233 resultados para residual peroxide
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Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
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Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
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The objective of this study was to evaluate the structure of Tanzania grassland grazed by goats managed with different residue leaf area index (RLAI) under intermittent stocking. The experiment was carried out from February to August, 2008. The treatments consisted of three different targets RLAI (0.8, 1.6 and 2.4) and 95% light interception (LI) criterion determined the rest period. Forage samples were collected at average height sampling points and weighed. Subsequently, a smaller sample was removed to separate the morphological components (leaf, stem and dead material) and to determine the structural and productive features. The canopy architecture was evaluated by the method of inclined point quadrat. The pre-grazing height in the paddocks were significantly different among treatments. RLAI influenced dry matter contents of green forage, leaf, stem and total, with the exception of dry matter of dead material, where the lowest values were observed for 0.8 RLAI. Thus, RLAI modifies canopy structure and is sensitive to canopy height changes throughout the year. Pasture regrowth is not compromised by residual leaf area indexes between 0.8 and 2.4, when climatic factors are not limiting.
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Dentre os reagentes alternativos, têm-se destacado o peróxido de hidrogênio, visando atender às demandas de produção de celulose ECF. Reagentes como cloro e dióxido de cloro reagem com a lignina residual, levando à formação de compostos organoclorados, fator negativo para as questões relacionadas ao meio ambiente. O fator kappa (FK) é determinante para a dosagem de dióxido de cloro em seqüencias de branqueamento que determinarão a alvura requerida e reduzirão a formação de compostos organoclorados no licor residual. O presente estudo avaliará o efeito da lignina residual através do número de permanganato, após o estágio D1, no branqueamento com peróxido de hidrogênio. Foram realizados cinco branqueamentos de polpas iguais por seqüências ECF em ensaios laboratoriais, variando-se o fator kappa entre eles. O branqueamento foi realizado com uma polpa kraft de eucalipto, prédeslignificada com oxigênio, utilizando a quantidade de reagentes requeridas para cada estágio, em sacos de polietileno e mantidas em banho de vapor com controle de temperatura pelo tempo requerido. A seqüência D(E+P)DP proposta foi comparada com a seqüência D(E+P)DD. Os métodos utilizados para realizar este estudo são os de procedimento padrão conforme as normas TAPPI e CPPA para branqueamento em laboratório de polpa celulósica. Foram avaliados os parâmetros de qualidade da polpa branqueada com os valores de alvura, viscosidade, número kappa, número de permanganato, reversão de alvura e custo do processo de branqueamento e a influência do fator kappa sobre cada uma das condições propostas. Os resultados foram interpretados com base para as polpas que atingiram a alvura objetivo de 90 %ISO. Verificou-se que o FK ideal obtido foi de 0,20 para as seqüências avaliadas. A lignina residual afetou negativamente o branqueamento de todas as sequências, sendo a sequência D(E+P)DP com FK de 0,20 e carga ...
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The new market, focused on sustainability and other environmental concerns, refers to innovations that seek alternative forms of production. In pulp and paper bleaching alternative reagents are studied, for example, hydrogen peroxide, in partial substitution of chlorine dioxide in order to reduce the formation of organochlorines. In this context, this study examined the burden of hydrogen peroxide (H2O2) on alkaline extraction stage (stage Ep) required for the bleaching of pulp with eucalyptus kraft pulp, pre-oxygen delignified to obtain equivalent brightness at 90 ± 0.5% ISO, as well as its effect on quality of pulp produced. The pulp was bleached by the sequence D(Ep)DP, with the application of factor kappa of 0.14 and varying the concentration of hydrogen peroxide in Ep stage three, five, seven and nine kilograms of reagent per ton of pulp absolutely drought. The final P stage was optimized with the use of six, nine and twelve pounds of hydrogen peroxide per ton of absolutely dry pulp to achieve the required brightness. The quality of the pulp produced was analyzed based on the kappa number, the brightness and the viscosity. The methods were performed according to standards set by the standard TAPPI (Technical Association of the Pulp and Paper Industry). The best result was obtained using the following D0Ep(7)D1P(6), which showed a viscosity of 19.9 cP, 89.6% ISO brightness, consumption of 94.9 kg / t of reagents and reagent costs of US$ 28.15, because it showed better pulp quality for a lower cost compared to the others. It was found that the greater the amount of hydrogen peroxide in alkaline extraction, the lower the kappa number and increased the amount of residual hydrogen peroxide. The higher the charge of hydrogen peroxide in Ep stage, the lower the need for hydrogen peroxide in the final P stage, reducing the cost of bleaching
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Pós-graduação em Zootecnia - FCAV
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Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
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Pós-graduação em Biopatologia Bucal - ICT
