Surface properties of polymers and competition adsorption of toluene and heptane on silica were studied using IR-visible sum frequency generation (SFG) vibrational spectroscopy. SFG is intrinsically surface sensitive because the second-order optical process is forbidden in media with inversion symmetry, such as bulk polymers and liquids. This nonlinear optical technique provides surface vibrational spectra under ambient conditions without the need of an ultra-high vacuum environment. Polymer surface properties, including surface relaxation temperature of poly(methyl methacrylate) (PMMA) and surface electronic states of poly[2-methoxy, 5-ethyl (2’-hexyloxy) para phenylenevinylene] (MEH-PPV), were investigated. It was found that there are significant differences between the surface and bulk properties for these polymers. For PMMA, a new surface structure relaxation was identified at 67°C, which does not match any known structure relaxation temperatures for bulk PMMA and is 40°C below the bulk glass transition temperature. For MEH-PPV, SFG electronic spectra, which were obtained by scanning the frequencies of incident visible and JR beams, indicated that the electronic states at the polymer/solid and air/polymer interfaces are red-shifted with respect to that of the bulk. Finally, SFG was employed to study the competition adsorption of toluene and heptane on silica surfaces. Experimental data showed that heptane adsorbed favorably compared to toluene. Using a Langmuir adsorption isotherm, the changes of Gibbs free energy for the adsorption processes were calculated to be —12.1 ± 1.8 (kJ/mol) for toluene and —16.5 ± 2.3 (kJ/mol) for heptane.

Surface properties of polymers and competition adsorption of toluene and heptane on silica were studied using IR-visible sum frequency generation (SFG) vibrational spectroscopy. SFG is intrinsically surface sensitive because the second-order optical process is forbidden in media with inversion symmetry, such as bulk polymers and liquids. This nonlinear optical technique provides surface vibrational spectra under ambient conditions without the need of an ultra-high vacuum environment. Polymer surface properties, including surface relaxation temperature of poly(methyl methacrylate) (PMMA) and surface electronic states of poly[2-methoxy, 5-ethyl (2’-hexyloxy) para phenylenevinylene] (MEH-PPV), were investigated. It was found that there are significant differences between the surface and bulk properties for these polymers. For PMMA, a new surface structure relaxation was identified at 67°C, which does not match any known structure relaxation temperatures for bulk PMMA and is 40°C below the bulk glass transition temperature. For MEH-PPV, SFG electronic spectra, which were obtained by scanning the frequencies of incident visible and JR beams, indicated that the electronic states at the polymer/solid and air/polymer interfaces are red-shifted with respect to that of the bulk. Finally, SFG was employed to study the competition adsorption of toluene and heptane on silica surfaces. Experimental data showed that heptane adsorbed favorably compared to toluene. Using a Langmuir adsorption isotherm, the changes of Gibbs free energy for the adsorption processes were calculated to be —12.1 ± 1.8 (kJ/mol) for toluene and —16.5 ± 2.3 (kJ/mol) for heptane.

Surface properties of polymers and competition adsorption of toluene and heptane on silica were studied using IR-visible sum frequency generation (SFG) vibrational spectroscopy. SFG is intrinsically surface sensitive because the second-order optical process is forbidden in media with inversion symmetry, such as bulk polymers and liquids. This nonlinear optical technique provides surface vibrational spectra under ambient conditions without the need of an ultra-high vacuum environment. Polymer surface properties, including surface relaxation temperature of poly(methyl methacrylate) (PMMA) and surface electronic states of poly[2-methoxy, 5-ethyl (2’-hexyloxy) para phenylenevinylene] (MEH-PPV), were investigated. It was found that there are significant differences between the surface and bulk properties for these polymers. For PMMA, a new surface structure relaxation was identified at 67°C, which does not match any known structure relaxation temperatures for bulk PMMA and is 40°C below the bulk glass transition temperature. For MEH-PPV, SFG electronic spectra, which were obtained by scanning the frequencies of incident visible and JR beams, indicated that the electronic states at the polymer/solid and air/polymer interfaces are red-shifted with respect to that of the bulk. Finally, SFG was employed to study the competition adsorption of toluene and heptane on silica surfaces. Experimental data showed that heptane adsorbed favorably compared to toluene. Using a Langmuir adsorption isotherm, the changes of Gibbs free energy for the adsorption processes were calculated to be —12.1 ± 1.8 (kJ/mol) for toluene and —16.5 ± 2.3 (kJ/mol) for heptane. / Science, Faculty of / Chemistry, Department of / Graduate

