京都大学 / 新制・課程博士 / 博士(工学) / 甲第23181号 / 工博第4825号 / 新制||工||1754(附属図書館) / 京都大学大学院工学研究科都市環境工学専攻 / (主査)教授 高岡 昌輝, 教授 橋本 訓, 准教授 大下 和徹 / 学位規則第4条第1項該当 / Doctor of Philosophy (Engineering) / Kyoto University / DFAM

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Bei der inversen Vulkanisation werden Polymere mit hohem Schwefelgehalt aus Alkenen und elementarem Schwefel hergestellt. Die Kontrolle über Eigenschaften wie die Molmasse oder die Löslichkeit der Polymere ist nicht etabliert. Bestehenden Strategien mangelt es an Vorhersagbarkeit oder sie erfordern große Variationen der Zusammensetzung der Polymere. Systematische Prinzipien zur Variation der Polymereigenschaften sind daher gesucht, um eine gezielte Materialentwicklung zu ermöglichen. Wir berichten über die inverse Vulkanisation von Norbornenylsilanen (NBS) mit einer unterschiedlichen Anzahl hydrolysierbarer Gruppen am Siliziumatom. Die inverse Vulkanisation von NBS-Mischungen mit anschließender Polykondensation ergab lösliche Copolymere mit hohem Schwefelgehalt (50 Masse-% S) und mit kontrollierbarer mittlerer Molmasse (MW), Polydispersität (Đ), Glasübergangstemperatur (TG) oder Null-Scher-Viskosität (η0). Die Polykondensation wurde in der Schmelze mit HCl als Katalysator durchgeführt, so dass kein Lösungsmittel erforderlich war. Die Reinigung durch Fällung ergab Polymere mit stark reduziertem Anteil an niedermolekularen Spezies.

It has been previously shown that micelles formed from surfactants with chiral head groups serve to induce a chiral reaction medium, leading to enhanced enantioselectivities in the reaction products. This utilization of chiral surfactants will offer an economical alternative to traditional chial solvents while simultaneously reducing organic waste. We have successfully dimethlated S-leucinol in an 85% yield, and have synthesized a hydrocarbon-based surfactant with this molecule as a head group. We have also formed polymeric surfactants that have polydimethylsiloxane as the hydrophobic portion with the (S)-dimethylleucinol as a head group. Tests of the solubility of these surfactants have been conducted. We also have done a reduction of a ketone in 95% ethanol and 1.3%-4% (w/v) surfactants, resulting in ee. 5.4%-6.6%.

Biogas, a gaseous mixture produced during decomposition of organic matter, is a renewable, easily generated and common byproduct of anaerobic digestion at wastewater treatment plants (WWTP), landfills and agricultural operations. There is growing interest in researching and utilizing the energy potential associated with its combustion. Siloxanes, a family of volatile organic silicon compounds, pose large impediments to biogas usage due to the formation and precipitation of silicon dioxide within combustion devices. Removal of siloxanes prior to combustion is therefore a growing endeavor. Research was performed to synthesize a representative gas stream produced from anaerobic digesters within WWTP. Methane, carbon dioxide and hydrogen sulfide were combined with humidity and gaseous siloxane in levels characteristically seen exiting anaerobic digesters. A methanol impinger train was utilized to sample the biogas composite. Gas chromatography-mass spectrometry (GC-MS) was used to determine gas-phase siloxane concentrations in the gas stream effluent for the purposes of confirming the generation of a consistent and reproducible biogas stream. / Master of Science

