International Telemetering Conference Proceedings / October 28-31, 1996 / Town and Country Hotel and Convention Center, San Diego, California / This paper presents a new architecture of the end-to-end ground system to reduce overall mission support costs. The present ground system of the Jet Propulsion Laboratory (JPL) is costly to operate, maintain, deploy, reproduce, and document. In the present climate of shrinking NASA budgets, this proposed architecture takes on added importance as it will dramatically reduce all of the above costs. Currently, the ground support functions (i.e., receiver, tracking, ranging, telemetry, command, monitor and control) are distributed among several subsystems that are housed in individual rack-mounted chassis. These subsystems can be integrated into one portable laptop system using established MultiChip Module (MCM) packaging technology. The large scale integration of subsystems into a small portable system will greatly reduce operations, maintenance and reproduction costs. Several of the subsystems can be implemented using Commercial Off-The-Shelf (COTS) products further decreasing non-recurring engineering costs. The inherent portability of the system will open up new ways for using the ground system at the “point-of-use” site as opposed to maintaining several large centralized stations. This eliminates the propagation delay of the data to the Principal Investigator (PI), enabling the capture of data in real-time and performing multiple tasks concurrently from any location in the world. Sample applications are to use the portable ground system in remote areas or mobile vessels for real-time correlation of satellite data with earth-bound instruments; thus, allowing near real-time feedback and control of scientific instruments. This end-to-end portable ground system will undoubtedly create opportunities for better scientific observation and data acquisition.

PhD thesis - Faculty of Science / The main aim of this thesis has been to study the way in which Fe(III) and Co(II) incorporation into Si-MCM-41 synthesis gels affects the properties of the unmodified material. Another aim was to investigate the influence of these hetero-atoms on the dispersion and particle size distribution as well as the catalytic activity of supported Au nanoparticles in the CO oxidation reaction. Si-MCM-41 has been successfully synthesized in this work using mixtures containing CTAB as a structure-directing agent (SDA) and water-glass as a SiO2 source. Replacement of water-glass with pre-calcined Si-MCM-41 for SiO2 source in the secondary synthesis step has produced Si-MCM-41 with improved structural properties (XRD, HRTEM and Raman spectroscopy), including restructured and more crystalline pore walls (Raman spectroscopy). The conventional shortcomings of Si-MCM-41 as a support for catalyticallyactive (transition) metal components such as low hydrothermal stability, low PZC, lack of cation exchange capacity and no reducibility have been partially addressed by modification with Fe(III) and Co(II). The premodification was achieved both during framework synthesis and after synthesis by the incipient wetness impregnation (IWI) method. As opposed to the one-pot synthesis of metal-containing derivatives, the IWI method gave materials with high metal loadings and maximal retention of the properties of pristine Si-MCM-41. On the other hand, metal incorporation during synthesis to a loading of ~8.8 wt% using aqueous solutions of metal precursors showed some collapse of the mesostructure. Consequently methods were sought to incorporate this amount of metal (and up to double, i.e., 16 wt%) with maximal retention of the MCM-41 characteristics. These methods included (i) using Si-MCM-41 as a SiO2 source, (ii) dissolving the metal precursors in an acid solution before inclusion into the synthesis gel, and (iii) using freshly precipitated alkali slurries of the metal precursors. The first method produced a highly ordered 16wt% Fe-MCM-41 material with excellent reducibility (TPR showed three well-resolved peaks) and pore-wall structure (Raman spectroscopy). Like the aqueous route, the acid-mediated metal incorporation route did not produce ordered materials at metal contents of ~16 wt%. The base precipitate route produced highly ordered composite materials up to 16 wt% metal content, with characteristics similar to those of Si-MCM-41 (XRD, BET and HRTEM), although some metal phases were observed as a separate phase on the SiO2 surface. Thus, metal-containing MCM-41 materials could be obtained with conservation of MCM-41 mesoporosity. Raman spectroscopic studies have shown that the effect of transition metal incorporation in MCM-41-type materials is to strengthen the pore walls (shift of Si-O-Si peaks to higher frequencies), while TPR studies revealed that the essentially neutral framework of Si-MCM-41 could be rendered reducible by transition metal incorporation. Gold-containing mesoporous