Studying dynamics of proteins in their biological milieu such as water is interesting because of their strong absorption in the terahertz range that contain information on their global and sub-global collective vibrational modes (conformational dynamics) and global dynamical correlations among solvent water molecules and proteins. In addition, water molecules dynamics within protein solvation layers play a major role in enzyme activity. However, due to the strong absorption of water in the gigahertz-to-terahertz frequencies, it is challenging to study the properties of the solvent dynamics as well as the conformational changes of protein in water. In response, we have developed a highly sensitive megahertz-to-terahertz dielectric spectroscopy system to probe the hydration shells as well as large-scale dynamics of these biomolecules. Thereby, we have deduced the conformation flexibility of proteins and compare the hydration dynamics around proteins to understand the effects of surface-mediated solvent dynamics, relationships among different measures of interfacial solvent dynamics, and protein-mediated solvent dynamics based on the complex dielectric response from 50 MHz up to 2 THz by using the system we developed. Comparing these assets of various proteins in different classes helps us shed light on the macromolecular dynamics in a biologically relevant water environment. / Doctor of Philosophy / Proteins are complicated biomolecules that exist in all living creatures and they are, mostly, involved in building up structures and cell functions in various biological systems. Not only their existence but also their complex movements and dynamics are vital to cell functions in living beings. Until recently, their chemical functions and dynamics have been extremely challenging to investigate and track in their native environments. Thanks to various efforts by researchers all over the world to learn more about their convoluted behavior, new techniques have arisen to study these properties. We, as a part of this community, have been able to develop highly sensitive megahertz-to-terahertz dielectric spectroscopy system to probe proteins and other biomolecules dynamics in picosecond to microsecond range. Using our benchmark system, we have been able to map the detailed dynamical properties of biomolecules as well as their exclusive hydration shell characterizations. In this work, we gathered details about three well-known proteins and biomolecules by studying their dielectric responses. Thus, we have been able to discuss the movements, relaxation processes and hydration shell properties of these molecules in liquid water as their basic native environment.

Master of Science / Department of Food Science / Karen A. Schmidt / This research sets out to determine how varying factors such as electromagnetic fluid conditioning (EFC) and varying protein and sugar contents can influence yogurt and skim milks overall quality. EFC uses magnets to alter the chemical and physical properties of skim milk in these studies. EFC has many different treatment parameters to optimize before this new processing technology can be industrialized. Treatment parameters include voltage, exposure time, flow rate, and magnetic field direction, as studied in this research. Voltage was altered 10 and 30 V for 2 and 10 minutes. This study showed that at 2 minutes that skim milk was not altered, but at both voltages at 10 minutes some changes occurred to surface tension and color properties (L* and a* values) of skim milk. For both voltages at 10 minutes, it was always the negative direction that experienced the most changes. A separate EFC experiment was done that set out to determine if pretreating skim milk with EFC, would have an effect on yogurt’s quality post fermentation throughout storage. Results indicated that EFC does alter the yogurt’s properties, but not in a desirable manner. Results were undesirable changes to the product’s firmness and syneresis when compared to the control sample. Dielectric spectroscopy is a rapid method to determine if varying protein and sugar contents has compromised yogurt’s quality. In the dielectric spectroscopy study, this research wanted to determine if varying protein and sugar contents influenced dielectric properties enough to where a model could be developed to predict yogurt’s firmness. Both of these methods, EFC and dielectric spectroscopy, are novel technologies to the dairy industry where, both have been very minimally tested on yogurt. This research proved to be a stepping stone to open further doors to research in these areas due to results indicating changes but not pin-pointing exactly what is going on due to these technologies.

