O objetivo global deste trabalho foi fornecer subsídios para melhor compreender como as políticas públicas voltadas às emissões veiculares, incluindo o uso de etanol combustível, podem afetar a composição química da atmosfera. O peróxido de hidrogênio (H2O2) é um dos oxidantes mais importantes presentes na troposfera, podendo participar de reações com uma variedade de compostos orgânicos e inorgânicos. Neste trabalho, a determinação de H2O2, etanol, acetaldeído e outras espécies orgânicas e inorgânicas, foi realizada na fase gasosa, água de chuva e em águas superficiais. Foi utilizado de forma pioneira o método fluorimétrico baseado na formação do fluoróforo 2,7-diclorofluoresceína para determinar H2O2 em amostras de águas naturais (LD = 2 nmol L-1 e LQ = 7 nmol L-1). Enquanto outros métodos demandam a análise imediata da amostra, neste caso, o fluoróforo permanece estável por cerca de 48 h, facilitando as análises e o trabalho de campo. A concentração de H2O2 na água de chuva de Ribeirão Preto coletada de 2014 a 2017 variou entre 5,8 e 96 mol L1, com média ponderada pelo volume (MPV) de 28,9 ± 1,3 µmol L-1 (n = 88). Foi observado que a radiação solar foi um parâmetro mais importante na formação de H2O2 do que no seu consumo. Enquanto as concentrações MPV de sulfato (pH < 5) e nitrato na água de chuva decresceram em torno de 35% em 2017 com relação a 2014, as concentrações de H2O2 praticamente dobraram no mesmo período. A correlação negativa entre essas espécies evidencia que as políticas nacionais destinadas a reduzir as emissões veiculares podem alterar a capacidade oxidativa da atmosfera. As concentrações de H2O2, etanol e acetaldeído na fase gasosa em Ribeirão Preto (RP) e São Paulo (SP) foram determinadas, utilizando de forma pioneira no Brasil, o método de coleta do condensado. As concentrações de etanol na atmosfera de RP (15,0 ± 6,6 ppbv, n = 19) e SP (22,0 ± 9,4 ppbv, n = 10) foram relativamente próximas, apesar da frota veicular de SP ser ~ 16 vezes maior. Essas concentrações de etanol são cerca de 21 vezes maiores que aquelas relatadas nos Estados Unidos devido ao elevado uso de etanol combustível no Brasil. As médias das concentrações de H2O2 e acetaldeído na atmosfera foram, respectivamente, de 2,10 ± 1,46 e 16,3 ± 6,0 ppbv em RP; e 1,29 ± 0,62 e 14,4 ± 5,4 ppbv em SP. A avalição diurna mostrou que enquanto a concentração de H2O2 aumentou com a radiação solar, a concentração de etanol diminuiu numa taxa próxima da produção de acetaldeído. Esses resultados indicam que o H2O2 pode ser um oxidante importante de etanol a acetaldeído em fase gasosa, sendo este último de elevada toxicidade para o ser humano. Os fluxos na interface ar-água nos locais estudados em RP e SP mostram que o corpo dágua funcionou como um sumidouro de H2O2. Já o fluxo de etanol foi variável, isto é, ora invasivo e ora evasivo, com evidências de uma importante produção fotoquímica dessa espécie no meio aquático. / The main objective of this work was to provide insights to better understand how the public policies focused on vehicular emissions, including the use of ethanol fuel, can affect the chemical composition of the atmosphere. Hydrogen peroxide (H2O2) is one of the most important oxidants in the troposphere and it can participate in reactions with a variety of organic and inorganic compounds. In this work, determination of H2O2, ethanol, acetaldehyde and other organic and inorganic species was carried out in the gas phase, rainwater and surface water. The fluorimetric method based on the formation of the 2, 7-dichlorofluorescein fluorophore was applied for the first time to determine H2O2 in natural water samples (LOD = 2 nmol L-1 and LOQ = 7 nmol L-1). While other methods require the immediate analysis of the sample, in this case, the fluorophore remains stable for about 48 h, facilitating the analyzes and fieldwork. H2O2 concentrations in rainwater of Ribeirão Preto collected between 2014 and 2017 ranged from 5.8 to 96 mol L-1, with a volume-weighted mean (VWM) of 28.9 ± 1.3 mol L-1 (n = 88). The solar radiation was observed to be a more important parameter in the formation of H2O2 than in its consumption. While the VWM concentrations of sulfate (pH <5) and nitrate in rainwater declined by approximately 35% in 2017 compared to 2014, H2O2 concentrations virtually doubled over the same period. The negative correlation between these species shows that national policies aimed at reducing vehicle emissions may modify the oxidizing capacity of the atmosphere. Gas phase H2O2, ethanol and acetaldehyde concentrations in Ribeirão Preto (RP) and São Paulo (SP) were determined using, for the first time in Brazil, the method of condensate collection. Ethanol concentrations in the atmosphere of RP (15.0 ± 6.6 ppbv, n = 19) and SP (22.0 ± 9.4 ppbv, n = 10) were relatively close, although the SP vehicle fleet is ~ 16 times higher. These ethanol concentrations are about 21 times higher than those reported in the United States due to the high use of ethanol fuel in Brazil. The mean concentrations of H2O2 and acetaldehyde in the atmosphere were, respectively, 2.10 ± 1.46 and 16.3 ± 6.0 ppbv in RP; and 1.29 ± 0.62 and 14.4 ± 5.4 ppbv in SP. Daytime variation showed that while H2O2 concentration increased with solar radiation, ethanol concentration decreased at a rate close to the one of acetaldehyde production. These results indicate that H2O2 may be an important oxidant of ethanol to acetaldehyde in the gas phase, the latter being highly toxic to humans. Fluxes in the air-water interface at the studied sites in RP and SP show that the water body worked as an H2O2 sink. On the other hand, ethanol fluxes were variable, i.e., sometimes invasive and sometimes evasive, with evidence of an important photochemical production of this species in the aquatic environment.

