This work explores the hydraulic performance of a wastewater lagoon system located in San Antonio, Bolivia. The system consists of one facultative pond and two maturation ponds in series and is managed through a locally elected water committee. A tracer study was performed on the primary facultative pond and an analysis of the solids accumulation on the bottom of the facultative lagoon was also performed. The results were used to generate residence time distribution curves and provide an estimate of mean residence time in the system. The data was used to examine hydraulic efficiency as it relates to short-circuiting and dead zones. A sludge study accumulation study was performed using the white towel method and the resulting measurements were interpolated to determine a total estimated sludge volume of 169 m3 (which is 8% of the facultative pond volume). An orange study was also performed to assess the surface flow pattern in the system. The results were compared with a computational 2-d model. The 2-d model incorporated the estimated sludge distribution and provided a good fit for the tracer dye concentrations measured in the field over the 12 day study period. Simple models such as the Tanks in Series and the Completely mixed model were evaluated and abandoned because of their inability to model the physical behavior in the system. The Completely mixed model did however perform better than the Plug flow model. After comparing the tracer results from the reactor models that were considered: Tanks in Series, Completely mixed fluid, manual interpolation and the results from the 2-d cfd flow simulation, the results that provided the best fit for the data over 12 days was the manual interpolation method at a flow rate of 98 m3/day and configuration D at 60 m3/day. However, because of uncertainty as to what depth to obtain a representative area for the 2-d simplification and sensitivity to flow; all four configurations were considered for estimating the MHRT at the lowest measured flow rate of 60 m3/day. The results at a flow rate of 60 m3/day varied between 10.88 and 13.04 days for the MHRT with a hydraulic efficiency that varied between 33-51.6% (accounting for sludge volume). This is much shorter than the actual nominal retention time of 37 days and the design nominal retention time of 26 days. As a result it was concluded that short-circuiting was occurring in the facultative lagoon.

Στην εργασία αυτή πραγματοποιήθηκε μια βιβλιογραφική ανασκόπηση σχετικά με τις ευαισθητοποιημένες ηλεκτροχημικές κυψελίδες και τα οργανικά φ/β, τις αρχές λειτουργίας τους,τα υλικά τους και τους τρόπους παρασκευής τους. Παρασκευάσαμε ηλεκτροχημικές κυψελίδες χρησιμοποιώντας διαφορετικές χρωστικές και αντιηλεκτρόδια. Όλες οι κυψελίδες δοκιμάστηκαν κάτω από διαφορετικές συνθήκες για την εύρεση των παραγόντων που επηρεάζουν την απόδοσή τους. Παράγοντες όπως το πάχος και η τραχύτητα του υμενίου, διαφορετικές χρωστικές και αντιηλεκτρόδια κτλ βελτιστοποιήθηκαν για την αύξηση τησ απόδοσης. Επίσης εξετάστηκε η σταθερότητα των κυψελίδων αυτών με το χρόνο. Τέλος εξετάστηκαν και εξηγήθηκαν οι παράγοντες για τη χαμηλή απόδοση των κυψελίδων. / In this study we make a comprehensive literature review on dye-sensitized nanostructured and organic solar cells, their operating principles, materials as well as their manufacturing methods. We have fabricated dye – sensitized electrochemical solar cells using different dyes and counter electrodes. All solar cells were tested under different conditions in order to find the factors limiting their efficiency. Factors like film thickness and roughness, different dyes and counter electrodes etc were changed in order to improve efficiency. The stability of these solar cells were also evaluated for different time intervals. The efficiency was rather low and the reasons for this are examined and explained thorougηly.

The research presented in this dissertation covers three separate topics of conservation as defined by the National Science Foundation: 1) Materials Stabilization, Strengthening, Monitoring, and Repair; 2. Understanding Material Degradation and Aging; and 3) Materials and Structural Characterization of Cultural Heritage Objects (the `technical study'). The first topic is addressed through a study to assess the consolidant tetraethoxysilane for the stabilization of alum treated wood. Falling under materials degradation studies is a study published in American Museum Novitates to understand how environmental conditions affect the aging of fossil resins from five different deposits. Two separate studies are included in technical study of cultural heritage objects which comprises the third research area of materials characterization. The first is a survey of red dyes used in Chinese paintings from the Ming Dynasty to the Early Republic (1364-1911). The second is a study of the pigments, dyes and binders used in Hawaiian barkcloth (kapa) from the 19th century.

