京都大学 / 0048 / 新制・課程博士 / 博士(地球環境学) / 甲第19419号 / 地環博第145号 / 新制||地環||29(附属図書館) / 32444 / 京都大学大学院地球環境学舎環境マネジメント専攻 / (主査)教授 藤井 滋穂, 教授 高岡 昌輝, 准教授 田中 周平 / 学位規則第4条第1項該当 / Doctor of Global Environmental Studies / Kyoto University / DFAM

El texto completo de este trabajo no está disponible en el Repositorio Académico UPC por restricciones de la casa editorial donde ha sido publicado. / The continuous flow intersections (CFI) increase the operational capacity of road systems with congestion problems, by using shared lanes located at the access points before the intersection. However, the CFI presents road safety risks that increase the likelihood of vehicle collision. This article proposes a geometric design composed of raised delineators at a traffic-light intersection, whose objective is to eliminate the points of primary conflicts caused by the left turns of the vehicles. To do this, a study was conducted to identify the different maneuvers present in a wide cross-type intersection in a commercial area located in the city of Lima. A total of 3219 vehicles was collected, of which 561 vehicles turned left demonstrating the high density of this type of maneuver. The effectiveness of the proposed design is validated using a microsimulation in the Vissim program. The results show that it was reduced from 58 to 8 points of conflict, increasing operational capacity by 34.97%. Finally, the risks caused by CFI decreased by 83%. / Revisión por pares

An introduction is given to the background theory and scientific literature of the major subject areas of interest in this thesis, namely the chemistry of free radical and anionic polymerisation, molecular weight control in each type of polymerisation, polymerisation reactors, computer simulation of polymerisation processes and polymer characterisation by gel permeation chromatography. A novel computer model has been devised, based on the analysis of the polymerisation process in terms of the reaction extent of each reactant and the use of generation functions to describe the concentration of living and dead polymeric species, for the free radical, solution polymerisation of methylmethacrylate in a CSTR. Both heat and mass balance expressions have been described. Conversion, Mn and Mw were monitored. To test the model a reactor was designed and constructed. A detailed description of the reactor and the experimental conditions used for the validation of the model are given. The results of these studies are presented and excellent agreement is shown between model predictions and experiments up to 30% conversion for Mn w and % conversion. A similar study is described for the anionic polymerisation of styrene in tetrahydrofuran as solvent, in a CSTR. In this work the computer model becomes 'stiff' when realistic rate constants are introduced in the kinetic expressions. Experimental difficulties were encountered in obtaining reproducible results in the anionic work. A new approach of using 'scavengers' as protecting agents for the living chains is described. A scavenger was successfully employed in the preparation of block copolymers using a tubular reactor. Block copolymerisation, in addition to providing a means of checking the number of the 'living' chains inside the reactor, is of interest in its own right. All the experimental findings are discussed in relation to the currently accepted views found in the scientific literature.

