Flax fibers are often used as reinforcement for thermoset and thermoplastic to produce biocomposite products. These products exhibit numerous advantages such as good mechanical properties, low density, and biodegradability. Thermoplastics are usually reinforced with flax fiber using injection molding technology and limited research has been done on compression molded thermoplastic biocomposite. Therefore, commercial thermoplastic high density polyethylene (HDPE) and polypropylene (PP) were selected for developing compression molded flax reinforced biocomposites in this research project. The main goal of this research was to develop compression molded biocomposite board using Saskatchewan flax fiber and investigate the effect of flax fiber and processing parameters (molding temperature and molding pressure) on the properties of biocomposite. <p>The fiber was cleaned and chemically treated with alkaline and silane solution that modified the fiber surface. Chemical treatments significantly increased the mechanical properties due to better fiber-polymer interfacial adhesion and also reduced the water absorption characteristics. The silane treatment showed better results than alkaline treatment. Differential scanning calorimetry (DSC) test and scanning electron microscopy (SEM) test were performed to study the thermal and morphological properties of the untreated and chemically treated flax fiber. Flax fiber and thermoplastic resin was mixed using a single-screw extruder to ensure homogenous mixing. HDPE- and PP-based biocomposites were developed through compression molding with three different pretreated flax fiber (untreated, alkaline, silane treated fiber), three levels of fiber content, two levels of molding temperature and two levels of molding pressure. <p>Increase in fiber content increased composite color index, density, water absorption, tensile strength, Youngs modulus, bending strength, and flexural modulus. However for the HDPE composites, tensile and bending strength decreased after 20% flax fiber loading. For the PP composites the, tensile and bending strength decreased after 10% flax fiber loading. Analysis of variance (ANOVA) was performed to quantitatively show the significant effects of the process variables (molding temperature, pressure, and fiber content) and their interactions on the response variables (physical and mechanical properties of biocomposites). The duncan multiple range test (DMRT) was also performed to compare the treatment means. Superposition surface methodology was adapted for both HDPE and PP composites to determine the optimum values of process variables.

<p>Fluorochlorozirconate (FCZ) glasses are a member of heavy metal fluoride glasses, and are derived from a well known ZBLAN glass. In this work, halogen salts of europium (Eu²⁺) and samarium (Sm³⁺) are used as dopants in FCZ glasses. FCZ glasses doped with Eu²⁺ and Sm³⁺ can be used in high resolution x-ray imaging for tissue scanning, and have been shown to behave as storage phosphors and/or x-ray scintillators.</p> <p>Glass transition (T_g), heat capacity (C_p) and glass crystallization (T_c) properties of Eu²⁺ and Sm³⁺ doped and undoped FCZ glasses with different amounts of relative Cl concentration, that is, with respect to the total Cl and F concentration have been investigated by conventional differential scanning calorimetry (DSC) and modulated differential scanning calorimetry (MDSC) techniques. MDSC experiments were performed at different heating rates to analyze the complex transitions and to get a better resolution of any overlapping transitions. The crystallization kinetics have also been studied by applying the Kissinger technique to multiple DSC scans in order to determine the thermal stability of FCZ glass samples used in this work. The apparent activation energy for the crystallization process was obtained by the crystallization peak temperature shift method in the conventional DSC mode. The specific heat capacity (C_p) has been measured as a function of composition, and the glass transition temperature (T_g) is evaluated from the smooth change in the heat capacity curve during the glass transformation. The observation of two possible glass transitions points to the presence of two phases in these FCZ glasses with higher relative Cl content.</p> <p>Optical transmission spectra of both doped and undoped FCZ glass samples have been measured by infrared spectroscopy and optical band gaps corresponding to an absorption coefficient of 10³ cm^-1 have been determined. A good correlation between X-ray luminescence and the glass structure is observed. While the integrated photoluminescence intensity increases linearly with the Sm³⁺ concentration, the integrated X-ray luminescence increases sublinearly. The importance of appropriate annealing conditions, such as temperature, time and ambient atmosphere, and their effect on the X-ray luminescence of rare earth (RE) doped FCZ glass samples have been investigated. Annealing conditions influence the formation of BaCl₂ nanocrystals in the glass and the properties of the resulting FCZ glass ceramics.</p>

