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Měření povrchového napětí kapalin / Surface tension measurementsHála, Ondřej January 2017 (has links)
The thesis deals with study of surface tension of liquids and measuring possibilities of this parameter. The paper is then focused on design of measuring apparatus based on pendant drop method. The apparatus is controlled with software written in Matlab. Several measurements are done at the end of this work, which confirm possibility to practical use of this apparatus for surface tension measurements. A part of this work is manual to use the apparatus and complete design documentation.
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Interfacial tension measurements of n-dodecane/CO2 from (298.15 to 573.15) K at pressures up to 10 MPa by pendant drop methodYang, Jian, Bi, Shengshan, Wu, Jiangtao 13 July 2022 (has links)
No description available.
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Avaliação da tensão superficial do PVB e da PA-6. / Evaluation of surface tension of poly(vinyl butyral) and nylon-6.Morais, Douglas 02 September 2008 (has links)
No laboratório de Análise, Processamento e Reologia de Materiais Poliméricos da Escola Politécnica da USP tem sido estudadas blendas de Poliamida-6 (PA-6) e filme de poli(vinil butiral) (PVB), como uma alternativa para reciclagem do filme de PVB oriundo do processo de separação dos componentes do vidro laminado pós-consumo. As propriedades mecânicas de uma blenda polimérica dependem da sua morfologia e, por sua vez, a morfologia depende das propriedades reológicas e da tensão interfacial entre os polímeros formadores da blenda, que para o caso de blendas envolvendo filme de PVB podem mudar em função da concentração de plastificante presente na composição do filme. Apesar da importância do seu conhecimento, a tensão interfacial entre PA-6 e filme de PVB não é conhecida. O presente trabalho teve como objetivo avaliar a tensão superficial do filme de PVB e da PA-6. O método utilizado foi o da gota pendente. Também estudou-se a influência da adição de plastificante na tensão superficial do filme de PVB. Os resultados mostraram que a tensão superficial dos polímeros estudados decresce com o aumento da temperatura (temperatura variando entre 240 e 260ºC). Em particular, para o filme de PVB a entropia de superfície ( (d/dT) ) apresentou um valor acima dos normalmente encontrados para polímeros fundidos. Este comportamento foi atribuído à estabilidade térmica do filme. O filme de PVB utilizado nos ensaios de tensão superficial foi caracterizado por Espectroscopia no Infravermelho (FTIR), Espectroscopia no Ultravioleta/Visível (UV-VIS), Espectroscopia Eletrônica para Análise Química (ESCA) e Análise Termogravimétrica (TG). Os resultados obtidos comprovaram que há mudanças na estrutura do PVB durante sua exposição a temperaturas elevadas, por longo período de tempo (condições do ensaio de tensão superficial). Foi observado, primeiramente, a evaporação do plastificante, seguida por perda de grupos polares (-OH, C=O e C-O-C) presentes na estrutura do PVB. A tensão superficial da Poliamida-6 foi determinada para temperaturas de 250 e 260ºC. Os resultados mostraram que a PA-6 manteve-se estável durante os ensaios. / In the Rheology and Polymer Processing Laboratory of Escola Politécnica of the University of São Paulo, Polyamide-6 / poly(vinyl butiral) film blends have been studied as an alternative for the recycling of post-consumption laminated glasses. The mechanical properties of these blends were studied and explained in light of their morphology. The morphology of polymer blends strongly depends on the rheological behavior of the blend and on the interfacial tension between the polymers forming the blend. In the case of Poliamide-6 (PA-6)/poly(vinyl butiral) (PVB) film blends, the interfacial tension depends on the plasticizer concentration present in PVB film. However, to our knowledge neither the PA-6/PVB film interfacial tension nor the surface tension of PVB film at temperatures above softening temperatures have been evaluated. In this work, the surface tension of poly(vinyl butyral) and polyamide was evaluated using the pendant drop method. Also it was tried to evaluate the surface tension of PVB film as a function of plasticizer content. The surface tension values obtained were in the same range as the ones obtained for other molten polymers: the surface tension decreases with increasing temperature (for temperatures ranging from 240 to 260°C). However, the value of PVB film surface entropy ((d/dT) where is the surface tension and T is the temperature) was much larger than values reported for other molten polymers. This result was attributed to thermal stability of PVB film during the surface tension measurement. The drops of PVB film after surface tension analysis were examined for any change in their functional groups using infrared spectroscopy (FITIR), ultraviolet-visible spectroscopy (UV/VIS), electron spectroscopy for chemical analysis (XPS/ESCA) and thermogravimetric analysis (TG). The results showed that changes in the chemical structure of PVB film occur during surface tension measurement. First, the plasticizer within the PVB film evaporates and, then, the PVB suffers reduction of polar units and creation of C=C bonds. The surface tension of PA-6 was evaluated for temperatures of 250 and 260°C. The PA-6 remained stable during tests.
