969 resultados para Three phase core type transformers


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Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

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In this work, siloxane-poly(propylene oxide) discs (PPO disc) prepared using the sol-gel process were used as solid phase in enzyme-linked immunosorbent assays (ELISA) for the detection of anti-hepatitis C virus (HCV) antibodies. The HCV RNA from serum (genotype 1b) was submitted to the RT-PCR technique and subsequent amplification of the HCV core 408 pb. This fragment was cloned into expression vector pET42a and expressed in Escherichia coli as recombinant protein with glutathione S-transferase (GST). Cell cultures were grown and induced having a final concentration of 0.4 x 10(-3) mol L-1 of IPTG. After induction, the cells were harvested and the soluble fraction was analyzed using polyacrilamide gel 15% showing a band with an approximate molecular weight of 44 kDa, the expected size for this GST-fused recombinant protein. The recombinant protein was purified and continued by immunological detection using HCV-positive serum and showed no cross-reactivity with positive samples for other infectious diseases. An ELISA was established using 1.25 ng of recombinant protein per PPO disc, a dilution of 1: 10,000 and 1:40 for a peroxidase conjugate and serum, respectively, and solutions of hydrogen peroxide and 3,3',5,5'-tetra-methylbenzidine in a ratio of 1: 1. The proposed methodology was compared with the ELISA conventional polystyrene-plate procedure and the performance of the PPO discs as a matrix for immunodetection gave an easy synthesis, good performance and reproducibility for commercial application. (c) 2007 Elsevier B.V. All rights reserved.

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It is shown that the appearance of a fixed-point singularity in the kernel of the two-electron Cooper problem is responsible for the formation of the Cooper pair for an arbitrarily weak attractive interaction between two electrons. This singularity is absent in the problem of three and few superconducting electrons at zero temperature on the full Fermi sea. Consequently, such three- and few-electron systems on the full Fermi sea do not form Cooper-type bound states for an arbitrarily weak attractive pair interaction.

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Low-energy muon-transfer cross sections and rates in collisions of muonic atoms with hydrogen isotopes are calculated using a six-state close-coupling approximation to coordinate-space Faddeev-Hahn-type equations. In the muonic case satisfactory results are obtained for all hydrogen isotopes and the experimentaly observed strong isotopic dependence of transfer rates is also reproduced. A comparison with results of other theoretical and available experimental works is presented. The present model also leads to good transfer cross sections in the well-understood problem of antihydrogen formation in antiproton-positronium collision.

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The development of chalcogenide glasses fibers for application in the infrared wavelength region between 1 and 10 μm is a big opportunity. More particularly, the possibility to generate efficient non linear effects above 2 μm is a real challenge. We present in this work the elaboration and optical characterizations of suspended core microstructured optical fibers elaborated from the As2S3 chalcogenide glass. As an alternative to the stack and draw process a mechanical machining has been used to the elaboration of the preforms. The drawing of these preforms into fibers allows reaching a suspended core geometry, in which a 2.5 μm diameter core is linked to the fiber clad region by three supporting struts. The zero dispersion wavelength is thus shifted towards 2 μm. At 1.55 μm our fibers exhibit a dispersion around -250 ps/nm/km. Their background level of losses is below 0,5 dB/m. By pumping them at 1.55 μm with a ps source, we observe self phase modulation as well as Raman generation. Finally a strong spectral enlargement is obtained with an average output power of - 5 dbm. © 2010 SPIE.

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A challenge in mesonic three-body decays of heavy mesons is to quantify the contribution of re-scattering between the final mesons. D decays have the unique feature that make them a key to light meson spectroscopy, in particular to access the Kn S-wave phase-shifts. We built a relativis-tic three-body model for the final state interaction in D+ → K -π+π+ decay based on the ladder approximation of the Bethe-Salpeter equation projected on the light-front. The decay amplitude is separated in a smooth term, given by the direct partonic decay amplitude, and a three-body fully interacting contribution, that is factorized in the standard two-meson resonant amplitude times a reduced complex amplitude that carries the effect of the three-body rescattering mechanism. The off-shell reduced amplitude is a solution of an inhomogeneous Faddeev type three-dimensional integral equation, that includes only isospin 1/2 K -π+ interaction in the S-wave channel. The elastic K-π+ scattering amplitude is parameterized according to the LASS data[1]. The integral equation is solved numerically and preliminary results are presented and compared to the experimental data from the E791 Collaboration[2, 3] and FOCUS Collaboration[4, 5].

