No description available.

No description available.

A highly self-ordered hexagonal array of cylindrical pores has been fabricated by anodizing a thin film of Al on substrate and subsequent growth of GaN and InGaN in these nanoholes has been performed. This AAO template-based synthesis method provides a low cost process to fabricate GaN-based nanomaterials fabrication. / Singapore-MIT Alliance (SMA)

The anodic films formed on CP-Ti in sulphuric and phosphoric acids using potentiodynamic polarization and potentiostatic anodizing were investigated. Single-barrier anodic films were created in sulphuric and phosphoric acids from 10 to 60 V. Oxygen evolution was initiated within both stages, leading to the suppression of current efficiency for the growth of anodic films. The crystalline phases assisted gas bubbles to develop within the film, resulting in the formation of the blister textures. The rupture of the anodic film was found from anodizing at 20 V in the sulphuric acid but occurred at 50 V in the phosphoric acid. The corrosion behaviour of the anodic oxide films formed on CP-Ti was studied in a 3.5% NaCl electrolyte. Ruptures and blisters of the films were found as a result of the release of a huge pressure by the bursting of oxygen bubbles. More ruptures were observed when anodizing to higher anodic voltages in the sulphuric and phosphoric acids. Further, the anodic films showed more ruptures after the anodized titanium specimens at higher anodic voltages were immersed for 60 days in the NaCl electrolyte compared with the immediate immersions. Additionally, the corrosion behaviours of the anodic films were examined by potentiodynamic polarization and electrochemical impedance spectroscopy. The corrosion resistance of the anodized titanium in the NaCl electrolyte increased with increased anodic voltage. Porous anodic films were formed on CP-Ti after anodizing at 100, 150 and 200 V for 900 s respectively. Nano-particulates were found within the pores; the size and quantity of the pores increased due to the dissolution of the particulates. The amorphous-to-crystalline transition was initiated during anodizing. It was revealed that the degree of crystallinity was greater at a higher voltage. An increased content of phosphorus species was incorporated into the porous oxide film as the voltage increased. The formation of anodic oxide films on CP-Ti in the NaTESi electrolyte was investigated. Barrier-type titanium anodic films generated after anodizing to 5, 10 and 20 V were of thickness 30, 37 and 67 nm respectively. Further, a porous anodic film of ~80.0 nm thickness was generated after anodizing to 40 V. Significant amounts of sodium species were found, which were incorporated into the anodic films. The current efficiency for the film growth was reduced at higher anodic voltages due to the formation of crystalline phases and more oxygen generation. The degree of crystallinity of the anodic film increased at higher voltages. The dielectric permittivity of the anodic film was estimated as ~2.35 according to EIS and the TEM evidence. The degradation test was carried out in a continuous climatic chamber with a humidity of 90% at 50 oC. The anodic films formed on CP-Ti in the NaTESi electrolyte showed an excellent degradation resistance. Single-lap bonding tests were operated for the study of the adhesion joint performance, and the bonding strength increased with increase of the voltage associated with a thicker anodic TiO2 coatings. The formation of anodic oxide films on the Ti6Al4V alloy in the NaTESi electrolyte at a constant current density of 20 mA cm-2 was studied. An anodic film with shallow pores was formed after anodizing to 10 V. Porous anodic films were created after anodizing to 20, 30 and 40 V respectively. Significant amounts of sodium species were incorporated into the films. The current efficiency for the anodic film growth increased from 10 to 30 V but decreased from 30 to 40 V due to oxygen evolution. The film thicknesses determined by RBS were ~15 nm, ~39 nm, ~1100 nm and 1800 nm for voltages of 10, 20, 30 and 40 V respectively. The film thickness at 10 V showed good agreement with 11 nm which was evident by TEM. The degree of crystallinity of the films was greater at a higher voltage. The dielectric permittivity of the film was ~118 according to the results of TEM and EIS. The degradation test was carried out in a continuous climatic chamber with a humidity of 90% at 50oC. Without the evidence of damages, the anodic films formed on Ti6Al4V alloy in the NaTESi electrolyte showed an excellent degradation resistance. In addition, it was evident that the film formed after anodizing to 40 V was crystallized at the thermal temperature of 50 oC. Single-lap bonding tests were employed to compare the strength of adhesively joined titanium alloy anodized with different film thicknesses, the results revealing a significant benefit from a thicker film. The ~100 nm thick 99.6% pure titanium layers were sputter-deposited on electropolished aluminium substrates by magnetron sputtering technique to investigate the anodic film growth behaviour of titanium in H3PO4. The TiO2 and the Ti layer were ruptured by the bursting of oxygen bubbles. The phosphoric acid electrolyte penetrated into the ruptured regions of the sputter-deposited titanium layer, leading to the growth of Al2O3. The thickness of TiO2 increased from 10 to 100 V but decreased from 100 to 150 V. Above 80 V, some regions of the titanium layer where were completely ruptured did not generate TiO2. Important structural details of anodic films with high quality images were obtained using the STEM-in-SEM technique, enabling the study of film morphologies, film thicknesses and oxygen bubble features. STEM-in-SEM would be used to study a large-scale morphology of the anodic film. Additionally, a 6-specimen carousel holder would provide an increase in productivity by ~20% compared with a conventional single-specimen STEM or TEM. An air-formed oxide film was stripped from CP-Ti substrate by chemical etching in the bromine-methanol electrolyte, exposing the bare titanium substrate and grain boundaries with defects. After that, pitting corrosion occurred on the bare titanium due to the attack of bromine. The corrosion pits propagated with etching time from 10 to 300 s and were displayed using white light interferometry. Increased surface roughness was identified with etching time due to the occurrence of more pitting corrosion attacks. Bromine species and TiBr4 compounds were detected by EDS and X-ray diffraction patterns, indicating that the dissolution of the titanium substrate was induced in each etching.

