906 resultados para Tin dioxido
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The tin alloys of tellurium are extremely hard and have very great tensile strength. It was thought that the reduction of the rate of grain growth of tin with the addition of tellurium accompanied this hardening and strengthening and such way found to be true.
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Powder metallurgy, the most recent innovation in metallurgical process, is not a new art; although not until recently did it become a matter of general interest, this being due not only to the products formed but also to the possibilities of future developments. The manufacture and application of metal powders is now beginning to take a position as a recognized part of the science of metallurgy.
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This thesis is concerned primarily with the production of metal powder compacts of iron and tin. In producing these compacts, the effects of processing variables on some of the essential properties of the pellets made were investigated.
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The art of Powder Metallurgy deals with the preparation of metal powders and their utilization. As a more pertinent definition, the following has been suggested: "Powder Metallurgy is the art of producing metal powders and shaped objects from individual, mixed, or alloyed metal powders, with or without the inclusion of non-metallic constituents".
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The purpose of this study was to determine the relative rate of corrosion of iron-tin alloys containing low percentages of tin. Since in the world today, a great deal of work is being done to develop large tin deposits and new methods devised to treat these ores, it is possible that the metal will become abundant and will obtain a more important position in the metal industry.
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In 1947, out of the 100,000 long tons of tin consumed in the United States, 25,000 tons went into solder. Tin plate took 39,000 tons while babbit, bronze and collapsible tubes accounted for approximately 17,000 tons. Solder ranked second to tin plate and required more than the next three major uses combined.
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In this investigation, attention is directed to the phases covered by a 28 per cent tin alloy. When the investigation was started, consideration was given to the possibility of making a Time - Temperature - Transformation curve for this particular alloy. As the work progressed and further research was carried on, this phase of the work was abandoned.
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Tin-containing fluoride solutions can reduce erosive tissue loss, but the effects of the reaction between tin and enamel are still not clear. During a 10-d period, enamel specimens were cyclically demineralized (0.05 M citric acid, pH 2.3, 6 x 5 min d(-1)) and remineralized (between the demineralization cycles and overnight). In the negative-control group, no further treatment was performed. Three groups were treated (2 x 2 min d(-1)) with tin-containing fluoride solutions (400, 1,400 or 2,100 ppm Sn2+, all 1,500 ppm F-, pH 4.5). Three additional groups were treated with test solutions twice daily, but without demineralization. Tissue loss was determined profilometrically. Energy-dispersive X-ray spectroscopy was used to measure the tin content on and within three layers (10 mum each) beneath the surface. In addition, scanning electron microscopy was conducted. All test preparations significantly reduced tissue loss. Deposition of tin on surfaces was higher without erosion than with erosion, but no incorporation of tin into enamel was found without demineralization. Under erosive conditions, both highly concentrated solutions led to the incorporation of tin up to a depth of 20 mum; the less-concentrated solution led to small amounts of tin in the outer 10 mum. The efficacy of tin-containing solutions seems to depend mainly on the incorporation of tin into enamel.
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OBJECTIVES: To determine the effect on resin composite-to-dentin bond strength of incorporation of an acidic tin-chloride pretreatment in two adhesive systems. MATERIALS AND METHODS: Human molars were ground to expose mid-coronal dentin. For microtensile bond strength (μTBS) testing, dentin was treated with Optibond FL or Clearfil SE according to one of six protocols (n = 22/group). Group 1: Phosphoric acid etching, Optibond FL Prime, Optibond FL Adhesive (manufacturer's instructions; control); Group 2: Tin-chloride pretreatment, Optibond FL Prime, Optibond FL Adhesive; Group 3: Phosphoric acid etching, tin-chloride pretreatment, Optibond FL Prime, Optibond FL Adhesive; Group 4: Clearfil SE Primer, Clearfil SE Bond (manufacturer's instructions; control); Group 5: Phosphoric acid etching, Clearfil SE Primer, Clearfil SE Bond; and Group 6: Tin-chloride pretreatment, Clearfil SE Primer, Clearfil SE Bond. The molars were then built up with resin composite (Clearfil Majesty Esthetic). After storage (1 week, 100 % humidity, 37 °C) the μTBS was measured and failure mode was determined. Additionally, pretreated dentin surfaces were evaluated using SEM and EDX. The μTBS results were analyzed statistically by a Welch Two Sample t-test and a Kruskal-Wallis test followed by exact Wilcoxon rank sum tests with Bonferroni-Holm adjustment for multiple testing (α = 0.05). RESULTS: When Optibond FL was used, partial or total replacement of phosphoric acid with tin-chloride decreased μTBS significantly. In contrast, when Clearfil SE was used, inclusion of a tin-chloride pretreatment in the adhesive procedure increased μTBS significantly. CONCLUSIONS: Tin-chloride pretreatment had a beneficial influence on the bond promoting capacity of the MDP-containing adhesive system Clearfil SE.