O parâmetro que determina o processo de transferência de oxigênio através da interface ar-água em escoamentos com superficie livre é o coeficiente de reaeração superficial, \'K IND.2\'. Existe um grande número de equações na literatura científica que realizam a previsão do coeficiente de reaeração, no entanto, a maioria dessas equações considera apenas algumas características hidráulicas do corpo de água como a velocidade e a profundidade, e ainda, como em sua maioria são de natureza empírica, acabam sendo adequadas para corpos de água específicos. Além destes dois parâmetros (velocidade e profundidade do escoamento), existem outros doze que são considerados importantes para estudos de reoxigenação em águas superficiais. É neste contexto que o objetivo deste trabalho foi estudar em condições de laboratório a influência da rugosidade do leito de um canal sobre o coeficiente de reaeração superficial. Além da rugosidade, foram variadas as condições de velocidade média do escoamento e profundidade da lâmina de água. A variação da rugosidade foi realizada através da implementação de obstáculos com geometria conhecida, dispostos transversalmente ao escoamento, e denominados como macro-rugosidades. Os resultados demonstraram evidências de que o coeficiente de reaeração superficial é controlado de forma significativa pela rugosidade do leito do canal. Foram desenvolvidos dois modelos matemáticos de natureza semi-empírica para a previsão do \'K IND.2\', os quais incorporam variáveis hidrodinâmicas e geométricas consideradas relevantes para o processo de transferência de massa na interface ar-água. / The parameter that determines the process of oxygen transfer through the air-water interface in flows with free surface is the superficial reaeration coefficient, \'K IND.2\'. There are a large quantity of equations in the cientific literature that perform the prevision of the reaeration coefficient; however, most of them consider only some of the hydraulic characteristics of water body; for example, the velocity and the depth. Most of these equations have empirical origin and are adequate just for a specific water body. In addition to these two parameters (velocity and depth of flow), there are another twelve important parameters in reoxygenation studies in superficial waters. In this context, the aim of this work was to study the influence of bed roughness of a channel on the superficial reaeration coefficient, under laboratory conditions. Besides the roughness, the conditions of mean velocity of the flow and depth of water were varied. The variation of roughness was done with implementation of obstacles with known geometry, arranged transversely to the flow direction, and called macro-roughness. The results have shown evidences that the surface reaeration coefficient is controlled significantly by the roughness of the channel bed. Two mathematical models of semi-empirical origin for the \'K IND.2\' prevision were developed, which incorporate hydrodynamic and geometric variables considered relevant in the process of mass transfer in air-water interface.