The relaxation characteristics of rubbery poly(ethylene oxide) [PEO] networks have been investigated as a function of network composition and architecture via dynamic mechanical analysis and broadband dielectric spectroscopy. A series of model networks were prepared via UV photopolymerization using poly(ethylene glycol) diacrylate [PEGDA] as crosslinker: variations in crosslink density were achieved either by the introduction of water in the prepolymerization reaction mixture, or by the inclusion of mono-functional acrylate such as poly(ethylene glycol) methyl ether acrylate [PEGMEA] or poly(ethylene glycol) acrylate [PEGA]. Copolymerization with mono-functional acrylate led to the insertion of flexible branches along the network backbone, and the corresponding glass-rubber relaxation properties of the copolymers (i.e., Tg, relaxation breadth, fragility) were a sensitive function of network architecture and corresponding fractional free volume. Relatively subtle variations in network structure led to significant differences in relaxation characteristics, and a systematic series of studies was undertaken to examine the influence of branch length, branch end-group, and crosslinker flexibility on viscoelastic response. Dielectric spectroscopy was especially useful for the elucidation of localized, sub-glass relaxations in the polymer networks: the imposition of local constraint in the vicinity of the crosslink junctions led to the detection of a distinctive fast relaxation process in the networks that was similar to a comparable sub-glass relaxation observed in crystalline PEO and in the confined regions of PEO nanocomposites. Gas permeation studies on the model PEGDA networks confirmed their utility as highly-permeable, reverse-selective membrane materials, and strategic control of the network architecture could be used to optimize gas separation performance. Dynamic mechanical and dielectric measurements have also been performed on a semicrystalline polyester, poly(trimethylene terephthalate) [PTT], in order to assess the influence of processing history on the resultant morphology and corresponding viscoelastic relaxation characteristics. Studies on both quenched and annealed PTT revealed the presence of a substantial fraction of rigid amorphous phase (RAP) material in the crystalline samples: dielectric measurements showed a strong increase in relaxation intensity above the glass transition indicating a progressive mobilization of the rigid amorphous phase with increasing temperature prior to crystalline melting.

The dynamic relaxation characteristics of Matrimid® (BTDA-DAPI) polyimide and several functionalized aromatic polyimides have been investigated using dynamic mechanical and dielectric methods. The functionalized polyimides were thermally rearranged to generate polybenzoxazole membranes with controlled free volume characteristics. All polyimides have application in membrane separations and exhibit three motional processes with increasing temperature: two sub-glass relaxations (ƴ and β transitions), and the glass-rubber (α) transition. For Matrimid, the low-temperature ƴ transition is purely non-cooperative, while the β sub-glass transition shows a more cooperative character as assessed via the Starkweather method. For the thermally rearranged polyimides, the ƴ transition is a function of the polymer synthesis method, thermal history, and ambient moisture. The β relaxation shows a dual character with increasing thermal rearrangement, the emerging lower-temperature component reflecting motions encompassing a more compact backbone contour. For the glass-rubber (α) transition, dynamic mechanical studies reveal a strong shift in Tα to higher temperatures and a progressive reduction in relaxation intensity with increasing degree of thermal rearrangement. The dynamic relaxation characteristics of poly(ether imide) and poly(methyl methacrylate) nanocomposites were investigated by dynamic mechanical analysis and dielectric spectroscopy. The nanoparticles used were native and surface-modified fumed silicas. The nanocomposites display a dual glass transition behavior encompassing a bulk polymer glass transition, and a second, higher-temperature transition reflecting relaxation of polymer chain segments constrained owing to their proximity to the particle surface. The position and intensity of the higher-temperature transition varies with particle loading and surface chemistry, and reflects the relative populations of segments constrained or immobilized at the particle-polymer interface. Dielectric measurements, which were used to probe the time-temperature response across the local sub-glass relaxations, indicate no variation in relaxation characteristics with particle loading. Nanocomposite studies were also conducted on rubbery poly(ethylene oxide) networks crosslinked in the presence of MgO or SiO2 nanoparticles. The inclusion of nanoparticles led to a systematic increase in rubbery modulus and a modest positive offset in the measured glass transition temperature (Tα) for both systems. The sizeable increases in gas transport with particle loading reported for certain other rubbery nanocomposite systems were not realized in these crosslinked networks.

