Current Search: Silica (x)
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Title
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EFFECT OF GERMANIUM DOPING ON ERBIUM SENSITIZATION IN THE ERBIUM DOPED SILICON RICH SILICA MATERIAL SYSTEM.
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Creator
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Ruhge, Forrest, Kik, Pieter, University of Central Florida
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Abstract / Description
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The continued size reduction in electronic integrated circuits has lead to a demand for on-chip high-bandwidth and low loss communication channels. Optical interconnects are considered an essential addition to the silicon electronics platform. A major challenge in the field of integrated Si photonics is the development of cost effective silicon compatible light sources. This thesis investigates the sensitization of group IV doped silica films emitting at 1.535μm for applications as...
Show moreThe continued size reduction in electronic integrated circuits has lead to a demand for on-chip high-bandwidth and low loss communication channels. Optical interconnects are considered an essential addition to the silicon electronics platform. A major challenge in the field of integrated Si photonics is the development of cost effective silicon compatible light sources. This thesis investigates the sensitization of group IV doped silica films emitting at 1.535μm for applications as silicon compatible light sources. Thin erbium-doped silica films containing excess silicon and germanium were deposited using a multi-gun sputter system. The composition of the deposited materials was verified by Rutherford Backscattering Spectrometry. Samples from each deposition were annealed in a controlled atmosphere tube furnace at temperatures between 500ºC and 1100ºC for 30 minutes. The photoluminescence spectra from the visible to the near-infrared region were acquired while pumping either near or far from the Er3+ absorption lines. Under both excitation conditions all samples annealed at temperatures below 1000ºC show clear emission at 1.535μm from Er3+ ions in the host material. In the current literature this is attributed to exciton mediated excitation of the Er3+. By contrast, in these studies indirect excitation was observed for samples annealed at temperatures well below the onset of nanocrystal nucleation and growth (between 500ºC and 1000ºC), suggesting excitation via small clusters or lattice defects. These findings could have significant implications in the further development of group IV sensitized silicon compatible gain media.
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Date Issued
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2006
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Identifier
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CFE0001439, ucf:47066
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Format
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Document (PDF)
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PURL
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http://purl.flvc.org/ucf/fd/CFE0001439
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Title
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Synthesis and Characterization of Antimicrobial Non-Color Forming Silica-Silver Nanocomposite.
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Creator
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Bazata, Joshua, Santra, Swadeshmukul, Moore, Sean, Jewett, Travis, University of Central Florida
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Abstract / Description
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Silver has been utilized for its antimicrobial properties for thousands of years in a variety of fields, extending the shelf life of food and water, rendering eating utensils sanitary, and more recently in biomedical applications such as silver based antiseptic creams. While effective as an antimicrobial agent at very low concentrations ((&)#181;g/mL), silver imparts a strong color to objects it is incorporated into, due to its high plasmonic efficiency. The goal of this study was to...
Show moreSilver has been utilized for its antimicrobial properties for thousands of years in a variety of fields, extending the shelf life of food and water, rendering eating utensils sanitary, and more recently in biomedical applications such as silver based antiseptic creams. While effective as an antimicrobial agent at very low concentrations ((&)#181;g/mL), silver imparts a strong color to objects it is incorporated into, due to its high plasmonic efficiency. The goal of this study was to determine if incorporating silver nanoparticles into a silica matrix could reduce or eliminate the plasmonic signal, while retaining the antimicrobial effects of the silver nanoparticles.Citrate capped silver nanoparticles (AgNP) were synthesized using a borohydride reduction method as outlined by Zheng et. al., and incorporated into silica nanoparticles using a method adapted from Fleger et. al. To test the antimicrobial efficacy of these synthesized silica coated silver nanoparticles (SiAgNP), minimum inhibitory concentration testing at three time points, 1, 4, and 8 hours, was carried out against E. coli and S. aureus using broth microdilution and Alamar Blue as an indicator of microbial growth. Efficacy was judged against uncoated AgNP and aqueous silver nitrate (AgNO3) solutions at equivalent Ag concentrations. Silica nanoparticles (SiNP) were utilized as a negative control. Further antimicrobial characterization using a bacterial viability assay revealed a time dependent killing trend in the SiAgNP, suggesting a controlled release of Ag+ from within the silica matrix. Efficacy of the SiAgNP was determined to fall between the most effective antimicrobial form of silver tested, AgNO3, and least effective, AgNP. However, the SiAgNP material exhibited no visible plasmon peak when UV-Visible spectrophotometric readings were taken, as well as remaining colorless when coated onto a ceramic substrate. Zeta potential revealed a high degree of colloidal stability of the SiAgNP. TEM imaging studies were carried out, verifying the presence of Ag within and on the silica nanoparticles, as well as the crystalline structure of the uncoated AgNP. It was determined that coating AgNP synthesized through borohydride reduction with silica through a St(&)#246;ber synthesis mechanism yields a material with enhanced antimicrobial effects compared to AgNP, but with no detectable plasmon signal, effectively producing a non-color forming silver based antimicrobial.
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Date Issued
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2015
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Identifier
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CFE0006208, ucf:51097
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Format
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Document (PDF)
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PURL
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http://purl.flvc.org/ucf/fd/CFE0006208
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Title
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Atomic-scale simulation of physical and chemical processes during space weathering and planet formation.
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Creator
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Quadery, Abrar, Schelling, Patrick, Britt, Daniel, Peale, Robert, Kara, Abdelkader, Sohn, Yongho, University of Central Florida
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Abstract / Description
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We investigate the mechanisms of space weathering and dust grain collisions, two topics of interests from planetary sciences, using atomic-scale simulations. Space weathering is the change in chemical and physical properties of minerals exposed to solar radiation and micrometeorite bombardment on surfaces of airless planetary bodies like the Moon and asteroids. An understanding of the connection between the surface evolution of the minerals and the underlying thermodynamic and kinetic factors...