No description available.

Die vorliegende Arbeit enthält neuartige Ergebnisse festkörperanalytischer Untersuchungen zu Synthese, Struktur und Eigenschaften von anodischen Konversionsschichten auf Vanadium und Zirkonium. Schwerpunkte sind die Darstellung anodischer Oxidschichten auf den Metallen Vanadium und Zirkonium sowie ihre Charakterisierung mit ausgewählten Methoden der Festkörperanalytik. Am Beispiel des Vanadiums wird die anodische Schichtbildung in Essigsäurebasiselektrolyten untersucht. Unter anderem wird anhand von Strom-Spannungs-Kennlinien das unterschiedliche anodische Verhalten der physikalisch ähnlichen Metalle Vanadium und Zirkonium diskutiert. Neben den Methoden der Röntgenbeugung, Infrarotspektroskopie, Photoelektronenspektroskopie und Elektronenmikroskopie wird die Ramanspektroskopie als ein geeignetes Mittel zur Unterscheidung der Oxidphasen verwendet. Die amorphen VOx-Schichten und kristallinen ZrO2- bzw. modifizierten Schichten wurden sowohl unter anodischen als auch unter elektrochemischen Plasmabedingungen erzeugt. Die Korrelation zwischen Schichtstruktur und Syntheseverfahren wird herausgearbeitet.

An equifield strength model has been established to elucidate the formation mechanism for the highly ordered alumina pore arrays and titanium oxide nanotubular arrays prepared via a common electrochemical methodology, anodisation. The fundamentals of the equifield strength model was the equilibrium between the electric field driven oxidation rate of the metal and electric field enhanced dissolution rate of oxide. During the anodic oxidation of metal, pore initiation was believed to generate based on dissolution rate difference caused by inhomogeneity near the metal/oxide interface. The ionic nanoconvection driven by the electric force exerted on the space charge layer in the vicinity of electrolyte/oxide interface is established to be the main driving force of the pore ordering at the early stage of the anodisation. While the equifield strength requirement governs the following formation of the single pore and the self-ordering of random distributed pore arrays during the anodisation process. Hexagonal patterned Al2O3 nanopore arrays and TiO2 nanotubular arrays have been achieved by anodisation of corresponding metal substrates in proper electrolytes. The two characteristic microstructural features of anodic aluminium oxide (AAO) and anodic titanium oxide (ATO) were investigated using scanning electron microscopy (SEM) and high resolution transmission electron microscopy (HRTEM). The observations of the hemispherical electrolyte/oxide and oxide/metal interfaces, uniform thickness of the oxide layer, as well as self-adjustment of the pore size and pore ordering can be well explained by the equifield strength model. Field enhanced dissociation of water is extremely important in determination of the porosity of anodic metal oxide. The porosity of AAO and ATO films was found to be governed by the relative dissociation rate of water which is dependent on anodisation conditions, such as electrolyte, applied voltage, current density and electric field strength. Using an empirical method, the relations between the porosity of the AAO (ATO) films and the anodisation parameters, such as electric field strength, current density and applied voltage, have been established. Besides, the extent that an external electric field can facilitate the heterolytic dissociation of water molecule has been estimated using quantum-chemical model computations combined with the experimental aspect. With these achievements, the fabrication of anodic metal oxide films can be understood and controlled more precisely. Additionally, the impacts of other factors such as the electrolyte type and the temperature effect on the morphology of the anodic products were also investigated. Some important experimental evidences on the pore diameters variation with applied voltage in the anodisation of aluminium and the titanium were obtained for future investigation of the anodic metal oxide formation processes.

