351 |
Compositional depth profiling : maximising spatial resolution through minimising sample damageWilkinson, David K. January 1997 (has links)
No description available.
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352 |
Thin films of flexible chain moleculesCallaway, Martin James January 1995 (has links)
No description available.
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353 |
Enhancement of fidelity of surface measurement systemsWang, W. L. January 1995 (has links)
No description available.
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354 |
A study of near-field optical imaging using an infrared microscopeQuartel, John Conrad January 1999 (has links)
No description available.
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355 |
Investigating probe-sample interactions in NSOMInglis, William January 2002 (has links)
No description available.
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356 |
Studies of reversed phase high performance liquid chromatography (RP-HPLC) stationary phasesWatson, Richard Charles January 1996 (has links)
No description available.
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357 |
The applications of SPM for pharmaceutical analysis of crystalline drugsDanesh, Ardeshir January 2000 (has links)
No description available.
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358 |
The dissolution of organic compoundsSanders, Giles January 1996 (has links)
No description available.
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359 |
Hot-wire chemical vapour deposition of carbon Nanotubes.Cummings, Franscious Riccardo January 2006 (has links)
<p>In this study we report on the effect of the deposition parameters on the morphology and structural properties of CNTs, synthesized by means of the hot-wire chemical vapour deposition technique. SEM, Raman and XRD results show that the optimum deposition conditions for the HWCVD synthesis of aligned MWCNTs, with diameters between 50 and 150 nm and lengths in the micrometer range are: Furnace temperature of 500 º / C, deposition pressure between 150 and 200 Torr, methane/hydrogen dilution of 0.67 and a substrateto- filament distance of 10 cm.</p>
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360 |
Investigating self-assembled protein nanotubes using atomic force microscopyNiu, Lijiang January 2009 (has links)
Self-assembled protein nanotubular materials are attractive as putative building blocks for a variety of applications. Knowledge of the three-dimensional structures and the physical properties of these protein nanotubes then becomes a prerequisite for their use in rational materials design. The main purpose of the work presented in this thesis is to investigate both the structural and mechanical properties of protein nanotubes utilizing atomic force microscopy (AFM). Several different protein nanotubes will be used as exemplars to develop AFM methods. AFM is capable of both visualizing and monitoring dynamic processes. Within this thesis, not only could the change in morphology of protein nanotubes be visualized by AFM, but also changes in their mechanical properties were monitored as dynamic processes. For example, changes in the morphology (in chapter 3) and flexibility (in chapter 4) of lysozyme fibrils during fibrillization were investigated. Chapters 4 to 6 describe a range of different methods to obtain the mechanical properties of protein nanotubes: the persistence length method (chapter 4), the adhesive interaction method (chapter 5) and the bending beam method (chapter 6). All of these had their own advantages. However, each method was found only to be suitable for protein nanotubes with elasticities within a defined range. The protein nanotubes investigated by AFM in the thesis included Salmonella flagellar filaments, lysozyme fibrils and diphenylalanine (FF) nanotubes. All of the investigated protein nanotube structures had Young’s moduli lying between that of gelatin and bone. This highlights their potential, in terms of mechanical properties, for a range of applications in drug-delivery systems and tissue-engineering scaffolds. In future, if a database of mechanical properties of protein nanotubes could be built up using the AFM methods developed and utilized within this thesis, the development of the applications of protein nanotubes will be accelerated, as the right protein nanotubes will be selected for appropriate applications.
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