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Ribeiro, Rafael Parra. "Efeito do tratamento de oxidação a plasma na produção de uma bicamada SiOx/SiOxCyHz." Universidade Estadual Paulista (UNESP), 2017. http://hdl.handle.net/11449/152465.
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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
Devido às suas propriedades mecânicas, soldabilidade e baixo custo, o aço carbono é um material amplamente utilizado nos mais diversos setores. Entretanto, o aço carbono é facilmente oxidado quando exposto ao ambiente. Para evitar esse problema, alguns trabalhos sugerem o desenvolvimento de revestimentos protetivos utilizando técnicas de deposição a plasma baseadas no composto hexametildisiloxano, HMDSO. A partir deste composto podese obter desde estruturas organosilicones até as inorgânicas pela alteração dos parâmetros de deposição. Revestimentos tipo óxido de silício são mais resistentes à corrosão que os organosilicones, porém sua estabilidade física é menor. Com o objetivo de associar as propriedades favoráveis de ambos os tipos de revestimentos, investigou-se, no presente trabalho, a possibilidade de revestir o aço carbono com sistemas bicamadas SiOx/SiOxCyHz através da combinação de metodologia de deposição e oxidação em plasmas de baixa pressão. Para tanto, filmes do tipo SiOxCyHz foram depositados a plasma de mistura de HMDSO (70%), O2 (20%) e Ar (10%) excitado por radiofrequência (150 W). A pressão total da atmosfera de deposição foi de 20 Pa. Os filmes foram depositados por 30 min e, posteriormente, expostos a plasmas de O2 (3,3 Pa, 10-300 W, 60 min) com o objetivo de criar uma camada superficial inorgânica. Foram investigados os efeitos da potência de excitação do plasma de O2 na espessura de camada, estrutura química e composição elementar das amostras. Avaliou-se também o efeito da potência do plasma de oxidação nas propriedades de barreira do revestimento depositado sobre aço carbono. Filmes como-depositados foram caracterizados como organosilicones. A exposição ao plasma de oxigênio foi observada remover hidrogênio, carbono e grupos metil da estrutura transformando-a em óxido de silício, sendo, todavia, o grau de conversão e a espessura da camada convertida fortemente dependentes da potência do plasma de oxidação. A resistência do sistema preparado sobre o aço carbono à corrosão foi observada depender da espessura final da camada e também da conectividade da estrutura convertida em sílica mais que do grau de conversão. A condição de tratamento eleita como ótima neste trabalho foi a conduzida com 50 W de potência por criar uma camada superficial inorgânica fina, compacta, com uma estrutura superficial similar a da sílica além de preservar a espessura do filme e aumentar as propriedades de barreira do sistema.
Due to its mechanical properties, welding and low cost, carbon steel is a material widely used in several sectors. However, carbon steel is easily oxidized when exposed to the environment. To avoid this problem, some work suggests the development of protective coating using plasma deposition techniques based on the compound hexamethyldisiloxane, HMDSO. From this compound it is possible to obtain from organosilicones structures to inorganic by changing the parameters of deposition. Silicon oxide type coatings are more resistant to corrosion than organosilicones, but their physical stability is lower. With the objective of associating the favorable properties of both types of coatings, the present work investigated the possibility of coating the carbon steel with SiOx/SiOxCyHz bilayer systems through the combination of deposition and oxidation methodology in low pressure plasmas. For that, SiOxCyHz films were deposited in a mixture plasma of HMDSO (70%), O2 (20%) and Ar (10%) excited by radiofrequency (150 W). The total pressure of the atmosphere of deposition was 20 Pa. The films were deposited for 30 min and subsequently exposed to O2 plasmas (3.3 Pa, 10-300 W, 60 min) to create an inorganic surface layer. The effects of the excitation power of the O2 plasma on the layer thickness, chemical structure and elemental composition of the samples were investigated. The effect of the oxidation plasma power was also evaluated in the barrier properties of the coating deposited on carbon steel. As-deposited films were characterized as organosilicones. Exposure to oxygen plasma was observed to remove hydrogen, carbon and methyl groups from the structure transforming it into a silicon oxide, however, the degree of conversion and the thickness of the converted layer is strongly dependent on the power of the oxidation plasma. The corrosion resistance of the system prepared on carbon steel was observed to depend on the final thickness of the layer and also on the connectivity of the structure converted to silica rather than the degree of conversion. The treatment condition chosen as optimal in this work was the one conducted with 50 W of power by creating a thin, compact, inorganic surface layer with a silica-like surface structure in addition to preserving the film thickness and increasing the barrier properties of the system.
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Queiroz, José Renato Cavalcanti de [UNESP]. "Filmes de SiOx crescidos em substrato de zircônia tetragonal policristalina estabilizada por ítria: influência na durabilidade da adesão a cimentos resinosos." Universidade Estadual Paulista (UNESP), 2011. http://hdl.handle.net/11449/105537.
Full textCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
Este estudo comparou o efeito de filmes à base de Si depositados pela técnica reactive magnetron sputtering com o uso do jateamento de partículas de alumina e a aplicação de primer na adesão de cimentos resinoso a superfície de zircônia. Blocos de zirconia (N=300) (4,5×4,5)mm foram sinterizados e regularizados com lixas de SiC (1200), sonicamente limpos com água destilada por 10 min e randomicamente divididos em 30 grupos (n=10) de acordo com 3 parâmetros: 1- cimento resinoso (Panavia/Kuraray; Multilink/Ivoclar; RelyX U100/3M); 2- tratamento de superfície (sem tratamentocontrole, Metal/Zirconia Primer, jateamento com partículas + Metal/Zirconia Primer, Filme A + Monobond S; Filme B + Monobond S); 3- termociclagem (TC). Parâmetros de rugosidade da superfície (Ra, Rz, Sdr) foram avaliados por Microscopia de Interferência e Microscopia Eletrônica de Varredura (MEV). Cilindros de cimento resinoso foram construídos (Ø: 2,4 mm; altura: 2 mm) sobre a superfície de zirconia. O ensaio de resistência adesiva ao cisalhamento foi realizado no momento inicial (24 h) e após a termociclagem (5o- 55oC, 6.000 ciclos) utilizando máquina de ensaio universal (1 mm/min). As superfícies fraturadas foram analisadas por microscopia ótica (30×) e MEV (100× e 2000×) para categorizar o modo de falha. Adicionais blocos de zirconia (15×15)mm confeccionados para análises por Espectroscopia por Retroespalhamento de Rutheford (RBS), e Trabalho de Adesão (WA) após os tratamentos de superfície. Os dados foram estatisticamente analisados por Anova 3-fatores e 11 teste Tukey (5%). Fotomicrografias revelaram microdefeitos nos filmes. Os resultados de Wa mostraram que os filmes melhoraram a molhabilidade da superfície. As análises por RBS mostraram que a concentração elementar dos filmes...
