74 resultados para H3PO4


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A study of several factors has been carried out in order to determine their influence on rare earth phosphates precipitation from H3PO4 solutions obtained after the treatment of the Kola phosphate rock.

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Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

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The development and maintenance of the sealing of the root canal system is the key to the success of root canal treatment. The resin-based adhesive material has the potential to reduce the microleakage of the root canal because of its adhesive properties and penetration into dentinal walls. Moreover, the irrigation protocols may have an influence on the adhesiveness of resin-based sealers to root dentin. The objective of the present study was to evaluate the effect of different irrigant protocols on coronal bacterial microleakage of gutta-percha/AH Plus and Resilon/Real Seal Self-etch systems. One hundred ninety pre-molars were used. The teeth were divided into 18 experimental groups according to the irrigation protocols and filling materials used. The protocols used were: distilled water; sodium hypochlorite (NaOCl)+eDTA; NaOCl+H3PO4; NaOCl+eDTA+chlorhexidine (CHX); NaOCl+H3PO4+CHX; CHX+eDTA; CHX+ H3PO4; CHX+eDTA+CHX and CHX+H3PO4+CHX. Gutta-percha/AH Plus or Resilon/Real Seal Se were used as root-filling materials. The coronal microleakage was evaluated for 90 days against Enterococcus faecalis. Data were statistically analyzed using Kaplan-Meier survival test, Kruskal-Wallis and Mann-Whitney tests. No significant difference was verified in the groups using chlorhexidine or sodium hypochlorite during the chemo-mechanical preparation followed by eDTA or phosphoric acid for smear layer removal. The same results were found for filling materials. However, the statistical analyses revealed that a final flush with 2% chlorhexidine reduced significantly the coronal microleakage. A final flush with 2% chlorhexidine after smear layer removal reduces coronal microleakage of teeth filled with gutta-percha/AH Plus or Resilon/Real Seal SE.

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Results obtained in a pilot-scale unit designed for COD removal and p-TBC (p-tert-butylcatechol) recovery from a butadiene washing stream (pH 14, 200,000 mg COD L-1, highly toxic) at a petrochemical industry are presented. By adding H3PO4, phase separation is achieved and p-TBC is successfully recovered (88 g L-1 of washing stream). Information (time for phase separation and organic phase characterization) was gathered for designing a future industrial unit. The estimated heat generation rate was 990 kJ min-1 and 15 min were enough to promote phase separation for a liquid column of approximately 1.15 m.

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This paper describes a sequential injection chromatography procedure for determination of picloram in waters exploring the low backpressure of a 2.5 cm long monolithic C18 column. Separation of the analyte from the matrix was achieved in less than 60 s using a mobile phase composed by 20:80 (v v-1) acetonitrile:5.0 mmol L-1 H3PO4 and flow rate of 30 μL s-1. Detection was made at 223 nm with a 40 mm optical path length cell. The limits of detection and quantification were 33 and 137 μg L-1, respectively. The proposed method is sensitive enough to monitor the maximum concentration level for picloram in drinking water (500 μg L-1). The sampling frequency is 60 analyses per hour, consuming only 300 μL of acetonitrile per analysis. The proposed methodology was applied to spiked river water samples and no statistically significant differences were observed in comparison to a conventional HPLC-UV method.

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Different types of activated carbon were prepared by chemical activation of brewer`s spent grain (BSG) lignin using H(3)PO(4) at various acid/lignin ratios (1, 2, or 3 g/g) and carbonization temperatures (300, 450, or 600 degrees C), according to a 2(2) full-factorial design. The resulting materials were characterized with regard to their surface area, pore volume, and pore size distribution, and used for detoxification of BSG hemicellulosic hydrolysate (a mixture of sugars, phenolic compounds, metallic ions, among other compounds). BSG carbons presented BET surface areas between 33 and 692 m(2)/g, and micro- and mesopores with volumes between 0.058 and 0.453 cm(3)/g. The carbons showed high capacity for adsorption of metallic ions, mainly nickel, iron, chromium, and silicon. The concentration of phenolic compounds and color were also reduced by these sorbents. These results suggest that activated carbons with characteristics similar to those commercially found and high adsorption capacity can be produced from BSG lignin. (C) 2009 Elsevier Ltd. All rights reserved.

