Tendo em vista a busca por matérias-primas de fontes renováveis e menos poluentes, e o crescente aproveitamento de subprodutos gerados por estas fontes, surgiu o interesse em estudar a síntese do carbonato de glicerina a partir da glicerina obtida como subproduto principal na fabricação de biodiesel. Sintetizou-se este composto no Laboratório de Química Orgânica Aplicada. Este tensoativo não é disponível no Brasil e possui propriedades cosméticas interessantes, que, no entanto, ainda devem ser mais exploradas na atualidade. No estudo, adicionou-se o carbonato a sabões líquidos obtidos a partir dos ácidos graxos provenientes dos óleos de soja e de mamona. Os sabões produzidos apresentaram baixa alcalinidade, reduzindo, assim, as adições de agentes químicos que podem ser agressivos à pele, como mostraram os resultados parciais. A partir do planejamento experimental, verifica-se a influência da temperatura e o tempo de reação da síntese do carbonato, assim como o tipo de catalisador utilizado. Análises de espectroscopia vibracional Raman e infravermelho, juntamente com ensaios de viscosidade, mostraram que a temperatura ideal para a carboxilação é de 140 °C, sendo que o tempo reacional deve ser de 6 a 7 h, utilizando-se como catalisador o sulfato de magnésio. Demonstrou-se também, a sensibilidade das duas técnicas na identificação dos picos das reações de síntese de carbonato de glicerila. Comparativamente, foram realizados testes de espuma dos sabões adicionados de carbonato de glicerila e de lauril sulfato de sódio. De um modo geral, a adição de carbonato de glicerila aos sabões propiciou a formação de uma espuma mais densa e persistente. A utilização de água dura reduziu o volume de espuma formado para todas as amostras. Comparando os dois óleos vegetais, soja e mamona, percebeu-se que os sabões produzidos a partir de óleo de mamona apresentaram menor formação de espuma. A adição de dietanolamina reduziu significativamente a estabilidade das espumas em todas as amostras. Estudos reológicos demonstraram que o tensoativo carbonato de glicerila é um fluido newtoniano, comportamento semelhante ao da glicerina pura. / In order to search for raw materials from cleaner and renewable sources, and the growing use of byproducts generated by these sources, has appeared the interest in studying the synthesis of glycerol carbonate from glycerol obtained as a main byproduct in the manufacture of biodiesel. This compound was synthesized at the Laboratory of Applied Organic Chemistry. This surfactant is not available in Brazil and has interesting cosmetic properties, which, however, should be more exploited at present. In the study, carbonate was added to liquid soaps from the fatty acids from soybean oil and castor oil. Soaps produced had low alkalinity, thereby reducing the additions of chemicals that can be aggressive to the skin, as partial results showed. From the experimental design, the influence of temperature and reaction time of the synthesis of carbonate is investigated, as well as the type of catalyst used. Analysis of partial Raman vibrational spectroscopy, together with viscosity experiments showed that the optimal temperature for carboxylation is 140 °C, and the reaction time should be from 6 to 7 h, using magnesium sulphate as the catalyst. It also demonstrated the sensitivity of both techniques in identifying the peaks of the reactions of synthesis of glycerol carbonate. In comparison,foam tests were made of soaps added glycerol carbonate and sodium laurylsulfate. Overall, the addition of glycerol carbonate to soap provided the formation of denser and persistent foam. The use of hard water reduced the volume of foam formed for all samples. Comparing the two vegetable oils, soy and castor bean, it was noticed that soaps produced from castor oil had lower foaming. The addition of diethanolamine significantly reduced the stability of foams in all samples. Rheological studies demonstrated that the surfactant glycerol carbonate is neuwtonian fluid, behavior similar to that of pure glycerin.

Managing soil hydrophobicity caused by localized dry spots (LDS) on sand based golf greens has become one of the greatest challenges for golf course superintendents and managers, especially as water restrictions intensify. The purpose of this study was to evaluate the effectiveness of thirteen soil surfactants in eliminating LDS and in maximizing root zone soil moisture on a sand based USGA golf green located on the California Central Coast. Potential water repellency of air dried cores (measured utilizing the water droplet penetration time (WDPT) method), phytotoxicity, and climate were analyzed during two experimental trials. Phytotoxicity data was collected for Trial I using visual quality ratings and for Trial II using a chlorophyll meter. Phytotoxicity decreased during Trial I. Differences in phytotoxicity as measured using chlorophyll index were not at all significant during Trial II (p = 1). Ten of the thirteen wetting agent treatments significantly (p < 0.001) decreased soil hydrophobicity compared with the other wetting agent treated plots and the non-treated control. More frequent application of Cascade Plus resulted in a more significant reduction in soil hydrophobicity. Increasing the application rates also resulted in the reduction of soil hydrophobicity. Wetting agent treatment 6-CP(10day) maintained the highest volumetric water content (VWC) but treatment 13-2079337 maintained the highest levels for wetting agents treated monthly.