This thesis describes the development of a new type of sensor for nitric oxide (NO) that can be used in a variety of combustion diagnostics and control applications. The sensor utilizes the absorption of ultraviolet (UV) radiation by the NO molecule to determine the concentration via optical absorption spectroscopy. UV radiation at 226.8 nm is generated by sum frequency mixing the outputs from a 395-nm external cavity diode laser (ECDL) and a 532-nm diode-pumped, intracavity frequency doubled Nd:YAG laser in a beta-barium borate (BBO) crystal. This radiation is used to probe the (v'=0, v"=0) band of the Α*Σ+ - Χ*π electronic transition of NO. The ECDL is tuned so that the UV radiation is in resonance with a specific energy level transition, and it is then scanned across the transition to produce a fully resolved absorption spectrum. Preliminary experiments were performed in a room-temperature gas cell in the laboratory to determine the accuracy of the sensor. Results from these experiments indicated excellent agreement between theoretical and experimental absorption line shapes as well as NO concentrations. Further experiments were performed at two actual combustion facilities to demonstrate the operation of the sensors in realistic combustion environments. Tests on a gas turbine auxiliary power unit (APU) at Honeywell Engines and Systems and on a well-stirred reactor (WSR) at Wright-Patterson Air Force Base produced excellent results despite the harsh temperatures and vibrations present. Overall, the sensitivity was estimated to be 0.8 parts per million (ppm) of NO (at 1000 K) for a 1 meter path length and the measurement uncertainty was estimated to be ±10%.

This thesis describes the development of a new type of sensor for nitric oxide (NO) that can be used in a variety of combustion diagnostics and control applications. The sensor utilizes the absorption of ultraviolet (UV) radiation by the NO molecule to determine the concentration via optical absorption spectroscopy. UV radiation at 226.8 nm is generated by sum frequency mixing the outputs from a 395-nm external cavity diode laser (ECDL) and a 532-nm diode-pumped, intracavity frequency doubled Nd:YAG laser in a beta-barium borate (BBO) crystal. This radiation is used to probe the (v'=0, v"=0) band of the Α*Σ+ - Χ*π electronic transition of NO. The ECDL is tuned so that the UV radiation is in resonance with a specific energy level transition, and it is then scanned across the transition to produce a fully resolved absorption spectrum. Preliminary experiments were performed in a room-temperature gas cell in the laboratory to determine the accuracy of the sensor. Results from these experiments indicated excellent agreement between theoretical and experimental absorption line shapes as well as NO concentrations. Further experiments were performed at two actual combustion facilities to demonstrate the operation of the sensors in realistic combustion environments. Tests on a gas turbine auxiliary power unit (APU) at Honeywell Engines and Systems and on a well-stirred reactor (WSR) at Wright-Patterson Air Force Base produced excellent results despite the harsh temperatures and vibrations present. Overall, the sensitivity was estimated to be 0.8 parts per million (ppm) of NO (at 1000 K) for a 1 meter path length and the measurement uncertainty was estimated to be ±10%.

Thorough understanding of interfaces requires an assessment of both the surface and bulk properties through the use of multiple techniques. In this thesis, infrared absorption, Raman scattering and sum frequency generation were used as vibrational probes of different features of interfacial systems including the ability to measure surface and bulk effects. Two-dimension correlation analysis was used to study the relationship between the spectral response of the different techniques. Attenuated total reflection absorption, bulk Raman scattering and sum frequency generation were used to study the adsorption of ethanol--water mixture on fused silica. With the use of two-dimension correlation analysis, interesting results were observed concerning the behavior of the surface in respect to the bulk. Surface concentration of ethanol were concluded to be higher than in the bulk indicative of competitive adsorption. Furthermore, at low concentration ethanol was shown to adsorb to the surface in dimers, to then form a bilayer of strongly oriented ethanol molecules at higher concentration. At highest concentration, this bilayer is disturbed, leaving only one layer at the surface of oriented ethanol molecules. The same spectroscopic techniques were applied to pressure sensitive adhesives of different composition while drying on a sapphire surface. The presence or absence of acrylic acid in the material was shown to alter the reorientation at the surface while drying. In the case where no acrylic acid is present, the orientation of the polymer at the surface was driven by the packing of the molecules at the surface. When acrylic acid was present in the pressure sensitive adhesive, reorientation occurred much faster and was caused by strong hydrogen bonding with the surface of the sapphire. An increase in acrylic acid composition, increased the rate of reorientation. An experimental set up was constructed to specifically study interfaces with a nonuniform distribution within the plane of the surface. This allows for concomitant measurement of polarized total internal reflection Raman scattering and sum frequency generation spectroscopy along with bright field imaging and cross polarized imaging. This set up was used to study the L-histidine crystal in situ adsorbed on fused silica. The polarized experiments along with calculations allowed for a more in-depth analysis of the crystal orientation effect on the birefringence, the Raman and the sum frequency generation. / Graduate