The main objective of this thesis is to efficiently disperse and align SWNTs in two different polymer matrices to obtain an orthotropic composite whose strength, stiffness and electrical properties depend on the orientation of the SWNTs. The SWNTs are successfully dispersed and aligned in a polyimide matrix and a polymer blend of UDMA/HDDMA. In-situ polymerization under sonication is used to disperse the SWNTs in polyimide matrix and sonication is used to disperse SWNTs in the UDMA/HDDMA matrix. In both cases, an electric field is used to align the SWNTs in the polymer matrices. In the polyimide, the SWNTs are aligned by electrospinning technique, and in (UDMA/HDDMA) the SWNTs are aligned by applying an AC electric field, while the composite is cured.The electrical and mechanical properties of randomly dispersed SWNT polyimide composites and SWNT/UDMA/HDDMA composite are measured. The dielectric constant and storage modulus of SWNT polyimide composite increased with SWNT concentration. Low percolation (0.06 wt%) and an increase of 113% in storage modulus with 0.2 wt% SWNTs, both indicate good dispersion of SWNTs in the polyimide matrix. The dielectric constants, conductivity for the unaligned SWNT/UDMA/HDDMA composite are isotropic. The electrical and mechanical properties of the randomly dispersed SWNT polyimide composite and SWNT/UDMA/HDDMA composite are used as references when analyzing the aligned counter parts. Different characterization methods are used to assess the alignment of the SWNTs in the polyimide and (UDMA/HDDMA) matrices. A variety of characterization techniques, i.e. microscopy, Raman spectroscopy, electrical conductivity, dynamic dielectric spectroscopy and dynamic mechanical analysis, indicate preferential alignment of SWNTs in two types of polymers: Polyimide and (UDMA/HDDMA). Optical microscope images showed alignment of the SWNTs in the UDMA/HDDMA composite. Inspection of the Raman spectra on aligned SWNT polyimide composite fibers and aligned SWNT/UDMA/HDDMA composite indicates a decrease in the intensity of the tangential peak of the SWNT with increase in the polarizer angle. The difference in the perpendicular and parallel Raman peaks indicate preferential alignment of SWNTs in both the polymer matrices. In the aligned polyimide composite, percolation transition is at 0.2 wt% SWNT concentrations when dielectric constant is measured parallel to the aligned SWNTs. But percolation transition is at 0.65 wt% SWNT concentrations when dielectric constant is measured perpendicular to the aligned SWNTs. Electrical measurements on aligned SWNT polyimide and UDMA/HDDMA composite are highly anisotropic. In both cases, the dielectric constant values parallel to the direction of SWNT alignment are higher than the values perpendicular to the direction of SWNT alignment. To analyze the resulting anisotropy in the dielectric constant, Bruggeman's effective medium approach is used. The effective medium theory predicts the effective dielectric constant of a composite with aligned anisotropic inclusions. The effective dielectric constant, perpendicular to the aligned inclusions and parallel to the aligned inclusions is estimated. The dielectric constant values of aligned SWNT polyimide and aligned SWNT/UDMA/HDDMA composites are compared to the experimental results. Both the values from the theory and experiment show anisotropy in dielectric constant. The theory indicated that the dielectric constant parallel to the aligned inclusions is highly influenced by the dielectric constant of the inclusion and the dielectric constant perpendicular to the aligned inclusions is highly influenced by the dielectric constant of the polymer matrix. Results from the different characterizing techniques indicate that SWNTs are successfully aligned in the polyimide matrix and (UDMA/HDDMA) matrix by electrospinning technique and by an AC electric field respectively.

This thesis presents an experimental study of the influence of an external field and alignment upon a colloid of a liquid crystal (octycyanobiphenyl denoted 8CB) and a silica gel of aerosil nano-particles. The first techniques used was an AC-calorimetry (alternating current heating) and the systems under investigation were firstly put under the influence of a magnetic field at John Hopkins University in Baltimore by professor Leheny's group. The experiments revealed changes in transition temperatures, nematic range and critical coefficient that could account for what we called a 'memory' of the above mentioned structures. The second technique, dielectric spectroscopy, was applied to the same very densities of mixture s mentioned in the first paragraph. The samples were applied in one procedure an increasingly higher alternating electric field. An overall increase of the capacitance of the sample was measured. The second experiment was to reproduce the application of the magnetic field from the AC-calorimetry experiment now with an electric field. In dielectric spectroscopy case, an increase in transition temperature after the application of the procedure was revealed.