<p>Fluorochlorozirconate (FCZ) glasses are a member of heavy metal fluoride glasses, and are derived from a well known ZBLAN glass. In this work, halogen salts of europium (Eu²⁺) and samarium (Sm³⁺) are used as dopants in FCZ glasses. FCZ glasses doped with Eu²⁺ and Sm³⁺ can be used in high resolution x-ray imaging for tissue scanning, and have been shown to behave as storage phosphors and/or x-ray scintillators.</p> <p>Glass transition (T_g), heat capacity (C_p) and glass crystallization (T_c) properties of Eu²⁺ and Sm³⁺ doped and undoped FCZ glasses with different amounts of relative Cl concentration, that is, with respect to the total Cl and F concentration have been investigated by conventional differential scanning calorimetry (DSC) and modulated differential scanning calorimetry (MDSC) techniques. MDSC experiments were performed at different heating rates to analyze the complex transitions and to get a better resolution of any overlapping transitions. The crystallization kinetics have also been studied by applying the Kissinger technique to multiple DSC scans in order to determine the thermal stability of FCZ glass samples used in this work. The apparent activation energy for the crystallization process was obtained by the crystallization peak temperature shift method in the conventional DSC mode. The specific heat capacity (C_p) has been measured as a function of composition, and the glass transition temperature (T_g) is evaluated from the smooth change in the heat capacity curve during the glass transformation. The observation of two possible glass transitions points to the presence of two phases in these FCZ glasses with higher relative Cl content.</p> <p>Optical transmission spectra of both doped and undoped FCZ glass samples have been measured by infrared spectroscopy and optical band gaps corresponding to an absorption coefficient of 10³ cm^-1 have been determined. A good correlation between X-ray luminescence and the glass structure is observed. While the integrated photoluminescence intensity increases linearly with the Sm³⁺ concentration, the integrated X-ray luminescence increases sublinearly. The importance of appropriate annealing conditions, such as temperature, time and ambient atmosphere, and their effect on the X-ray luminescence of rare earth (RE) doped FCZ glass samples have been investigated. Annealing conditions influence the formation of BaCl₂ nanocrystals in the glass and the properties of the resulting FCZ glass ceramics.</p>

Flax fibers are often used as reinforcement for thermoset and thermoplastic to produce biocomposite products. These products exhibit numerous advantages such as good mechanical properties, low density, and biodegradability. Thermoplastics are usually reinforced with flax fiber using injection molding technology and limited research has been done on compression molded thermoplastic biocomposite. Therefore, commercial thermoplastic high density polyethylene (HDPE) and polypropylene (PP) were selected for developing compression molded flax reinforced biocomposites in this research project. The main goal of this research was to develop compression molded biocomposite board using Saskatchewan flax fiber and investigate the effect of flax fiber and processing parameters (molding temperature and molding pressure) on the properties of biocomposite. <p>The fiber was cleaned and chemically treated with alkaline and silane solution that modified the fiber surface. Chemical treatments significantly increased the mechanical properties due to better fiber-polymer interfacial adhesion and also reduced the water absorption characteristics. The silane treatment showed better results than alkaline treatment. Differential scanning calorimetry (DSC) test and scanning electron microscopy (SEM) test were performed to study the thermal and morphological properties of the untreated and chemically treated flax fiber. Flax fiber and thermoplastic resin was mixed using a single-screw extruder to ensure homogenous mixing. HDPE- and PP-based biocomposites were developed through compression molding with three different pretreated flax fiber (untreated, alkaline, silane treated fiber), three levels of fiber content, two levels of molding temperature and two levels of molding pressure. <p>Increase in fiber content increased composite color index, density, water absorption, tensile strength, Youngs modulus, bending strength, and flexural modulus. However for the HDPE composites, tensile and bending strength decreased after 20% flax fiber loading. For the PP composites the, tensile and bending strength decreased after 10% flax fiber loading. Analysis of variance (ANOVA) was performed to quantitatively show the significant effects of the process variables (molding temperature, pressure, and fiber content) and their interactions on the response variables (physical and mechanical properties of biocomposites). The duncan multiple range test (DMRT) was also performed to compare the treatment means. Superposition surface methodology was adapted for both HDPE and PP composites to determine the optimum values of process variables.

