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.

A waterflood has been used as a secondary recovery process to maintain the reservoir pressure and displace the oil towards the producer. However, the existence of high-permeability zones (thief zones) can cause early water breakthrough and excessive water production, thus, leaving a significant amount of oil bypassed in heterogeneous reservoirs. In this work, thermally active (Bright Water®) and pH-sensitive polymers have been proposed as an in-depth conformance tool with detailed simulation studies. Thermally active polymers are triggered by temperature change, whereas pH-sensitive polymers are triggered by pH change. Upon activation, polymers provide high resistance to subsequent fluid flow and divert the flow into adjacent unswept zones. As a result, this leads to improved sweep efficiency, low oil-water-ratio, and incremental oil recovery. The modeling of a pH-sensitive polymer was based on the principles of the microgel modeling procedure developed by Huh et al. (2005). In addition, a modified model was developed to calculate equilibrium swelling ratio explicitly in terms of pH and ionic strength of solution instead of using a root-finding algorithm. Thermal active polymers were modeled in terms of gelation reaction, gel viscosity, gel adsorption, and permeability reduction factor. Thermally active and pH-sensitive polymers were coupled with UTGEL reservoir simulator in an attempt to assess applicability of these gels as a conformance tool. Sensitivity analysis studies were conducted through 3D synthetic models to investigate technical feasibility of thermally active and pH-sensitive polymers as an in-depth conformance tool. Results indicated that incremental oil recovery and conformance control depend on the polymer concentration, slug size, permeability contrast between matrix and thief zone, vertical to horizontal permeability ratio (kv/kh), treatment location, oil-to-water viscosity ratio, and adsorption level, among others. It is concluded in this study that the permeability contrast between matrix and thief zones appears to be one of the most important parameters that impacts treatment performance. Therefore, a high permeability contrast is a prerequisite to achieve technically and economically successful treatment. / text

This dissertation discusses the effect of synthesis route and ortho-position group on the thermal and transport properties of thermally rearranged polymers. Thermally rearranged polymers are polybenzoxazoles formed via the solid state rearrangement of ortho-functional polyimides. In this study, polymers were derived from 3,3'-dihydroxy-4,4'-diamino-biphenyl and 2,2'-bis-(3,4-dicarboxyphenyl) hexafluoropropane dianhydride (HAB-6FDA). These HAB-6FDA polymers were synthesized using chemical and thermal imidization, and hydroxyl, acetate, propanoate, or pivalate ortho-position groups were considered. In these polymers, gas permeability increases as a function of conversion for all samples. The polyimide synthesis route does not affect the thermal or transport properties. However, the precursor ortho-position group strongly influences the thermal and transport properties of TR polymers. Additionally, it was determined that an increase in gas diffusivity was the primary cause of increased permeability as a function of thermal rearrangement. / text

