519 resultados para Voltametria cíclica
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Adsorptive stripping voltammetry carried out in a homogeneous ternary solvent composed of N,N-dimethylformamide, water and ethanol, with alpha-benzoinoxime (alphaBO) as the complexing agent for Mo(VI) and a 0.5 mol L-1 acetic acid - sodium acetate buffer as supporting electrolyte was successfully used for the determination of molybdenum in polyvitamin-polymineral tablets. Tablet samples were analyzed and the results were compared with those obtained both by graphite furnace atomic absorption and by recovery tests, with good correlations, indicating that this may be considered as an alternative procedure for routine determination of Mo(VI) in pharmaceutical samples.
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Universidade Estadual de Campinas . Faculdade de Educação Física
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La rotació cíclica d'antibiòtics (RCA) consisteix a restringir de forma determinada i establerta un antibiòtic o classe d'antibiòtics durant un determinat període de temps, per a tornar a reintroduir-lo posteriorment. D'aquesta manera es pretén evitar l'aparició de resistències bacterianes derivades d'un ús continuat del mateix. En aquest treball, proposem la RCA com una estratègia per al control d'infeccions per gèrmens multirresistents i veure la seva influència en els gèrmens més freqüents que intervenen en les pneumònies nosocomials (NN). A través del registre ENVIN es van recollir les dades de tots els pacients ingressats a la UCI de l'Hospital Universitari la Fe durant dotze mesos consecutius. Es van dividir en 4 cicles de 3 mesos de durada cadascun d'ells. En el primer cicle es va restringir ampicilina/sulbactam, amikacina, cefalosporines i vancomicina; en el segon cicle carbapenems, amikacina i linezolid; en el tercer cicle tigeciclina, quinolones, tobramicina i linezolid i al quart i últim cicle, piperacilina/tazobactam, tobramicina i teicoplanina. Es va comparar amb els tres mesos previs al inici del treball, al qual l'ús d'antibiòtics va ser lliure. El temps global de l'estudi va ser de 15 mesos. El percentatge d'aïllaments d´Acinetobacter spp en el període basal va ser del 46,15% (n=6), de Pseudomonas aeruginosa 15,38% (n=2) i d'Escherichia coli 7, 69% (n=1). Al final de l'estudi els gèrmens aïllats van ser en un 8,57% (n=3) Acinetobacter spp i en un 37,14% (n=13) Pseudomonas aeruginosa.
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O objetivo do trabalho foi verificar o consumo e o custo de alimentos para recuperação da atividade ovariana luteal cíclica (AOLC) em vacas mestiças Holandês x Zebu com anestro. Foram usadas 18 vacas, não-gestantes, não-lactantes, magras, apresentando ovários sem função luteal, de tamanho normal e sem folículos palpáveis na superfície. Doze animais permaneceram em confinamento e receberam alimentação para ganho de peso até o reinício da AOLC. Os seis animais restantes, constituindo o grupo controle, receberam alimentação de mantença para o baixo peso apresentado e permaneceram em anestro durante o período experimental. A AOLC foi avaliada pela concentração de progesterona no soro sangüíneo (coleta de sangue a cada sete dias), pelo exame dos ovários por palpação retal a cada 12 dias, e observação visual dos sinais do estro três vezes ao dia. A recuperação da AOLC nas vacas com anestro exigiu um consumo médio de 722,4 kg de matéria seca, 50,4 kg de proteína bruta e 402,4 kg de NDT, relativos à ingestão média de 2.374,2 kg de volumoso e 194,1 kg de concentrado. O custo desses alimentos somado à perda estimada da produção de leite numa vaca de 3.000 litros de leite/lactação, provocada pelo prolongamento do intervalo de partos, foi equivalente a 1.364,2 litros de leite (preço recebido pelo produtor = R$ 0,20/litro). Esse custo elevado da recuperação do anestro onera o custo final da produção de leite, tendo em vista a alta incidência de anestro nos rebanhos brasileiros.