The Department of Energy funded a project to determine if the specific heat of thermal energy storage materials could be improved by adding nanoparticles. The standard thermal energy storage materials are molten salts. The chosen molten salt was a sodium nitrate and potassium nitrate eutectic, commercially called Hitec Solar Salt. Two nanoparticle types were chosen, alumina and silica. The nanoparticle composite materials were fabricated by mixing the components in an aqueous solution, mixing that solution for a set amount of time using a sonic mixer, then removing the water from the aqueous solution, leaving the composite molten salt behind as a fine white powder. The thermal properties of the composite and plain material were measured using two techniques: American Society for Testing and Materials (ASTM) 1269E and Modulating Differential Scanning Calorimetry (MDSC). These two techniques measured the specific heat and the heat of fusion of the plain and composite materials. The results of all the ASTM and MDSC measurements suggest that the addition of the nanoparticles using the given manufacturing technique increased the specific heat of the molten salt by approximately 20 percent, with both measurement techniques showing approximately the same level of increase. The silica and the alumina improved the specific heat by nearly the same amount over the base material. The heat of fusion did not seem to be significantly altered compared to the observed heat of fusion value of the unmodified material. It was also observed that the nitrate and silica composite material's specific heat decreased if the material was raised to a temperature above 400C. The specific heat was observed to decrease over time, even when the temperature was well below 400C. It is unknown why this occurred. The nitrate plus alumina composite and the plain nitrate were stable to a temperature of 450C for the test duration.

Interactions of simvastatin with zwitterionic dipalmitoyl phosphotidylcholine (DPPC) multilamellar liposomes were investigated as a function of temperature and simvastatin concentration. And acyl chain length effect on the simvastatin-model membrane interactions was monitored with DPPC and dimyristoyl phosphotidylcholine (DMPC) lipids. All studies were carried out by two non-invasive techniques, namely Fourier transform infrared (FTIR) spectroscopy, and differential scanning calorimetry (DSC). The results showed that as simvastatin concentration increased, the main phase transition temperature decreased, the main phase transition curve broadened, and the characteristic pretransition was disappeared for both DMPC and DPPC model membranes. All concentrations of simvastatin disordered and decreased the fluidity of phospholipid membranes. Analysis of C=O stretching band showed that simvastatin either strengthen the existing hydrogen bonds of the glycerol skeleton closer to the head groups or caused the formation of new hydrogen bonds. A dehydration effect caused by simvastatin around the PO2- functional groups in the polar part of the lipids was monitored. This dehydration effect in the gel phase was more profound than in the liquid crystalline phase for 1, 6, and 12 mol% of simvastatin concentrations. DSC peaks broadened and shifted to lower temperature values by increasing the simvastatin concentration. For both lipids, simvastatin-induced lateral phase separation was observed in the DSC thermograms. Any change caused by the acyl chain length difference of DMPC and DPPC lipids was not observed on the simvastatin-membrane interactions. Also, for both of the lipids similar trends were observed in the FTIR and DSC results. More profound effects of simvastatin on the less stable DMPC membranes were observed.

Interactions of cholesterol reducing agent simvastatin with charged model membranes were investigated. Effects of cholestrol reducing agent simvastatin on the phase transition behaviour and physical properties of the anionic dipalmitoyl phosphatidylglycerol (DPPG) multilamellar liposome were studied as a function of temperature and simvastatin concentration. Moreover the effect of acyl chain length on the simvastatin model membrane interactions was monitored using dipalmitoyl phosphatidylglycerol (DPPG) and dimyristoyl phosphatidylglycerol (DMPG) lipids. All experiments were carried out by two non-invasive techniques namely Fourier Transform Infrared (FTIR) Spectroscopy and Differential Scanning Calorimetry (DSC). The observations made in the this study clearly showed that simvastatin interacts with the lipids of multilamellar liposomes and induces some variations in the structure of membranes. These effects are seen in the thermotropic phase transition profile of the membranes, on membrane order, acyl chain flexibility, lipid head group structures and membrane fluidity. The analysis of the C-H stretching region of FTIR spectra showed that, as simvastatin concentration increased, the phase transition curve broadened, pretransition temperature diminished, membrane order and membrane fluidity increased for anionic DPPG membrane. Moreover analysis of the C=O stretching and PO2 - stretching bands showed that simvastatin caused dehydration effect by decreasing of hydrogen bonding capacity in the glycerol backbone and also around the lipid head groups. DSC studies showed that as the simvastatin concentration increased, DSC curves broadened. In addition, simvastatin-induced lateral phase separation was observed in the DSC thermograms. In the second part of the study, the effect of acyl chain length on the simvastatin - membrane interactions was investigated for DPPG and DMPG lipid membranes. All parameters used in the FTIR studies are compared for DMPG and DPPG membranes. Similar results were observed for both membranes, except for the CH2 antisymmetric stretching band frequency at gel phase. Results showed that there are no significant effect of acyl chain length on simvastin - membrane interactions.