Adsorption layers of soluble surfactants enable and govern a variety of phenomena in surface and colloidal sciences, such as foams. The ability of a surfactant solution to form wet foam lamellae is governed by the surface dilatational rheology. Only systems having a non-vanishing imaginary part in their surface dilatational modulus, E, are able to form wet foams. The aim of this thesis is to illuminate the dissipative processes that give rise to the imaginary part of the modulus. <br><br> There are two controversial models discussed in the literature. The reorientation model assumes that the surfactants adsorb in two distinct states, differing in their orientation. This model is able to describe the frequency dependence of the modulus E. However, it assumes reorientation dynamics in the millisecond time regime. In order to assess this model, we designed a SHG pump-probe experiment that addresses the orientation dynamics. Results obtained reveal that the orientation dynamics occur in the picosecond time regime, being in strong contradiction with the two states model. <br><br> The second model regards the interface as an interphase. The adsorption layer consists of a topmost monolayer and an adjacent sublayer. The dissipative process is due to the molecular exchange between both layers. The assessment of this model required the design of an experiment that discriminates between the surface compositional term and the sublayer contribution. Such an experiment has been successfully designed and results on elastic and viscoelastic surfactant provided evidence for the correctness of the model. <br><br> Because of its inherent surface specificity, surface SHG is a powerful analytical tool that can be used to gain information on molecular dynamics and reorganization of soluble surfactants. They are central elements of both experiments. However, they impose several structural elements of the model system. During the course of this thesis, a proper model system has been identified and characterized. The combination of several linear and nonlinear optical techniques, allowed for a detailed picture of the interfacial architecture of these surfactants. / Amphiphile vereinen zwei gegensätzliche Strukturelemente in einem Molekül, eine hydrophile Kopfgruppe und ein hydrophobe, meist aliphatische Kette. Aufgrund der molekularen Asymmetrie erfolgt eine spontane Adsorption an der Wasser-Luft Grenzfläche. Die Adsorptionsschicht verändert die makroskopischen Eigenschaften des Materials, z.B. die Grenzflächenspannung wird erniedrigt. Amphiphile sind zentrale Bauelemente der Kolloid- und Grenzflächenforschung, die Phänomene, wie Schäume ermöglichen. <br><br> Eine Schaumlamelle besteht aus einem dünnen Wasserfilm, der durch zwei Adsorptionsschichten stabilisiert wird. Die Stabilität der Lamelle wird durch die Grenzflächenrheologie entscheidend geprägt. Die wesentliche makroskopische Größe in diesem Zusammenhang ist das so genannte Grenzflächendilatationsmodul E. Es beschreibt die Fähigkeit des Systems die Gleichgewichtsgrenzflächenspannung nach einer Expansion oder Dilatation der Adsorptionschicht wieder herzustellen. Das Modul E ist eine komplexe Größe, in dem der Imaginärteil direkt mit der Schaumstabilität korreliert. <br><br> Diese Arbeit widmet sich der Grenzflächenrheologie. In der Literatur werden zwei kontroverse Modelle zur Interpretation dieser Größe diskutiert. Diese Modelle werden experimentell in dieser Arbeit überprüft. Dies erfordert die Entwicklung neuer experimenteller Aufbauten basierend auf nichtlinearen, optischen Techniken. Mit diesen Experimenten konnte eines der Modelle bestätigt werden.

A new measurement technique called fiber optic reflectometer (FOR) was developed to investigate multiphase flows. The principle and setup of the FOR technique were introduced and applied to various experiments. Based on the coherently mixed signal between the Fresnel reflection off the fiber-liquid interface and the scattered signal off the object, such as a gas bubble, and a solid particle, this single probe technique is capable of simultaneously measuring the velocity of the object with a high accuracy and the phase of the fluid. In addition, bubble diameter, velocity, and void fraction were measured directly. By means of a simple modification of the FOR technique, solute concentration and refractive index change were measured with a greatly improved accuracy. This modified technique was used for measuring of a NaCl concentration in deionized water to validate a new normalization technique. In the second part of this thesis, a plunging breaking wave in deep water has been studied. Using the wave focusing method, a strong plunging breaker was generated with accuracy in the deep water condition in a two-dimensional wave tank. It was possible to describe the breaking process in detail using a high speed camera with a frame rate of 500 or 1000 fps. Four kinds of experimental techniques were employed or developed to investigate the plunging breaker. Bubble image velocimetry (BIV) and particle image velocimetry (PIV) were used to measure the velocity fields. The velocity fields of the highly aerated region were obtained from the BIV measurements. In addition, the modified PIV technique is capable of measuring the velocities in the entire flow field including the aerated region. Mean and turbulent properties were obtained by the ensemble average. The mean velocity, mean vorticity, and mean kinetic energy were examined over the entire flow field. In addition, the Reynolds stresses and turbulent kinetic energy were calculated with high temporal and spatial resolutions. Free surface elevation was obtained from wave gauge measurements. BIV and PIV images were also used to obtain the free surface elevation and the boundary of the aerated region for more accurate results. The FOR technique was used to obtain the void ratio at each splash-up region. Compressibility of the plunging breaker was considered. Mass flux, momentum flux, kinetic energy, and Reynolds stresses at each FOR station were recalculated using the void ratio obtained from the FOR measurements. All terms at the first splash-up region were highly overestimated more than 100 percent unless the void ratio was applied to the calculation of fluxes and energies. Compared with the fully developed first splash-up region, the overestimation at the second and third splash-up was less significant. However, most terms were overestimated by 20~30 percent when the void ratio was not considered.