This study compared the effect of si-based nanofilm deposition using reactive magnetron sputtering to application of air-abrasion (alumina particles) and zirconia primers on the adhesion of resin cements to zirconia. Zirconia (Nblocks=300) (4.5 mm × 3.5 mm × 4.5 mm) were sintered, ground finished to 1200 SiC paper and cleaned ultrasonically in distilled water for 10 min. The blocks were randomly divided into 30 groups (n=10) according to 3 testing parameters: 1- Resin Cements (Panavia/Kuraray; Multilink/Ivoclar; RelyX U100/3M); 2- Surface conditioning (no conditioning-control, Metal/Zirconia Primer, air-abrasion + Metal/Zirconia Primer, Sibased film A + Monobond S; Si-based film B + Monobond S); 3- Aging (with and without). Surface roughness parameters (Ra, Rz, Sdr) before and after surface conditioning were evaluated using interference microscopy (IM). Rutheford Backscattering Spectroscopy (RBS), Scanning Electron Microscopy (SEM), and Work of Adhesion (WA) analyses were performed after surface treatments. Resin cements were incrementally built up (Ø: 2.4 mm; height: 4 mm) on the zirconia surfaces. Bonded specimens were then thermocycled (5o-55oC, 6,000 cycles). Shear bond strength (SBS) was performed using the Universal Testing Machine (1 mm/min). After fracture, the surfaces were analyzed using an optical microscopy (30 ×), SEM (100 × and 2000 ×) to categorize the failure modes. The data were statistically evaluated using 3-way ANOVA and Tukey's test (5%). Scanning Electron Microscopy showed micro defects on Si-based nanofilms surface. The result to Wa showed that surface coated with Si-based nanofilms improved wetability when compared to the other surface treatments. RBS analysis showed that was produced films with different chemical elemental concentration. While air-abraded... (Complete abstract click electronic access below)
Queiroz, José Renato Cavalcanti de. "Filmes de SiOx crescidos em substrato de zircônia tetragonal policristalina estabilizada por ítria : influência na durabilidade da adesão a cimentos resinosos /." São José dos Campos : [s.n.], 2011. http://hdl.handle.net/11449/105537.
Full textCoorientador: Marcos Massi
Banca: Luiz Felipe Valandro
Banca: Argemiro Soares da Silva Sobrinho
Banca: Rodrigo Othavio de Assunção e Souza
Banca: Marco Cícero Bottino
Resumo: Este estudo comparou o efeito de filmes à base de Si depositados pela técnica reactive magnetron sputtering com o uso do jateamento de partículas de alumina e a aplicação de primer na adesão de cimentos resinoso a superfície de zircônia. Blocos de zirconia (N=300) (4,5×4,5)mm foram sinterizados e regularizados com lixas de SiC (1200), sonicamente limpos com água destilada por 10 min e randomicamente divididos em 30 grupos (n=10) de acordo com 3 parâmetros: 1- cimento resinoso (Panavia/Kuraray; Multilink/Ivoclar; RelyX U100/3M); 2- tratamento de superfície (sem tratamentocontrole, Metal/Zirconia Primer, jateamento com partículas + Metal/Zirconia Primer, Filme A + Monobond S; Filme B + Monobond S); 3- termociclagem (TC). Parâmetros de rugosidade da superfície (Ra, Rz, Sdr) foram avaliados por Microscopia de Interferência e Microscopia Eletrônica de Varredura (MEV). Cilindros de cimento resinoso foram construídos (Ø: 2,4 mm; altura: 2 mm) sobre a superfície de zirconia. O ensaio de resistência adesiva ao cisalhamento foi realizado no momento inicial (24 h) e após a termociclagem (5o- 55oC, 6.000 ciclos) utilizando máquina de ensaio universal (1 mm/min). As superfícies fraturadas foram analisadas por microscopia ótica (30×) e MEV (100× e 2000×) para categorizar o modo de falha. Adicionais blocos de zirconia (15×15)mm confeccionados para análises por Espectroscopia por Retroespalhamento de Rutheford (RBS), e Trabalho de Adesão (WA) após os tratamentos de superfície. Os dados foram estatisticamente analisados por Anova 3-fatores e 11 teste Tukey (5%). Fotomicrografias revelaram microdefeitos nos filmes. Os resultados de Wa mostraram que os filmes melhoraram a molhabilidade da superfície. As análises por RBS mostraram que a concentração elementar dos filmes... (Resumo completo, clicar acesso eletrônico abaixo)
Abstract: This study compared the effect of si-based nanofilm deposition using reactive magnetron sputtering to application of air-abrasion (alumina particles) and zirconia primers on the adhesion of resin cements to zirconia. Zirconia (Nblocks=300) (4.5 mm × 3.5 mm × 4.5 mm) were sintered, ground finished to 1200 SiC paper and cleaned ultrasonically in distilled water for 10 min. The blocks were randomly divided into 30 groups (n=10) according to 3 testing parameters: 1- Resin Cements (Panavia/Kuraray; Multilink/Ivoclar; RelyX U100/3M); 2- Surface conditioning (no conditioning-control, Metal/Zirconia Primer, air-abrasion + Metal/Zirconia Primer, Sibased film A + Monobond S; Si-based film B + Monobond S); 3- Aging (with and without). Surface roughness parameters (Ra, Rz, Sdr) before and after surface conditioning were evaluated using interference microscopy (IM). Rutheford Backscattering Spectroscopy (RBS), Scanning Electron Microscopy (SEM), and Work of Adhesion (WA) analyses were performed after surface treatments. Resin cements were incrementally built up (Ø: 2.4 mm; height: 4 mm) on the zirconia surfaces. Bonded specimens were then thermocycled (5o-55oC, 6,000 cycles). Shear bond strength (SBS) was performed using the Universal Testing Machine (1 mm/min). After fracture, the surfaces were analyzed using an optical microscopy (30 ×), SEM (100 × and 2000 ×) to categorize the failure modes. The data were statistically evaluated using 3-way ANOVA and Tukey's test (5%). Scanning Electron Microscopy showed micro defects on Si-based nanofilms surface. The result to Wa showed that surface coated with Si-based nanofilms improved wetability when compared to the other surface treatments. RBS analysis showed that was produced films with different chemical elemental concentration. While air-abraded... (Complete abstract click electronic access below)
Doutor
Dresch, Mauro André. "Aplicação de catalisadores PtSn/C e membranas Nafion-SiO2 em células a combustível de etanol direto em elevadas temperaturas." Universidade de São Paulo, 2014. http://www.teses.usp.br/teses/disponiveis/85/85134/tde-06102014-102906/.
Full textThis work has as objective to evaluate anodes and electrolytes in direct ethanol fuel cells (DEFC) operating at high temperature (130 ºC). As anode materials, electrocatalysts based on PtSn/C were prepared by Modified Polyol Method with various Pt:Sn atomic ratios. Such methodology promotes selforganized electrocatalysts production with narrow particle size distribution and high alloying degree. The eletrocatalysts were characterized by XRD, and CO stripping. The results showed that these materials presented high alloying degree and Eonset CO oxidation at lower potential as commercial materials. As electrolyte, Nafion-SiO2 hybrids were synthesized by sol-gel reaction, by the incorporation of oxide directly into the ionic aggregates of various kinds of Nafion membranes. The synthesis parameter, such sol-gel solvent, membrane thickness and silicon precursor concentration were studied in terms of silica incorporation degree and hybrid mechanical stability. Finally, the optimized anodes and electrolytes were evaluated in DEFC operating at 80 130 ºC temperature range. The results showed a significant improvement of the DEFC performance (122 mW cm-2), resulted from the acceleration of ethanol oxidation reaction rate due to anode material optimization and high temperature operation once the use of hybrids possibilities the increase of temperature without a significant conductivity loses. In this sense, the combination of optimized electrodes and electrolytes are a promising alternative for the development of these devices.
Dresch, Mauro André. "Síntese e caracterizção eletroquímica de membranas híbridas Nafion-SIO2 para a aplicação como eletrólito polimérico em células a combustível tipo PEM." Universidade de São Paulo, 2009. http://www.teses.usp.br/teses/disponiveis/85/85134/tde-26092011-141218/.