This thesis is made as it is submitted as a sum of published papers by the candidate. Aluminium hydroxides including gibbsite, boehmite and diaspore, are the major components, while iron hydroxides/oxides and kaolinite are the major impurities in bauxite. The dehydroxylation pathways during thermal activation of bauxite have been debated for decades. Phase transformation during thermal activation or calcination of bauxite to achieve high yields of alumina has been an important goal for the refining industry. This study deals with natural and synthetic aluminium and iron hydroxides using vibrational spectroscopy in conjunction with X-ray diffraction and electron microscopy, followed by the characterisation of the phase transformation in activated bauxite. In the Raman spectra, gibbsite shows four bands at 3617, 3522, 3433 and 3364 cm-1, and bayerite shows seven bands at 3664, 3652, 3552, 3542, 3450, 3438 and 3420 cm-1 in the hydroxyl stretching region. Five bands at 3445, 3363, 3226, 3119 and 2936 cm-1 for diaspore and four at 3371, 3220, 3085 and 2989 cm-1 for boehmite are present. The far infrared spectrum of boehmite resembles that of diaspore in the 300-400 cm-1 region. Boehmite has two characteristic bands at 366 and 323 cm-1 while diaspore has five at 354, 331, 250, 199 and 158 cm-1. The far infrared spectrum of gibbsite resembles that of bayerite in the 230-300 cm-1 region. Gibbsite shows three characteristic bands at 371, 279 and 246 cm-1 whereas bayerite shows six at 383, 345, 326, 296, 252 and 62 cm-1. The far infrared spectra are in-harmony with the FT-Raman spectra, allowing the study and differentiation of the stretching of AlO4 units to characterize these four alumina phases. The surface properties of kaolinite and gibbsite are studied using Fourier transform infrared photoacoustic spectroscopy (FTIR-PAS). The FTIR-PAS spectra of kaolinite are recorded at mirror velocities of 0.05, 0.1, and 0.2 cm s-1, and compared to the gibbsite spectra recorded at mirror velocity of 0.2 cm s-1. It is found that the hydroxyl surface spectra are a function of depth. For the FTIR spectroscopy of thermal dehydroxylation of goethite to form hematite, the intensity of hydroxyl stretching and bending vibrations decreased with the extent of dehydroxylation of goethite. Infrared absorption bands clearly show the phase transformation between goethite and hematite, in particular the migration of excess hydroxyl units from goethite to hematite. Data from the band component analysis of FT-IR spectra indicate that the hydroxyl units mainly affect the a- plane in goethite and the equivalent c- plane in hematite. A larger amount of non-stoichiometric hydroxyl unit is found to be associated with a higher aluminium substitution. A shift to a higher wavenumber of bending and hydroxyl stretching vibrations is attributed to the effects of aluminium substitution associated with non-stoichiometric hydroxyl units on the a-b plane relative to the b-c plane of goethite. The dehydroxylation pathways of both the aluminium hydroxides and the impurities are intensively studied. Gibbsite completely decomposed at 250 °C, followed by boehmite and kaolinite at 500 °C. No phase transformations were observed for hematite, anatase, rutile or quartz up to 800 °C. Small amounts of gibbsite transformed to boehmite but the majority transformed to chi (χ) alumina, a disordered transition alumina phase, after dehydroxylation at 250 °C. The dehydroxylation pathways of crystalline gibbsite follow the orders: (a) gibbsite (&lt250 °C) to boehmite (250-450 °C) to gamma alumina (γ) (500-800 °C); or (b) gibbsite (&lt250 °C) to chi alumina (χ) (250-800 °C) to chi (χ) + kappa alumina (κ) (700-800 °C). Boehmite completely altered to gamma alumina (γ), while kaolinite altered to metakaolinite at 500 °C. The vibrational spectroscopy including FT-IR and FT-Raman, is a rapid, accurate and non-destructive technique in characterising both single and mixed mineral phases. In particular, the vibrational spectroscopy has shown its advantages over other techniques in terms of its sensitivity to hydroxyl groups. Future work on the simulation of bauxite dehydroxylation with emphasis on the studies of transition aluminas is proposed. The application of the advanced technique synchrotron x-ray spectroscopy, in addition to those techniques used in the present study, is recommended.

This dissertation focuses on the synthesis and characterization of high performance polymers, especially polyimides, polybenzoxazoles and polybenzimidazoles for gas separation applications. An abundance of monomers and novel polymers were synthesized and fabricated into membranes. Thermally rearranged polybenzoxazoles and their precursor polyimides were systematically studied with regard to size of pendant functional groups, thermal rearrangement conversion, and relationship of backbone structure/gas transport properties. 3,3'-Diamino-4,4'-dihydroxybiphenyl was synthesized using an economical route. Meta and para oriented polyimides with different ortho-functionality were synthesized and these polymers were thermally rearranged into polybenzoxazoles. The polar hydroxyl functional groups on the polyimide backbone diminished the meta/para isomer effect of the permeability coefficients of the polymers and only a small difference between meta- and para-oriented polyhydroxyimides in permeability coefficients was observed. The TR polybenzoxazoles derived from meta/para-oriented isomeric polyimides with ortho functionality had similar gas separation properties, especially for CO2/CH4 separation, and it is hypothesized that this is due to a lack of intersegmental mobility distinction between the two isomeric TR polymers. The TR polymers derived from the polyimides with acetate ortho-functional groups had significantly better gas separation properties than ones derived from the precursor with hydroxyl ortho-functional groups. Polybenzimidazoles were also investigated for use as gas separation membranes. Polybenzimidazoles are some of the most thermally stable polymers. However, commercial polybenzimidazoles do not have good solubility in common solvents. The solubility issue was solved by incorporating sulfonyl linkages into the polybenzimidazole backbone using a 3,3',4,4'-tetraaminodiphenylsulfone (TADPS) monomer. 3,3',4,4'-Tetraaminodiphenylsulfone was synthesized by a novel route with higher overall yield and less steps than the traditional synthetic method. The TADPS based polybenzimidazoles also demonstrated better thermal stability than commercial polybenzimidazole. The meta/para oriented isomer effect on gas transport properties is discussed. TADPS-based polybenzimidazoles exhibited H2/CO2 gas separation properties near or surpassing the upper bound with H2 permeabilities from 3.6 to 5.7 Barrer and selectivities from 10.1 to 32.2 at 35 °C. / Ph. D.