Nos dias de hoje um grande número de pesticidas é utilizado em colheitas, agricultura, transporte de sementes, entre outros. Esses pesticidas são moléculas orgânicas que apresentam em sua estrutura grupos funcionais capazes de formar ligações com íons metálicos, que de forma natural ou por intervenção humana, são encontradas no solo. Estas espécies entram em contato no meio ambiente, e assim, interagem formando ligações, dando forma aos chamados compostos de coordenação, ou complexos. A formação destes complexos pode alterar significativamente as propriedades dos pesticidas e dos íons metálicos, podendo acentuar seu caráter tóxico, sua persistência e degradação. Neste trabalho foram escolhidos dois pesticidas que são bons exemplos deste tipo de molécula. O fungicida Thiram, que apresenta em sua estrutura átomos de enxofre, e assim interage com uma gama de íons metálicos; e o herbicida picloram, que é um derivado piridínico, o qual apresenta um átomo de nitrogênio com pares de elétrons livres e capazes de formar ligações, e um grupamento ácido na posição dois do anel também capaz de interagir com íons metálicos. Com o intuito de se entender melhor como ocorre estas interações, realizou-se este trabalho onde observou-se a complexação dos pesticidas thiram e picloram com quatro íons metálicos previamente selecionados, zinco, cobre, cádmio e chumbo. Dessa forma, deu-se início a um estudo de complexação utilizando o método de Voltametria de Redissolução Anódica em modo de Pulso Diferencial, a fim de se avaliar a ocorrência desta complexação. Para isso, contamos com duas ferramentas muito utilizadas para a avaliação da capacidade complexante de amostras, os métodos de linearização de Scatchard e Langmuir. Com a técnica utilizada foram levantadas curvas de titulação de amostras contento os pesticidas, e a partir dos dados obtidos aplicou-se os cálculos de Langmuir e Scatchard para se obter dois parâmetros importantes, a constante de estabilidade condicional do complexo formado, K\', e a concentração de ligante que participa da reação de complexação em solução, [L]T. Os dados obtidos com ambos pesticidas foram satisfatórios, indicando a ocorrência de complexos. Porém, observou-se que essa interação é maior entre o fungicida thiram e os respectivos metais do que com o herbicida picloram. As constantes de estabilidade condicional para o fungicida thiram se encontram com Log de K\' entre 6 e 7, enquanto as mesmas para os complexos formados entre o herbicida picloram e os íons metálicos se encontram entre 5 e 6. Para se confirmar as medidas de voltametria de redissolução anódica, foram realizadas medidas de espectroscopia na região do ultravioleta visível, bem como medidas de voltametria cíclica e de pulso diferencial. / Nowadays, numerous pesticides are used in crops, agriculture, transport of seeds, among others. These pesticides are organic molecules that present functional groups in their structure which are capable of forming connections with metallic ions, which, whether naturally or by human intervention, are found in the soil. These species enter in contact in the environment, and thus, they interact forming connections, giving form to the so called compound of coordination, or complex. The formation of these complexes can alter significantly the properties of both the pesticides and the metallic ions, being able to enhance toxic character, persistence and degradation. In this work, two pesticides were chosen for being good examples of this type of molecule. The fungicide Thiram, which presents atoms of sulfur in its structure, and thus interact with a range of metallic ions; and the herbicide picloram, a derived pyridinic, which presents a nitrogen atom with pairs of free electrons and capable of forming binding, and an acid group in the position two of the ring, also capable of interacting with metallic ions. In order to better understand how these interactions occur, this work focused where the complexation of pesticides thiram and picloram was observed with four metallic ions previously selected, zinc, copper, cadmium and lead. Hence, a study of complexation was started using the method of Differential Pulse Anodic Stripping Voltammetry, in order to evaluate the occurrence of the complexation. For that, we counted on two tools very frequently used for the viii evaluation of the metal-binding capacity of samples, namely, the linearization methods of Scatchard and Langmuir. Titration curves of the samples containing the pesticide were obtained using the technique, and starting from the data, the calculations of Langmuir and Scatchard were applied in order to obtain two important parameters, stability conditional constant of the formed compound, K\', as well as the ligand concentration that participates in the reaction complexation in solution, [L]T. The data obtained with both pesticides were satisfactory, indicating the occurrence of complexes. However, it was observed that the interaction is larger between the fungicide thiram and the respective metals than with the herbicide picloram. The constants of conditional stability for the fungicide thiram are with LogK\' between 6 and 7, while the same ones for the compounds formed between the herbicide picloram and the metallic íons are between 5 and 6. To confirm the measures of anodic stripping voltammetry, spectroscopy measures were carried out in the area of the visible ultraviolet, as well as measures of cyclic voltammetry and of differential pulse.