L'interface (0001) alpha-quartz hydroxylé/eau liquide est modélisée par dynamique moléculaire dans le formalisme de la théorie de la fonctionnelle de la densité (DFT-MD). Poursuivant une étude déjà publiée sur la structure et la réactivité acido-basique de cette interface, nous élargissons l'analyse aux effets d'ions simples et de pH sur la structure et les propriétés de l'interface avec une attention particulière aux phénomènes d'adsorption ainsi qu'aux modifications de l'eau interfaciale et des sites de surface. Nous caractérisons en particulier les changements dans la réactivité de surface dus à la présence d'ions (cations alcalins et halogénures) par calcul direct de pKa et détaillons la structure de la double couche électrique dans le cas de paires d'ions.Nous cherchons de plus à calculer les spectres SFG (Sum Frequency Generation) vibrationnels à ces interfaces, ce qui serait une première pour une interface solide/liquide traitée au niveau DFT-MD. L'approche théorique de cette spectroscopie vibrationnelle non linéaire du second ordre permettrait de proposer une interprétation claire des bandes d'élongation O-H, alors que les études expérimentales continuent à diverger sur ce sujet. / We use Density-Functional-Theory-based molecular dynamics simulations to investigate the hydroxylated (0001) alpha-quartz/liquid water interface. As a follow up of an already published study on the structural and acid/base properties of this interface, we now focus on simple ion and pH effects on these properties and characterize adsorption behaviors and interfacial changes on both solid and liquid sides. In particular, we directly calculate surface pKa's in presence of ions (alkaline cations and/or halide anions) and provide microscopic details on the structure of the electric double layer when ion pairs are concerned.Besides, we try to apply DFT-MD simulations to the computation of vibrational Sum-Frequency Generation spectra at a solid/liquid interface. Indeed, calculations would be necessary to provide a clear interpretation of the vibrational bands in the OH stretching region since experimental band assignment is still a matter of debate.

The molecular structure and charge on solid surfaces in aqueous environments is of fundamental importance to various scientific research and applications, yet remain not sufficiently understood. The research herein uses sum frequency generation spectroscopy to reveal the molecular structure of the mineral and polymer surfaces, and also probes the water molecules near the charged aqueous interfaces to get information about the surface charge. The application of visible-infrared sum-frequency generation spectroscopy to polymer thin-films requires a careful interpretation of the results, as the electric field magnitude and phase at each interface must be determined in a manner that takes thin film interference effects into account. A straightforward method that has a concise analytic solution in the case of a single thin film that exhibits interference effects was proposed. This method enabled selective probing of transparent thin-films using sum frequency generation spectroscopy, hence eliminated the ambiguity of the contribution of signal from two interfaces. The method was then extended to multiple polarization schemes, enabling easier and more comprehensive study of the molecular orientation on thin-films. Nonlinear vibrational spectroscopy has also been used to study the temperature-dependent surface structure of polydimethylsiloxane when exposed to water and a perfluorinated hydrophobic liquid. Quantitative analysis of the methyl plane orientation was performed using a combination of vibrational peak ratios and peak amplitudes that enable proposed structures to be identified. For both environments, the tilt and twist of the methyl plane was found to increase with temperature in a reversible manner. This has been attributed to be a consequence of the backbone reorganization due to temperature-dependent density changes. At charged aqueous interfaces, the structure of water adjacent to solid interface is sensitive to the surface potential. As a result, close inspection of signals originating from these water molecules can be used to reveal the surface charge density. Nonlinear vibrational spectroscopy was used to monitor the water O-H stretching band over a temperature range of 10-75°C to account for the increase in surface potential from deprotonation. It has been demonstrated that the behavior at the silica surface is a balance between increasing surface charge, and a decreasing contribution of water molecules aligned by the surface charge. Together with a model that accounts for two different types of silanol sites, the change in enthalpy and entropy for deprotonation at each site were reported. The surface charge density of untreated polydimethylsiloxane surface in water with various ionic strengths was also determined. It was found that the surface charge could be explained with an ion adsorption model. A relationship between the surface potential and measured nonlinear optics response that is valid at high potentials and low ionic strength was proposed. Finally, a universal method was demonstrated to derive the surface potential with nonlinear optics by modulating the coherence length. / Graduate / 2022-09-07

Reversed-phase liquid chromatography (RPLC) is a widely used technique for analytical separations but routinely requires empirical optimization. Gaining a better understanding of the molecular reasons for retention may mean more efficient separations with fewer trial and error runs to obtain optimized separations. Vibrationally resonant sum frequency generation (VR-SFG) is a surface specific technique that has allowed for in situ examination of model RPLC stationary phases under various solvent and pressure conditions. In order to improve on past work with model RPLC stationary phases two challenges had to be overcome. First, improved vibrational mode assignments of the C18 stationary phase were needed for proper understanding of this model system. Second, the synthesis of back-surface reference mirrors used in these VR-SFG experiments allowed us to better correct the relative intensities of the various spectral peaks present in typical spectra. After examination of model RPLC systems under various conditions, we have found that these model substrates have a significant amount of interference from nonresonant signal. This interference of resonant and nonresonant signals on fused silica surfaces has not been previously examined and further studies of the model RPLC stationary phase must properly deal with the non-negligible nonresonant interference that is present. We have seen changes in the VR-SFG spectra of these model systems under a variety of conditions including elevated pressure, however the changes are mostly due to nonresonant interference. These spectral changes, although apparently not solely from structural changes, need to be investigated further to better understand the molecular basis of retention in model RPLC systems.

No description available.