The air-water interface is abundant in the environment, thus it is an important proxy for atmospheric processes such as the uptake and transfer of molecules, heterogeneous reactions, photochemistry, and cloud condensation. This thesis aims to elucidate the role of semi-soluble and insoluble organic coatings on atmospheric processes at the air-water interface. Using glancing-angle LIF it was found that monolayer coatings of 1-octanol and of octanoic acid have opposing effects on the ozonation rate of pyrene at the air-water interface. LIF was also coupled with a Profile Analysis Tensiometer (PAT-1) to measure the effect of stearic acid coating compression on the uptake of HCl to a water droplet. Due to preliminary issues with this novel technique, no significant uptake suppression was observed. The oxidation of benzene by OH radical was also explored briefly, as were the photophysics of photosensitizers and the angle dependence of Raman signal from a D2O pendent droplet.

The air-water interface is abundant in the environment, thus it is an important proxy for atmospheric processes such as the uptake and transfer of molecules, heterogeneous reactions, photochemistry, and cloud condensation. This thesis aims to elucidate the role of semi-soluble and insoluble organic coatings on atmospheric processes at the air-water interface. Using glancing-angle LIF it was found that monolayer coatings of 1-octanol and of octanoic acid have opposing effects on the ozonation rate of pyrene at the air-water interface. LIF was also coupled with a Profile Analysis Tensiometer (PAT-1) to measure the effect of stearic acid coating compression on the uptake of HCl to a water droplet. Due to preliminary issues with this novel technique, no significant uptake suppression was observed. The oxidation of benzene by OH radical was also explored briefly, as were the photophysics of photosensitizers and the angle dependence of Raman signal from a D2O pendent droplet.

If air is entrained in a bottom outlet of a dam in an uncontrolled way, the resulting air pockets may cause problems such as blowback, blowout and loss of discharge capacity. In order to provide guidance for bottom outlet design and operation, this study examines how governing parameters affect air entrainment, air-pocket transport and de-aeration and the surrounding flow structure in pipe flows. Both experimental and numerical approaches are used. Air can be entrained into the bottom outlet conduit due to vortex formation at the intake if the intake submergence is not sufficient. The influent of the intake entrance profiles and channel width on the critical submergence were studied in the experiment. The experimental study was performed to investigate the incipient motion of air pockets in pipes with rectangular and circular cross sections. The critical velocity is dependent on pipe slope, pipe diameter, pipe roughness and air-pocket volume. If the pipe is horizontal, air removal is generally easier in a rectangular pipe than in a circular pipe. However, if the pipe is downward-inclined, air removal is easier in a circular pipe. When a bottom outlet gate opens, air can become entrained into the conduit in the gate shaft downstream of the gate. Using FLUENT software, the transient process of air entrainment into a prototype bottom outlet during gate opening is simulated in three dimensions. The simulations show in the flow-pattern changes in the conduit and the amount of air entrainment in the gate shaft. The initial conduit water level affects the degree of air entrainment. A de-aeration chamber is effective in reducing water surface fluctuations at blowout. High-speed particle image velocimetry (HSPIV) were applied to investigate the characteristics of the flow field around a stationary air pocket in a fully developed horizontal pipe flow. The air pocket generates a horseshoe vortex upstream and a reverse flow downstream. A shear layer forms from the separation point. Flow reattachment is observed for large air pockets. The air―water interface moves with the adjacent flow. A similarity profile is obtained for the mean streamwise velocity in the shear layer beneath the air pocket. / <p>QC 20140211</p>

