143 resultados para Dessorção
Resumo:
The MCM-41 mesoporous synthesis was done using rice hulls ash and chrysotile as natural alternative silica sources. For the using of these sources, chemical and thermic treatments were done in both materials. After chemical and thermic treatments, these materials were employed on the MCM-41 mesoctructures synthesis. The natural materials treated and employed in the synthesis were characterized by several techniques such as X-ray diffraction, N2 adsorption and desorption, scanning electronic microscopy and thermogravimetric analysis. MCM-41 standart samples synthetized with aerosil 200 commercial sílica were used to evaluation. The formed material from rice hulls ash showed values from BET specific area about 468 m².g-1, N2 adsorption and desorption isotherms and loss mass similar to reference materials. The silica from chrysotile calcined and leached was employed to mesoporous materials synthesis. The BET specific area showed values about 700 m².g-1, N2 adsorption and desorption isotherms type IV and loss mass similar to mesoporous materials. The formed material from calcined and leached chrysotile, without calcination, applied to phenol remotion carried high performance liquid chromatography and evaluated with organophilic clays with different treatments. By the characterization techniques were proved that mesoporous materials with lesser order that reference samples. The material formed from rice hulls ash without the calcination step achieved better adsorption results than organophilic clays
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Biodiesel is an alternative fuel, renewable, biodegradable and nontoxic. The transesterification of vegetable oils or animal fat with alcohol is most common form of production of this fuel. The procedure for production of biodiesel occurs most commonly through the transesterification reaction in which catalysts are used to accelerate and increase their income and may be basic, acid or enzyme. The use of homogeneous catalysis requires specific conditions and purification steps of the reaction products (alkyl ester and glycerol) and removal of the catalyst at the end of the reaction. As an alternative to improve the yield of the transesterification reaction, minimize the cost of production is that many studies are being conducted with the application of heterogeneous catalysis. The use of nano-structured materials as catalysts in the production of biodiesel is a biofuel alternative for a similar to mineral diesel. Although slower, can esterify transesterified triglycerides and free fatty acids and suffer little influence of water, which may be present in the raw material. This study aimed at the synthesis, characterization and application of nano-structured materials as catalysts in the transesterification reaction of soybean oil to produce biodiesel by ethylic route. The type material containing SBA-15 mesoporous lanthanum embedded within rightly Si / La = 50 was used catalyst. Solid samples were characterized by X-ray diffraction, thermogravimetric analysis, infrared spectroscopy, nitrogen adsorption and desorption. For the transesterification process, we used a molar ratio of 20:1 alcohol and oil with 0.250 g of catalyst at 60°C and times of 6 hours of reaction. It was determined the content of ethyl esters by H-NMR analysis and gas chromatography. It was found that the variable of conversion obtained was 80%, showing a good catalytic activity LaSBA-15 in the transesterification of vegetable oils via ethylic route
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In this study, was used a very promising technique called of pyrolysis, which can be used for obtaining products with higher added value. From oils and residues, since the contribution of heavier oils and residues has intensified to the world refining industry, due to the growing demand for fuel, for example, liquid hydrocarbons in the range of gasoline and diesel. The catalytic pyrolysis of vacuum residues was performed with the use of a mesoporous material belonging the M41S family, which was discovered in the early 90s by researchers Mobil Oil Corporation, allowing new perspectives in the field of catalysis. One of the most important members of this family is the MCM-41, which has a hexagonal arrangement of mesopores with pore diameters between 2 and 10 nm and a high specific surface area, making it very promising for use as a catalyst in petroleum refining for catalytic cracking, and their mesopores facilitate the access of large hydrocarbon molecules. The addition of aluminum in the structure of MCM-41 increases the acidity of the material, making it more positive for application in the petrochemical industry. The mesoporous material of the type Al-MCM41 (ratio Si / Al = 50) was synthesized by hydrothermal method starting from the silica gel, NaOH and distilled water added to the gel pseudobohemita synthesis. Driver was used as structural CTMABr. Removal of organic driver (CTMABr) was observed by TG / DTG and FTIR, but this material was characterized by XRD, which was observed the formation of the main peaks characteristic of mesoporous materials. The analysis of adsorption / desorption of nitrogen this material textural parameters were determined. The vacuum residues (VR's) that are products of the bottom of the vacuum distillation tower used in this study are different from oil fields (regions of Ceará and Rio de Janeiro). Previously characterized by various techniques such as FTIR, viscosity, density, SARA, elemental analysis and thermogravimetry, which was performed by thermal and catalytic degradation of vacuum residues. The effect of AlMCM-41 was satisfactory, since promoted a decrease in certain ranges of temperature required in the process of conversion of hydrocarbons, but also promoted a decrease in energy required in the process. Thus enabling lower costs related to energy expenditure from degradation during processing of the waste
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The production of synthesis gas has received renewed attention due to demand for renewable energies to reduce the emissions of gases responsible for enhanced greenhouse effect. This work was carried out in order to synthesize, characterize and evaluate the implementation of nickel catalysts on MCM-41 in dry reforming reactions of methane. The mesoporous molecular sieves were synthesized using as silica sources the tetraethyl orthosilicate (TEOS) and residual glass powder (PV). The sieves were impregnated with 10% nickel to obtain the metallic catalysts (Ni/MCM-41). These materials were calcined and characterized by Thermogravimetric Analysis (TG), Infrared spectroscopy (FTIR), X-ray Diffraction (XRD), Temperature-Programmed Reduction (TPR) and N2 Adsorption/Desorption isotherms (BET/BJH). The catalytic properties of the samples were evaluated in methane dry reforming with CO2 in order to produce synthesis gas to be used in the petrochemical industry. The materials characterized showed hexagonal structure characteristic of mesoporous material MCM-41 type, being maintained after impregnation with nickel. The samples presented variations in the specific surface area, average volume and diameter of pores based on the type of interaction between the nickel and the mesoporous support. The result of the the catalytic tests showed conversions about 91% CO2, 86% CH4, yelds about 85% CO and 81% H2 to Ni/MCM-41_TEOS_C, and conversions about 87% CO2, 82% CH4, yelds about 70% CO and 59% H2 to Ni/MCM-41_PV_C. The similar performance confirms that the TEOS can be replaced by a less noble materials
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Dissertação (mestrado)—Universidade de Brasília, Faculdade UnB Planaltina, Mestrado em Ciências de Materias, 2016.