Clean water is essential to life. Growth in world population, changing diets, and a warming climate are driving an increase in the demand for water. Better management of water resources will help prevent scarcity, but in order to fully meet the future demand for safe, clean drinking water, new water treatment technologies are needed. This dissertation investigates a technology which is not well understood; the combination of ozone and ultrasound as potentially an efficient technology. Since nearly all previously published studies of combined ozone/ultrasound utilized batch reactors, a continuous flow reactor was constructed for this research. 1,4-Dioxane, henceforth referred to as dioxane, was chosen to evaluate the effectiveness of the combined ozone/ultrasound process. Dioxane is commonly detected in surface and groundwater and is a suspected human carcinogen. A recalcitrant contaminant, it resists direct oxidation by chlorine, oxygen, ozone, and biological treatment. It is miscible in water and doesn't sorb readily to organic matter, so it spreads rapidly in groundwater contamination plumes. It also resists air stripping and filtration, including reverse osmosis. For these reasons, dioxane makes an excellent candidate to measure the effectiveness of advanced oxidation processes, such as combined ozone/ultrasound. The treatment of dioxane by advanced oxidation processes has been studied extensively in the past. However, only one study has been published using combined ozone/ultrasound, and it was done in a batch reactor operating at a high ultrasonic frequency. The reactor built for this study also permitted reactor pressurization effects to be studied in a manner that has not been reported before for the combined ozone/ultrasound process. In this study, the combination of ozone and ultrasound was found to cause synergistic removal of dioxane from drinking water; the removal achieved by the combination significantly exceeded the sum of the removal achieved by ozone and ultrasound separately. In fact, the combination of ozone and ultrasound was found to remove more than double the dioxane that would be removed by doing both treatment processes separately. Ultrasound (20 kHz) was ineffective in removing dioxane alone, achieving less than 20% removal. At 16 mg/L, ozone alone was found to achieve removal of up to 86% after a 16 minute treatment time, but appears sensitive to matrix effects, especially pH. When ultrasound was combined with just 1.2 mg/L of aqueous ozone, over 90% removal occurred after a 16 minute treatment. Removal of dioxane was found to be driven not by ozone itself, but by radicals, suggesting that the decomposition of ozone is responsible for the generation of radical species and subsequent removal of dioxane. Ultrasound was found to increase the decomposition of ozone and appeared to be driving increased mass transfer of ozone into the aqueous phase. Modest reactor pressure appears to aid dioxane removal, but further increases in pressure did not appear to further enhance removal. An empirical model was constructed using a form similar to the Chick & Watson model for disinfection. Given inputs of initial aqueous ozone concentration, initial dioxane concentration, treatment time, and ultrasonic power, the model is able to predict effluent concentrations of dioxane with a relative root mean squared error of less than 5%. Additionally, RCT and mass balance analyses were performed, and both analysis techniques suggested that the removal of dioxane is dependent on the consumption of aqueous ozone. Spiked drinking water is representative of water that has undergone conventional treatment but requires a polishing step, and the combined ozone/ultrasound has shown promise as a polishing technology. Owing to its recalcitrance, prevalence, and mobility, dioxane represents a real and challenging groundwater contaminant, and combined ozone/ultrasound has shown promise as a groundwater treatment option. Additionally, the process is capable of dioxane removal in a pH range of 4-10. This pH independence, coupled with its ability to degrade recalcitrant contaminants, suggests that combined ozone/ultrasound holds promise as an industrial wastewater treatment option, too. The removal achieved by both ozone and combined ozone/ultrasound was an order of magnitude greater than what has been reported in previously published reports. However, a comparison of cost effectiveness relative to other advanced oxidation processes remains an area for future study. Finally, the combined ozone/ultrasound process holds promise as a drinking water treatment option in remote areas, since it requires only electricity. As a promising technology for polishing water for reuse, treating contaminated groundwater, treating industrial wastewater, and potentially improving access to safe drinking water in remote areas, combined ozone/ultrasound could aid in meeting global water demand in the future. / Civil Engineering