Show moreWe investigate the mechanisms of space weathering and dust grain collisions, two topics of interests from planetary sciences, using atomic-scale simulations. Space weathering is the change in chemical and physical properties of minerals exposed to solar radiation and micrometeorite bombardment on surfaces of airless planetary bodies like the Moon and asteroids. An understanding of the connection between the surface evolution of the minerals and the underlying thermodynamic and kinetic factors is still missing. We address this issue and determine the time evolution of Frenkel defects in the silicate minerals olivine ((Mg,Fe)$_2$SiO$_4$) and orthopyroxene ((Mg,Fe)SiO$_3$) using molecular dynamics with a pair potential. Defect diffusion and clustering are observed in both the minerals. Cation diffusion occurs more readily in olivine than in orthopyroxene and leads to faster annealing in the former. In orthopyroxene, diffusion of anion defects, especially oxygen interstitials, occurs more rapidly and also exhibits anisotropy, which hinders the annealing process. This difference in defect evolution may explain the experimental observation that surface modifications due to irradiation is more pronounced in orthopyroxene than in olivine. Dust grain collision is the dominant process in the initial stage of planet formation, however, the mechanisms by which dust grains grow to larger aggregates and eventually to kilometer sized planetesimal is still not understood. We explore the role of surface chemistry in energy dissipation and grain adhesion during collision of amorphous silica (SiO$_2$) nanograins using molecular dynamics with a reactive potential, namely ReaxFF. We found nonhydroxylated amorphous silica nanoparticles stick with higher probability than their hydroxylated counterpart. This difference is attributed to the preponderance of unsatisfied dangling bonds on the dry silicate surface which facilitate bond formation during collision, and thereby provide a mechanism for energy dissipation. The speed below which sticking occurs in the dry nanograins is much higher than that found in Earth-based experiments, which suggests any experimental study of dust grain collision should take into account of the chemical environment. We probe into the nanograin collisions further and carry out atomistic simulatons of collisions of molten silica nanograins. We observed in the molten state, amorphous silica is more sticky than it is in the solid phase. This happens due to increased viscoelastic energy dissipation. The result may explain how rocky planets originated from the inner rings of the protoplanetay disks where temperatures were as high as $\sim$ 2000 K. In order to increase the range of materials that could be simulated with ReaxFF potential, and also to examine the different oxidation states of iron associated with nanophase iron formation during space weathering, we made attempt to develop ReaxFF potential for fayalite (Fe$_2$SiO$_4$). We found out fundamental limitations of ReaxFF model to describe three-component minerals. However, during the fitting process we developed a model for iron silicide (FeSi), and made attempt to improve the silica model to obtain better elastic properties. We report here the fitting processes and the observed limitations of ReaxFF model.
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Date Issued
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2017
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Identifier
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CFE0006907, ucf:51691
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Format
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Document (PDF)
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PURL
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http://purl.flvc.org/ucf/fd/CFE0006907
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Title
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Mixed Valence Copper(Cu)/Silica Nanocomposite: Synthesis, Characterization and Systematic Antimicrobial Studies.
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Creator
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Young, Mikaeel, Santra, Swadeshmukul, Self, William, Moore, Sean, University of Central Florida
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Abstract / Description
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Copper (Cu) compounds are widely used as effective agricultural bactericides. Continuous use of these materials has led to Cu accumulation in soil over time. The United States Environmental Protection Agency (US EPA) is concerned about potential Cu contamination in the environment. Improving biocidal efficacy of Cu is an attractive alternative, allowing reduction of Cu amount per application. In this research, we focused on making water-soluble mixed-valence Copper/Silica composite nanogel ...
Show moreCopper (Cu) compounds are widely used as effective agricultural bactericides. Continuous use of these materials has led to Cu accumulation in soil over time. The United States Environmental Protection Agency (US EPA) is concerned about potential Cu contamination in the environment. Improving biocidal efficacy of Cu is an attractive alternative, allowing reduction of Cu amount per application. In this research, we focused on making water-soluble mixed-valence Copper/Silica composite nanogel (CuSiNG) material. The objective is to improve the efficacy of Cu by manipulating Cu valence states. It has been shown in the literature that Cu (0) and Cu (I) states are more potent that Cu (II) states in terms of their antimicrobial efficacy. It is hypothesized that mixed valence Cu will exhibit improved efficacy over Cu (II). A water-soluble mixed valence Cu/silica nanogel (MV-CuSiNG) composite has been synthesized and characterized. Structure, morphology, crystallinity and composition of the MV-CuSiNG material was characterized using High-Resolution Transmission Electron Microscopy (HRTEM), HRTEM Selected Area Electron Diffraction (SAED) and X-ray Photoelectron Spectroscopy (XPS). Amount of Cu loading in MV-CuSiNG composite material was estimated by Atomic Absorption Spectroscopy (AAS). To confirm presence of Cu (I) in the MV-CuSiNG material, Neocuproine (Nc, a Cu (I) specific chelator) assay was used. Antimicrobial efficacy of MV-CuSiNG and CuSiNG was evaluated against X.alfalfae, B.subtilis and E.coli using Kocide(&)#174; 3000 ((")Insoluble Cu (II)(") compound), Copper sulfate ((")Soluble Cu (II)(") compound) and Cuprous chloride (Copper (I) compound) as positive controls and silica (")seed(") particles (without Cu loading) as negative control. Antimicrobial studies included observing bacterial growth inhibition and determining the Minimum Inhibitory Concentration (MIC). Improved antimicrobial efficacy was observed in MV-CuSiNG when compared to CuSiNG and other controls. For the assessment of plant safety of MV-CuSiNG and CuSiNG materials, phytotoxicity studies were conducted using Vinca sp and Hamlin orange under environmental conditions. It was observed that MV-CuSiNG material was safe to plants at commercially used (standard) spray application rate.
