As unidades industriais de produção de poliolefinas operam de maneira contínua, mas precisam produzir diferentes tipos de grades poliméricos (polímeros com diferentes especificações, para diferentes aplicações). As condições de operação do reator são mantidas por um certo período de tempo para produzir um determinado grade, e periodicamente as condições são alteradas para produzir lotes de outros grades. Estas transições permitem produzir diferentes grades usando o mesmo reator, mas exige mudanças nas condições operacionais e, como consequência, o polímero produzido durante uma transição fica fora da especificação. Assim, é desejável que as transições sejam realizadas no menor tempo possível, de maneira a produzir a menor quantidade de polímero fora da especificação. Estratégias mais eficientes de operar a transição podem ser obtidas através da solução de um problema de otimização dinâmica. Neste trabalho uma função objetivo integral quadrática foi minimizada, utilizando técnicas sequenciais dinâmicas para resolução da otimização. Os resultados foram primeiramente simulados e depois otimizados para a homopolimerização e copolimerização. No caso da homopolimerização, as otimizações mostraram que para aumentar o MI é preciso aumentar a concentração de hidrogênio na alimentação. Já na copolimerização, para aumentar o MI foi preciso diminuir a concentração de hidrogênio na alimentação e aumentar a vazão de comonômero; e para diminuir a densidade foi preciso aumentar a vazão de comonômero. Observou-se que as propriedades instantâneas têm dinâmica mais rápida e agressiva que as cumulativas. Os resultados mostraram que quando a parametrização não era adequada a solução se afastava do ótimo. Foi possível notar que atuar durante 2 tempos de residência já traz uma redução significativa do tempo para o término da transição e da massa de produto fora da especificação. O perfil das propriedades da transição no sentido grade 1 - grade 2 se mostrou diferente do grade 2 - grade 1, concluindo que o perfil de uma transição depende fortemente da direção da mudança nas propriedades. / Polyolefin plants operate under continuous production, but they need to supply many types of polymer grades (polymer with different specification, used in different applications). The operating conditions are maintained constant during the production of a certain grade and need to change periodically to produce another grade. Grade transitions allow the production of different polymer grades in a single reactor, but as they require changes in the operating conditions, there is a large production of off-specification polymer. Therefore, a desired transition drives the polymer properties to the new grade in a short period of time, producing a small amount of off-specification polymer. Efficient strategies to operate the transition can be obtained by solving a problem of dynamic optimization. In this work, a quadratic integral objective function was minimized by using dynamic sequential techniques for solving optimization. The results were first simulated and then optimized for the homopolymerization and copolymerization. In the case of homopolymerization, optimizations showed that to increase the MI is necessary to increase the hydrogen concentration in the feed. In the copolymerization, to increase the MI was necessary to reduce the concentration of hydrogen in the feed and increase the comonomer flow rate; and to decrease the density was necessary to increase the comonomer flow rate. It was observed that the instantaneous properties have faster and aggressive dynamics compared to the cumulative properties. The results showed that when the parameterization was not adequate the solution moves away from the optimum. It was observed that to act for 2 residence times makes a significant reduction in the transition time completion and in the mass of product out of specification. The trajectories of the transition properties towards grade 1 - grade 2 showed different behavior compared to grade 2 - grade 1 transition, concluding that the profile of a transition depends strongly on the direction of change in the properties.

