Made available in DSpace on 2016-03-15T19:36:57Z (GMT). No. of bitstreams: 1 Alexandre Pastro Alves.pdf: 1203203 bytes, checksum: a4482af4edaf66d6d70071a940528a5a (MD5) Previous issue date: 2009-02-04 / Fundo Mackenzie de Pesquisa / Nanocomposites are polymeric hybrid materials where inorganic substances of nanometric dimensions are dispersed in a polymeric matrix. The fillers present area of raised surface, promoting better dispersion in the polymeric matrix and therefore an improvement of the physical properties of the composite that depends on the homogeneity of the material. The nanocomposites preparation with polymeric matrix allows in many cases to find a relation enters a low cost, due to the use of lesser amount of filler, and a raised performance level. In this work nanocomposites were obtained with pseudobohemite synthesized by sol-gel process and high density polyethylene with different concentrations of pseudobohemite. The nanocomposites were prepared by intercalation for fusing and characterized by thermal and mechanical tests. The results showed an increase in the values of hardness, tensile strength and compression strength, and an increase in the temperature of thermal distortion (HDT) and in the glass transition temperature (Tg) evidencing the interaction of nanofiller with the polymeric matrix. / Nanocompósitos poliméricos são materiais híbridos onde substâncias inorgânicas de dimensões nanométricas estão dispersas em uma matriz polimérica. As cargas apresentam área de superfícial elevada, promovendo melhor dispersão na matriz polimérica e por isso uma melhoria das propriedades físicas do compósito que depende da homogeneidade do material. A preparação de nanocompósitos com matriz polimérica permite em muitos casos encontrar uma relação entre um baixo custo, devido à utilização de menor quantidade de carga, e um elevado nível de desempenho. Neste trabalho foram obtidos nanocompósitos com pseudoboemita sintetizada pelo processo sol-gel e polietileno de alta densidade com diferentes concentrações de pseudoboemita. Os nanocompósitos foram preparados por intercalação por fusão e caracterizados por meio de ensaios térmicos e mecânicos. Os resultados mostraram um aumento nos valores de dureza, de resistência à tração e resistência à compressão, um aumento na temperatura de distorção térmica (HDT) e na temperatura de transição vítrea (Tg) evidenciando a interação da nanocarga com a matriz polimérica.

La miniaturisation des pièces est une étape importante pour la progression de la microtechnologie dans plusieurs domaines (connectique, médical, optique, microsystèmes mécaniques). Pour cela, le moulage par microinjection, semble être la solution clé pour la production à grande échelle de micro-composants de polymères. Pour les polymères semi-cristallins, la cristallisation, sous fort taux de cisaillement et sous des vitesses de refroidissement élevées (about 100 K/s), induit des morphologies et des propriétés spécifiques. Elle prend donc une importance considérable dans le processus de microinjection par rapport au moulage par injection classique où les épaisseurs injectées sont généralement supérieures à 1 mm. Ces microstructures ont une grande influence sur les propriétés mécaniques du produit final. La prédiction de ces propriétés à partir de la description de la microstructure est un défi technique et scientifique. Durant cette thèse, deux polymères semi-cristallins ont été microinjectés, le polyéthylène haute densité et le polyamide 12. Les analyses obtenues par la microscopie otiques montrent que les morphologies cristallines varient entre les micro- et les macro-pièces. Tandis que la morphologie de ‘peau-cœur' est présente dans les macropièces, les micropièces présentent une morphologie plutôt particulière. Les analyses combinées de diffusion et de diffraction des rayons X (SAXS et WAXS) avec un microfaisceau synchrotron, nous ont permis de déterminer la microstructure induite par le processus de microinjection dans toute l'épaisseur des pièces. Nous avons constaté que la morphologie et les orientations cristallines induites sont très dépendantes des conditions d'injection ou de microinjection. Une diminution de l'épaisseur, de la vitesse et de la température du moule, augmente l'orientation cristalline en limitant la relaxation des chaînes de polymères. / The components miniaturization is an important step in the evolution of micro technology in several domain (connectivity, medical, optical, mechanical, microsystems). For this purpose, the micro-injection molding seems to be the key solution for the large-scale micro-polymer components production.The crystallization of the semi-crystalline polymers under high shear and cooling rates (about 100 K / s), induces specific properties and morphologies, consequently, it takes a substantial importance in the process of micro-injection compared to conventional injection molding where the usually injected thicknesses is over 1 mm. These micro-structures have a great influence on the mechanical propertie of the final product. The prediction of the final product's properties based on the illustration of the micro-structure is a technical and scientific challenge. In this thesis, two semi-crystalline polymers were micro-injected, the high density polyethylene and the polyamide 12. The obtained analyzes with the use of an optical microscope showed that the Morphology of Crystals vary between micro-and macro-pieces. While the morphology of 'peau-cœur' is present in the macro-pieces, the micro-parts have a particular morphology. The combined analysis of diffusion and X-ray diffraction (WAXS and SAXS) along with the synchrotron microbeam, has allowed us to determined the micro-structure induced by the micro-injection process throughout the thickness of the pieces.We have identified that the morphology and the induced crystal's orientation are very dependent on the conditions of injection or micro-injection. The decrease of the thickness,speed and temperature of the mold will increase the crystal orientation by limiting the relaxation of the polymer chains.