Full textIn this work, the effect of sol-gel synthesis parameters on the preparation and polarization response of Nafion-SiO2 hybrids as electrolytes for proton exchange membrane fuel cells (PEMFC) operating at high temperatures (130 oC) was evaluated. The inorganic phase was incorporated in a Nafion matrix with the following purposes: to improve the Nafion water uptake at high temperatures (> 100 oC); to increase the mechanical strength of Nafion and; to accelerate the electrode reactions. The hybrids were prepared by an in-situ incorporation of silica into commercial Nafion membranes using an acid-catalyzed sol-gel route. The effects of synthesis parameters, such as catalyst concentration, sol-gel solvent, temperature and time of both hydrolysis and condensation reactions, and silicon precursor concentration (Tetraethylorthosilicate TEOS), were evaluated as a function on the incorporation degree and polarization response. Nafion-SiO2 hybrids were characterized by gravimetry, thermogravimetric analysis (TGA), scanning electron microscopy and X-ray dispersive energy (SEM-EDS), electrochemical impedance spectroscopy (EIS), and X-ray small angle scattering (SAXS). The hybrids were tested as electrolyte in single H2/O2 fuel cells in the temperature range of 80 130 oC and at 130 oC and reduced relative humidity (75% and 50%). Summarily, the hybrid performance showed to be strongly dependent on the synthesis parameters, mainly, the type of alcohol and the TEOS concentration.
Vecchi, Pierpaolo. "Caratterizzazione elettrica e spettroscopia superficiale di film sottili a base di silicio." Bachelor's thesis, Alma Mater Studiorum - Università di Bologna, 2018. http://amslaurea.unibo.it/16338/.
Full textMcConkie, Thomas O. "Curious Growth of a Buried SiO2 Layer." BYU ScholarsArchive, 2012. https://scholarsarchive.byu.edu/etd/3755.
Full textQuiroga, Jean-Manuel. "Étude des propriétés optiques de multicouches a-Si:H/a-SiO2." Grenoble 1, 1998. http://www.theses.fr/1998GRE10124.
Full textAndrade, Gessie Maria Silva de. "Oxidação parcial de metano a compostos oxigenados (HCHO e CH3OH) sobre catalizadores oxidos MoOx/MgO-SiO2 e VOx-SiO2." [s.n.], 2003. http://repositorio.unicamp.br/jspui/handle/REPOSIP/267468.
Full textTese (doutorado) - Universidade Estadual de Campinas, Faculdade de Engenharia Quimica
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Resumo: A utilização cada vez maior do gás natural como combustível deve-se ao aumento da demanda de energia nos países em crescimento acompanhado da disponibilidade crescente das reservas de gás em relação às de petróleo, o que pode tomá-Io uma fonte de energia de grande importância neste século XXI. O metano é o componente presente em maior quantidade no gás natural, constituindo mais de 90% da fração dos hidrocarbonetos. Um dos processos mais utilizados para funcionalização das moléculas de hidrocarbonetos, tais como o metano, é a oxidação parcial. Desta forma, no presente estudo foi realizada a oxidação parcial do metano a compostos oxigenados (HCHO e CH30H) a pressão atmosférica utilizando catalisadores de óxidos redutíveis de MoOx/MgO-Si02 e VOx/MgO-Si02 com a finalidade de investigar a influência da introdução de MgO no suporte dos catalisadores e da concentração superficial de Mo+n e V+n na atividade e seletividade destes catalisadores, assim como o efeito da razão CH4:O2 na cinética desta reação. Os óxidos mistos de MgO- Si02 foram preparados em razões atômicas preestabelecidas (Mg:Si = 1:0, 3:1,2:1, 1:1, 1:3, 1:2 e 0:1), secos e calcinados a 400 K por 12 horas e 1050 K por 5 horas, respectivamente. O método para a introdução da fase ativa Mo ou V nos suportes foi a impregnação incipiente, obedecendo-se seis diferentes percentagens em peso de Mo+6 ou V+5 nos sólidos finais: 0,1%, 1,67%, 2,2 %, 3,25%, 4,82%, 6,4%, os quais foram caracterizados por difração de raios-X, adsorção de N2 e adsorção seletiva de O2. Os principais produtos observados para a reação em estudo foram HCHO, CO, CO2, sendo que HCHO e CH30H (produtos de oxidação parcial) foram favorecidos por altas razões molares de CH4:O2. A formação de CH3OH foi observada em teores moderados de óxidos metálicos (0:l[Mg:Si]/0,I%Mo e 0:1[Mg:Si]/3,25%Mo), os quais apresentaram consideráveis seletividades para esse produto (32% e 18%, respectivamente). Os resultados obtidos para as constantes de velocidade demonstraram que para baixas conversões, a seletividade para HCHO se aproxima de 100%, enquanto a seletividade para CO2 se manteve em valores baixos, próximos de zero, mostrando que em condições diferenciais (conversão de CH4 < 10%) a velocidade de formação de HCHO é maior que a velocidade de formação de CO2
Abstract: Methane is the major component of natural gas, often present as more than 90% of the gas. Current1y it is primarily used as a fuel. In the chemical industry it is used in the production of synthesis gas, hydrogen, and in the manufacture of the halogen derivatives of methane, acetylene, hydrogen cyanide, technical carbon, and many other products. The direct conversion of methane to formaldehyde and methanol in a single catalytic step in sufficient1y high yield would give rise to new opportunities in the conversion of natural gas to other useful fuels and chemicals. Both the homogeneous and heterogeneous processes have been studied under various conditions although progress toward obtaining a yield that would make such a process industrially viable has been very slow. The majority of these studies have involved metal oxide catalysts. In this work, the selective oxidation of methane to oxygenated compounds (HCHO e CH3OH) at atmospheric pressure was studied on MoOxfMgO-SiO2 and VOx/MgO-SiO2. The mixed oxides of magnesia and silica were prepared in different atom ratios (Mg:Si = 1:0, 3:1,2:1, 1:1, 1:3, 1:2 or 0:1), dried at 400 K for 12 h and calcined at 1050 K for 5 h. The active phase, Mo (H24Mo7N6O24) or V (H4NO3 V), was added to the supports by the incipient wetness method. The percentages of Mo or V added to the mixed oxides were 0,1%, 1,67%,2,2%,3,25%,4,82% or 6,4%. The solids were characterized by X-ray diffraction, BET surface area and oxygen chemisorption. The objective of the present work was to study the influence of the introduction of MgO in the supports, of the amount of Mo and V on the surface of the supports and of the CH4:O2 molar ratios. Both supported Mo and V oxides were active in the conversion of methane to C1-oxygenates and Cox. The main products of the oxidation reaction were HCHO, CO and CO2. The partial oxidation products (HCHO, CH30H) were favored by high CH4:O2 molar ratios and formaldehyde was the first oxidation product, which was further oxidized to CO. The vanadium oxide catalysts were more active than the molybdenum oxide catalysts in conversion of methane. However, the higher reaction rate also resulted in a further oxidation of HCHO to CO
Doutorado
Desenvolvimento de Processos Químicos
Doutor em Engenharia Química
Soares, Liliana do Amaral. "Cu/SiO2 : catalisador reciclável para a síntese one pot de triazóis." reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2013. http://hdl.handle.net/10183/97958.
Full textThe search for new technologies has inspired the science in all areas of chemistry and one of the most studied research fields lays on the search for natural product's mimetics. A good example, among different efforts for simple and efficient new methods of synthesis, is the click chemistry and its Cu catalysed 1,3-dipolar cycloaddition, once this reaction permits quick acess to 1,4-disubstituted-1,2,3-triazoles. In this work we synthesized a copper catalyst through the sol-gel methodology, so called Cu-silica and tested it in the 1,3-cycloaddition reaction, using different starting materials and energy sources. At first we applied this catalyst in a multicomponent reaction in which benzyl bromides, sodium azide and different acetylenes and the reaction was heated for 12 hours or 10 minutes under microwave irradiation (50W), providing the 1,2,3-triazoles with 95% of yield. Further we changed the benzyl halides for boronic acids; we didn’t have success using non-classical heating systems (microwave or ultrasound), however under traditional heating at 50º C for 48 hours we got the product in 91% yield. Finally we developed a new one-pot metodology to obtain 1,2,3-triazoles from alchools. This procedure consists in a two-step continuous system embracing three transformations wihtin 25 hours with an overall yield of 60%.
