Biomedical subjects

Hans-Jürgen Butt

Publications and source records attributed to Hans-Jürgen Butt.

14 recordsLinked to original sources

PubMed2006

Microstructures by solvent drop evaporation on polymer surfaces: dependence on molar mass.

When a solvent drop evaporates from a polymer surface, it leaves behind a characteristic structure, typically a crater. We deposited toluene drops with a microsyringe onto planar polystyrene (PS) surfaces and analyzed the surface topography after drying. For low molar mass PS (Mw = 20.9-24.3 kDa) dotlike protrusions with a ridge at the periphery formed on the polymer surface. With increasing molar mass the central region decreased in height. At Mw = 29.6-643 kDa a craterlike structure with a depression in the center and a ridge was observed. At even higher molar mass, irregular structures without rotational symmetry occurred. We explain the observed dependence on the molar mass with a different degree of entanglement, leading to different dissolution rates and different diffusion constants.

Journal Article↗

PubMed2006

On the adhesion between fine particles and nanocontacts: an atomic force microscope study.

In this study we measured the adhesion forces between atomic force microscope (AFM) tips or particles attached to AFM cantilevers and different solid samples. Smooth and homogeneous surfaces such as mica, silicon wafers, or highly oriented pyrolytic graphite, and more rough and heterogeneous surfaces such as iron particles or patterns of TiO2 nanoparticles on silicon were used. In the first part, we addressed the well-known issue that AFM adhesion experiments show wide distributions of adhesion forces rather than a single value. Our experiments show that variations in adhesion forces comprise fast (i.e., from one force curve to the next) random fluctuations and slower fluctuations, which occur over tens or hundreds of consecutive measurements. Slow fluctuations are not likely to be the result of variations in external factors such as lateral position, temperature, humidity, and so forth because those were kept constant. Even if two solid bodies are brought into contact under precisely the same conditions (same place, load, direction, etc.) the result of such a measurement will often not be the same as that of the previous contact. The measurement itself will induce structural changes in the contact region, which can change the value for the next adhesion force measurement. In the second part, we studied the influence of humidity on the adhesion of nanocontacts. Humidity was adjusted relatively fast to minimize tip wear during one experiment. For hydrophobic surfaces, no signification change in adhesion force with humidity was observed. Adhesion force versus humidity curves recorded with hydrophilic surfaces either showed a maximum or continuously increased. We demonstrate that the results can be interpreted with simple continuum theory of the meniscus force. The meniscus force is calculated based on a model that includes surface roughness and takes into account different AFM tip (or particle) shapes by a two-sphere model. Experimental and theoretical results show that the precise contact geometry has a critical influence on the humidity dependence of the adhesion force. Changes in tip geometry on the sub-10-nm length scale can completely change adhesion force versus humidity curves. Our model can also explain the differences between earlier AFM studies, where different dependencies of the adhesion force on humidity were observed.

Journal Article↗

PubMed2005

Direct measurements of particle-bubble interactions.

The essence of mineral flotation is the formation of strong particle-bubble aggregates. Hydrodynamics and DLVO forces hinder the particle-bubble approach, however the presence of a hydrophobic surface results in hydrophobic attraction and strong aggregate formation. In this article we review literature where the colloid probe technique has been used to investigate flotation, primarily particle-bubble interactions in aqueous solution. In some instance particles-bubble interactions have used to quantify the hydrophobic force, whilst hydrophobic forces are crucial for particle-bubble attachment, studies of hydrophobic forces are not the main focus of this article.

Colloids↗

PubMed2005

Surface and capillary forces encountered by zinc sulfide microspheres in aqueous electrolyte.

The colloid probe technique was used to investigate the interactions between individual zinc sulfide (ZnS) microspheres and an air bubble in electrolyte solution. Incorporation of zinc ions into the electrolyte solution overcomes the disproportionate zinc ion dissolution and mimics high-volume-fraction conditions common in flotation. Determined interaction forces revealed a distinct lack of long-ranged hydrophobic forces, indicated by the presence of a DLVO repulsion prior to particle engulfment. Single microsphere contact angles were determined from particle-bubble interactions. Contact angles increased with decreasing radii and with surface oxidation. Surface modification by the absorption of copper and subsequently potassium O-ethyldithiocarbonate (KED) reduced repulsive forces and strongly increased contact angles.