Aerobic granular sludge has been regarded as a promising alternative to the conventional activated sludge which has been used for a century in that granular sludge offers advantages in high biomass retention, fast sludge-water separation, and small footprint requirement. However, this technology has been rarely applied in continuous flow reactors (CFRs) which are the most common type of bioreactors used in water resource recovery facilities across the world. Hence, the overarching goal of this study is to provide advanced understanding of biogranulation mechanism to enable industrial application of this technology. The lack of long-term stability study in CFRs has restricted its full-scale acceptability. The high settling velocity-based selection pressure has been regarded as the ultimate driving force towards biogranulation in sequential batch reactors (SBRs). In this study, this physical selection pressure was firstly weakened and then eliminated in CFRs to investigate its role in maintaining the long-term structural stability of aerobic granules. Given the fact that implementing settling velocity-based selection pressure only can cultivate biogranules in SBRs but not in completely stirred tank reactors (CSTRs), the essential role of feast/famine conditions was investigated. Seventeen sets of data collected from both literature and this study were analyzed to develop a general understanding of the granulation mechanisms. The outcome indicated that granulation is more sensitive to the feast/famine conditions than to the settling velocity-based selection pressure. The theory was tested in a CFR with 10-CSTR chambers connected in series to provide feast/famine conditions followed by a physical selector separating the slow-settling bioflocs and fast-settling biogranules into feast and famine zones, respectively. Along with successful biogranulation, the startup performance interruption problem inherent in SBRs was also resolved in this innovative design because the sludge loss due to physical washout selection was mitigated by returning bioflocs to the famine zone. Then, a cost-effective engineering strategy was put forward to promote the full-scale application of this advanced technology. With this generalized biogranulation theory, pure culture biogranules with desired functions for high value-added bioproducts were also investigated and achieved for the first time in this study, which paves a new avenue to harnessing granulation technology for intensifying waste valorization bioprocesses. / Doctor of Philosophy / Nowadays, the rapid population growth and unprecedented urbanization are overloading the capacity of many wastewater resource recovery facilities (WRRFs). Therefore, there is a need to develop a cost-effective strategy to upgrade the treatment capacity of existing WRRFs without incurring major capital investment. Because conventional activated sludge comes with loose structure and poor settleability, replacing them with dense aerobic granular sludge offers the opportunity to intensify the capacity of existing WRRF tankage and clarifiers through better retention of high bacterial mass that offers not only a fast pollutant removal rate but also a high water-solids separation rate. The aerobic granulation technology turns traditional activated sludge into granular sludge by inducing microbial cell-to-cell co-aggregation. Although this technology has been developed for more than 20 years, its application in full-scale WRRFs is still limited because majority of WRRFs are constructed with continuous flow reactors in which the aerobic granulation mechanism largely remains unknown. Besides, the long-term stability of aerobic granules in continuous flow reactors also remain unstudied, further constraining the full-scale application of the technology. The sensitivity of aerobic granulation to physical selection and biological selection was analyzed in this study. The results concluded that aerobic granulation is more sensitive to the latter but not to the former. Subsequently, this theory was tested in a novel bioreactor setup that creates feast/famine conditions for biological selection. A physical selector was installed at the end of the bioreactor to separate and return the fast- and slow- settling bioparticles to the feast and famine zones, respectively. This unique reactor design and operational strategy provided an economical approach to retrofitting current WRRFs for achieving treatment capacity upgrading without major infrastructure alternation. It also protected the bioreactor startup performance by enhancing the stability of WRRFs in the future application. Last but not least, this updated understanding of aerobic granulation theory was for the first time extrapolated to and verified with the formation of pure culture biogranules harnessed in this study for value-added bioproduct valorization from waste materials.

Although concepts of the XDL intersection or CFI (Continuous Flow Intersection) have been around for approximately four decades, users do not yet have a simplified procedure to evaluate its traffic performance and compare it with a conventional intersection. Several studies have shown qualitative and quantitative benefits of the XDL intersection without providing accessible tools for traffic engineers and planners to estimate average control delays, and queues. Modeling was conducted on typical geometries over a wide distribution of traffic flow conditions for three different design configurations or cases using VISSIM simulations with pre-timed signal settings. Some comparisons with similar conventional designs show considerable savings in average control delay, and average queue length and increase in intersection capacity. The statistical models provide an accessible tool for a practitioner to assess average delay and average queue length for three types of XDL intersections. Pre-timed signal controller settings are provided for each of the five intersections of the XDL network. In this research, a "real-time" traffic signal control strategy is developed using genetic algorithms and neural networks to provide near-optimal traffic performance for XDL intersections. Knowing the traffic arrival pattern at an intersection in advance, it is possible to come up with the best signal control strategy for the respective scenario. Hypothetical cases of traffic arrival patterns are generated and genetic algorithms are used to come up with near-optimal signal control strategy for the respective cases. The neural network controller is then trained and tested using pairs of hypothetical traffic scenarios and corresponding signal control strategies. The developed neural network controller produces near-optimal traffic signal control strategy in "real-time" for all varieties of traffic arrival patterns. / Master of Science

