Carbon nanotubes (CNTs) have extraordinary electrical and mechanical properties, and many potential applications have been proposed, ranging from nanoscale devices to reinforcement of macroscopic structures. However, due to their small sizes, characterization of their mechanical properties and deformation behaviours are major challenges. Theoretical modelling of deformation behaviours has shown that multi-walled carbon nanotubes (MWCNTs) can develop ripples in the walls on the contracted side when bent above a critical curvature. The rippling is reversible and accompanied by a reduction in the bending stiffness of the tubes. This behaviour will have implications for future nanoelectromechanical systems (NEMS). Although rippling has been thoroughly modelled there has been a lack of experimental data thus far. In this study, force measurements have been performed on individual MWCNTs and vertically aligned carbon nanofibers (VACNFs). This was accomplished by using a custom-made atomic force microscope (AFM) inside a scanning electron microscope (SEM). The measurements were done by bending free-standing MWCNTs/VACNFs with the AFM sensor in a cantilever-to-cantilever fashion, providing force-displacement curves. From such curves and the MWCNT/VACNF dimensions, measured from SEM-images, the critical strain for the very onset of rippling and the Young’s modulus, E, could be obtained. To enable accurate estimations of the nanotube diameter, we have developed a model of the SEM-image formation, such that intrinsic diameters can be retrieved. We have found an increase in the critical strain for smaller diameter tubes, a behaviour that compares well with previous theoretical modelling. VACNFs behaved very differently, as they did not display any rippling and had low bending stiffnesses due to inter-wall shear. We believe that our findings will have implications for the design of future NEMS devices that employ MWCNTs and VACNFs. / <p>Artikel 2 Image formation mechanisms tidigare som manuskript, nu publicerad: urn:nbn:se:kau:diva-16425 (MÅ 150924)</p>

Eukaryotic cells face a considerable challenge organizing a complicated interior with spatial and temporal precision. They do so, in part, through the deployment of the microtubule- based molecular motors kinesin and dynein, which translate chemo-mechanical force production into the movement of diverse cargo. Many aspects of kinesin’s motility mechanism are now known in detail, whereas fundamental aspects of dynein’s motility mechanism remain unclear. An important unresolved question is how dynein couples rounds of ATP binding and hydrolysis to changes in affinity for its track, a requisite for a protein that takes steps. Here we report a sub- nanometer cryo-EM reconstruction of the high affinity state of dynein’s microtubule binding domain in complex with the microtubule. Using molecular dynamics flexible fitting, we determined a pseudoatomic model of the high affinity state. When compared to previously reported crystal structure of the free microtubule binding domain, our model revealed the conformational changes underlying changes in affinity. Surprisingly, our simulations suggested that specific residues within the microtubule binding domain may tune dynein’s affinity for the microtubule. We confirmed this observation by directly measuring dynein’s motile properties using in vitro single molecule motility assays, which demonstrated that single point mutations of these residues dramatically enhance dynein’s processivity. We then sought to understand why dynein has been selected to be a restrained motor, and found that dynein-driven nuclear oscillations in budding yeast are defective in the context of highly processive mutants. Together, these results provide a mechanism for the coupling of ATPase activity to microtubule binding and release by dynein, and the degree to which evolution has fine-tuned this mechanism. I conclude with a roadmap of future approaches to gain further insight into dynein’s motility mechanism, and describe our work developing materials and methods towards this goal.

Oxidation developed from the surfaces into the cores of the microwaved particles. Metallic particles were also formed during microwave exposure. Lihir gold ore, in which gold was finely disseminated in pyrite and marcasite, was an extremely refractory gold ore. Without pretreatment, only 37-39% of the gold could be extracted with sodium cyanide. However, this was improved after the head ores or floatation concentrates were pretreated by microwave radiation. 74.581.2% of the gold was extracted from the microwave treated head ore. The hydrometallurgical pretreatment of pyrite and marcasite in a microwave field and a conventional heating environment was also investigated.I,n a nitric acid solution, pyrite and marcasite can be rapidly leached. Reaction temperature and the concentration of HNO3 had a significant influence on decomposition rate. Marcasite had a substantially higher i decomposition rate than pyrite. Microwave heating could promote the dissociation of marcasite and pyrite, compared with conventional heating. This was caused by special volumetric heating during microwave exposure that may induce local overheating or improve the interactions between the high dielectric loss minerals and the leaching solution. Kinetic investigations show that the decomposition of both the minerals in a nitric acid medium is controlled by chemical reactions on the surfaces of particles. The decomposition is a second order reaction with respect to nitric acid concentration. Less than 5- 7% of the decomposed sulphur was transformed into elemental sulphur during the leaching of both the minerals