The purpose of this dissertation is to advance the understanding of SrS-based a. c. thin film electroluminescent (ACTFEL) devices. The role of traps in the bulk phosphor layer in the light emission mechanism from ACTFEL devices is studied, characterized and modeled. Experiments were performed to observe the response of the ACTFEL devices to tailored voltage excitations. A physical model was developed to describe the optoelectronic processes taking place in the phosphor; analytical equations were written and numerically simulated to plot the flux and luminance responses of the device to similarly tailored voltage excitations. The voltage excitation parameters such as amplitude, rise times and fall times were varied both experimentally and in simulations and their effect on the opto-electronic response of the device was studied. Thermally stimulated luminance studies were performed to determine critical device parameters. Theoretical predictions matched the experimental data in a qualitative manner. A much improved quantitative accuracy is obtained when the role of dipoles in the EL mechanisms is incorporated into the model.

Medidas de corrente termoestimuladas e de carga a temperatura constante, sob campo elétrico constante externo, foram realizadas no intuito de identificar além de cargas espaciais existentes em amostras comerciais de PVDF, também estudar o pico anômolo de corrente que se apresentou nas medidas isotérmicas. Este pico desaparecia em medidas subseqüentes, mas sua recuperação, apesar de lenta, foi registrada, principalmente se a amostra era conservada em ambiente úmido. Uma série de medidas feitas em diferentes umidades relativas do ar, cuidadosamente controladas, evidenciou que este fenômeno estava diretamente ligado à água absorvida pela amostra do ambiente externo. O efeito mostrou também ser fortemente dependente do campo aplicado. Um modelo baseado em dissociação iônica da água, provavelmente fracamente ligada a estrutura do polímero, foi desenvolvido, levando em consideração que o coeficiente de dissociação depende do campo elétrico, bem como do tempo de extração dos portadores dissociados da amostra. Nesta cinética controladora da corrente, é considerada também recombinação bi-iônica. / Thermally stimulated current and depolarization measurements were carried on commercially available samples of PVDF. The measurements were conducted under constant temperature and constant applied field in order to investigate an anomolous peak which appears in isothermal measurements, and also identify the presence of space charge. This peak is observed only in the first measurements, but it can recover if the sample is stored in a humid environment. Series of measurements was carried out with carefully controlled relative humidity from which one can conclude that the peak is directly linked to water absorved by the sample. This effect is shown to depend strongly on the applied electric field. A theoretical model based on ionic dissociation of water molecules - probably weakly attached to the polymer structure is developed to explain the experimental results. In the model, the dissociation coefficient and the time of escape of dissociated carriers are assumed to depend on the electric field. Bi-ionic recombination is also assumed to play an important role in the control of the kinetics of the process.

Chemotherapy regimens, one of the most common cancer treatments, are often dictated by dose-limiting toxicities. Also, the largest hurdle for translating novel biological therapies such as siRNA into the clinic is lack of an efficient delivery mechanism to get the therapeutic into malignant cells. Both of these situations would benefit from a minimally-invasive controlled release system that only delivers a therapeutic to the site of malignant tissue. This thesis presents work towards the creation of such a delivery platform using two novel material components: a thermally responsive poly[N-isopropylacrylamide-co-acrylamide] (NIPAAm-co-AAm) hydrogel and gold-silica nanoshells. Thermally responsive hydrogels undergo a physical property transition at their lower critical solution temperature (LCST). When transitioning from below to above the LCST, the hydrogel material expels large amounts of water and absorbed molecules. This phase change can be optically triggered by embedded gold-silica nanoshells, which rapidly transfer near-infrared (NIR) light energy into heat energy due to the surface plasmon resonance phenomena. When this material is loaded with absorbed drug molecules, drug release can be externally triggered by exposure to an NIR laser. Initial characterization of this material was accomplished using bulk hydrogel-nanoshell composites. Poly(NIPAAm-co-AAm)-nanoshell composites were synthesized via free radical polymerization. The LCST of the poly(NIPAAm-co-AAm) hydrogels was determined to be from 39-45 deg C, or slightly above physiologic temperature. The material was swollen in a drug solution of either doxorubicin (a common chemotherapeutic) or a 21bp dsDNA olgio (a model molecule for siRNA). Composites were then exposed to an 808 nm laser, which was found to trigger release of the therapeutics from the composite material. Further work has been done in translating this composite material to nano-scale sized particles, such that it could be injected intravenously, passively accumulate in tumor tissue, and be externally triggered to release therapeutics by exposure to an NIR laser. Sub-micron composite particles were synthesized using dissolvable gelatin templates with 500 nm wells. Analysis by transmission electron microscopy (TEM) indicates that these particles consist of gold nanoshells surrounded by a hydrogel coating. Dynamic light scattering (DLS) measurements were used to show that these particles display the same thermal properties as seen in the bulk material: collapsing in response to increased temperatures or NIR light exposure. Ultimately, the work in this thesis advances the development of a minimally-invasive, optically-triggered drug delivery platform.