A series of detailed laboratory investigations were conducted to examine low solubility gas transfer across wind-forced wavy air-water interfaces. The study focuses on the increase in gas flux associated with the microphysical interfacial wind momentum exchange and the complex wave coupled hydrodynamics. Key elements of the laboratory investigations included the measurement of hydrodynamic behaviour within the aqueous viscous sub-layer using a particle image velocimetry (PIV) system and the development of a Laser Induced Fluorescent (LIF) system capable of measuring reliable dissolved oxygen concentration profiles to within 28??m of the air-water interface. Major achievements and findings included: 1. The first phase resolved gas flux measurements along wind forced microscale waves, indicating the highest mean gas fluxes are located in the wave troughs. This finding demonstrated the relative importance of wave orbital straining in gas flux enhancement; a wave coupled hydrodynamic process whose significance has previously been neglected. 2. The relative contributions to gas flux from wind shear, wave orbital straining, increased surface area of the waves, parasitic capillary ripples and microscale breaking are quantified with respect to friction velocity, wave steepness and an efficiency of microscale wave breaking. The parasitic capillary ripples are shown to have a negligible role in gas enhancement. A hybrid model is developed to estimate the gas flux based on both wind and wave characteristics. 3. Gas enhancement due to microscale wave breaking and the significance of the highly localised subduction at the toe of the spilling region on the leeward face of the wave crests was investigated using data from the LIF experiments. The highly localised subduction was shown to substantially reduce the thickness of the diffusion sub-layer, resulting in an increase in gas flux when waves transitioned from the incipient breaking to the microscale breaking wave form. 4. Consideration of previously unidentified optical distortions in LIF imagery due to non-linear effects is presented that is critical for robust LIF data processing and experimental design. A formal mathematical description of optical distortions has been developed and presented.

The surface behavior of biologically or atmospherically relevant chemical compounds in aqueous solution has been studied using surface-sensitive X-ray photoelectron spectroscopy (XPS). The aim is to provide information on the molecular-scale composition and distribution of solutes in the surface region of aqueous solutions. In the first part, the distribution of solutes in the surface region is discussed, where in particular single molecular species are studied. Concentration-dependent studies on succinic acid and various alkyl-alcohols, where also parameters such as pH and branching are varied, are analyzed using different approaches that allow the quantification of surface concentrations. Furthermore, due to the sensitivity of XPS to the chemical state, reorientation of linear and branched alkyl-alcohols at the aqueous surface as a function of concentration is observed. The results are further discussed in terms of hydrophilic and hydrophobic interactions in the interfacial region, where the three-dimensional hydrogen bonded water structure terminates. In the second part, mixed solutions of compounds, both ionic and molecular, are inspected. Again concentration, but also co-dissolution of other chemical compounds, are varied and differences in the spatial distribution and composition of the surface region are discussed. It is found that the guanidinium ion has an increased propensity to reside at the surface, which is explained by strong hydration in only two dimensions and only weak interactions between the aromatic π-system and water. Ammonium ions, on the other hand, which require hydration in three dimensions, are depleted from the surface region. The presence of strongly hydrated electrolytes out-competes neutral molecules for hydrating water molecules leading to an enhanced abundance of molecules, such as succinic acid, in the interfacial region. The partitioning is quantified and discussed in the context of atmospheric science, where the impact of the presented results on organic loading of aerosol particles is emphasized.

L’interface air-eau est un milieu où la tension de surface intervient en permanence pour minimiser l’énergie de la surface. Cette force est à l’origine des phénomènes capillaires que les organismes semi-aquatiques exploitent. L’objectif de cette thèse est d’étudier l’importance de ces phénomènes dans l’écologie des organismes semi-aquatiques en prenant les gyrins comme modèle. Les résultats montrent que le ménisque bipolaire produit par les gyrins est responsable d’auto-assemblables statiques entre individus immobiles. Les gyrins utilisent également différents types de nage pour minimiser les forces de résistance qu’ils rencontrent, notamment la force liée à la production d’onde. L’étude expérimentale de la perception d’objets immobiles suggère la perception des ménisques par les gyrins. L’écholocation grâce aux ondes de surface, supposée dans la littérature, ne peut cependant être exclue. / The surface tension at the air-water interface is responsible for capillary phenomena minimizing surface energies. Semi-aquatic organisms have evolved to exploit this capillarity. The purpose of this thesis is to study the importance of capillary phenomena in the ecology of semi-aquatic organisms using whirligig beetles as a model. Results show that the bipolar meniscus produced around whirligig beetles is responsible for static self-assembly between individuals. These insects use different types of swimming to minimize resistance forces, especially the wave drag. The experimental study of the detection of immobile objects suggests that whirligig beetles perceive the menisci. Echolocation using surface waves, assumed in literature, cannot however be excluded.