Feed intake assessment is a valuable tool for herd management decisions. The use of markers, either internal or external, is currently the most used technique for estimating feed intake in production animals. Three experiments were conducted with beef and dairy cattle. In dairy cows fed a corn silage based diet with 45% concentrate, the average fecal recovery (FR) of TiO2 was higher than FR of Cr2O3 and both FR were more than unity. The FR was unaffected by the fecal sampling procedure but, estimates for dry-matter digestibility (DMD) and fecal output (FO) were affected. The Cr2O3 + indigestible acid detergent fiber (iADF) marker pair produced accurate dry-matter intake (DMI) estimates. In steers fed diets with different forage sources FR of TiO2 was close to 1 and this marker produced adequate FO estimates. The FR was affected by the forage source that composed the diet and none of the marker pairs produced accurate DMI estimates. In young Nelore bulls fed corn silage or Tifton-85 hay based diets with varying F:C ratios, the average FR of internal markers acetyl bromide lignin (ABL), indigestible neutral detergent fiber (iNDF), iADF and cutin was different from 100%. Markers Cr2O3 and TiO2 had FR lower and higher than 100%, respectively. The combination of internal and external markers to estimate DMI produced satisfactory and accurate results, particularly Cr2O3 based pairs with iNDF and iADF. Internal markers ABL and cutin deserve more attention. The GRAB sampling procedures yielded accurate DMD, FO and DMI estimates, which were as good as or better than BULK sampling procedures. Regardless of the fecal sampling method and the composition of the diet, it is necessary to establish the FR of the markers to be used in each experiment, in order to obtain correct estimates. None of the markers had complete FR consistent throughout the 3 experiments. Cutin and ABL had lower than unity FR on all diets and failed to produce accurate DMD estimates. When either one was paired with Cr2O3 or TiO2, DMI estimates were also not accurate. Of the indigestible fibers, iNDF and iADF, the later was more accurate in estimating DMI when paired with Cr2O3. Consistently throughout the experiments, FR was lower than and higher than unity for internal and external markers, respectively. Corrected FO estimates were accurate for Cr2O3 on various diets under GRAB sampling. The same was not true for TiO2, which even after FR correction was applied failed to produce accurate FO estimates consistently. The method of dosing the external markers is extremely important and greatly affects and determines results. Whichever the method, it must allow the animals to display normal feeding behavior and not affect performance. The GRAB sampling procedures can replace TFC (once FR is established) which may open new possibilities for pasture based or collectively housed animals. / A determinação do consumo de alimentos é uma valiosa ferramenta na hora da tomada de decisões de manejo do rebanho. O uso de marcadores, sejam internos ou externos, é atualmente a técnica mais utilizada para estimar o consumo em animais de produção. Três experimentos foram conduzidos. Em vacas de leite alimentadas com silagem de milho com 45% de concentrado, a recuperação fecal (RF) média de TiO2 foi maior do que a RF de Cr2O3 e ambas foram maiores do que a unidade. A RF não foi afetada pelo método de coleta de fezes, mas, as estimativas de digestibilidade da matéria seca e produção fecal (PF) foram. A dupla de marcadores Cr2O3+i fibra detergente ácido indigestível (iADF) produziu estimativas de consumo de matéria seca (CMS) acuradas. Em novilhos alimentados com diferentes fontes de forragem, a RF do TiO2 foi próxima a 1 e este marcador produziu estimativas de PF adequadas. A RF foi afetada pela fonte de forragem que compunha a dieta e nenhum dos marcadores produziu estimativas de CMS acuradas. Em tourinhos Nelore alimentados com dietas compostas de silagem de milho ou feno de Tifton-85 e diferentes relações de volumoso:concentrado, a RF média dos marcadores internos lignina brometo de acetila (LBA), fibra detergente ácido indigestível (iFDN), (iFDA) e cutina foi diferente de 100%. Os marcadores Cr2O3 e TiO2 tiveram RF menor e maior que 100%, respectivamente. A combinação de marcadores internos e externos para estimar o CMS produziu resultados acurados e satisfatórios, principalmente as duplas Cr2O3 e iFDN ou iFDA. Os marcadores internos LBA e cutina merecem mais estudos. O método de coleta GRAB produziu estimativas de DMS, PF e CMS acuradas, as quais foram iguais ou melhores que as produzidas pelo método de coleta BULK. Independentemente do método de coleta de fezes e da composição da dieta, é necessário estabelecer a RF real dos marcadores que serão usados em experimento para obter estimativas corretas. Nenhum dos marcadores teve RF completa e consistente nos 3 experimentos. A cutina e LBA tiveram RF menor do que a unidade em todas as dietas e falharam em produzir estimativas acuradas de DMS. Quando qualquer dos dois foi pareado com Cr2O3 ou TiO2 as estimativas de CMS também não foram acuradas. Das fibras indigestíveis, iFDN e iFDA, a segunda foi mais acurada em estimar o CMS quando pareada com Cr2O3. As estimativas de PF corrigida foram acuradas para Cr2O3 em diferentes dietas sob metodologia de coleta GRAB. O mesmo não foi observado para o TiO2, que produziu estimativas enviesadas inclusive após a correção. O método de dosagem dos marcadores externos é extremadamente importante já que afeta e determina em grande medida os resultados. Qualquer que seja o método, este deve permitir ao animal comportar-se e alimentar-se normalmente sem comprometer seu desempenho. Os métodos de coleta GRAB podem substituir a coleta total de fezes (CTF) (após determinação da RF) o que poderá abrir novas possibilidades para estudos com animais em pastagem ou alojados em baias coletivas.