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Avaliação da tensão superficial do PVB e da PA-6. / Evaluation of surface tension of poly(vinyl butyral) and nylon-6.Douglas Morais 02 September 2008 (has links)
No laboratório de Análise, Processamento e Reologia de Materiais Poliméricos da Escola Politécnica da USP tem sido estudadas blendas de Poliamida-6 (PA-6) e filme de poli(vinil butiral) (PVB), como uma alternativa para reciclagem do filme de PVB oriundo do processo de separação dos componentes do vidro laminado pós-consumo. As propriedades mecânicas de uma blenda polimérica dependem da sua morfologia e, por sua vez, a morfologia depende das propriedades reológicas e da tensão interfacial entre os polímeros formadores da blenda, que para o caso de blendas envolvendo filme de PVB podem mudar em função da concentração de plastificante presente na composição do filme. Apesar da importância do seu conhecimento, a tensão interfacial entre PA-6 e filme de PVB não é conhecida. O presente trabalho teve como objetivo avaliar a tensão superficial do filme de PVB e da PA-6. O método utilizado foi o da gota pendente. Também estudou-se a influência da adição de plastificante na tensão superficial do filme de PVB. Os resultados mostraram que a tensão superficial dos polímeros estudados decresce com o aumento da temperatura (temperatura variando entre 240 e 260ºC). Em particular, para o filme de PVB a entropia de superfície ( (d/dT) ) apresentou um valor acima dos normalmente encontrados para polímeros fundidos. Este comportamento foi atribuído à estabilidade térmica do filme. O filme de PVB utilizado nos ensaios de tensão superficial foi caracterizado por Espectroscopia no Infravermelho (FTIR), Espectroscopia no Ultravioleta/Visível (UV-VIS), Espectroscopia Eletrônica para Análise Química (ESCA) e Análise Termogravimétrica (TG). Os resultados obtidos comprovaram que há mudanças na estrutura do PVB durante sua exposição a temperaturas elevadas, por longo período de tempo (condições do ensaio de tensão superficial). Foi observado, primeiramente, a evaporação do plastificante, seguida por perda de grupos polares (-OH, C=O e C-O-C) presentes na estrutura do PVB. A tensão superficial da Poliamida-6 foi determinada para temperaturas de 250 e 260ºC. Os resultados mostraram que a PA-6 manteve-se estável durante os ensaios. / In the Rheology and Polymer Processing Laboratory of Escola Politécnica of the University of São Paulo, Polyamide-6 / poly(vinyl butiral) film blends have been studied as an alternative for the recycling of post-consumption laminated glasses. The mechanical properties of these blends were studied and explained in light of their morphology. The morphology of polymer blends strongly depends on the rheological behavior of the blend and on the interfacial tension between the polymers forming the blend. In the case of Poliamide-6 (PA-6)/poly(vinyl butiral) (PVB) film blends, the interfacial tension depends on the plasticizer concentration present in PVB film. However, to our knowledge neither the PA-6/PVB film interfacial tension nor the surface tension of PVB film at temperatures above softening temperatures have been evaluated. In this work, the surface tension of poly(vinyl butyral) and polyamide was evaluated using the pendant drop method. Also it was tried to evaluate the surface tension of PVB film as a function of plasticizer content. The surface tension values obtained were in the same range as the ones obtained for other molten polymers: the surface tension decreases with increasing temperature (for temperatures ranging from 240 to 260°C). However, the value of PVB film surface entropy ((d/dT) where is the surface tension and T is the temperature) was much larger than values reported for other molten polymers. This result was attributed to thermal stability of PVB film during the surface tension measurement. The drops of PVB film after surface tension analysis were examined for any change in their functional groups using infrared spectroscopy (FITIR), ultraviolet-visible spectroscopy (UV/VIS), electron spectroscopy for chemical analysis (XPS/ESCA) and thermogravimetric analysis (TG). The results showed that changes in the chemical structure of PVB film occur during surface tension measurement. First, the plasticizer within the PVB film evaporates and, then, the PVB suffers reduction of polar units and creation of C=C bonds. The surface tension of PA-6 was evaluated for temperatures of 250 and 260°C. The PA-6 remained stable during tests.
