An ancient technology of solar-driven water evaporation and distillation has recently been revived due to the concept of interfacial solar evaporation and the development of photothermal materials. There have been many research interests in improving solar light harvesting and solar-to-water evaporation efficiency within these systems, including new photothermal materials search, structural engineering, and thermal management. The application horizon of both solar-driven water evaporation and distillation has been broadly expanded beyond their conventional domain, including now wastewater treatment, seawater desalination, steam sterilization, electric generation, and chemicals/fuels productions. This dissertation focused on designing of photothermal materials and their applications to clean water production. More specifically: (1) a bi-layered porous rGO membrane with a polystyrene (PS) foam as the heat insulator was designed and proved to be effective for reducing heat conduction to the bulk water and to improve the solar-to-water evaporation efficiency, (2) a tandem-structured SiC-C ceramic monolith was prepared and demonstrated to be mechanically and chemically stable to withstand physical or chemical cleaning during long-term use in real seawater and wastewater, (3) in order to simultaneously treat the contaminated water and get clean distillate water, multi-functional SiC foam modified with mesoporous Au/TiO2 nanocomposites has been prepared, which was demonstrated to possess both photocatalytic reduction and oxidation abilities for complex wastewater treatment, and (4) when the water source was contaminated by VOCs, another efficient multi-functional photothermal material was designed with a honeycomb ceramic plate as the matrix material, and a CuFeMnO4 nanocomposite coating layer acting as both photothermal material and Fenton agent for VOCs removal. Therefore, the light absorption property of photothermal material could be improved by using a porous structure, tandem-structure, porous foam or 3D structure. The solar-to-water evaporation efficiency was improved by including a heat insulator and the reduction of the water channels’ dimension. The ceramic-based material showed potential for long-term use with high mechanical strength to endure physical cleaning. Multi-functional photothermal materials were successfully developed for complex wastewater treatment and clean water generation.

京都大学 / 新制・課程博士 / 博士(理学) / 甲第23598号 / 理博第4760号 / 新制||理||1682(附属図書館) / 京都大学大学院理学研究科化学専攻 / (主査)教授 寺西 利治, 教授 若宮 淳志, 教授 倉田 博基 / 学位規則第4条第1項該当 / Doctor of Science / Kyoto University / DGAM

La demande énergétique de l’humanité augmente rapidement et ne montre aucun signe de ralentissement. Parallèlement à cette problématique, l'utilisation abusive de combustibles fossiles est l'une des principales causes d'augmentation de la concentration de CO₂ dans l'atmosphère. Ces problèmes doivent être résolus en termes de limitation des émissions de CO₂ et de recherche de sources d'énergie renouvelables pour remplacer les combustibles fossiles. De nos jours, l’énergie solaire est l’une des sources d’énergie renouvelables les plus efficaces. La conversion de l'énergie de la lumière solaire en électricité dans le photovoltaïque ou en énergie chimique par le biais de processus photocatalytiques implique invariablement un transfert d'énergie photo-induit et un transfert d'électrons. Dans ce contexte, l'objectif de la thèse est d'étudier les processus photo-induits dans les photosystèmes moléculaires utilisant la photolyse par flash laser. Le premier thème de cette thèse porte sur l’étude du transfert monoélectronique dans des systèmes de dyades donneur-accepteur en vue d’optimiser l’efficacité de la séparation des charges et de son application dans la cellule solaire organique photovoltaïque. Le deuxième thème de cette thèse porte sur l’étude de deux systèmes modèles de photosynthèse artificielle étudiés pour la possibilité d’une accumulation de charge par étapes. Ensuite, différents systèmes photocatalytiques, développés pour la photoréduction du CO₂, ont été étudiés. La compréhension des processus photo-induits devraient permettre l’amélioration de l'efficacité de la réduction du CO₂ dans les systèmes photocatalytiques pratiques. / The energy demand of humanity is increasing rapidly, and shows no signs of slowing. Alongside this issue, abuse using fossil fuels is one of the main reasons which leads to an increase in atmospheric CO₂ concentration. These problems have to be solved in terms of both limiting CO₂ emission and finding renewable energy sources to replace fossil fuels. Nowadays, solar energy appears as one of the most effective renewable energy sources. Conversion of solar light energy to electricity in photovoltaics or to chemical energy through photocatalytic processes invariably involves photoinduced energy transfer and electron transfer. In this context, the aim of the thesis focuses on studying photoinduced processes in molecular photosystems using laser flash photolysis. The first theme of this thesis focus on studying single electron transfer in Donor-Acceptor Dyad systems towards optimization efficiency of charge separation and application in the photovoltaic organic solar cell. In the second theme of this thesis, two model systems of artificial photosynthesis were investigated to assess the possibility of stepwise charge accumulation on model molecules. A fairly good global yield of approximately 9% for the two charge accumulation on MV²⁺ molecule was achieved. Then, different photocatalytic systems, which have developed for CO₂ reduction, were studied. Understanding of the photoinduced processes is an important step toward improving the efficiency of reduction of CO₂ in practical photocatalytic systems.