Introdução: O dióxido de titânio (TiO2) é um corante encontrado na forma de partículas em diversos produtos industrializados. Muitos estudos, a maioria envolvendo o trato respiratório, alertam sobre os efeitos prejudiciais advindos da exposição ao TiO2. Embora partículas da dieta, tais como o TiO2, sejam ingeridas diariamente, ainda existem poucos estudos investigando seus efeitos sobre o trato gastrointestinal. Objetivos: O objetivo principal desse trabalho é investigar a ação de nano (NP) e micropartículas (MP) de TiO2 sobre a resposta inflamatória no intestino delgado de camundongos. Material e Métodos: Camundongos Bl 57/6 foram divididos em 2 grupos experimentais, os quais receberam NP TiO2 (66 nm) ou MP TiO2 (260 nm) a uma dose de 100 mg/Kg/dia, e um grupo controle, o qual recebeu água destilada. O tratamento foi administrado por gavagem, durante 10 dias, uma vez ao dia. Ao final, o intestino delgado foi coletado para a análise de citocinas (IL-1b, IL-4, IL-6, IL-8, IL-10, IL-12, IL-13, IL-17, IL-23, TNFa, IFNg e TGFb) por ELISA e quantificação de células T CD4+, T CD8+, células dendríticas e natural killers por imunohistoquímica. Resultados: Os resultados demonstram maior concentração de citocinas IL-12, TNFa, IFNg, IL-4, IL-23 e TGFb, e células T CD4+ nos grupos que receberam TiO2. O aumento de citocinas foi mais importante no íleo, onde há maior concentração de células M, as quais representam a principal via de captação de partículas no intestino. Conclusão: As partículas de TiO2 provocaram uma resposta pró-inflamatória, predominantemente do tipo Th1, no intestino delgado dos camundongos, especialmente no íleo. Esses dados representam uma evidência in vivo do potencial inflamatório de partículas de TiO2 sobre o trato gastrointestinal / Introduction: Titanium dioxide (TiO2) is a white pigment widely found as micro and nano-sized particles added to food, drugs, cosmetics, etc. Studies involving the pulmonary tract warn about adverse effects resulting from exposure to TiO2, emphasizing its inflammatory potential. Although the gastrointestinal tract is considerably exposed to TiO2 particles at daily basis there are few information regarding its adverse effects on intestine. Objectives: We aimed to investigate the effects of TiO2 nanoparticles (NP) and microparticles (MP) on inflammatory response in the small intestine of mice. Methods: Bl 57/6 mice received suspensions containing TiO2 (100 mg/Kg/day) as TiO2 NP (66 nm), or TiO2 MP (260 nm) by gavage for 10 days, once a day; control group received only distilled water. At the end of the treatment, the small intestine were extracted for assessment of cytokines (IL-1b, IL-4, IL-6, IL-8, IL-10, IL-12, IL-13, IL-17, IL-23, TNFa, IFNg e TGFb) by ELISA and quantification of inflammatory cells (T CD4+, T CD8+, dendritic cells, and natural killer) by immunohistochemistry. Results: We found increased levels of T CD4+ cells and cytokines (IL-12, TNFa, IFNg, IL-4, IL-23, and TGFb) on groups receiving TiO2 when compared to control group. Cytokines production was more important on the ileum, local presenting greater concentration of M cells, which represent the main pathway of particles uptake on gut. Conclusion: Our findings indicate that TiO2 particles induce a Th1 mediated inflammatory response on small bowel in mice. These results represent an in vivo evidence of the inflammatory potential of TiO2 particles on the gastrointestinal tract

Orientadores: Jacobus Willibordus Swart, Angélica Denardi de Barros / Dissertação (mestrado) - Universidade Estadual de Campinas, Faculdade de Engenharia Elétrica e de Computação / Made available in DSpace on 2018-08-26T06:34:57Z (GMT). No. of bitstreams: 1 Cesar_RodrigoReigota_M.pdf: 3932101 bytes, checksum: b4dd2542176f2f405f73883dd504a69a (MD5) Previous issue date: 2014 / Resumo: Com a escassez de água potável e com a sua contaminação frequente, a monitoração da mesma tornou-se importante. Dentre os muitos contaminantes, temos o chumbo (Pb). Este no passado foi muito utilizado em encanamentos residenciais, causando a contaminação da água. O chumbo pode causar danos á saúde humana desencadeando desde disfunções nos rins, aborto até alguns tipos de câncer. Dessa forma a criação de um dispositivo do tipo ISFET (Transistor de Efeito de Campo Sensível a Íon), que detecta a presença de cátions e ânions em água, está sendo desenvolvido para a detecção específica do chumbo. Para tal fim, foram utilizados filmes finos de óxido de titânio (TiO2) como dielétrico de porta e foi utilizado fosfato de cério fibroso (CeP) como membrana seletiva (material desenvolvidos no Laboratório de Química do Estado Solido - LQES[1]). Os filmes finos de TiO2 foram obtidos por dois métodos: i) deposição de titânio metálico por sputtering seguido pelo processo de oxidação térmica rápida (rapid thermal process - RTP); ii) deposição do óxido de titânio por sputtering. Foi escolhido o dióxido de titânio (TiO2) devido as suas características como: alta constante dielétrica, capacidade de formar pontes de hidrogênio e