Friction of Methyl-Branched Fatty Acid Layers at Low and High Sliding Speeds.

The friction of methyl-branched fatty acids was studied with a surface forces apparatus (SFA) with attachments for low-speed (µm/s) and high-speed (cm/s) sliding. The systems studied were isooleic acid, a mixture of unsaturated C-18 isomers with one methyl group located along the chain, and isostearic acid, which consisted of saturated C-18 isomers with one methyl branch. The methyl group was expected to disrupt the close packing of the molecules in the pure substance and when adsorbed on a surface. The friction forces and friction coefficients were compared with results for stearic and oleic acid. Isostearic acid showed low friction at low speeds. At high speeds, a peak was found in the friction coefficient of both isostearic and isooleic acid layers, whereas a gradual increase in friction coefficient with speed was seen for oleic acid, suggesting different relaxation times of the structures formed on the surfaces.

Ion-Specific Effects of Divalent Ions on the Structure of Polyelectrolyte Brushes.

Polyelectrolyte brushes consist of charged polymer chains attached on one end to a surface at high densities. They are relevant for many practical applications ranging from biosensors to drug delivery to colloidal stability. Their structure and functionality can be dramatically influenced by multivalent counterions in the solution environment. In this work, the surface forces apparatus (SFA) and atomic force microscopy (AFM) were used to investigate the effects of three alkaline earth divalent cations, Mg2+, Ca2+, and Ba2+, on the structures of polystyrenesulfonate (PSS) brushes tethered to mica and silicon oxide surfaces. While all these ions caused significant shrinkage of the height of the PSS brushes, strong ion-specific effects were observed. Mg2+ and Ca2+ caused homogeneous shrinkage; Ba2+ led to pinned-micelle like inhomogeneous structures. Isothermal titration calorimetry (ITC) demonstrated that this ion specificity was mainly caused by the difference in binding energy between sulfonate groups and the divalent cations. Considering the abundance of divalent cations in industrial processes, natural environments, and biological systems, the understanding of strong ion-specific effects of divalent counterions is of great importance for theoretical studies and various applications involving polyelectrolytes.

Effects of Imprinted 3D Surface Patterning on Localized Changes in the Tribology of Human Stratum Corneum.

Natural surfaces may exhibit remarkable surface properties due to their structure. In the case of skin, its surface topography (microrelief) influences many of its perceived sensorial properties (shine, color, touch). Imprinted patterns can modify the original microrelief, inducing a completely new set of perceived properties. To explore the effects of superimposed biomimetic surface textures on the friction of skin, human stratum corneum was prepared with and without an imprinted regular, micrometer-sized, 3D grid pattern. Atomic Force Microscopy (AFM) and optical profilometry indicated that the inherent, smaller-scale roughness of the stratum corneum remained when lines with heights of 20-200 µm and spacings of 600-2000 µm were introduced, but it was somewhat reduced on the grid lines. Surface Forces Apparatus (SFA) friction experiments on stratum corneum were performed at low speed (µm/s, back-and-forth sliding) and at more realistic, high speed (cm/s, rotational sliding). Two stratum corneum surfaces in contact did not adhere to one another, and they had a friction coefficient µ of 0.1, or lower, at low sliding speed. An interesting loading-unloading hysteresis was observed, with lower friction force on unloading, in particular, when the contact was on a grid line of the patterned samples. This suggests that the patterning locally induced different mechanical properties of the stratum corneum and that its recovery was not immediate on unloading. When one stratum corneum surface slid against a rigid glass surface, the friction coefficient was always higher than that when two stratum corneum surfaces were in contact. At high sliding speed, much higher friction coefficients were found between one stratum corneum surface and a rigid, smooth surface, µ ≥ 1. The results demonstrate that topograpic patterning by imprinting clearly modifies the tribological response of stratum corneum. This approach provides a simple method for exploring the development of biomimetic modifications of skin texture.

Detection of Liquid Penetration of a Micropillar Surface Using the Quartz Crystal Microbalance.