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Date Issued
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2013
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Identifier
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CFE0005282, ucf:50550
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Format
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Document (PDF)
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PURL
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http://purl.flvc.org/ucf/fd/CFE0005282
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Title
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EFFECTS OF SOURCE WATER BLENDING FOLLOWING TREATMENT WITH SODIUM SILICATE AS A CORROSION INHIBITOR ON METAL RELEASE WITHIN A WATER DISTRIBUTION SYSTEM.
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Creator
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Lintereur, Phillip, Duranceau, Steven, University of Central Florida
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Abstract / Description
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A study was conducted to investigate and quantify the effects of corrosion inhibitors on metal release within a pilot distribution system while varying the source water. The pilot distribution system consisted of pre-existing facilities from Taylor et al (2005). Iron, copper, and lead release data were collected during four separate phases of operation. Each phase was characterized by the particular blend ratios used during the study. A blended source water represented a water that had been...
Show moreA study was conducted to investigate and quantify the effects of corrosion inhibitors on metal release within a pilot distribution system while varying the source water. The pilot distribution system consisted of pre-existing facilities from Taylor et al (2005). Iron, copper, and lead release data were collected during four separate phases of operation. Each phase was characterized by the particular blend ratios used during the study. A blended source water represented a water that had been derived from a consistent proportion of three different source waters. These source waters included (1) surface water treated through enhanced coagulation/sedimentation/filtration, (2) conventionally treated groundwater, and (3) finished surface water treated using reverse osmosis membranes. The corrosion inhibitors used during the study were blended orthophosphate (BOP), orthophosphate (OP), zinc orthophosphate (ZOP), and sodium silicate (Si). This document was intended to cite the findings from the study associated with corrosion treatment using various doses of sodium silicate. The doses were maintained to 3, 6, and 12 mg/L as SiO2 above the blend-dependent background silica concentration. Sources of iron release within the pilot distribution system consisted of, in the following order of entry, (1) lined cast iron, (2) un-lined cast iron, and (3) galvanized steel. Iron release data from these materials was not collected for each individual iron source. Instead, iron release data represented the measurement of iron upon exposure to the pilot distribution system in general. There was little evidence to suggest that iron release was affected by sodium silicate. Statistical modeling of iron release suggested that iron release could be described by the water quality parameters of alkalinity, chlorides, and pH. The R2 statistic implied that the model could account for only 36% of the total variation within the iron release data set (i.e. R2 = 0.36). The model implies that increases in alkalinity and pH would be expected to decrease iron release on average, while an increase in chlorides would increase iron release. The surface composition of cast iron and galvanized steel coupons were analyzed using X-ray photoelectron spectroscopy (XPS). The surface analysis located binding energies consistent with Fe2O3, Fe3O4, and FeOOH for both cast iron and galvanized steel. Elemental scans detected the presence of silicon as amorphous silica; however, there was no significant difference between scans of coupons treated with sodium silicate and coupons simply exposed to the blended source water. The predominant form of zinc found on the galvanized steel coupons was ZnO. Thermodynamic modeling of the galvanized steel system suggested that zinc release was more appropriately described by Zn5(CO3)2(OH)6. The analysis of the copper release data set suggested that treatment with sodium silicate decreased copper release during the study. On average the low, medium, and high doses decreased copper release, when compared to the original blend source water prior to sodium silicate addition, by approximately 20%, 30%, and 50%, respectively. Statistical modeling found that alkalinity, chlorides, pH, and sodium silicate dose were significant variables (R2 = 0.68). The coefficients of the model implied that increases in pH and sodium silicate dose decreased copper release, while increases in alkalinity and chlorides increased copper release. XPS for copper coupons suggested that the scale composition consisted of Cu2O, CuO, and Cu(OH)2 for both the coupons treated with sodium silicate and those exposed to the blended source water. Analysis of the silicon elemental scan detected amorphous silica on 3/5 copper coupons exposed to sodium silicate. Silicon was not detected on any of the 8 control coupons. This suggested that sodium silicate inhibitor varied the surface composition of the copper scale. The XPS results seemed to be validated by the visual differences of the copper coupons exposed to sodium silicate. Copper coupons treated with sodium silicate developed a blue-green scale, while control coupons were reddish-brown. Thermodynamic modeling was unsuccessful in identifying a controlling solid that consisted of a silicate-based cupric solid. Lead release was generally decreased when treated with sodium silicate. Many of the observations were recorded below the detection limit (1 ppb as Pb) of the instrument used to measure the lead concentration of the samples during the study. The frequency of observations below the detection limit tended to increase as the dose of sodium silicate increased. An accurate quantification of the effect of sodium silicate was complicated by the observations recorded below detection limit. If the lead concentration of a sample was below detection limit, then the observation was recorded as 1 ppb. Statistical modeling suggested that temperature, alkalinity, chlorides, pH, and sodium silicate dose were important variables associated with lead release (R2 = 0.60). The exponents of the non-linear model implied that an increase in temperature, alkalinity, and chlorides increased lead release, while an increase in pH and sodium silicate dose were associated with a decrease in lead release. XPS surface characterization of lead coupons indicated the presence of PbO, PbO2, PbCO3, and Pb3(OH)2(CO3)2. XPS also found evidence of silicate scale formation. Thermodynamic modeling did not support the possibility of a silicate-based lead controlling solid. A solubility model assuming Pb3(OH)2(CO3)2 as the controlling solid was used to evaluate lead release data from samples in which lead coupons were incubated for long stagnation times. This thermodynamic model seemed to similarly describe the lead release of samples treated with sodium silicate and samples exposed to the blended source water. The pH of each sample was similar, thus sodium silicate, rather than the corresponding increase in pH, would appear to be responsible if a difference had been observed. During the overall study, the effects of BOP, OP, ZOP, and Si corrosion inhibitors were described by empirical