As unidades industriais de produção de poliolefinas operam de maneira contínua, mas precisam produzir diferentes tipos de grades poliméricos (polímeros com diferentes especificações, para diferentes aplicações). As condições de operação do reator são mantidas por um certo período de tempo para produzir um determinado grade, e periodicamente as condições são alteradas para produzir lotes de outros grades. Estas transições permitem produzir diferentes grades usando o mesmo reator, mas exige mudanças nas condições operacionais e, como consequência, o polímero produzido durante uma transição fica fora da especificação. Assim, é desejável que as transições sejam realizadas no menor tempo possível, de maneira a produzir a menor quantidade de polímero fora da especificação. Estratégias mais eficientes de operar a transição podem ser obtidas através da solução de um problema de otimização dinâmica. Neste trabalho uma função objetivo integral quadrática foi minimizada, utilizando técnicas sequenciais dinâmicas para resolução da otimização. Os resultados foram primeiramente simulados e depois otimizados para a homopolimerização e copolimerização. No caso da homopolimerização, as otimizações mostraram que para aumentar o MI é preciso aumentar a concentração de hidrogênio na alimentação. Já na copolimerização, para aumentar o MI foi preciso diminuir a concentração de hidrogênio na alimentação e aumentar a vazão de comonômero; e para diminuir a densidade foi preciso aumentar a vazão de comonômero. Observou-se que as propriedades instantâneas têm dinâmica mais rápida e agressiva que as cumulativas. Os resultados mostraram que quando a parametrização não era adequada a solução se afastava do ótimo. Foi possível notar que atuar durante 2 tempos de residência já traz uma redução significativa do tempo para o término da transição e da massa de produto fora da especificação. O perfil das propriedades da transição no sentido grade 1 - grade 2 se mostrou diferente do grade 2 - grade 1, concluindo que o perfil de uma transição depende fortemente da direção da mudança nas propriedades. / Polyolefin plants operate under continuous production, but they need to supply many types of polymer grades (polymer with different specification, used in different applications). The operating conditions are maintained constant during the production of a certain grade and need to change periodically to produce another grade. Grade transitions allow the production of different polymer grades in a single reactor, but as they require changes in the operating conditions, there is a large production of off-specification polymer. Therefore, a desired transition drives the polymer properties to the new grade in a short period of time, producing a small amount of off-specification polymer. Efficient strategies to operate the transition can be obtained by solving a problem of dynamic optimization. In this work, a quadratic integral objective function was minimized by using dynamic sequential techniques for solving optimization. The results were first simulated and then optimized for the homopolymerization and copolymerization. In the case of homopolymerization, optimizations showed that to increase the MI is necessary to increase the hydrogen concentration in the feed. In the copolymerization, to increase the MI was necessary to reduce the concentration of hydrogen in the feed and increase the comonomer flow rate; and to decrease the density was necessary to increase the comonomer flow rate. It was observed that the instantaneous properties have faster and aggressive dynamics compared to the cumulative properties. The results showed that when the parameterization was not adequate the solution moves away from the optimum. It was observed that to act for 2 residence times makes a significant reduction in the transition time completion and in the mass of product out of specification. The trajectories of the transition properties towards grade 1 - grade 2 showed different behavior compared to grade 2 - grade 1 transition, concluding that the profile of a transition depends strongly on the direction of change in the properties.

Foi desenvolvido modelo matemático para o processo de produção de álcoois etoxilados em um reator batelada com spray da fase líquida na fase gasosa. O modelo considera a cinética da polimerização iônica e a transferência de massa de óxido de eteno entre as fases gasosa e líquida. A cinética foi estudada a partir de dados previamente obtidos em laboratório. Para modelagem da transferência de massa, foram utilizados dados de bateladas industriais. Foram testados vários modelos de transferência de massa encontrados na literatura, sendo que o modelo que se mostrou mais adequado para este reator industrial foi o de gotas com circulação interna. A partir do modelo obtido da cinética e da transferência de massa, foi analisada a influência de parâmetros de projeto, como a vazão de recirculação de líquido, a relação entre a altura e o raio do reator e o tipo de spray na produtividade deste. Observou-se que a maior vazão de recirculação aumenta a produtividade do reator, assim como o aumento da altura do reator. O tipo e o diâmetro da gota do spray também influenciam a produtividade do reator. / A mathematical model for the production of ethoxylated alcohols in a spray tower loop reactor was developed. The model considers the reaction as an ionic polymerization and the ethylene oxide mass transfer from the vapor phase to the liquid phase. The kinetics was obtained from a laboratory scale reactor data. The mass transfer model was obtained from the industrial reactor data. Several models for the mass transfer of ethylene oxide from gas phase to the liquid droplets were tested, and it was found that the most appropriate mass transfer model for this industrial reactor was the internally well-mixed drop model. From the kinetics and the mass transfer model, the influence of the pump recirculation flow rate, the ratio between the reactor height and radius and the spray performance was analyzed. The results show that higher reactor productivity can be obtained using higher recirculation flow and higher reactor height. The spray nozzle performance and the drop diameter also influence the reactor productivity.