Baigiamojo darbo tikslas – nustatyti paviršinio aktyvumo medžiagų micelių susidarymo koncentracijas ir įvertinti tirpalų rūgštinių-bazinių savybių pokyčius paviršinio aktyvumo medžiagų ir rūgštinių dažiklių vandeniniuose tirpaluose. Kritinė micelių susidarymo koncentracija nustatyta atlikus tirpalų elektrinio laidumo ir šviesos absorbcijos matavimus, naudojantis konduktometriniu bei spektrofotometriniu tyrimo metodais. Dažiklių rūgštinių-bazinių savybių kitimas vandeniniuose tirpaluose įvertintas nustačius dažiklio disociacijos konstantų neigiamo logaritmo vertes ir termodinaminius parametrus. Paviršinio aktyvumo medžiagų, tokių kaip natrio dodecilsulfato, dodeciltrimetilamonio chlorido ir joninio tirpalo 1-dodecil-3-metilimidazolio chlorido kritinės micelių susidarymo koncentracijos buvo nustatytos Žaliojo B dažiklio vandeniniuose bei buferiniuose tirpaluose. Nustatyta, kad paviršinio aktyvumo savybe pasižyminčių medžiagų kritinės micelių susidarymo koncentracijų vertės priklauso nuo tirpalo pH, o didinant tirpalo joninę jėgą jos mažėja. Rūgštinio Oranžinio 7 ir Rūgštinio Mėlynojo 80 dažiklių disociacijos konstantų neigiamo logaritmo pKr vertės kito priklausomai nuo vandeninio tirpalo temperatūros, pH vertės ir naudotų skirtingos prigimties paviršinio aktyvumo medžiagų. Nustatyta, kad Rūgštinio Oranžinio 7 dažiklio rūgštinės savybės stipriausiai išreikštos, kai tirpale buvo amfoterinės paviršinio aktyvumo medžiagos – kokoamidopropilbetaino, o Rūgštinio Mėlynojo 80 -... [toliau žr. visą tekstą] / The aim of this work was to determinate the critical micelle concentration of surfactants and to evaluate the variation of acidic-basic properties of acidic dyes and surfactants solutions. The critical micelle concentration was determinated by the measurements of electrical conductivity and absorption, using electrical conductivity and UV-vis absorption spectrometry methods. The variation of acidic-basic properties of dyes in aqueous solutions was evaluated by estimation the values of the negative logarithm of dissociation constant of the dye and thermodynamic parameters of dyes-surfactants solution. The critical micelle concentration of sodium dodecyl sulfate, dodecyltrimethylammonium chloride and 1-dodecyl-3-methylimidazolium chloride was determinated in aqueous and phosphate buffered solutions of the Janus Green B dye. The value of critical micelle concentration of anionic, cationic surfactants and ionic compound depends on the pH value of the solutions, it can be observed that increasing the ionic strength of solution the value of critical micelle concentration decreases. The values of the negative logarithm of dissociation constant of Acid Orange 7 and Acid Blue 80 dyes varied depending on the temperature of aqueous solution, the pH value and the nature of used surfactants. It was estimated, that the lowest value of pKa of Acid Orange 7 dye was then the amphoteric surfactant - cocamidopropyl betaine was used in the dye solution and for Acid Blue 80 dye – nonionic... [to full text]

No description available.