Ray, Samuel L. "Evaluation of a High School Sheltered Instruction Observation Protocol (SIOP) Implementation." DigitalCommons@USU, 2011. https://digitalcommons.usu.edu/etd/848.
Full textLi, Bin, and 李斌. "A study of integrated semiconductor thin-film sensors on sio2/si substrate." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2001. http://hub.hku.hk/bib/B30446752.
Full textLi, Bin. "A study of integrated semiconductor thin-film sensors on sio2/si substrate." Hong Kong : University of Hong Kong, 2001. http://sunzi.lib.hku.hk/hkuto/record.jsp?B23000995.
Full textFeltrin, Jucilene. "Estabilização a elevadas temperaturas da fase anatase com partículas submicrométricas de SiO2." reponame:Repositório Institucional da UFSC, 2012. http://repositorio.ufsc.br/xmlui/handle/123456789/100746.
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Este estudo descreve rotas desenvolvidas para obter a estabilidade da fase anatase em temperaturas acima de 900oC, através da mistura via seco de titânia e estabilizantes (quartzo e sílica amorfa), prensagem e tratamento térmico em condições industriais típicas da cerâmica de revestimento. A avaliação das fases obtidas após tratamento térmico foi realizada por difração de raios-X e por microscopia eletrônica de varredura. Em termos de processamento, as composições que revelaram maior estabilidade da fase anatase foram aquelas em que se utilizou uma titânia com maior tamanho de partícula e com dopante quartzo. Após a avaliação dos resultados foram estudados os possíveis mecanismos de formação da fase anatase e como estes foram afetados pela adição dos dopantes. Por fim, propõe-se uma rota para a estabilização da fase anatase a partir das características da titânia, dopantes e tratamento térmico. A obtenção da fase anatase em revestimentos cerâmicos é promissora e está sendo amplamente estudada por diversos pesquisadores devido à propriedade fotocatalítica deste material, capaz de degradar uma grande variedade de poluentes orgânicos tóxicos em substâncias menos inofensivas.
Abstract : This study describes routes developed to obtain the anatase phase stability at temperatures above 900oC, by blending via dried and titania stabilizers (quartz and amorphous silica), pressing and heat treatment in typical industry conditions of ceramic coating. The evaluation of the phase obtained after heat treatment was carried out by X-ray diffraction and scanning electron microscopy. In terms of processing, the compositions that showed increased stability of anatase, were those which used a titania with higher particle size and with dopant quartz. After the evaluation of the results, we studied the possible mechanisms formation of the anatase phase and how they were affected by the addition of dopants. Finally, a route is proposed for stabilizing the anatase phase from the characteristics of titania, doping and thermal treatment. The anatase phase coatings are being extensively studied by many researchers due to photocatalytic property of the material, capable of degrading a variety of toxic organic pollutants into less harmless substances.
Kramerová, Nina. "Vliv mineralizátorů na slinování a fázové transformace v soustavě Li2O-Al2O3-SiO2." Master's thesis, Vysoké učení technické v Brně. Fakulta chemická, 2010. http://www.nusl.cz/ntk/nusl-216638.
Full textThyssen, Vivian Vazquez. "Catalisadores Ni/MgO-SiO2 aplicados na reação de reforma a vapor de glicerol." Universidade de São Paulo, 2016. http://www.teses.usp.br/teses/disponiveis/75/75134/tde-29062016-162740/.
Full textNi catalysts (10wt%) supported on MgO-SiO2 were assessed in glycerol steam reforming reaction. The effects of MgO as additive and preparation method were evaluated on physico-chemical and textural materials properties; as their activity, selectivity, stability and carbon formation in glycerol steam reforming. The catalysts were prepared with different amounts of MgO (10wt%, 30wt% and 50wt%) on commercial SiO2 by dry process (physical mixture) and wet process (sequential impregnation with water, ethanol and acetone as solvents). Samples were characterized by energy dispersive X-ray spectroscopy, nitrogen physisorption, X-ray diffraction, thermogravimetry, in situ X-ray diffraction with O2, temperature programmed reduction with H2, in situ X-ray diffraction with H2, temperature programmed desorption with H2 and scanning electron microscopy. It was observed that the Ni(II) interacts differently with supports with different MgO content, and the polarity of impregnation solvent used in preparation process influences on catalysts properties. In order to evaluated the activity, selectivity and carbon deposition, the catalysts were tested in glycerol steam reforming reaction at 600oC for 5h and water:glycerol molar ratio of 12:1. After reaction, carbon deposits obtained during the catalytic process were characterized by thermogravimetry, X-ray diffraction and scanning electron microscopy. Mixed matrices catalysts were active in glycerol steam reforming and showed similar selectivity for the gaseous products (H2, CH4, CO and CO2), with a high H2 yield. It was observed that the addition of MgO increased Ni(II) dispersion on material, which influenced on the quantity of carbon deposited during reaction. Polarity of impregnation solvent had also influence on metallic dispersion, and smaller the solvent polarity, higher the dispersion obtained in the catalyst, and lower the carbon deposition on reaction. The material that showed the best catalytic performance in H2 yield and carbon deposition, was the catalyst prepared with 30wt% of MgO with ethanol as impregnation solvent.
Nezval, David. "Výpočty interakce systému grafen/SiO2 s adsorbovanými atomy a molekulami pomocí DFT metod." Master's thesis, Vysoké učení technické v Brně. Fakulta strojního inženýrství, 2015. http://www.nusl.cz/ntk/nusl-231953.
Full textSanjon, Elvira Prisca [Verfasser], Barbara Akademischer Betreuer] Drossel, and Michael [Akademischer Betreuer] [Vogel. "A molecular dynamics investigation of tetrahedral liquids and aqueous solutions in bulk (SiO2 ) and confinements (SiO2, H2O, water-octanol mixtures) / Elvira Prisca Sanjon ; Barbara Drossel, Michael Vogel." Darmstadt : Universitäts- und Landesbibliothek Darmstadt, 2018. http://d-nb.info/1173899154/34.
Full textSanjon, Elvira Prisca Verfasser], Barbara [Akademischer Betreuer] Drossel, and Michael [Akademischer Betreuer] [Vogel. "A molecular dynamics investigation of tetrahedral liquids and aqueous solutions in bulk (SiO2 ) and confinements (SiO2, H2O, water-octanol mixtures) / Elvira Prisca Sanjon ; Barbara Drossel, Michael Vogel." Darmstadt : Universitäts- und Landesbibliothek Darmstadt, 2018. http://d-nb.info/1173899154/34.
Full textKrishnamoorthy, Soumya. "Development of a ZnO/SiO₂/Si high sensitivity interleukin-6 biosensor." College Park, Md. : University of Maryland, 2007. http://hdl.handle.net/1903/6702.
Full textThesis research directed by: Electrical Engineering. Title from t.p. of PDF. Includes bibliographical references. Published by UMI Dissertation Services, Ann Arbor, Mich. Also available in paper.
Santos, Daniele Cristina Almeida Hummel Pimenta. "Obtenção e caracterização de materiais dopados SiO2-CdSe a partir de sonogeis de silica." [s.n.], 1994. http://repositorio.unicamp.br/jspui/handle/REPOSIP/265224.