Particle Nucleation is the forcing function in the Emulsion Polymerization processes and it plays an important role in dictating the final properties of the latex produced. Identification of the main nucleation sites and characterizing them in terms of their size and composition is important for elucidating the mechanism of particle nucleation. This research focuses on identifying the most likely nucleation locus in emulsion polymerization processes by characterizing the initial conditions of the reaction mixture. In order to achieve this objective, a methodology was devised, which used a non-reacting model emulsion system instead of the original emulsion. The model emulsion system selected has the same dispersion properties as that of the monomer emulsion system, but different optical properties. The model emulsion system enabled the study of the distribution of the emulsifier using Uv vis spectroscopy. This approach also eliminated the time constraint associated with sampling during a polymerization reaction. A quantitative deconvolution using the turbidity equation, was done on the transmission Uv vis spectra of the emulsions. This enabled the characterization of the emulsions in terms of their particle size distribution, particle number and the composition of the droplet populations comprising them. The studies conducted provide the experimental evidence for a previously unidentified nano-droplet population of size range 30 to 100nm in diameter. To further support this experimental evidence, calculations were performed to obtain the emulsifier distribution over the nano-droplet population. The calculations suggest the probability of existence of the nano-droplet population to be much higher than the probability of the existence of the swollen micelles. The results, depending upon the emulsification conditions, indicate the presence of about 15 % to 80% of the dispersed phase in the nano-droplet population. The large interfacial area offered by the nano-droplet population due to their high particle numbers and high percentage of the dispersed oil phase in them, make them the most probable particle nucleation loci in emulsion polymerization processes. Designed experiments were performed to experimentally observe the changes in the nano-droplet populations. The effects of the process variables, namely pH, surfactant concentration and temperature, on the size and compositional characteristics of the nano-droplet population were investigated. The results suggested that the surfactant to oil ratio was the dominating factor governing the size and the weight percent of the dispersed phase in the nano-droplet population.

La réduction de la traînée est un phénomène d'écoulement qui, par la présence de très petites quantités d'additifs (polymères ou tensio-actifs) dans un fluide quelconque, consiste en une réduction significative du frottement à la paroi en régime turbulent. Certaines solutions d'additifs, en interagissant avec la structure de la turbulence conduisent à une réduction du frottement pouvant aller jusqu'à 90 % par rapport au solvant pur. Ceci induit une réduction de la puissance de pompage de l'ordre de 30 %. La réduction de la traînée peut trouver son application dans des systèmes de chauffage et de refroidissement urbains, dans le domaine pétrolier (pipelines), ... Dans ce travail de thèse une contribution à l'étude de ce type d'écoulement a été menée. Une solution réductrice de la traînée à base de « CTAC/NaSal » à faible concentration a été largement explorée. La rhéométrie, la vélocimétrie par images de particules (PIV) et des modèles numériques sont utilisés. Ainsi, les solutions de tensio-actifs ont été caractérisées rhéologiquement. Plusieurs paramètres influençant la réduction de la traînée en conduite ont été étudiés. Le phénomène de glissement à la paroi a été abordé par une étude dans une géométrie de Couette. Enfin, un modèle de comportement rhéologique issu des mesures rhéologiques a été testé par Simulation Numérique Directe (DNS). Les principaux résultats qui ressortent de ce travail montrent que le mécanisme de la réduction de la traînée est conditionné par plusieurs paramètres par contre, le glissement à la paroi n'est pas forcement responsable de la réduction de la traînée.

Herein are presented collective studies of amino acid-based surfactants, also known as lipoamino acids, at liquid interfaces. Chapter III describes an investigation of domain morphology of N-Stearoylglutamic acid (N-SGA) Langmuir monolayers at the air/water interface by epifluorescence microscopy. Anisotropic feather-like domains were observed in L-enantiomeric monolayers while symmetric circular domains were found in racemic N-SGA monolayers. At a surface pressure of 30 mN/m the enantiomeric domains melted at 31 ??C while the racemic domains melted at 27 ??C. This result is exactly opposite to the behavior found in bulk crystals where the racemate melts at a higher temperature. These results were explained in terms of different molecular packing and hydrogen bonding between bulk crystals and two-dimensional thin films for enantiomeric and racemic compounds. Chapter IV summarizes the investigations of hydrogen bonding in N-acyl amino acid monolayers by vibrational sum-frequency spectroscopy (VSFS). The intermolecular hydrogen bonding interaction between the adjacent molecules through amide-amide groups in N-stearoylalanine (N-SA) is characterized by an NH stretch peak at 3311 cm-1. This is the first time that the amide NH stretching signals have been detected with the VSFS technique. A similar peak was detected at 3341 cm-1on N-SGA monolayer. The higher frequency indicates that the H-bond strength is weaker due to the larger size of the glutamic acid residue. The NH stretch mode can thus be used as a fingerprint of hydrogen bonding among amide-amide groups. A peak at 3050 cm-1 due to hydrogen bonding among carboxyl groups was also resolved from the VSFS spectra. Molecular models of intermolecular hydrogen bonding were proposed.