nanocomposites were prepared by both direct synthesis and post-synthetically. Catalysts prepared by direct hydrothermal synthesis were always accompanied by formation of large Au particles because of the need to calcine the materials at 500 oC in order to remove the occluded surfactant template. The presence of transition metal components in Me-MCM-41 (Me = Fe and Co) has been found to play a significant role in the particle size distribution and also the dispersion of Au nanoparticles when these materials were used as supports. In general, a base metal-containing support was found to produce smaller Au nanoparticles than the corresponding siliceous support. It has been proposed that the transition metal components serve as anchoring or nucleation sites for the Au nanoparticles, which are likely to sinter during calcination. The anchoring sites thus retard the surface mobility of Au at calcination temperatures above their TTammann. The use of the Au/Me-MCM-41 materials as catalysts in the CO oxidation reaction has led to the following observations: (i) catalyst on metal-containing supports showed better activity than those on Si-MCM-41, probably due to the induced reducibility in metal-MCM-41, (ii) catalysts prepared by direct synthesis showed inferior activity owing to large Au particles, (iii) increasing Au content improves the catalytic performance, (iv) increasing the Fe content of the support at constant Au improves the catalytic performance, and (v) changing the base metal component of the support from Fe to Co led to a significant improvement in catalytic activity. The similarity of the apparent activation energies (Ea) for the 5 wt% Au-containing 5 wt% Fe- and 5 wt% Co-MCM-41 suggested that the difference in catalytic activity is associated with the number of active sites possessed by each catalyst system. The observed order of catalytic activity of these 5 wt% Au-containing systems in terms of the support type is: Co-MCM-41 > Fe-MCM-41 > Si-MCM-41. This was further supported by the average Au particle size, which, in terms of the support, followed the order Co-MCM-41 < Fe-MCM-41 < Si-MCM-41. Thus, metal-support interactions between Au and MCM-41 have been enhanced by introducing Fe(III) and Co(II), which also induced framework charge, ion exchange capacity (IEC) and reducibility in the neutral siliceous support.

Made available in DSpace on 2014-12-17T15:41:45Z (GMT). No. of bitstreams: 1 MariaJFCpdf.pdf: 4931245 bytes, checksum: 45a7ea893d17f478c73adf56787579aa (MD5) Previous issue date: 2008-12-22 / Coordena??o de Aperfei?oamento de Pessoal de N?vel Superior / The present work reports the study of nanoporous structures, aiming at their use in research directed to the current demand of the petroleum industry to value heavy oil. Initially, two ways were chosen for the synthesis of porous structures from the molecular sieves of type Si-MCM-41. In the first way, the structure MCM-41 is precursory for heteroatom substitutes of silicon, generating catalyst of the type Al-MCM-41 from two different methods of incorporation of the metal. This variation of the incorporation method of Aluminum in the structure of Si-MCM-41 was carried out through the conventional procedure, where the aluminum source was incorporated to the gel of synthesis, and the procedure post-synthesis, where the Aluminum source was incorporated in catalyst after the synthesis of Si-MCM-41. In the second way, the MCM-41 acts as a support for growth of nanocrystals of zeolite embedded in their mesoporous, resulting in hybrid MCM-41/ZSM-5 catalyst. A comparative analysis was carried through characterizations by XRD, FTIR, measures of acidity through n-butylamine adsorption for TGA, SEM-XRF and N2 adsorption. Also crystalline aluminosilicate with zeolitic structure MFI of type ZSM-5 was synthesized without using organic templates. Methodologies to the preparation of these materials are related by literature using conventionally reactants that supply oxides of necessary silicon and aluminum, as well as a template agent, and in some cases co-template. The search for new routes of preparation for the ZSM-5 aimed at, above all, the optimization of the same as for the time and the temperature of synthesis, and mainly the elimination of the use of organic templates, that are material of high cost and generally very toxic. The current study is based on the use of the H2O and Na+ cations playing the role of structural template and charge compensation in the structure. Characterizations by XRD, FTIR, SEM-XRF and N2 adsorption were also conducted for this material in order to compare the samples of ZSM-5 synthesized in the absence of template and those used industrially and synthesized using structuring / O presente trabalho relata o estudo de estruturas nanoporosas, visando o uso em pesquisas que atendam a atual demanda da ind?stria do petr?leo, de valorizar ?leos pesados. Inicialmente, optou-se por duas vertentes para a s?ntese