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The effect of interfacial tension in CO<sub>2</sub> assisted polymer processingHongbo, Li 29 September 2004 (has links)
No description available.
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Stabilized Nanobubbles for Diagnostic ApplicationsHernandez, Christopher 01 June 2018 (has links)
No description available.
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Dynamics of Surfactants at Soft Interfaces using Droplet-Based MicrofluidicsRiechers, Birte 21 December 2015 (has links)
No description available.
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Dynamique et rhéologie interfaciales à haute fréquence d'une goutte oscillante / Interfacial dynamics and rheology of an oscillating drop at high frequencyAbi Chebel, Nicolas 11 December 2009 (has links)
Ce travail présente une étude de la dynamique interfaciale de gouttes oscillantes dans une plage étendue de fréquences, en particulier dans le domaine des hautes fréquences. Nous avons développé une méthode de caractérisation de la dynamique des oscillations de gouttes, en présence d’un forçage externe imposé, sous la forme de variations de volume périodiques de faible amplitude sur une goutte attachée à l’extrémité d’un capillaire. Cette méthode permet d’identifier les modes d’oscillation des gouttes et d’en mesurer les fréquences et les taux d’amortissement. Cette méthode a été appliquée à différents systèmes liquide-liquide, en l’absence ou en présence de surfactants. Dans ce dernier cas, elle permet d’évaluer l’effet du comportement viscoélastique des interfaces sur la dynamique des oscillations. Ainsi 3 types d’interfaces ont été identifiés. Pour les interfaces de premier type (heptane/eau sans ajout de surfactant), chaque mode propre est modélisé par un oscillateur linéaire peu amorti. Les fréquences propres et les taux d’amortissement sont bien prédits par la théorie linéaire. Les interfaces de types 2 et 3 sont obtenues en ajoutant du pétrole brut à la phase dispersée. Les surfactants naturellement présents dans le pétrole (asphaltènes, résines) s’adsorbent à l’interface et lui confèrent des propriétés viscoélastiques. Pour les interfaces jeunes (type 2, moins de 20 minutes de vieillissement), les fréquences propres mesurées restent bien prédites par la théorie, qui considère des interfaces non contaminées, tandis que les taux d’amortissement sont de loin supérieurs aux valeurs théoriques. D’autre part, les interfaces vieillies (type 3) présentent des modes propres différents avec des fréquences de résonance supérieures à celles des interfaces jeunes. Dans ce cas, la dynamique de l’interface à haute fréquence est régie par l’élasticité du réseau formé par les espèces amphiphiles du pétrole brut. Les oscillations libres d’une goutte en ascension dans une phase externe stagnante, pour un système liquide-liquide sans ajout de surfactants, ont été étudiées. Les valeurs mesurées de la fréquence d’oscillation des 4 premiers modes sont en adéquation avec la théorie linéaire. Cependant les valeurs mesurées du taux d’amortissement sont très élevées par rapport aux valeurs théoriques, pour une interface non contaminée. En effet, des espèces résiduelles adsorbées à l’interface provoquent l’apparition d’un gradient de tension interfaciale par effet Marangoni et par suite une production de vorticité plus intense dans les couches-limites, ce qui conduit à l’augmentation de l’amortissement des oscillations. / We present an experimental study of oscillating drop interfacial dynamics at a wide frequency range, especially at high frequency. A characterization method of drops oscillation dynamics has been developed. The oscillations are generated by imposing low amplitude periodic variation of volume to a drop which is attached to a capillary tip. The present method is based on the identification of the drop eigenmodes and the determination of their frequencies and damping rates. It has been applied to characterize several liquid-liquid systems. Three types of interface have been identified. For interfaces of type 1 (heptane/water without added surfactant), each eigenmode is modelled by a weakly damped linear oscillator. Eigenfrequencies and damping rates are well predicted by the linear theory. Interfaces of Types 2 and 3 are obtained by adding crude oil to the disperse phase. Oil native surfactants (asphaltenes, resins) adsorb on the drop interface and provide the latter with viscoelastic behaviour. For young interfaces (type 2 with aging time below 20 minutes), eigenfrequencies remain well predicted by the theory, which deals with non contaminated interfaces, whereas the measured damping rates are significantly higher than the theoretical values. On the other hand, aged interfaces (type 3) exhibit different eigenmodes, of which eigenfrequencies are much higher than the resonance frequencies measured for the young interfaces. At high frequency, the dynamics of aged interfaces are governed by the elasticity of the network constituted by the crude oil amphiphilic species, while the dynamics of young interfaces are governed by interfacial tension. Freely decaying oscillations of a rising drop in a liquid at rest without added surfactant were also considered. Measured frequencies for the first four eigenmodes are in good agreement with the linear theory. However, measured damping rates are much higher than the theoretical rates for non contaminated interfaces. In fact, residual adsorbed species at the heptane/water interface induce Marangoni effects and thus gradients of interfacial tension. Therefore, vorticity production within the boundary layers is enhanced, which explains the observed increase of the oscillation damping rates.