The aim of this study was to understand the contribution of Linear Alkylbenzene Sulfonates (LAS) to the decline of Mediterranean coastal forest exposed to marine aerosols. LAS are a group of synthetic anionic surfactants widely used in the composition of household or industrial detergents and agrochemicals. This study was part of a large project (RISICO) aiming the assessment of the environmental impact of the LAS at multiple levels: biodegradation in the coastal waters, sorption – desorption processes in the sediments, toxicity to the aquatic life and toxicity to the coastal forest (by aerosolisation of the sea water). Previous studies pointed out this group of surfactants as the main cause of the coastal forest decline. However, the quantification of this surfactant in the environmental samples (mainly sea water and foliar deposition) was done using non-specific analytical methods as methylene blue active substances (MBAS), leading to overestimation of the environmental concentrations of LAS. The work hypothesis was that at actual environmental concentrations, the LAS does not play a key role in the foliar uptake of the sea salt deposited on the coastal vegetation by the marine aerosols, therefore the LAS may not be the main cause of the coastal forest decline. The research involved both greenhouse experiments and field measurements. The experimental work was conducted on young Mediterranean trees (Laurus nobilis L., Quercus ilex L. and Pinus halepensis P. Mill.) and investigated the synergistic toxic effects of exposure to simulated marine aerosol contaminated with surfactants. An array of endpoints was used including photosynthetic activity, relative water content, foliar deposition and uptake of salt and LAS, and pigments analysis. The results of those experiments revealed that LAS itself did not have phytotoxic effects. Nevertheless, the surfactant was shown to enhance the foliar uptake of the salt in the tested species, especially in Pinus halepensis, confirming the conclusions of previous studies regarding the sensitivity of this species to polluted marine aerosols. The field work was conducted in San Rossore National Park (Italy) and Porquerolles Island (France) and was focused on evaluating the health status of the Mediterranean forest (Quercus ilex L., Pinus halepensis Mill. and Pinus pinaster Aiton.) and also on quantification of LAS in coastal aerosols using highly specific analytical methods, like the mass spectrometry (MS). The frequencies and extent of injuries in the coastal trees were found to be correlated to the salt but not with the LAS content of the leaves. The concentrations of LAS in the Pinus and Quercus leaves were comparable in the two studied sites but the concentrations of salt were extremely high in San Rossore, suggesting that other factors may determine the excessive salt foliar uptake. The parallel MS and MBAS carried out in the same set of aerosol samples revealed that MBAS measurements were not relevant for LAS concentrations in the marine aerosols. Projecting the experimental results to the real LAS and salt exposure of the coastal forest, we concluded that LAS may play a marginal role in coastal vegetation decline.

