Thesis (Ph. D.)--Civil and Environmental Engineering, Georgia Institute of Technology, 2006. / Yiacoumi, Sotira, Committee Chair ; Tsouris, Costas, Committee Co-Chair ; Pavlostathis, Spyros, Committee Member ; Tannenbaum, Rina, Committee Member ; Sherrill, David, Committee Member.

The behavior of 2D materials has become of great interest in the wake of development of electrochemical double-layer capacitors (EDLCs) and the discovery of monolayer graphene by Geim and Novoselov. This study aims to analyze the response variance of 2D electrode materials for EDLCs prepared through the liquid-phase exfoliation method when subjected to differing conditions. Once exfoliated, samples are tested with a series of structural characterization methods, including tunneling electron microscopy, atomic force microscopy, Raman spectroscopy, and x-ray photoelectron spectroscopy. A new ionic liquid for EDLC use, 1-butyl-1-methylpyrrolidinium tris(pentafluoroethyl)trifluorophosphate is compared in performance to 6M potassium hydroxide aqueous electrolyte. Devices composed of liquid-phase exfoliated graphene / MoS2 composites are analyzed by concentration for ideal performance. Device performance under cold extreme temperatures for the ionic fluid is presented as well. A brief overview of by-layer analysis of graphene electrode materials is presented as-is. All samples were tested with cyclic voltammetry, galvanostatic charge-discharge, and electrochemical impedance spectroscopy, with good capacitive results. The evolution of electrochemical behavior through the altered parameters is tracked as well.

In this research we have investigated electrochemical and impedance characteristics of liquid phase exfoliated graphene electrodes. The exfoliated graphene electrodes were characterized in Electrochemical Double Layer Capacitors (EDLCs) geometry. Liquid phase exfoliation was performed on bulk graphite powder in order to produces few layer graphene flakes in large quantities. The exfoliation processes produced few layer graphene based materials with increased specific surface area and were found to have suitable electrochemical charge storage capacities. Electrochemical evaluation and performance of exfoliated graphene electrodes were tested with Cyclic Voltammetry, constant current charging discharging and Electrochemical Impedance Spectroscopy (EIS) at ambient conditions. We have used several electrolytes in order to evaluate the effect of electrolyte in charge storage capacities. Specific capacitance value of ~ 47F/g and ~ 262F/g was measured for aqueous and ionic electrolytes respectively. These values are at least an order of magnitude higher than those obtained by using EDLC's electrodes fabricated with the bulk graphite powder. In addition these EDLC electrodes give consistently good performance over a wide range of scan rates and voltage windows. These encouraging results illustrate the exciting potential for high performance electrical energy storage devices based on liquid phase exfoliated graphene electrodes.

Abstract The dissertation considers the time fractional diffusion equation (TFDE) with the Dirichlet boundary condition in the sub-diffusion case, i.e. the order of the time derivative is α ∈ (0,1). In the thesis we have studied the solvability of TFDE by the method of layer potentials. We have shown that both the single layer potential and the double layer potential approaches lead to integral equations which are uniquely solvable. The dissertation consists of four articles and a summary section. The first article presents the solution for the time fractional diffusion equation in terms of the single layer potential. In the second and third article we have studied the boundary behaviour of the layer potentials for TFDE. The fourth paper considers the spline collocation method to solve the boundary integral equation related to TFDE. In the summary part we have proved that TFDE has a unique solution and the solution is given by the double layer potential when the lateral boundary of a bounded domain admits C1 regularity. Also, we have proved that the solution depends continuously on the datum in the sense that a nontangential maximal function of the solution is norm bounded from above by the datum in L2(ΣT). If the datum belongs to the space H1,α/2(ΣT), we have proved that the nontangential function of the gradient of the solution is norm bounded from above by the datum in H1,α/2(ΣT).