This thesis presents the investigation of the liquid crystal (LC) - particle suspensions. Particles from nano- to micro-size, spherical to two-dimensional shapes, with different functionality are dispersed into nematic and smectic phases. The aim is to create ordered nanoparticle (NP) assemblies and thereby modify the common properties of the liquid crystal, such as dielectric anisotropy and electro-optical, revealing any interaction between particles and LC properties. It is found that for concentrations (>0.5vol%), the ferroelectric NPs have increased the sensitivity of the nematic liquid crystal to the electric field through electro-optical responses, which is seen by an enhancement in the dielectric anisotropy. This could be induced by the coupling of the electrical dipole moments in the spherical NPs with the LC director field. The electro-optical properties of the chiral smectic (SmC*) phase (tilt angle Θ, switching time τ_s and spontaneous polarisation P_s) are found to be independent of the concentration and sizes of the doped NPs. The relaxation frequency f_R of the Goldstone mode is faster in the ferroelectric NPs suspensions of 2.0vol% compared to the paraelectric NPs. In the graphene oxide (GO) - nematic LC (5CB) suspensions, the small GO sizes of mean size 560 nm are more easily dispersible than larger flakes of 2.8 micro metre mean size. As the GO concentration is increased, each of the threshold voltage and splay elastic constant dramatically increases, reaching saturation at ≈1.0wt%. The field driven switching-on time is practically not affected, while the purely elastically driven switching-off time is strongly sped-up. Interestingly, thermotropic and lyotropic LC phases are exhibited in the GO-5CB suspensions when heating the thermotropic liquid crystal into its isotropic phase. The isotropic phase of 5CB acts as a solvent for the GO particles, forming a lyotropic nematic phase with largely reduced birefringence. It is found that the nematic to isotropic phase transition is shifted toward higher temperature for the GO-5CB system compared to the BaTiO3-5CB system. Dispersions of different sizes of GO flakes are prepared in isotropic and nematic fluid media. The dielectric relaxation behaviour of GO-dispersions was examined for a wide temperature range (25-60 ℃) and frequency range (100 Hz-2 MHz). The mixtures containing GO flakes were found to exhibit varying dielectric relaxation processes, depending on the size of the flakes and the elastic properties of the dispersant fluid. The relaxation frequencies in the isotropic media were lower compared to the nematic medium. Relaxation frequencies (~10 kHz) are observed in the GO-isotropic media, which are reduced as the size of the GO flakes are decreased, are anticipated to be inherited from GO flakes. However, the fast relaxations (~100 kHz) that are observed in the nematic suspensions could imply strongly slowed down molecular relaxation modes of the nematogenic molecules. Finally, the phase diagram of lyotropic LC as a function of the lateral dimensions of the GO flakes, their concentration, geometrical confinement configuration and solvent polarity was investigated. Polarising optical microscopy was used to determine isotropic-biphasic-nematic phase evolution. The confinement volume and geometry of the sample relative to the GO size are shown to be vital to the observation of the lyotropic phase. GO LCs have the potential for a range of applications from display technologies to conductive fibres. The confinement related LC phase transition is critical toward their applications. It is also found that the stability of the LC phase is higher for the solvent of higher dielectric constant.

The key features of dynamics of ultraslowing glass forming systems are their universality in diversity. Its origin is recognized as one of the greatest challenges of condensed matter physics and materials engineering in the XXI century. Similar phenomena are observed on approaching the glass transition in low molecular weight supercooled liquids, polymers, colloidal fluids as well as in solids, for instance in orientationally disordered crystals, spin glass-like magnetic, vortex glasses. Pre-vitreous dynamics is also proposed as a general reference for the category of complex liquids/soft matter systems. The upsurge of the primary relaxation time or related dynamical properties is the basic physical phenomena of the still mysterious previtreous behavior. This means a much more pronounced slowing down than the Arrhenius pattern observed far above the glass transition temperature. Portraying this behavior constitutes one of key checkpoints for theoretical models developed to unwind the glass transition puzzle. However, none of the aforementioned features can answer the understanding that governs the increase of relaxation time in liquids upon cooling. In this thesis we focus on the above questions studying the dynamics of some materials for which their molecules can retain a translational order being orientationally disordered between them upon cooling, which are referred to plastic phases or orientationally disordered (OD) crystalline phases. The work presented in this thesis potentially extends the knowledge of dynamics of OD phases and orientationally glasses (OG), a research topic which has gained interest during the last decades. Through this study, especial attention has been devoted to the phenomenological equations accounting to the temperature dependence of the mean relaxation time describing the orientational dynamics .The study was carried out by the use of BDS as well as two complementary experimental