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The vast majority of commercial gas separation membrane systems are polymeric because of processing feasibility and cost. However, polymeric membranes designed for gas separations have been known to have a trade-off between permeability and selectivity as shown in Robeson's upper bound curves. The search for membrane materials that transcend Robeson's upper bound has been the critical issue in research focused on membranes for gas separation in the past decade. To that end, many researchers have explored the idea of mixed matrix membranes (MMMs). These membranes combine a polymer matrix with inorganic molecular sieves such as zeolites. The ideal filler material in MMMs should have excellent properties as a gas adsorbent or a molecular sieve, good dispersion properties in the polymer matrix of submicron thickness, and should form high quality interfaces with the polymer matrix. In order to increase gas permeance and selectivity of polymeric membranes by fabricating MMMs, we have fabricated mixed matrix membranes using carbon nanotubes (CNTs) and nano-sized mesoporous silica. Mixed matrix membranes containing randomly oriented CNTs showed that addition of nanotubes to a polymer matrix could improve its selectivity properties as well as permeability by increasing diffusivity. Overall increases in permeance and diffusivity for all tested gases suggested that carbon nanotubes can provide high diffusivity tunnels in the CNT within the polymer matrix. This result agreed well with molecular simulation estimations. In order to prepare ordered CNTs membranes, we have developed a simple, fast, commercially attractive, and scalable orientation method. The oriented CNT membrane sample showed higher permeability by one order of magnitude than the value predicted by a Knudsen model. This CNT membrane showed higher selectivities for CO₂ over other gas molecules because of preferential interaction of CO₂ with the amine functionalized nanotubes, demonstrating practical applications in gas separations. Recently, mesoporous molecular sieves have been used in MMMs to enhance permeability or selectivity. However, due to their micrometer scale in particle size, the composite membrane was extremely brittle and tended to crack at higher silica loading. In this study, we have developed fabrication techniques to prepare MMMs containing mesoporous MCM-41 nanoparticles on the order of ~50 nm in size. This smaller nanoparticle lead to higher polymer/particle interfacial area and provides opportunity to synthesize higher loading of molecular sieves in polymer matrix up to ~80 vol%. At 80 vol% of nano-sized MCM-41 silica loading, the permeability of the membrane increased dramatically by 300 %. Despite these increases in permeability, the separation factor of the MMMs changed only slightly. Therefore, these nanoscale molecular sieves are more suitable for commercialization of MMMs with very thin selective layers than are micro-sized zeolites or molecular sieves. / Ph. D.

Polyimides epitomize one of the most versatile high-performance engineering polymers. Polyimides are inherently mechanically robust, chemically inert, and thermooxidatively stable to 400+ °C depending on their chemical structure, enabling their function in numerous aerospace, electronic, medical, and flame-retardant applications. Polyimides can be highly modular even within synthetic limitations, which promotes and sustains innovative research. One recent interest concerns the innovation of fire suppression foams. Aqueous film-forming foams (AFFFs) are regularly sought when engaging liquid fuel (gasoline, jet fuel) fires. AFFFs utilize perfluorinated compounds (PFCs) like perfluorooctanesulfonic acid (PFOS) and perfluorooctanoic acid (PFOA), which exhibit toxicity, bioaccumulation, and persistence in the environment resulting in the presence of fluorosurfactant chemicals in environments either through direct or secondary exposure via chemical migration. Recently, the USEPA has even detected PFAS in drinking water at hundreds of military training facilities and civilian airports. While fluorinated compounds provide desirable thermooxidative stability and excellent fire retardancy, the environmental impact imposed by these chemicals strongly encourages research that targets the complete removal of PFCs in conventional formulations. This thesis focuses on the fundamental development of water-soluble sulfonated polyimide (sPI) and poly(amic acid) (sPAA) systems for next-generation polymer-based fire suppression foams. The use of sulfonated monomers and poly(amic acid) salt formation enables tunable structures and water solubilities. The polymers maintain competitive thermal stabilities to conventional polyimides and, when combined with readily available, non-toxic surfactants (SDS), produce stable foams. The MIL-F-24385F performance requirement evaluates foam quality/stability, drainage time, and burnback resistance to access viability and provides comparison to other systems; preliminary testing shows that sPI/sPAA formulations perform well. Solution rheology offers insights into fundamental scaling relationships of specific viscosity vs. concentration in both salt and salt-free solution that are important to future foam development. Additionally, the structural nature of the sPIs/ sPAAs allows for their modification with phosphonium moieties or siloxanes, which are slated to have positive effects on performance. Overall, these sPIs and sPAAs provide a promising platform for the future direction of fire suppression foams. / Master of Science / High-performance polymers are used in the most demanding of engineering applications. Polyimides represent one of the most versatile high-performance polymers. Polyimides are mechanically strong, chemically inert, and resistant to extreme temperatures depending on their chemical structure, allowing their use in numerous aerospace, electronic, medical, and flame-retardant applications. Polyimides are synthetically versatile, which enables the discovery of new uses after decades of research. One new targeted application is fire suppression foams. Aqueous film-forming foams (AFFFs) are the standard when battling liquid fuel (gasoline, jet fuel) fires. AFFFs contain perfluorinated compounds (PFCs), which are toxic and persist in the environment; they migrate easily to affect indirectly exposed ecosystems. Recently, the USEPA has even detected PFAS in drinking water at hundreds of military training facilities and civilian airports. While AFFFs with PFCs are highly effective, replacement materials are needed. This thesis focuses on the fundamental development of water-soluble sulfonated polyimide (sPI) and poly(amic acid) (sPAA) systems for fire suppression foams. The polymers remain thermally stable, and when combined with readily available surfactants (SDS), produce stable foams. Preliminary fire testing shows that sPI/sPAA formulations perform well against military specifications. Solution rheology (study of flow) explores the solution behavior of sPI, which offers insights into fundamental concentration-viscosity relationships that are important to future foam development. Additionally, the structural nature of the sPIs/ sPAAs allows for their modification with phosphonium groups or siloxanes, which changes their characteristics. Overall, these sPIs and sPAAs are initially promising for the future direction of fire suppression foams.