As silicon-based transistor technology continues to scale ever downward, anticipation of the fundamental limitations of ultimately-scaled devices has driven research into alternative device technologies as well as new materials for interconnects and packaging. Additionally, as power dissipation becomes an increasingly important challenge in highly miniaturized devices, both the implementation and verification of high mobility, high thermal conductivity materials, such as low dimensional carbon nanomaterials, and the experimental investigation of heat transfer in the nanoscale regime are requisite to continued progress. This work furthers the current understanding of structure-property relationships in low dimensional carbon nanomaterials, specifically carbon nanotubes (CNTs) and graphene, through use of combined thermal conductance and transmission electron microscopy (TEM) measurements on the same individual nanomaterials suspended between two micro-resistance thermometers. Through the development of a method to measure thermal contact resistance, the intrinsic thermal conductivity, [kappa], of multi-walled (MW) CNTs is found to correlate with TEM observed defect density, linking phonon-defect scattering to the low [kappa] in these chemical vapor deposition (CVD) synthesized nanomaterials. For single- (S) and double- (D) walled (W) CNTs, the [kappa] is found to be limited by thermal contact resistance for the as-grown samples but still four times higher than that for bulk Si. Additionally, through the use of a combined thermal transport-TEM study, the [kappa] of bi-layer graphene is correlated with both crystal structure and surface conditions. Theoretical modeling of the [kappa] temperature dependence allows for the determination that phonon scattering mechanisms in suspended bi-layer graphene with a thin polymeric coating are similar to those for the case of graphene supported on SiO₂. Furthermore, a method is developed to investigate heat transfer through a nanoscale point contact formed between a sharp silicon tip and a silicon substrate in an ultra high vacuum (UHV) atomic force microscope (AFM). A contact mechanics model of the interface, combined with a heat transport model considering solid-solid conduction and near-field thermal radiation leads to the conclusion that the thermal resistance of the nanoscale point contact is dominated by solid-solid conduction. / text

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Titanium carbide (TiC) and titanium carbonitride (Ti(C,N)) are both common components in hard, wear resistant ceramic-metal composites, or cermets. In this study the intermetallic nickel aluminide (Ni3Al) has been used as a binder for the production of TiC and Ti(C,N) based cermets. These cermets offer several improved characteristics relative to conventional WC-based ‘hardmetals’, such as lower mass and improved oxidation resistance, which are also combined with high fracture resistance, hardness and wear resistance. The cermets were produced using an in-situ, reaction sintering procedure to form the stoichiometric Ni3Al binder, with the binder contents varied from 20 to 40 vol%. However, for high N content Ti(C,N) cermets, the wettability of molten Ni3Al is relatively poor, which leads to materials with residual porosity. Therefore various amounts of Mo2C (1.25, 2.5, 5 and 10 vol%) were incorporated into the Ti(C0.3,N0.7)-Ni3Al cermets, with the aim of improving the densification behaviour. Mo2C was found to improve upon the wettability during sintering, thus enhancing the densification, especially at the lower binder contents. The tribological behaviour of TiC and Ti(C,N) cermets have been evaluated under reciprocating sliding conditions. The wear tests were conducted using a ball-on-flat sliding geometry, with a WC-Co sphere as the counter-face material, for loads from 20 to 60 N. The wear response was characterised using a combination of scanning electron microscopy, energy dispersive X-ray spectroscopy, and focused ion beam microscopy. Initially, two-body abrasive wear was observed to occur, which transitions to three-body abrasion through the generation of debris from the cermet and counter-face materials. Ultimately, this wear debris is incorporated into a thin tribolayer within the wear track, which indicates a further transition to an adhesive wear mechanism. It was found that Mo2C additions had a positive effect on both the hardness and indentation fracture resistance of the samples, but had a detrimental effect on the sliding wear response of the cermets. This behaviour was attributed to increased microstructural inhomogeneity with Mo2C additions.

