991 resultados para 1 Cor 15, 20-28


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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

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Pós-graduação em Agronomia (Energia na Agricultura) - FCA

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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

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As argamassas podem ser consideradas como um conjunto de partículas sólidas em suspensão (agregado miúdo), aglomerantes e água (pasta de cimento). Sendo assim, seu comportamento reológico durante a cura pode ser influenciado por fatores como a granulometria, composição e teor de água incorporado. Este trabalho estudou as características reológicas de seis composições de argamassas, em função do teor de cinza volante, como material de atividade pozolânica, em substituição parcial do cimento. A argamassa estudada utilizou como base agregado o resíduo da construção civil (RCC), devidamente caracterizado por difratometria e fluorescência de raios-X. Formularam-se composições de argamassas para os ensaios reológicos com adição de resíduo de construção civil (RCC) nas proporções de 95, 90, 85, 80, 75 e 70%; cinzas volantes (CV) 0, 5, 10, 15, 20 e 25% e 5% de Cimento Portland Comum (CP II- E 32), sendo que em cada amostra foi incorporado 35% de água. Utilizou-se o viscosímetro modelo VT 550, com sensor tipo cilindros coaxiais SV1 – Haake a temperatura de 28ºC. Para avaliar o tempo de cura do material programou-se uma taxa de cisalhamento constante 53,4 s-1 em 1h e 45min, sendo avaliado o torque em intervalos de 15min. Para a elaboração das curvas de fluxo e curvas de histerese, utilizou-se a taxa de cisalhamento entre 0 e 600 s-1 no intervalo de tempo de 120s. Os resultados mostraram que a incorporação de cinza volante foi o principal fator para aumento do torque no tempo de cura das argamassas e mudança do comportamento de reópetico para tixotrópico, nos traços analisados. Os dados experimentais das formulações propostas ajustaram-se ao modelo reológico de Herschel-Bulkley.

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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

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This study aimed to evaluate the effect of chloprostenol administration, at early or intermediary puerperium, under uterine involution, intrauterine fluid accumulation and ovarian activity return. 30 Murrah postpartum buffaloes were randomly divided into three groups: CONT (saline, n = 10); CLO2 (chloprostenol at days 2 and 5 postpartum, n = 10) and; CLO15 (chloprostenol at days 15 and 20 postpartum, n = 10). Gynecological exams were performed at days 2, 7, 14, 21 and 28 postpartum, when uterine involution degree (1 to 3 scale, by transrectal palpation), intrauterine fluid accumulation (0 to 3 scale, by ultrasound exam) and ovarian activity (B-mode ultrasound exam) were evaluated. CLO2 group presented higher uterine involution (2.00 +/- 0.23, 1.66 +/- 0.23, 1.58 +/- 0.23 for groups CLO2, CONT and CLO15, respectively) and faster ovarian activity return in relation to groups CONT and CLO15 (P < 0.05). Groups CLO2 and CLO15 showed lower intrauterine fluid accumulation compared to CONT group (2.04 +/- 0.20, 1.58 +/- 0.20, 1.92 +/- 0.20 for groups CONT, CLO2 and CLO15, respectively; P < 0.05). Prostaglandin analogue administration in postpartum buffalo benefited uterine involution, lochia expulsion and ovarian activity return, improving reproductive efficiency in this specie.

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β-(1→3)-Glucanases were produced by Trichoderma harzianum Rifai PAMB-86 cultivated on botryosphaeran in a bench-fermenter and optimised by the response surface method. Maximal enzyme titres occurred at 5 days, initial pH 5.5 and aeration of 1.5vvm. β-(1→3)-The β-glucanolytic enzyme complex produced by T. harzianum Rifai PAMB- 86 was fractionated by gel filtration into 2 fractions (F-I, F-II), and employed to produce gluco-oligosaccharides from algal paramylon ((1→3)-β-D-glucan) and lichen pustulan ((1→6)-β-D-glucan). Both enzymes attacked paramylon to the extent of ~15-20% in 30 min releasing glucose and laminaribiose as major end-products, and laminarioligosaccharides of degree of polymerization (DP) ≥3. Only F-I degraded pustulan resulting in ~2% degradation at 30 min, with glucose, gentiobiose and gentio-oligosaccharides of DP ≥4 as major products. The difference in the nature of the hydrolysis products can be explained by the substrate specificities of each enzyme fraction, and the structural differences of the β-D-glucans attacked.

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Pós-graduação em Agronomia (Entomologia Agrícola) - FCAV

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The aim of this in vitro study was to evaluate the trans-enamel and transdentinal cytotoxic effects of two in-office tooth bleaching techniques that employ bleaching gels containing 20% and 38% of H2 O2 on cultured odontoblast-like cell line (MDPC-23). Sixty enamel/dentin discs were obtained from bovine central incisors and placed individually in artificial pulp chambers. Six groups were formed according to the following enamel treatments: G1- 20% H2 O2 (1 application); G2- 20% H2 O2 (2 applications); G3- 38% H2 O2 (1 application); G4- 38% H2 O2 (2 applications); G5- 38% H2 O2 (3 applications); and G6- control (no treatment). In G1 and G2, the bleaching gel was left in contact with the enamel surface for 45 min in each application. However, in G3, G4, and G5 the bleaching gel was applied for only 10 min per application. After the last application, the extracts were collected and applied on previously cultured cells (30.000 cells/cm2 ) for 24 h. Cell metabolism was evaluated by the MTT assay and cell morphology was analysed by scanning electron microscopy. Cell metabolism decreased by 96.29%; 96.11%; 96.42%; 95.62%; and 97.18% in G1, G2, G3, G4, and G5, respectively. All treated groups differed significantly from non-treated control group (G6) (p < 0.05). However, the difference in cell metabolism among treated groups was not significant statistically. In addition, significant morphological cell alterations were observed in all treated groups. Under the tested experimental conditions, the extracts collected after both tooth bleaching techniques evaluated in this study caused severe toxic effects on cultured odontoblast-like cell MDPC-23.

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