Semi-batch crystallization experiments have been performedboth in a loop reactor and in stirred tank reactors.Hydrochloric acid was fed to a stirred solution of sodiumbenzoate, and benzoic acid immediately formed. Benzoic acid isformed in excess of the solubility making the solutionsupersaturated. The loop reactor is U-shaped. In one leg a propeller stirrerwas placed to circulate the solution and in the other a turbinestirrer was placed in front of the feed point to vary the localmixing intensity. The objective was to analyse the relativeimportance of different levels of mixing on the product sizedistribution. The importance of mixing as well as scaling-upeffects on the product size distribution were studied in threestirred tank reactors of volumes 2.5 L, 10 L, and 200 L. Thestirred tank reactors had different geometry and were equippedwith either a marine propeller or a pitched blade turbine. The weight mean size generally increases with increasingtotal feeding time and increasing mixing intensity. The weightmean size increases by locating an extra turbine impeller atthe feed point in the 10 L stirred tank reactor. The turbineimpeller provides the desired feed point mixing intensitywithout raising the mixing intensity of the whole tank. The weight mean size increases with decreasing feed pipediameter in the loop reactor and for low feed rates in the 10 Lstirred tank reactor. The weight mean size increasessignificantly by changing the feed pipe opening from circularto rectangular with a constant cross-sectional area at equalfeed rates. Backmixing is visually observed in the largest feedpipe diameter in the loop reactor, thus, reducing the weightmean size. However, backmixing is not considered to be adominant phenomenon in the present work. Mesomixing time constants have been calculated according tothe turbulent dispersion mechanism and the inertial-convectivemechanism. The time constants for mesomixing are generallylonger than the time constant for micromixing. Thus, the ratioof the mesomixing and the micromixing time constants shows aninfluence of mesomixing as is shown by the experimentalresults. The experimental results are best described by theinertial-convective disintegration mechanism showing that thefeed plume mixing increases with decreasing feed pipe diameterand increased feed point mixing. The weight mean size is not strongly affected by the reactorvolume. However, the mixing conditions in the reactors have astrong influence on the weight mean size. No suggestedscaling-up rule can satisfactorily predict the weight mean sizein the different volumes. No single physical parameter, such asthe local energy dissipation rate, the mean energy dissipationrate or the circulation time, can satisfactorily explain theexperimental results. A new dimensionless mixing parameter, TR,has been defined as the ratio of the total feeding time and themesomixing time constant. The mesomixing time constant isdefined as the shortest dimension of the feed pipe divided bythe resultant bulk velocity passing the feed pipe entrance. Theexperimental results from both the loop reactor and the stirredtank reactors of different volumes can be correlated with TR.The weight mean size increases with increasing TR. <b>Keywords</b>: reaction crystallization, precipitation,benzoic acid, macromixing, mesomixing, micromixing,semi-batch, loop reactor, backmixing, colour experiments,scaling-up. <b>Keywords</b>: reaction crystallization, precipitation,benzoic acid, macromixing, mesomixing, micromixing,semi-batch, loop reactor, backmixing, colour experiments,scaling-up.