estabilidade química. Os filmes de TiO2, foram caracterizados estruturalmente por espectroscopia Raman; apresentando picos relacionados à estrutura cristalina rutilo, o que foi através do índice de refração igual a 2.4 encontrado na elipsometria. A microscopia de força atômica (AFM) e microscópio óptico mostraram a uniformidade do filme de CeP, dessa maneira sendo possível determinar qual é o melhor método de deposição da solução de CeP. Para testar qual método de deposição que resultou no melhor filme fino de TiO2, foram desenvolvidos capacitores com estrutura Si/TiO2e Si/SiO2/TiO2 no CCS (Centro de Componentes Semicondutores). Dessa maneira foram realizadas as medidas capacitância por tensão (CxV) e corrente por tensão (IxV) para vários tempos de recozimento. Levando-se em consideração o menor valor de densidade de carga, tensão de banda plana próximo ou igual a -0,9 V e o maior valor da constante dielétrica foi possível determinar que para ambos os métodos de deposição a melhor estrutura é a de Si/TiO2, com 10 minutos de recozimento para o filme obtido por RTP e com 15 minutos para o filme obtido por sputtering. Com a melhor condição elétrica de funcionamento dos capacitores foi desenvolvido o Eletrólito-Isolante-Semicondutor (EIS). A partir da curva CxV dos dispositivos EIS sem a membrana de CeP e com o óxido de Ti obtido por RTP, foi possível determinar a sensibilidade de 45mV/pH para soluções com diferentes valores de pH e sensibilidade igual a 42mV/100ppm para soluções com diferentes concentrações de chumbo. Com a membrana seletiva o dispositivo mostrou sensibilidade de 40mV/100ppm para soluções com concentrações diferentes de chumbo. O dispositivo EIS com óxido obtido por sputtering teve sensibilidade de 96mV/pH na detecção de pH, sendo está sensibilidade maior que a obtida pelo EIS obtido por RTP. Ao testar soluções com diferentes concentrações de chumbo, o dispositivo sem a membrana seletiva mostrou uma sensibilidade de 30mV/100ppm. Neste caso, o EIS com membrana seletiva mostrou uma sensibilidade de 20mV/100ppm / Abstract: With the shortage of drinking water and with their frequent contamination, monitoring the same became important. Among the many contaminants, we have lead (Pb). This in the past it was widely used in residential plumbing, one of the ways that caused water contamination. Lead can cause damage to human health from kidney dysfunction, causing abortion and even some types of cancer. In this way the creation of a device of type ISFET (Sensitive Field Effect Transistor for ion), which detects the presence of cations and anions in water, is being developed for the specific detection of lead. For this purpose, we used thin titanium dioxide (TiO2) films as dielectric and fibrous cerium phosphate (CeP) was used as selective membrane (material developed in the laboratory of Solid State Chemistry-LQES[1]). The TiO2 thin films were obtained by two methods: 1) metallic titanium was deposited by sputtering then was oxidized by rapid thermal oxidation process (RTP); 2) Consist in titanium oxide deposition by sputtering. Titanium dioxide was chosen due to it quality was dielectric constant, ability to form hydrogen bonds and chemical stability. TiO2 thin films were structurally characterized by Raman Spectroscopy showing peaks related to rutile crystal structure, which has been proven through the refractive index equal to 2.4 found on elipsometria. The atomic force microscopy (AFM) and optical microscope showed the uniformity of the CeP film, thus being able to determine what the best method of deposition of CeP solution. To test which method has the best TiO2 thin film capacitors were developed with Si/TiO2 and Si/SiO2/TiO2 structure on CCS (Centre of Semiconductor Components). In this way were carried out the measures capacitance of versus voltage (CxV) and current versus tension (IxV) for various annealing times. Taking into consideration the smallest value of charge density, flat-band voltage near -0.9V and the greatest value of dielectric constant, it was possible to determine that for both methods of deposition the best structure is the Si/TiO2, with 10 minutes of annealing for the film obtained by RTP and with 15 minutes to the film obtained by sputtering. With the best electrical capacitors operating condition was developed the Electrolyte-Insulator-Semiconductor (EIS). From the curves CxV without the membrane of CeP and the titanium oxide obtained by RTP, it was possible to determine the sensitivity of 45mV/pH for pH detection and sensitivity of 42mV/100ppm for lead detection. With the selective membrane the EIS showed a sensitivity of 40mV/100ppm for lead detection. The EIS device with TiO2 obtained by sputtering showed a sensitivity of 96mV/pH for pH detection and sensitivity of 30mV/100ppm for lead detection. The EIS with selective membrane showed a sensitivity of 20mV/100 ppm for lead detection / Mestrado / Eletrônica, Microeletrônica e Optoeletrônica / Mestre em Engenharia Elétrica

