Effects of argon plasma treatment on the interfacial adhesion of PBO fiber/bismaleimide composite and aging behaviors

This paper is concerned with the influence of argon plasma on the interfacial adhesion of PBO fiber/bismaleimide composites and aging behaviors. The interlaminar shear strength (ILSS) was greatly increased to 62.3 MPa with an increase of 39.7% after treatment for 7 min at 80 Pa, 200 W. A small amount of O and N atoms was incorporated onto the fiber surface, but the plasma caused C-O bonds to break and generated OC-N groups. The fiber surface roughness increased, contributing much to the wettability. However, long-time treatment excessively destroyed the inherent and newly created structures. The SEM images suggested that the fracture shifted from the interface to the matrix. The modification effects degraded with storage time in the air and the ILSS decreased to approximately 54.0 MPa after 10-30 days. The composite had low water absorption of 2.0 wt% and a high retention of 90% in the ILSS at moisture conditions.     

Regulation of the elastic modulus of polyurethane microarrays and its influence on gecko-inspired dry adhesion

We studied the influence of the elastic modulus on the gecko-inspired dry adhesion by regulating the elastic modulus of bulk polyurethane combined with changing the size of microarrays. Segmented polyurethane (PU) was utilized to fabricate micro arrays by the porous polydimethyl siloxane (PDMS) membrane molding method. The properties of the micro arrays, such as the elastic modulus and adhesion, were investigated by Triboindenter. The study demonstrates that bulk surfaces show the highest elastic modulus, with similar values at around 175 MPa and decreasing the arrays radius causes a significant decrease in E, down to 0.62 MPa. The corresponding adhesion experiments show that decrease of the elastic modulus can enhance the adhesion which is consistent with the recent theoretical models.     

Strengthening of liquid crystalline polymer by functionalized carbon nanotubes through interfacial interaction and homogeneous dispersion

Multiwalled carbon nanotubes (MWCNTs) were functionalized with two types of chemical moieties (i.e. carboxylic, ? COOH and hydroxyl benzoic acid groups, ‐HBA) on their sidewalls in order to improve their interaction with a liquid crystalline polymer (LCP) and dispersion in LCP. We have investigated the rheological, mechanical, dynamic mechanical, and thermal properties in detail with variation of HBA‐functionalized MWCNTs in the LCP matrix. Effect of the dispersion state of the functionalized MWCNTs in the LCP matrix on the rheological behavior was also studied. The composites containing HBA‐functionalized MWCNTs showed higher complex viscosity, storage, and loss modulus than the composites with the same loading of raw MWCNTs and MWCNT‐COOH. It was suggested that the HBA‐functionalized MWCNTs exhibited a better dispersion in the polymer matrix and formed stronger CNT‐polymer interaction in the composites than the raw MWCNTs and MWCNT‐COOH, which was also confirmed by FESEM and FTIR studies. As a result, the overall mechanical performance of the HBA‐MWCNT‐LCP composites could be improved significantly. For example, the addition of 4 wt% HBA‐MWCNT to LCP resulted in the considerable improvements in the tensile strength and modulus of LCP (by 66 and 90%, respectively). Copyright © 2010 John Wiley & Sons, Ltd.     

Nanoscale viscoelastic properties and adhesion of polydimethylsiloxane for tissue engineering简

It has shown that altering crosslink density of biopolymers will regulate the morphology of Mesenchymal Stem Cells （MSCs） and the subsequent MSCs differentia- tion. These observations have been found in a wide range of biopolymers. However, a recent work published in Nature Materials has revealed that MSCs morphology and differen- tiation was unaffected by crosslink density of polydimethyl- siloxane （PDMS）, which remains elusive. To understand such unusual behaviour, we use nanoindentation tests and modelling to characterize viscoelastic properties and sur- face adhesion of PDMS with different base：crosslink ratio varied from 50：1 （50D） to 10：1 （10D）. It has shown that lower crosslink density leads to lower elastic moduli. De- spite lower nanoindentation elastic moduli, PDMS with lowest crosslink density has higher local surface adhesion which would affect cell-biomaterials interactions. This work suggests that surface adhesion is likely another important physical cue to regulate cell-biomaterials interactions.     

Tuning Molecular Adhesion via Material Anisotropy

Cell adhesion with extracellular matrix depends on the collective behaviors of a large number of receptor‐ligand bonds at the compliant cell‐matrix interface. While most biological tissues and structures, including cells and extracellular matrices, exhibit strongly anisotropic material properties, existing studies on molecular adhesion via receptor‐ligand bonds have been largely limited to isotropic materials. Here the effects of transverse isotropy, a common form of material anisotropy in biological systems, in modulating the adhesion behavior of a cluster of receptor‐ligand bonds are investigated. The results provide a theoretical basis to understand cell adhesion on anisotropic extracellular matrices and to explore the possibility of controlling cell adhesion via anisotropy design in material properties. The combined analysis and simulations show that the orientation of material anisotropy strongly affects the apparent softness felt by the adhesive bonds, thereby altering their ensemble lifetime by several orders of magnitude. An implication of this study is that distinct cellular behaviors can be achieved through remodeling of material anisotropy in either extracellular matrix or cytoskeleton. Comparison between different loading conditions, together with the effects of material anisotropy, yields a rich array of out‐of‐equilibrium behaviors in the molecular interaction between reactant‐bearing soft surfaces, with important implications on the mechanosensitivity of cells.     