This dissertation focuses on the spectroscopic and thermodynamic characterization of the unusual metal-RNA cluster found in the P5abc subdomain of the Tetrahymena group I intron. The P5abc subdomain is a part of the P4-P6 domain found in the Tetrahymena thermophila group I intron selfsplicing RNA. From both X-ray crystal structures of the P4-P6 domain, a remarkable cluster of Mg2+ or Mn2+ ions was found in the P5abc subdomain (Cate et al. 1996; Juneau et al. 2001). It is believed that the metal ion core in the P5abc subdomain stabilizes the active conformation of the RNA (Cate et al. 1996). An understanding of the role of these metal ions in facilitating the correct structure of the P5abc subdomain provides insight into how metal ions help overcome the folding barriers of complex RNA structures. Under solution conditions, the properties of this uncommon metal ion core and its influence on the truncated P5abc subdomain structure have been investigated. Both EPR spectroscopy and thermal denaturation experiments have been employed to search for a spectroscopic signature of metal ion core formation and also determine the thermodynamic contribution of the metal ion core on the stability of the folded P5abc structure. A spectroscopic signature of metal ion core formation was assigned for the P5abc subdomain by EPR microwave power saturation studies. Power saturation studies of the P5abc subdomain, P4-P6 domain and corresponding mutants reveal that the addition of 5 equivalents of Mn2+ are required for the wild type P5abc subdomain to form the metal ion core under solution conditions in 0.1 M NaCl. Results from both domain and subdomain microwave power saturation studies suggest that this technique can be applied for detecting clustering of Mn2+ ions in other RNA structures. The thermodynamic consequence of this metal ion core was probed by thermal denaturation techniques including UV-Vis spectroscopy and differential scanning calorimetry (DSC). DSC experiments were utilized to directly determine the thermodynamic contribution of the metal ion core. This value was determined to be an average of &#8710;&#8710;G of -5.3 kcal/mol and is consistent with &#8710;&#8710;G values obtained for other RNA tertiary structures.

In der vorliegenden Arbeit werden M(II)-Formiat-Komplexe mit M=Cu, Ni, Zn beschrieben. Das themogravimetrische Verhalten dieser Komplexe wird vorgestellt. TG-MS-Untersuchungen geben erste Hinweise auf das Metallisierungsverhalten obiger Spezies. Die Charakterisierung der entsprechenden Komplexe erfolgte durch die Elementaranalyse, IR-Spektroskopie sowie in einzelnen Fällen durch die Einkristallröntgendiffraktometrie.

Owing to their excellent infrared transmittance and good rheological properties, selenium based chalcogenide glasses have been materials of choice for a number of technological applications. However, chalcogenide glasses can undergo substantial structural relaxation even at room temperature due to their low glass transition temperatures. The origins of these dynamic processes and their correlation to the glass structure is therefore of fundamental and practical interest. In particular, a deep understanding of the dynamic response near the glass transition region could help elucidate the mechanism of these structural relaxation processes. The correlation between structure and dynamic properties of selenium based glass systems were therefore investigated. NMR and Raman spectroscopy measurements reveal that the structure of AsₓSe₁₋ₓ glass follow the chain crossing model in selenium-rich glasses but contain increasing amounts of cage molecules in arsenic-rich compositions. This structural pattern leads to systematic extrema in physical properties at the stoichiometric composition As₄₀Se₆₀.The dynamic response of AsₓSe₁₋ₓ glasses investigated by heat capacity spectroscopy shows two minima in melt fragility as a function of composition which correlate well with the dimensionality of the glassy network. The structure evolves from 2D to 3D during crosslinking of selenium chains by arsenic but reduces into a 2D layer-like structure at the stoichiometric composition. Upon precipitation of arsenic-rich cages the network first reverts back to 3D and eventually becomes a mix of 2D and 0D structural units. The presence of molecular clusters in the network is evidenced by a strong bimodal dynamic response at high arsenic contents. NMR and Raman spectroscopy measurements of GeₓSe₁₋ₓ glasses suggest a structure composed of aggregated tetrahedral units and long selenium chains with little or no connectivity. Distinct dynamic responses of these two separated structural motifs are revealed by heat capacity spectroscopy. A non-Gaussian distribution of the imaginary heat capacity peak provided further evidence for the structural heterogeneity. This behavior is consistent with high temperature NMR measurements which show that the dynamic response of floppy selenium chains is distinct from that of rigid tetrahedral units. Finally, heat capacity spectroscopy applied to pure selenium provides strong evidence for the microscopic origin of the non-exponential structural relaxation, a universal feature of fragile glasses. The evolution of the imaginary heat capacity peak shape during annealing shows a non-monotonic trend which remarkably matches model predictions based on the enthalpy landscape. These results indicate that the non-exponential character of the relaxation process is linked to density fluctuations in the glass.