Full textTese (doutorado) - Universidade Estadual de Campinas, Faculdade de Engenharia Mecanica
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Resumo: O processo de obtenção de materiais pela via sol-gel tem-se mostrado muito interessante na obtenção de novos materiais como atesta o grande número de trabalhos desenvolvidos na última década. A possibilidade de obter materiais sólidos monolíticos assim como pós, filmes e fibras a partir de uma mistura no estado líquido à temperatura ambiente através de reações de agregação e polimerização é particularmente interessante. A fácil manipulação da composição química precursora permite criar materiais compósitos com propriedades ópticas, eletrônicas, químicas, mecânicas especiais para aplicações em alta tecnologia. Em particular, os materiais compostos de uma matriz vítrea com inclusão de nanocristais semicondutores apresentam propriedades ópticas não-lineares e são considerados de grande importância tecnológica em aplicações estratégicas, como comunicação e processamento de informações. Neste trabalho apresentamos os resultados da obtenção de materiais compostos por partículas semicondutoras imersas numa matriz ele sílica gel. As matrizes hospedeiras foram preparadas por hidrólise do tetraetilortosilicato (TEOS) com adição de nitrato de cádmio. Como agente controlador da cinética ele secagem (drying control chemical additive -DCCA) foram usadas a formamida e a N-N-dimetilformamida. O processo de preparação incluiu a aplicação de doses pré-determinadas de ultrasom de alta potência. As matrizes foram caracterizadas através de técnicas de análise térmica (ADT e ATG), adsorção de gases (BET), picnometria de mercúrio, microscopia eletrônica de varredura (SEM) e espalhamento de raios X a baixos ângulos (SAXS). A impregnação do "sonogel" seco com uma solução de KSeCN realizada em condições de vácuo, permitiu a formação de nanocristais de seleneto de cádmio (CdSe) e melhorou as propriedades mecânicas da matriz. Xerogéis vermelhos e transparentes foram obtidos e caracterizados por espectroscopia óptica de absorção, microscopia eletrônica por transmissão (TEM) e SAXS. Os resultados desses estudos levam a propor um modelo estrutural para estes materiais consistente em uma matriz porosa contendo nanocristais de seleneto de cádmio, apresentando uma distribuição de tamanhos bimodal que depende da concentração de selênio na solução usada para a difusão líquida. O deslocamento das bandas de absorção óptica para grandes energias ("blue shift") revela o confinamento quântico nos nanocristais de seleneto de cádmio
Abstract: The sol-gel process has proved to be extremely interesting in the production of new materiaIs. This is clearly indicated by the great number of publications in this area in the last decade. The possibility of obtaining monolithic solid materials and also powders, films and fibers from a liquid mixture of components at room temperature via aggregation and polymerization reactions is particularly interesting. The easy way in which chemical composition can be modified allows the preparation of composite materiais with specific optical, electronic, chemicalor mechanical properties designed for special applications in modern tecnology. In particular, materiaIs consisting in a vitreous matrix with embedded nanocrystals of semiconductor compounds are known to present non-linear optical properties wich makes them very important in strategic technological applications, such as communications and data processing. In this work we present the results of the preparation of materials consisting of semiconducting nanoparticles embedded in a silica gel matrix. The host matrices were prepared by hydrolysis of tretaethylortosilicate (TEOS) with the addition of cadmium nitrate. Two different additives were used as a drying control agent (DCCA) : formamide and N-Ndimethylformamide. The preparation process included the use of pre-determined doses of high power ultrasound. The matrices were characterized by thermal analyses (TGA and DTA), gas adsorption techniques (BET), mercury picnometry, scanning electron microscopy (SEM) and small angle X ray scattering (SAXS). The impregnation of the dry "sonogels" using a KSeCN solution under vacuum, led to the formation of CdSe nanocrystals and improved the mechanical properties of the matrix. Typically red, transparent xerogels were obtained and characterized by optical absorption spectroscopy, transmission electron microscopy (TEM), and SAXS. The results of this study lead to propose a structural model for these materials, consisting of a porous matrix containing CdSe nanocrystals with a bimodal size distribution that depends on the selenium content in the solution used for the liquid diffusion. The shift in the optical absorption band towards higher energies (blue shift) revcals the quantum confinement in the nanosized particles of cadmium selenide
Doutorado
Doutor em Engenharia Mecânica
Taghi, Khani Arefeh. "Characterization of growth of GaAs on Si/SiO2 via a thin layer of perovskite." Thesis, University of Sheffield, 2015. http://etheses.whiterose.ac.uk/11433/.
Full textBohnlein, Ivy Briana 1974. "Wounded Knee in 1891 and 1973: Prophets, protest, and a century of Sioux resistance." Thesis, The University of Arizona, 1998. http://hdl.handle.net/10150/278658.
Full textDong, Tianqi. "A study of infrared femtosecond laser irradiation on monolayer graphene on SiO2/Si substrate." Thesis, University of Cambridge, 2018. https://www.repository.cam.ac.uk/handle/1810/275642.
Full textWilliams, Michael Shawn. "An Investigation of Internalizing Social-Emotional Characteristics in a Sample of Lakota Sioux Children." DigitalCommons@USU, 1997. https://digitalcommons.usu.edu/etd/6306.
Full textKalinová, Helena. "Vliv mineralizátorů na šířku intervalu slinování a fázové transformace v soustavě Li2O-Al2O3-SiO2." Master's thesis, Vysoké učení technické v Brně. Fakulta chemická, 2008. http://www.nusl.cz/ntk/nusl-216345.
Full textGodinho, Vanda. "Synthesis and characterization of magnetron sputtered thin films of the Ti-Al-Si-N(O) system." Doctoral thesis, Universite Libre de Bruxelles, 2011. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/209969.
Full textIn each chapter the individual conclusions from that particular chapter are presented, a summary of the most relevant conclusions and achievements is listed below.
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Doctorat en Sciences de l'ingénieur
info:eu-repo/semantics/nonPublished
Ribeiro, Renata Uema. "Nanopartículas de Co suportadas em SiO2 : síntese, caracterização e propriedades catalíticas para a reforma a vapor do etanol." Universidade Federal de São Carlos, 2007. https://repositorio.ufscar.br/handle/ufscar/3982.
Full textUniversidade Federal de Sao Carlos
Colloidal Co Nanoparticles (Co-NPs) were used to prepare supported Co catalysts. The Co- NPs were obtained by thermal decomposition of the precursor Co2(CO)8 in the presence of oleic acid and trioctylphosphine oxide (TOPO), in an inert atmosphere (Ar). The Co- NPs/SiO2 were obtained by impregnation of a colloidal suspension of nanoparticles on the support no-porous SiO2. The effect of the solvent (ethanol and methanol) used in the step of precipitation of the particles, and by tuning the oleic acid/precursor ratio in the catalytic properties for the steam reforming of ethanol were investigated. The catalysts were characterized by Specific Superficial Area (SBET) and Fourier Transform Infrared Spectroscopy of the CO adsorbed (FTIR-CO). By tuning the oleic acid/precursor ratio it was possible to obtain particles sizes in the 2 and 17nm range. The results of FTIR-CO showed that the samples present the band of CO lineally adsorbed in the same position independent of the synthesis conditions, suggesting similar electronic density of the sites of Co. The results of adsorption of H2 and CO suggest that the fraction of acessible sites of Co so much to H2, as to CO, depends on the particles sizes and the residual oleic acid . Then with the increase of the particles sizes, there is a maximum of accessible sites of Co. For the same particle size, it is obtained an increase of the number of accessible sites of Co, using methanol as solvent for precipitation, suggesting smaller recovering. The catalysts prepared with Co-NPs present profiles of similar catalytic activity for the steam reforming of ethanol. Starting from reaction data a mechanism was proposed: in low temperatures, the molecule of ethanol adsorbs in the catalyst surface and it suffers dehydrogenation producing acetaldehyde. The increase of the temperature favors the formation of species CH4 and CO, suggesting the crack of the C-C bond of acetaldehyde for the formation of these products. The activity for the reforming reactions on the Co-NPs/SiO2 begins in approximately 350ºC, suggesting that the activation of the water occurs in this temperature. Therefore it is suggested the oxidation of adsorbed species CHx and CO for the formation of the products CO e CO2, respectively, occurred in temperatures above 350ºC. The catalytic activity depends on the fraction of accessible sites of Co. The reactions results demonstrate that the catalysts prepared with methanol presented higher catalytic activity for the reforming reaction, possibly due to the presence of a larger number of accessible sites of Co.