<p>Semi-batch crystallization experiments have been performedboth in a loop reactor and in stirred tank reactors.Hydrochloric acid was fed to a stirred solution of sodiumbenzoate, and benzoic acid immediately formed. Benzoic acid isformed in excess of the solubility making the solutionsupersaturated.</p><p>The loop reactor is U-shaped. In one leg a propeller stirrerwas placed to circulate the solution and in the other a turbinestirrer was placed in front of the feed point to vary the localmixing intensity. The objective was to analyse the relativeimportance of different levels of mixing on the product sizedistribution. The importance of mixing as well as scaling-upeffects on the product size distribution were studied in threestirred tank reactors of volumes 2.5 L, 10 L, and 200 L. Thestirred tank reactors had different geometry and were equippedwith either a marine propeller or a pitched blade turbine.</p><p>The weight mean size generally increases with increasingtotal feeding time and increasing mixing intensity. The weightmean size increases by locating an extra turbine impeller atthe feed point in the 10 L stirred tank reactor. The turbineimpeller provides the desired feed point mixing intensitywithout raising the mixing intensity of the whole tank.</p><p>The weight mean size increases with decreasing feed pipediameter in the loop reactor and for low feed rates in the 10 Lstirred tank reactor. The weight mean size increasessignificantly by changing the feed pipe opening from circularto rectangular with a constant cross-sectional area at equalfeed rates. Backmixing is visually observed in the largest feedpipe diameter in the loop reactor, thus, reducing the weightmean size. However, backmixing is not considered to be adominant phenomenon in the present work.</p><p>Mesomixing time constants have been calculated according tothe turbulent dispersion mechanism and the inertial-convectivemechanism. The time constants for mesomixing are generallylonger than the time constant for micromixing. Thus, the ratioof the mesomixing and the micromixing time constants shows aninfluence of mesomixing as is shown by the experimentalresults. The experimental results are best described by theinertial-convective disintegration mechanism showing that thefeed plume mixing increases with decreasing feed pipe diameterand increased feed point mixing.</p><p>The weight mean size is not strongly affected by the reactorvolume. However, the mixing conditions in the reactors have astrong influence on the weight mean size. No suggestedscaling-up rule can satisfactorily predict the weight mean sizein the different volumes. No single physical parameter, such asthe local energy dissipation rate, the mean energy dissipationrate or the circulation time, can satisfactorily explain theexperimental results. A new dimensionless mixing parameter, TR,has been defined as the ratio of the total feeding time and themesomixing time constant. The mesomixing time constant isdefined as the shortest dimension of the feed pipe divided bythe resultant bulk velocity passing the feed pipe entrance. Theexperimental results from both the loop reactor and the stirredtank reactors of different volumes can be correlated with TR.The weight mean size increases with increasing TR.</p><p><b>Keywords</b>: reaction crystallization, precipitation,benzoic acid, macromixing, mesomixing, micromixing,semi-batch, loop reactor, backmixing, colour experiments,scaling-up.</p><p><b>Keywords</b>: reaction crystallization, precipitation,benzoic acid, macromixing, mesomixing, micromixing,semi-batch, loop reactor, backmixing, colour experiments,scaling-up.</p>

Foi desenvolvido modelo matemático para o processo de produção de álcoois etoxilados em um reator batelada com spray da fase líquida na fase gasosa. O modelo considera a cinética da polimerização iônica e a transferência de massa de óxido de eteno entre as fases gasosa e líquida. A cinética foi estudada a partir de dados previamente obtidos em laboratório. Para modelagem da transferência de massa, foram utilizados dados de bateladas industriais. Foram testados vários modelos de transferência de massa encontrados na literatura, sendo que o modelo que se mostrou mais adequado para este reator industrial foi o de gotas com circulação interna. A partir do modelo obtido da cinética e da transferência de massa, foi analisada a influência de parâmetros de projeto, como a vazão de recirculação de líquido, a relação entre a altura e o raio do reator e o tipo de spray na produtividade deste. Observou-se que a maior vazão de recirculação aumenta a produtividade do reator, assim como o aumento da altura do reator. O tipo e o diâmetro da gota do spray também influenciam a produtividade do reator. / A mathematical model for the production of ethoxylated alcohols in a spray tower loop reactor was developed. The model considers the reaction as an ionic polymerization and the ethylene oxide mass transfer from the vapor phase to the liquid phase. The kinetics was obtained from a laboratory scale reactor data. The mass transfer model was obtained from the industrial reactor data. Several models for the mass transfer of ethylene oxide from gas phase to the liquid droplets were tested, and it was found that the most appropriate mass transfer model for this industrial reactor was the internally well-mixed drop model. From the kinetics and the mass transfer model, the influence of the pump recirculation flow rate, the ratio between the reactor height and radius and the spray performance was analyzed. The results show that higher reactor productivity can be obtained using higher recirculation flow and higher reactor height. The spray nozzle performance and the drop diameter also influence the reactor productivity.