Heart failure is expected to ail over 8 million people in America by 2030 leaving many in need of cardiac replacement. To accommodate this large volume of people, ventricular assist devices (VADs) are necessary to provide mechanical circulatory support. Current VADs exhibit issues such as thrombosis and hemolysis caused by large local pressure drops and turbulent flow within the pump. Multiple disk centrifugal pumps (MDCPs) use shearing and centrifugal forces to produce laminar flow patterns and eliminate large pressure drops within the pump which greatly reduce risks that are in current VADs. The MDCP has a shaft drive system (SDS) that causes leakage between the motor and housing that when implanted can cause blood loss, infection, thrombosis and hemolysis. To eliminate these adverse effects, a magnetic external motor-driven system (MEMDS) was implemented. An efficiency study was performed to examine the efficacy of the MEMDS by comparing the hydraulic work of the MDCP to the power required to run the pump. This was done by measuring inlet and outlet pressures, outlet flow rate and input current at various input voltages and resistances. The results showed the MDCP could produce physiologic flow characteristics with a flow rate of 4.90 L/min and outlet pressure of 61.33 mmHg at an impeller speed of 989.79 rpm. Other VADs generate flow rates around 5 L/min at rotational speeds of 2400 rpm for centrifugal pumps and 12000 rpm for axial pumps. When compared to the SDS, the MEMDS exhibited similar efficiencies of 3.89% and 3.50% respectively. This study shows promise in the advancement of MDCP.

Over the last two centuries, the discovery and application of catalysts has had a substantial impact on how and what chemicals are produced.Given their broad significance, our group has focused on developing new catalyst systems that are recoverable and reusable, in an attempt to reduce concomitant costs. Our efforts have centered on constructing a recyclable chiral heterogeneous catalyst capable of effecting asymmetric hydrogenations of olefins with high stereoselectivity. A class of phosphinoimidazoline ligands, developed by researchers at Boehringer-Ingelheim, known as BIPI ligands, have proven efficacious in the asymmetric reduction of alkenes. However, these chiral ligands are homogeneous and coordinated to precious metals, rendering them irrecoverable and expensive. To address these issues, our group has derivatized the BIPI ligand-metal complex and immobilized it to the surface of graphene oxide as well as polystyrene. Their efficacy and recyclability toward the asymmetric hydrogenation of a functionalized olefin have been evaluated. Another facet of our work has included developing a cost effective synthetic process to artemisinin, the gold standard drug in the treatment of malaria.As a natural product, artemisinin’s worldwide supply remains highly unpredictable, contributing to great price volatility.Combining the benefits of catalysis and the advantages of continuous flow chemistry, our research has sought to develop an economical approach to convert a biosynthetic precursor, artemisinic acid, to artemisinin in three chemical transformations. High-throughput experimentation allowed us to screen a prodigious number of catalysts and identify those effective in the asymmetric hydrogenation artemisinic acid to dihydroartemisinic acid, the first step in the transformation. This screening directed us to an inexpensive, heterogeneous ruthenium catalyst. The second step of the process includes the photooxygenation of dihydroartemisinic acid, which involves photochemically generated singlet oxygen. We have evaluated a commercially available heterogeneous photocatalyst packed in a transparent bed, surrounded by light emitting diodes in the continuous photooxygenation of dihydroartemisinic acid to dihydroartemisinic acid hydroperoxide. The third and final step, an acid induced hock cleavage, initiates an intricate cascading reaction that installs an endoperoxide bridge to deliver artemisinin. Our process afforded a 57% yield from dihydroartemisinic acid to artemisinin.