Nanopartículas coloidais de Co (Co-NPs) foram utilizadas na preparação de catalisadores de Co suportados. As Co-NPs foram obtidas por decomposição térmica do precursor octacarbonil dicobalto (Co2(CO)8), na presença de ácido oléico e óxido de trioctilfosfina (TOPO), sob atmosfera inerte (Ar). Os catalisadores Co-NPs/SiO2 foram obtidos por impregnação de uma suspensão coloidal de nanopartículas sobre o suporte. O efeito do solvente (etanol e metanol) utilizado na etapa de precipitação das partículas, e a variação da razão ácido oléico/precursor nas propriedades catalíticas para a reforma a vapor do etanol foram investigados. Os catalisadores foram caracterizados por meio de Área Superficial Específica (SBET) e Espectroscopia de Reflectância Difusa na Região do Infravermelho com Transformada de Fourier do CO adsorvido (FTIR-CO). Variando-se a razão ácido oléico/precursor foi possível obter uma faixa de tamanho de partículas entre 2 e 17nm. Os resultados de FTIR-CO revelaram que as amostras apresentam a banda do CO linearmente adsorvido na mesma posição independente das condições de síntese, sugerindo similar densidade eletrônica dos sítios de Co. Os resultados de quimissorção de H2 e CO sugerem que a fração de sítios de Co acessíveis tanto ao H2, como ao CO, dependem do tamanho das partículas e do ácido oléico residual. Assim, com o aumento do tamanho das partículas, têmse um máximo de sítios de Co acessíveis. Para um mesmo tamanho de partícula obtém-se um aumento do número de sítios de Co acessíveis, quando se utiliza metanol como solvente de precipitação das partículas, sugerindo menor recobrimento pelo ácido oléico. Os catalisadores preparados com Co-NPs apresentam perfis de atividade catalítica semelhante para a reação de reforma a vapor do etanol. A partir de dados de reação um mecanismo foi proposto: em temperaturas baixas a molécula de etanol adsorve na superfície do catalisador e sofre desidrogenação, produzindo acetaldeído. O aumento da temperatura favorece o aparecimento de espécies CH4 e CO, sugerindo a quebra da ligação C-C do acetaldeído para a formação destes produtos. A atividade para as reações de reforma sobre os Co-NPs/SiO2 inicia-se em aproximadamente 350ºC, sugerindo que a ativação da água ocorre nesta faixa de temperatura. Com isso, sugere-se que a oxidação de espécies adsorvidas CHx e CO para a formação dos produtos CO e CO2, respectivamente, ocorra em temperaturas acima de 350ºC. A atividade catalítica depende da fração de sítios de Co acessíveis. Desta forma, os resultados obtidos mostram que o catalisador preparado com metanol apresentou maior atividade catalítica para a reação de reforma, possivelmente devido à presença de um número maior de sítios do Co acessíveis.
Vršecký, Michal. "Studium mechanizmu koroze žáruvzdorných materiálů v soustavě SiO2-Al2O3 taveninami a struskami s vysokým obsahem alkálií a vanadu." Master's thesis, Vysoké učení technické v Brně. Fakulta chemická, 2008. http://www.nusl.cz/ntk/nusl-216208.
Full textRichter, Laura. "A VLBI polarisation study of 43 GHZ SiO masers towards VY CMA /." Link to this resource, 2005. http://eprints.ru.ac.za/784/.
Full textRichter, Laura. "A VLBI polarisation study of 43 GHZ SiO masers towards VY CMA." Thesis, Rhodes University, 2006. http://hdl.handle.net/10962/d1005284.
Full textYazhenskikh, Elena. "Development of a new database for thermodynamic modelling of the system Na2O-K2O-Al2O3-SiO2." [S.l.] : [s.n.], 2005. http://deposit.ddb.de/cgi-bin/dokserv?idn=977928454.
Full textWaechtler, Thomas, Nina Roth, Robert Mothes, Steffen Schulze, Stefan E. Schulz, Thomas Gessner, Heinrich Lang, and Michael Hietschold. "Copper Oxide ALD from a Cu(I) -Diketonate: Detailed Growth Studies on SiO2 and TaN." Universitätsbibliothek Chemnitz, 2009. http://nbn-resolving.de/urn:nbn:de:bsz:ch1-200901741.
Full text© 2009 The Electrochemical Society. All rights reserved.
Hanif, Raza. "Microfabrication of Plasmonic Biosensors in CYTOP Integrating a Thin SiO2 Diffusion and Etch-barrier Layer." Thèse, Université d'Ottawa / University of Ottawa, 2011. http://hdl.handle.net/10393/19880.
Full textBaganha, César Chiesorin. "Considerações sobre a origem da emissão luminosa de Nanocristais de Si em Matriz de SiO2." reponame:Repositório Institucional da UFPR, 2010. http://hdl.handle.net/1884/23720.
Full textClavel, Rojo Luis. "Respuesta ósea a la vitrocerámica del sistema CaSiO3 SiO2 Ca3(PO4). Estudio experimental “in vivo”." Doctoral thesis, Universidad de Murcia, 2011. http://hdl.handle.net/10803/83365.
Full textŠimíková, Michaela. "Selektivní růst kovových materiálů." Master's thesis, Vysoké učení technické v Brně. Fakulta strojního inženýrství, 2009. http://www.nusl.cz/ntk/nusl-228773.
Full textSilva, Mariane Capellari Leite da. "Caracterização físico-química de SiC sintetizado pelo processo Acheson a partir de diferentes fontes de SiO2." Universidade de São Paulo, 2015. http://www.teses.usp.br/teses/disponiveis/97/97134/tde-06052015-165740/.
Full textCurrently, there is a strong demand for ceramics as structural materials to replace metals and alloys with high hardness for use in hostile environments. Among structural ceramics families, silicon carbide stands out due to its unique properties combination: high corrosion/oxidation resistance, high abrasion resistance, low density, high hardness, high thermal conductivity, good thermal shock resistance and maintenance of the majority of these properties at elevated temperatures. The Acheson process is industrially the main synthesis process of silicon carbide, consisting of two solid electrodes connected to compacted graphite powder, surrounded by a mixture of silica and petroleum coke, wherein the heating is performed electrically between 2200 to 2600 oC [SOMIYA, 1991]. The formation of SiC depends on the partial pressure of gases, temperature, reactants grain size, the properties of each individual grain as well as the contact area and the degree of mixing between SiO2 and C [LIDSTAD, 2002]. The SiC produced by the Acheson process contains impurities from the raw materials, such as Al, Fe, Ti and Na, which during the synthesis are influenced by the temperature gradient. Metal or carbides particles of these impurities are distributed in SiC matrix, being found as the temperature decreases, with exception of Al that forms solid solution with SiC by replacing the Si atoms in the crystal lattice [WEIMER, 1997]. The objectives of this work was the characterization and evaluation of the influence of raw materials and process conditions on the behavior of silicon carbide synthesized by Acheson process. It was observed, through chemical, mineralogical and microstructural analyzes, that the distribution of impurities along the cross section of synthesized SiC is independent of the raw material precursor, and these are concentrated in the most distant regions of the graphite core, but its contents are superior to SiC synthesized from a less pure raw material, which also showed a change in the beginning of the SiC oxidation process, at least 50 ° C lower, than the synthesized SiC from raw material with higher purity.
Bertram, Rodney L. "Sheltered Instruction: A Case Study of Three High School English Teachers' Experiences with the SIOP Model." Thesis, University of North Texas, 2011. https://digital.library.unt.edu/ark:/67531/metadc67959/.
Full textJohnson, Norman C. "Assessing Cognitive Abilities in a Sample of Sioux Children Utilizing Traditional and Nonverbal Measures of Intelligence." DigitalCommons@USU, 2006. https://digitalcommons.usu.edu/etd/6238.
