Prof. Dr. Roland Bennewitz

A computationally lean model for the coarse-grained description of contact mechanics of hydrogels is proposed and characterized. It consists of a simple bead-spring model for the interaction within a chain, potentials describing the interaction between monomers and mold or confining walls, and a coarse-grained potential reflecting the solvent-mediated effective repulsion between non-bonded monomers. Moreover, crosslinking only takes place after the polymers have equilibrated in their mold. As such, the model is able to reflect the density, solvent quality, and the mold hydrophobicity that existed during the crosslinking of the polymers. Finally, such produced hydrogels are exposed to sinusoidal indenters. The simulations reveal a wavevector-dependent effective modulus E∗(q) with the following properties: (i) stiffening under mechanical pressure, and a sensitivity of E∗(q) on (ii) the degree of crosslinking at large wavelengths, (iii) the solvent quality, and (iv) the hydrophobicity of the mold in which the polymers were crosslinked. Finally, the simulations provide evidence that the elastic heterogeneity inherent to hydrogels can suffice to pin a compressed hydrogel to a microscopically frictionless wall that is undulated at a mesoscopic length scale. Although the model and simulations of this feasibility study are only two-dimensional, its generalization to three dimensions can be achieved in a straightforward fashion.

Event related potentials (ERPs) represent a noninvasive means for studying sensory and cognitive processes that occur in response to particular stimuli. Here we report on a phase measure for estimating single trial interaction of late somatosensory potentials (LSPs) following a tribological well defined mechanical stimulation of the human fingertip. Stimuli are presented via a programmable Braille-display with actively switchable pins which was slid along the apex of the passive fingertip, i.e., the fingertip rested stationarily in a finger holding system with circular opening at the bottom. The event was the raising and the lowering of either one, three or five lines of pins. Differences were identified by measures based on instantaneous phase synchronization to the stimuli across trials, in particular the wavelet phase synchronization stability (WPSS) measure for single trial sequences of LSPs. In particular, we show that the higher the friction the stronger and more localized the induced phase coherency is. We concluded that the WPSS analysis of single sequences of LSPs represents a reliable method which allows for the quantification of brain responses upon distinct tactile stimuli.

The tribological properties of poly (ether ether ketone) (PEEK) were investigated at different length scales in order to elucidate commonalities and differences in friction and wear. To achieve this goal, the PEEK/steel tribo-system was studied by block-on-ring, block-on-disc, cone-on-disc, and cylinder-on-disc tests as well as by asperity scratching. For better comparability, asperities were prepared from the counter-body steel of the macroscopic experiments. Friction and wear properties were compared on the basis of the pv level. Friction coefficients in macro sliding can be related to the interfacial shear strength in asperity scratching by material's yield pressure. The study confirms that friction and wear of PEEK at different scales can be correlated, despite differences of characteristic velocity and pressure in different experiments.

A model for the contact area of a single asperity sliding in a groove after repeated cycles is presented. Based only on the asperity geometry and on data from friction experiments, the model predicts the area of the asymmetric elliptical contact of the asperity sliding in its own groove. It thus allows to determine the shear stress of the steel–polymer couple in the relevant geometry without need for further microscopy of indenter or groove. The model was validated by experiments with an indenter manufactured from slide bearing steel and polyether-ether ketone (PEEK) as substrate. In experiments of 1000 repeated cycles, the contact area was found to vary with varying load and sliding velocity, while the shear stress was 20.5 MPa at a normal pressure of 50–70 MPa, independent of velocity when friction heating is still negligible. Model and experimental confirmation advance single-asperity friction experiments into an efficient method to extract shear stress and contact area for an understanding of sliding friction in metal-polymer contacts.

