It is the objective of this work to focus on heat dissipation in gallium nitride based solid-state logic devices as well as optoelectronic devices, a major technical challenge. With a direct band gap that is tunable through alloying between 0.7-3.8 eV, this material provides an enabling technology for power generation, telecommunications, power electronics, and advanced lighting sources. Previously, advances in these areas were limited by the availability of high quality material and growth methods, resulting in high dislocation densities and impurities. Within the last 40 years improvements in epitaxial growth methods such as lateral epitaxial overgrowth (LEO), hydride vapor phase epitaxy (HVPE), molecular beam epitaxy (MBE), and metal organic chemical vapor deposition (MOCVD), has enabled electron mobilities greater than 1600 cm2V/s, with dislocation densities less than 109/cm2. Increases in device performance with improved materials have now been associated with an increase in power dissipation (>1kW/cm2) that is limiting further development. In the following work thermophysical material of III-V semiconducting thin films and associated substrates are presented. Numerical modeling coupled with optical (micro-IR imaging and micro-Raman Spectroscopy) methods was utilized in order to study the heat carrier motion and the temperature distribution in an operating device. Results from temperature mapping experiments led to an analysis for design of next generation advancements in electronics packaging.

The proton exchange membrane fuel cells should have three major advantages: 1. micro-phase separation, 2. mechanical properties and 3. thermal stability. According to the recent literature and the material of core benzene ring poly (arylene ether)s studied by our group, this paper synthesize a series of the locally and densely sulfonated polymer. We use core benzene ring as the diol monomer and the containing CF3 groups as the fluorine monomer to synthesis poly (arylene ether)s via nucleophilic displacement reactions, and then use the different concentrations synthesized sulfonated polymer by sulfonic acid reaction. According to NMR¡¦s result we confirmed that the structure of synthetic materials is correct. By using GPC we get that the KP1, KP2, and KP3¡¦s molecular weight about 20000 (g/mol) ; The thermal stability up to 530OC for 5% loss in TGA under nithtrogen, to prove thisseries of polymer excellent thermal stability. After sulfonation, SKP1, SKP2 and SKP3¡¦s decomposition temperature decreased about 200OC ~ 250OC ranging with increasing degree of sulfonation. By DSC analysis, K1, K2 and K3 monomer's Tg followed up with the increase of the benzene ring number, however, the polymer does not have any apparent peak. About the Proton conductive, SKP2C IEC 2.23mequiv / g, water uptake 94%, the highest proton conductivity can be as high as 68.2 mS / cm, has been similar to Nafion 117 of 70 mS / cm.

Proton Exchange Membrane Fuel Cell has the potential to become an important energy conversion technigne. Lots of efforts oriented toward the electrochemical conversion of energy using proton exchange membrane (PEM) fuel cells have been enormously accelerated with the hope to promote as an alternative power source for transport and portable purposes. However, they still suffer from such disadvantages as limited operation temperature, high cost, insufficient durability and high methanol permeability.Good membranes should meet several strict requirements as follows; reasonable proton conductivity, high stability and durny the performance of a fuel cell environment,outstanding mechanical toughness, high heat endurance, and impermeability to fuel gas or liquid. Presently,a lot of references have mentioned some sulfonatied polymer sulfonated of poly(ether ether ketone) (SPEEK), sulfonatedpolysulfone (SPSF), sulfonated polysulfide sulfone(SPSS), and polybenzimidazole(PBI) and so on.To achieve high proton conductivity usually match with a high degree of sulfonation that means owning a large Ion Exchange Capacity, IEC.But which in turn leads to a decrease in the electrochemical¡Bdimensional stability¡Bwater uptake¡Boxidative stability. Therefore they suffer from such disadvantages as limited operation range of temperature.Three aromatic poly(arylene ether)s P4b¡BP4c¡BP4d were synthesized from the polymer consists nine of polyaromatic groups with bisfluoride monomer at studying long time in our laboratory with S1¡BS2¡BS3 diol monomer.The molecular weight of the polymer (Mw:1.49¡Ñ105~5.3¡Ñ105 g/mol ,PDI: 1.82~2)This polymer has high strength,thermal stability and all of polymers own very high Td ,which are over than 500oC.We sulfonatied the polymer in order to apply as the proton exchange membrane of a fuel cell.The results showed after sulfonation of P4b¡BP4c¡BP4d.All IEC reaches 3.9~1(meq/g).According to above result, we propose the aromatic poly(arylene ether)s is good matenal can be used on all application as a proton exchange membrane.

