Submitted by Claudinei Pracidelli (cpracide@ipen.br) on 2015-08-07T14:31:04Z No. of bitstreams: 0 / Made available in DSpace on 2015-08-07T14:31:04Z (GMT). No. of bitstreams: 0 / De modo geral, os materiais termoplásticos são sensíveis à radiação ultravioleta (UV), a qual provoca mudanças em suas estruturas químicas, afetando suas propriedades, principalmente as mecânicas, e características de aparência. A radiação ultravioleta (10-400 nm), em especial na faixa entre 290- 400 nm, é bastante agressiva aos materiais plásticos resultando na quebra de cadeias e/ou reticulação. Para aplicações agrícolas, são fatores críticos para envelhecimento: a radiação solar total, temperatura, umidade relativa do ar, esforço mecânico, presença de agroquímicos, poluição do ar e a combinação desses fatores. Os aditivos estabilizantes de luz são adicionados aos plásticos para aumentar a durabilidade do produto final. Existem diversos sistemas estabilizantes de luz, desenvolvidos de acordo com a resina, aplicação final, tipo de cultivo e outras características. Além dos estabilizantes convencionais, como por exemplo, benzofenona, benzotriazol e as moléculas do tipo aminas estericamente bloqueadas (HALS), existem também aditivos inorgânicos baseados em nanotecnologia. Este estudo avalia diferentes sistemas de aditivos: HALS, nano carbonato de cálcio (nCaCO3 ou NPCC), nano óxido de zinco (nZnO) e nano dióxido de titânio (nTiO2), aplicados a 0,25 % e 0,75 % (em massa) em polietileno de baixa densidade linear (PEBDL) e copoliéster alifático aromático. As amostras foram envelhecidas em QUV-B simulando 6 meses de exposição à intempérie. Foram realizados testes de resistência à tração, termogravimetria (TG), calorimetria exploratória diferencial (DSC), índice de carbonila, espectroscopia na região do infravermelho com transformada de Fourier (FT-IR), microscopia eletrônica de varredura (MEV), microscopia de força atômica (AFM) e espectroscopia de absorção na região de ultravioleta e visível (UV-VIS). As propriedades das amostras não envelhecidas foram comparadas as envelhecidas para avaliar o desempenho dos vários sistemas de aditivos sobre o comportamento da degradação das amostras. Como resultado deste estudo, concluiu-se que há viabilidade da aplicação de nanopartículas como aditivos estabilizantes de luz (anti-UV), em especial o nZnO. Contudo, a aditivação do tipo HALS ainda mostrou-se mais eficaz, considerando os polímeros, sistemas de aditivação e proporções utilizadas. / Tese (Doutorado em Tecnologia Nuclear) / IPEN/T / Instituto de Pesquisas Energeticas e Nucleares - IPEN-CNEN/SP

Submitted by Claudinei Pracidelli (cpracide@ipen.br) on 2016-04-08T12:32:34Z No. of bitstreams: 0 / Made available in DSpace on 2016-04-08T12:32:34Z (GMT). No. of bitstreams: 0 / A casca da castanha de caju (CCC), um resíduo agrícola da produção de castanha, proveniente da região nordeste do Brasil foi caracterizada e submetida ao processo de pirólise lenta. As propriedades do bio-carrvão, do bio-óleo e dos gases produzidos foram investigados e potenciais aplicações foram propostas. A CCC foi caracterizada pela seguintes técnicas: análise elementar CHNS, umidade total, conteúdo de cinzas, matérias voláteis, poder calorífico superior e por análise termogravimétrica. A análise termogravimétrica sob fluxo de nitrogênio mostrou que a decomposição é dominada pela degradação da hemicelulose e celulose na faixa de 250 a 350oC e pela decomposição da lignina na faixa de 400 a 500oC. Na presença de ar, o perfil de degradação é semelhante, porém observa-se uma maior degradação da lignina. A pirólise lenta da casca da castanha de caju foi realizada em um reator tipo batelada aquecido por chama ar-GLP sob diferentes fluxos (mL min-1) de nitrogênio ou ar. O sólido obtido (bio-carvão), líquido (fase aquosa + bio-óleo) e a fase gás foram quantificados e caracterizados por diferentes técnicas. Os experimentos realizados sob fluxo de nitrogênio apresentaram um rendimento de cerca de 30, 40 e 30% em massa paras as fases sólido, líquida e gás, respectivamente. Sob fluxo de ar ocorreu uma diminuição no rendimento da fase líquida, principalmente na produção de bio-óleo, e um aumento da fase gás. Os bio-carvões produzidos apresentaram elevados teores de carbono, na faixa de 70-75% em massa, poder calorífico na faixa de 25 a 28 MJ kg-1, características de carbono amorfo, sem morfologias definidas e ausência de poros. Os espectros FTIR de bio-óleos produzidos sob fluxo de nitrogênio apresentaram um aumento da intensidade relativa das bandas cerca de 1700 cm-1 (ν C=O) e 1230 cm-1 (ν C-O) em comparação com os produzidos sob fluxo de ar, o que sugere a presença de grandes quantidades de compostos oxigenados de carbono, como aldeídos, cetonas e ácidos carboxílicos. As análises das fases gás mostraram a predominância de CO2 e CO a temperaturas inferiores a 400ºC e a formação preferencial de H2 acima desta temperatura. / Dissertação (Mestrado em Tecnologia Nuclear) / IPEN/D / Instituto de Pesquisas Energeticas e Nucleares - IPEN-CNEN/SP