Magister Scientiae - MSc (Chemistry) / Drinking water with high concentrations of inorganic and organic contaminants can cause adverse health defects. Specifically methyl orange dye is an organic water contaminant that has been known (along with others like methyl blue etc.) to have an increase in our water systems over the past few years due to increasing demand in industrial processes. It is therefore of utmost importance to remediate organic contaminants and ultimately enable prevention. The contaminants can be removed by photocatalysis. Anatase TiO2 is known for its photocatalytic degradation of environmental pollutants and photoelectro-chemical conversion of solar energy. However its application is limited since it is a wide band gap semiconductor, (Eg = 3.2 eV). The following study deals with the enhancement of the photocatalytic properties of TiO2 for remediation of organic water contaminants.

Microplastic (MP) pollution has recently been recognized as a threat to the biosphere including humans due to its widespread distribution, persistent nature and infinitesimal size. This study focused on the solid phase degradation of microplastic residues (particularly low density polyethylene, LDPE) in water through heterogeneous photocatalysis process by designed photocatalysts of zinc oxide nanorods (ZnO NRs) and platinum nanoparticles deposited on zincoxide nanorods (Pt NPs-ZnO NRs) under visible light irradiation. These photocatalysts were assessed following standard protocol (ISP 10678: 2010), and characterized using SEM, EDX andoptical spectroscopies (UV-VIS and PL). Deposition of Pt-NPs on ZnO NRs for certain minutes has been found optimum that enhanced the photodegradation process about 38% under UV irradiation and 16.5% under visible light irradiation by improving of both electrons-holes pair separation process and visible light absorption. Photocatalytic degradation of LDPE films was confirmed by FTIR spectroscopy, dynamic mechanical analyzer (DMA), optical and electron microscopes. When LDPE film irradiated in presence of Pt-ZnO, degradation was found quicker than ZnO alone of similar concentration which exhibited formation of a large number of wrinkles, cracks and cavities on the film surface. Dynamic mechanical analyzer (DMA) test indicated stiffness and embrittlement of exposed LDPE films in presence of photocatalysts. Thus, the present work provides a new insight about modified catalysts for the degradation of microplastics in water using visible light.

