer were investigated by dynamic water contact angle measurements and polarization-modulation infrared reflection-absorption spectroscopy.

Microwave versus Conventional Heating in the Grafting of Alkyltrimethoxysilanes onto Silica Particles

The scope of this work is the comparative analysis in terms of grafting rate, structure of the grafted layer, and wetting behavior of three series of silica nanoparticles modified with alkyltrimethoxysilanes by using conventional heating with and without acid catalysis, and microwave irradiation. A comprehensive characterization of the grafted layer by means of Fourier transform infrared (FTIR), microanalysis, and solid state NMR techniques has shown that microwave irradiation provokes a pronounced increase in the loading rate compared to conventional heating. This microwave effect is outstanding in the case of the reactions with methyltrimethoxysilane, because of the acceleration of the condensation rate. Moreover, solid state NMR spectra ((29)Si and (13)C) strongly suggest structural differences in the grafted layer obtained by the two heating sources. The wetting behavior of the modified nanoparticles was studied, concluding that these changes in the structure of the grafted layer induced by the synthetic procedure do not determine the values of the dynamic water contact angles.

Transparent water repellent silica films by sol–gel process

Non-wettable surfaces with high contact angles and facile sliding angle of water droplets have received tremendous attention in recent years. The present paper describes the room temperature (∼27 °C) synthesis of dip coated water repellent silica coatings on glass substrates using iso-butyltrimethoxysilane (iso-BTMS) as a co-precursor. Emphasis is given to the influence of the hydrophobic reagent (iso-BTMS) on the water repellent properties of the silica films. Silica sol was prepared by keeping the molar ratio of tetraethoxysilane (TEOS) precursor, methanol (MeOH) solvent, water (H 2O) constant at 1:16.53:8.26 respectively, with 0.01 M NH 4F throughout the experiment and the molar ratio of iso-BTMS/TEOS ( M) was varied from 0 to 0.965. The effect of M on the surface structure and hydrophobicity has been researched. The static water contact angle values of the silica films increased from 65° to 140° and water sliding angle values decreased from 42° to 16° with an increase in the M value from 0 to 0.965. The water repellent silica films are thermally stable up to a temperature of 280 °C and above this temperature the film shows hydrophilic behavior. The water repellent silica films were characterized by the Fourier Transform Infrared (FT-IR) Spectroscopy, Scanning Electron Microscopy (SEM), Atomic Force Microscopy (AFM), % of optical transmission, thermal and chemical aging tests, humidity tests, static and dynamic water contact angle measurements.

Sliding behavior of water drops on sol–gel derived hydrophobic silica films

Control on the wettability of solid state materials is a classical and key issue in surface engineering. Optically transparent methyltriethoxysilane (MTES)-based silica films with water sliding angle as low as 9° were successfully prepared by two-step sol–gel co-precursor method. The emphasis is given to the effect of trimethylethoxysilane (TMES) as a co-precursor on water sliding behavior of silica films. The coating sol was prepared with molar ratio of methyltriethoxysilane (MTES), methanol (MeOH), acidic water (0.01 M, oxalic acid) and basic water (12 M, NH 4OH) kept constant at 1:12.73:3.58:3.58 respectively, and the molar ratio of TMES/MTES (M) was varied from 0 to 0.22. The static water contact angle as high as 120° and the water sliding angle as low as 9° was obtained by keeping the molar ratio (M) of TMES/MTES at 0.22. When the modified films were cured at temperature higher than 280 °C, the films became superhydrophilic. Further, the humidity study was carried out at a relative humidity of 90% at 30 °C over 60 days. We characterized the water repellent silica films by Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), atomic force microscopy (AFM), % of optical transmission, humidity tests and static and dynamic water contact angle (CA) measurements.