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Procurou-se conhecer o ganho de peso necessário e o peso mínimo para restabelecimento da atividade ovariana luteal cíclica (AOLC) em vacas adultas, mestiças Holandês x Zebu, não-lactantes, magras e com ovários inativos, anestro adquirido após longo período de restrição alimentar. Seis animais, com peso médio de 322,0 ± 27,0 kg, receberam dieta de mantença para o baixo peso apresentado (grupo I) e 12 animais, com peso médio de 315,0 ± 29,4 kg, foram alimentados para ganho de peso até a recuperação da AOLC (grupo II). O sangue foi coletado (dosagem de progesterona-RIA), e os animais, pesados semanalmente. A AOLC foi avaliada pela concentração de progesterona no sangue, exame dos ovários por palpação retal a cada 12 dias e observação visual do estro três vezes ao dia. O reinício da AOLC ocorreu nos animais do grupo II quando pesaram em média 392,7 ± 29,4 kg. A média do ganho de peso total nesse grupo foi de 77,7 ± 11,2 kg, correspondendo a 24,7 ± 4,5% do peso desses animais em anestro, ou 37,7% dos 206,2 kg perdidos na fase de restrição alimentar para adquirir anestro. Os seis animais do grupo I permaneceram em anestro. Os resultados mostram a influência do nível alimentar sobre a função luteal ovariana e a necessidade de ganho de peso para o restabelecimento do ciclo estral em vacas mestiças leiteiras, magras e em anestro.
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Objetivou-se neste trabalho verificar se a restrição alimentar no pós-partoem vacas Girolanda, multíparas, de bom escore de condição corporal (ECC = 3,5 a 4,5) ao parto será suficiente para impedir o reinício da atividade ovariana luteal cíclica (AOLC) pós-parto.Os animais foram distribuídos em três tratamentos: Grupo I (n = 15), mantença; Grupo II (n = 10) e Grupo III (n = 13), sendo que os grupos II e III receberam restrição alimentar até 90 e 180 dias pós-parto, respectivamente. As pesagens e avaliações do ECC foram efetuadas logo após o parto, e depois semanalmente. A AOLC foi avaliada por palpação retal, observação de cio e concentração de progesterona no leite. Os intervalos do parto ao primeiro cio foram de 53,1, 63,2 e 51,2 dias (P>0,05), respectivamente para os Grupos I, II e III, que apresentaram perdas de peso de 7,3 kg, 57,0 kg e 63,7 kg nesse período; e de 14,2 kg, 63,8 kg e 78,4 kg do parto até 90 dias pós-parto, repectivamente. Em vacas Girolanda de bom escore de condição corporal ao parto, a perda de 15,2% do peso nos três primeiros meses de lactação, e de 16,3% do peso até 180 dias pós-parto, não é suficiente para atrasar o reinício ou interromper a AOLC nos respectivos períodos.
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This paper describes the construction and performance of homemade electrodes for voltammetric purpose using cheap materials, like pipette tips and asbestos fiber. A good cost-to-benefit relation makes this devices specially designed for student use, expecting to improve the broadcasting of electroanalytical methods in Brazilian schools.
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This work describes the construction of a home-made low-cost reactor, using easily available materials, capable of destroying efficiently dissolved organic matter. Just 30 minutes of irradiation were sufficient to destroy more than 99% of the humic acids present in a solution of 4 mg C L-1. Copper speciation was evaluated in natural waters of different salinities to test the reactor's efficiency in destroying organically complexed metal species. The effect of the organic matter concentration, salinity, dissolved oxygen and temperature in the photo-oxidation process is discussed.
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The theoretical aspects of square wave voltammetry were discussed. Reversible, irreversible and quase-reversible electrode reactions were analyzed and the correlations between parameters like frequency, period, square wave potential and amplitude were showed. In this way, diagnostic relationships allow to characterize the electrode process. The analytical applications were discussed in base of the increment in the analytical response (current) due to the characteristics of the developed equations and the unique mode of collecting the electrode response, i.e., the direct and reverse signals. Finally, recent advances in the basic theory, as the applications to the hydrodynamic electrode and the ultramicroelectrode were also analyzed, and the multiple pulses square wave voltammetry was also introduced.