Orientadores: Francisco das Chagas Marques, Ana Flávia Nogueira / Dissertação (mestrado) - Universidade Estadual de Campinas, Instituto de Física Gleb Wataghin / Made available in DSpace on 2018-08-26T08:45:20Z (GMT). No. of bitstreams: 1 Coutinho_NataliadeFaria_M.pdf: 12394800 bytes, checksum: 1d28bb92259a5c9eb6848a0fe678b6b3 (MD5) Previous issue date: 2014 / Resumo: A demanda mundial de energia elétrica tem crescido muito nas últimas décadas, o que tem levado a uma busca mais expressiva por fontes de energia renováveis e sustentáveis. Deste modo, as células solares, que através do efeito fotovoltaico convertem a energia proveniente do sol em energia elétrica, tem ganhado atenção. Dentre os vários tipos de células solares, se encontram as células solares sensibilizadas por corante, DSSC, que têm ganhado interesse de estudiosos da área por apresentarem uma possibilidade de geração de energia elétrica a baixo custo. Para que essas células ganhem competitividade no mercado, é necessário que suas eficiências aumentem, e é nesse ramo de pesquisa que o presente trabalho se coloca. Este trabalho foi baseado no estudo e otimização da eficiência de células solares sensibilizadas por corante, onde verificamos a influência de vários fatores na eficiência das células. Dentre eles, se encontram o processo de manufatura das células, o pós-tratamento de TiCl4 sobre o filme nanoestruturado de TiO2, a composição da pasta de TiO2 e do eletrólito líquido, o método de deposição da Pt no contra-eletrodo, e a utilização de uma camada espalhadora de luz com nanopartículas de TiO2 da ordem de 200nm. Além disso, um estudo a respeito do efeito de uma blocking layer de TiO2 entre o FTO e o filme nanoestruturado de TiO2, depositada pela técnica conhecida como atomic layer deposition, ALD, também foi realizado, o que levou a um aumento na eficiência das células. Através desses estudos, conseguimos aumentar a eficiência das células em até 90% se comparado às primeiras células que produzimos (de 3,9% a 7,4%), atingindo valores de tensão de circuito aberto Voc, densidade de corrente de curto-circuito Jsc, fator de preenchimento FF e eficiência ? de até 0,71V, 14,38mA/cm2, 0,67 e 7,4%, respectivamente. Deste modo, uma melhora significativa na performance das células foi observada, chegando a resultados comparáveis aos obtidos por diversos grupos de pesquisa em todo o mundo / Abstract: World demand for electricity has grown in the last decades, which has led to a more expressive search for renewable and sustainable energy sources. Consequently, solar cells have been getting attention because of their capacity to convert energy from the sun into electrical energy through the photovoltaic effect. Among the various types of solar cells, there are the dye-sensitized solar cells, DSSC, which have gained interest of the solar cell community for having a possibility of power generation at low cost. In order to these cells get market competitiveness, it is necessary to increase their efficiency, and this is the research field that the present work is placed into. This thesis was based on the study and optimization of dye-sensitized solar cells efficiency, where we could see the influence of various factors in cells efficiency. Among these, there are the cells manufacturing process, the post-treatment on nanostructured TiO2 films using a TiCl4 solution, the composition of the TiO2 paste and the liquid electrolyte, the method of Pt deposition at the counter electrode, and the use of a reflecting layer with 200nm TiO2 nanoparticles. In addition, a study of the effect of a TiO2 blocking layer between the FTO and the nanostructured TiO2 film deposited by the technique known as atomic layer deposition, ALD, was also performed, which led to an increase in cells efficiency. Through these studies, we could increase cells efficiency by up to 90% compared to the first cells we produced (from 3,9% to 7,4%), reaching values of open circuit voltage Voc, short circuit current density Jsc, fill factor FF and efficiency _ of up to 0,71V, 14,38mA/cm2, 0,67 and 7,4%. Thus, a significant improvement in cells performance was observed, reaching results comparable to that obtained by many research groups around the world / Mestrado / Física / Mestra em Física

Orientador: Wilson de Figueiredo Jardim / Tese (doutorado) - Universidade Estadual de Campinas, Faculdade de Engenharia Civil / Made available in DSpace on 2018-08-01T21:14:54Z (GMT). No. of bitstreams: 1 Teixeira_ClaudiaPolideAlmeidaBarea_D.pdf: 9723868 bytes, checksum: af66f37d0f1ef9ed84d053f79363e4df (MD5) Previous issue date: 2002 / Resumo: Estudou-se a degradação de fenol em soluções preparadas em laboratório utilizando Processos Oxidativos Avançados (POA) que combinam Ti02, H202, 03, reagente de Fenton e UV. Os ensaios foram realizados utilizando um reator fotoquímico modelo Advantage 12 (Trojan) e a eficiência da mineralização dos compostos orgânicos presentes foi monitorada pela análise de COD (Carbono Orgânico Dissolvido). Observou-se que a maioria dos oxidantes testados se mostrou ineficazes na degradação de fenol quando