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The research projects presented in this thesis are mainly focused toward green chemistry and engineering: developing innovative strategies to minimize waste, improve process efficiency and reduce energy consumption. Specifically, the work was centered on the design and applications of green solvents and processes for the sustainable production of pharmaceuticals. The first project was focused on the use of CO₂ to enhance Suzuki coupling reactions of substrates containing unprotected primary amines. This work established that exceptionally challenging substrates like halogenated amino pyridines (i.e. 4-amino-2-bromopyridine and 4-amino-2-chloropyridine) are suitable substrates for Suzuki coupling reactions under standard conditions using CO₂ pressures, without the need for protection/deprotection steps which are traditionally considered to be necessary for these reactions to proceed cleanly. The second project explored the use of water at elevated temperatures (WET) for the sustainable and selective removal of protecting groups. The favorable changes that occur in the physiochemical properties (i.e. density, dielectric constant and ionization constant) of water at elevated temperatures and pressures make it an attractive solvent for the development of sustainable, environmentally green processes for the removal of protecting groups. The water-mediated selective removal of protecting groups such as N-Boc, N-Acetyl and O-Acetyl from a range of organic model compounds was successfully achieved by tuning the temperature (125 to 275°C) or properties of water. The third project investigated the use of Organic-Aqueous Tunable Solvents (OATS) for the rhodium catalyzed hydroformylation of p-methylstyrene. This enables the reactions to be carried out efficiently under homogeneous conditions, followed by a carbon dioxide (CO₂) induced heterogeneous separation. Modest pressures of CO₂ induced the aqueous-rich phase (containing the catalyst) to separate from the organic-rich phase (containing the reactant), thus enabled an easy separation and recycling of catalyst. The use of Al(OtBu)₃ as a potent catalyst toward continuous Meerwein-Ponndorf-Verley (MPV) reductions was established in the fourth project. The MPV reduction of model compounds like benzaldehyde and acetophenone to their corresponding alcohols was investigated in continuous mode as a function of temperature and catalyst loading. These results established a roadmap for the pharmaceutical industry to document the implementation of continuous flow processes in their manufacturing operations.

Monitored natural attenuation has been particularly used at sites where petroleum hydrocarbons and chlorinated solvents have contaminated soil and groundwater. One of the important aspects of the methodology that has been recognized recently is that the mass removal rates, the most important parameter to determine effectiveness of the methodology, is controlled by the groundwater flow regime and the aquifer heterogeneity. Considering this recognition, the primary objective of this study is to quantitatively describe the relationship between the natural attenuation rates and aquifer heterogeneity using numerical simulation techniques. To represent different levels of aquifer heterogeneity, the hydraulic conductivity distribution (ln K) is statistically simulated with the numerical algorithm, Turning Bands Random Field Generator, by changing the statistical parameters, Coefficient of Variation (CV) and correlation length (h) and Visual MODFLOW and RT3D software programs are used for the simulation of groundwater flow and chlorinated solvent transport. Simulation results showed that degradation rates and the shape of the contaminant plumes show variations for different heterogeneity levels. Increasing CV resulted in the decrease in the transport of the plume and shrinkage in the areal extend. On the other hand, &ldquo / h&rdquo / determined the shape and the size of the plume through its affect on mechanical dispersion. For a given &ldquo / h&rdquo / , degradation rates increased with increasing CV, but change in &ldquo / h&rdquo / did not show a regular trend. Such findings are expected to be beneficial when assessing the effectiveness of natural attenuation process for a selected site during the feasibility studies without need for detailed site characterization.

Progress in the microelectronics industry is driven by smaller and faster transistors. As feature sizes in integrated circuits become smaller and liquid chemical waste becomes an even greater environmental concern, gas expanded liquids (GXLs) may provide a possible solution to future device fabrication limitations relative to the use of liquids. The properties of GXLs such as surface tension can be tuned by the inclusion of high pressure gases; thereby, the reduced surface tension will allow penetration of cleaning solutions into small features on the nanometer scale. In addition, the inclusion of the gas decreases the amount of liquid necessary for the photoresist and etch residue removal processes. This thesis explores the role of CO2-based GXLs for photoresist and etch residue removal. The gas used for expansion is CO2 while the liquid used is methanol. The cosolvent serving as the removal agent is tetramethyl ammonium hydroxide (TMAH) which upon reacting with CO2 becomes predominantly tetramethyl ammonium bicarbonate (TMAB).

Diss. (sammanfattning) Uppsala : Sveriges lantbruksuniversitet, 2005. / Härtill 6 uppsatser.

19 Dec 2004. / Published through the Information Bridge: DOE Scientific and Technical Information. "IS-T 1948" Jamie Marie Rintelman. 12/19/2004. Report is also available in paper and microfiche from NTIS.

Thesis (Ph. D.)--University of Wisconsin--Madison, 1971. / Typescript. Vita. Description based on print version record. Includes bibliographical references.