Collagen is an important structural protein in living organisms and plays an indispensable role in connecting cells and tissues, such as in musculature, bone, and ligament. The stability and conformation of collagen are, however, strongly influenced by ambient temperature and constitutes an interesting subject of study. Thermally induced conformation change of collagen has been investigated by techniques such as differential scanning calorimetry (DSC) and second harmonic generation. DSC is a powerful method in uncovered important thermal dynamics properties including phase change, enthalpy, and thermal stability of the collagen. However, due to its collective nature, no localized information can be found. For comparison, second harmonic generation, which reflects structural symmetry, can be combined with laser scanning microscopy to investigate localized variation. It has been shown in previous studies that the thermal stability of collagen is strongly influenced by the water content within collagen. For comparison, we are investigating the conformational change of collagen under a vacuum stat with second harmonic microscopy so as to isolate environmental effects, particularly those from water and oxygen. In this way, we have found the conformational change of collagen takes place at a much higher temperature and activation energy. Additionally, the high spatial resolution achieved also allows many further possibilities.

<p>Cancer is currently the second leading cause of death in the United States. Although many treatment options exist, some of the most common, including radiotherapy and chemotherapy, are restricted by dose-limiting toxicities. In addition, the largest hurdle for translating novel biological therapies such as siRNA into the clinic is lack of an efficient delivery mechanism to get the therapeutic into malignant cells. This work aims to improve this situation by engineering a minimally invasive controlled release system that specifically delivers therapeutics to the site of malignant tissue. This platform consists of two novel material components: a thermally responsive poly[N-isopropylacrylamide-co-acrylamide] (NIPAAm-co-AAm) hydrogel and gold-silica nanoshells. Therapeutic molecules are encapsulated within a poly(NIPAAm-co-AAm) hydrogel carrier, leading to increased serum stability, circulation time, and decreased exposure to off-site tissues. Additionally, gold-silica nanoshells embedded within this hydrogel will be used to optically trigger therapeutic release from the carrier. This hydrogel-nanoshell composite material was designed to be swollen under physiologic conditions (37 oC), and expel large amounts of water and absorbed molecules at higher temperatures (40-45 oC). This phase transition can be optically triggered by embedded gold-silica nanoshells, which rapidly transfer near-infrared (NIR) light energy into heat due to the surface plasmon resonance phenomena. NIR light can deeply penetrate biological tissue with little attenuation or damage to tissue, and upon exposure to such light a rapid temperature increase, hydrogel collapse, and drug expulsion will occur. Ultimately, these drug-loaded hydrogel-nanoshell composite particles would be injected intravenously, passively accumulate in tumor tissue due to the enhanced permeability and retention (EPR) effect, and then can be externally triggered to release their therapeutic payload by exposure to an external NIR laser. This dissertation describes the synthesis, characterization, and validation of such a controlled therapeutic delivery platform.</p><p>Initial validation of poly(NIPAAm-co-AAm)-gold nanoshell composites to act as a material in site-specific cancer therapeutic delivery was accomplished using bulk hydrogel-nanoparticle composite disks. The composite material underwent a phase transition from a hydrated to a collapsed state following exposure to NIR light, indicating the ability of the NIR absorption by the nanoshells to sufficiently drive this transition. The composite material was loaded with either doxorubicin or a DNA duplex (a model nucleic acid therapeutic), two cancer therapeutics with differing physical and chemical properties. Release of both therapeutics was dramatically enhanced by NIR light exposure, causing 2-5 fold increase in drug release. Drug delivery profiles were influenced by both the molecular size of the drug as well as its chemical properties. </p><p>Towards translation of this material into in vivo applications, the hydrogel-nanoshell composite material was synthesized as injectable-sized particles. Such particles retained the same thermal properties as the bulk material, collapsing in size from ~330 nm to ~270 nm upon NIR exposure. Furthermore, these particles were loaded with the chemotherapeutic doxorubicin and NIR exposure triggered a burst release of the drug payload over only 3 min. In vitro, this platform provided increased delivery of doxorubicin to colon carcinoma cells compared to free-drug controls, indicating the irradiated nanoshells may increase cell membrane permeability and increase cellular uptake of the drug. This phenomena was further explored to enhance cellular uptake of siRNA, a large anionic therapeutic which cannot diffuse into cells easily. </p><p>This work advances the development of an injectable, optically-triggered delivery platform. With continued optimization and in vivo validation, this approach may offer an novel treatment option for cancer management.</p> / Dissertation