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The primary goal of this research was to evaluate the effects of light on soymilk, including the oil component. Soybean oil with added chlorophyll a (0, 1, and 2μg/ml), a photosensitizer, was exposed to light (no light [control], broad-spectrum light) and narrow-band wavelengths (430nm, 450nm, and 660nm] for 4h. Chlorophyll completely degraded under broad-spectrum light and 430nm treatments; 64% degradation occurred at 660nm. Oil with chlorophyll addition resulted in significantly higher peroxide values and malondialdehyde concentrations with light exposure to broad spectrum and 430nm wavelengths. Light at 430 and 660 nm degraded chlorophyll and increased risk of oxidation in soybean oil. Soymilk contains low concentrations of chlorophyll, the photosensitizer riboflavin, as well as highly susceptible oxidizable substrates from the soy oil. Soymilk (1% fat from soybean oil) was packaged under a positive flow hood into 5 high density polyethylene (HDPE) packages and stored for 36 days at 4°C under fluorescent lighting (1122 lux ± 439 lux). Control packaging had no light protective additive (LPA; positive (foil-wrapped) and negative control) and the experimental packaging treatments had three levels of LPA (low, medium, high). Chemical and sensory analyses to measure oxidation changes were completed on the product at days, 1, 4, 8, 15, 22, 29, and 36. HDPE packages with high LPA protected the sensory quality of the product as well as the positive control (foil-wrapped) packages for a minimum of 15 days. High-LPA HDPE protected soymilk for 29 days from degradation of riboflavin and limited development of aldehyde end-products associated with photooxidation. Soymilk was treated with food grade TiO2 at levels of 0, 0.5, and 1.0% by weight. TiO2 significantly whitened the product as demonstrated by L* values. TiO2-treated soymilks resulted in significantly improved hedonic scores for appearance, smell, taste, mouthfeel, and aftertaste compared to control soymilk. However, in a second experiment, overall acceptability of TiO2-treated soymilk, at additions of 0.1%, 0.3%, and 0.5% TiO2, was not higher than control soy milk. / Ph. D.

In this thesis, we focused on understanding the synthesis of titanium dioxide (TiO2) films and nitrogen doped TiO2 films using an atmospheric pressure Dielectric Barrier Discharge (DBD). The first part of the work was dedicated to the deposition of TiO2 films by cold plasma DBD with titanium tetraisopropoxide as precursor in a single-step process at room temperature. The deposition rate was about 70 nm·min-1. The photocatalytic degradation rate for the degradation of methylene blue (MB) under ultra violet (UV) irradiation of the TiO2 film after annealing was close to a reference anatase TiO2 spin coated film. Moreover, the TiO2 films showed a good photocatalytic stability. The second part of the study focused on the optimization and the understanding of the effect of the plasma parameters (gas flow rate and power) on the morphology of the TiO2 films and on the investigation of the deposition mechanisms. The morphology of the film changed from granular to compact film by either increasing the total flow rate or decreasing the plasma power. In other words, adapting the energy density in the plasma allowed the control of the morphology of the TiO2 films. To our knowledge, it was the first time that the energy density parameters of the plasma were used to control the morphology of TiO2 films. The photocatalytic degradation rate for the degradation of MB under UV irradiation of the annealed TiO2 film turned out to be about 2 and 15 times higher than the one of the commercial TiO2 film and the as-deposited TiO2 films, respectively. In order to extend the light utilization to the visible light range, TiO2 films were doped with nitrogen using a room temperature argon/ammonia plasma discharge. XPS and SIMS results confirmed that the nitrogen has been incorporated in the TiO2 lattice mostly in Ti-N state. This was further confirmed by Raman spectroscopy and XRD. The plasma properties and the doping mechanism were studied by Optical Emission Spectroscopy. It is suggested that the NH radicals played a key role in the doping of TiO2. The concentration of nitrogen in the N-TiO2 coatings could be tuned by adapting the ratio of NH3 in the plasma or the plasma power. The band gap of our N-TiO2 coatings is lower than the one of undoped TiO2 coating. The photocatalytic degradation rate for N-TiO2 coating was more than 4 times higher than the one of the undoped TiO2 coating. / Doctorat en Sciences / info:eu-repo/semantics/nonPublished

Titanium dioxide, TiO₂, materials have received much attention in recent years due to their potential use as intercalation negative electrodes for rechargeable lithium-ion batteries. The aim of this doctoral work was to synthesise and characterise new titanium dioxide nanomaterials and to investigate their electrochemical behaviour. Three morphologies of TiO₂(B) phase: micro-sized (bulk), nanowires and nanotubes, were synthesised. All three exhibit properties which make them excellent hosts for lithium intercalation. The nanotubes show the best capability of accommodating lithium in the structure, being able to host over one molar equivalent of lithium at low current rates (5 mA g⁻¹). The lithium insertion mechanism in the TiO₂(B) was studied using powder neutron diffraction. In addition, the nature of the irreversible capacity of the nanotubes was studied and ways of reducing it proposed. Nanotubes of another titanium dioxide polymorph, anatase, were synthesised and characterised. Their electrochemical performance was compared with that of commercially available counterparts with different morphologies and particle sizes. The interrelation between particle size/morphology and electrochemical properties has been established. The insertion of lithium which leads to phase variations was studied using in situ Raman microscopy and neutron powder diffraction. It has been demonstrated that doping of the TiO₂(B) nanotubes with vanadium improves their electronic conductivity which is essential for practical applications. Remarkably good electrochemical performance is exhibited by the 6% V-doped TiO₂(B) nanotubes.