models. Statistically, the model represented the expected value, or mean average, function. If these models are to be used to predict a dose for copper release, then the relationship between the expected value function and the 90th percentile must be approximated. The USEPA Lead and Copper Rule (LCR) regulates total copper release at an action level of 1.3 mg/L. This action level represents a 90th percentile rather than a mean average. Evaluation of the complete copper release data set suggested that the standard deviation was proportional to the mean average of a particular treatment. This relationship was estimated using a linear model. It was found that most of the copper data sub-sets (represented by a given phase, inhibitor, and dose) could be described by a normal distribution. The information obtained from the standard deviation analysis and the normality assumption validated the use of a z-score to relate the empirical models to the estimated 90th percentile observations. Since an analysis of the normality and variance (essentially contains the same information as the standard deviation) are required to assess the assumptions associated with an ANOVA, an ANOVA was performed to directly compare the effects of the inhibitors and corresponding doses. The findings suggested that phosphate-based inhibitors were consistently more effective than sodium silicate when comparing the same treatment levels (i.e. doses). Among the phosphate-based inhibitors, the effectiveness of each respective treatment level was inconsistent (i.e. there was no clear indication that any one phosphate-based inhibitor was more effective than the other). As the doses increased for each inhibitor, the results generally suggested that there was a corresponding tendency for copper release to decrease.
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Date Issued
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2008
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Identifier
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CFE0002383, ucf:47737
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Format
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Document (PDF)
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PURL
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http://purl.flvc.org/ucf/fd/CFE0002383
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Title
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Experimental and numerical investigation of a novel adsorption bed design for cooling applications.
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Creator
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Abdelhady, Ramy, Chow, Louis, Mansy, Hansen, Das, Tuhin, Duranceau, Steven, University of Central Florida
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Abstract / Description
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A global challenge is to develop environmentally friendly, affordable, compact and sustainable technologies to provide heating and cooling power. Adsorption cooling (AC) technology is one of the most promising ways to solve the environmental issues and cut down the energy consumption related to the traditional air conditioning and refrigeration systems. However, AC systems still suffer from poor heat and mass transfer inside the adsorption bed, which is the main obstacle to commercialization...
Show moreA global challenge is to develop environmentally friendly, affordable, compact and sustainable technologies to provide heating and cooling power. Adsorption cooling (AC) technology is one of the most promising ways to solve the environmental issues and cut down the energy consumption related to the traditional air conditioning and refrigeration systems. However, AC systems still suffer from poor heat and mass transfer inside the adsorption bed, which is the main obstacle to commercialization of adsorption cooling units. The main goal of this study is designing an efficient adsorption cooling cycle. In this research work, an in-depth scaling analysis of heat and mass transfer in an adsorption packed bed has been performed to identify and quantify how the effective thermal diffusivity of an adsorption bed and the surface diffusion rate of an adsorbate in a nanoporous adsorbent affect the specific cooling power of an adsorption cooling system. The main goal of this study is to derive new scaling parameters that can be used to specify the optimal bed dimensions and select the appropriate adsorbate/adsorbent pair to achieve the maximum cooling power. As the choice of a suitable working pair is critical for an adsorption cooling cycle, an experimental setup is designed and built to measure the adsorption kinetics and isotherms of any working pair accurately. This setup is also able to measure the dynamic performance of an adsorption bed. The equilibrium uptakes of Fuji silica-gels Type-RD and RD-2060 (manufactured by Fuji Silysia, Japan), which are commonly used in adsorption cooling systems, are measured experimentally. Based on the adsorption rate and the adsorbent temperature measured simultaneously, a new approach is proposed to measure the surface diffusivity in the temperature and pressure ranges typical of those during the operating conditions of adsorption cooling systems. In addition, the experimental measurements from the lab-scale adsorption bed are used to validate the numerical models that are commonly used for estimating the SCP of AC cycle. By using the scaling parameters driven from the scaling analysis, a newly designed packed bed for use in AC systems is proposed and evaluated in this research. The proposed design consists of repeated packed bed cells (modules). Each module is an open-cell aluminum foam packed with silica gel to enhance the overall thermal conductivity of the bed from 0.198 to 5.8 W/m.K. the experimental test rig is used to evaluate the performance on the new adsorption bed. The effect of pores per inch (PPI) of the foam, silica-gel particle size, bed height and adsorption isotherm of different types of silica gel on the bed performance are investigated.
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Date Issued
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2019
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Identifier
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CFE0007422, ucf:52702
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Format
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Document (PDF)
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PURL
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http://purl.flvc.org/ucf/fd/CFE0007422
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Title
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Novel copper loaded core-shell silica nanoparticles with improved copper bio-availability : Synthesis, characterization and study of antibacterial properties.
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Creator
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Maniprasad, Pavithra, Santra, Swadeshmukul, Self, William, Naser, Saleh, University of Central Florida
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Abstract / Description
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A novel core-shell silica based antimicrobial nanoparticle was synthesized. The St(&)#246;ber silica shell has been engineered to accommodate copper. Synthesis of the core-shell Cu-silica nanoparticle (C-S CuSiNP) involves preparation of base-hydrolyzed St(&)#246;ber silica (")seed(") particles first, followed by the acid-catalyzed seeded growth of the Cu-silica shell layer around the core. Scanning electron microscopy and transmission electron microscopy showed monodispersed, spherical...