techniques. We show distortion-sensitive and derivative-based empirical analysis of the validity of leading equations for portraying the previtreous evolution of primary relaxation time. A new method for studying the dynamics of glass forming systems is introduced and the minimization procedure is validated and discussed. We present the results divided in two topics, the dynamics of the pure compounds and mixed crystals and the derivative analysis through different existing models. In the first topic we focus on the dynamics of the pure compounds and mixed crystals formed between cycloheptanol and cyclooctanol as well as the a-relaxation dynamics of 1-cyano-adamantane and its mixtures with 1-chloro-adamantane. The second topic is divided in two groups of models, linearized and non-linearized models. In the linearized models we show the application of the derivative based, distortion-sensitive analysis to liquid crystals (LC) and OD phases. We also discuss the results concerning to the cases of the olygomeric liquid epoxy resin (EPON828), neopentylalcohol and neopentylglycol mixture, isooctylcyanobiphenyl and propylene carbonate. The possible empirical correlations between one of the linearized models with the universal pattern for the high frequency wing of the loss curve for primary relaxation time for LCs and OD phases is also shown. In the final part we show that the form of the equation recently introduced by Mauro et al. does not allow a similar straightforward linearization procedure. Unlike the previous models, the involved parameters are not correlated with the slope and the intercept of a linear function. In order to solve this problem, we have introduced the concept of the enthalpy space. The evidences of the existence of crossovers as well as quantitative descriptions are discussed. We show also a new procedure for detecting the crossover in a very easy way. A new kind of crossovers which seems to be impossible to be detected by the classical Stickel transformation is presented. / La principal característica de la dinámica de sistemas vítreos viscosos, es su universalidad en la diversidad. Su origen es uno de los mayores desafíos de la física de la materia condensada y de la ingeniería de materiales en el siglo XXI. La fenomenología típica de las fases vítreas se observan cerca de la transición vítrea en líquidos subenfriados de bajo peso molecular, polímeros, fluidos coloidales, así como en los sólidos con fases orientacionalmente desordenadas. La imposibilidad de explicar las causas del gran aumento del tiempo de relajación al enfriar un líquido, constituye uno de los problemas más importantes no resueltos en materia condensada. Con el objetivo de dar respuesta a dicha interrogante, se han propuesto modelos termodinámicos y dinámicos que han resultado inconsistentes. En esta tesis nos centramos en dicha problemática, estudiando la dinámica orientacional de algunos materiales que al ser enfriados pueden conservar un orden traslacional mientras que se conserva el desorden orientacional de las moléculas que los forman. Dichas fases se conocen como fases plásticas u orientacionalmente desordenadas (OD). El trabajo presentado en esta tesis amplía el conocimiento de la dinámica de dichas fases, un tema de investigación cuyo interés ha aumentado durante las últimas décadas. Se ha dedicado una atención especial a las ecuaciones fenomenológicas que describen la dependencia del tiempo de relajación con la temperatura. El estudio se ha llevado a cabo mediante el uso de espectroscopía dieléctrica de banda ancha, así como mediante el uso de técnicas experimentales complementarias. Se ha introducido un nuevo método para el estudio de la dinámica de los sistemas que dan lugar a fases vítreas. El método ha sido validado y discutido. Los resultados de esta tesis se presentan divididos en dos temas, por un lado, la dinámica de compuestos puros y de los cristales mixtos y, por otro, el análisis mediante el método derivativo aplicado a los diferentes modelos físicos existentes. En el primer tema nos centramos en la dinámica de los compuestos puros y los cristales mixtos formados por cicloheptanol y ciclooctanol, así como la dinámica de la relajación alfa en 1-ciano-adamantano y sus mezclas con 1-cloro-adamantano. El segundo tema se divide en dos grupos de modelos, los modelos lineales y no lineales. En los modelos lineales se muestra la aplicación del procedimiento de derivativo en los cristales líquidos (CL) y las fases OD. También se discuten los resultados relativos a los casos de la resina líquida (EPON828), la mezcla neopentil-alcohol y neopentil-glicol, el carbonato de propileno, así como el CL isooctilcianobifenil. Se discute también la existencia de posibles correlaciones empíricas entre uno de los modelos lineales con el patrón universal para la parte de alta frecuencia de la curva de pérdidas dieléctricas de la relajación primaria para las fases CL y OD. En la parte final se muestra que la forma de la ecuación introducida recientemente por Mauro et al. no permite la linearización mediante el método derivativo. A diferencia de los modelos anteriores, los diferentes parámetros no están correlacionados con la pendiente y el origen de coordenadas de una función lineal. Para resolver este problema, hemos introducido el concepto del espacio entálpico. Se analiza también la existencia de cambios de comportamiento dinámicos y se aportan descripciones cuantitativas. Se muestra también un nuevo procedimiento para detectar los cambios dinámicos de una manera fácil, que permite incluso detectar aquéllos que son obviados mediante el método clásico de Stickel.