In current enterprises, simulations are being utilized to lessen the cost of product advancement.  Along this line, there is an awesome enthusiasm for enhancing precision and accuracy of simulations. For an accurate and reliable simulation, it is essential to use an accurate material model and provide it with accurate material information. In exhibit industries, orthotropic materials are being simulated utilizing isotropic material model, as orthotropic material model requires more material data which is not promptly accessible. This proposal intends to test and identify orthotropic materials and simulate them using orthotropic material model in ABAQUS. Materials utilized as a part of this proposal are Aluminium, LDPE, PET. Required material data was gotten by performing Uni-directional tensile tests, DIC, and an algorithm we developed in light of Inverses method. To get highly accurate material data from DIC, a few kinds of patterns were examined, and a superior pattern was resolved for camera configuration being utilized.

The course of polymer film functioning has been a crucial concern in the advent of packaging technology. The thesis project aims towards obtaining an understanding of mechanical properties for a class of these materials, namely LDPE and PET. A constitutive understanding of this behavior in the case of LDPE is acquired through incorporating a plastic stress strain relationship in an iterative approach with focus put on the sensitivity of a few parameters by following a simple linear curve-fit technique in a way that the global as well as the local response are predictable. FE-models also developed in this way are validated with experimental data. An inverse analysis testing validity or usefulness of DIC technique in identifying a material model is done and some discussions are drawn towards this area. A relative numerical study with respect to experimentally obtained global response for tearing of these polymers is done through use of a similar material model developed from tensile tests and the challenges faced in this area have been addressed.

This thesis is intended to identify the mode I and mode II fracture toughness to characterize the thin laminate interface by using the Double Cantilever Beam test (DCB) and End Notched Flexure test (ENF). This study’s thin laminate was Polyethylene Terephthalate and Low-Density Polyethylene (PET-LDPE), which is mostly used by packaging industries in the manufacturing of packages to store liquid food. As PET-LDPE film is very flexible and difficult to handle, DCB and ENF tests cannot be performed directly so, sheet metal (Aluminium) was used as carrier material. PET-LDPE film is placed between two aluminum plates to reduce the flexibility and perform the tests. Therefore, the Aluminium plate was also studied to find the constitutive parameters (young’s modulus (E) and mixed hardening parameters (Plastic properties)) under the tensile test and three-point bending test. From the test response, energy release rate calculation has been done for different Pre-crack lengths to validate the DCB and ENF experimental setup, study the different Pre-crack lengths, and characterize the laminate interface. Finite Element simulation (FE simulation) for those tests were carried out in AbaqusTM2020. When needed, the force versus displacement response from FE simulation was optimized against experimental response to find the required constitutive parameters (Young’s modulus, Hardening parameters, and PET-LDPE material properties). Implementing of optimization algorithm and automated simulation has been done with the help of MATLAB code. In contrast, MATLAB works as a server, and Abaqus works as a client and connected two interfaces to run the optimization. The results obtained from experiments and FE simulations were compared to the results found in the literature.

