844 resultados para magnesium carbonate


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O cenário mundial de crescimento está favorecendo uma demanda cada vez maior por petróleo e gás. Para se adequar a esta demanda crescente, as companhias petroleiras têm perfurado em regiões de águas profundas e com caráter geológico particular, como os depósitos carbonáticos recém explorados no Brasil pela Petrobras e que entraram em produção a partir de 2008. Para a produção de hidrocarbonetos é preciso um conhecimento profundo das rochas que os contém. Isto se deve ao fato que os sensores usados para detectar hidrocarbonetos no processo conhecido como perfilagem de poço na indústria petroleira são influenciados em suas medições pelas características das rochas. No caso deste trabalho, carbonatos do pré-sal, aparece uma complicação adicional em termos litológicos que é a presença do mineral Estevensita que não é comumente encontrado em ambientes carbonáticos. Em função de não haver uma forma de detectar sem ambiguidades o mineral Estevensita (rico em magnésio) com a Dolomita (também rica em magnésio), e levando-se em consideração o fato de que a Estevensita fecha os poros da rocha (rocha não reservatório) enquanto a Dolomita normalmente pode ser uma excelente rocha reservatório é de fundamental importância conhecer se o magnésio é proveniente da Estevensita ou do processo de dolomitização do carbonato (substituição de cálcio por magnésio). Não existe hoje em dia uma metodologia de perfilagem de poço que possa indicar a proveniência do magnésio. Estevensita ou Dolomita? Rocha reservatório ou não-reservatório? O objetivo deste trabalho é prover respostas às perguntas acima. Desenvolver uma forma de analisar os minerais presentes no pré-sal através da perfilagem e espectroscopia de poço e fazer a separação entre os diversos constituintes das rochas encontradas no pré-sal. O pré-sal brasileiro é constituído por litologia carbonática complexa, sendo a seção rifte formada por coquinas e a seção sag por microbialitos. Estas rochas foram depositadas antes da deposição da camada de sal no fim do Aptiano. Para atingir o resultado esperado neste trabalho serão utilizadas medições convencionais e não convencionais no laboratório com rochas análogas ao pré-sal e minerais puros tais como a Estevensita a fim de determinar respostas padrão para serem utilizados em programas de análise de registros de perfilagem. O produto final deste trabalho é desenvolver um procedimento para determinação de litologia no pré-sal brasileiro através de registros a cabo (wireline) ou enquanto se perfura (Logging While Drilling - LWD)

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In March 2006, a dead, male bottlenose dolphin (Tursiops truncatus) was found in the salt marsh in Charleston, South Carolina, United States. During necropsy, an enterolith was found completely obstructing the intestinal lumen. Further examination of the enterolith revealed a stingray spine nidus. Most terrestrial enteroliths are composed primarily of struvite (magnesium ammonium phosphate); however, the majority of the enterolith discovered in the stranded dolphin was composed of calcium phosphate carbonate. This case provides an interesting comparison of the variation in the mineral composition between terrestrial and marine enteroliths.

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The use of microbial induced precipitation as a soil improvement technique has been growing in geotechnical domains where ureolytic bacteria that raise the pH of the system and induce calcium carbonate (CaCO3) precipitation are used. For many applications, it is useful to assess the degree of CaCO 3 precipitation by non-destructive testing. This study investigates the feasibility of S-wave velocity measurements to evaluate the amount of calcite precipitation by laboratory testing. Two sets of cemented specimen were tested. The first were samples terminated at different stages of cementation. The second were samples that went through different chemical treatments. These variations were made to find out if these factors would affect the S-wave velocity- cementation relationship. If chemical reaction efficiency was assumed to be constant throughout each test, the relationship between S-wave velocity (Vs) and the amount of CaCO3 precipitation was found to be approximately linear. This correlation between S-wave velocity and calcium carbonate precipitation validates its use as an indicator of the amount of calcite precipitation © 2011 ASCE.

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The performance of porous blocks containing three different reactive magnesia-based cements - namely magnesia alone, magnesium oxide: Portland cement (PC) in 1:1 ratio, cured in ambient conditions, and magnesia alone, cured at elevated carbon dioxide conditions, in hydrochloric acid and magnesium sulfate solution - was investigated. Different aggressive chemical solution conditions were used, to which the samples were exposed for up to 12 months and then tested for strength and microstructure. The performance was also compared with that of standard PC-based blocks. The results showed the significant resistance to chemical attack offered by magnesia, both alone and with PC blend in the porous blocks when cured under ambient carbon dioxide conditions, and confirmed the much poorer performance of blocks made from PC alone. The blocks of solely magnesia cured in elevated carbon dioxide conditions, at 20% concentration, showed slightly lower resistance to acid attack than PC; however, the resistance to sulfate attack was much higher. © 2012 Thomas Telford Ltd.