Journal Article↗

PubMed2005

Morphosynthesis of strontianite nanowires using polyacrylate templates tethered onto self-assembled monolayers.

Strontianite nanowires have been synthesized on self-assembled monolayers (SAM) in the presence of polyacrylate templates. The morphology of this product exhibits characteristic differences from that of products obtained in the absence of polyacrylate. It is demonstrated that the template-induced crystallization process involves the interaction between the SAM surface, polyacrylate (a dissolved polyelectrolyte), and the cations/anions in solution. By the combination of these components, hierarchically ordered mineral hybrid structures are formed.

Journal Article↗

PubMed2005

Microdrops on atomic force microscope cantilevers: evaporation of water and spring constant calibration.

The evaporation of water drops with radii approximately 20 microm was investigated experimentally by depositing them onto atomic force microscope (AFM) cantilevers and measuring the deflection versus time. Because of the surface tension of the liquid, the Laplace pressure inside the drop, and the change of interfacial stress at the solid-liquid interface, the cantilever is deflected by typically a few hundred nanometers. The experimental results are in accordance with an analytic theory developed. The evaporation process could be monitored with high accuracy even at the last stage of evaporation because (1) cantilever deflections can be measured with nanometer resolution and (2) the time resolution, given by the inverse of the resonance frequency of the cantilever of approximately 0.3 ms, is much faster than the typical evaporation time of 1 s. Experimental results indicate that evaporation of the last thin layer of water is significantly slower than the rest of the drop, which can be due to surface forces. This drop-on-cantilever system can also be used to analyze the drop impact dynamics on a surface and to determine the spring constant of cantilevers.

Journal Article↗

PubMed2004

Rupture force between the third strand and the double strand within a triplex DNA.

The rupture force to separate the third strand and the duplex within a triplex DNA was measured by means of atomic force spectroscopy. The tip and the sample surfaces were functionalized by oligodeoxyribonucleotides 5'-TTCTTCTTTCTTTTCCTTTTCTTTCTTCTTACTTCTCTCTCTC TCTCTCT-SH-3'. The sample surface was hybridized with 5'-AAGAAGAAAGAAAAGGAAAAGAAAGAAGAA-3' to form a double strand DNA on the surface prior to the force measurements. These sequences form triple helices with 30 base pairs under a pH of 5.8 and in the presence of 2.0 mM spermine. Signals of rupture of single and multiple triplex DNA were observed in the force distance curves. Rupture force histograms revealed a force of 42.6 +/- 1.9 pN from 24 independent measurements at a tip velocity of 400 nm/s to separate the third strand from duplex DNA. The velocity dependence of the rupture force quantum indicates a thermal dissociation process similar to that of rupturing a ds-DNA. The number of rupture events was controlled by adding oligonucleotides 5'-AAGAAGAAAGAAAAGGAAAAGAAAGAAGAA-3' either to reduce or to initiate triplex formation.

Base Sequence↗

PubMed2004

Equilibrium interaction of solid surfaces across a polymer melt.

Forces across polymer melts are poorly understood despite their importance for adhesion and fabricating composite materials. Using an atomic force microscope (AFM), this interaction was measured for poly(dimethyl siloxane) (PDMS). The structure of the polymer at the surface changed during the first approximately 10 h. Afterward, short-range attractive forces were observed with short-chain PDMS (M(w) = 4200 g/mol). Using PDMS with a molecular weight (M(w) = 18 000 g/mol) above the entanglement limit, we measured a monotonically decaying repulsive force, which indicates that a quasi-immobilized layer had formed at the solid surface. Due to the small radius of curvature of the tip, forces could be measured in equilibrium.

Dimethylpolysiloxanes↗

PubMed2004

Tilt of atomic force microscope cantilevers: effect on spring constant and adhesion measurements.

In atomic force microscopy, the cantilevers are mounted under a certain tilt angle alpha with respect to the sample surface. In this paper, we show that this increases the effective spring constant by typically 10-20%. The effective spring constant of a rectangular cantilever of length L can be obtained by dividing the measured spring constant by cos2 alpha(1 - 2D tan alpha/L). Here, alpha is the tilt angle and D is the size of the tip. In colloidal probe experiments, D has to be replaced by the radius of the attached particle. To determine the effect of tilt experimentally, the adhesion force between spherical borosilicate particles and planar silicon oxide surfaces was measured at tilt angles between 0 degrees and 35 degrees. The experiments revealed a significant decrease of the mean apparent adhesion force with a tilt of typically 20-30% at alpha = 20 degrees. In addition, they demonstrate that the adhesion depends drastically on the precise position of contact on the particle surface.