de estruturas porosas a partir da peneira molecular do tipo Si-MCM-41. Na primeira vertente, a estrutura MCM-41 ? precursora para hetero?tomos substituintes do sil?cio, gerando catalisadores do tipo Al-MCM-41 a partir de dois diferentes m?todos de incorpora??o do metal. Essa varia??o do m?todo de incorpora??o do Alum?nio na estrutura do Si-MCM-41 se deu atrav?s do procedimento convencional, no qual a fonte de alum?nio foi incorporada ao gel de s?ntese e do procedimento p?s-s?ntese, no qual a fonte de Alum?nio foi incorporada ao catalisador ap?s a s?ntese do Si-MCM-41. Na segunda vertente, o MCM-41 age como suporte para o crescimento de nanocristais de ze?lita embutidos nos seus mesoporos, resultando no catalisador h?brido MCM-41/ZSM-5. Uma an?lise comparativa foi realizada atrav?s de caracteriza??es por XRD, FTIR, medidas de acidez atrav?s de dessor??o de n-butilamina por TGA, SEM-XRF e Adsor??o de N2. Tamb?m foi sintetizado um aluminossilicato cristalino com estrutura zeol?tica MFI do tipo ZSM-5, na aus?ncia total de direcionador org?nico. Metodologias relacionadas ? prepara??o desses materiais s?o relatadas pela literatura utilizando-se convencionalmente reagentes que forne?am os ?xidos de sil?cio e de alum?nio necess?rios, bem como um agente direcionador, e em alguns casos at? co-direcionadores. A busca por novas rotas de prepara??o para a ZSM-5 visou, sobretudo, a otimiza??o da mesma no que se refere ao tempo e ? temperatura de s?ntese, e principalmente a elimina??o do uso dos direcionadores org?nicos, que s?o materiais de alto custo e geralmente muito t?xicos. O atual estudo se baseia na utiliza??o da H2O e dos c?tions Na+ desempenhando o papel de direcionamento estrutural e compensa??o de cargas na estrutura. Caracteriza??es por XRD, FTIR, SEM-XRF e Adsor??o de N2 tamb?m foram realizadas para esse material, a fim de comparar as amostras de ZSM-5 sintetizadas na aus?ncia do direcionador e aquelas utilizadas industrialmente e sintetizadas utilizando estruturantes

The total amount of plastic wastes produced by our society has been growing rapidly. The low biodegradability of these wastes creates a serious environmental problem that is directing the governments and environmental agencies to take serious measures to solve the problem of the plastic wastes. Landfilling or incineration of these wastes are not the right solutions, because the former has the danger of leaching and soil impregnation of its degradation products and the latter produce air pollution problems due to the possible emissions of toxic and acid gases. An alternative approach to the solution of problem caused by these wastes is the recycling of them by chemical recovery. In this method, the waste plastics are thermally non-catalytically or catalytically degraded into gases and oils. In this study, pure and aluminum containing ordered mesoporous materials MCM-type and SBA-type, were synthesized using different aluminum sources and aluminum loadings in order to be tested in catalytic degradation of polypropylene. These catalysts, except aluminum containing SBA-type catalysts, were synthesized by hydrothermal synthesis method. Aluminum containing SBA-type catalysts were synthesized by impregnation method. Tetraethyl orthosilicate was used as the Si source and aluminum nitrate, aluminum sulphate and aluminum isopropoxide were used as the Al source. It was observed that these materials had high surface areas and exhibited Type IV isotherms. In MCM-type materials, the aluminum incorporated more effectively into the structure at low concentrations but not effectively at high concentrations. On the other hand, in SBA-type catalysts, the aluminum incorporation into structure was very effective. 27Al MAS NMR spectra of the catalysts exhibited a mixture of tetrahedral and octahedral aluminum. TEM images showed well-ordered hexagonal arrays of mesopores. As an initial step, the activation energy value of polypropylene pyrolysis reaction in the presence of synthesized catalysts was determined by the help of a thermal analyzer and these TGA results showed a marked reduction in the degradation temperature. In the case of using aluminum containing MCM-type materials, the activation energy values decreased to about 68-126 kJ/mol. On the other hand, when aluminum containing SBA-type catalysts were used, the activation energy values decreased from 172 kJ/mol to a value in the range of 51 &ndash / 89 kJ/mol. Heavier molecules degraded into lighter hydrocarbons in the presence of catalysts and they gave high ethylene selectivity among the gaseous products. Additionally, butane selectivity increased with the use of catalysts. SBA-type catalysts showed higher selectivity to lighter hydrocarbons (&lt / C14). C7 selectivity among the liquid products was high when aluminum isopropoxide was used in the synthesis of catalysts and C18 selectivity increased significantly when aluminum nitrate was used in the synthesis of MCM-type catalysts.