No description available.

The crystallization and melting behaviors of an ethylene/1-hexene copolymer and series of narrow molecular weight linear polyethylene and poly(ethylene oxide) fractions were studied using a combination of ultra-fast and conventional differential scanning calorimetry, optical microscopy, small angle X-ray scattering, and wide angle X-ray diffraction. In the case of linear polyethylene and poly(ethylene oxide), the zero-entropy production melting temperatures of initial lamellae of isothermally crystallized fractions were analyzed in the context of the non-linear Hoffman-Weeks method. Using the Huggins equation, limiting equilibrium melting temperatures of 141.4 ± 0.8oC and 81.4 ± 1.0oC were estimated for linear polyethylene and poly(ethylene oxide), respectively. The former and the latter are about 4oC lower and 12.5oC higher than these predicted by Flory/Vrij and Buckley/Kovacs, respectively. Accuracy of the non-linear Hoffman-Weeks method was also examined using initial lamellar thickness literature data for a linear polyethylene fraction at different crystallization temperatures. The equilibrium melting temperature obtained by the Gibbs-Thomson approach and the C2 value extracted from the initial lamellar thickness vs. reciprocal of undercooling plot were similar within the limits of experimental error to those obtained here through the non-linear Hoffman-Weeks method. In the next step, the Lauritzen-Hoffman (LH) secondary nucleation theory was modified to account for the effect of stem length fluctuations, tilt angle of the crystallized stems, and temperature dependence of the lateral surface free energy. Analysis of spherulite growth rate and wide angle X-ray diffraction data for 26 linear polyethylene and 5 poly(ethylene oxide) fractions revealed that the undercooling at the regime I/II transition, the equilibrium fold surface free energy, the strength of the stem length fluctuations and the substrate length at the regime I/II transition are independent of chain length. The value of the equilibrium fold surface free energy derived from crystal growth rate data using the modified Lauritzen-Hoffman theory matches that calculated from lamellar thickness and melting data through the Gibbs-Thomson equation for both linear polyethylene and poly(ethylene oxide). Larger spherulitic growth rates for linear polyethylene than for poly(ethylene oxide) at low undercooling is explained by the higher secondary nucleation constant of poly(ethylene oxide). While the apparent friction coefficient of a crystallizing linear polyethylene chain is 2 to 8 times higher than that of a chain undergoing reptation in the melt state, the apparent friction coefficient of a crystallizing poly(ethylene oxide) chain is about two orders of magnitude lower. This observation suggests that segmental mobility on the crystal phase plays a significant role in the crystal growth process. In case of the statistical ethylene/1-hexene copolymer, the fold surface free energies of the copolymer lamellae at the time of crystallization and melting increase with increasing undercooling, approaching the same magnitude at high undercooling. As a result of this temperature dependence, the experimental melting vs. crystallization temperature plot is parallel to the Tm = Tc line and the corresponding Gibbs-Thomson plot is non-linear. This behavior is attributed to the fact that longer ethylene sequences form a chain-folded structure with lower concentration of branch points on the lamellar surface at lower undercooling, while shorter ethylene sequences form lamellar structures at higher undercooling exhibiting a higher concentration of branch points on the lamellar surface. Branch points limit the ability of lamellar structures to relax their kinetic stem-length fluctuations during heating prior to melting. / Ph. D. / Morphology of semi-crystalline polymers is strongly affected by their crystallization conditions. Thermodynamic and kinetic models allow us to understand the crystallization mechanism of a semi-crystalline polymer and relate its crystallization conditions to the final morphology. In this research, we studied the molar mass dependence of the crystallization and melting behaviors of narrow molecular weight distribution linear polyethylene (LPE) and poly(ethylene oxide) (PEO) fractions using a modified Lauritzen-Hoffman (LH) secondary nucleation theory. We have shown that the equilibrium melting temperature of LPE and PEO fractions found from the non-linear Hoffman-Weeks method are within the experimental uncertainty identical with these measured directly for extended chain crystals or derived from a Gibbs-Thomson analysis. The value of the equilibrium fold surface free energy derived from crystal growth rate data using the modified LH theory matches that calculated from lamellar thickness and melting data through the Gibbs-Thomson equation for both LPE and PEO. We reported that the higher segmental mobility of PEO in the crystalline phase leads to significantly lower apparent chain friction coefficients during crystal growth compared to LPE. We also studied the role of short-chain branching in the crystal growth kinetics of ethylene/1-hexene copolymers. We observed that the fold surface free energies during crystallization and during melting are both function of the undercooling while the ratio of the former to the latter decreases with increasing undercooling. We proposed that this behavior may be related to the concentration of short-chain branches at the surface of the lamellae, where higher concentration leads to lower relaxation.