Adhesion and friction studies of Au nanoparticle‐textured surfaces with colloidal tips

Surface roughness plays an important role in affecting the adhesive force and friction force in microelectromechanical systems (MEMS)/nanoelectromechanical systems (NEMS). One effective approach of reducing adhesion and friction of contacting interfaces is to create textured surface, which is especially beneficial for MEMS'/NEMS' production yield and product reliability. In this article, we present a convenient method to fabricate the nano‐textured surfaces by self‐assembling Au nanoparticles (NPs) on the silicon (100) surfaces. The nanoparticle‐textured surfaces (NPTS) with different packing density and texture height were prepared by controlling the assembling time and the size of Au NPs. The morphologies and chemical states of NPTS were characterized by atomic force microscope (AFM), field emission scanning electron microscope, and XPS. The adhesion and friction on the NPTS were studied by AFM with colloidal tip. The results show that the nano‐textured surfaces have effectively reduced adhesive force and friction force compared with the 3‐aminopropyl trimethoxysilane self‐assembled monolayer surfaces. The lowered adhesion and friction were attributed to the reduced real area of contact between NPTS and colloidal tip. The adhesion and friction of the NPTS are varying with the texture packing density and dependent on both the texture height and asperities spacing, which are related to the size and coverage ratio of NPs on surfaces. Copyright © 2011 John Wiley & Sons, Ltd.     

Molecular and nanoscale factors governing pressure‐sensitive adhesion strength of viscoelastic polymers

Pressure‐sensitive adhesives (PSAs) are finding increasing applications in various areas of industry and medicine. PSAs are a special class of viscoelastic polymers that form strong adhesive joints with substrates of varying chemical nature under application of light external bonding pressures (1–10 Pa) over short periods of time (1–5 s). To be a PSA, a polymer should possess both high fluidity under applied bonding pressure, to form good adhesive contact, and high cohesive strength and elasticity, which are necessary for resistance to debonding stresses and for dissipation of mechanical energy at the stage of adhesive bond failure under detaching force. For rational design of novel PSAs, molecular insight into mechanisms of their adhesive behavior is necessary. As shown in this review, strength of PSA adhesive joints is controlled by a combination of diffusion, viscoelastic, and relaxation mechanisms. At the molecular level, strong adhesion is the result of a narrow balance between two generally conflicting properties: high cohesive strength and large free volume. These conflicting properties are difficult to combine in a single polymer material. Individually, high cohesive interaction energy and large free volume are necessary but insufficient prerequisites for PSA strength. Evident correlations are observed between the adhesive bond strengths of different PSAs, and their relaxation behaviors are described by longer relaxation times. Innovative PSAs with tailored properties can be produced by physical mixing of nonadhesive long‐ and short‐chain linear parent polymers, with groups at the two ends of the short chains complementary to the functional groups in the recurring units of the long chains. Although chemical composition and molecular structure of such innovative adhesives are unrelated to those of conventional PSAs, their mechanical properties and adhesive behaviors obey the same general laws, such as the Dahlquist's criterion of tack. © 2012 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys, 2012     

Gecko‐Inspired Controllable Adhesive Structures Applied to Micromanipulation

Gecko‐inspired angled elastomer micropillars with flat or round tip endings are presented as compliant pick‐and‐place micromanipulators. The pillars are 35 μm in diameter, 90 μm tall, and angled at an inclination of 20°. By gently pressing the tip of a pillar to a part, the pillar adheres to it through intermolecular forces. Next, by retracting quickly, the part is picked from a given donor substrate. During transferring, the adhesion between the pillar and the part is high enough to withstand disturbances due to external forces or the weight of the part. During release of the part onto a receiver substrate, the contact area of the pillar to the part is drastically reduced by controlled vertical or shear displacement, which results in reduced adhesive forces. The maximum repeatable ratio of pick‐to‐release adhesive forces is measured as 39 to 1. It is found that a flat tip shape and shear displacement control provide a higher pick‐to‐release adhesion ratio than a round tip and vertical displacement control, respectively. A model of forces to serve as a framework for the operation of this micromanipulator is presented. Finally, demonstrations of pick‐and‐place manipulation of micrometer‐scale silicon microplatelets and a centimeter‐scale glass cover slip serve as proofs of the concept. The compliant polymer micropillars are safe for use with fragile parts, and, due to exploiting intermolecular forces, could be effective on most materials and in air, vacuum, and liquid environments.