utilizados em separado ou mesmo de forma combinada, sem a presença da radiação UV. O uso combinado de H2O2/UV se mostrou eficaz na degradação de soluções de fenol com CCOD = 100 mg.L-1 e a relação CH20/CCOD = 6/1 foi a mais eficiente para esta concentração de feno!. Neste caso os valores de EE/O variaram entre 23,5 e 34,7 kWh.m-3 e os valores de degradação entre 188 e 299 mgC.h-1. A vazão de recirculação da solução dentro do reator fotoquímico influencia a sua hidrodinâmica e, conseqüentemente, a eficiência do processo de degradação dos compostos orgânicos presentes. Para o reator utilizado, os melhores resultados foram obtidos com a vazão de 22 L.min-1 para os sistemas homogêneos e de 8 L.min-1 para os sistemas heterogêneos. Sistema de tratamento em batelada, utilizando um volume de solução variando entre 3 a 10 vezes o volume do reator se mostrou adequada para avaliar a tratabilidade dos efluentes e teve comportamento semelhante à utilização de sistemas com alimentação contínua. Os estudos de caso com diferentes efluentes industriais, apresentados no anexo, mostram que os POA são uma alternativa de tratamento para efluentes cujo tratamento convencional não seja possível ou mesmo adequado, como aqueles contendo compostos tóxicos, recalcitrantes, misturas complexas e/ou muito concentradas / Abstract: The degradation of phenol solutions was studies using AOP (Advanced Oxidation Processes) in the presence of Ti02, H2O2, 03, Fenton's reagent and UV. Experimental tests were performed using a photochemical reactor Advantage 12 (Trojan) and the efficiency was monitored by DOC (dissolved Organic Carbon) analysis. It was observed that the use of one oxidant alone yielded low mineralization rates, the same observed for the vast majority of combined oxidants. The use ofH202/UV showed higher efficiency in the degradation of 100 mgC.L-1 phenol solutions in the ratio CH20/CCOD = 6/1. Under this condition, values of EE/O between 23,5 and 34,7 kWh.m-3 and degradation rates between 188 and 299 mgC.h-1 were obtained. The recirculation flow rate used in the experiments control the reactor hydrodynamic and the quantum efficiency. Using this reactor, better results were obtained with 22 L.min-l to the homogeneous systems and 8 L.min-l to the heterogeneous systems. The utilization of batch systems using a total volume of3 up to 10 times the volume of the reactor showed to be valid in terms to evaluate the treatability of the effluents, yielding similar results to the ones obtained under continuous flow. Experiments with different industrial eft1uents presented as Case Studies show that AOPs are an alternative viable option to wastewater treatment, specially when conventional alternatives showed poor performance, such as in the ones containing toxic compounds, recalcitrant, complex mixtures and/or very concentrated solutions / Doutorado / Saneamento e Ambiente / Doutor em Engenharia Civil

L’hydrogénation du CO2 par voie catalytique hétérogène représente une stratégie pertinente pour atténuer les émissions. Cette thèse a pour but de contribuer à la compréhension des facteurs physico-chimiques qui déterminent l’activité de catalyseurs Ru/TiO2 en conditions douces (= 200 °C, 1 atm). Des nanoparticules de RuO2 de 2 nm sont utilisées comme précurseurs de la phase active de Ru métallique. Ces nanoparticules calibrées sont combinées avec plusieurs supports de TiO2 présentant diverses cristallinités, textures, stabilité et compositions, dans le but de comprendre les paramètres qui dictent l’activité des catalyseurs Ru/TiO2. Les interactions spécifiques entre le support de TiO2 et les nanoparticules de RuO2 sont mises en évidence via différentes techniques avancées incluant la tomographie et la microscopie électronique en transmission environnementale à pression atmosphérique. Il apparait que le paramètre clé conférant une activité catalytique élevée est la stabilisation épitaxiale de RuO2 sur le TiO2 rutile lors de l’étape d’activation qui précède la réduction vers la forme Ru métallique. / The hydrogenation of CO2 performed through heterogeneous catalysis is a pertinent strategy for mitigating CO2 emissions. This thesis aims to contribute to the understanding of the physico-chemical factors related to the catalytic performance of Ru/TiO2 catalysts at mild conditions (= 200 °C, 1 atm). Pre-synthesized 2 nm-RuO2 nanoparticles (NPs) are used to serve as precursors for active metallic Ru. These calibrated NPs are coupled with various tailor made TiO2 supports with different crystallinity, textural properties, stability and composition to understand parameters that dictate the activity of Ru/TiO2 catalysts. The specific RuO2-TiO2 interactions and RuO2 NPs migration phenomenon are demonstrated using various techniques including the state-of-the-art tomography and environmental transmission electron microscopy at atmospheric pressure. The important parameter for the better catalytic performance is found to be the epitaxial stabilization of RuO2 on rutile TiO2 prior to the formation of active Ru phase.