This thesis was about finding a recovery method for TiO2, using a TiO2 recovery technology, which was high enough to be economical ($10 - $15 per 1,000 gallons) to be adopted by wastewater treatment plants. When comparing recovery technologies, the top three which were investigated further through experimentation were a centrifuge, sedimentation tank, and microfilter membrane. Upon experimentation and research, the TiO2 recovery efficiencies of these technologies were 99.5%, 92.5%, and 96.3%, respectively. When doing economic analysis on these technologies comparing TiO2 efficiencies and capital and operational costs, the centrifuge was the most preferred economic option. Also, its cost did were in the economical range ($10 - $15/1,000 gallons) which makes even this technology economical. Besides that, important and valuable information about TiO2: settling behavior, particle size and zeta potential, interactions with COD, and filter operations (particle characterization) were discovered for future research and future testing on this issue. / Includes bibliography. / Thesis (M.S.)--Florida Atlantic University, 2015. / FAU Electronic Theses and Dissertations Collection

In nature, cells are not randomly clustered to form tissues. The tissue is a more complicated system with functions that go beyond what any single cell type could accomplish. While studying single-cell mechanics and dynamics is relevant from an investigative point of view, this approach loses, or fail to gather information about the tissue. The tissue investigated in this study is the neurosensory retina which seeing as extension of the brain is a very convenient model for the central nervous system due to its accessibility. The retina is constantly subjected to different mechanical stresses from development to adulthood. Although the majority of the phenomena where mechanical stresses are involved are well-studied, the mechanics behind them is not well understood. However, knowledge about the ability of the retina to adjust to mechanical stresses is essential, for example, for improving retinal surgery. Establishing a method to mechanically probe the retina is a challenge due to the extremely delicate nature of this multilayered neural tissue and to the short-time survival ex vivo. The organotypic tissue culture is a powerful tool because it allows to maintain with high accuracy the complex multicellular anatomy and the microenvironment of the original tissue. One of the limitations of the organotypic culture techniques has been until recently due to the ability to use only post-natal/juvenile tissues for long-term culture. The importance of using adult tissue is incontestable when the investigation focuses on age-related pathologies such as vitreous shrinkage or macula degeneration. In this work, TiO2 nanotube arrays are presented as the innovative substrate for long-term organotypic culture of adult neural tissue. The retinal whole-mount of adult guinea pig and the brain slices of adult mouse were cultures for 14 days without showing any sign of edema or swelling. Furthermore, in order to study the behavior of the retinal tissue under shear stress new set-ups were designed. For the first time, the behavior of the retinal layers were observed showing that the retina does not act as an homogeneous material in response to an applied stress. The methods developed here can be used for future quantitative studies, to provide an exact knowledge of retinal biomechanics which will help retinal surgeons to optimize their methods.

Novel, tailored titanium dioxide pigments with controllable nanoscale morphological features were shown to significantly enhance the optical and strength properties of paper. The opacifying power of synthesized polycrystalline TiO2 particles in a cellulose matrix was found experimentally to be superior to that of a commercial rutile pigment, depending on the crystal structure of the synthesized particles. High aspect ratio polycrystalline rutile pigments composed of a linear linkage of several individual rutile crystals gave 6% more opacity than the commercial rutile pigment. Theoretical light scattering calculations using the T-Matrix Method showed the light scattering efficiency of linearly arranged polycrystalline rutile particles to depend on number and size of crystals composing the particle and confirmed the higher efficiency of the synthesized polycrystalline rutile pigments over commercial rutile. The opacifying power of hollow polycrystalline rutile particles was found experimentally to be superior to that of a commercial rutile pigment in a highly pressed bleached fiber matrix, depending on cavity size, while the opacifying power of silica-rutile titania core-shell particles was found comparable to commercial rutile at constant titania loading. The light scattering efficiency of titania core-shell particles was shown to be dependant on the light scattering efficiency of the core material. The overall particle shape and aspect ratio of titania core-shell and hollow nanoparticles were shown to be tunable by choosing an appropriate template and coating thickness in layer-by-layer or sol-gel templating synthesis. Inorganic-cellulose core-shell and hollow cellulose nanoparticles were prepared by self-encapsulation with regenerated cellulose via precipitation of cellulose in a polyacrylic acid hydrogel layer surrounding inorganic particle templates in 4-Methylmorpholine N-oxide (NMMO) monohydrate solution. This discrete encapsulation of inorganic pigments with a thin, uniform cellulose shell was found to increase the bondability improvement between the particles and a polysaccharide substrate. The crystallinity of several carbohydrate polymers was shown to significantly affect the bondability of encapsulated core-shell particles.