Ce travail de thèse porte sur la synthèse de cristaux liquides semiconducteurs, obtenus à partir de molécules associant des unités à caractère donneur-accepteur-donneur (DAD) et substituées aux deux extrémités par une chaîne oligosiloxane. Le fort pouvoir microségrégeant des oligosiloxanes a pour effet de stabiliser, pour l'ensemble des matériaux, une phase smectique unique (désordonnée) sur une gamme de température remarquablement large (>300°C). Pour des raisons de géométrie, les partie D et A doivent se nanostructurer en phase smectique pour conduire à la formation d'une structure à lamelles D/A alternées, favorable pour des applications photovoltaïques. Les matériaux ont fait l'objet de nombreuses études, notamment pour caractériser leurs propriétés structurales, photophysiques et de transport de charge. Ces matériaux ont ainsi révélé l'existence d'un transport de charge ambipolaire avec des valeurs de mobilité de l'ordre de 10-3 cm2/Vs en phase smectique. Les tests préliminaires de conversion photovoltaïque montre l'existence d'un très faible rendement, qui démontre l'importance d'un travail ultérieur d'optimisation des conditions de dépôts et du contrôle de l'orientation des couches smectiques sur les substrats.

The synthesis of 2,4,6,8-Tetramethylcyclotetrasiloxane (D4H), and Poly(methylhydrosiloxane) (PMHS) average molecular weight 1700-3200 g/mol, were functionalized with different repeat units of methoxy polyethylene glycol (PEG) (n = 8,12,17). These compounds act as polymer electrolytes with a backbone of siloxane and they were prepared via hydro-silylation reaction to be functionalized with different molecular weights of Ally-PEG. The compounds were confirmed by FT-IR, 1H-NMR and 13C NMR spectroscopy. A hydro-silylation reaction between the functionalized AllyPEG of different molecular weights produced four compounds with a low glass transition temperature that could improve comb like polymer electrolytes conductivity by reducing crystalline phase of PEO. Another way to increase the percentage of the amorphous phase of PEO is to blend it with other polymers. The blending method is considered to be an important method to improve the ionic conductivities and dimensional stability of polymer electrolytes. The main advantages of the blend systems are the simplicity of preparation and the ease to control the physical properties. A high molecular weight of poly 2- vinyl pyridine (Mw=200,000) was added to improve the dimensional stability. Differential scanning calorimetry (DSC) thermal analysis shows that all the blend systems will exhibit an increase in the glass transition temperature by increasing the salt content. The other novel synthesis of polymer electrolytes are triglyme borane and borosilicate. They were synthesized via hydro-boration. These compounds were characterized and confirmed by FT-IR, 1H-NMR 13C NMR spectroscopy. The ionic conductivity of both systems, pure and blend, of different compositions were determined at four temperatures i.e. 25°C, 40°C, 55°C and 70°C. A maximum ionic conductivity value of the siloxane blend is 9.1x10-4 S cm-1 and the pure triglyme borane is 2.14x10-3 S cm-1 at ambient temperature. The ratios of ethylene oxide to lithium salt of siloxane blend and pure triglyme borane were 10:1 and 35:1 respectively. These ratios were the highest conductivity obtained in all the electrolyte systems. The ionic conductivity increases with increasing temperature and salt content to reach optimum concentration. This behavior results in ionic transport, which is supported by the segmental motion of the polymer matrix host.