The main purpose of this thesis is to improve the fundamental knowledge of non-isothermal tempering of martensite phase and its effects on the reduction in hardness (softening) with respect the base metal occurring at the heat affected zone (HAZ) of resistance spot welded dual-phase (DP) steels. This thesis also aims at understanding the influence of HAZ-softening on the joint performance of various DP steel grades. The tempering of martensite occurring at the sub-critical HAZ (SC-HAZ) of resistance spot welded DP600, DP780 and DP980 steels has been systematically evaluated by microhardness testing through Vickers indentation and the degree of tempering has been correlated to the HAZ-softening. From the joint performance analysis of similar and dissimilar steel grade combinations assessed through standardized testing methods, three important issues have been targeted: a) the joint strength (maximum load to failure), b) the location of failure (failure mode), and c) the physical characteristic of the weld that determines certain type of failure (weld nugget size). In addition, a partial tensile test has been conducted in order to evaluate the initiation of failure in dissimilar steel grade combinations. It has been shown that HAZ-softening lowered the weld size at which transition from interfacial to pullout failure mode takes place along with increased load-bearing capacity and higher energy absorption. Thus, it is concluded from mechanical testing that HAZ-softening benefits the lap-shear tensile joint performance of resistance spot welded DP steels by facilitating pullout failures through failure initiation at the SC-HAZ (tempered region). Instrumented nanoindentation testing was employed to further investigate HAZ-softening along the SC-HAZ by evaluating individual phases of ferrite matrix and tempered martensite islands. Although the ferrite matrix presented a slight reduction in hardness at nanoscale, higher reduction in hardness (softening) resulted for tempered martensite; thus confirming that tempered martensite is the major contributor to softening at micro-scale. A comparison between nanohardness and microhardness testing made at different distances from the line of lower critical temperature of transformation (Ac1) allowed revealing the actual extension of the SC-HAZ. In this regard, good correlation was obtained between nanohardness results along the SC-HAZ and the microstructural changes analyzed by electron microscopy (i.e., the tempering of martensite occurring at various distances far from Ac1 was correlated to low temperature tempering of dual phase steels). An in-depth analysis of the tempering of martensite phase at high temperature in DP steel subjected non-isothermal conditions i.e., rapid heating, extremely short time at peak temperature and rapid cooling (resistance spot welding), has been carried out mainly through analytical transmission electron microscopy (TEM). In addition, an isothermal tempering condition (i.e., slow heating and long time at peak temperature) in DP steel has been evaluated for complementing the analysis. Both non-isothermal and isothermal conditions have been correlated to the softening behaviour. TEM analysis of the base metal in the DP steel indicated that the morphology of the martensite phase is dependent on its carbon content, and its tempering characteristics are similar to that of equal carbon containing martensitic steel. The isothermally tempered structure is characterized by coarsening and spheroidization of cementite (θ) and complete recovery of the martensite laths; whereas precipitation of fine quasi-spherical intralath θ-carbides, coarser plate-like interlath θ-carbides, decomposition of retained austenite into elongated θ-carbides, and partial recovery of the lath structure were observed after non-isothermal tempering of DP steel. This difference in tempering behaviour is attributed to synergistic effect of delay in cementite precipitation due to higher heating rate, and insufficient time for diffusion of carbon that delays the third stage of tempering process (cementite coarsening and recrystalization) during non-isothermal. The finer size and the plate-like morphology of the precipitated carbides along with the partial recovery of the lath structure observed after non-isothermal tempering strongly influenced the softening behaviour of DP steel. The chemical analysis of θ-carbides through extraction replicas for three different DP steels revealed that the chemistry of the carbides is inherited from the parent DP steel during non-isothermal tempering at high temperature confirming that non-isothermal tempering DP steel is predominantly controlled by carbon diffusion.