Magister Scientiae - MSc / An electrolytic cell was designed and constructed for the preparation of TiO2 nanotubes. Conditions of anodic oxidation were established to reproducibly prepare TiO2 nanotubes of average length 35-50 μm vertically orientated relative to the plain of a pure titanium metal sheet. A non-aqueous solution of ethylene glycol containing small percentage of ammonium fluoride was used as the electrolyte with an applied voltage of 60 V. The morphology and dimensions of the nanotube arrays were studied by scanning (SEM) and transmission (TEM) electron microscopy. The effect of calcination under different conditions of temperature and atmosphere (nitrogen, argon and air) were assessed by both X-ray diffraction (XRD) and cyclic voltammetry (CV). Cyclic voltammetry studies were made possible by construction of a specially designed titanium electrode upon which the nanotubes were prepared. CV studies established a positive correlation between crystallinity and conductivity of the nanotubes. Doping of the nanotubes with nitrogen and carbon was established by elemental analysis, X-ray photoelectron spectroscopy (XPS) and Rutherford back scattering (RBS). The effect of nonmetal doping on the band gap of the TiO2 nanotubes was investigated by diffuse reflectance spectroscopy (DRS). / South Africa

A thorough study on the distribution of defect-related active energy levels has been performed on nanocrystalline TiO2. Films have been deposited on thick-alumina printed circuit boards equipped with electrical contacts, heater and temperature sensors, to carry out a detailed thermally stimulated currents analysis on a wide temperature range (5-630 K), in view to evidence contributions from shallow to deep energy levels within the gap. Data have been processed by numerically modelling electrical transport. The model considers both free and hopping contribution to conduction, a density of states characterized by an exponential tail of localized states below the conduction band and the convolution of standard Thermally Stimulated Currents (TSC) emissions with gaussian distributions to take into account the variability in energy due to local perturbations in the highly disordered network. Results show that in the low temperature range, up to 200 K, hopping within the exponential band tail represents the main contribution to electrical conduction. Above room temperature, electrical conduction is dominated by free carriers contribution and by emissions from deep energy levels, with a defect density ranging within 10(14)-10(18) cm(-3), associated with physio- and chemi-sorbed water vapour, OH groups and to oxygen vacancies.

Ce travail se résume en deux objectifs principaux. Le premier concerne l'élaboration de matériaux nanohybrides de dioxyde de titane (sous forme sphérique ou tubulaire) décoré par des allotropes de carbone (fullerène fonctionnalisé ou graphène). Le deuxième objectif consiste à l'évaluation de ces différents nanomatériaux dans la photodégradation de l'acide formique (AF) sous irradiation UV. Un effet bénéfique des allotropes de carbone sur l'activité photocatalytique des nanohybrides a été observé suite à l'augmentation de la durée de vie des paires électron-trou photogénérées. Dans un premier temps, la méthode d'élaboration et la teneur en fullerène fonctionnalisé ont été optimisées conduisant ainsi à l'élaboration de nanomatériaux révélant des propriétés photocatalytiques améliorées par rapport au TiO2 nanotube seul. Une corrélation entre les propriétés texturales, les propriétés photoélectriques et la constante de vitesse de dégradation de l'AF a été établie afin d'élucider les causes de l'amélioration de l'activité photocatalytique. Dans un second temps, une étude détaillée portant sur l'élaboration d'une nouvelle génération de nanocomposites combinant nanotubes de TiO2 et oxyde de graphène (OG) a été menée. Le degré de réduction de l'oxyde de graphène influence fortement l'activité photocatalytique. Ainsi, l'addition d'OG ou OG réduit aux nanotubes de TiO2 influence positivement les performances intrinsèques en photodégradation de l'acide formique en facilitant le transfert de photoélectrons de la bande de conduction du TiO2 vers l'oxyde de graphène. Finalement, l'étude des matériaux composites combinant l'oxyde de graphène et diverses compositions anatase/rutile a permis de mettre en évidence une synergie entre le OG et les deux phases TiO2 / Two main objectives were achieved in the present work. The first objective concerns the elaboration of nanohybrid materials formed by combining titanium dioxide (in spherical or tubular form) with carbon allotropes (functionalized fullerene or graphene). The second objective consists in evaluating these different nanomaterials in the photodegradation of formic acid (FA) under UV irradiation. A beneficial effect of the different carbon allotropes on the photocatalytic activity of the resulting nanohybrids was observed and ascribed to an increased lifetime of photogenerated electron-hole pairs. In a first step, the elaboration method of functionalized fullerenes and their content were optimized leading to the development of nanomaterials showing improved photocatalytic properties compared to TiO2 nanotube alone. Textural properties, photoelectric properties and the FA degradation rate constant were correlated in order to determine the reasons for the photocatalytic activity improvement. In a second step, a detailed study about the development of a new generation of nanocomposites combining TiO2 nanotubes and graphene oxide (GO) was carried out. The degree of reduction of GO strongly influences the photocatalytic activity. Thus, the addition of reduced GO or GO to TiO2 nanotubes improves the intrinsic photodegradation performance of formic acid by facilitating the transfer of photoelectrons from the conduction band of TiO2 to graphene oxide. Finally, composite materials combining graphene oxide and various anatase/rutile compositions were analyzed showing a synergy between GO and the two TiO2 phases