MCM7, une des sous unités de l'ADN hélicase MCM, est poly-ubiquitinylée quand elle est sur la chromatine en réplication ou en réparation. Pendant la réplication, l'ubiquitinylation dégradative de MCM7 provoque son départ de la chromatine. La proto-oncoprotéine Int6 interagit avec les formes ubiquitinylées de MCM7 pour les protéger de la dégradation. Son absence entraîne la déstabilisation de MCM7 et l'apparition de lésions à l'ADN. La capacité d'Int6 à réguler la dégradation de MCM7 et peut-être d'autres facteurs semble donc primordiale pour la stabilité génomique. Suite à une irradiation causant des cassures de l'ADN, l'ubiquitinylation de MCM7 la stabilise et est stimulée par BRCA1, un suppresseur de tumeur doté d'une activité ubiquitine ligase. Cette stabilisation participerait au rôle de MCM7 dans le signalement des lésions de l'ADN. Ces travaux ajoutent MCM7 à la liste des protéines dont l'ubiquitinylation régule le métabolisme de l'ADN pour maintenir l'intégrité génomique.

Im Rahmen dieser Diplomarbeit sollten die Moeglichkeiten einer kationisch initiierten Polymerisation im Zeolithkanal ueberprueft werden.

La miniaturització de la industria microelectrònica és un fet del tot inqüestionables i la tecnologia CMOS no n'és una excepció. En conseqüència la comunitat científica s'ha plantejat dos grans reptes: En primer lloc portar la tecnologia CMOS el més lluny possible ('Beyond CMOS') tot desenvolupant sistemes d'altes prestacions com microprocessadors, micro - nanosistemes o bé sistemes de píxels. I en segon lloc encetar una nova generació electrònica basada en tecnologies totalment diferents dins l'àmbit de les Nanotecnologies. Tots aquests avanços exigeixen una recerca i innovació constant en la resta d'àrees complementaries com són les d'encapsulat. L'encapsulat ha de satisfer bàsicament tres funcions: Interfície elèctrica del sistema amb l'exterior, Proporcionar un suport mecànic al sistema i Proporcionar un camí de dissipació de calor. Per tant, si tenim en compte que la majoria d'aquests dispositius d'altes prestacions demanden un alt nombre d'entrades i sortides, els mòduls multixip (MCMs) i la tecnologia flip chip es presenten com una solució molt interessant per aquests tipus de dispositiu. L'objectiu d'aquesta tesi és la de desenvolupar una tecnologia de mòduls multixip basada en interconnexions flip chip per a la integració de detectors de píxels híbrids, que inclou: 1) El desenvolupament d'una tecnologia de bumping basada en bumps de soldadura Sn/Ag eutèctics dipositats per electrodeposició amb un pitch de 50µm, i 2) El desenvolupament d'una tecnologia de vies d'or en silici que permet interconnectar i apilar xips verticalment (3D packaging) amb un pitch de 100µm. Finalment aquesta alta capacitat d'interconnexió dels encapsulats flip chip ha permès que sistemes de píxels tradicionalment monolítics puguin evolucionar cap a sistemes híbrids més compactes i complexes, i que en aquesta tesi s'ha vist reflectit transferint la tecnologia desenvolupada al camp de la física d'altes energies, en concret implantant el sistema de bump bonding d'un mamògraf digital. Addicionalment s'ha implantat també un dispositiu detector híbrid modular per a la reconstrucció d'imatges 3D en temps real, que ha donat lloc a una patent. / The scaling down of microelectronic's industry is a fact completely unquestionable and the technology CMOS is not an exception. Consequently, the scientific community has considered two great challenges: In first place to bring the technology CMOS the most far away possible ('Beyond CMOS') while developing advanced systems such as microprocessors, micro - nanosystems or pixel systems. On the other hand to begin a new electronic generation based on technologies totally different inside the Nanotechnologies