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The electrochemical behavior of paraquat on Pt, Au and carbon fiber ultramicroelectrodes were studied in laboratory samples by square wave voltammetry at high frequencies. The results showed two reversible peaks for paraquat reduction, in agreement to the literature data. The first peak was associated to the reduction of paraquat molecule in solution, with the further adsorption of the intermediate on the electrode surface. This adsorbed species undergoes to electroreduction in a reaction associated to the second voltammetric peak. The variation in pH and square wave parameters showed the best conditions to reduce paraquat as pH 5.0, frequency as high as 1000 s-1, scan increment of 2 mV and square wave amplitude of 50 mV. At such conditions, a variation of paraquat concentrations from 4.3 x 10-6 to 1.66 x 10-4 mol L-1 presented values for the detection limit equal to 3.9, 6.2 and 20.3 ppb on Pt, Au and carbon, respectively, at 1000 s-1. These values are quite below17 the allowed limit of paraquat in drinking water.
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The anodic voltammetric behavior of 4-chlorophenol (4-CF) in aqueous solution has been studied on a Boron-doped diamond electrode using square wave voltammetry (SWV). After optimization of the experimental conditions, 4-CF was analyzed in pure and natural waters using a Britton-Robinson buffer with pH = 6.0 as the supporting electrolyte. Oxidation occurs at 0.80 V vs Ag/AgCl in a two-electron process controlled by adsorption of the species. The detection limits obtained were 6.4 µg L-1 in pure water and 21.5 µg L-1 for polluted water taken from a local creek, respectively. The combination of square wave voltammetry and diamond electrodes is an interesting and desirable alternative for analytical determinations.
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The aim of this work is to discuss some selected applications of square wave voltammetry published in the last five years. The applications focused here cover several electroanalytical fields such as: determination of pesticides; molecules with biological activity; metals and other environmental pollutants. Special attention is given to the work developed in the Grupo de Materiais Eletroquímicos e Métodos Eletroanalíticos - IQSC - USP concerning the utilization of square wave voltammetry, with different kinds of electrodes, for the determination of pesticides in natural waters and active principles in pharmaceutical formulations. The new methodology is simple, fast and sensitive when compared with the traditional ones such as chromatography and spectrophotometry. The satisfactory results obtained provide alternative procedures for the quality control of drugs and the monitoring of pesticides in natural environments.
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This work reports the use of square wave voltammetry (SWV) to analyse the electrochemical reduction of dichlorvos (2, 2-dichlorovinyl-dimethylphosphate) in spiked pure and natural waters. SWV measurements were carried out in 0.5 mol L-1 Na2SO4 aqueous solutions at pH 5, prepared with water originated from three different sources, namely, one sample of purified water and others from two urban creeks in São Carlos County. In all cases, two reduction peaks were observed, at potentials of -0.15 and -1.05 V vs Ag/AgCl, with both current and potential being dependent on pesticide concentration. This allowed the calculation of the following detection limits: 1.0, 2.5 and 3.0x10-8 mol L-1 for purified, Gregorio creek and Monjolinho creek waters, respectively, in a working range between 2.0x10-7 and 1.4x10-6 mol L-1. Recovery measurements found values higher than 80% in all cases, for an added concentration of 4.0 x 10-7 mol L-1 of dichlorvos in each solution. All analytical experiments were performed in triplicate and showed a standard deviation always less than 3%.
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A boron-doped diamond electrode is used for determination of Mn(II) in atmospheric particulate matter by square wave cathodic stripping voltammetry. The analytical curve was linear for Mn(II) concentrations between 5.0 and 37.5 µg L-1, with quantification limit of 3.6 µg L-1. The precision was evaluated by the relative standard deviation, with values between 5.1% and 9.3%. The electrode is free of adsorption, minimizing memory effects. Samples collected in the workplace atmosphere of a foundry had Mn(II) concentrations between 0.4 and 4 µg m-3. No significant differences were observed between the proposed method and inductively coupled plasma optical emission spectroscopy.
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This work illustrates the modeling procedure for a solvent mixture using the simplex- centroid approach. The selected experiment was the optimization of the peak current observed in the direct determination of nickel by anodic stripping voltammetry (ASV) in a solvent mixture composed of N,N-dimethylformamide, ethanol and water. The text is presented in a tutorial way, showing in detail the several steps which must be followed in such a process. Since not all possible mixtures lead to a measurable instrumental response, pseudocomponents had to be used to rescale the experimental design. This also allows to show how to apply this tool, usually troublesome for non-specialists in mixture modeling procedures.