Research in nanoparticle-reinforced composites is predicated by the promise for exceptional properties. However, to date the performance of nanocomposites has not reached its potential due to processing challenges such as inadequate dispersion and patterning of nanoparticles, and poor bonding and weak interfaces. The main objective of this dissertation is to improve the physical properties of polymer nanocomposites at low nanoparticle loading. The first step towards improving the physical properties is to achieve a good homogenous dispersion of carbon nanofibers (CNFs) and single wall carbon nanotubes (SWNTs) in the polymer matrix; the second step is to manipulate the well-dispersed CNFs and SWNTs in polymers by using an AC electric field. Different techniques are explored to achieve homogenous dispersion of CNFs and SWNTs in three polymer matrices (epoxy, polyimide and acrylate) without detrimentally affecting the nanoparticle morphology. The three main factors that influence CNF and SWNT dispersion are: use of solvent, sonication time, and type of mixing. Once a dispersion procedure is optimized for each polymer system, the study moves to the next step. Low concentrations of well dispersed CNFs and SWNTs are successfully manipulated by means of an AC electric field in acrylate and epoxy polymer solutions. To monitor the change in microstructure, alignment is observed under an optical microscope, which identifies a two-step process: rotation of CNFs and SWNTs in the direction of electric field and chaining of CNFs and SWNTs. In the final step, the aligned microstructure is preserved by curing the polymer medium, either thermally (epoxy) or chemically (acrylate). The conductivity and dielectric constant in the parallel and perpendicular direction increased with increase in alignment frequency. The values in the parallel direction are greater than the values in the perpendicular direction and anisotropy in conductivity increased with increase in AC electric field frequency. There is an 11 orders magnitude increase in electrical conductivity of 0.1 wt% CNF-epoxy nanocomposite that is aligned at 100 V/mm and 1 kHz frequency for 90 minutes. Electric field magnitude, frequency and time are tuned to improve and achieve desired physical properties at very low nanoparticle loadings.

Through past research, it is known that carbon nanotubes have the potential of enhancing the thermal performance of heat transfer fluids. The research is of importance in electronics cooling, defense, space, transportation applications and any other area where small and highly efficient heat transfer systems are needed. However, most of the past work discusses the experimental results by focusing on the effect of varying concentration of carbon nanotubes (CNTs) on the thermal performance of CNT nanofluids. Not much work has been done on studying the effect of processing variables. In the current experimental work, accurate measurements were carried out in an effort to understand the impact of several key variables on laminar flow convective heat transfer. The impact of ultrasonication energy on CNT nanofluids processing, and the corresponding effects on flow and thermal properties were studied in detail. The properties measured were viscosity, thermal conductivity and the convective heat transfer under laminar conditions. Four samples of 1 wt % multi walled carbon nanotubes (MWCNT) aqueous suspensions with different ultrasonication times were prepared for the study. Direct imaging was done using a newly developed wet-TEM technique to assess the dispersion characteristics of CNT nanofluid samples. The results obtained were discussed in the context of the CNT nanofluid preparation by ultrasonication and its indirect effect on each of the properties. It was found that the changes in viscosity and enhancements in thermal conductivity and convective heat transfer are affected by ultrasonication time. The maximum enhancements in thermal conductivity and convective heat transfer were found to be 20 % and 32 %, respectively, in the sample processed for 40 minutes. The thermal conductivity enhancement increased considerably at temperatures greater than 24 °C. The percentage enhancement in convective heat transfer was found to increase with the axial distance in the heat transfer section. Additionally, the suspensions were found to exhibit a shear thinning behavior, which followed the Power Law viscosity model.