<p>Aim and Objectives: To assess the effect of bleaching on the marginal integrity of Class V composite resin restorations. To determine the effect of a 6% hydrogen peroxide over the counter and a 38% hydrogen peroxide in-office vital bleaching treatment products on the microleakage of Class V composite restorations.</p>

Thèse numérisée par la Division de la gestion de documents et des archives de l'Université de Montréal

The purpose of the research work, presented in this thesis is to offer a detailed atomic level study of interfaces created by adsorption of organic molecules on metals and metal oxides to point out significant impact of substrate, dye structure as well as different mediators on the charge transfer at these interfaces, which is proven to influence the device performance to a great extent. Adsorption of organic photosensitive molecules on metals and metal-oxides is the main focus of this thesis. Phthalocyanines which are organic semiconductors offer a broad range of properties, such as thermal and chemical stability, high charge mobility and strong absorption coefficient in the visible and near-IR regions, which make them very attractive to be applied in various systems and devices. Fuel cells, organic field-effect transistors (OFETs), organic light emitting diodes (OLEDs) and solar cells are examples of phthalocyanine’s applications. The main focus of this work is to characterize the interfaces of Dye Sensitized Solar Cells (DSSCs). DSSC was invented by Michael Grätzel and Brian O’Regan in 1988. At the heart of this cell there is an oxide which is coated by a photosensitive dye. Under illumination, an electron is excited from HOMO to LUMO of the molecule, which can be further transferred to the conduction band of the oxide by a proper energy level alignment. The original state of the dye is regenerated by electron donation via the electrolyte, which usually is an organic solvent containing a redox couple e.g., iodide/triiodide. The iodide is regenerated by reduction of triiodide at the counter electrode. To improve the functionality of the cell, different additives can be added to the electrolyte. To mimic the interfaces of this cell, molecular layers of MPc (M: Fe, Zn, Mg) are adsorbed on both metallic surfaces, Au(111) and Pt(111), and rutile TiO2(110). Layers of iodine were inserted between metallic substrates and dyes to investigate the electronic properties and charge transfer at these multi-interface systems. 4-tert-butyl pyridine is a significant additive to the electrolyte and has proven to enhance the cell’s performance. This molecule was also adsorbed on Pt(111) and TiO2(110). Phthalocyanines were deposited by organic molecular beam deposition and 4TBP was evaporated at room temperature. Surface structures and reconstructions were confirmed by LEED measurements. Surface sensitive synchrotron radiation based spectroscopy methods, XPS and NEXAFS were applied to characterize these surfaces and interfaces. STM images directly give a topographical and electronic map over the surface. All measurements were carried out in UHV condition. When MPc was adsorbed on Au(111) and TiO2(110), charge transfer from molecule to substrate is suggested, while the opposite holds for MPc adsorbed on Pt(111). Moreover, stronger interaction between MPc and Pt(111) and TiO2(110) compared to Au(111) also demonstrates the effect of substrate on the charge transfer at the interface. The stronger interaction observed for these two substrates disturbed the smooth growth of a monolayer; it also resulted in bending of the molecular plane. Interaction of MPc with metallic surfaces was modified by inserting iodine at the interface. Another substrate-related effect was observed when MgPc was adsorbed on TiO2(110);  and -cross linked surfaces, where the surface reconstruction directly affect the molecular configuration as well as electronic structure at the interface. Besides, it is shown that the d-orbital filling of the central metal atom in MPc plays an important role for the properties of the molecular layer as well as charge transfer at the interface. Upon adsorption of 4TBP on Pt(111), C-H bond is dissociatively broken and molecules is adsorbed with N atoms down. Modification of surface by iodine, prevent this dissociation. In the low coverage of iodine, there is a competition between 4TBP and iodine to directly bind to Pt(111). Investigation on the adsorption of 4TBP on TiO2(110) illustrated that these molecules in low coverage regime, prefer the oxygen vacancy sites and their adsorption on these sites, results in a downward band bending at the substrate’s surface. / <p>QC 20131203</p>