Orientador: Carlos Alberto Gasparetto / Tese (doutorado) - Universidade Estadual de Campinas, Faculdade de Engenharia de Alimentos / Made available in DSpace on 2018-08-08T22:28:21Z (GMT). No. of bitstreams: 1 Ohata_SueliMarie_D.pdf: 1133009 bytes, checksum: d9e555381242748bb00e413dc46b8c7d (MD5) Previous issue date: 2007 / Resumo: Os reatores de recirculação representam uma tecnologia alternativa muito atraente para o processo de hidrogenação, tecnologia esta ainda não totalmente desenvolvida para a hidrogenação de óleos vegetais. Os reatores convencionais utilizados no processo de hidrogenação possuem agitação mecânica, sistema de injeção de hidrogênio na base, e necessitam de condições mais severas de operação, como a temperatura e a pressão. Em um reator que opera num sistema de recirculação, um ejetor tipo Venturi e utilizado, o qual proporciona uma grande transferência de massa entre as fases presentes, dispensando a agitação mecânica, alem de requerer quantidades menores de catalisador, demandar menos hidrogênio e trabalhar com pressão, temperatura e tempo de reação menor. Foram encontradas poucas informações na literatura a respeito do processo de hidrogenação de óleos vegetais através do reator de recirculação, desta forma, o objetivo deste trabalho foi analisar o processo de hidrogenação de óleo de soja em um reator de recirculação através da modelagem e simulação. Para a formulação do modelo que descreve este sistema, foram considerados os fenômenos de transferência de massa, alem da cinética da reação. A partir das equações obtidas, propos-se uma metodologia para solucionar o sistema de equações diferenciais que descrevem o sistema. Foram propostos dois modelos para o estudo: reator em batelada, resolvido analiticamente e uma associação de um reator CSTR em serie com um PFR com dispersão axial, resolvido pelo método da colocação ortogonal. Ambos os modelos descreveram adequadamente o processo de hidrogenação nas condições estudadas / Abstract: Loop reactors represent a very attractive alternative technology to the hydrogenation process, but this technology was not totally developed for the hydrogenation of vegetable oils. The conventional reactors used for the hydrogenation process have mechanical agitation, system of injection of hydrogen in the basis and they need more severe conditions of operation, as the temperature and the pressure. In a reactor that operates in a system loop, an ejector type Venturi is used, which provides an high mass transfer rate between the present phases, without mechanical agitation, needs less catalyst, demands less hydrogen and works with lower values of pressure, temperature and time of reaction. There is very little information in the literature about the hydrogenation process of vegetable oils in a loop reactor, thus, the purpose of this study was to analyse of the process of hydrogenation of soybean oil in a loop reactor by modelling and simulation. For the formulation of the model that describes this system, the phenomena of mass transfer and kinetics of the reaction were considered. From the balance equations, a method was considered to solve the system of differential equations that describe the system. Two models of reactors were proposed for the study: batch reactor, solved analytically and an association of a reactor CSTR in series with a PFR with axial dispersion, solved by orthogonal collocation method. Both models described the process of hydrogenation appropriately in the studied conditions / Doutorado / Doutor em Engenharia de Alimentos