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In this work we report our achievements in the elaboration and optical characterizations of low-losses suspended core optical fibers elaborated from As2S3 glass. For preforms elaboration, alternatively to other processes like the stack and draw or extrusion, we use a process based on mechanical drilling. The drawing of these drilled performs into fibers allows reaching a suspended core geometry, in which a 2 μm diameter core is linked to the fiber clad region by three supporting struts. The different fibers that have been drawn show losses close to 0.9 dB/m at 1.55 μm. The suspended core waveguide geometry has also an efficient influence on the chromatic dispersion and allows its management. Indeed, the zero dispersion wavelength, which is around 5 μm in the bulk glass, is calculated to be shifted towards around 2μm in our suspended core fibers. In order to qualify their nonlinearity we have pumped them at 1.995 μm with the help of a fibered ns source. We have observed a strong non linear response with evidence of spontaneous Raman scattering and strong spectral broadening. © 2011 SPIE.

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Pós-graduação em Engenharia e Ciência de Alimentos - IBILCE

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O mapeamento geológico realizado na área de Nova Canadá, porção sul do Domínio Carajás, Província Carajás, possibilitou a individualização de duas unidades de caráter máfico e intrusivas nos granitoides do Complexo Xingu e, mais restritamente, na sequência greenstone belt do Grupo Sapucaia. São representadas por diques de diabásio isotrópicos e por extensos corpos de anfibolito, com os últimos descrevendo texturas nematoblástica e granoblástica, de ocorrência restrita à porção SW da área. Ambos apresentam assinatura de basaltos subalcalinos de afinidade toleítica, sendo que os diques de diabásio são constituídos por três variedades petrográficas: hornblenda gabronorito, gabronorito e norito, sendo essas diferenças restritas apenas quanto à proporção modal de anfibólio, orto- e clinopiroxênio, já que texturalmente, as mesmas não apresentam diferenças significativas. São formados por plagioclásio, piroxênio (orto- e clinopiroxênio), anfibólio, minerais óxidos de Fe-Ti e olivina, apresentam um padrão ETR moderadamente fracionado, discreta anomalia negativa de Eu, ambiente geotectônico correspondente a intraplaca continental, e assinaturas dos tipos OIB e E-MORB. Já os anfibolitos são constituídos por plagioclásio, anfibólio, minerais opacos, titanita e biotita, mostram um padrão ETR horizontalizado, com anomalia de Eu ausente, sendo classificados como toleítos de arco de ilha e com assinatura semelhante aos N-MORB. Os dados de química mineral obtidos nessas unidades mostram que, nos diques de diabásio, o plagioclásio não apresenta variações composicionais significativas entre núcleo e borda, sendo classificados como labradorita, com raras andesina e bytownita; o anfibólio mostra uma gradação composicional de Fe-hornblenda para actinolita, com o aumento de sílica. Nos anfibolitos, o plagioclásio mostra uma grande variação composicional, de oligoclásio à bytownita nas rochas foliadas, sendo que nas menos deformadas, sua classificação é restrita à andesina sódica. O piroxênio, presente apenas nos diabásios, exibe considerável variação em sua composição, revelando um aumento no teor de magnésio nos núcleos, e de ferro e cálcio, nas bordas, permitindo classificá-los em augita, pigeonita (clinopiroxênio) e enstatita (ortopiroxênio). Os diabásios apresentam titanomagnetita, magnetita e ilmenita como os principais óxidos de Fe-Ti, permitindo reconhecer cinco formas distintas de ilmenita nessas rochas: ilmenita treliça, ilmenita sanduíche, ilmenita composta interna/externa, ilmenita em manchas e ilmenita individual. Feições texturais e composicionais sugerem que a titanomagnetita e os cristais de ilmenita composta externa e individual foram originados durante o estágio precoce de cristalização. Durante o estágio subsolidus, a titanomagnetita foi afetada pelo processo de oxi-exsolução, dando origem a intercrescimentos de magnetita pobre em titânio com ilmenita (ilmenitas treliça, em mancha, sanduíche e composta interna). Os anfibolitos possuem a ilmenita como único mineral óxido de Fe e Ti ocorrendo, portanto, sob a forma de ilmenita individual, onde encontra-se sempre associada ao anfibólio e à titanita. Os valores mais elevados de suscetibilidade magnética (SM) estão relacionados aos gabronoritos e noritos, os quais exibem maiores conteúdos modais de minerais opacos e apresentam titanomagnetita magmática em sua paragênese. A variedade hornblenda gabronorito define as amostras com valores intermediários de SM. Os menores valores de SM são atribuídos aos anfibolitos, que são desprovidos de magnetita. A correlação negativa entre valores de SM com os conteúdos modais de minerais ferromagnesianos indica que os minerais paramagnéticos (anfibólio e piroxênio) não possuem influência significativa no comportamento magnético dos diabásios, enquanto nos anfibolitos a tendência de correlação positiva entre estas variáveis pode sugerir que estas fases são as principais responsáveis pelos seus valores de SM. Dados geotermobarométricos obtidos a partir do par titanomagnetita-ilmenita nos diabásios indicam que estes se formaram em condições de temperatura (1112°C) e Fo2 (-8,85) próximas daquelas do tampão NNO.