Structure and Conformation of Methyl-Terminated Poly(ethylene oxide)-Bis[methylenephosphonate] Ligands Adsorbed to Boehmite (AlOOH) from Aqueous Solutions. Attenuated Total Reflection Infrared (ATR-IR) Spectra and Dynamic Contact Angles

A ligand with a bisphosphonate headgroup and methyl-terminated poly(ethylene oxide) 550 tail has been adsorbed to a boehmite (AlOOH) particle film from aqueous solutions at 9, 18, 26, and 40 degrees C with a range of coverages. In situ attenuated total reflectance infrared (ATR-IR) spectra of the PEO-modified boehmite particle films has been used to monitor surface coverage. PEO-related IR absorptions showed variation in band shape with coverage and temperature which reflect changes in the configuration and crowding of PEO ligand tails. The integrated absorbance of PEO-related absorptions arising from CH(2) wagging and twisting vibrations indicated the average conformation about the C-C and C-O bonds. At all values of coverage and temperature, the PEO tails of the PEO-phosphonate ligands were found to have a predominantly gauche conformation about C-C bonds and a predominantly trans conformation about C-O bonds. The proportion of PEO with this predominant configuration, termed TGT, was found to vary with coverage and temperature and was most prevalent for PEO-modified boehmite surfaces with a ligand coverage of approximately 0.95 at 18 degrees C. Dynamic water contact angle measurements showed that PEO-modified surfaces with the greatest proportion of PEO in the TGT configuration were also the most hydrophilic, thus indicating that PEO in the TGT configuration was more hydrated or polar than other configurations. Variation in the proportion of PEO in the TGT configuration with temperature and coverage have been used to explain the variable resistance to protein adhesion reported for PEO-modified surfaces. Factors influencing the configuration of surface-bound PEO with changes in ligand coverage and temperature have been discussed.

Porous superhydrophobic silica films by sol–gel process

Wettability of solid surfaces is a crucial concern in our daily life as well as in engineering and science. The present research work describes the room temperature synthesis of adherent and porous superhydrophobic silica films on glass substrates using methyltriethoxysilane (MTES) as hydrophobic reagent by sol–gel process. The coating sol was prepared by keeping the molar ratio of tetraethoxysilane (TEOS), methanol (MeOH), water (H 2O) constant at 1:22.09:6.25, respectively, with 0.01 M NH 4F catalyst throughout the experiments and the MTES/TEOS molar ratio ( M) was varied from 0 to 0.43. The static water contact angle as high as 160° and water sliding angle as low as 3° was obtained for silica film prepared from M = 0.43. The surface morphological study showed the porous structure with pore sizes ranging from 250 to 300 nm. The superhydrophobic silica films retained their superhydrophobicity up to a temperature of 290 °C and above this temperature the films became superhydrophilic. The prepared silica films were characterized by Scanning Electron Microscopy (SEM), Atomic Force Microscopy (AFM), Fourier Transform Infrared (FT-IR) spectroscopy, percentage of optical transmission, humidity test and static and dynamic water contact angle measurements.

Control on wetting properties of spin-deposited silica films by surface silylation method

Control on the wettability of solid materials by liquid is a classical and key issue in surface engineering. Optically transparent water-repellent silica films have been spin-deposited on glass substrates at room temperature (∼27 °C). The wetting behavior of silica films was controlled by surface silylation method using dimethylchlorosilane (DMCS) as a silylating reagent. A coating sol was prepared by keeping the molar ratio of methyltrimethoxysilane (MTMS) precursor, methanol (MeOH) solvent, water (H 2O) constant at 1:8.8:2.64 respectively, with 4 M NH 4OH as a catalyst throughout the experiments and the amount of DMCS in hexane was varied from 0 to 12 vol.%. It was found that with an increase in vol.% of DMCS, the water contact angle values of the films increased from 78° to 136°. At 12 vol.% of DMCS, the film shows static water contact angle as high as 136° and water sliding angle as low as 18°. The hydrophobic silica films retained their water repellency up to a temperature 295 °C and above this temperature the films show superhydrophilic behavior. These results are compared with our earlier research work done on silylation of silica surface using hexamethyldisilazane (HMDZ) and trimethylchlorosilane (TMCS). The hydrophobic silica films were characterized by taking into consideration the Fourier transform infrared (FT-IR) spectroscopy, thermo gravimetric-differential thermal (TG-DT) analyses, scanning electron microscopy (SEM), atomic force microscopy (AFM), % of optical transmission, thermal and chemical aging tests, humidity tests, static and dynamic water contact angle measurements.