Show moreA novel core-shell silica based antimicrobial nanoparticle was synthesized. The St(&)#246;ber silica shell has been engineered to accommodate copper. Synthesis of the core-shell Cu-silica nanoparticle (C-S CuSiNP) involves preparation of base-hydrolyzed St(&)#246;ber silica (")seed(") particles first, followed by the acid-catalyzed seeded growth of the Cu-silica shell layer around the core. Scanning electron microscopy and transmission electron microscopy showed monodispersed, spherical shaped nanoparticles with smooth surface morphology. Characterization of particle size distribution in solution by the Dynamic Light Scattering (DLS) technique was fairly consistent with the electron microscopy results. Loading of Cu to nanoparticles was confirmed by the SEM-Energy Dispersive X-Ray Spectroscopy (EDS) and Atomic Absorption Spectroscopy (AAS). Antibacterial efficacy of C-S CuSiNP was evaluated against E.coli and B.subtilis using Cu hydroxide ((")Insoluble(") Cu compound) and copper sulfate as positive control and silica (")seed(") particles (without Cu loading) as negative control. Minimum Inhibitory Concentration (MIC) of C-S CuSiNP was evaluated by measuring the fluorescent intensity of resorufin to determine the decrease in viable cells with increase in copper concentration in C-S CuSiNP. The MIC value of C-S CuSiNP against both E.coli and B.subtilis was estimated to be 4.9 ppm. Bac-light fluorescence microscopy based assay was used to count relative population of the live and dead bacteria cells. Antibacterial study clearly shows that C-S CuSiNP is more effective than insoluble Cu hydroxide particles and copper sulfate at equivalent metallic Cu concentration, suggesting more soluble Cu in C-S CuSiNP material due to its core-shell design.
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Date Issued
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2011
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Identifier
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CFE0004479, ucf:49300
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Format
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Document (PDF)
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PURL
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http://purl.flvc.org/ucf/fd/CFE0004479
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Title
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Trace Contaminant Control: An In-Depth Study of a Silica-Titania Composite for Photocatalytic Remediation of Closed-Environment Habitat Air.
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Creator
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Coutts, Janelle, Yestrebsky, Cherie, Clausen, Christian, Sigman, Michael, Elsheimer, Seth, Wheeler, Raymond, University of Central Florida
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Abstract / Description
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This collection of studies focuses on a photocatalytic oxidation (PCO) system for the oxidation of a model compound, ethanol (EtOH), using an adsorption-enhanced silica-titania 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 in closed-environment habitats.The first goal was to distinguish the...
Show moreThis collection of studies focuses on a photocatalytic oxidation (PCO) system for the oxidation of a model compound, ethanol (EtOH), using an adsorption-enhanced silica-titania 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 in closed-environment habitats.The first goal was to distinguish the effect of photon flux (i.e., photons per unit time reaching a surface) from that of photon 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 (?peak = 365 nm) at its maximum light intensity or a UV-C germicidal lamp (?peak = 254 nm) at three levels of light intensity. The STC-catalyzed oxidation of ethanol was found to follow zero-order kinetics with respect to CO2 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 photonic efficiency (63.3 vs. 50.1 nmol CO2 (&)#181;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 temperature from 25(&)deg;C to 65(&)deg;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 photonic efficiency (42.7 vs. 82.5 nmol CO2 (&)#181;mol photons-1); as well as a decrease in intermediate acetaldehyde (ACD) evolution in the effluent. By elevating the reactor temperature to 45(&)deg;C, an ~32% increase in photonic efficiency was obtained over the use of UV-C irradiation at room temperature. Increasing the reactor temperature 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 STC-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 photonic 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 show great promise for this technology as part of a trace contaminant control system for niche applications such as air processing onboard the ISS or other new spacecrafts.
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Date Issued
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2013
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Identifier
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CFE0005092, ucf:50741
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Format
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Document (PDF)
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PURL
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http://purl.flvc.org/ucf/fd/CFE0005092
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Title
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Agglomeration, Evaporation and Morphological Changes in Droplets with Nanosilica and Nanoalumina Suspensions in an Acoustic Field.
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Creator
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Tijerino Campollo, Erick, Kumar, Ranganathan, Deng, Weiwei, Chow, Louis, Basu, Saptarshi, University of Central Florida
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Abstract / Description
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Acoustic levitation permits the study of droplet dynamics without the effects of surface interactions present in other techniques such as pendant droplet methods. Despite the complexities of the interactions of the acoustic field with the suspended droplet, acoustic levitation provides distinct advantages of controlling morphology of droplets with nanosuspensions post precipitation. Droplet morphology is controlled by vaporization, deformation and agglomeration of nanoparticles, and therefore...