area.All these advances require a research and constant innovation in the rest of complementary areas such as Packaging. Any packaging system has to satisfy three functions in a basic way: Electrical interface of the system with the exterior, to provide a mechanical support to the system and to provide a way of heat dissipation. In order to satisfy the requirements of advanced systems with high number of I/Os, the multichip modules (MCMs) and the flip chip technology are presented as a very interesting solution.The goal of this thesis consist of developing a multichip module technology based on flip chip interconnections for the integration of hybrid pixel detectors, which includes: 1) The development of a bumping technology based on electrodeposited Sn/Ag eutectic solder bumps with a pitch of 50µm, and 2) The development of a technology of gold vias in silicon that allows to interconnect and to stack chips vertically (3D packaging) with a pitch of 100µm.Finally this high capacity of flip chip interconnection has allowed that traditional monolithic pixel systems can evolve towards hybrid systems more compact and complex, and that in this thesis has been reflected transferring the technology developed in the field of the high energies physics, implanting the bump bonding system of a digital mammography system in particular. Additionally also a modular hybrid detecting device (CMOS Image Sensor) has been implanted for the reconstruction of 3D images in real time, which has caused a patent.

Since it was discovery in 1992 by researchers at Mobil Oil Corporation, which mesoporous molecular sieves MCM-41 type has aroused great interest in the scientific community because their main properties, high surface area (700-1500 m2g-1), uniform size distribution pores and high capacity ion exchange, where the presence of exchange sites allows functionalize the surface of these materials for specific applications. In this work mesoporous molecular sieve MCM-41 modified with rare earth elements, for example: cerium, lanthanum and praseodymium and the aluminum metal were synthesized direct via by non-hydrothermal method. The insertion of metal in MCM-41 structure aimed to generate acid sites on the sample surface to be applied in the reaction of oleic acid esterification model in order to obtain biodiesel. The synthesized samples were characterized by X-ray diffraction (XRD), thermogravimetry (TG/DTG), infrared spectroscopy (FTIR), nitrogen adsorption, determination of surface acidity and scanning electron microscopy (SEM). The results show that the incorporation of metals in the MCM-41 structure is possible, but the inclusion of rare earth elements is a difficult process, forming mesoporous materials with lower degree of organization. All the synthesized catalysts were evaluated their catalytic activity in the esterification reaction of oleic acid with methanol. The conversion of methyl oleate was determined by titration by the acidity index of the reaction medium. All catalysts showed activity, but the best performers were 40AlMCM-41 and LaMCM-41 with 47.6 and 36.5% conversion to methyl oleate, respectively. These were then evaluated for their catalytic activities greater detail, by varying the reaction time (2, 3, and 4 h), reaction temperature (130, 165 and 200 °C) and molar ratio oleic acid/methanol (1:8, 1:14 and 1:20). The reaction conditions which optimize conversion to methyl oleate, within the range studied, are T = 200 °C, AO/MeOH = 1:8 and t = 3 h, reaching 91.1 and 81.3% conversion for catalysts LaMCM-41 and 40AlMCM-41, respectively, under the conditions: t = 2 h, T = 200 °C, AO / MeOH = 1:8 and 5% catalyst. / Coordenação de Aperfeiçoamento de Pessoal de Nível Superior / Desde sua descoberta em 1992 pelos pesquisadores