Graphene, a two-dimensional nanomaterial, has been given much attention since it was first isolated in 2004. Driving this intensive research effort are the unique properties of this one atom thick sheet of carbon, in particular its electrical, thermal and mechanical properties. While the technological applications proposed for graphene abound, its low-cost production in large scales is still a matter of interrogation. Simple methods to obtain few-layered graphene flakes of high structural quality are being investigated with the exfoliation of graphite taking a prominent place in this arena. From the many suggested approaches, the most promising involve the use of liquid media assisted by intercalants and shear forces acting on the basal layers of graphite. In this thesis, it is discussed how a novel method was developed to produce flakes with consistent lateral dimensions that are also few-layered and retain the expected structural and chemical characteristics of graphene. Here, the source material was a commercially available graphiteintercalated compound, also known as expandable graphite. Several exfoliation-inducing tools were investigated including the use of blenders, homogenizers, and ultrasonic processors. To aid in this process, various solvents and intercalants were explored under different reactive conditions. The more efficient approach in yielding defect-free thin flakes was the use of thermally expanded graphite in boiling dimethylformamide followed by ultrasonic processing and centrifugation. In parallel, a method to fraction the flakes as a function of their lateral size was developed. Ultimately, it was possible to obtain samples of graphene flakes with a lateral dimension of a few micrometers (<5 μm) and thickness of 1-3 nm (i.e. <10 layers).

Thermally expandable microspheres are polymeric core/shell particles in which a volatile hydrocarbon is encapsulated by a thermoplastic shell. When these microspheres are heated, they expand and increase their volume dramatically. This volume increase is retained upon cooling, leading to a density reduction from around 1100 kg m-3 to about 30 kg m-3. Since the development in the early 1970´s, microspheres have been used extensively by the industry as a foaming agent or light weight filler. In this thesis, microspheres with a poly(acrylonitrile-co-methacrylonitrile) shell have been synthesized through free radical suspension polymerization. The microspheres have been characterized with respect to particle morphology and expansion properties in order to deepen the understanding of the microspheres. It was found that the monomer feed ratio and the polymerization temperature are very important parameters with respect to the expansion properties. Excellent expansion could only be accomplished when polymerizing at 62 °C, with the acrylonitrile feed, fAN, being around 60 mol%, even though core/shell microspheres are formed over a much wider range of fAN. Furthermore, no expansion was achieved when polymerizing at 80 °C, even though no noticeable differences were found, compared to the corresponding sample polymerized at 62 °C. It was also shown that the expansion properties can be modified by replacing the encapsulated hydrocarbon by another hydrocarbon with a different boiling point. Not only is the boiling point important, the structure of the hydrocarbon is also important. Isooctane which is highly branched was found to give superior expansion compared to linear or cyclic hydrocarbons having a similar boiling point. Crosslinking of the polymer shell has proven to be very important for the expansion properties. Both the amount and the structure of the crosslinker are important parameters. Especially the maximum expansion can be improved by the crosslinking of the polymer shell. This originates in an increase in the shape persistence of the expanded microspheres at elevated temperatures. By the combination of crosslinkers that are incorporated separately into the polymer shell, the onset temperature of expansion can be increased significantly. Finally, the surface of microspheres has been modified by grafting poly(glycidyl methacrylate) from the surface by ARGET ATRP. Given that the reaction conditions are appropriate, such modifications can be performed with only limited effects on the expansion properties of the microspheres.

Thesis (M.S.)--Ohio University, June, 1988. / Title from PDF t.p.

Thesis (Ph. D.)--University of Missouri-Columbia, 2003. / Typescript. Vita. Includes bibliographical references (leaf 177). Also available on the Internet.

Thesis (Ph. D.)--University of Missouri-Columbia, 2003. / Typescript. Vita. Includes bibliographical references (leaf 177). Also available on the Internet.

No description available.