The use of size and shape tunable quantum confinement nanocrystals has many potential applications for use in semiconductors, optics and sensors. The synthesis of lead sulfide (PbS) and copper indium diselenide (CuInSe���) nanoparticles are of particular interest for use in semiconductor, optoelectronics and bio-medical applications. The continuous synthesis of lead sulfide (PbS) and copper indium diselenide (CuInSe���) nanocrystals was undertaken in this work. Quality colloidal nanocrystal synthesis requires three components: precursors, organic surfactants and solvents. The synthesis of the nanocrystals can be thought of as a nucleation event, followed by a subsequent growth period. Both the nucleation and growth rates were found to be dependent upon factors such as temperature, growth time, and precursor concentration. For a continuous flow system the residence time (at nucleation and growth conditions) was also found to be important. In order to separate the nucleation and growth events, injection techniques were employed to achieve rapid nucleation of nanocrystals with final size dictated by the growth temperature and/or residence time through the growth zone of the reaction system. Experimental parameters to investigate the size, shape, and composition of synthesized nanocrystals included injection temperature, growth temperature, residence time, and concentration of organic surfactants. Size tunability was accomplished for both PbS and CuInSe��� nanocrystals where particle sizes less than 10 nm were achieved and the resulting nanocrystal compositions were found to be at the approximate stoichiometric ratios for both PbS and CuInSe���. The materials used for the process tubing and pumps were found to be important as chlorinated reaction byproducts were found to react with the stainless steel tubing and pump heads. Post processing was also found to be important in order to remove any possible reaction by-products and residual precursors from the surface of synthesized nanocrystals. When at least one dimension of the nanocrystal approaches the exciton Bohr radius, the bandgap for the nanocrystal increases. UV-VIS spectroscopy was used to optically characterize synthesized PbS nanocrystals from our continuous flow synthesis. The absorption spectra for the particles demonstrated an absorption onset showing a large blueshift compared to that of bulk PbS. The blueshift matches closely with literature reports of the quantum confinement effect that would be desired when synthesizing PbS nanoparticles at diameters that are less than the PbS exciton Bohr radius of 18 nm. / Graduation date: 2013

Sustainable chemical processes are becoming increasingly important in all fields of synthetic chemistry. Catalysis can play an important role in developing environmentally benign chemical processes, and transition metals have an important role to play in the area of green chemistry. In particular, palladium(II) catalysis includes many key features for successful green chemistry methods, as demonstrated by a number of eco-friendly oxidation reactions catalyzed by palladium(II). The aim of the work presented in this thesis was to develop novel and greener palladium(II)-catalyzed coupling reactions. In striving to achieve this aim, the first open-vessel, room-temperature palladium(II)-catalyzed oxidative Heck reaction, using oxygen from the air as the reoxidant of palladium, was developed. In a further investigation of the palladium(II)-catalyzed oxidative Heck reaction, base-free conditions for the transformation were identified and suitable conditions for microwave-assisted oxidative Heck reactions were established. A convenient and low-cost palladium(II)-catalyzed method for the synthesis of styrene derivatives, by coupling arylboranes with vinyl acetate, was developed. The reaction mechanism was studied using ESI-MS, which enabled the detection of cationic palladium intermediates in ongoing productive reactions, and a plausible catalytic cycle was proposed. In an attempt to make the oxidative Heck and the styrene synthesis reactions more attractive from an industrial point of view, conditions for continuous flow synthesis were identified. The results were generally good and rapid synthesis of the desired products was obtained. The first palladium(II)-catalyzed C–P bond-forming Hirao-type reaction, employing arylboranes instead of the commonly used aryl halides, was developed. An ESI-MS study was performed, and a plausible catalytic pathway was suggested. Finally, a novel method for synthesizing aryl ketones from benzoic acids and nitriles, via palladium(II)-catalyzed decarboxylation of the benzoic acids, was established. Further, the reaction mechanism was studied by ESI-MS and a plausible catalytic route presented.