Full textRICHARD, GONZALEZ DE LINARES BENEDICTE. "Contribution a l'etude d'un procede d'imagerie radiologique utilisant le photoconducteur a memoire bi : :(12)sio::(20)." Paris 6, 1987. http://www.theses.fr/1987PA066095.
Full textSouza, André Machado Ribeiro de. "A influência da morfologia do MgO nas propriedades catalíticas do SiO2/MgO para a formação de 1,3-Butadieno a partir de etanol." Universidade Federal de São Carlos, 2016. https://repositorio.ufscar.br/handle/ufscar/8013.
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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
Ethanol has been largely studied in the past few decades as a substitute to fossil fuels in the synthesis of a large variety of chemicals. 1,3-Butadiene, one of these compounds, is an important chemical intermediate and also a monomer for some polymers such as synthetic rubbers. It is mainly produced as a by-product from naphtha steam cracking, which has ethylene as the major product. As crude oil prices have been fluctuating in the latest years and with the discovery of shale gas in the US, a promising source for ethylene, there is an urgency for developing alternative routes to produce 1,3-Butadiene. Several studies have been carried since the 1940s trying to create viable processes and using many different catalysts, indicating MgO/SiO2 - with or without the addition of transition metals - as being the most promising one. However, there is still a lot of missing information on how does the interaction between silica and magnesia affect the yields and selectivity. In the present work it was studied how the morphology of the MgO affects the interaction with the SiO2 to generate active sites. The MgO with different morfologies were synthesized and then wet-kneaded with SiO2 to provide catalysts with different MgO/SiO2 ratio. The samples were calcined and catalytic tests were carried out. X-Ray Diffraction, Temperature Programmed Desorption of CO2 and Scanning Electron Microscopy were also performed on the catalysts. The obtained micrographs for the oxides confirmed the successful preparation of different morphologies, and the results for catalytic tests showed that there is some influence from the morphology over conversion and selectivity of SiO2/MgO. For the MgO morphologies at the temperature of 425 oC, ethanol conversions between 11.7% and 21.9% were obtained for different samples, with selectivities for butadiene between 5.6% and 30.4%. For SiO2/MgO catalysts, in the same temperature, different yields were obtained for distinct morphologies and Mg:Si ratios. For 3:1 catalysts, yields between 21.5% and 34.3% were observed, while for 7:1 catalysts the yields vary from 18.5% to 35.4%. Catalytic properties could not be clearly correlated to the TPD-CO2 and specific surface area, indicating that they are dependant on a complex set of factors, among them the accessibility of the surface for the SiO 2 contact. Variation of the silica content for all morphologies showed that the SiO2/MgO ratio is extremely important for the preparation of active and selective catalysts for the production of 1,3-butadiene.
O etanol vem sendo largamente estudado, recentemente, como um substituto aos combustíveis fósseis na síntese de diversos produtos industriais. O 1,3-Butadieno (BD), um destes compostos, é um importante intermediário químico e monômero para alguns polímeros e borrachas sintéticas. BD atualmente é produzido principalmente como um subproduto do craqueamento a vapor do nafta, que tem o etileno como principal produto. Flutuações no preço do petróleo e a descoberta de grandes reservas de shale gas nos Estados Unidos fazem com que haja uma necessidade de busca de rotas alternativas para a produção do BD. Muitos estudos vêm sendo realizados desde os anos 1940, utilizando diferentes catalisadores, indicando o MgO/SiO2 - com ou sem a adição de metais de transição - como o mais promissor. No entanto, ainda falta informação sobre a forma como a interação entre a sílica e a magnésia afeta os resultados da reação. No presente trabalho foi verificada a influência que a morfologia do MgO tem sobre a interação com SiO2 para formação de sítios ativos. As amostras de MgO com diferentes morfologias foram sintetizadas e, então, adicionadas de sílica para gerar os catalisadores com diferentes razões MgO/SiO2. Após calcinação, testes reacionais foram realizados. As amostras de MgO e SiO2 /MgO foram caracterizadas por Difração de Raios-X, Dessorção a Temperatura Programada de CO 2 (TPD-CO2) e Microscopia Eletrônica de Varredura (MEV). As imagens de MEV dos óxidos permitiram confirmar a síntese das diferentes morfologias de MgO, e resultados para testes de atividade catalítica mostram uma influência da morfologia na atividade e seletividade do SiO2/MgO. Para os MgO, em uma temperatura de 425 oC, foram obtidas conversões entre 11.7% e 21.9% para diferentes morfologias, com seletividades para BD entre 5.6% e 30.4%. Para os catalisadores SiO2/MgO, na mesma temperatura, foram obtidos rendimentos variáveis com a morfologia e com o teor Mg:Si. Para os catalisadores 3:1, foram observados rendimentos entre 21.5% e 34.3%, enquanto que para os catalisadores 7:1 puderam ser observados rendimentos variando entre 18.5% e 35.4%. As propriedades catalíticas não puderam ser claramente correlacionadas com os dados de TPD-CO2 e área superficial específica, evidenciando que estas são dependentes de um complexo conjunto de fatores, dentre eles a acessibilidade da superfície para o contato com o SiO2 . A variação do teor de sílica mostra que a razão SiO 2/MgO é extremamente importante para obtenção de catalisadores ativos e seletivos para formação do 1,3-butadieno.
Lian, Cheng-Wei, and 連承偉. "A Buried Silicon Nanocrystal Based High Gain Coefficient SiO2/SiOX/SiO2 Strip-Loaded Waveguide Amplifier on the Si Substrate." Thesis, 2008. http://ndltd.ncl.edu.tw/handle/39948804785714057250.
Full text國立臺灣大學
光電工程學研究所
96
In this thesis, we simulate the SiO2/SiOX/SiO2/Quartz-substrate strip-loaded waveguide and the SiO2/SiOX/SiO2/Si-substrate strip-loaded waveguide. The Effective-Index Method (EIM), the Beam Propagation Method (BPM), and the Finite Element Method (FEM) are used to simulate the waveguide structure. Subsequently, we fabricate these two type waveguides and measure the optical gain and loss coefficients by fitting the one dimensional amplifier equation of the Variable Stripe Length (VSL) method. We observe that the Si-rich SiOX strip-loaded waveguide with silicon (Si) nanocrystal contributed amplified spontaneous emission (ASE) at 750-850 nm with the associated spectral linewidth of 140 nm is characterized. The ASE spectrum is red-shifted 6 nm to PL spectrum because of mode guiding. The peak wavelength of ASE spectrum is blue shift with longer pumping length. Because of the longer pumping length, the mode guiding is stronger and the peak wavelength becomes stable. The optical gain and loss coefficients of the SiO2/SiOX/SiO2/Quartz-substrate strip-loaded waveguide are 70 and 5 cm-1, respectively. The optical gain and loss coefficients of the SiO2/SiOX/SiO2/Si-substrate strip-loaded waveguide are 106.7 and 21 cm-1, respectively. The optical loss coefficient of the Si-substrate device is larger than the Quartz-substrate device which is due to the optical mode leakage to Si substrate. The optical net modal gain coefficient of Si-substrate device is larger than Quartz-substrate device which is due to the better mode confinement. The small-signal amplification of up to 11.73 dB for 795 nm small laser signal under He-Cd laser pumping of 43.7 mW at the wavelength of 325 nm is obtained from the SiO2/SiOX/SiO2/Si-substrate strip-loaded waveguide amplifier with a length of 1 cm.
Lian, Cheng-Wei. "A Buried Silicon Nanocrystal Based High Gain Coefficient SiO2/SiOX/SiO2 Strip-Loaded Waveguide Amplifier on the Si Substrate." 2008. http://www.cetd.com.tw/ec/thesisdetail.aspx?etdun=U0001-3007200823324700.
Full textWu, Ming-Shing, and 吳銘興. "A-SiOx Thin Film Growth in Magnetron Plasma System." Thesis, 1993. http://ndltd.ncl.edu.tw/handle/26585093717171697201.