Master of Science / Department of Chemical Engineering / Larry E. Erickson / The damage that can be inflicted by ultraviolet radiation has gained widespread interest. Traditionally sunscreens are made of organic and inorganic components that block two of the three types of ultraviolet radiation, UVA and UVB. This report is a literature review of several articles that have investigated the effects of inorganic UV filters; specifically titanium dioxide and cerium dioxide. There are concerns about absorption of titanium dioxide into the skin and the adverse reactions that could occur, but it was found that there is little to no absorption. Similarly the photostability of titanium dioxide is a concern; this was found to be remedied in part by a surface treatment to the titanium dioxide. The combination of titanium dioxide and carnauba wax was also studied and found to enhance the properties of both the organic and inorganic filters. Ceria was studied as a possible replacement for titanium dioxide. It was found to have similar ultraviolet shielding properties while minimizing the photocatalytic activity and photocytotoxicity seen in titanium dioxide.

This study focuses on the visible light response of hetero-structures of TiO2-graphene- MoS2 for solar energy harvestings. The commercial P25 TiO2 nano-particles, and selfprepared layered reduced graphene oxides (RG) and MoS2 were assembled for the targeted hetero-structure materials as visible-light responsible solar harvesting cocatalysts. The hydrothermal method was applied for nano-material synthesis, the reduction of graphene oxides, and bonding formation. Multiple characterization methods (SEM-TEM, XRD, XPS, UV-VIS, PL, FT-IR, TGA) have been applied to understand the electron-hole pair separation and recombination, and performance tuning in their visible-light photo-catalysis rhodamine B (Rh.B) degradations process Compared to TiO2, an obvious red shift of light absorption (from 3.1 eV to 2.6 eV) of the as-prepared RG-TiO2 was observed by UV-vis analysis, and an enhanced photocatalytic degradation of the Rhodamine B (Rh.B) using the as-prepared RG-TiO2 was also observed in a Xe lamp exposure test. The explication of these two approaches to photocatalytic improvements were concluded as the energy gap changing, the formation of Ti-O-C chemical bonds between TiO2 and RG for charge transfer and the reduction of the band gap, as well as a likelihood of up-conversion photoluminescence mechanism (UCPL). The synthesis temperature was found to be critical factor to control binding formation and agglomeration of nano-materials. The lower and higher temperatures induced ineffective formations of preferable bonding structures and the significant agglomeration. The optimal synthesis temperature was found to be within 120 ℃-150 ℃ in the TiO2-RG system. For better understanding of the Ti-O-C bonding, a heterostructure of TiO2 nanotube arrays with GO (TNA-GO) was synthesized using the Langmuir-Blodgett (LB) assembly method. The band gap of this assemble was very close to the previous TiO2-RG synthesized below 120 ℃, which is very close to that of TiO2 nano-particles. This lead to the conclusion on the significance of the Ti-O-C bonding in the visible-light-responsible photo-catalysis solar harvestings. This study revealed the fundamental mechanisms on the bonding formations and the significant visible-light-response of hetero-structcures between commercial-available, inexpensive and non-toxic TiO2 and layered materials, such as the zero-band-gap graphene and the smaller-band-gap MoS2. This mechanisms understanding will greatly sustain applications of economical-effective and environmental-safe TiO2.

Due to climate change and its effects, alternative renewable energy sources are needed in the future human society. In the work of this thesis, the Dye-sensitized Solar Cell (DSC) has been investigated and characterized. DSCs are appealing as energy conversion devices, since they have high potential to provide low cost solar light to electricity conversion. The DSC is built up by a working electrode consisting of a conductive glass substrate with a dye-sensitized mesoporous TiO2 film, a counter electrode with a catalyst and, in between, the electrolyte which performs the charge transport by means of a redox mediator. The aim of this thesis was to develop and evaluate cheap and environmentally friendly materials for the DSC. An alternative polymer-based counter electrode catalyst was fabricated and evaluated, showing that the PEDOT catalyst counter electrode outperformed the platinum catalyst counter electrode. Different organic dyes were evaluated and it was found that the dye architecture affected the performance of the assembled DSCs. A partly hydrophilic organic triphenylamine dye was developed and applied in water-based electrolyte DSCs. The partly hydrophilic dye outperformed the reference hydrophobic dye. Small changes in dye architecture were evaluated for two similar dyes, both by spectroscopic and electrochemical techniques. A change in the length of the dialkoxyphenyl units on a triphenylamine dye, affected the recombination and the regeneration electron transfer kinetics in the DSC system. Finally, three water soluble cobalt redox couples were developed and applied in water-based electrolyte DSCs. An average efficiency of 5.5% (record efficiency of 5.7%) for a 100% water-based electrolyte DSC was achieved with the polymer-based catalyst counter electrode and an organic dye with short dimethoxyphenyl units, improving the wetting and the regeneration process.