This collection of studies focuses on a PCO system for the oxidation of a model compound, ethanol, using an adsorption-enhanced silica-Ti02 composite (STC) as the photocatalyst; studies are aimed at addressing the optimization of various parameters including light source, humidity, temperature, and possible poisoning events for use as part of a system for gaseous trace-contaminant control system in closed-environment habitats. The first goal focused on distinguishing the effect of photon flux (i.e., photons per unit time reaching a surface) from that ofphoton energy (i.e., wavelength) of a photon source on the PCO of ethanol. Experiments were conducted in a bench-scale annular reactor packed with STC pellets and irradiated with either a UV -A fluorescent black light blue lamp O·max=365 nm) at its maximum light intensity or a UV -C germicidal lamp O.·max=254 nm) at three levels of light intensity. The STC-catalyzed oxidation of ethanol was found to follow zero-order kinetics with respect to C02 production, regardless of the photon source. Increased photon flux led to increased EtOH removal, mineralization, and oxidation rate accompanied by lower intermediate concentration in the effluent. The oxidation rate was higher in the reactor irradiated by UV -C than by UV-A (38.4 vs. 31.9 nM s-1 ) at the same photon flux, with similar trends for mineralization (53.9 vs. 43.4%) and reaction quantum efficiency (i.e., photonic efficiency, 63.3 vs. 50.1 nmol C02 ~mol photons-1 ). UV-C irradiation also led to decreased intermediate concentration in the effluent compared to UV -A irradiation. These results demonstrated that STC-catalyzed oxidation is enhanced by both increased photon flux and photon energy. The effect of temperature and relative humidity on the STC-catalyzed degradation of ethanol was also determined using the UV-A light source at its maximum intensity. Increasing ii temperature from 25°C to 65°C caused a significant decrease in ethanol adsorption (47.1% loss in adsorption capacity); minimal changes in EtOH removal; and ·a dramatic increase in mineralization (37.3 vs. 74.8%), PCO rate (25.8 vs. 53.2 nM s-1 ), and reaction quantum efficiency (42.7 vs. 82.5 nmol C02 J..Lmol phontons-1 ); intermediate acetaldehyde (ACD) evolution in the effluent was also decreased. By elevating the reactor temperature to 45°C, a -32% increase in reaction quantum efficiency was obtained over the use ofUV-C irradiation at room temperature; this also allowed for increased energy usage efficiency by utilizing both the light and heat energy of the UV-A light source. Higher relative humidity (RH) also caused a significant decrease (16.8 vs. 6.0 mg EtOH g STCs-1 ) in ethanol adsorption and dark adsorption 95% breakthrough times (48.5 vs.16.8 hours). Trends developed for ethanol adsorption correlated well with studies using methanol as the target VOC on a molar basis. At higher RH, ethanol removal and ACD evolution were increased while mineralization, PCO rate, and reaction quantum efficiency were decreased. These studies allowed for the development of empirical formulas to approximate EtOH removal, PCO rate, mineralization, and ACD evolution based on the parameters (light intensity, temperature, and RH) assessed. Poisoning events included long-term exposure to low-VOC laboratory air and episodic spikes of either Freon 218 or hexamethylcyclotrisiloxane. To date, all poisoning studies have shown minimal (0-6%) decreases in PCO rates, mineralization, and minimal increases in ACD evolution, with little change in EtOH removal. These results, while studies are still ongoing, show great promise of this technology for use as part of a trace contaminant control system for niche applications such as air processing onboard the ISS or other new spacecrafts.

<p> </p> <p>ndoor air quality (IAQ) due to the presence of airborne microorganisms or bioaerosols (0.01-10 μm) in indoor spaces has been a concern for many years; however, it gained significant attention during the COVID-19 pandemic. Photocatalytic oxidation (PCO) has shown promising potential to kill microorganisms (removal/disinfection) and has already been in use within HVAC systems to treat volatile organic compounds (VOCs) (treatment). The main motivation of this work is to understand whether PCO devices can be used for bioaerosol removal in indoor spaces by integrating them with HVAC systems. Among the various factors that influence the adoption of PCO for large-scale bioaerosol removal, this work specifically tries to investigate two factors 1) whether the commercially available PCO reactors for treatment can be used for removal/disinfection or not, and 2) how to setup a standardized experimental setup for evaluating the removal efficiency of these systems. Generally, most of the commercial PCO devices use UV- based photocatalysis, so the removal efficiency is a combination of inactivation by UV and the reactive oxygen species produced by photocatalytic reactions (pure photocatalytic effect).</p> <p>In this work, the bioaerosol transport and the photon transport in a reactor is hypothesized as central to using the photocatalytic effect to inactivate microorganisms. This study uses analytical models to estimate the collection efficiency of the bioaerosols inside the honeycomb channels as a function of non-dimensional aspect ratios and velocity typical of HVAC systems. Subsequently, the collection efficiency results are overlaid with the prior literature results on photon transport inside such channels to present a limiting case for the removal efficiency of these systems. Another crucial factor for the performance of PCO systems is to investigate about the bioaerosol remediation on a photocatalyst substrate. Since there are many challenges associated with the numerical modeling of this phenomenon, this work developed a standardized experimental setup at the Herrick Laboratories, Purdue to investigate these interactions and further validate the previous hypothesis .The setup is constructed to systematically characterize the bioaerosol flowing through the airstream and measure data crucial to the PCO reactor performance, such as fluence rate field, number concentration (#/cm3), and viable concentration (CFU or PFU/m3) of the microorganisms upstream and downstream of the treatment sections. </p> <p>The collection efficiency (CE) of bioaerosols in honeycomb channels with velocities typical to HVAC systems were estimated using analytical models, and the results were presented in dimensionless aspect ratios (AR= Lch/ Dch). Based on the CE modeling results, the highest CE for aspect ratio 25 was less than 20% for the entire bioaerosol size range. From the prior literature results on photon transport, it was found that the intensity of the light reduced significantly for aspect ratios less than or equal to 6. Based on these results, it was found that the existing honeycomb geometries weren’t effective for PCO disinfection in operating conditions typical of HVAC systems. Since there aren’t any existing well-established methods to experimentally investigate these kinds of systems, this work will present the details about the development of the proposed methods inspired from prior literature for general air cleaning devices and small-scale PCO experiments. Furthermore, a detailed discussion about the important subsystems such as aerosol generation subsystem, sampling subsystem, and reactor subsystem which is crucial to investigating the hypotheses is presented in this thesis. Finally, some preliminary results on each of these characterization experiments to test the hypotheses has been presented in this thesis.</p>