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Extension du modèle de tracé de rayons vectoriels complexes et application à la caractérisation d'une particule non-sphérique / Extension of vectorial complex ray model and its application to the metrology of non-spherical particlesMa, Zelong 31 January 2018 (has links)
Cette thèse est dédiée à l'extension du Tracé de Rayons Vectoriels Complexes (TRVC) développé au laboratoire et son application à la caractérisation des particules non-sphériques. Dans divers domaines de recherche, tels que la mécanique des fluides et la combustion, nous devons mesurer les caractéristiques des particules. Parmi les différents types de techniques de mesure, la métrologie optique est largement utilisée grâce à sa précision et sa fiabilité. Cependant, la forme des particules est souvent considérée comme sphérique principalement à cause du manque de moyens pour prédire avec précision l'interaction de la lumière avec de grandes particules non-sphériques. TRVC a été développé pour répondre à ces besoins. Il est basé sur le modèle de rayons mais une amélioration radicale a été apportée dans ce nouveau modèle par l'introduction d'une nouvelle propriété dans la notion de rayons lumineux - la courbure de front d'onde. Dans cette thèse, le modèle est appliqué à réexaminer la théorie d'Airy. Il a été montré que TRVC prédit mieux les intensités et les positions des lobes secondaires dans les arcs-en-ciel d'une particule sphérique que la théorie d'Airy. Ensuite, TRVC est appliqué à l'étude des propriétés des arcs-en-ciel formés par les ellipsoïdes allongé et aplati. Il est montré que TRVC peut prédire analytiquement les positions et les intensités de lobes secondaires dans les arcs-en-ciel d’une particule sphéroïdale lorsqu’elle est éclairée par une onde plane dans le plan symétrique. Les pics dus à l'effet focal d'une particule sphéroïdale aplatie ont également été évalués analytiquement en utilisantle facteur de divergence de TRVC. Un système de mesure est aussi mis en place dans le laboratoire pour la diffusion de la lumière par des gouttes pendantes. Il a été montré que le rapport des intensités des deux premiers arcs-en-ciel est sensible à l'ellipticité d'un sphéroïde équivalent. Ceci ouvre un champ d'application potentiel pour caractériser la déformation d'une goutte pendante. / This thesis is dedicated to the extension of Vectorial Complex Ray Model (VCRM)developed in the laboratory and its application in the characterization of large nonspherical particles. In various research domains, such as the uid mechanics and the combustion field, we need to measure the characteristics of the particles. Among di_erent kinds of measurement techniques, the optical metrology is largely employed due to its advantage of being accurate, reliable and non-intrusive. However, in many optical techniques, the shape of the particles is assumed to be spherical. The main reason of this limit is due to the lack of theoretical model to describe with precision the interaction of light with large non-spherical particles. The Vectorial Complex Ray Model has been developed to reply this demand. It is based on the ray model but a radical improvement has been done by introducing a new property the wave front curvatures in the ray model. In this thesis, the model is firstly applied to reexamine the Airy theory. It is shown that even in the case of spherical particle VCRM predicts better the intensity and positions of supernumerary bows of rainbow than the Airy theory. Then VCRM is applied to investigate the properties of the rainbows formed by a spheroidal (prolate or oblate) particle. It is shown that VCRM can predict analytically the positions and the intensity of supernumerary bows and the peaks due to the focal effect when it is illuminated by a plane wave in the symmetrical plane.The theoretical research results have been also applied to the experimental characterization of a pendant drop. The intensity ratio of the two first orders of rainbow is shown sensible to the aspect ratio of the equivalent spheroid and it opens a potential to develop a measurement technique to characterize the deformation of pendant drop.
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