Philosophiae Doctor - PhD / Emerging micropollutants such as bisphenol-A and 2-nitrophenol present a great threat in drinking water due to their adverse effects. Most conventional technologies in water and wastewater treatment are not designed to eliminate these xenobiotics; instead pollutants are merely transferred from one phase to another. Advanced oxidation technologies (AOTs) however, have been identified as suitable routes for the degradation of these potential damaging substances based on free radical mechanisms and use of less expensive chemicals. Moreover, due to the structural complexity of wastewater and the existence of pollutants as mixtures, no single advanced oxidation technology can convincingly remove all forms of contaminants and then most often than not, a combination of treatment processes is required for an effective purification process. Besides, the problem of adequate degradation of emerging contaminants in the environment, when AOT(s) are used individually, they present inherent problems. For instance, powder TiO₂ photocatalysts obstruct light penetration, thus prevent effective interaction of UV light with the target pollutants, and particulates present problems of post-filtration and recovery of catalyst particles after treatment. Additionally, TiO₂ has a high band gap energy, high electron-hole recombination rate, and is prone to aggregation of the suspended particles. Similarly, the dielectric barrier discharge (DBD) system produces ultra violet light and hydrogen peroxide within the plasma zone which is not fully maximised for the mineralization of persistent organic pollutants. Rapid oxidation and aggregation of nano zero valent iron particles in photo-Fentons process reduce the particles mobility and affect its performance. In the same vein, the jet loop reactor (JLR) system is characterised by low impingement yield, which is responsible for low mineralization rate. In light of this background, this research investigated the degradation of bisphenol-A and 2- nitrophenol in aqueous solution using the following combined advanced oxidation methods: DBD/supported TiO₂ or Ag doped TiO₂ photocatalysts, DBD/photo-Fenton induced process and JLR/UV/H₂O₂. The target was to assess the performance of each single system and then identify the best combined AOTs capable of significantly mineralizing the target compounds. Firstly, two materials were developed namely supported TiO₂ and stabilized nano zero valent Fe. The TiO₂ photocatalyst supported on a stainless steel mesh was synthesised using sol-gel solution of 8 % PAN/DMF/TiCl₄. The influence of calcination temperature and holding time on the formation of nanocrystals was investigated. Afterwards, various amounts of metallic silver were deposited on the (optimum) supported TiO₂ photocatalyst using thermal evaporation. The catalysts were characterized by several analytical methods; HRSEM, HRTEM, EDS, SAED, FTIR, TGA-DSC, UV-vis/diffuse reflectance spectroscopy, XRD, BET, and XPS. The photocatalytic activity of the prepared catalysts was determined using methylene blue as a model pollutant under ultra-violet light irradiation. Secondly, the TiO2 photocatalyst and 2.4 % Ag doped TiO₂ nanocomposites obtained as optimums (in section 1) were combined with the DBD to decompose BPA or 2-NP in aqueous solution. Moreover, the photo-Fenton process was applied for degradation of the model pollutants, and different dosages of stabilized nZVI (in the range of 0.02 -1.00 g) were added to the DBD system to induce the photo-Fenton process and improve BPA or 2-NP degradation efficiency. Finally, a jet loop reactor (JLR) presenting advanced mixing by the “impinging effect” was explored to decompose BPA or 2-NP in aqueous solution as a function of inlet applied pressure, solution pH, and initial concentration of BPA or 2-NP. Subsequently, different concentrations of hydrogen peroxide (H₂O₂) were added to the JLR to enhance the mineralization process. Furthermore, a combination of JLR with in-line UV light and H₂O₂ were further utilised to decompose BPA or 2-NP in aqueous solution. The residual concentration of the model compounds and intermediates were analysed using high performance liquid chromatography (HPLC) and liquid chromatography mass spectrometry (LCMS). The concentration of the ozone, hydrogen peroxide and hydroxyl radicals generated by the DBD in the presence or absence of a catalyst was monitored using Ultraviolet-visible spectroscopy and Photoluminescence spectroscopy. The