A quantitative characterization of the wetting states of droplets on hydrophobic textured surfaces requires direct measurement of the liquid penetration into surface cavities, which is challenging. Here, the use of quartz crystal microbalance (QCM) technology is reported for the characterization of the liquid penetration depth on a micropillar-patterned surface. The actual liquid-air interface of the droplet was established by freezing the droplet and characterizing it using a cryogenically focused ion beam/scanning electron microscope (cryo FIB-SEM) technique. It was found that a direct correlation exists between the liquid penetration depth and the responses of the QCM. A very small frequency shift of the QCM (1.5%) was recorded when the droplet was in the Cassie state, whereas a significant frequency shift was observed when the wetting state changed to the Wenzel state (where full liquid penetration occurs). Furthermore, a transition from the Cassie to the Wenzel state can be captured by the QCM technique. An acoustic-structure-interaction based numerical model was developed to further understand the effect of penetration. The numerical model was validated by experimentally measured responses of micropillar-patterned QCMs. The results also show a nonlinear response of the QCM to the increasing liquid penetration depth. This research provides a solid foundation for utilizing QCM sensors for liquid penetration and surface wettability characterization.

Brief history of intermolecular and intersurface forces in complex fluid systems.

We review the developments of ideas, concepts, and theories of intermolecular and intersurface forces and how these were influenced (or ignored) by observations of nature and, later, systematic experimentation. The emphasis of this review is on the way things gradually changed: experimentation replaced rhetoric, measurement and quantification replaced hand waving, energy replaced force in calculations, discrete atoms replaced the (continuum) aether, thermodynamics replaced mechanistic models, randomness and probability replaced certainty, and delicate experiments on the subnanoscale revealed fascinating self-assembling structures and complex behavior of even the simplest systems. We conclude by discussing today's unresolved challenges: how complex "dynamic" multicomponent--especially living biological--systems that receive a continuous supply of energy can be far from equilibrium and not even in any steady state. Such systems, never static but evolving in both space and time, are still far from being understood both experimentally and theoretically.

Direct nanomechanical measurement of an anchoring transition in a nematic liquid crystal subject to hybrid anchoring conditions.

We have used a surface forces apparatus to measure the normal force between two solid curved surfaces confining a film of nematic liquid crystal (5CB, 4'-n-pentyl-4-cyanobiphenyl) under hybrid planar-homeotropic anchoring conditions. Upon reduction of the surface separation D, we measured an increasingly repulsive force in the range D = 35-80 nm, reaching a plateau in the range D = 10-35 nm, followed by a short-range oscillatory force at D < 5 nm. The oscillation period was comparable to the cross-sectional diameter of the liquid crystal molecule and characteristic of a configuration with the molecules parallel to the surfaces. These results show that the director field underwent a confinement-induced transition from a splay-bend distorted configuration at large D, which produces elastic repulsive forces, to a uniform planar nondegenerate configuration with broken homeotropic anchoring, which does not produce additional elastic forces as D is decreased. These findings, supported by measurements of the birefringence of the confined film at different film thicknesses, provide the first direct observation of an anchoring transition on the nanometer scale.

Surface characterization and protein interactions of segmented polyisobutylene-based thermoplastic polyurethanes.

The surface properties and biocompatibility of a class of thermoplastic polyurethanes (TPUs) with applications in blood-contacting medical devices have been studied. Thin films of commercial TPUs and novel polyisobutylene (PIB)-poly(tetramethylene oxide) (PTMO) TPUs were characterized by contact angle measurements, X-ray photoelectron spectroscopy, and atomic force microscopy (AFM) imaging. PIB-PTMO TPU surfaces have significantly higher C/N ratios and lower amounts of oxygen than the theoretical bulk composition, which is attributed to surface enrichment of PIB. Greater differences in the C/N ratios were observed with the softer compositions due to their higher relative amounts of PIB. The contact angles were higher on PIB-PTMO TPUs than on commercial polyether TPUs, indicating lower surface energy. AFM imaging showed phase separation and increasing domain sizes with increasing hard segment content. The biocompatibility was investigated by quantifying the adsorption of fouling and passivating proteins, fibrinogen (Fg) and human serum albumin (HSA) respectively, onto thin TPU films spin coated onto the electrode of a quartz crystal microbalance with dissipation monitoring (QCM-D). Competitive adsorption experiments were performed with a mixture of Fg and albumin in physiological ratio followed by binding of GPIIb-IIIa, the platelet receptor ligand that selectively binds to Fg. The QCM-D results indicate similar adsorbed amounts of both Fg and HSA on PIB-PTMO TPUs and commercial TPUs. The strength of the protein interactions with the various TPU surfaces measured with AFM (colloidal probe) was similar among the various TPUs. These results suggest excellent biocompatibility of these novel PIB-PTMO TPUs, similar to that of polyether TPUs.

Structure and Functionality of Polyelectrolyte Brushes: A Surface Force Perspective.

