The adhesion and removal of particles from surfaces is a contemporary problem in many industrial applications like Semiconductor manufacturing, Bioaerosol removal, Pharmaceuticals, Adhesives and Petroleum industry. The complexity of the problem is due to the variety of factors like roughness, temperature, humidity, fluid medium etc. that affect pull-off of particles from surfaces. In particle removal from surfaces using fluid motion, the dynamic effects of particle separation will play an important role. Thus it is essential to study the dynamic effects of particle removal. Velocity of pull-off and force duration effects are two important dynamic factors that might affect pull-off. Particle adhesion studies can be made using the Atomic Force Microscope (AFM). The velocity of pull-off and force duration can be varied while making the AFM measurements. The objective of the current work is to obtain the dependence of pull-off force on pull-off velocity. Experiments were conducted using AFM and the data obtained from the experiments is processed to obtain plots for pull-off force vs. particle size and pull-off force vs. pull-off velocity. The pull-off force is compared with the predictions of previous contact adhesion theories. A velocity effect on pull-off force is observed from the experiments conducted.

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The diploma thesis deals with force-distance spectroscopy method as a tool for determining pull-off force on graphit/graphene sheets under varied conditions. There is described also a contact angle method which is used to idetify contact angles of water on six investigated samples. Results of both method were discussed with respect to utilization of force-distance spectroscopy in wetting measurements of materials. Finally it was carried out modification of graphen sheet by local anodic oxidation.

<p>Flotation is a critical operation in the isolation of valuable minerals from natural ore. Before flotation, chemical collectors are routinely added to ground ore slurries. Collectors selectively bind to mineral-rich particles, increasing their hydrophobicity thus promoting selective flotation. Conventional collectors are small surfactants with a short hydrocarbon tail (2-6 carbons) and a head group, such as xanthate. In this work, much larger hydrophobic polystyrene nanoparticles are evaluated as potential flotation collectors. Experiments involving both clean model mineral suspensions and complex ultramafic nickel ores confirm that conventional water-soluble molecular collectors could be partially or completely replaced by colloidal hydrophobic nanoparticle flotation collectors.</p> <p>The ability of nanoparticles to induce flotation has been demonstrated by floating hydrophilic, negatively charged glass beads with cationic polystyrene nanoparticle collectors. Mechanisms and key parameters such as nanoparticle hydrophobicity and nanoparticle adsorption density have been identified. Electrostatic attraction promotes the spontaneous deposition of the nanoparticles on the glass surfaces raising the effective contact angle to facilitate the adhesion of beads to air bubbles. The pull-off force required to detach a glass sphere from the air/water interface of a bubble into the water was measured by micromechanics. Coating with nanoparticles allows the beads to attach remarkably firmly on the air bubble. As little as 10% coverage of the bead surfaces with the most effective nanoparticles could promote high flotation efficiencies, whereas conventional molecular collector requires 25% or higher coverage for a good recovery. Contact angle measurements of modified glass surfaces with a series of nanoparticles that covered a range of surface energies were used to correlate the nanoparticle surface properties with their ability to promote flotation of glass beads. Factors influencing nanoparticle deposition on glass, such as nanoparticle dosage, nanoparticle size, conditioning time have been investigated with a quartz crystal microbalance (QCM). Deposition kinetics has been analyzed according to Langmuir kinetics model.</p> <p>Surface functionalized nanoparticles enhance the ability of nanoparticle collectors to selectively deposit onto surfaces of the desired mineral particles in the presence of gangue materials. Poly (styrene-co-vinylimidazole) based nanoparticle collectors have been developed to selectively deposit onto nickel mineral (pentlandite) in the presence of Mg/Si slime. Flotation tests of ultramafic nickel ores with these nanoparticle collectors have shown improvements in both pentlandite recovery and selectivity.</p> / Doctor of Philosophy (PhD)

The problem of a thin elastomeric layer confined between two stiff adherends arises in numerous applications such as microelectronics, bio-inspired adhesion and the manufacture of soft biomedical products. A common requirement is that the debonding of the elastomeric layer from the adherends be controlled to avoid undesirable failure modes. This level of control may necessitate understanding the collective role of the interfacial adhesion, material properties, part geometries, and loading conditions on the debonding. Analytical and numerical approaches using the finite element method and a cohesive zone model (CZM) for the interfacial debonding are used in this dissertation to delineate the role of the afore-mentioned parameters on the initiation and propagation of debonding for both rigid and non-rigid adherends. Extensively studied in the dissertation is the debonding of a semi-infinite relatively stiffer adherend from an elastomer layer with its other surface firmly bonded to a rigid base. The adherend is pulled upwards by applying normal displacements either on its entire unbonded surface or on the edge of its part overhanging from the elastomer layer. The adherend and the elastomeric layer materials are assumed to be linear elastic, homogeneous and isotropic and the elastomer is assumed to be incompressible. Viscoelasticity of the elastomer is considered in the first part of the work. Plane strain deformations of the system with a bilinear traction-separation (TS) relation in the CZM are analyzed. Two non-dimensional numbers, one related to the layer confinement and the other to the interfacial TS parameters, are found to determine if debonding initiates at interior points in addition to at corner points on the adherend/elastomer interface, and if adhesion-induced instability is exhibited. This work is extended to axisymmetric problems in which debonding can take place at both interfaces. Motivated by an industrial demolding problem, numerical experiments are conducted to derive insights into preferential debonding at one of the two interfaces, including for curved adherends. Results reported herein should help engineers design an elastomer layer sandwiched between two adherends for achieving desired failure characteristics. / Ph. D.

The adhesive and frictional response of an AFM tip connected to a substrate through supramolecular host–guest complexes is investigated by dynamic Monte Carlo simulations. Here, the variation of the pull-off force with the unloading rate recently observed in experiments is unraveled by evidencing simultaneous (progressive) breaking of the bonds at fast (slow) rates. The model reveals the origin of the observed plateaus in the retraction force as a function of the tip-surface distance, showing that they result from the tip geometrical features. In lateral sliding, the model exhibits a wide range of dynamic behaviors ranging from smooth sliding to stick-slip at different velocities, with the average friction force determined by the characteristic formation/rupture rates of the complexes. In particular, it is shown that for some molecular complexes friction can become almost constant over a wide range of velocities. Also, we show the possibility of exploiting the ageing effect through slide-hold-slide experiments, in order to infer the characteristic formation rate. Finally, our model predicts a novel ‘‘antiageing’’ effect which is characterized by a decrease of the static friction force with the hold time. Such an effect is explained in terms of enhancement of adhesion during sliding, especially observed at high driving velocities.