results revealed that the optimal thermal conditions to obtain well supported uniformly grown, highly active crystalline TiO₂ catalysts with high specific surface area was 350 ºC at a 3 h holding time in N2 atmosphere with a flow rate of 20 mL/min. Pyrolysis temperature and holding time played an important role on the crystalline nature and photocatalytic activity of the catalyst. Moreover, 2.4 % Ag doped TiO₂ nanocomposites exhibited higher photocatalytic activity for methylene blue degradation than the undoped supported TiO₂ nanocrystals. The results indicated that combining DBD with 2.4 % Ag doped TiO₂ nanocomposites achieved 89 % and 81 % removal efficiency for BPA or 2-NP compared to 67.22 % or 56.8 % obtain when using the DBD system alone. The 2.4 % Ag doped TiO₂ nanocomposites demonstrated excellent activity and offered photochemical stability after four repeated applications.In the case of the photo-Fenton induced process, nano zero valent iron particles (nZVI) stabilized with polyethylene glycol were synthesised using a modified borohydride reduction method. The HRSEM, BET, XRD, and XPS analysis confirmed the formation of filamentous, high surface area iron nanoparticles in the zero valent state. Unlike combined DBD/Ag doped TiO2 nanocomposites, 100 % or complete removal of BPA or 2-NP in aqueous solution was achieved with DBD/nZVI system within 30 minutes compared to 67.9 % (BPA) or 56.8 % (2-NP) with DBD alone after 80 minutes. The removal efficiency was attributable to the production of an increased concentration of OH radicals as well as existence of a synergetic effect in the combined DBD/nZVI system. Five new transformation products namely: 4-nitrophenol (C₆H₅NO₃), 4-nitrosophenolate (C₆H₄NO₂), 4-(prop-1-en-2-yl) cyclohexa-3,5-diene-1,2-dione, (C₉H₈O₂), 4-(2- hydroxylpropan-2-yl)cyclohexane-3,5-diene-1,2-dione (C₉H₁₀O₃), and 1,2-dimethyl-4-(2- nitropropan-2-yl)benzene (C₉H₁₀NO₄) were identified during the degradation of BPA. While, three aromatic intermediate compounds such as 2-nitro-1,3,5-benzenetriolate (C₆H₂NO₅), 2- nitro-1,4-benzoquinone (C₆H₃NO₄), and 2,5-dihydroxyl-1,4-benzoquinone (C₆H₄O₄) respectively were identified during the degradation of 2-NP for the first time in the DBD with JT14 or JT17 using LC-MS. These intermediate compounds have never been reported in the literature, thereby expanding the number of BPA or 2-NP intermediates in the data base in the DBD/JT14 or DBD/nZVI system. BPA degradation proceeded via ozonation, hydroxylation, dimerization, and decarboxylation and nitration step, while 2-NP proceeded via hydroxylation, nitration and denitration respectively. Furthermore, maximum removal efficiency of BPA or 2-NP in aqueous solution using JLR alone under the optimum solution pH (3), inlet pressure (4 bar), flow rate (0.0007 m3/s) was 14.0 % and 13.2 % respectively after 80 minutes. A removal efficiency of 34.9 % was recorded for BPA while 33.2 % was achieved for 2-NP using combined JLR/UV under the same conditions as JLR alone. For the combined JLR/H₂O₂ under optimum conditions of inlet pressure (4 bar), solution pH (3) and peroxide dosage (0.34 g/L), a 51.3 % and 50.1 % removal efficiency was achieved for BPA and 2-NP respectively under same conditions relative to JLR alone. Combination of JLR/UV/H₂O₂ achieved 77.7 % (BPA) or 76.6 % (2- NP) removal efficiency under the same conditions. The combined JLR/UV/H₂O₂ process was found to be most effective combination under the optimized operating parameters due to existence of a synergetic index value of 6.42 or 6.84. This implies that JLR should be coupled with UV and H₂O₂ to achieve greater mineralization efficiency instead of using the system individually. The obtained experimental data of these combined treatment processes fitted the pseudo-first order kinetic models. The combination of the JLR/UV/H₂O₂ was found to be energy efficient and could effectively degrade BPA or 2-NP in aqueous solution to a greater extent than the JLR, JLR/UV or JLR/H₂O₂ system. However, the total organic