The unique functionality of polyelectrolyte brushes depends on several types of specific interactions, including solvent structure effects, hydrophobic forces, electrostatic interactions, and specific ion interactions. Subtle variations in the solution environment can lead to conformational and surface structural changes of the polyelectrolyte brushes, which are mainly discussed from a surface-interaction perspective in this Focus Review. A brief overview is given of recent theoretical and experimental progress in the structure of polyelectrolyte brushes in various environments. Two important techniques for surface-force measurements are described, the surface forces apparatus (SFA) and atomic force microscopy (AFM), and some recent results on polyelectrolyte brushes are shown. Lastly, this Focus Review highlights the use of these surface-grafted polyelectrolyte brushes in the creation of functional surfaces for various applications, including nonfouling surfaces, boundary lubricants, and stimuli-responsive surfaces.

Adsorption, lubrication, and wear of lubricin on model surfaces: polymer brush-like behavior of a glycoprotein.

Using a surface force apparatus, we have measured the normal and friction forces between layers of the human glycoprotein lubricin, the major boundary lubricant in articular joints, adsorbed from buffered saline solution on various hydrophilic and hydrophobic surfaces: i), negatively charged mica, ii), positively charged poly-lysine and aminothiol, and iii), hydrophobic alkanethiol monolayers. On all these surfaces lubricin forms dense adsorbed layers of thickness 60-100 nm. The normal force between two surfaces is always repulsive and resembles the steric entropic force measured between layers of end-grafted polymer brushes. This is the microscopic mechanism behind the antiadhesive properties showed by lubricin in clinical tests. For pressures up to approximately 6 atm, lubricin lubricates hydrophilic surfaces, in particular negatively charged mica (friction coefficient mu = 0.02-0.04), much better than hydrophobic surfaces (mu > 0.3). At higher pressures, the friction coefficient is higher (mu > 0.2) for all surfaces considered and the lubricin layers rearrange under shear. However, the glycoprotein still protects the underlying substrate from damage up to much higher pressures. These results support recent suggestions that boundary lubrication and wear protection in articular joints are due to the presence of a biological polyelectrolyte on the cartilage surfaces.

Multivalent ions induce lateral structural inhomogeneities in polyelectrolyte brushes.

Subtle details about a polyelectrolyte's surrounding environment can dictate its structural features and potential applications. Atomic force microscopy (AFM), surface forces apparatus (SFA) measurements, and coarse-grained molecular dynamics simulations are combined to study the structure of planar polyelectrolyte brushes [poly(styrenesulfonate), PSS] in a variety of solvent conditions. More specifically, AFM images provide a first direct visualization of lateral inhomogeneities on the surface of polyelectrolyte brushes collapsed in solutions containing trivalent counterions. These images are interpreted in the context of a coarse-grained molecular model and are corroborated by accompanying interaction force measurements with the SFA. Our findings indicate that lateral inhomogeneities are absent from PSS brush layers collapsed in a poor solvent without multivalent ions. Together, AFM, SFA, and our molecular model present a detailed picture in which solvophobic and multivalent ion-induced effects work in concert to drive strong phase separation, with electrostatic bridging of polyelectrolyte chains playing an essential role in the collapsed structure formation.

High-frequency measurements of interfacial friction using quartz crystal resonators integrated into a surface forces apparatus.

A quartz crystal resonator covered with a thin sheet of mica was integrated into a surface forces apparatus. The shifts in resonance frequency and bandwidth were monitored as the mica surface came into contact with a spherical lens approached from above. We compare experiments where the lens was either coated with a second mica sheet or just had a silver layer evaporated onto its surface. For the contact with the silver surface, strong maxima in bandwidth occurred during the formation and the disruption of the contact. No such maxima were seen when approaching and separating two mica surfaces. We attribute this increased dissipation to sliding and rolling friction, involving plastic deformation of the metal surface under oscillatory load.

Preparing contamination-free mica substrates for surface characterization, force measurements, and imaging.

Due to its perfect cleavage that provides large areas of molecularly smooth, chemically inert surfaces, mica is the most commonly used natural substrate in measurements with the surface forces apparatus (SFA), in atomic force microscopy (AFM), and in many adsorption studies. However, preparing mica surfaces that are truly clean is not easy since mica is a high-energy surface that readily adsorbs water, organic contaminants, and gases from the atmosphere. Mica can also become charged on cleaving, which makes it prone to picking up oppositely charged particles or mica flakes from the surroundings. High refractive index particles, such as metals, will adhere to mica through van der Waals forces. Recent articles have demonstrated that particle contamination is obtained when inappropriate cutting and handling procedures for the mica are used. In this paper, we show that both particle and other critical contamination is easy to detect and provide proper steps to take during the sample preparation process.