da Mobil Oil Corporation, peneiras moleculares mesoporosas do tipo MCM-41 tem despertado grande interesse no meio científico devido suas principais propriedades, elevada área superficial (700 – 1500 m2g-1), distribuição uniforme de tamanho de poros e elevada capacidade de troca iônica, onde a presença de sítios de troca permite funcionalizar a superfície destes materiais para aplicações especificas. Nesse trabalho peneiras moleculares mesoporosas MCM-41 modificadas com os elementos terras raras cério, lantânio e praseodímio e com o metal alumínio foram sintetizados via direta pelo método não-hidrotérmico. A inserção dos metais na estrutura da MCM-41 teve o objetivo de gerar sítios ácidos na superfície das amostras para serem aplicados na reação modelo de esterificação do ácido oleico visando à obtenção de biodiesel. As amostras sintetizadas foram caracterizadas por difração de raios X (DRX), termogravimetria (TG/DTG), espectroscopia no infravermelho (FTIR), adsorção de nitrogênio, determinação da acidez superficial e microscopia eletrônica de varredura (MEV). Os resultados mostram que a incorporação dos metais na estrutura da MCM-41 é possível. Porém a inserção dos elementos terras raras é um processo difícil, formando materiais mesoporosos com menor grau de organização. Todos os catalisadores sintetizados tiveram suas atividades catalíticas avaliadas na reação de esterificação do ácido oleico com metanol. A conversão do ácido oleico foi determinada por titulometria, através do índice de acidez do meio reacional. Todos os catalisadores se mostraram ativos, porém os que apresentaram melhor desempenho foram 40AlMCM-41 e LaMCM-41 com 47,6 e 36,5 % de conversão do ácido oleico, respectivamente. Estes então tiveram suas atividades catalíticas avaliadas em maior detalhe, variando-se o tempo reacional (2, 3 e 4 h), temperatura de reação (130, 165 e 200 ºC) e razão molar ácido oleico/metanol (1:8, 1:14 e 1:20), alcançando 91,1 e 81,3 % de conversão para os catalisadores LaMCM-41 e 40AlMCM-41, respectivamente, nas condições: t = 2 h, T = 200 ºC, AO/MeOH = 1:8 e 5 % de catalisador.

Submitted by Automa??o e Estat?stica (sst@bczm.ufrn.br) on 2016-06-03T23:35:59Z No. of bitstreams: 1 IzabelCristinaMedeirosCosta_DISSERT.pdf: 7508849 bytes, checksum: baba9399e7458c8670380f1bc49a950c (MD5) / Approved for entry into archive by Arlan Eloi Leite Silva (eloihistoriador@yahoo.com.br) on 2016-06-07T00:21:16Z (GMT) No. of bitstreams: 1 IzabelCristinaMedeirosCosta_DISSERT.pdf: 7508849 bytes, checksum: baba9399e7458c8670380f1bc49a950c (MD5) / Made available in DSpace on 2016-06-07T00:21:16Z (GMT). No. of bitstreams: 1 IzabelCristinaMedeirosCosta_DISSERT.pdf: 7508849 bytes, checksum: baba9399e7458c8670380f1bc49a950c (MD5) Previous issue date: 2015-11-30 / Conselho Nacional de Desenvolvimento Cient?fico e Tecnol?gico (CNPq) / Neste trabalho foi realizado um estudo dos par?metros de s?ntese da ze?lita MCM-22 (estrutura MWW) com o intuito de otimizar a obten??o deste material e aumentar sua acessibilidade, tanto pelo aumento de superf?cie externa, quanto pela gera??o de mesoporos. Foram realizadas s?nteses de rela??o Si/Al= 15 e Si/Al=50 sob condi??es est?ticas em diferentes temperaturas e com indu??o por sementes, as quais resultaram em MCM-22 pura e cristalina de rela??o Si/Al= 15 em 3 dias e Si/Al=50 em 11 dias. A redu??o do teor de hexametileneimina (HMI) foi estudada na s?ntese em agita??o. As condi??es de redu??o foram de 30 % de HMI na s?ntese padr?o de 7 dias e em s?ntese empregando sementes com tempos de 1, 2, 3 e 4 dias. Redu??o de 45 % de HMI com adi??o de ?gua-m?e e tempos de 2, 4, 5 e 7 dias. Quanto ao aumento de acessibilidade na MCM-22, buscou-se aumentar a velocidade de cristaliza??o e redu??o do tempo, com o objetivo de se obter