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Trabalho Final de Mestrado para obtenção do grau de Mestre em Engenharia Química e Biológica

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use of additives (Mg/P and nitrification inhibitor dicyandiamide - DCD), on nitrous oxide emission during swine slurry composting. The experiment was run in duplicate; the gas was monitored for 30 days in different treatments (control, DCD, Mg/P and DCD + Mg/P). Nitrous oxide emissions rate (mg of N2O-N.day-1) and the accumulated emissions were calculated to compare the treatments. Results has shown that emissions of N-N2O were reduced by approximately 70, 46 and 96% through the additions of DCD, MgCl2.6H2O + H3PO4 and both additives, respectively, compared to the control. Keywords Composting; swine slurry; additives; nitrous

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A alcalinidade excessiva das águas destinadas à fertirrigação pode criar uma série de inconvenientes, que vão desde o entupimento dos emissores, pela precipitação de carbonatos, até a redução da disponibilidade dos micronutrientes para as culturas. Com o propósito de auxiliar a tomada de decisão quanto ao manejo da alcalinidade dessas águas, desenvolveu-se o ALKA 1.0, um software em CLIPPER 5.2, que pode ser rodado em microcomputadores IBM-PC/XT/AT/PENTIUM ou outros 100% compatíveis. A partir do fornecimento do pH original da água de irrigação, da sua alcalinidade total ou subdividida em CO3(2-) e HCO3- (em mmol L-1), e da lâmina de irrigação utilizada durante o ciclo da cultura, o ALKA 1.0 fornece as quantidades de HCl, HNO3, H2SO4 e H3PO4 que devem ser adicionadas à água de irrigação para que o seu pH atinja o valor estipulado pelo usuário. Além do volume de cada ácido a ser adicionado, o programa fornece a quantidade de nutrientes introduzidas pelos ácidos, na dosagem recomendada, bem como o custo total de cada uma das possíveis escolhas. Para tal, cadastram-se, inicialmente, a densidade e a pureza (%p/p) de cada ácido, bem como seu custo por litro. O ALKA 1.0 oferece, ainda, a opção de adições mistas dos diversos ácidos, visando não só à remoção da alcalinidade excessiva da água, mas também a um balanço adequado à cultura em questão dos nutrientes (N, P, S) adicionados via ácido. Por fim, o ALKA 1.0 oferece a possibilidade de trabalhar-se com bancos de dados, pré-cadastrados, que contêm informações sobre as origens (localidades) e fontes (rios, poços, lagos, açudes e outros) de diversas águas, além do seu pH e alcalinidade total. Desta forma, podem-se conhecer as características de manejo da alcalinidade dessas águas em função de características definidas pelo usuário, tais como um município em particular, determinada fonte, pH, e outros. O ALKA 1.0 foi validado com uma mistura sintética de CO3(2-) e HCO3-, com pH 9,19, em que se verificou a eficiência dos cálculos efetuados para o abaixamento do pH para 7,0, 6,5 e 5,5; e com amostras de águas naturais, para o abaixamento do pH para 6,5 e 6,0; obtendo-se resultados bastante satisfatórios. A redução do pH das amostras naturais para 5,0 não foi eficiente.

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Zeolites are hydrated crystalline aluminosilicate minerals of natural occurrence, structured in rigid third dimension net that can be used as slow release plant-nutrient source. The main objective of this study was to evaluate the effects of plant growth substrate under zeolite application, enriched with N, P and K, on dry matter yield and on nutrient contents in consecutive crops of lettuce, tomato, rice, and andropogon grass. The experiment was carried out in a greenhouse, with 3 kg pots with an inert substrate, evaluated in a randomized block design with three replications. Treatments consisted of four types of enrichment of concentrated natural zeolite: concentrated zeolite (Z) only, zeolite + KNO3 (ZNK), zeolite + K2HPO4 (ZPK) and zeolite + H3PO4 + apatite (ZP), and a control grown in substrate fertilized with a zeolite-free nutrient solution. Four levels of enriched zeolite were tested: 20, 40, 80, and 160 g/pot. Four successive crops were grown on the same substrate in each pot: lettuce, tomato, rice, and andropogon grass. Results indicated that N, P and K enriched zeolite was an adequate slow-release nutrient source for plants. The total dry matter production of above-ground biomass of four successive crops followed a descending order: ZP > ZPK > ZNK > Z.

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The objective of this work was to determine the contribution of dissolved organic carbon (DOC) from a biochar mineral complex (BMC), so as to better understand the interactions between DOC, biochar, clay, and minerals during thermal treatment, and the effects of BMC on amended soils. The BMC was prepared by heating a mixture of a H3PO4-treated saligna biochar from Acacia saligna, clays, other minerals, and chicken manure. The BMC was applied to a sandy loam soil in Western Australia, where wheat was grown. Liquid chromatography-organic carbon detection (LC-OCD) tests were carried out on water extracts from the untreated biochar, the BMC, the BMC-amended soil, and on a control soil to measure the DOC concentration. LC-OCD tests provide a fingerprint of the DOC, which allows the fractions of DOC to be determined. Thermal processing enhanced the reaction of the A. saligna biochar with manure, clays and minerals, and affected the distribution of the DOC fractions. Notably, the process leads to immobilization of hydrophobic DOC and to an increase in the concentration of low-molecular-weight neutrals in the BMC. The application of the BMC to soil increases the DOC in the amended soil, especially the biopolymer fraction.