Show moreAcoustic levitation permits the study of droplet dynamics without the effects of surface interactions present in other techniques such as pendant droplet methods. Despite the complexities of the interactions of the acoustic field with the suspended droplet, acoustic levitation provides distinct advantages of controlling morphology of droplets with nanosuspensions post precipitation. Droplet morphology is controlled by vaporization, deformation and agglomeration of nanoparticles, and therefore their respective timescales are important to control the final shape. The balance of forces acting on the droplet, such as the acoustic pressure and surface tension, determine the geometry of the levitated droplet. Thus, the morphology of the resultant structure can be controlled by manipulating the amplitude of the levitator and the fluid properties of the precursor nanosuspensions. The interface area in colloidal nanosuspensions is very large even at low particle concentrations. The effects of the presence of this interface have large influence in the properties of the solution even at low concentrations.This thesis focuses on the dynamics of particle agglomeration in acoustically levitated evaporating nanofluid droplets leading to shell structure formation. These experiments were performed by suspending 500(&)#181;m droplets in a pressure node of a standing acoustic wave in a levitator and heating them using a carbon dioxide laser. These radiatively heated functional droplets exhibit three distinct stages, namely, pure evaporation, agglomeration and structure formation. The temporal history of the droplet surface temperature shows two inflection points. Morphology and final precipitation structures of levitated droplets are due to competing mechanisms of particle agglomeration, evaporation and shape deformation. This thesis provides a detailed analysis for each process and proposes two important timescales for evaporation and agglomeration that determine the final diameter of the structure formed. It is seen that both agglomeration and evaporation timescales are similar functions of acoustic amplitude (sound pressure level), droplet size, viscosity and density. However it is shown that while the agglomeration timescale decreases with initial particle concentration, the evaporation timescale shows the opposite trend. The final normalized diameter hence can be shown to be dependent solely on the ratio of agglomeration to evaporation timescales for all concentrations and acoustic amplitudes. The experiments were conducted with 10nm silica, 20nm silica, 20nm alumina and 50nm alumina solutions. The structures exhibit various aspect ratios (bowls, rings, spheroids) which depend on the ratio of the deformation timescale (tdef) and the agglomeration timescale (tg).
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Date Issued
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2012
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Identifier
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CFE0004610, ucf:49914
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Format
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Document (PDF)
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PURL
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http://purl.flvc.org/ucf/fd/CFE0004610
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Title
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TOWARDS DIRECT WRITING OF 3-D PHOTONIC CIRCUITS USING ULTRAFAST LASERS.
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Creator
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Zoubir, Arnaud, Richardson, Martin, University of Central Florida
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Abstract / Description
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The advent of ultrafast lasers has enabled micromachining schemes that cannot be achieved by other current techniques. Laser direct writing has emerged as one of the possible routes for fabrication of optical waveguides in transparent materials. In this thesis, the advantages and limitations of this technique are explored. Two extended-cavity ultrafast lasers were built and characterized as the laser sources for this study, with improved performance over existing systems. Waveguides are...
Show moreThe advent of ultrafast lasers has enabled micromachining schemes that cannot be achieved by other current techniques. Laser direct writing has emerged as one of the possible routes for fabrication of optical waveguides in transparent materials. In this thesis, the advantages and limitations of this technique are explored. Two extended-cavity ultrafast lasers were built and characterized as the laser sources for this study, with improved performance over existing systems. Waveguides are fabricated in oxide glass, chalcogenide glass, and polymers, these being the three major classes of materials for the telecommunication industry. Standard waveguide metrology is performed on the fabricated waveguides, including refractive index profiling and mode analysis. Furthermore, a finite-difference beam propagation method for wave propagation in 3D-waveguides is proposed. The photo-structural modifications underlying the changes in the material optical properties after exposure are investigated. The highly nonlinear processes of the light/matter interaction during the writing process are described using a free electron model. UV/visible absorption spectroscopy, photoluminescence spectroscopy and Raman spectroscopy are used to assess the changes occurring at the atomic level. Finally, the impact of laser direct writing on nonlinear waveguide applications is discussed.
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Date Issued
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2004
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Identifier
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CFE0000236, ucf:46252
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Format
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Document (PDF)
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PURL
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http://purl.flvc.org/ucf/fd/CFE0000236
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Title
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ADDITIVE LITHOGRAPHY FABRICATION AND INTEGRATION OF MICRO OPTICS.
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Creator
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Pitchumani, Mahesh, Johnson, Eric, University of Central Florida
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Abstract / Description
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Optical elements are the fundamental components in photonic systems and are used to transform an input optical beam into a desired beam profile or to couple the input beam into waveguides, fibers, or other optical systems or devices. Macroscopic optical elements are easily fabricated using grinding and polishing techniques, but few methods exist for inexpensive fabrication of micro optical elements. In this work we present an innovative technique termed Additive Lithography that makes use of...
Show moreOptical elements are the fundamental components in photonic systems and are used to transform an input optical beam into a desired beam profile or to couple the input beam into waveguides, fibers, or other optical systems or devices. Macroscopic optical elements are easily fabricated using grinding and polishing techniques, but few methods exist for inexpensive fabrication of micro optical elements. In this work we present an innovative technique termed Additive Lithography that makes use of binary masks and controlled partial exposures to sculpt photoresist into the desired optical surface relief profile. We explore various masking schemes for fabricating a variety of optical elements with unprecedented flexibility and precision. These masking schemes used in conjunction with the additive lithographic method allows us to carefully control the photoresist exposure and reflow processes for fabricating complex aspheric lens elements, including aspheric elements whose fabrication often proves highly problematic. It will be demonstrated that employing additive lithography for volume sculpting followed by controlled reflow can also allow us to fabricate refractive beam shaping elements. Finally we will discuss the dry etching techniques used to transfer these optical elements into the glass substrate. Thus the additive lithography technique will be demonstrated as an inexpensive, high throughput and efficient process in the fabrication of micro optical elements.
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Date Issued
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2006
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Identifier
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CFE0000914, ucf:46761
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Format
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Document (PDF)
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PURL
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http://purl.flvc.org/ucf/fd/CFE0000914
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Title
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THE EFFECT OF COLLOIDAL STABILITY ON THE HEAT TRANSFER CHARACTERISTICS OF NANOSILICA DISPERSED FLUIDS.
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Creator
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Venkataraman, Manoj, Kumar, Ranganathan, University of Central Florida
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Abstract / Description
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Addition of nano particles to cooling fluids has shown marked improvement in the heat transfer capabilities. Nanofluids, liquids that contain dispersed nanoparticles, are an emerging class of fluids that have great potential in many applications. There is a need to understand the fundamental behavior of nano dispersed particles with respect to their agglomeration characteristics and how it relates to the heat transfer capability. Such an understanding is important for the development and...