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Pós-graduação em Agronomia (Produção Vegetal) - FCAV
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O presente trabalho foi realizado nas dependências da FURP (Fundação para o Remédio Popular) de Américo Brasiliense - SP, com o objetivo de validar o método de determinação para residual de detergente alcalino nos equipamentos de revestimento de comprimidos. O trabalho foi desenvolvido no laboratório do Controle de Qualidade da FURP. A validação de limpeza é um tema pouco visto durante o curso de graduação em Farmácia - Bioquímica, porém bastante importante dentro da Indústria Farmacêutica. O processo de limpeza dos equipamentos utilizados na indústria farmacêutica deve ser validado para garantir a qualidade dos produtos. Determinar o residual de um produto de limpeza em um equipamento assegura que o agente de limpeza usado no processo, no caso o detergente alcalino, esteja em uma quantidade dentro do limite aceitável após a limpeza do equipamento. Primeiramente, validou-se o método analítico utilizado para determinar a quantidade de resíduo através da condutividade. Foram analisados os parâmetros linearidade, precisão e especificidade, que se encontraram dentro do limite permitido. Também foi realizado o estudo de recuperação (recovery) do resíduo de detergente do equipamento para confirmar a eficácia da técnica de amostragem juntamente com o método analítico quantitativo escolhido. Após a validação da metodologia analítica quantitativa e o estudo de recuperação foi possível definir um procedimento adequado para a análise do residual de detergente alcalino nos equipamentos submetidos ao processo de limpeza. Juntamente com o setor de Garantia da Qualidade, também foi realizado o estudo de validação da limpeza dos equipamentos da linha de sólidos da FURP (unidade Américo Brasiliense), neste estudo foi avaliado se o procedimento de limpeza estava sendo eficiente e também foi possível fazer a determinação de residual de detergente alcalino presente no equipamento após amostragem com swab, ...
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Pós-graduação em Agronomia - FEIS
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Pós-graduação em Agronomia - FEIS
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Aim To assess the initial cytotoxicity and the late phenotype marker expression of odontoblast-like cells (MDPC-23) subjected to less aggressive in-office bleaching therapies. Methodology A 17.5% hydrogen peroxide (H2O2) gel was applied for 45, 15 or 5 min to enamel/dentine discs adapted to trans-wells positioned over cultured MDPC-23 cells. No treatment was performed on the negative control. Immediately after bleaching, the cell viability, gene expression of inflammatory mediators and quantification of H2O2 diffusion were evaluated. The ALP activity, DSPP and DMP-1 gene expression and mineralized nodule deposition (MND) were assessed at 7, 14 or 21 days post-bleaching and analysed statistically with Mann–Whitney U-tests (α = 5%). Results H2O2 diffusion, proportional to treatment time, was observed in all bleached groups. Reductions of approximately 31%, 21% and 13% in cell viability were observed for the 45-, 15- and 5-min groups, respectively. This reduction was significant (P < 0.05) for the 45- and 15-min groups, which also presented significant (P < 0.05) over-expression of inflammatory mediators. The 45-min group was associated with significant (P < 0.05) reductions in DMP-1/DSPP expression at all periods, relative to control. The ALP activity and MND were reduced only in initial periods. The 15-min group had less intense reduction of all markers, with no difference to control at 21 days. Conclusions The 17.5% H2O2 applied to tooth specimens for 5 min caused no alteration in the odontoblast-like cells. When this gel was applied for 45 or 15 min, a slight cytotoxicity, associated with alterations in phenotypic markers, was observed. However, cells were able to recover their functions up to 21 days post-bleaching.
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To evaluate the effect of the oxidative stress on human dental pulp cells (HDPCs) promoted by toxic concentrations of hydrogen peroxide (H2O2) on its odontoblastic differentiation capability through time. Methods HDPCs were exposed to two different concentrations of H2O2 (0.1 and 0.3 μg/ml) for 30 min. Thereafter, cell viability (MTT assay) and oxidative stress generation (H2DCFDA fluorescence assay) were immediately evaluated. Data were compared with those for alkaline phosphatase (ALP) activity (thymolphthalein assay) and mineralized nodule deposition (alizarin red) by HDPCs cultured for 7 days in osteogenic medium. Results A significant reduction in cell viability and oxidative stress generation occurred in the H2O2-treated cells when compared with negative controls (no treatment), in a concentration-dependent fashion. Seven days after H2O2 treatment, the cells showed significant reduction in ALP activity compared with negative control and no mineralized nodule deposition. Conclusion Both concentrations of H2O2 were toxic to the cells, causing intense cellular oxidative stress, which interfered with the odontogenic differentiation capability of the HDPCs. Clinical significance The intense oxidative stress on HDPCs mediated by H2O2 at toxic concentrations promotes intense reduction on odontoblastic differentiation capability in a 7-day evaluation period, which may alter the initial pulp healing capability in the in vivo situation.
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Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)