After introducing fundamentals of catalysis with noble metal surfaces especially Pt metal for CO oxidation and subsequent developments on nano-crystalline Pt metals supported on oxide supports, an idea of Pt ion in reducible oxide supports acting as adsorption sites is proposed in chapter 1. Idea of red-ox cycling of an ion in an oxide matrix is presented taking Cu ion in YBa2Cu3O7 as an example. Noble metal ions in reducible oxides such as CeO2 or TiO2 acting as adsorption sites and hence a red-ox catalyst was arrived at from chemical considerations. Among several reducible oxide supports, TiO2 was chosen from crystal structure and electronic structure considerations. A good redox catalyst for auto exhaust and related applications should have high oxygen storage capacity (OSC). Any new material that can work as a redox catalyst should be tested for its OSC. Therefore we designed and fabricated a temperature programmed reduction by hydrogen (H2¬TPR) system to measure OSC. This is presented in chapter 2. We have synthesized a number of oxides by solution combustion method. Structures were determined by powder XRD and Rietveld refinement methods. Fe2O3, Fe2-xPdxO3-δ, Cu1-xMnAl1+xO4, LaCoO3, LaCo1-xPdxO3-δ, CeO2, Ce1¬xPdxO2-δ, TiO2, Ti1-xPdxO2-δ and many other oxide systems were synthesized and their structures were determined. OSC of these systems were determined employing the H2/TPR system. TPR studies were carried out for several redox cycles in each case. Except Pd ion substituted CeO2 and TiO2 other oxide systems decomposed during redox cycling. Pd ion substituted TiO2 gave highest OSC and also it was stable paving way to choose this system for further study. In chapter 3, we have described lattice oxygen of TiO2 activation by the substitution of Pd ion in its lattice. Ti1-xPdxO2-x (x = 0.01 to 0.03) have been synthesized by solution combustion method crystallizing in anatase TiO2 structure. Pd is in +2 oxidation state and Ti is in +4 oxidation state in the catalyst as seen by XPS. Pd is more ionic in TiO2 lattice compared to Pd in PdO. Oxygen storage capacity defined by ‘amount of oxygen that is used reversibly to oxidize CO’ is as high as 5100 μmol/g of Ti0.97Pd0.03O1.97. Oxygen is extracted by CO to CO2 in absence of feed oxygen even at room temperature. Rate of CO oxidation is 2.75 μmol.g-1.s-1 at 60 0C over Ti0.97Pd0.03O1.97 and C2H2 gets oxidized to CO2 and H2O at room temperature. Catalyst is not poisoned on long time operation of the reactor. Such high catalytic activity is due to activated lattice oxygen created by the substitution of Pd ion as seen from first-principles density functional theory (DFT) calculations with 96 atom supercells of Ti32O64, Ti31Pd1O63, Ti30Pd2O62 and Ti29Pd3O61. The compounds crystallize in anatase TiO2 structure with Pd2+ ion in nearly square planar geometry and TiO6 octahedra are distorted by the creation of weakly bound oxygens. Structural analysis of Ti31Pd1O63 which is close to 3% Pd ion substituted TiO2 shows that bond valence of oxygens associated with both Ti and Pd ions in the lattice is 1.87. A low bond valence of oxygen is characteristic of weak oxygen in the lattice compared to oxygens with bond valence 2 and above in the same lattice. Thus, the exact positions of activated oxygens have been identified in the lattice from DFT calculations. Pt has two stable valencies: +2 and +4. Ti ion in TiO2 is in +4 state. Is it possible to substitute Pt exclusively in +2 or +4 state in TiO2? Implications are that Pt in +2 will have oxide ion vacancies and Pt in +4 states will not have oxide ion vacancies. Indeed we could synthesize Pt ion substituted TiO2 with Pt in +2 and +4 states by solution combustion method. In chapter 4, we have shown the positive role of an oxide ion vacancy in the catalytic reaction. Ti0.97Pt2+0.03O1.97 and Ti0.97Pt4+0.03O2 have been synthesized by solution combustion method using alanine and glycine as the fuels respectively. Both are crystallizing in anatase TiO2 structure with 15 nm average crystallite size. X-ray photoelectron spectroscopy (XPS) confirmed Pt ions are only +2 state in Ti0.97Pt0.03O1.97 (alanine) and only in +4 state in Ti0.97Pt0.03O2 (glycine). CO oxidation rate with Ti0.97Pt2+0.03O1.97 is over 10 times higher compared to Ti0.97Pt4+0.03O2. The large shift in 100 % hydrocarbon oxidation to lower temperature was observed by Pt2+ ion substituted TiO2 from that by Pt4+ ion substituted TiO2. After reoxidation of the reduced compound by H2 as well as CO, Pt ions are stabilized in mixed valences, +2 and +4 states. The role of oxide ion vacancy in enhancing catalytic activity has been demonstrated by carrying out the CO oxidation and H2 + O2 recombination