Show moreAddition of nano particles to cooling fluids has shown marked improvement in the heat transfer capabilities. Nanofluids, liquids that contain dispersed nanoparticles, are an emerging class of fluids that have great potential in many applications. There is a need to understand the fundamental behavior of nano dispersed particles with respect to their agglomeration characteristics and how it relates to the heat transfer capability. Such an understanding is important for the development and commercialization of nanofluids. In this work, the stability of nano particles was studied by measuring the zeta potential of colloidal particles, particle concentration and size. Two different sizes of silica nano particles, 10 nm and 20 nm are used in this investigation at 0.2 vol. % and 0.5 vol. % concentrations. The measurements were made in deionized (DI) water, buffer solutions at various pH, DI water plus HCl acid solution (acidic pH) and DI water plus NaOH solution (basic pH). The stability or instability of silica dispersions in these solutions was related to the zeta potential of colloidal particles and confirmed by particle sizing measurements and independently by TEM observations. Low zeta potentials resulted in agglomeration as expected and the measured particle size was greater. The heat transfer characteristics of stable or unstable silica dispersions using the above solutions were experimentally determined by measuring heat flux as a function of temperature differential between a nichrome wire and the surrounding fluid. These experiments allowed the determination of the critical heat flux (CHF), which was then related to the dispersion characteristics of the nanosilica in various fluids described above. The thickness of the diffuse layer on nano particles was computed and experimentally confirmed in selected conditions for which there was no agglomeration. As the thickness of the diffuse layer decreased due to the increase in salt content or the ionic content, the electrostatic force of repulsion cease to exist and Van der Waal's force of agglomeration prevailed causing the particles to agglomerate affecting the CHF. The 10nm size silica particle dispersions showed better heat transfer characteristics compared to 20nm dispersion. It was also observed that at low zeta potential values, where agglomeration prevailed in the dispersion, the silica nano particles had a tendency to deposit on the nickel chromium wire used in CHF experiments. The thickness of the deposition was measured and the results show that with a very high deposition, CHF is enhanced due to the porosity on the wire. The 10nm size silica particles show higher CHF compared to 20nm silica particles. In addition, for both 10nm and 20nm silica particles, 0.5 vol. % concentration yielded higher heat transfer compared to 0.2 vol. % concentration. It is believed that although CHF is significantly increased with nano silica containing fluids compared to pure fluids, formation of particle clusters in unstable slurries will lead to detrimental long time performance, compared to that with stable silica dispersions.
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Date Issued
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2005
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Identifier
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CFE0000837, ucf:46676
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Format
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Document (PDF)
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PURL
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http://purl.flvc.org/ucf/fd/CFE0000837
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Title
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Harmful Algal Bloom Mitigation using Recycle Concrete Aggregate coated with Fixed-Quat.
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Creator
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Ezeodurukwe, Ikenna, Lee, Woo Hyoung, Randall, Andrew, Sadmani, A H M Anwar, University of Central Florida
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Abstract / Description
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Human activities generate surplus nutrients which may lead to algal bloom events in water resources along with serious ecological problems and thus substantial economic losses. Particularly, harmful algal blooms (HABs) represent toxic cyanobacterial blooms which produce cyanotoxins. The primary concerns of HABs are the exposures to a wide variety of cyanotoxins via ingestion of contaminated drinking water, inhalation during recreational activities, and consumption of contaminated fish and...
Show moreHuman activities generate surplus nutrients which may lead to algal bloom events in water resources along with serious ecological problems and thus substantial economic losses. Particularly, harmful algal blooms (HABs) represent toxic cyanobacterial blooms which produce cyanotoxins. The primary concerns of HABs are the exposures to a wide variety of cyanotoxins via ingestion of contaminated drinking water, inhalation during recreational activities, and consumption of contaminated fish and shellfish. However, conventional physical and chemical methods are not always possible to efficiently handle these HABs events. It is urgent to develop viable and rapid solutions to control HABs in field and mitigate the effects of HABs in fresh water, particularly in those that serve as sources of drinking water supply.(&)nbsp;Quaternary ammonium compounds (Quats) represent a wide range of cationic compounds with different formulation that constitutes products for agriculture, domestic and medical and industry. As organic antimicrobial compounds, Quats can be used as alternatives to existing chemical-based technique for HABs control due to its less toxicity and its affinity to variety of surface. In this study, recycled concrete aggregate (RCA) from a regional construction and demolition (C(&)D) waste recycling facility was used as a sustainable and environmentally friendly substrate and coated with a composite of silica-quaternary ammonium compounds (Fixed-Quat).(&)nbsp;Then, the algistatic capabilities of imparting antimicrobial properties of Quats to the RCA surface, which involve the covalent attachment of the biocides to the surfaces (sol-gel technique), were evaluated with HABs-causing algal species, Microcystis aeruginosa. Chlorophyll-a was measured to determine the efficiency of HABs mitigation using Fixed-Quat coated RCA in terms of photosynthetic inactivation of the selected algae. OD660 and pH were measured as key parameters to monitor algal cell growth and cement hydration. Notably, a 61% reduction of chlorophyll-a within 6 hours and complete removal of chlorophyll-a within 8 hours were achieved, indicating that Fixed-Quat coated RCA would be efficient in growth inhibition of Microcystis aeruginosa. Overall, with an appropriate design for field application and further evaluations like lifetime of Quat coating and potential recovery of treated algae, the Fixed-Quat antimicrobial coated RCA would be a promising and sustainable(&)nbsp;alternative to conventional HABs mitigation methods in various aquatic systems.