In Canadian remote northern communities most electricity is generated by burning diesel fuel. However, because it is expensive to import fuel into remote communities the cost of electricity is very high. Waste management is also difficult in remote northern communities. The goal of this thesis was to investigate the co-gasification of refuse waste materials and biomass as a means of reducing solid waste volumes while also using locally available materials for power generation. As part of this research, thermo-gravimetric analysis (TGA) was investigated as a potential means of characterizing refuse derived fuels (RDF). Laboratory sample preparation of RDF for TGA had not been thoroughly considered. Laboratory sample preparation is important since RDF is very heterogeneous compared to other solid fuels and since TGA typically requires a very small sample size. A TGA method was applied to a variety of materials prepared from a commercially available RDF using a variety of procedures. The repeatability of the experimental results was related to the sample preparation methods. Cryogenic ball milling was found to be an appropriate means of preparing RDF samples for TGA. Applicability of the TGA method to the determination of the renewable content of RDF was considered. Air-blown auto-thermal gasification experiments using materials representative of waste and biomass were performed at 725°C, 800°C, and 875°C, using a 0.15 m internal diameter bubbling fluidized bed gasifier located at NRCan CametENERGY in Ottawa, Ontario. Commercially prepared RDF and PET scrap were used to represent waste materials. Commercially produced hardwood pellets were used to represent biomass. The co-gasification of hardwood pellets and commercially produced RDF indicated that each fuel make a contribution to the results which is proportional to its fraction in the feed mixture. Inclusion of the RDF in the fuel mixture led to bed agglomeration at the 875°C temperature condition. Higher temperatures were found to provide better conversion of the fuel to gas, and the limitation which inclusion of RDF places on the operating temperature of the gasifier negatively affects conversion of biomass. Results obtained with RDF suggested that utilization of mixed waste for a thermal conversion process located in a Canadian remote northern community is probably not a viable option. It was then decided to target plastic waste in particular. Plastic could be source-separated, collected, and gasified alongside biomass. Polyethylene terephthalate (PET), which is often used for food and beverage containers, was chosen to represent plastic. Initially, attempts were made to co-gasify mixtures of PET pellets and hardwood pellets. These attempts failed due to the formation of coke above the bed. To alleviate these problems hardwood-PET composite pellets were manufactured and these were gasified at 725°C, 800°C, and 875°C. Inclusion of PET in the pellets dramatically increased the amount of tar produced during gasification.