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OBJECTIVES To evaluate the effect of a tin-containing fluoride (Sn/F) mouth rinse on microtensile bond strength (μTBS) between resin composite and erosively demineralised dentin. MATERIALS AND METHODS Dentin of 120 human molars was erosively demineralised using a 10-day cyclic de- and remineralisation model. For 40 molars, the model comprised erosive demineralisation only; for another 40, the model included treatment with a NaF solution; and for yet another 40, the model included treatment with a Sn/F mouth rinse. In half of these molars (n = 20), the demineralised organic matrix was continuously removed by collagenase. Silicon carbide paper-ground, non-erosively demineralised molars served as control (n = 20). Subsequently, μTBS of Clearfil SE/Filtek Z250 to the dentin was measured, and failure mode was determined. Additionally, surfaces were evaluated using SEM and EDX. RESULTS Compared to the non-erosively demineralised control, erosive demineralisation resulted in significantly lower μTBS regardless of the removal of demineralised organic matrix. Treatment with NaF increased μTBS, but the level of μTBS obtained by the non-erosively demineralised control was only reached when the demineralised organic matrix had been removed. The Sn/F mouth rinse together with removal of demineralised organic matrix led to significantly higher µTBS than did the non-erosively demineralised control. The Sn/F mouth rinse yielded higher μTBS than did the NaF solution. CONCLUSIONS Treatment of erosively demineralised dentin with a NaF solution or a Sn/F mouth rinse increased the bond strength of resin composite. CLINICAL RELEVANCE Bond strength of resin composite to eroded dentin was not negatively influenced by treatment with a tin-containing fluoride mouth rinse.
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OBJECTIVES The study investigated the modification of composite-to-enamel bond strength by pre-treatment of enamel with a concentrated, acidic SnCl2-solution. METHODS Six groups of flat human enamel specimens (n=44 per group) were treated as follows: OB-H: H3PO4 etching, Optibond FL application (primer+adhesive; manufacturer's instructions); OB-S: SnCl2 pre-treatment, Optibond FL application (primer+adhesive); OB-HS: H3PO4 etching+SnCl2 pre-treatment, Optibond FL application (primer+adhesive); CF-N: Clearfil SE application (primer+bond; manufacturer's instructions); CF-H: H3PO4 etching, Clearfil SE application (primer+bond); CF-S: SnCl2 pre-treatment, Clearfil SE application (primer+bond). Enamel specimens were then built up with resin composite (Clearfil Majesty Esthetic) and stored (100% humidity, 37 °C, 1 week). μTBS-measurement and failure mode analysis of one-half of the specimens were performed immediately after storage, while the other half was analysed after a thermocycling procedure (8500 cycles; 5 °C and 55 °C; dwell time 30s). Additional specimens were prepared for SEM- and EDX-analysis. RESULTS Highest values were measured for OB-H before and after thermocycling, lowest values for CF-N. Compared to OB-H treatment, OB-S treatment reduced μTBS before/after thermocycling by 23%/28% and OB-HS treatment by 8%/24% (except for OB-SH before (n.s.), all p≤0.001 compared to OB-H). In the Clearfil SE treated groups pre-treatment increased μTBS significantly compared to CF-N (before/after: CF-H: +46%/+70%; CF-S: +51%/42%; all p≤0.001). CONCLUSION Pre-treatment with H3PO4 or SnCl2 markedly increased the μTBS of Clearfil SE to enamel. However, thermocycling partly reduced the gain in μTBS obtained by SnCl2 pre-treatment. CLINICAL SIGNIFICANCE The application of an acidic and highly concentrated SnCl2 solution is a good option to increase the μTBS between enamel and a resin composite mediated by an adhesive system containing the multifunctional monomer MDP.
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Tin is a notable anti-erosive agent, and the biopolymer chitosan has also shown demineralisation-inhibiting properties. Therefore, the anti-erosive/anti-abrasive efficacy of the combination of both compounds was tested under in situ conditions. Twenty-seven volunteers were included in a randomised, double-blind, three-cell crossover in situ trial. Enamel specimens were recessed on the buccal aspects of mandibular appliances, extraorally demineralised (6 × 2 min/day) and intraorally treated with toothpaste slurries (2 × 2 min/day). Within the slurry treatment time, one-half of the specimens received additional intraoral brushing (5 s, 2.5 N). The tested toothpastes included a placebo toothpaste, an experimental NaF toothpaste (1,400 ppm F(-)) and an experimental F/Sn/chitosan toothpaste (1,400 ppm F(-), 3,500 ppm Sn(2+), 0.5% chitosan). The percentage reduction of tissue loss (slurry exposure/slurry exposure + brushing) compared to placebo was 19.0 ± 47.3/21.3 ± 22.4 after use of NaF and 52.5 ± 30.9/50.2 ± 34.3 after use of F/Sn/chitosan. F/Sn/chitosan was significantly more effective than NaF (p ≤ 0.001) and showed good efficacy against erosive and erosive-abrasive tissue loss. This study suggests that the F/Sn/chitosan toothpaste could provide good protection for patients who frequently consume acidic foodstuffs.