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PAH (N-(4-aminobenzoyl)glycin) clearance measurements have been used for 50 years in clinical research for the determination of renal plasma flow. The quantitation of PAH in plasma or urine is generally performed by colorimetric method after diazotation reaction but the measurements must be corrected for the unspecific residual response observed in blank plasma. We have developed a HPLC method to specifically determine PAH and its metabolite NAc-PAH using a gradient elution ion-pair reversed-phase chromatography with UV detection at 273 and 265 nm, respectively. The separations were performed at room temperature on a ChromCart (125 mmx4 mm I.D.) Nucleosil 100-5 microm C18AB cartridge column, using a gradient elution of MeOH-buffer pH 3.9 1:99-->15:85 over 15 min. The pH 3.9 buffered aqueous solution consisted in a mixture of 375 ml sodium citrate-citric acid solution (21.01 g citric acid and 8.0 g NaOH per liter), added up with 2.7 ml H3PO4 85%, 1.0 g of sodium heptanesulfonate and completed ad 1000 ml with ultrapure water. The N-acetyltransferase activity does not seem to notably affect PAH clearances, although NAc-PAH represents 10.2+/-2.7% of PAH excreted unchanged in 12 healthy subjects. The performance of the HPLC and the colorimetric method have been compared using urine and plasma samples collected from healthy volunteers. Good correlations (r=0.94 and 0.97, for plasma and urine, respectively) are found between the results obtained with both techniques. However, the colorimetric method gives higher concentrations of PAH in urine and lower concentrations in plasma than those determined by HPLC. Hence, both renal (ClR) and systemic (Cls) clearances are systematically higher (35.1 and 17.8%, respectively) with the colorimetric method. The fraction of PAH excreted by the kidney ClR/ClS calculated from HPLC data (n=143) is, as expected, always <1 (mean=0.73+/-0.11), whereas the colorimetric method gives a mean extraction ratio of 0.87+/-0.13 implying some unphysiological values (>1). In conclusion, HPLC not only enables the simultaneous quantitation of PAH and NAc-PAH, but may also provide more accurate and precise PAH clearance measurements.

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O objetivo do trabalho foi avaliar o efeito da adição de um concentrado zeolítico enriquecido com N, P e K ao substrato de cultivo sobre o crescimento, produção de matéria seca, área foliar, teores e extração de N, P e K e os teores de clorofila do limoeiro 'Cravo'. O porta-enxerto foi cultivado por 93 dias em tubetes de 150 cm³ com substrato orgânico compostado de casca de coco e carvão vegetal (3:1) ao qual se adicionou o concentrado zeolítico. Este foi obtido com a concentração da zeólita natural (Z) e enriquecimento desta com KNO3 (ZNK), e também com a acidificação com H3PO4 e mistura com apatita (ZP). Utilizou-se uma mistura de 30%ZNK + 70%ZP nas doses de: 0; 2,5; 5; 10 e 15 g por planta. Os resultados indicaram que o fornecimento de nutrientes através do mineral zeólita adicionado ao substrato orgânico comprovou ser alternativa viável para a obtenção de porta-enxertos no sistema de produção em ambiente protegido. A adição de 6,4 g do concentrado zeolítico enriquecido com NPK aumentou significativamente a produção de matéria seca, área foliar, altura e diâmetro de caule. Este aumento foi de 37,5% em relação à testemunha que não recebeu o concentrado zeolítico. Houve aumentos nos teores e extração de N, P e K com o fornecimento da zeólita enriquecida. As leituras dos teores de clorofila relacionaram-se com os teores de N, indicando ser esta uma alternativa para o diagnóstico do estado nutricional para a cultura.

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Phosphates have been used for lead immobilization in soils but the influence of soil type is not fully understood. In this work, lead chemical behaviour in two Brazilian latosoils (LA and LV) was studied via treatment with phosphates. The Pb concentration in Toxicity Characteristic Leaching Procedure (TCLP) solutions was decreased in all treatments. After treatment with H3PO4 the Pb concentration in the LA remained within the regulatory limit established by EPA. The ecotoxicological results with Daphnia pulex showed that this treatment reduced the lead bioavailability. Sequential extraction analyses showed that the lead was transferred from the most available to the residual fraction. Relevant decrease of soluble lead was observed in all phosphate treatments.