cristais de menor tamanho. Alguns agentes foram empregados para acelerar a obten??o da MCM-22, foram estes as sementes, ?gua-m?e, incremento de temperatura e dissolu??o da s?lica. Com rela??o ainda ao aumento de acessibilidade na MCM-22, foram estudados tratamentos ?cidos para retirada de alum?nio e gera??o de mesoporos e a silaniza??o de proto-unidades zeol?ticas, que atua tamb?m na forma??o de mesoporos e na diminui??o dos cristais. O tratamento com ?cido ox?lico de concentra??o 0,5 mol/ L resultou na forma??o de mesoporos de 3 nm e a s?ntese empregando a silaniza??o de proto-unidades zeol?ticas de pr?-cristaliza??o de tr?s dias resultou na redu??o de 70 % no tamanho dos cristais e em poros mais abertos, com alguns destes com di?metros na faixa de mesoporos (2,6 nm). / In this paper a synthesis parameters study was conducted in order to optimize the obteinment of MCM-22 (MWW structure) and increase its accessibility, getting higher external surface and generating mesopores. Syntheses with Si / Al = 15 and Si / Al = 50 ratios were performed under static conditions at different temperatures and with seeds induction, which resulted in MCM-22 pure and crystalline (Si / Al ratio = 15) after 3 days and Si / Al = 50 after 11 days. The reduction of hexamethyleneimine content (HMI) was studied in the stirring synthesis and a HMI reduction of 47% was possible through the mother liquor reuse, in addition, a specific area of 481 m? / g has been obtained in the fourth synthesis day. Regarding the increase of accessibility of the MCM-22 zeolite skeins of MCM-22 plates with about 2 ?m were obtained, through the use of dissolved silica, addition of seeds, increased temperature and synthesis time of 2 days. A significant value of specific area was found for this material, around 500 m? / g. Also with respect to the increase of MCM-22 accessibility, treatment with oxalic acid concentration of 0.5 mol / L and silanization of proto-zeolitic units resulted in the mesopores formation . Furthermore, silanization still favored reduction of 70 % in crystal size and a specific area of 566 m? / g.

Submitted by Automa??o e Estat?stica (sst@bczm.ufrn.br) on 2017-06-13T18:57:00Z No. of bitstreams: 1 AndersonJoelSchwanke_TESE.pdf: 68952400 bytes, checksum: 183df356ba12677a33625fdc1a455ae1 (MD5) / Approved for entry into archive by Arlan Eloi Leite Silva (eloihistoriador@yahoo.com.br) on 2017-06-13T23:49:01Z (GMT) No. of bitstreams: 1 AndersonJoelSchwanke_TESE.pdf: 68952400 bytes, checksum: 183df356ba12677a33625fdc1a455ae1 (MD5) / Made available in DSpace on 2017-06-13T23:49:01Z (GMT). No. of bitstreams: 1 AndersonJoelSchwanke_TESE.pdf: 68952400 bytes, checksum: 183df356ba12677a33625fdc1a455ae1 (MD5) Previous issue date: 2016-12-05 / Conselho Nacional de Desenvolvimento Cient?fico e Tecnol?gico (CNPq) / Coordena??o de Aperfei?oamento de Pessoal de N?vel Superior (CAPES) / A s?ntese das ze?litas hier?rquicas de estrutura MWW foram realizadas empregando estrat?gias de soft e hard templates. Os materiais foram caracterizados por diversas t?cnicas como DRX, TG, ICP, Isotermas de adsor??o de N2, MEV, MET e, UV-Vis e FTIR com piridina adsorvida. A estrat?gia por soft template foi realizada empregando surfactantes com diferentes tamanhos de cadeia em diferentes tratamentos (suave e agressivo). Foi observado que o tamanho do surfactante em sinergia de tratamento (suave ou agressivo) influencia na arquitetura final gerando materiais pilarizados, desorganizados e desilicados. De uma forma geral, foi observado que o tratamento agressivo danifica a estrutura, por?m cria regi?es de acessibilidade devido ? quebra de algumas l?minas MWW, resultando em uma atividade catal?tica para convers?o de frutose a 5-hidroximetilfurfural (5-HMF) semelhante aos materiais com tratamento