Ce travail porte sur l’étude électrochimique de l’interface formée par une électrode d’or plongée dans le liquide ionique 1-butyl-3-methylimidazolium dicyanamide ou [BMIm][DCA]. Ce liquide ionique a été sélectionné car outre sa conductivité intrinsèque, il permet de solubiliser aisément des sels de métaux de transition à température ambiante. Les liquides ioniques sont, par définition, des sels liquides en dessous de 100 °C et la plupart d’entre eux sont liquides à température ambiante. Etant donné que les liquides ioniques sont constitués majoritairement d’ions, la description de la double couche électrique telle que décrite dans les électrolytes traditionnels doit être reconsidérée.<p>Deux grandes thématiques fondamentales sont abordées dans ce travail :le comportement de la double couche électrique à l’interface liquide ionique / Doctorat en Sciences / info:eu-repo/semantics/nonPublished

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This master thesis deals with supercapacitors based on electrical double layer and proper carbon electrodes for this type of supercapacitors. In theoretical part of work is described theory of supercapacitors, energy storage principles and their properties. In the next part are described carbon materials, their properties and electrochemical methods of measurements that we used. In the experimental part is described preparation of electrodes, results and conclusion.

<p>Urea has been widely used as a crop fertilizer to increase crop yield. The low nutrient use efficiency (NUE) of urea, however, is a challenge. Coated fertilizers are considered a solution not only for enhancing the NUE but also for alleviating soil and water pollution. In this paper, the physical properties of coated fertilizers were analyzed, including their particle size distribution, fracture force, thermal behavior, envelope density, and apparent density (regular fertilizer: pure urea and the Anderson 12-6-6; slow release fertilizer: Osmocote 14-14-14, the Anderson 18-6-12; controlled release fertilizer: Environmentally smart nitrogen (ESN), Florikan 14-14-14, Everris 17-3-6). The granules’ closed and open pore number, pore volume, and total porosity were analyzed using X-ray micro-tomography (XRCT). The results demonstrated that pure urea and Florikan have a similar median particle size, around 4 mm, while ESN and Osmocote have a similar median particle size of around 3 mm. Finally, Everris, the Andersons 18-6-12, and the Andersons 12-6-6, have a similar median particle size of roughly 2.5 mm. The fracture pressure of ESN (4.58±0.98 MPa) and the NPK combination fertilizers (Florikan: 9.40±1.46 MPa and Osmocote: 8.94±2.09 MPa) were higher than pure urea. The envelope and apparent density of pure urea (envelope: 1.22±0.02 kg/m³ and apparent: 1.27±0.01 kg/m³) and ESN (envelope: 1.26±0.03 kg/m³ and apparent: 1.27±0.00 kg/m³) are similar, while all NPK fertilizers have a significantly higher density (envelope: 1.68–1.87 kg/m³ and apparent: 1.83–2.09 kg/m³). ESN had higher internal pore space and a higher total pore volume than pure urea, while NPK combination fertilizer showed lesser pores and significantly smaller pore volumes. The physical properties were also significantly different when comparing urea and NPK compound fertilizers, mainly because of the differences in their nutrient coatings and manufacturing methods. The coating of the urea increases the granule strength but does not alter the thermal properties; however, the overall porosity of the granules is influenced by the coating. In this thesis core, different binders were used to alter the internal structure of the urea granule to control the dissolution behavior and to make it a slow-release fertilizer. The layered agglomeration technique was used to manufacture the granules. The core of the granule was made by granulating technical urea powder in a drum granulator, with corn starch as the binder. A second layer of urea was added to the core by drum granulation in order to obtain a nutrient release pattern that matches with the crop demand. Corn starch, PEG 4000, and corn starch hydrogel were used as binders for the second layer. The density, thermal properties, strength, and internal porosity were measured to compare with market urea and coated slow-release fertilizer granules. All the dissolution rates of the double layer granules were slower than for market urea. Among these granule types, the dissolution rate curve of the granule with starch hydrogel in the second layer better matched the crop demand curve than those of the other two types of granules. Moreover, the strength of the double layer granules with hydrogel was the greatest of the three double layer granules. So, overall, the double layer granule manufactured with corn starch in the core and starch hydrogel in the second layer performed the best. Although the pattern of dissolution of the double layer granule was similar to the crop nitrate demand curve, a soil-based study is needed to verify the nitrate release characteristics.<br></p><ul> </ul>

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京都大学 / 0048 / 新制・課程博士 / 博士(工学) / 甲第21125号 / 工博第4489号 / 新制||工||1698(附属図書館) / 京都大学大学院工学研究科合成・生物化学専攻 / (主査)教授 杉野目 道紀, 教授 吉田 潤一, 教授 松田 建児 / 学位規則第4条第1項該当 / Doctor of Philosophy (Engineering) / Kyoto University / DGAM