Full textWu, Bing-Chien, and 吳秉謙. "A Study of Photodetectors Based on AZO/SiOx/n-Si Heterojunction Structure." Thesis, 2016. http://ndltd.ncl.edu.tw/handle/08015171370439565657.
Full textLiu, Li-Hao, and 劉力豪. "Study of Laser Annealing of a-Si/a-SiOx Multi-layer by Raman Scattering." Thesis, 2006. http://ndltd.ncl.edu.tw/handle/12322213673272379151.
Full text國立臺灣海洋大學
光電科學研究所
93
Abstract: This research used a continuous wave Argon ion laser for annealing an a-Si/a-SiOx multi-layer sample and measured Raman spectrum at the same spot with reduced laser power. By subtracting amorphous silicon contribution to laser annealed multilayer’s Raman spectrum,the microcrystalline silicon’s Raman signature can be obtained. The evolution of microcrystalline silicon’s Raman peak position and width with the accumulated laser exposure was analyzed to deduce the growth process of microcrystalline silicon nanoparticles.
Chang, Ming-Chieh, and 張民杰. "Study of SiOx Dielectric Film with Hydrogen Content for a-IGZO-TFT Device." Thesis, 2012. http://ndltd.ncl.edu.tw/handle/08695751884636984221.
Full text國立交通大學
平面顯示技術碩士學位學程
100
Nowadays, poly-silicon and amorphous-silicon generally have been used for active layer of TFT (Thin Film Transistor) device technology of TFT LCD (Liquid Crystal Display). Poly-silicon-TFT has high field-effect mobility of over 100Vs/cm2, but it has disadvantage of high running cost and bad processing uniformity. Moreover, amorphous silicon has lower process cost for less process steps, but its field-effect mobility is less than 1Vs/cm2. Recently, a-IGZO TFTs (amorphous Indium Gallium Zinc Oxide Thin Film Transistor) have attracted considerable attentions for their superior electrical properties including great field-effect mobility from 10Vs/cm2 to 20Vs/cm2, sub-threshold swing, and high on/off current ratio. Furthermore, a-IGZO film, which is deposited at low temperature with an amorphous phase, exhibits good uniformity and can be fabricated on plastic substrates for flexible electronic or AMOLED (Active Matrix Organic Light Emitting Display) driving TFT. This thesis discussed SiOx dielectric film with low hydrogen content for a-IGZO-TFTs. If hydrogen content of SiOx film was high, a-IGZO film will be transformed from semiconductor to conductor in the application of TFT device. It is important that hydrogen content of SiOx film is reduced when SiOx film is deposited. Therefore, hydrogen ion generated by SiH4 must be reduced when deposited SiOx film. The proposed process of a-IGZO-TFT utilized low hydrogen contents SiOx film as etching stop layer and passivation layer to produce top gate and bottom gate transistor components. Experimental results showed that a-IGZO film exhibit intrinsic semiconductor characteristic, which is main claim of the dissertation.
Ho, Chia-chi, and 何家齊. "Cooper Gate Electrode Fabrication and SiOx Gate Dielectric Properties on a-Si:H TFTs Electrical Characterization." Thesis, 1996. http://ndltd.ncl.edu.tw/handle/07587454817268626490.
Full text國立交通大學
材料科學與工程研究所
84
In this thesis we used low resistivity Cu/TiW double layered gate metal fabrication a-Si:H THT.Using low resistivity Cu metal as gate can effectively reduce RC delay in gate line and at the same time prevent the production of hillocks and whisker.In this way,Cu/TiW gate utilizes a complete chemical wet etching process.While Cu etched by various ratio of CH3COOH and Al etchant,we find that CH3COOH 70~80% buffer Aletchant have a uniform etching morphology,small side etch distance and excellent taper shape.The TFT with Cu/TiW double-layered gate metal provides good electrical performance,such as the small threshold voltage(1.2V),low subthreshold swing(0.24V/dec.) and high mobility (0.8cm^2/V.s). SiH4-N2O based and TEOS-O2 based oxide are fabricated in a-Si:H TFT as gate dielectric to investigate the oxide gate dielectric properties on the a-Si:H TFT performance.We find that PE-TEOS oxide have better step coverage than silane-based oxide and the surface of PE-TEOS oxideis more smooth.The breakdown strength for TEOS oxide is 8.5 MV/cm and 8 MV/cm for silane-based oxide.The value have high enough for TFT device.Both have been used a TFTs gate dielectric,and the best electrical performance is Vth about 5V, S=0.4 V/dec.,and ufe=0.6cm^2/V.s.The TFTs electrical performance with silane-based oxide are improved accompanying with oxide properties that with fewer hydrogen related bonds and rigid structure.The Vth shift decrease with the oxide gate insulator that with fewer hydrogenrelated bonds.But the subthreshold swing shift shows an inverted tendency that may resulting from the interface bonding structure related to O atoms induced weak silicon bond structure.The TFTs electrical performance with TEOS-based oxide gate insulator have similar result that oxide with complete Si-O bonding has better performance.But the oxide deposited under high power will producing a large amount of fixed charge trap in oxide by plasmadamage and resulting in high threshold voltage. SiNx TFTs with CA a-Si:H and H2 plasma treatment SiNx surface TFTs have been prepare.CA a-Si:H TFTs have many interface layers in a-Si:H and more interface states are build up resulting in decrease in ufe and increase in S.When gate bias is applied,the S will reach a saturation value and ufe will increase.The reson still not clear,maybe cause by the release of the strain in a-Si:H.from breaking weak bonds for H2 plasma treatment SiNx surface TFT when gate bias is performed both S and mobility decrease.Because the plasma damage the interface,an unstable interface is produced.All the sample have worse electrical properties than conventional SiNx TFTs.The instablity in oxide gate dielectric a-Si:H THT mainly come from the trap defect centers in oxide and state creation at or near the interface.
Lu, Chi-Chang, and 呂其璋. "Silicon Oxide (SiOx) Film Deposition Using Radio-Frequency Atmospheric-Pressure Plasma Jet With a Spiral Electrode." Thesis, 2010. http://ndltd.ncl.edu.tw/handle/71087727569830978254.
Full text國立交通大學
機械工程學系
98
Thin film deposition of silicon oxide (SiOx) using a radio-frequency (13.56 MHz) coaxial argon atmospheric-pressure plasma jet (RF-APPJ) has been investigated experimentally in this thesis. A stable, arc-free swirling APPJ was produced with a spiral powered electrode covered by a quartz tube, which makes the addition of oxygen (up to 10%) possible without extinguishing the discharge. This APPJ was employed to deposit silicon oxide thin films using a precursor, hexamethyldisiloxane (HMDSO), diluted in an argon carrier gas, into the post-discharge region. Test conditions included variations of treatment passes, input power (35-50 W), treatment distances (3-7.5 mm), oxygen additions (0-10%), and substrate temperatures (25-300 oC). Results show that deposition rate increased with increasing treatment passes, input power, oxygen addition and decreased with increasing substrate temperatures and treatment distances. The variation of oxygen addition and substrate temperature greatly affected the properties of silicon oxide thin films. The deposition rate of the silicon oxide thin film was 37.5 nm/min using pure argon plasma with 50 W RF power, 300 oC substrate temperature and 5 mm treatment distance. When oxygen addition increases to 0.8%, the deposition rate increases to 275 nm/min. However, oxygen addition is more than 2%, highly porous, particle-like structure was formed. FTIR and XPS measurements show that quantity of carbon atoms, the degree of porosity and deposition rate in the film decrease with increasing substrate temperature. However, the hardness of the film surface increases with increasing substrate temperature. In summary, we have successfully deposited and characterized the silicon oxide films formed in the post-discharge region of a RF-APPJ using argon mixed with oxygen. Recommendations for the future study are also outlined at the end of the thesis.