suave. Para as ze?litas com pilares mistos de Si/Nb, a inser??o do metal aumenta a acidez de Lewis devido a incorpora??o de ni?bio. O ni?bio se encontra como esp?cies mononucleares tetra?dricamente coordenado com o sil?cio nos pilares e o seu aumento gradual da quantidade de ni?bio nos pilares acaba por diminuir a mesoporosidade interlamelar. O uso de part?culas de carbono tipo BP 2000 como hard templates em ze?litas tipo MCM-22 foi efetivo e no controle de morfologia microesf?rica. Isto se deve ao procedimento de s?ntese utilizado, em modo din?mico, e particularmente, a forma tortuosa das dos aglomerados de part?culas prim?rias do carbono BP 2000 que interage com os n?cleos zeol?ticos. O crescimento dos cristais se d? em orienta??es aleat?rias, na forma de castelo de cartas com regi?es de meso e macroporos acess?veis em toda a microesfera as quais possuem tamanhos entre 6-10 ?m. O controle da morfologia na forma de microesferas n?o afeta a atividade catal?tica comparado ? s?ntese tradicional da MCM-22. As microesferas na forma acidificadas foram impregnadas com ni?bio e demonstraram sinergia entre a acidez da ze?lita e o metal apresentando atividade catal?tica superior para a convers?o de frutose a 5-HMF ? sua forma acidificada nos primeiros 45 minutos de rea??o. Foi demonstrado que as estrat?gias por soft e hard template s?o atrativas e potencias para a cria??o de porosidade hier?rquica em ze?litas de estrutura MWW. / A s?ntese das ze?litas hier?rquicas de estrutura MWW foram realizadas empregando estrat?gias de soft e hard templates. Os materiais foram caracterizados por diversas t?cnicas como DRX, TG, ICP, Isotermas de adsor??o de N2, MEV, MET e, UV-Vis e FTIR com piridina adsorvida. A estrat?gia por soft template foi realizada empregando surfactantes com diferentes tamanhos de cadeia em diferentes tratamentos (suave e agressivo). Foi observado que o tamanho do surfactante em sinergia de tratamento (suave ou agressivo) influencia na arquitetura final gerando materiais pilarizados, desorganizados e desilicados. De uma forma geral, foi observado que o tratamento agressivo danifica a estrutura, por?m cria regi?es de acessibilidade devido ? quebra de algumas l?minas MWW, resultando em uma atividade catal?tica para convers?o de frutose a 5-hidroximetilfurfural (5-HMF) semelhante aos materiais com tratamento suave. Para as ze?litas com pilares mistos de Si/Nb, a inser??o do metal aumenta a acidez de Lewis devido a incorpora??o de ni?bio. O ni?bio se encontra como esp?cies mononucleares tetra?dricamente coordenado com o sil?cio nos pilares e o seu aumento gradual da quantidade de ni?bio nos pilares acaba por diminuir a mesoporosidade interlamelar. O uso de part?culas de carbono tipo BP 2000 como hard templates em ze?litas tipo MCM-22 foi efetivo e no controle de morfologia microesf?rica. Isto se deve ao procedimento de s?ntese utilizado, em modo din?mico, e particularmente, a forma tortuosa das dos aglomerados de part?culas prim?rias do carbono BP 2000 que interage com os n?cleos zeol?ticos. O crescimento dos cristais se d? em orienta??es aleat?rias, na forma de castelo de cartas com regi?es de meso e macroporos acess?veis em toda a microesfera as quais possuem tamanhos entre 6-10 ?m. O controle da morfologia na forma de microesferas n?o afeta a atividade catal?tica comparado ? s?ntese tradicional da MCM-22. As microesferas na forma acidificadas foram impregnadas com ni?bio e demonstraram sinergia entre a acidez da ze?lita e o metal apresentando atividade catal?tica superior para a convers?o de frutose a 5-HMF ? sua forma acidificada nos primeiros 45 minutos de rea??o. Foi demonstrado que as estrat?gias por soft e hard template s?o atrativas e potencias para a cria??o de porosidade hier?rquica em ze?litas de estrutura MWW.