Networking multiple "smart" displays together is an affordable way of creating large high-resolution display systems. In this work I propose a new structure and data distribution paradigm for displays of this nature. I model my work on the peer-to-peer style of content distribution, as opposed to the traditional client-server model for this kind of system. In taking a peer-to-peer approach, I present a low-cost and scalable system without the inherent constraints imposed by the client-server model. I present a new class of applications specifically designed for this peer-to-peer style of display system, and provide an easy-to-use framework for developers to use in creating this type of system. / Graduate / 0984

Networking multiple "smart" displays together is an affordable way of creating large high-resolution display systems. In this work I propose a new structure and data distribution paradigm for displays of this nature. I model my work on the peer-to-peer style of content distribution, as opposed to the traditional client-server model for this kind of system. In taking a peer-to-peer approach, I present a low-cost and scalable system without the inherent constraints imposed by the client-server model. I present a new class of applications specifically designed for this peer-to-peer style of display system, and provide an easy-to-use framework for developers to use in creating this type of system. / Graduate / 0984

After three decades of commercialization, graphite remains the preferred active material for intercalation-type Li-ion battery anodes. Still, the characterization of staging continues to be elusive at the sub-micro- and nano-scales, the typical dimensions of graphite crystallites. Here, the intercalation of Al-based anions in graphitic materials was studied using X-ray powder diffraction (XRD) and Raman spectroscopy. While, in the first case, the analysis was done ex-situ and in mm3-samples, a more localized view was provided by the laser probe which could, furthermore, interrogate the electrochemical process in real-time (in-situ). To do this, an electrochemical cell for Raman studies was custom-made for Al batteries working with non-aqueous electrolytes. Two C materials were used: natural graphite (NG) and processed expandable graphite (EG). Owing to the smaller flake size, higher graphitization degree and larger crystallites of the NG, the Al/NG cells exhibited better performance than the Al/EG ones. Interestingly, discrepancies were observed in the stage numbers estimated from XRD and Raman. These were thought to arise from the, respectively, long- and short-range atomic order scales that are analyzed by those two techniques. To confirm this, in-situ Raman multi-point studies were performed. The results show the presence of domains with mixed stage graphite intercalation when the cells were fully charged, explaining the staging discrepancies.

Termiskt expanderbara mikrosfärer är ihåliga polymera partiklar i vilka en flyktig drivgas har kapslats in. När mikrosfärerna upphettas förgasas drivgasen, vilket ökar trycket i mikrosfärerna så att de expanderar och deras volym ökar avsevärt. Denna unika egenskap gör att expanderade mikrosfärer har en låg densitet och är lämpliga för applikationer där låg vikt är väsentligt, och för att förändra ytstrukturer, så som i till exempel konstläder och textiler. Syftet med denna studie har varit att utveckla ett stabilt system för suspensionspolymerisation för att ge en liten mikrosfär (~20 μm efter expansion) som expanderar vid relativt höga temperaturer. Detta har uppnåtts genom att undersöka effekterna av förändringar i stabiliseringssystemet. Komponenterna som varierades var mängden silika (LX), kondensationsoligomeren mellan adipinsyra och dietanolamin (KO), olika formuleringar och mängd av dilauryl peroxid, samt mängden m(III)nitrat. Ytterligare tester gjordes runt effekten av tvärbindning, tillsats av monomeren metyl metakrylat (MMA), samt tillsats av salt (NaCl). Ett stabilt system för polymerisation i 1L-skala med en homogen dispersion uppnåddes med en av dilauryl peroxide formuleringarna tillsammans med en större mängde LX och KO. Studien visar även att kvoten mellan LX och KO har en signifikant effekt på systemets stabilitet och att mängden av både LX och KO påverkar partikelstorleken. / Thermally expandable microspheres are hollow polymeric particles in which a blowing agent has been encapsulated. Upon heating the blowing agent will vaporize, causing the internal pressure to increase, thereby expanding the microspheres. This unique expandable property reduces the density of the microspheres tremendously and makes them excellent for many applications, as for example as light weight fillers and to alter surface textures, such as in artificial leather and textiles. The purpose of this study has been to develop a viable system for the suspension polymerization of a small microsphere (~20 μm when expanded) expanding at fairly high temperatures. This has been accomplished by investigating the effect of changes in the stabilization system. Components of the stabilization system that have been varied were the amounts of silica (LX), condensation oligomer from adipic acid and diethanol amine (KO), and m(III)nitrate, as well as different formulations and amounts of the initiator dilauryl peroxide. Additional tests were performed concerning the effect of the crosslinking, adding the monomer methyl methacrylate (MMA), and the addition of salt (NaCl). A system for polymerization in 1L-scale was accomplished where it was found that one of the dilauryl peroxide formulations together with a higher amount of LX and KO provided a stable system giving homogeneous dispersions in which the microspheres have the desired expansion properties. Also, the ratio between LX and KO had a significant effect on the stability of the system and the amount of both LX and KO affects the particle size.