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Una planta AIP es cualquier sistema propulsivo capaz de posibilitar la navegación de un vehículo submarino bajo la superficie del mar de forma completamente independiente de la atmósfera terrestre. El uso a bordo de submarinos de plantas AIP basadas en la reacción química entre un hidrocarburo y oxígeno (ambos almacenados en el interior del submarino) da lugar a la producción en grandes cantidades de agua y CO2, residuos que necesitan ser eliminados. En concreto, la producción de CO2 en grandes cantidades (y en estado gaseoso) constituye un auténtico problema en un submarino navegando en inmersión, ya que actualmente no resulta viable almacenarlo a bordo, y su eliminación tiene que llevarse a cabo de forma discreta y con un coste energético reducido. Actualmente, hay varias alternativas para eliminar el CO2 producido en la propulsión de un submarino navegando en inmersión, siendo la más ventajosa la disolución de dicha sustancia en agua de mar y su posterior expulsión al exterior del submarino. Esta alternativa consta básicamente de 3 etapas bien definidas: • Etapa 1.- Introducir agua de mar a bordo del submarino, haciendo bajar su presión desde la existente en el exterior hasta la presión a la que se quiere realizar el proceso de disolución. • Etapa 2.- Llevar a cabo el proceso de disolución a presión constante e independiente de la existente en el exterior del submarino. • Etapa 3.- Expulsar fuera del submarino el agua de mar saturada de CO2 haciendo subir su presión desde la correspondiente al proceso de disolución hasta la existente en el exterior. Para ejecutar las etapas 1 y 3 con un coste energético aceptable, resulta necesaria la instalación de un sistema de recuperación de energía, el cual basa su funcionamiento en aprovechar la energía producida en la caída de presión del flujo de agua entrante para elevar la presión del flujo de agua saliente saturada de CO2. El sistema arriba citado puede implementarse de 3 formas alternativas: • Recuperación de doble salto mediante máquinas hidráulicas de desplazamiento positivo. • Recuperación directa mediante cilindros estacionarios dotados de pistones internos. • Recuperación directa mediante cilindros rotativos sin pistones internos. Por otro lado, para ejecutar la etapa 2 de forma silenciosa, y sin ocupar excesivo volumen, resulta necesaria la instalación de un sistema de disolución de CO2 en agua de mar a baja presión, existiendo actualmente 2 principios funcionales viables: • Dispersión de finas burbujas de gas en el seno de una masa de agua. • Difusión directa de CO2 a través de una inter-fase líquido/gas estable sin procesos de dispersión previos. Una vez dicho todo esto, el objetivo de la tesis consiste en llevar a cabo dos estudios comparativos: uno para analizar las ventajas/inconvenientes que presentan las 3 alternativas de recuperación de energía citadas y otro para analizar las ventajas/inconvenientes que presentan los sistemas de disolución de CO2 en agua de mar basados en los 2 principios funcionales mencionados. En ambos estudios se van a tener en cuenta las singularidades propias de una instalación a bordo de submarinos. Para finalizar este resumen, cabe decir que la ejecución de los estudios arriba citados ha exigido el desarrollo de un código software específico (no disponible en la bibliografía) para llevar a cabo la simulación numérica de los distintos sistemas presentados en la tesis. Este código software se ha desarrollado bajo una serie de restricciones importantes, las cuales se listan a continuación: • Ha sido necesario tener en cuenta fluidos de trabajo multi-componente: agua de mar con CO2 disuelto. • El fluido de trabajo se encuentra normalmente en estado líquido, habiendo sido necesario considerar fenómenos de cambio de fase únicamente en etapas incipientes. • La algoritmia se ha diseñado de la forma más simple posible, al objeto de facilitar el subsiguiente proceso de programación y reducir al máximo el tiempo de ejecución en máquina. • La algoritmia arriba citada se ha diseñado para llevar a cabo análisis de tipo comparativo solamente, y no para obtener resultados extremadamente precisos en términos absolutos.
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Segun Gutiérrez del Caño, p. 673, Silvestre Esparsa imprimió entre 1628 y 1660