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The composite nature of mineralized natural materials is achieved through both the microstructural inclusion of an organic component and an overall microstructure that is controlled by templating onto organic macromolecules. A modification of an existing laboratory technique is developed for the codeposition of a CaCO3-gelatin composite with a controllable organic content. First, calibration curves are developed to determine the organic content of a CaCO3-gelatin composite from infrared spectra. Second, a CaCO3-gelatin composite is deposited on either glass coverslips or demineralized eggshell membranes using an automated alternating soaking process. Electron microscopy images and use of the infrared spectra calibration curves show that by altering the amount of gelatin in the ionic growth solutions, the final organic component of the mineral can be regulated over the range of 1-10%, similar to that of natural eggshell. © 2012 Materials Research Societ.

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Upon heating, hydrated magnesium carbonates (HMCs) undergo a continuous sequence of decomposition reactions. This study aims to investigate the thermal decomposition of various commercially produced HMCs classified as light and heavy, highlight their differences, and provide an insight into their compositions in accordance with the results obtained from thermal analysis and microstructure studies. An understanding of the chemical compositions and microstructures, and a better knowledge of the reactions that take place during the decomposition of HMCs were achieved through the use of SEM, XRD, and TG/differential thermal analysis (DTA). The quantification of their CO 2 contents was provided by TG and dissolving the samples in HCl acid. Results show that variations exist within the microstructure and decomposition patterns of the two groups of HMCs, which do not exactly fit into the fixed stoichiometry of the known HMCs in the MgO-CO2-H2O system. The occurrence of an exothermic DTA peak was only observed for the heavy HMCs, which was attributed to their high CO2 contents and the relatively delayed decomposition pattern. © 2013 Akadémiai Kiadó, Budapest, Hungary.

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Codoping of p-type GaN nanowires with Mg and oxygen was investigated using first-principles calculations. The Mg becomes a deep acceptor in GaN nanowires with high ionization energy due to the quantum confinement. The ionization energy of Mg doped GaN nanowires containing passivated Mg-O complex decreases with increasing the diameter, and reduces to 300 meV as the diameter of the GaN nanowire is larger than 2.01 nm, which indicates that Mg-O codoping is suitable for achieving p-type GaN nanowires with larger diameters. The codoping method to reduce the ionization energy can be effectively used in other semiconductor nanostructures. (C) 2010 American Institute of Physics.

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Organic light emitting diodes employing magnesium doped electron acceptor 3, 4, 9, 10 perylenetetracarboxylic dianhydride (Mg: PTCDA) as electron injection layer and silver as cathode were demonstrated. As compared to Mg: Ag cathode, the combination of the Mg: PTCDA layer and silver provided enhanced electron injection into tris (8-quinolinolato) aluminium. The device with 1: 2 Mg: PTCDA and Ag showed an increase of about 12% in the maximum current efficiency, mainly due to the improved hole-electron balance, and an increase of about 28% in the maximum power efficiency, as compared to the control device using Mg: Ag cathode. The properties of Mg: PTCDA composites were studied as well.

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Bright organic electroluminescent devices are developed using a metal-doped organic layer intervening between the cathode and the emitting layer. The typical device structure is a glass substrate/indium-tin oxide (ITO)/copper phthalocyanine (CuPc)/NN'-bis-(1-naphthl)-diphenyl-1,1'-biphenyl-4,4'-diamine (NPB)/Tris(8-quinolinolato) aluminum(Alq(3))/Mg-doped CuPc/Ag. At a driving voltage of 11 V, the device with a layer of Mg-doped CuPc (1:2 in weight) shows a brightness of 4312 cd/m(2) and a current efficiency of 2.52 cd/A, while the reference device exhibits 514 cd/m(2) and 1.25 cd/A.

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Molar-tooth carbonate refers to a sort of rock that has ptygmatical folded structure comparable to the ivory. This kind of carbonate exists in a special time range (from Middle to Neoproterozoic). Its origin and the possibility to use it in stratigraphic correlation of the paleocontinent is the key task of the IGCP447, a project on Proterozoic molar tooth carbonates and the evolution of the earth (2001-2005). The importance lies in that the molar-tooth structure is the key to solving problems related to Precambrian biological and global geochemical events. The molar-tooth structure is associated with microorganisms. Development and recession of such carbonates have relations with the evolution process of early lives and abrupt changes in sea carbonate geochemistry. In recent years, based on researches on petrology, geochemistry and Sr isotope of molar-tooth carbonate in the Jilin-Liaoning and Xuzhou-Huaiyang area, the authors hold that it can be used as a marker for stratigraphic sequence and sedimentary facies analyses.