This thesis is focused on the fabrication and characterization of self-assembled arrays of magnetic iron oxide (Fe3O4, γ-Fe2O3 and Fe1-xO) nanoparticles. The synthesis of spherical and cubic iron oxide nanocrystals, with sizes between 5 and 30 nm and narrow size distributions, is demonstrated, along with a rigorous morphological characterization of the cubic nanoparticles. The transformation of core|shell Fe1-xO|Fe3-δO4 particles into single-phase Fe3-δO4 particles is studied in detail. It is found that anti-phase boundaries in the particles result in the emergence of anomalous magnetic properties i.e. exchange bias, and a reduced saturation magnetization compared to that of bulk Fe3O4. Cubic nanocrystals are assembled into arrays possessing an exceptionally high degree of translational ordering and a high degree of crystallographic alignment. A combination of electron microscopy and small-angle X-ray scattering is used in the characterization of the 3D nanostructures. The directional (anisotropic) interactions in the 3D structures are modeled in an attempt to find a link between the nanocrystal morphology and the corresponding mesostructure. Here, the cohesive van der Waals energy is estimated for a system of nanocubes with a variable truncation. The assembly of nanocubes in magnetic fields of various strengths is systematically investigated. A perturbed mesocrystal growth habit is observed at intermediate fields, whereas at high field strengths, the assembly is dominated by ferrohydrodynamic instabilities. Last, magnetometry is used to study the collective magnetic properties of self-assembled nanocrystals. The magnetic susceptibility in a weak magnetic field is studied as a function of film thickness and particle size. An increase in the tendency to form ferromagnetic couplings  with decreasing film thickness can be established. This 2D to 3D crossover of the magnetic properties of the nanoparticle arrays can be related to a change in the magnetic vortex states.

This thesis is an investigation of methods to remediate methicillin-resistant Staphylococcus pseudintermedius (MRSP) biofilms through conventional and microfluidic-based in vitro assays. MRSP biofilm related infections are a major concern for veterinary clinicians as they may complicate remediation by the immune system or antimicrobials. Novel antimicrobials that have been found to reduce biofilm growth in other staphylococci were assessed in both mono- and combination therapy against MRSP biofilm. Quantitative assay results (p < 0.05) suggest fosfomycin alone and in combination with clarithromycin can significantly reduce biofilm formation. Morphological examination using scanning electron microscopy and atomic force microscopy further demonstrated the effectiveness of fosfomycin alone on biofilm formation on orthopaedic screws and mica sheets. Fabricated microfluidic assays were utilized to assess multiple concentrations of antimicrobial therapy against pre-formed biofilm under physiologically relevant conditions in a quick and repeatable manner. Results demonstrated the usefulness of microfluidic platforms in determining minimum biofilm eradication concentrations.

Recent studies of fcc metals with dense twins (~10 nm spacing) have revealed impressive mechanical properties, along with improved ductility and electrical conductivity in comparison to nanocrystalline metals with similar feature sizes. Many important fcc metals could benefit from these “nanotwinned” microstructures, however, not all fcc metals readily form such twins. The tendency of fcc metals to form twin boundaries is related to the twin boundary energy; those with low twin boundary energy, such as silver (Ag), easily form twins. Increasing twin boundary energy interferes with twin formation, to the point that in metals with high twin boundary energy, like aluminum (Al), twins are quite rare. This thesis focuses on the synthesis of nanotwinned Ag and Al via physical vapor deposition. Nanotwinned Ag is readily fabricated, however, a template approach had to be developed to induce twins in Al. The microstructures and their relationships to observed mechanical properties are also discussed. Grain boundaries interfere with dislocation transmission by posing a slip system discontinuity between grains. Twin boundaries are a special class of grain boundaries in which the grains on either side of the boundary are related by mirror symmetry. Twin boundaries inhibit dislocation transmission, providing strength in the same manner as grain boundaries. However, their symmetrical structure reduces the free volume and grain boundary energy. Accordingly, coherent twin boundaries are often more energetically stable than grain boundaries, and their coherency allows plasticity mechanisms to remain active under conditions where such mechanisms may be inhibited at grain boundaries. Hence, twin boundaries may provide a metal with unique combinations of high strength and good ductility, conductivity, and thermal stability.