Ultrahydrophobic silica films by sol–gel process

Wettability of solid surfaces is a crucial concern in our daily life as well as in engineering and science. The present research work describes the room temperature (27 °C) synthesis of adherent and water repellent silica films on glass substrates using vinyltrimethoxysilane (VTMS) as a hydrophobic reagent by a single step sol–gel process. The silica sol was prepared by keeping the molar ratio of tetraethoxysilane (TEOS), methanol (MeOH), water (H2O) constant at 1:14.69:5, respectively, with 0.01 M NH4F throughout the experiments and the VTMS/TEOS molar ratio (M) was varied from 0 to 0.97. The effects of M on the surface structure and hydrophobicity have been researched. The static water contact angle as high as 144° and water sliding angle as low as 14° was obtained for silica film prepared from M = 0.97. The hydrophobic silica films retained their hydrophobicity up to a temperature of 255 °C and above this temperature the films became superhydrophilic. The prepared silica films were characterized by Scanning Electron Microscopy (SEM), Atomic Force Microscopy (AFM), Fourier Transform Infrared (FT-IR) spectroscopy, humidity test and static and dynamic water contact angle measurements.

ABC Triblock Surface Active Block Copolymer with Grafted Ethoxylated Fluoroalkyl Amphiphilic Side Chains for Marine Antifouling/Fouling-Release Applications

An amphiphilic triblock surface-active block copolymer (SABC) possessing ethoxylated fluoroalkyl side chains was synthesized through the chemical modification of a polystyrene-block-poly(ethylene-ran-butylene)-block-polyisoprene polymer precursor. Bilayer coatings on glass slides consisting of a thin layer of the amphiphilic SABC spray coated on a thick layer of a polystyrene-block-poly(ethylene-ran-butylene)-block-polystyrene (SEBS) thermoplastic elastomer were prepared for biofouling assays with the green alga Ulva and the diatom Navicula. Dynamic water contact angle analysis and X-ray photoelectron spectroscopy (XPS) were used to characterize the surfaces. Additionally, the effect of the Young's modulus of the coating on the release properties of sporelings (young plants) of the green alga Ulva was examined through the use of two different SEBS thermoplastic elastomers possessing modulus values of an order of magnitude in difference. The amphiphilic SABC was found to reduce the settlement density of zoospores of Ulva as well as the strength of attachment of sporelings. The attachment strength of the sporelings was further reduced for the amphiphilic SABC on the "low"-modulus SEBS base layer. The weaker adhesion of diatoms, relative to a PDMS standard, further highlights the antifouling potential of this amphiphilic triblock hybrid copolymer.

Preparation of photochromic poly(vinylidene fluoride-co-hexafluoropropylene) fibers by electrospinning

Photochromic poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-co-HFP) fibers were prepared by electrospinning from a solution of copolymer and ester-functionalized nitrospiropyran (SPEST) molecules. The surface and internal features of the electrospun (ES) fibers were characterized by scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR) and wide-angle X-ray diffraction (WAXD). The strong segregation of fluorine-rich groups on the fiber surface, which occurs during and/or after the electrospinning process, is driven by the lower surface tension for fluorine-rich groups and leads to encapsulation of SPEST predominantly near the core of the fibers, as confirmed by both X-ray photoelectron spectroscopy (XPS) and dynamic water contact angle (CA) measurements. The photochromic behavior of the spiropyran is preserved in the polymeric fibers, as confirmed by steady-state absorption and emission spectroscopy. Both isomeric forms of the photochrome in SP-PVDF-co-HFP were emissive, an effect that is thought to be due to the steric and/or electrostatic restrictions on the ring-opening reaction imposed by the fiber.

Immobilization of Biomolecules on the Surface of Electrospun Polycaprolactone Fibrous Scaffolds for Tissue Engineering

To make polycaprolactone (PCL) more suitable for tissue engineering, PCL in the form of electrospun fibrous scaffolds was first modified with 1,6-hexamethylenediamine to introduce amino groups on their surface. Various biomolecules, i.e., collagen, chitosan, and Gly-Arg-Gly-Asp-Ser (GRGDS) peptide, were then immobilized on their surface, with N,N'-disuccinimidylcarbonate being used as the coupling agent. Dynamic water contact angle measurement indicated that the scaffold surface became more hydrophilic after the aminolytic treatment and the subsequent immobilization of the biomolecules. The appropriateness of these PCL fibrous scaffolds for the tissue/cell culture was evaluated in vitro with three different cell lines, e.g., mouse fibroblasts (L929), human epidermal keratinocytes (HEK001), and mouse calvaria-derived preosteoblastic cells (MC3T3-E1). Both the neat and the modified PCL fibrous scaffolds released no substances in the levels that were harmful to these cells. Among the various biomolecule-immobilized PCL fibrous scaffolds, the ones that had been immobilized with type I collagen, a Arg-Gly-Asp-containing protein, showed the greatest ability to support both the attachment and the proliferation of all of the investigated cell types, followed by those that had been immobilized with GRGDS peptide.