M. Tech (Department of Chemistry, Faculty of Applied and Computer Sciences) Vaal University of Technology. / In this study, analytical method for determining the chlorinated phenols in water was developed using High Performance Liquid Chromatography. The following four compounds which are 2, 4, 6- Trichlorophenol (2, 4, 6 TCP), 3-chlorophenol (3CP), 2, 4- Dichlorophenol (2, 4 DCP) and 4-chloro-3-methylphenol (4C3MP) were identified and quantified with a High Performance Liquid Chromatography (HPLC). The validation parameters tested were,: linearity, trueness, precision, detection limit of quantitation, sensitivity, specificity, selectivity. The linear calibration ranges of five standard solution from 1-10 ppm. The linearity ranges between 0.9298-0.9813. The activated carbon based on the waste macadamia nutshell activated carbon (MAC) was investigated for its potential uses as an adsorbent for chlorinated phenols removal and compared with grafted macadamia nutshell activated carbon (GMAC). The adsorbent was characterized with Fourier transform infrared spectrophotometer (FTIR), scanning electron microscope (SEM) and thermo gravimetric analysis (TGA). The parameters such as pH, temperature, contact time, concentration and adsorbent were investigated by adsorption technique. The strata C18E has been used before for the same reason and therefore the research was based on mimic the functional group of solid phase extraction (SPE) into macadamia activated carbon (MAC). The functional groups in SPE C18E are benzene and octadecyl. MAC was grafted with strata C18E functional groups to compare its potential with the SPE. The pseudo-first-order and pseudo-second-order kinetic models were applied to verify the experimental data. The pseudo-second order exhibited the best fit for the kinetic studies for MAC adsorption. Chemical removal of chlorinated phenols from wastewater is necessary to reduce harmful products on the environment and human health. Chlorinated phenols have been previously listed as some of the highest priority contaminants and as well as mainly important capability carcinogenic toxins released from chemical plants. Their availability in water supplies was perceived by their bad taste and smell. The acceptable chlorinated phenols concentration in portable water is 1 (mg/l) base on the approval of world health organization. The permanent checking of chlorinated phenols in environmental samples has a greater significance and stresses highly effectiveness, common selectively and great sensitively methods. The maximum uptake of Phenol using weighed mass of MAC was found to be 78 % and for GMAC was 84% for both 2,4,6TCP. t=250 min, pH=5, Co=1mg/l, T = 25 oC and m = 0.3 g/l were the optimum condition for Phenol-MAC system and GMAC system. Over all analysis of equilibrium model analysis indicates the fitness of Langmuir isotherm model to Phenol MAC adsorption system, suggesting a monolayer adsorption of phenol on the surface of MAC. Phenol adsorption capacity of MAC was found to be decreasing with increase in temperature suggesting that the adsorption process was exothermic in nature, which was further supported by the negative values of change in enthalpy. Characterization of MAC and GMAC confirmed the mesoporous texture, highly carbonaceous nature and a higher effective surface area of 912 m2/g. The highest phenol uptake capacity of GMAC was found to be 8.0049 mg/g. The optimal conditions for various process parameters are t = 250 min, pH=5, Co=1mg/l, T = 25 oC and m = 0.3 g/l were the optimum condition for Phenol-GMAC system. Like Phenol-MAC system, the kinetics studies confirmed that Phenol-GMAC adsorption system can be described by pseudo- second-order kinetics model. Equilibrium model analysis indicates the fitness of Langmuir isotherm model to Phenol-MAC adsorption system, suggesting a monolayer adsorption of phenol on the surface of GMAC. Phenol adsorption capacity of GMAC was found to be decreasing with increase in temperature suggesting that the adsorption process was exothermic in nature, which was further supported by the negative values of change in enthalpy. The negative values of Gibb’s free energy suggested that adsorption of phenol onto GMAC was a spontaneous process.

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Nenhuma / Investigamos neste trabalho as propriedades elétricas e térmicas de 1)compositos resina epóxi/nanotubos de carbono de paredes múltiplas concêntricas (MWNT) manufaturados com 0,1, 0,5 e 1% em massa de MWNT dispersos aleatoriamente na resina; 2)de compósitos reina/buckpaper; 3) de buckpaper (tecido de MWNT).