Success of acid fracturing depends on uneven etching along the fracture surfaces caused by heterogeneities such as variations in local mineralogy and variations in leakoff behavior. The heterogeneities tend to create channeling characteristics, which provide lasting conductivity after fracture closure, and occur on a scale that is neither used in laboratory measurements of acid fracture conductivity, which use core samples that are too small to observe such a feature, nor in typical acid fracture simulations in which the grid block size is much larger than the scale of local heterogeneities. Acid fracture conductivity depends on fracture surface etching patterns. Existing acid fracture conductivity correlations are for random asperity distributions and do not consider the contribution of channels to the conductivity. An acid fracture conductivity correlation needs the average fracture width at zero closure stress. Existing correlations calculate average fracture width using dissolved rock equivalent width without considering the effect of reservoir characteristics. The purpose of this work is to develop an intermediate-scale acid fracture model with grid size small enough and the whole dimension big enough to capture local and macro heterogeneity effects and channeling characteristics in acid fracturing. The model predicts pressure field, flow field, acid concentration profiles, and fracture surface profiles as a function of acid contact time. By extensive numerical experiments with the model, we develop correlations of fracture conductivity and average fracture width at zero closure stress as a function of statistical parameters of permeability and mineralogy distributions. With the model, we analyzed the relationships among fracture surface etching patterns, conductivities, and the distributions of permeability and mineralogy. From result analysis, we found that a fracture with channels extending from the inlet to the outlet of the fracture has a high conductivity because fluid flow in deep channels needs a very small pressure drop. Such long and highly conductive channels can be created by acids if the formation has heterogeneities in either permeability or mineralogy, or both, with high correlation length in the direction of the fracture, which is the case in laminated formations.

This thesis describes the synthesis of a low modulus, thermally conductive thermal interface materials (TIM) using metal decorated nanotubes as fillers. TIMs are very important in electronics because they act as a thermally-conductive medium for thermal transfer between the interface of a heat sink and an electronic package. The performance of an electronic package decreases with increasing operating temperature, hence, there exists a need to create a TIM which has high thermal conduction to reduce the operating temperature. The TIM in this study is made from metal decorated multi-walled carbon nanotubes (MWCNT) and Vinnapas®BP 600 polymer. The sample was functionalized using mild oxidative treatment with nitric acid (HNO3) or, with N-Methly-2-Pyrrolidone (NMP). The metals used for this experiment were copper (Cu), tin (Sn), and nickel (Ni). The metal nanoparticles were seeded using functionalized MWCNTs as templates. Once seeded, the nanotubes and polymer composites were made with or without sodium dodecylbenzene sulfonate (SDBS), as a surfactant. Thermal conductivity (k) measurement was carried out using ASTM D-5470 method at room temperature. This setup best models the working conditions of a TIM. The TIM samples made for this study showed promise in their ability to have significant increase in thermal conduction while retaining the polymer’s mechanical properties. The highest k value that was obtained was 0.72 W/m-K for a well dispersed aligned 5 wt percent Ni@MWCNT sample. The Cu samples underperformed both Ni and Sn samples for the same synthesis conditions. This is because Cu nanoparticles were significantly larger than those of Ni and Sn. They were large enough to cause alloy scattering and too large to attach to the nanotubes. Addition of thermally-conductive fillers, such as exfoliated graphite, did not yield better k results as it sunk to the bottom during drying. The use of SDBS greatly increased the k values of the sample by reducing agglomeration. Increasing the amount of metal@MWCNT wt percent in the sample had negative or no effect to the k values. Shear testing on the sample shows it adheres well to the surface when pressure is applied, yet it can be removed with ease.