The work presented here report findings in (1) infrared detectors based on p-GaAs/AlGaAs heterojunctions, (2) J and H aggregate sensitized heterojunctions for solar cell and photon detection applications, (3) heterojunctions sensitized with quantum dots as low cost solar energy conversion devices and near infrared photodetectors. (1)A GaAs/AlGaAs based structure with a graded AlGaAs barrier is found to demonstrate a photovoltaic responsivity of ~ 30mA/W (~ 450mV/W) at the wavelength of 1.8 mm at 300K. Additionally the graded barrier has enhanced the photoconductive response at 78 K, showing a responsivity of ~ 80mA/W with a D*=1.4×108 Jones under 1V bias at 2.7 mm wavelength. This is an approximately 25 times improvement compared to the flat barrier detector structure, probably due to the improved carrier transport, and low recapture rate in the graded barrier structure. However, these graded barrier devices did not indicate a photoresponse with photoconductive mode at 300K due to high shot noise. Additionally, two generation-recombination noise components and a 1/f noise component were identified. A series of GaAs/AlGaAs multilayer hetero-junction structures were tested as thermal detectors. A superlattice structure containing 57% Al fraction in the barrier and 3 × 1018 cm-3 p-doped GaAs emitter showed the highest responsivity as a thermal detector with a TCR of ~ 4% K-1, at 300K. (2)The photovoltaic properties of heterojunctions with J-/ H- aggregated dye films sandwiched between n– and p-type semiconductors were investigated for potential application as solar cells and IR detectors. Films of cationic dye Rhodamine-B-thiocyanate adsorbed on Cu2O substrate are found to form organized dye layers by self-assembled J- aggregation, resulting in large red-shifts in the photo -response. Additionally, cells sensitized with a pentamethine cyanine dye exhibited a broad spectral response originating from J- and H-aggregates. The photocurrent is produced by exciton transport over relatively long distances with significant hole-mobility as well as direct sensitized injection at the first interface. (3) A ZnO/PbS-QD/Dye heterostructure had enhanced efficiency compared to ZnO/Dye heterostructure as a solar cell. Furthermore, a ZnO/PbS-QD structure has demonstrated UV and NIR responses with 4×105V/W (390 nm) and 5.5×105 V/W (750 nm) under 1V bias at 300K.

The arrangement of soft materials through solution processing techniques is a topic of profound importance for next generation solar cells; the resulting morphology has a major influence on construction, performance and lifetime. This thesis investigates the connections between the soft matter physics of colloidal systems and solid state dye sensitised (SSDS) and bulk heterojunction (BHJ) solar cells. A study of aqueous titanium dioxide nanoparticulate suspensions was carried out in order to observe how suspension structure can be controlled by altering the inter-colloid potential via pH-induced electrostatic charging. Measurements were performed at volume fractions between 0.025% and 8.2% with the solution pH set to 3.1, 3.5 or 4.5 before mixing. Suspensions with a volume fraction above 4% formed self-supporting gels regardless of the set pre-mix pH. These gels displayed shear thinning behaviour with a power law exponent of 0.8, a yield stress of 11(1) Pa and rheological response consistent with an aggregated fractal network. At lower volume fractions, suspensions exhibited consolidation interpreted as the collapse of a gel of fractal clusters with a fractal dimension of 2.36. The velocity of the suspension/supernatant interface exhibited delayed sedimentation behaviour, as well as further fractal-based power law scalings with volume fraction. Lower volume fraction suspensions were explored using dynamic light scattering. Limited aggregation of ‘stable’ suspensions was observed when compared to primary aggregate radii measured from electron microscopy images. To connect suspension structure and cell manufacture, the behaviour of more concentrated suspensions was observed during the drying of thin films, a process which forms an essential part of a SSDS solar cell. Lowering the pH of the suspension after mixing from 4 to 3 resulted in an ordering of observed crack domains. An increase in film delamination was also observed. Rates of mass loss during drying followed the expected three phase process, although there was an unexpected increase in rate during the initial phase (where rate is usually constant in time). Dynamic light scattering was found to be a useful but demanding technique for studying cluster formation in titanium dioxide suspensions. A non-linear fitting technique utilising the method of moments was thoroughly explored using computer simulated datasets. The algorithm reduced the systematic error in fitted parameters for moderately polydisperse (0:2 < < 0:4) datasets as compared to the commonly applied linear algorithm. The fitting algorithm was also robust to bad initial estimates of parameters. Finally, test solar cells have been built using blends of titanium dioxide and poly-3-hexylthiophene. Device performance was reduced with blend standing time after mixing but could be improved by remixing the blend before spin coating, implicating a reversible process (e.g. aggregation of titanium dioxide or crystallisation of P3HT) in the loss of performance. Addition of a titanium dioxide hole blocking layer before spin coating reduced cell performance. Combining the above studies and these device designs provides a future platform for continuation of this work in the context of real devices.