O Distrito Grafitífero Aracoiába-Baturité apresenta depósitos do tipo gnaisse grafitoso (minério disseminado) e veio (minério maciço) com diferentes origens genéticas e com características físicas e ambientes geológicos de formação próprios. O minério tipo gnaisse grafitoso é de origem sedimentar, singenético, com teores de 1,5 a 8% de C, que se distribuem ao longo de duas extensas faixas paralelas, hospedadas na Subunidade Baturité, que constitui um importante metalotecto regional. A associação de grafita metamórfica disseminada em metassedimentos da Sequência Acarápe constitui um geoindicador de antiga bacia sedimentar neoproterozóica e, também, pode ser considerado como zona de geosutura resultante do subsequente fechamento de um oceano primitivo. As rochas desta subunidade correspondem na paleogeografia da Sequência Acarápe aos fácies de sopé de talude e de planície abissal. O minério tipo veio (fluido depositado) é epigenético e, com teores entre 20% e 70% de C, forma corpos tabulares e bolsões, controlados em escala local por estruturas de alívio (falhas, fraturas, zonas de contato, eixos de dobras etc.) que permitiram a percolação de soluções penumatolíticas relacionadas ao corpo plutônico de Pedra Aguda. As variações dos valores das relações entre isótopos estáveis de carbono (δ13C) na grafita do minério disseminado são de -26,72 a -23,52 e do minério maciço de -27,03 a -20,83, revelando sinal de atividades biológicas (bioassinaturas) e permitem afirmar que a grafita das amostras acima são derivadas de matéria orgânica. Foram apresentados os principais guias de prospecção para grafita e testados os seguintes métodos geofísicos: Eletro-Resistividade; GPR - Ground Penetrating Radar; Magnetometria; VLF (Very Low Frequency); e Polarização Induzida Espectral (IPS) / Resistividade (ER). A conjugação dos métodos de Polarização Induzida Espectral (IPS) e Eletro Resistividade (ER) foi o que demonstrou a melhor eficiência. Com relação à determinação do teor de carbono por termogravimetria (ATG), que é o método mais utilizado para este elemento. Verificou-se, que as faixas de queima atribuídas ao carbono no minério do Distrito de Aracoiába-Baturité (340 a 570C e de 570 a 1050C) eram diferentes das faixas do minério de Minas Gerais (350C a 650C e 650C a 1.050C). Esta constatação indica a necessidade de se determinar previamente as faixas de temperatura para cada região pesquisada. / The Aracoiába-Baturité Graphite-bearing District has graphitic gneiss deposits (disseminated ore) and vein (solid ore) with different genetic origins and their own physical characteristics and geological environments. The graphite gneiss ore is of sedimentary, syngenetic origin, with 1.5% to 8% C content, which is distributed along two long parallel belts, hosted in the Baturité Sub-unit, which consists of a major regional metallotect. The association of metamorphic graphite disseminated in metasediments of the Acarápe Sequence consists of a geoindicator of an old Neo-Proterozoic sedimentary basin and also can be considered a geosuture zone, the result of the subsequent closing of a primitive ocean. The rocks of this subunit correspond in the paleogeography of the Acarápe Sequence to the facies of the bottom of a slope and of an abyssal plain. The vein ore (deposited fluid) is epigenetic and, with C contents of between 20% and 70%, forms tabular bodies and pockets, controlled on a local scale by relief structures (faults, fractures, contact zones, fold axes, etc.), which allowed seepage of pneumatolithic solutions relating to the plutonic body of Pedra Aguda. The variations in the values of the ratios between stable carbon isotopes (δ13C) in the graphite of the disseminated ore are -26.72 to -23.52 and of the solid ore -27.03 to -20.83, showing a sign of biological activities (biosignatures), and it can be said that the graphite of the above samples is derived from organic matter. The main prospecting guides for graphite were presented and the following geophysical methods tested: Electro-resistivity (ER); Ground Penetrating Radar (GPR); Magnetometry; Very Low Frequency (VLF); and Spectral Induced Polarization (SIP) / Electro-resistivity (ER). It was found that the combination of the Spectral Induced Polarization (SIP) and Electro-resistivity (ER) methods proved the most efficient. In relation to determining the carbon content using thermogravimetry (TG), which is the most commonly used method for this element, it was found that the bands of burning attributed to the carbon in the ore in the Aracoiába-Baturité District (340 to 570C and from 570oC to 1050C) were different from the bands of the ore in Minas Gerais (350C to 650C and 650C to 1050C). This finding suggests the need to determine beforehand the temperature ranges for each region studied.

In the past decade, tremendous progress has been made in organic field effecttransistors. Fused oligothiophenes and anthracene molecules are fascinatingmacromolecules having unique optoelectronic properties. These compounds are successfully employed as active components in optoelectronic devices including field effect transistors. Our goal is to design and synthesize conjugated molecular materials, which are highly functionalized through structural modifications in order to enhance their electronic, photonic, and morphological properties. The main desire is to synthesize novel organic fused-arenes having efficient charge carrier mobilities, as well as to optimize optical properties for organic field effect transistors (OFETs). Novel series of fused arene molecules of 9,10-di(thiophen-3-yl)anthracene (1), trans-2,5-(dianthracene-9- vinyl)thiophene (2), trans-5,5’-(dianthracene-9-yl)vinyl)- 2,2’-bithiophene (3), 5,5’-di(2 thiophene)-2,2’-bithiophene (4) , 9,10-(divinyl)anthracene core with 1- phenylcarboxypyrene (6) and polymers of poly(anthracene-co-bithiophene) (5) and poly(anthracene) (7) have been synthesized as promising materials for organic field effect transistors (OFETs). These compounds were confirmed and characterized by 1H-NMR, FT-IR, and elemental analysis. Their optical, thermal, and electronic properties were investigated using UV-Vis and photoluminescence spectroscopy, and thermogravimetric analysis respectively. Future studies will focus on evaluating OFETs performance of these material.

Made available in DSpace on 2014-10-09T12:27:04Z (GMT). No. of bitstreams: 0 / Made available in DSpace on 2014-10-09T13:56:34Z (GMT). No. of bitstreams: 1 14386.pdf: 115351 bytes, checksum: e171f39a0d4e19bac211bcd02845aa90 (MD5) / Dissertacao (Mestrado) / IPEN/D / Instituto de Pesquisas Energeticas e Nucleares - IPEN-CNEN/SP