This work investigates how HV impulses affect the behavior of partial discharge (PD) activity and the low voltage dielectric response of oil-impregnated paper insulation. It also investigates how the change in the PD activity is related to the degradation level of oil-impregnated paper insulation. In order to accomplish these objectives, the ageing were done under three different electrical stress conditions, i.e. HV impulses following an early stage 50 Hz AC PD activity, a prolonged PD activity at a 50 Hz AC stress alone, and a combination of HV impulses and a prolonged PD activity at a 50 Hz AC stress. In order to predict the level of deterioration caused by each ageing stress condition, the dielectric spectroscopy (DS) measurements in a frequency range of 1.0 mHz to 1.0 kHz were performed before and after subjecting a test object to each of the ageing stress conditions.      The investigations were mainly done on the test samples consisting of a cavity deliberately introduced between the layers of oil-impregnated paper. Additionally, the investigation about the effect of HV impulses alone on the DS results was done on aged oil-impregnated paper transformer bushing.      The PD experimental results presented in this thesis indicate that HV impulses below the impulse breakdown stress following an early stage AC PD activity will neither cause a significant change in phase resolved partial discharge (PRPD) patterns nor damage oil-impregnated paper insulation to a level that can be noticed with visual observations. On the other hand, a prolonged PD activity at a 50 Hz AC stress can cause the change in PRPD patterns by decreasing the total PD charge and the number of PD pulses, but cannot quickly damage the oil-impregnated paper insulation as it would do when it is combined with HV impulses. In addition to that, the results show that the combination of both, HV impulses and a prolonged PD activity at a 50 Hz AC stress can cause a high drop in the PD parameters (total PD charge and number of PD pulses).       The DS results show that HV impulses below the impulse breakdown stress following an early stage 50 Hz AC PD activity will not cause a significant increase in the real part of the complex capacitance and in the dissipation factor as they will do when they are combined with a prolonged PD activity at a 50 Hz AC stress. Further, the dielectric spectroscopy results obtained every three hours during the ageing of oil-impregnated paper insulation by a prolonged PD activity at an AC stress show that the dissipation factor will increase, but the PD parameters (total PD charge and the repetition rate) will decrease with time of PD application. For a case of the aged oil-impregnated paper transformer bushing, HV impulses of amplitudes up to 200 kV did not result in the change in the dissipation factor curve before removing insulating oil from the bushing. However, after removing about 2.5 liters of insulating oil from the bushing, HV impulses resulted in the change in the dissipation factor curve. The magnitudes of the dissipation factor curves appeared to be much higher in the middle frequencies region, i.e. the frequencies between 10 mHz and 100 Hz. After refilling the bushing with the same insulating oil, the loss peak shifted towards the higher frequencies.      To understand how the ageing by-products initiated by PDs in the small cavity can modify the geometry of oil-impregnated paper insulation; the model of oil-impregnated paper insulation, comprising of a small cavity, was implemented in Finite Element Method (FEM) software (COMSOL Multiphysics 4.2a). The comparison between the simulation and experimental results show that PD by-products will result in two zones, i.e. aged and unaged zones, and the aged zone will grow with time of PD application; thereby increasing the dissipation factor. On the other hand, in order to interpret  the change in the dissipation factors for the dielectrics in aged oil-impregnated paper transformer bushing after had been exposed to HV impulses, a model of a part of the condenser body (oil-paper insulation) was also implemented in the FEM software (COMSOL Multiphysics 4.2a). To model a condition of low insulating oil level in the bushing, a part of oil subdomains was replaced with the air dielectric properties. A comparison between the simulation and experimental dissipation factor curves indicate that HV impulses will produce the by-products (ions), which will increase the conductivity of air when the bushing has low insulating oil level. On refilling the bushing with the same insulating oil, the insulating oil will take these ions and the reactions between the aged insulating oil by-products (such as acids) and the ions, may produce more ions, thereby increasing further the conductivity of the insulating oil. / <p>QC 20140303</p>

Kyoto University (京都大学) / 0048 / 新制・課程博士 / 博士(工学) / 甲第15371号 / 工博第3250号 / 新制||工||1489(附属図書館) / 27849 / 京都大学大学院工学研究科機械理工学専攻 / (主査)教授 中部 主敬, 教授 小寺 秀俊, 教授 田畑 修 / 学位規則第4条第1項該当