Vapor-Phase Formation of Alkyl Isocyanate-Derived Self-Assembled Monolayers on Titanium Dioxide

Titanium dioxide (TiO2) surfaces were modified at atmospheric pressure by exposure to the vapor of alkyl isocyanates having different alkyl chain lengths (CH3[CH2]nN=C=O, where n = 3, 4, 7, 11, 15, and 17). Dynamic water contact angle measurements, X-ray photoelectron spectroscopy, and atomic force microscopy confirmed that the vapor-phase treatment produced self-assembled monolayers (SAMs) of the isocyanate molecules on the TiO2 surface through a carbamate linkage without any marked changes in surface morphology. The thickness and hydrophobicity of the isocyanate-derived SAMs depend on both the alkyl chain length and process temperature. As a control, an oxidized silicon (SiO2/Si) surface was treated under the same conditions. Water contact angle hysteresis for the SAM-covered TiO2 surfaces is greater than that observed for SAM-covered SiO2/Si surfaces, suggesting that SAMs on TiO2 surfaces are disordered and/or insufficiently cover the surfaces. This leads to their water sensitivity. Desorption kinetics are also strongly affected by the alkyl chain length, and the SAMs of adsorbed molecules with n = 15 and 17 are relatively stable among these six isocyanate-derived SAMs.

Protein adsorption resistant surface on polymer composite based on 2D- and 3D-controlled grafting of phospholipid moieties

To prepare the biocompatible surface, a phosphorylcholine (PC) group was introduced on this hydroxyl group generated by surface hydrolysis on the polymer composite composed of polyethylene (PE) and poly (vinyl acetate) (PVAc) prepared by supercritical carbon dioxide. Two different procedures such as two-dimensional (2D) modification and three-dimensional (3D) modification were applied to obtain the steady biocompatible surface. 2D modification was that PC groups were directly anchored on the surface of the polymer composite. 3D modification was that phospholipid polymer was grafted from the surface of the polymer composite by surface-initiated atom transfer radical polymerization (SI-ATRP) of 2-methacryloyloxyethyl phosphorylcholine (MPC). The surfaces were characterized by X-ray photoelectron spectroscopy, dynamic water contact angle measurements, and atomic force microscope. The effects of the poly(MPC) chain length on the protein adsorption resistivity were investigated. The protein adsorption on the polymer composite surface with PC groups modified by 2D or 3D modification was significantly reduced as compared with that on the unmodified PE. Further, the amount of protein adsorbed on the 3D modified surface that is poly(MPC)-grafted surface decreased with an increase in the chain length of the poly(MPC). The surface with an arbitrary structure and the characteristic can be constructed by using 2D and 3D modification. We conclude that the polymer composites of PE/PVAc with PC groups on the surface are useful for fabricating biomedical devices due to their good mechanical and surface properties.

Surface characterization on binary nano/micro-domain composed of alkyl- and amino-terminated self-assembled monolayer

The binary alkyl- and amino-terminated self-assembled monolayers (SAMs) composed of nano/micro-sized domains was prepared though a self-assembly technique. In addition, the wetting and electrostatic property of the binary SAMs was investigated by the analysis of the static and dynamic water contact angle and zeta-potentials measurement. The binary SAMs were also characterized by atomic force microscope (AFM), Kelvin probe force microscope (KPFM) and X-ray photoelectron spectroscopy (XPS). The domains on the binary SAMs were observed in topographic and surface potential images. The height of domain and the surface potential between octadecyltrichlorosilanes (OTS)-domain and n-(6-aminohexl)aminopropyl-trimethoxysilane (AHAPS)-SAM were about 1.1 nm and −30 mV. These differences of height and surface potential correspond to the ones between OTS and AHAPS. In XPS N 1s spectra, we confirmed the formation of binary SAMs by an amino peak observed at 399.15 eV. The dynamic and the static water contact angles indicated that the wetting property of the binary SAMs was depended on the OTS domain size. In addition, static water contact angles were measured under the conditions of different pH water and zeta-potential also indicated that the electrostatic property of the binary SAMs depended on OTS domain size. Thus, these results showed that the wetting and electrostatic property on the binary SAMs could be regulated by controlling the domain size.