The "slot-drill" completion method, which utilizes a mechanically cut high-conductivity "slot" in the target formation created using a tensioned abrasive cable, has been proposed as an alternative stimulation technique for shale-gas and other low/ultra-low permeability formations. This thesis provides a comprehensive numerical simulation study on the "slot drill" completion technique. Using a Voronoi gridding scheme, I created representative grid systems for the slot-drill completion, as well as for the case of a vertical well with a single fracture, the case of a horizontal well with multiple hydraulic fractures, and various combinations of these completions. I also created a rectangular slot configuration, which is a simplified approximation of the actual "slot-drill" geometry, and investigated the ability of this rectangular approximation to model flow from the more complicated (actual) slot-drill configuration(s). To obtain the maximum possible diagnostic and analytical value, I simulated up to 3,000 years of production, allowing the assessment of production up to the point of depletion (or boundary-dominated flow). These scenarios provided insights into all the various flow regimes, as well as provided a quantitative evaluation of all completion schemes considered in the study. The results of my study illustrated that the "slot-drill" completion technique was not, in general, competitive in terms of reservoir performance and recovery compared to the more traditional completion techniques presently in use. Based on my modeling, it appears that the larger surface area to flow that multistage hydraulic fracturing provides is much more significant than the higher conductivity achieved using the slot-drill technique. This work provides quantitative results and diagnostic interpretations of productivity and flow behavior for low and ultra-low permeability formations completed using the slot-drill method. The results of this study can be used to (a) help evaluate the possible application of the "slot-drill" technique from the perspective of performance and recovery, and (b) to establish aggregated economic factors for comparing the slot-drill technique to more conventional completion and stimulation techniques applied to low and ultra-low permeability reservoirs.

Polycondensation reaction was carried out for synthesizing rigid-rod polymer hPBI. Various molar ratios (50:1, 25:1, and 15:1) of 2-hydroterephthalic acid and 5-hydroisophthalic acid were also introduced in the synthesis for articulated rigid-rod polymer a-hPBI. The polymers were further derivatized with 1,3-propanesulton for pendants of lithium ionomer to become water soluble polyelectrolytes hPBI-PS(Li+) and a-hPBI-PS(Li+), respectively. Lithium salt doped cast film of the rigid-rod polyelectrolyte hPBI-PS(Li+) showed a room-temperature DC conductivity parallel to film surface as high as 4.02¡Ñ10-3 S/cm. Molecular weight of the rigid-rod polyelectrolyte was low indicating a small molecular aspect ratio. In cast film, the molecules were randomly distributed and highly isotropic facilitated Li cations mobility for a high film conductivity. The conductivity was also insensitive to the anion of lithium salt. No apparent layered structure was revealed by scanning electron microscope suggesting that the cast films had near three-dimensionally isotropic structure and conductivity.

In this study, electrically conductive coating materials composed of epoxy resin and carbon black (CB) were prepared by applying two different mixing techniques (Grinding and Mechanical Mixing). The effect of carbon black addition, ultrasonication, mixing type and surface modification of carbon black on the morphologies, electrical and mechanical properties of the composites were investigated. According to test results, Grinding Method is much more efficient and for this method, percolation concentration was found as 2 vol %. The electrical resistivity value obtained at this composition is around 107 ohm.cm. Also, for the samples prepared by Grinding Method, the hardness increased by adding conductive filler, but the impact energy and adhesive strength decreased with increasing carbon black content. Ultrasonication was applied to the samples containing 2 vol % CB obtained by Grinding Method to reduce the electrical resistivity further. Three different ultrasonic mixing times were tried, however, no positive effect was observed on electrical and mechanical properties. Since the addition of carbon black has a negative effect on the processability of the mixture, it was aimed to obtain desired conductivity value at lower percolation concentration by modifying carbon black surface with different silane coupling agents and formamide. The best result in terms of electrical conductivity was obtained for the materials produced with formamide treated carbon black by Grinding Method. At 1 vol % concentration, the electrical resistivity was found as approximately 106 ohm.cm which is three orders smaller than the resistivity of materials prepared with untreated carbon black.