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Verificou-se o deslocamento de atrazina no perfil do solo, em função do movimento da água e do tempo de aplicação, e possíveis influencias de fluxos preferenciais sobre a lixiviação. O trabalho foi conduzido em uma Terra Roxa Estruturada eutrófica de textura argilosa, em Piracicaba-SP, no período de junho de 92 a fevereiro de 93. Foram instalados 2 experimentos, sendo um com a cultura do milho irrigado (experimento 1) e o outro em solo nu (experimento 2). O experimento 1 foi instalado em uma área de 1000m2 sobre a qual se demarcou duas parcelas de 12m x 12m separadas uma da outra por 18m. Uma parcela foi irrigada e a outra fertirrigada . O experimento 2 foi instalado em duas parcelas de 7m x 7m, separadas uma da outra por 5m. Em uma das parcelas do experimento 2 aplicou-se previamente 1000kg de calcario/ha para elevar a saturação de bases para 88%, alem de 500kg de gesso/ha. Cada parcela do experimento 2 foi constituída de 3 linhas de instrumentos e os resultados obtidos para cada linha foram comparados entre si para verificação de fluxo preferencial. A atrazina foi aplicada na dosagem de 6,3l/ha no experimento 1 e 6kg do principio ativo/ha no experimento 2. Os resultados mostraram intensa lixiviação da atrazina em todo o perfil do solo ate 150cm de profundidade já na primeira coleta efetuada 7 dias apos a aplicação. A parcela 2 do experimento 2 , apesar de não ter recebido calcario, mostrou perdas de atrazina por lixiviação muito maiores que a parcela 1. O solo apresentou pequena capacidade de adsorção de atrazina (máximo em torno de 10% na camada de 0-30cm).
Resumo:
Com os objetivos de avaliar a distribuição, persistência e degradação dos herbicidas no solo, na água e seu escape para outros corpos de água e avaliar os mecanismos de absorção/dessorção no solo, foi instalado um experimento de campo no Município de Pelotas no Rio Grande do Sul, utilizando-se os herbicidas propanil e clomazone na cultura de arroz alagado. O processo adotado para amostrar os produtos no solo foi aperfeiçoado, com a introdução de tubos de PVC perfurados que permitiam a ocorrência dos processos de troca no solo. Foram feitas as isotermas de adsorção para o propanil e clomazone, ajustadas por quatro modelos distintos. Fez-se também analise química dos grãos para os elementos N, P, K, Ca, Mg, S, Cu, Mn, Zn, determinando-se o teor de proteína bruta.Os resultados obtidos para o clomazone mostram que não houve contaminação ambiental pelo produto uma vez que nao foi detectada sua presença nas amostras de solo e agua do experimento. A ocorrência do propanil somente foi detectada nas amostras de solo coletadas com os tubos perfurados aos 30 e 120 dias após a emergência das plantas. Dos modelos de curvas de adsorção testados e comparados pelo método dos resíduos padronizados, o modelo de Freundlich foi o que melhor descreveu o comportamento dos dois produtos.
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O trabalho apresenta possíveis consequências da utilização do pesticida Paraquat na agricultura a partir de resultados da execução em laboratório de ensaios de batelada (adsorção e dessorção) e de coluna em um solo (Cambissolo) de Bom Jardim, RJ. A avaliação dos parâmetros de transporte (fator de retardamento e dispersão hidrodinâmica), obtidos pelos ensaios, mostrou que o Paraquat se comportou como sendo de elevada capacidade de adsorção ao solo estudado. Embora a taxa de dessorção tenha sido pequena, a mesma não pode ser desconsiderada tendo em vista os processos de erosão hídrica. Conclui-se, portanto, que o Paraquat apresenta baixo risco de contaminação de águas subterrâneas por lixiviação, sendo provavelmente o maior risco de contaminação via escoamento superficial, devendo tal ser mais investigado visando subsidiar o uso sustentável da área.