The Reversible Addition Fragmentation Chain Transfer (RAFT) process using the new RAFT agent benzyldithiophenyl acetate is shown to be a powerful polymerization tool to synthesize novel well-defined amphiphilic diblock copolymers composed of the constant hydrophobic block poly(butyl acrylate) and of 6 different hydrophilic blocks with various polarities, namely a series of non-ionic, non-ionic comb-like, anionic and cationic hydrophilic blocks. The controlled character of the polymerizations was supported by the linear increase of the molar masses with conversion, monomodal molar mass distributions with low polydispersities and high degrees of end-group functionalization. <br><br> The new macro-surfactants form micelles in water, whose size and geometry strongly depend on their composition, according to dynamic and static light scattering measurements. The micellization is shown to be thermodynamically favored, due to the high incompatibility of the blocks as indicated by thermal analysis of the block copolymers in bulk. The thermodynamic state in solution is found to be in the strong or super strong segregation limit. Nevertheless, due to the low glass transition temperature of the core-forming block, unimer exchange occurs between the micelles. Despite the dynamic character of the polymeric micellar systems, the aggregation behavior is strongly dependent on the history of the sample, i.e., on the preparation conditions. The aqueous micelles exhibit high stability upon temperature cycles, except for an irreversibly precipitating block copolymer containing a hydrophilic block exhibiting a lower critical solution temperature (LCST). Their exceptional stability upon dilution indicates very low critical micelle concentrations (CMC) (below 4∙10^-4 g∙L^-1). All non-ionic copolymers with sufficiently long solvophobic blocks aggregated into direct micelles in DMSO, too. Additionally, a new low-toxic highly hydrophilic sulfoxide block enables the formation of inverse micelles in organic solvents. <br><br> The high potential of the new polymeric surfactants for many applications is demonstrated, in comparison to reference surfactants. The diblock copolymers are weakly surface-active, as indicated by the graduate decrease of the surface tension of their aqueous solutions with increasing concentration. No CMC could be detected. Their surface properties at the air/water interface confer anti-foaming properties. The macro-surfactants synthesized are surface-active at the interface between two liquid phases, too, since they are able to stabilize emulsions. The polymeric micelles are shown to exhibit a high ability to solubilize hydrophobic substances in water. / Amphiphile sind Moleküle, die aus einem hydrophilen und einem hydrophoben Molekülteil aufgebaut sind. Beispiele für Amphiphile sind Tenside, deren makromolekulares Pendant amphiphile Block-Copolymere sind, die häufig auch als Makro-Tenside bezeichnet sind. Ihre Lösungseigenschaften in einem selektiven Lösungsmittel, i.e., ein für einen Block gutes und für den anderen schlechtes Lösungsmittel, sind analog zu denen von Tensiden. Die Unverträglichkeit der Polymersegmente führt zu einer von hydrophoben Wechselwirkungen getriebenen Mikrophasenseparation, d.h. zur Selbstorganisation der amphiphilen Makromoleküle zu Mizellen unterschiedlichster Form, während die kovalente Bindung zwischen den Blöcken eine Makrophasenseparation verhindert. Aufgrund ihres besonderen strukturellen Aufbaus adsorbieren Makro-Tenside an Grenzflächen, was zahlreiche Anwendungen, z.B. zur (elektro)sterischen Stabilisierung von Emulsionen und Dispersionen findet. <br><br> Die vorliegende Arbeit demonstriert, dass die neuen kontrollierten radikalischen Polymerisationen wie die RAFT-Methode („Reversible Addition Fragmentation Chain Transfer“) für die Synthese von neuen wohldefinierten amphiphilen Diblock-Copolymerstrukturen sehr gut geeignet sind. Eine Reihe von neuen amphiphilen Diblock-Copolymeren wurde mittels RAFT synthetisiert, mit einem konstanten hydrophoben Block und verschiedenen hydrophilen Blöcken unterschiedlichster Polaritäten. Die engen Molmassenverteilungen und der lineare Aufstieg der Molmassen mit dem Umsatz belegen den kontrollierten Charakter der Polymerisation. <br><br> Die thermodynamisch favorisierte Selbstorganisation der synthetisierten Blockcopolymere in Wasser führt zur Bildung von Mizellen, deren Eigenschaften aber von der Präparationsmethode stark abhängig sind. Korrelationen zwischen den Mizelleigenschaften und der Blockcopolymerstruktur zeigen, dass die Mizellgröße vor allem von der Länge des hydrophoben Blocks kontrolliert wird, wohindagegen die Natur des hydrophilen Blocks der entscheidende Faktor für die Mizellgeometrie ist. Die gebildeten Mizellen sind besonders stabil gegenüber Verdünnung und Temperaturzyklen, was ein großer Vorteil für eventuelle Anwendungen ist. Wegen der niedrigen Glasübergangstemperatur des hydrophoben Blocks findet ein Austausch von Makromolekülen zwischen den Mizellen statt, d.h. es handelt sich um dynamische Mizellsysteme. <br><br> Das Potential der neuen Makrotenside für Anwendungen wurde untersucht. Die Polymermizellen zeigen eine hohe Kapazität wasserunlösliche Substanzen in Wasser zu solubilisieren. Die Blockcopolymere sind grenzflächenaktiv, d.h. sie adsorbieren an Wasser / Luft oder Wasser / Öl Grenzflächen. Entsprechend sind die Blockcopolymere in der Lage, Emulsionen zu stabilisieren oder als Antischaumsubstanzen zu wirken.

<p>The aim of this study was to compare the water quality of raw wastewater and treated sewage effluents from three different sewage treatment plants in the Western Cape, South Africa. The treatment plants investigated are on the same river system. Sewage treatment plant 1 and 2 use older technologies, while sewage treatment plant 3 has been upgraded and new technologies (membrane bioreactor) were incorporated in the treatment processes. The first objective was to determine the occurrence of total coliforms, Escherichia coli (E. coli) and fluoroquinolone and sulfamethoxazole antibiotic residues in raw wastewater and treated sewage effluents. Bacteria in treated sewage effluents can result in diseases such as dysentery, gastroenteritis, and typhoid upon exposure. A chromogenic test was used to screen for coliforms and E. coli. Enzyme linked Immunosorbent Assays (ELISA) were used to quantitate antibiotic residues (fluoroquinolones and sulfamethoxazole) in raw wastewater and treated sewage effluents. This study showed that bacteria are present in raw wastewater and residual bacteria are released with treated sewage effluents from sewage treatment plants.</p>

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