Journal Article↗

PubMed2004

Using the atomic force microscope to study the interaction between two solid supported lipid bilayers and the influence of synapsin I.

To measure the interaction between two lipid bilayers with an atomic force microscope one solid supported bilayer was formed on a planar surface by spontaneous vesicle fusion. To spontaneously adsorb lipid bilayers also on the atomic force microscope tip, the tips were first coated with gold and a monolayer of mercapto undecanol. Calculations indicate that long-chain hydroxyl terminated alkyl thiols tend to enhance spontaneous vesicle fusion because of an increased van der Waals attraction as compared to short-chain thiols. Interactions measured between dioleoylphosphatidylcholine, dioleoylphosphatidylserine, and dioleoyloxypropyl trimethylammonium chloride showed the electrostatic double-layer force plus a shorter-range repulsion which decayed exponentially with a decay length of 0.7 nm for dioleoylphosphatidylcholine, 1.2 nm for dioleoylphosphatidylserine, and 0.8 nm for dioleoyloxypropyl trimethylammonium chloride. The salt concentration drastically changed the interaction between dioleoyloxypropyl trimethylammonium chloride bilayers. As an example for the influence of proteins on bilayer-bilayer interaction, the influence of the synaptic vesicle-associated, phospholipid binding protein synapsin I was studied. Synapsin I increased membrane stability so that the bilayers could not be penetrated with the tip.

Adsorption↗

PubMed2003

Surface roughness and hydrodynamic boundary slip of a newtonian fluid in a completely wetting system.

The influence of surface roughness on the boundary condition for the flow of a Newtonian fluid near a hard wall has been investigated by measurement of the hydrodynamic drainage force. The degree of slip is found to increase with surface roughness. This leads to the conclusion that in most practical situations boundary slip takes place, leading to a reduction of the drainage force.

Journal Article↗

PubMed2002

Rupture of molecular thin films observed in atomic force microscopy. I. Theory.

In atomic force microscope studies of molecular thin films, a defined jump of the tip through the film is often observed once a certain threshold force has been exceeded. Here, we present a theory to describe this film rupture and to relate microscopic parameters to measurable quantities. We assume that the tip has to overcome an activation energy before the film ruptures. A universal relation between the force dependence of the activation energy and the approaching velocity of the tip is derived. Two complementary models for calculating the activation energy are presented: a continuum nucleation model and a discrete molecular model. Both models predict a narrow distribution of yield forces in agreement with experimental results.

Journal Article↗

PubMed2002

Rupture of molecular thin films observed in atomic force microscopy. II. Experiment.

In atomic force microscope studies of thin films often a defined jump of the tip through the film is observed once a certain threshold force has been exceeded. In particular, on lipid bilayers this is regularly observed. In a previous paper [H.-J. Butt and V. Franz, Phys. Rev. E 66, 031601 (2002)] we presented two complementary models to describe film rupture. The aim of this study was to verify these models. Experiments were done with solid supported bilayers consisting of dioleoyloxypropyl-trimethylammonium chloride (DOTAP) and dioleoylphosphatidylserine (DOPS) in aqueous solutions and with propanol. Both models describe experimental results adequately. In particular, a narrow distribution of yield forces and an increase of the mean yield force with increasing loading rate is correctly predicted. For the lipid bilayers spreading pressures of roughly 20 mN/m (DOTAP) and 5 mN/m (DOPS) were measured. Line tensions for the edge of a lipid bilayer ranged between 3 (DOTAP) and 6 pN (DOPS).

Journal Article↗

PubMed2002

Hydrodynamic force measurements: boundary slip of water on hydrophilic surfaces and electrokinetic effects.

The hydrodynamic drainage force of aqueous medium between smooth hydrophilic surfaces was measured with the colloidal probe technique up to shear rates of typically 10(4) s(-1). Measured force curves were compared to simulations. To reach agreement between experimental and simulated force curves, the hydrodynamic force had to be fitted with a model allowing for boundary slippage. Boundary slip was characterized by a slip length of 8-9 nm. Force measurements with charged surfaces could be simulated taking only hydrodynamic and electrostatic double-layer forces into account.

Journal Article↗