Friction forces between human fingertip and a Braille display were recorded simultaneously with electroencephalographic (EEG) signals related to the somatosensory cortex. The correlation between frictional stimuli and event-related EEG signals was analyzed. Raising and lowering the dots of the Braille display caused significant N50 and P110 waves in the event-related EEG signal, but variations in the force stimulus by a factor of two between different Braille pattern did not cause significant differences in the EEG responses related to early tactile processing. Raising and lowering the dots of the Braille display triggers a characteristic temporal development of friction due to viscoelastic skin relaxation.

Friction force microscopy was performed with oxidized or gold-coated silicon tips sliding on Au(111) or oxidized Si(100) surfaces in ultrahigh vacuum. We measured very low friction forces compared to adhesion forces and found a modulation of lateral forces reflecting the atomic structure of the surfaces. Holding the force-microscopy tip stationary for some time did not lead to an increase in static friction, i.e., no contact ageing was observed for these pairs of tip and surface. Passivating layers from tip or surface were removed in order to allow for contact ageing through the development of chemical bonds in the static contact. After removal of the passivating layers, tribochemical reactions resulted in strong friction forces and tip wear. Friction, wear, and the re-passivation by oxides are discussed based on results for the temporal development of friction forces, on images of the scanned area after friction force microscopy experiments, and on electron microscopy of the tips.

Molecular layering of liquids in nanometer-scale confinement is demonstrated for typical lubricant constituents such as polyalphaolefins (PAO) and an ester by means of atomic force microscopy. Layering is observed in force vs. distance curves for poly-(1-decene) tetramers (PAO6) and undecamers (PAO40) and for a 2-ethylhexyl monoester on graphite, mica, and polished steel surfaces and is compared to the layering of hexadecane and 1-hexadecene. On graphite surfaces, the confined molecules are oriented parallel to the surfaces for all liquids, resulting in layers with a thickness comparable to the diameter of the alkyl chains. On mica, confined hexadecane molecules also lie parallel to the surface, while the molecules in the first layer of 1-hexadecene and PAOs take a more upright orientation. Confinement on the oxidized polished steel surfaces results in a molecular layering which most often resembles the layering on graphite and differs significantly from layering on the ionic oxide mica.

Friction and wear of a commercially available polyetheretherketone were investigated by two different testing approaches, namely the standard pin-on-disc (POD) configuration and an unidirectional pin-on-flat (POF) scratch test, in a wide range of pv-products from 0.001 to 8 MPa m/s under dry sliding condition. It was found that the steady state friction coefficient gained from POD tests slightly decreases with increasing sliding velocity from 0.1 to 1 m/s, further increase in the velocity to 4 m/s results in an obvious raise of the friction coefficient. It is assumed that this increase can be attributed to the high interfacial temperature induced strong adhesion between PEEK surface and steel counterbody. No obvious difference of the friction coefficients between POD and POF tests is noted in the studied range. With respect to the wear rate, the wear rate measured from POD increases with monotonously increasing velocity. Possible reasons for these observations are discussed based on the analysis of the worn surfaces of polymer samples and transfer films formed on the steel counterface as well as the investigations on the thermal characteristics of different tribo-systems.

Water-soluble shape-persistent cyclodextrin (CD) polymers with amino-functionalized end groups were prepared starting from diacetylene-modified cyclodextrin monomers by a combined Glaser coupling/click chemistry approach. Structural perfection of the neutral CD polymers and inclusion complex formation with ditopic and monotopic guest molecules were proven by MALDI–TOF and UV–vis measurements. Small-angle neutron and X-ray (SANS/SAXS) scattering experiments confirm the stiffness of the polymer chains with an apparent contour length of about 130 Å. Surface modification of planar silicon wafers as well as AFM tips was realized by covalent bound formation between the terminal amino groups of the CD polymer and a reactive isothiocyanate–silane monolayer. Atomic force measurements of CD polymer decorated surfaces show enhanced supramolecular interaction energies which can be attributed to multiple inclusion complexes based on the rigidity of the polymer backbone and the regular configuration of the CD moieties. Depending on the geometrical configuration of attachment anisotropic adhesion characteristics of the polymer system can be distinguished between a peeling and a shearing mechanism.