No description available.

Nanoestructuras de alumina anódica porosa (AAP) têm sido tradicionalmente fabricadas por duas etapas de anodização a temperaturas relativamente baixas (de 0 até 5°C), e usadas como máscaras ideais para formação de vários materiais nanoestruturados. Neste sentido, o objetivo do trabalho foi estudar sistematicamente a formação e a fabricação de nanoestruturas de AAP autoorganizadas por uma só etapa de anodização e posterior aplicação na síntese de nanopartículas e nanofios metálicos. As nanoestruturas auto-organizadas de AAP foram obtidas por apenas uma etapa de anodização em ácido oxálico (H2C2O4) a temperatura ambiente; diferentemente dos processos convencionais onde são utilizados duas ou mais etapas de anodização. As características estruturais dos filmes de AAP foram moduladas através do controle dos parâmetros da concentração da solução, temperatura e potencial de polarização. O procedimento principal, para a obtenção de AAP auto-organizadas apenas por uma etapa de anodização, foi o pós-processamento de abertura dos poros através de um processo de corrosão química. Os resultados obtidos neste trabalho mostraram que o diâmetro médio dos poros apresentou uma dependência linear com a temperatura, potencial e tempo de corrosão química e foi constante em relação à concentração da solução eletrolítica. No entanto, a análise estrutural via microscopia eletrônica de varredura (MEV), mostrou que a circularidade e a ordem dos nanoporos sobre a superfície anodizada melhoraram com o aumento da concentração do eletrólito. A estrutura de AAP com um arranjo hexagonal de poros regularmente distribuídos foi obtida quando a anodização foi realizada em 0,3M de H2C2O4, a 45V e 20°C de temperatura seguido de uma corrosão química a temperatura de 17°C por 102 minutos. Adicionalmente foram obtidos nanopartículas e nanofios metálicos utilizando-se as nanoestruturas de AAP como moldes. Como os filmes de AAP são isolantes a obtenção das nanopartículas e nanofios foi realizado através de um processo de eletrodeposição de corrente alternada (CA). Os resultados deste trabalho mostraram que nanoestruturas de AAP autoorganizadas podem ser fabricadas por uma etapa de anodização controlando o tempo de corrosão química. Os resultados apresentados neste trabalho mostram-se vantajosos em relação aos reportados na literatura, já que normalmente as nanoestruturas de AAP são obtidas mediante processos de anodização em duas etapas e tempos longos de anodização. / Nanostructures of porous anodic alumina (PAA) have been traditionally manufactured by two steps anodization at relatively low temperatures (0 to 5°C) and used as templates suitable for the formation of various nanostructured materials. In this sense, the goal of this work was the fabrication of self-organized porous Anodic alumina nanostructures (AAP) by a one anodization step and subsequent application in the synthesis of metal nanowires and nanoparticles. The self-organized nanostructures of PAA were obtained by just one anodization step in oxalic acid (H2C2O4) at ambient temperature unlike to conventional processes where they are used two or more anodization steps. The structural characteristics of PAA films were modulated through control of the solution concentration, temperature and potential of polarization. The key procedure to obtain the periodic organized PAA by only one step anodization was the post-processing of pore opening through a process of corrosion chemistry. The results of this work showed that the average diameter of pores presented a linear dependence with temperature, time of chemical corrosion, polarization potential and it was constant relative to the concentration of the electrolyte solution. However, the structural analysis via scanning electron microscopy (SEM) showed that the roundness and the order of nanoporos over the anodized surface improved with the electrolyte concentration increasing. The PAA structure with a hexagonal arrangement of pores was obtained when the anodization was held in 0.3 M of H2C2O4, 45V, and 20°C of temperature followed by a chemical corrosion at 17°C of temperature for 102 minutes. Additionally it was obtained nano particles and nano metal wires using the PAA structures as molds. Since the PAA films are insulating, the nanoparticles and nanowire were obtained through an electrodeposition process using alternating current. The results of this work have shown that self-organized PAA nanostructures can be fabricated by one anodization step controlling the time of chemical etching process. The results presented in this work are advantageous in relation to reported in the literature, since normally the structures of PAA are obtained by two step anodization and for long anodization time.