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Date Issued
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2018
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Identifier
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CFE0007400, ucf:52066
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Format
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Document (PDF)
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PURL
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http://purl.flvc.org/ucf/fd/CFE0007400
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Title
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THE APPLICATION OF TWO-PHOTON ABSORBING PROBES IN LYSOSOMAL, ZINC ION SENSING AND FOLATE RECEPTOR-TARGETED BIOIMAGING.
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Creator
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WANG, XUHUA, Belfield, Kevin D., University of Central Florida
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Abstract / Description
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Two-photon fluorescence microscopy (2PFM) has become a powerful technique for bioimaging in non-invasive cancer diagnosis and also investigating the mechanization and original of a variety of diseases by tracking various biological processes. Because the fluorescence emission by two photon absorbing (2PA) is directly proportional to the square of the intensity of excitation light, this intrinsic property of 2PA provides 2PFM great advantages over traditional one-photon fluorescence microscopy...
Show moreTwo-photon fluorescence microscopy (2PFM) has become a powerful technique for bioimaging in non-invasive cancer diagnosis and also investigating the mechanization and original of a variety of diseases by tracking various biological processes. Because the fluorescence emission by two photon absorbing (2PA) is directly proportional to the square of the intensity of excitation light, this intrinsic property of 2PA provides 2PFM great advantages over traditional one-photon fluorescence microscopy (1PFM), including high 3D spatial localization, less photodamage and interference from biological tissue because of using longer wavelength excitation (700-1300 nm). However, most 2PA probes are hydrophobic and their photostabilities are questionable, severely limiting their biological and medical applications. In addition, probes with significant specificity for certain organelles for tracking cellular processes or metal ions for monitoring neural transmission are somewhat rare. Moreover, it is also very significant to deliver the probes to specific disease sites for early cancer diagnosis. In order to increase the water solubility of probes, polyethylene glycol (PEG) was introduced to a fluorene-based 2PA probe LT1 for lysosomal 2PFM cell imaging. The 2PFM bioimaging application of the novel two-photon absorbing fluorene derivative LT1, selective for the lysosomes of HCT 116 cancer cells is described in Chapter II. Linear and nonlinear photophysical and photochemical properties of the probe were investigated to evaluate the potential of the probe for 2PFM lysosomal imaging. After the investigation of the cytotoxicity of this new probe, colocalization studies of the probe with commercial lysosomal probe Lysotracker Red in HCT 116 cells were conducted. A high colocalization coefficient (0.96) was achieved and demonstrated the specific localization of the probe in lysosomes. A figure of merit, FM, was introduced by which all fluorescent probes for 2PFM can be compared. LT1 was demonstrated to have a number of properties that far exceed those of commercial lysotracker probes, including much higher 2PA cross sections, good fluorescence quantum yield, and, importantly, high photostability, all resulting in a superior figure of merit. Consequently, 2PFM was used to demonstrate lysosomal tracking with LT1. In addition to lysosomes, it is also very significant to investigate the physiological roles of free metal ions in biological processes, especially Zn2+, because Zn2+ normally serves either as the catalytic elements in enzymatic activity centers or as structural elements in enzymes and transcription factors. However, biocompatible and effective Zn2+ probes for 2PFM bioimaging are infrequent. In Chapter III, 2PFM bioimaging with a hydrophilic 2PA Zn2+ sensing fluorescent probe, bis(1,2,3-triazolyl)fluorene derivative, is described. 2PFM bioimaging of the probe in living HeLa cancer cells was demonstrated. The results revealed a significant fluorescence increase upon introduction of Zn2+ into the cancer cells, and a reversible Zn2+ binding to the probe was also demonstrated, providing a robust probe for two-photon fluorescence zinc ion sensing. Early cancer diagnosis is another critical application for 2PFM, but there are still huge challenges for this new technique in clinical areas. Most 2PA probes with large two-photon absorbing cross sections and fluorescence quantum efficiency are synthetically more accessible in hydrophobic forms. In order to increase the efficiency of the probes and minimize the effect of the probe on the human body, delivery of the probe specifically to cancer sites is desired. The synthesis and characterization of narrow dispersity organically modified silica nanoparticles (SiNPs), diameter ~30 nm, entrapping a hydrophobic two-photon absorbing fluorenyl dye, are reported in Chapter IV. The surface of the SiNPs was functionalized with folic acid to specifically deliver the probe to folate receptor (FR) over-expressing HeLa cells, making these folate 2PA dye-doped SiNPs potential candidates as probes for two-photon fluorescence microscopy (2PFM) bioimaging. In vitro studies using FR over-expressing HeLa cells demonstrated specific cellular uptake of the functionalized nanoparticles. However, when the concentration of the dye in SiNPs increased for higher signal output, the fluorescence quantum efficiency of a probe normally decreases because of self-quenching. In Chapter V, a near-infrared (NIR) emitting probe is reported to overcome this limitation through both aggregate-enhanced fluorescence emission and aggregate enhanced two-photon absorption. The dye was encapsulated in SiNPs and the surface of the nanoparticles was functionalized with PEG followed by a folic acid derivative to specifically target folate receptors. NIR emission is important for deep tissue imaging. In vitro studies using HeLa cells that upregulate folate receptors indicated specific cellular uptake of the folic acid functionalized SiNP nanoprobe. Meanwhile, the probe was also investigated for live animal imaging by employing mice bearing HeLa tumors for in vivo studies. Ex vivo 2PFM tumor imaging was then conducted to achieve high quality 3D thick tissue tumor images.
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Date Issued
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2011
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Identifier
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CFE0003640, ucf:48891
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Format
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Document (PDF)
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PURL
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http://purl.flvc.org/ucf/fd/CFE0003640