A técnica de microencapsulamento consiste em englobar um núcleo com o material que se deseja proteger com uma casca sólida que tem a finalidade de proteger o núcleo. A técnica de evaporação de solvente consiste em realizar duas emulsões, contendo o núcleo que se deseja encapsular, o polímero que formará a cápsula dissolvido em solvente e um meio de dispersão. Para o processo, a modificação de parâmetros e condições de processo são capazes de aumentar a eficiência do microencapsulamento. Foram produzidas microcápsulas de poliestireno contendo água deionizada com o objetivo de analisar o efeito da relação núcleo cápsula, temperatura de evaporação, presença de cloreto de sódio e surfactante na eficiência do processo de microencapsulamento, quando comparados a uma amostra padrão. Adicionalmente, as amostras foram caracterizadas por microscopia eletrônica de varredura (MEV) e análise termogravimétrica (TG). Foi encontrado que a relação núcleo: cápsula ideal para a produção de microcápsulas é de 2:1, com eficiência de 61,47 %. A análise termogravimétrica indicou também que a relação 2:1 apresentava melhor eficiência pois continha uma maior quantidade de material do núcleo. As imagens de MEV mostraram que a microcápsula formada possui superfície lisa. A adição de tensoativo e a redução da temperatura de evaporação aumentaram a eficiência para 76,83 % e 79,25 % respectivamente. / The microencapsulation technic consist in envelop a core with the material to protect by a solid shell that protects the core for the external environment.The solvent evaporation techtnic consist into two emulsion, the core that wants to be encapsulated, the polimers for the shell solved into a organic solvent and a dispesion media. For the process, the modification of process parameters are able to improve the yeld of the microencapsulation. It was produced polystyrene microcapsules with deionized water to evaluate the effect of core: shell ratio, evaporation temperature, the presence of sodium chloride and the surfactant in the efficiency microencapsulation process, when compared to a standard sample. Additionally, samples were characterized by scanning electron microscopy (SEM) and thermal gravimetric analysis (TG). It was found that the ideal core:shell ratio for the production of microcapsules is 2: 1, with 61.47% of yelding. Thermogravimetric analysis also indicated that the 2:1 ratio had better efficiency since it contained a larger amount of the core material. The SEM images showed that the formed microcapsule has smooth surface. The addition of surfactant and reducing the evaporation temperature increased the efficiency of 76.83% and 79.25% respectively.

Orientador: Cristiano Soleo de Funari / Resumo: Aproximadamente 3,7 x 109 toneladas de resíduos agrícolas são produzidos anualmente no mundo. Por ser uma das grandes potências agrícolas atualmente, grandes quantidades de resíduos agrícolas são geradas constantemente no Brasil. Uma das principais culturas produzidas no país é a soja. Além de seu uso na pecuária, utilizada na alimentação animal, assim como para alimentação humana, a soja desperta grande interesse do ponto de vista farmacológico, por ser uma das principais fontes de isoflavonas, uma forma de fitoestrogênio, sendo umas das espécies listadas na RENISUS. Este trabalho teve como objetivo investigar o perfil químico dos resíduos provenientes da cultura da soja (caules, folhas e vagens) por meio de uma abordagem analítica verde. Os extratos foram obtidos em triplicata por maceração dinâmica a 30 °C, com acetona e etanol, com e sem adição de ácido. O solvente acetonitrila foi utilizado como solvente de referência, pois é comumente empregado tanto para a extração como para a separação de isoflavonas presentes em grãos de soja. Os extratos foram analisados por cromatografia líquida de alta eficiência acoplada a um espectrofotômetro de untravioleta/visível (HPLC-PAD/UV) e a comparação da eficiência de extração entre os solventes testados foi feita com base em número total de picos, área total sob os picos e rendimento da extração. Os solventes verdes etanol e acetona mostraram-se mais eficientes do que o solvente de referência acetonitrila. Posteriormente, uma estratég... (Resumo completo, clicar acesso eletrônico abaixo) / Abstract: Approximately 3.7 x 109 tonnes of agricultural waste is produced annually in the world. Because it is one of the great agricultural powers today, large amounts of agricultural residues are constantly generated in Brazil. One of the main crops produced in the country is soy. In addition to its use in livestock and human nutrition, the soybean awakes great interest from the pharmacological point of view, being one of the main sources of isoflavones, a form of phytoestrogen, being one of the species listed in RENISUS. The objective of this work was to investigate the chemical profile of residues from soybean (shoots, leaves and pods) using a green analytical approach. The extracts were obtained in triplicate by dynamic maceration at 30 ° C, with acetone and ethanol, with and without acid addition. The solvent acetonitrile was used as reference solvent, since it is commonly used both for the extraction and the separation of isoflavones present in soybean grains. The extracts were analyzed by high performance liquid chromatography coupled to an untraviolet/visible spectrophotometer (HPLC-PAD/UV) and the comparison of the extraction efficiency among the solvents tested was done based on total number of peaks, total area under peaks and extraction yield. The green solvents ethanol and acetone were more efficient than the reference solvent acetonitrile. Subsequently, a strategy for the identification of compounds in mixture, based on data obtained by high performance liquid chromatog... (Complete abstract click electronic access below) / Mestre

In this thesis we use density functional theory (DFT) to study the solvent mediated interactions between solvophobic, solvophilic and patchy nanostructures namely rectangular cross section blocks. We calculate both the density profiles and local compressibility around the blocks and the results obtained for our model system provide a means to understanding the basic physics of solvent mediated interactions between nanostructures, and between objects such as proteins in water, that possess hydrophobic and hydrophilic patches. Our results give an improved understanding of the behaviour of liquids around solvophobic objects and solvophobicity (hydrophobicity) in general. Secondly, we look into the physics incorporated in standard mean-field DFT. This is normally derived by making what appears to be a rather drastic approximation for the two body density distribution function: ρ(2)(r,r′) ≈ ρ(r)ρ(r′), where ρ(r) is the one-body density distribution function. We provide a rationale for why the DFT often does better than this approximation would make you expect. Finally, we develop a lattice model to understand the nature of the pattern formation exhibited by certain systems of particles deposited on liquid-air interfaces and in particular the nature of the transitions between the different patterned structures that are observed. This is done using Monte Carlo computer simulations and DFT and links the observed microphase ordering with the micellisation process seen e.g. in surfactant systems.