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Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

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This study evaluated the effect of the core substrate type (dentin and composite resin) on the retention of crowns made of yttrium oxide stabilized tetragonal zirconia polycrystal (Y-TZP), submitted to three inner surface conditionings. For this purpose, 72 freshly extracted molars were embedded in acrylic resin, perpendicular to the long axis, and prepared for full crowns: 36 specimens had crown preparations in dentin; the remaining 36 teeth had the crowns removed, and crown preparations were reconstructed with composite resin plus fiber posts with dimensions identical to the prepared dentin. The preparations were impressed using addition silicone, and 72 Y-TZP copings for the tensile test were produced. Cementation was performed with a dual-cured cement containing phosphate monomers. For cementation, the crown preparation (dentin or resin) was conditioned with the adhesive system, and the ceramic was subjected to one of three surface treatments: isopropyl alcohol, tribochemical silica coating, or thin low-fusing glassy porcelain layer application plus silanization. After 24 hours, all specimens were submitted to thermocycling (6000 cycles) and placed in a special tensile testing device in a universal testing machine to determine failure loads. The failure modes of all samples were analyzed under a stereomicroscope. Two-way analysis of variance showed that the surface treatment and substrate type (alpha=0.05) affected the tensile retention results. The dentin substrate presented the highest tensile retention values, regardless of the surface treatment. When the substrate was resin, the tribochemical silica coating and low-fusing glaze application plus silanization groups showed the higher retention values.

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A method using Liquid Phase Microextraction for simultaneous detection of citalopram (CIT), paroxetine (PAR) and fluoxetine (FLU), using venlafaxine as internal standard, in plasma by high performance liquid chromatography with fluorescence detection was developed. The linearity was evaluated between 5.0 and 500 ng mL(-1) (r > 0.99) and the limit of quantification was 2.0, 3.0 and 5.0 ng mL-1 for CIT. PAR and FLU, respectively. Therefore, it can be applied to therapeutic drug monitoring, pharmacokinetics or bioavailability studies and its advantages are that it necessary relatively inexpensive equipment and sample preparation techniques.

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In this article were studied two xanthone derivatives known as 1,5-dihydroxy-8-methoxyxanthone (I) and 1,3,7-trihydroxy-8-methoxyxanthone (II), which show one water molecule into their crystal structures. In xanthone I, there are water wires contributing to build up channel-like cavities along the c axis, whereas in xanthone II the water is surrounded by three xanthone molecules forming a cage-type structure. The geometries of I and II were optimized using the density functional theory method with B3LYP functional, and the results were compared with crystal structure. Both theoretical and experimental investigations reveal a concordance between structural parameters, with the xanthone core presenting an almost flat conformation and substituents adopting the more stable orientations. In the two compounds, the hydroxyl group linked at position 1 is involved in a resonance-assisted hydrogen bond with the carbonyl group. Besides, the supramolecular arrangement of the host/guest systems are stabilized mainly by classical intermolecular hydrogen bonds (O-H center dot center dot center dot O) involving xanthone-to-water and xanthone-to-xanthone. In addition, C-H center dot center dot center dot O weak hydrogen bonds, as well as pi-pi interactions play an important role to stabilize the crystal self-assembly of xanthones I and II. The results reported here underline the role of inclusion of water molecules and their different arrangement into the crystal structure of two xanthone host/guest systems.

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Lodenafil carbonate is a new phosphodiesterase Type 5 (PDE5) inhibitor used in treatment of erectile dysfunction. Objective: The present study was conducted to evaluate the safety, tolerability, and pharmacokinetics of lodenafil carbonate after administering ascending (1 - 100 mg) single oral doses to healthy male volunteers (n = 33). Methods: The study was an open-label, dose-escalation, Phase I clinical trial involving the administration of single oral doses of lodenafil carbonate. Lodenafil carbonate was administered sequentially, escalating in single doses of 1 mg - 100 mg with a washout period of at least 1 week between each dose. The progression to the next dose was allowed after clinical and laboratory exams, Ambulatory Monitoring of Arterial Pressure (AMAP) without relevant clinical modifications and adverse events without clinical relevancy. Blood samples were collected at pre-dose, 0.25, 0.5, 0.75, 1, 1.25, 1.5, 1.75, 2, 2.5, 3, 3.5, 4, 4.5, 5, 6, 7, 8, 10, 12, 14, 16, 20 and 24 h post-dosing. Plasma samples for measurement of lodenafil carbonate and lodenafil were analyzed by liquid chromatography coupled to tandem mass spectrometry. Results: No serious adverse events were observed, and none of the subjects discontinued the study due to intolerance. The AMAP measurements, clinical and laboratory exams and ECG revealed no significant changes even at higher doses. Lodenafil carbonate was not detected in any samples, indicating that it acts as a prodrug. The mean lodenafil pharmacokinetic parameters for t(max) and t(1/2) were 1.6 (+/- 0.4) h and 3.3 (+/- 1.1) h, respectively. This study demonstrated that lodenafil carbonate was well tolerated and showed a good safety profile in healthy male volunteers.