reaction in presence and in absence of O2. There is no deactivation of the catalyst by long time CO to CO2 catalytic reaction. We analyzed the activated lattice oxygens upon substitution of Pt2+ ion and Pt4+ ion in TiO2, using first-principles density functional theory (DFT) calculations with supercells Ti31Pt1O63, Ti30Pt2O62, Ti29Pt3O61 for Pt2+ ion substitution in TiO2 and Ti31Pt1O64, Ti30Pt2O62, Ti29Pt3O61 for Pt4+ ion substitution in TiO2. We find that the local structure of Pt2+ ion has a distorted square planar geometry and that of Pt4+ ion has an octahedral geometry similar to Ti4+ ion in pure TiO2. The change in coordination of Pt2+ ion gives rise to weakly bonded oxygens and these oxygens are responsible in high rates of catalytic reaction. Thus, the high catalytic activity results from synergistic roles of oxide ion vacancy and weakly bonded lattice oxygen. In chapter 5, we have shown high rates of H2 + O2 recombination reaction by Ti0.97Pd0.03O1.97 catalyst coated on honeycomb monolith made up of cordierite material. This catalyst was coated on γ¬Al2O3 coated monolith by solution combustion method using dip-dry-burn process. This is a modified conventional method to coat catalysts on honeycombs. Formation of Ti0.97Pd0.03O1.97 catalyst on monolith was confirmed by XRD. Form the XPS spectra of Pd(3d) core level in Ti1-xPdxO2-δ, Pd ion is the formed to be +2 state. Ti0.97Pd0.03O1.97 showed high rates of H2 + O2 recombination compared to 2 at % Pd(metal)/γ-Al2O3, Ce0.98Pd0.02O2-δ, Ce0.98Pt0.02O2-δ, Ce0.73Zr0.25Pd0.02O2-δ and Ti0.98Pd0.02O1.98. Activation energy of H2 + O2 recombination reaction over Ti0.97Pd0.03O1.97 is 7.8 kcal/mole. Rates of reaction over Ti0.97Pd0.03O1.97 are in the range of 10 – 20 μmol/g/s at 60 0C and 4174 h-1 space velocity. Rate is orders of magnitude higher compared to noble metal catalysts. From the industrial point of view, solvent-free hydrogenation of aromatic nitro compounds to amines at nearly 1 bar pressure is an important process. In chapter 6, we showed that Ti0.97Pd0.03O1.97 is a good –nitro to –amine conversion catalyst under solvent-free condition at 1.2 – 1.3 bar H2 pressure. Nitrobenzene, p-nitrotoluene and 2-chloro-4-nitrotoluene are taken for the catalytic reduction reaction. The amine products were analyzed by gas chromatography and mass spectrometry (GCMS). Further, confirmation of compounds was done by FTIR, 1H NMR and 13C NMR. In presence of alcohol as solvent, 100% conversion of aromatic nitro compounds to amines took place at higher temperature and it required more times. In n-butanol solvent, 100% conversion of nitrobenzene and p-nitrotoluene occurred within 10 h and 12 h at 105 °C respectively. We have compared solvent-free reduction of p-nitrotoluene over different catalysts at 90 °C. Catalytic activity for reduction of p¬nitrotoluene over Ti0.97Pd0.03O1.97 is much higher than that reaction over 3 atom % Pd on TiO2 and Pd metal. Turnover frequencies (TOF) for nitrobenzene and 2-chloro-4-nitrotoluene conversion are 217 and 20 over Ti0.97Pd0.03O1.97 respectively. With increase of temperature, TOF of aromatic nitro compound reduction is also increased. We have compared the solvent-free reduction of aromatic nitro compound over Ti0.97Pd0.03O1.97 with others in the literature. Upto 3 cycles of reduction reaction, there was no degradation of Ti0.97Pd0.03O1.97 catalyst and stability of catalyst structure was analyzed by XRD, XPS and TEM images. Catalyst is stable under reaction condition and the structure is retained with Pd in +2 state. Finally, we have proposed the mechanism of -nitro group reduction reaction based on the structure of Ti0.97Pd0.03O1.97. Instead of handling nano-crystalline materials we proceeded with coating our catalysts on cordierite honeycombs. In chapter 7, we have shown high catalytic activity towards Heck reaction over Ce0.98Pd0.02O2-δ and Ti0.97Pd0.03O1.97 coated on cordierite monolith. XRD patterns of Ce0.98Pd0.02O2¬δ coated on cordierite monolith were indexed to fluorite structure. Heck reaction of aryl halide with olefins over Ce0.98Pd0.02O2-δ and Ti0.97Pd0.03O1.97 coated on cordierite monolith were carried out at 120 °C. The products were first analyzed by GCMS and for the confirmation of compounds, we have recorded 1H NMR and 13C NMR. Heck reaction was carried out with different solvents and different bases for choosing the good base and a solvent. Hence, we have chosen K2CO3 as base and N,N¬dimethylformamide (DMF) as solvent. We have compared the rates of Heck reactions over these two catalysts and Ti0.97Pd0.03O1.97 catalyst showed much higher catalytic activity than Ce0.98Pd0.02O2-δ. With increase of temperature from 65 °C to 120 °C, the catalytic activity of Ti0.97Pd0.03O1.97 on Heck reaction is also increased. The catalyst was reused for next Heck reaction without significant loss of activity. A mechanism for Heck reaction of aryl halide with alkyl acrylate has been proposed based on the structure of Ti0.97Pd0.03O1.97. In chapter 8, we have provided a critical review of the work presented in the thesis. Critical issues such as noble metal ion doping in TiO2 vs noble metal ion substitution, difficulty of proving the substitution of low % noble metal ion in TiO2, need for better experimental methods to study noble metal ion in oxide matrix have been discussed. Finally, conclusions of the thesis are presented.