No description available.

<p> Photocatalytic TiO2 coated paper was prepared as antibacterial paper to investigate bactericidal activity of TiO2 in the presence of UV light. When TiO2 exposed to UV light, it produced hydroxyl radicals which were strong oxidative groups and could damage the cell wall causing death of bacteria. The goal of this work was to develop a promising method for microbiological examination of antibacterial paper and to test the disinfection properties of photocatalytic TiO2 coated paper after UV illumination.</p> <p> Three different methods were modified to test antibacterial effect of TiO2 coated paper. The disk diffusion method, the washing method, and the membrane filter method. It was found that disk diffusion technique would not work because of insolubility of TiO2 in water but it could be used for any other antibacterial paper that consisted water soluble agent. The results from membrane filter method agreed with those of washing method showing the reduction of E.coli colonies for TiO2 coated paper after exposure to UV, comparing to blank paper.</p> <p> With use of washing method, it was shown that by changing some functions such as: increasing TiO2 content on the paper, increasing UV irradiation time or UV intensity, survival ratio of the bacteria decreased.</p> / Thesis / Master of Applied Science (MASc)

<p dir="ltr">Nature moves small things by chemical energy. Inspired by this, catalytic reactions driven microswimmers have been designed and believed to be promising to help transport drugs and other cargos at microscales. However, decorating the microswimmers with drugs and cargos would make them heavy and hard to move. An alternative solution to this would be designing self-pumping devices that can pump the fluid and things carried by the fluid all together without external resources. In this work, we have presented the first full numerical model of electrochemically-powered self-pumping in the Pt-Au coated polycarbonate membrane reported by Jun and Hess [1]. The simulations demonstrate that autonomous flow in self-pumping membranes is an electro-osmotic flow driven by a self-generated electric field. The injection and consumption of H⁺ on Pt and Au respectively lead to a charge asymmetry and an associated electric field that acts on the electric double layers (EDL) coating the pore walls driving fluid move, i.e. self-electro-osmosis. Key parameters controlling the performance of self-pumping are pore radius and background pH values, as they affect the EDL overlap and ionic strength. Other parameters such as porosity and pore length can both be tuned to find the local optimum for a membrane design. By tuning these parameters, the trade-off between increased ionic current and increased ionic strength could be balanced, contributing to an optimum self-pumping performance. When inclination or deformation occurs in cylindrical pores, the self-pumping flow does not significantly deviate from the trend. Membranes with complicated shape of contracting/expanding pores and cross-linked connecting pores should follow same pattern as cylindrical pores with similar pore size. In addition, if we replace the Pt/Au catalytic pairs by TiO₂/Au photocatalytic pairs, self-pumping membrane could be driven by light. The geometry of pore enhances the light absorption, enabling self-pumping membrane achieving high flow rate at large porosity with relatively large pores. At the end, we provide experimental evidence of self-pumping flow on TiO₂-Au plates as well as self-pumping membrane driven by light.</p>