carbon (TOC) reduction value by all combined DBD and JLR system recorded was not completely achieved due to the formation of recalcitrant intermediate compounds under the applied conditions. In conclusion, this study is reporting for the first time a combination of supported 2.4 % Ag doped TiO₂ nanocomposites with dielectric barrier discharge system for BPA/2-NP degradation in aqueous solution; a combination jet loop reactor based on impingement with in-line UV lamp and H2O2 for successfully decomposing BPA or 2-NP in aqueous solution; as well as a combination of dielectric barrier discharge system and stabilised nano zero valent iron particles, which induced a photo-Fenton process for highly effective removal of BPA or 2-NP in aqueous solution. This study conclusively supports the hypothesis that combined advanced oxidation technologies offer a sustainable and highly efficient means of achieving partial or complete removal of BPA or 2-NP in aqueous solutions. Considering all the combinations of AOTs investigated in this study, the novel DBD/photo-Fenton-induced process under optimised operating parameters was found to be the most efficient in the elimination of BPA or 2-NP in aqueous solutions. The combination of DBD with photo- Fenton like process offers a promising advanced waste water purification technology in the immediate future. Based on these findings, it is recommended that DBD should be redesigned to prevent loss of ozone and JLR system reconfigured to increase impingement and cavitational yield in order to have an effective combination treatment strategy for waste water purification especially in large scale waste water management. / National Research Foundation (NRF) and Water Research Commission, South Africa

Orientadores: Rubens Maciel Filho, Jose Carlos Costa da Silva Pinto, Priamo Albuquerque Melo Junior / Dissertação (mestrado) - Universidade Estadual de Campinas, Faculdade de Engenharia Química / Made available in DSpace on 2018-08-10T00:03:32Z (GMT). No. of bitstreams: 1 Lucca_EneidaAparecidade_M.pdf: 1657459 bytes, checksum: 56b6b6c35a2802734e03ed28ceb76c67 (MD5) Previous issue date: 2007 / Resumo: Reatores tubulares do tipo loop são amplamente empregados nas indústrias de poliolefinas. No caso da produção de polipropileno, compõem a tecnologia Spheripol. São constituídos de duas seções tubulares interconectadas por um ponto de alimentação e por uma bomba, que promove a recirculação da massa reacional. O simulador dinâmico desenvolvido nesse trabalho é capaz de estimar valores de diversas variáveis chave no monitoramento do processo; dentre elas, o XS e o MFI. As validações feitas mostraram que o simulador é capaz de representar de forma acurada os dados experimentais disponíveis em uma planta real de polimerização, inclusive para ¿N¿ reatores em série / Abstract: Tubular loop reactors are widely used in the polyolefins industries. In the particular case of polypropylene production, loop reactors are part of the Spheripol technology. Loop reactors are composed of two tubular reactors that are connected by a feed point and a pump that is responsible for promoting recirculation of the reaction mass. The dynamic simulator developed here is able to estimate values of several important variables used to monitor the industrial process, like the XS and the MFI. The model was validated with actual industrial data obtained for different reactor configurations, including ¿N¿ reactors in series / Mestrado / Engenharia de Processos / Mestre em Engenharia Química

Diploma thesis will be dealt with the utilization of ozone wastewater treatment. Experimental part will be focused on study of ozone utilization in two different reactors (bubble column, jet loop reactor). Reactors will be compared by overall mass transfer coefficient and saturation concentration. Ozonization will be applied because of biological resistent and toxic compound 2-mercaptobenzothiazole disposal. Changes of biological decomposition will be measured and assessed by respirometric measurements.