The objective of my work was to develop HDPE clay nanocomposites for packaging with superior barrier (gas and water) properties by economical processing technique. This work also represents a comparative study of thermoplastic nanocomposites for packaging based on linear low density polyethylene (LLDPE), high density polyethylene (HDPE) and Nylon12. In this study properties and processing of a series of linear low density polyethylene (LLDPE), high density polyethylene (HDPE) and Nylon 12 nanocomposites based on Na-MMT clay and two different aspect ratio grades of kaolinite clay are discussed.

M. Tech. (Civil Engineering, Faculty of Engineering and Technology), Vaal University of Technology) / Modified asphalt concrete is one of the important construction materials for flexible pavements. The addition of polymers and natural hydrocarbon modifiers to enhance the properties of asphalt concrete over a wide temperature range in paving applications has been the common practice. Currently these modified asphalt mixtures are relatively expensive. However, recycled polymers and rubber added to asphalt have also shown similar results in improving the performance of road pavements. In this study, an attempt has been made to use low density polyethylene (LDPE) obtained from plastic waste and crumb rubber obtained from worn out vehicle tyres. The aim was to optimise the proportions of LDPE in the bitumen binder using the ‘wet process’ and crumb rubber aggregates in the hot mix asphalt (HMA) using the ‘dry process’. The Marshall method of bituminous mix design was carried out for varying percentages of LDPE namely 2%, 4%, 6%, 8% and 10% by weight of bitumen binder and 1%, 2%, 3%, 4% and 5% crumb rubber by volume of the mineral aggregates. The characteristics of bitumen modified with LDPE were evaluated. The modified asphalt mix was also evaluated to determine the different mix characteristics. The results from laboratory studies in terms of the rheological properties of the LDPE modified bitumen binder showed an increase in viscosity, softening point and stiffness of the binder. The optimum Marshall stability values for HMA mixtures containing 2% crumb rubber tyre and 4% LDPE were found to be 30% higher than the conventional asphalt concrete mix. The wheel tracking test done at 50ºC was 9.81mm rut depth showing a good rutting resistance of the optimized mixture compared to the conventional asphalt mixes. The Modified Lottman test gave a Tensile Strength Ratio value of 0.979 which indicates a low degree of moisture susceptibility of the modified asphalt mix. The above results showed improved properties of the asphalt mixture. The economic assessment done using the present worth of costs indicated a reduction in maintenance cost due to the extended service life of the modified asphalt pavement.

LIBS é um método baseado na espectrometria de emissão óptica que emprega a microamostragem por ablação por laser e formação de um microplasma para a determinação dos elementos químicos presentes na amostra. Neste trabalho, o método foi avaliado para a análise de embalagens plásticas produzidas com polietileno de alta densidade e polipropileno. A construção de curvas de calibração com amostras dos polímeros contendo diferentes concentrações de Cd, Cr e Pb e a determinação desses analitos, assim como os efeitos da taxa de repetição do laser, número de pulsos, fluência e diâmetro de focalização foram estudados. O sistema LIBS utilizado foi composto por um laser pulsado de Nd:YAG operando a 064 nm, com pulsos de 5 ns e máxima energia de 360 mJ/pulso. Os sinais de emissão foram coletados por um conjunto de lentes acoplado por fibra óptica ao espectrômetro com montagem Echelle e detector ICCD. Os parâmetros instrumentais foram ajustados em 10 pulsos acumulados, 2 \'mü\'s de atraso e 6 \'mü\'s de integração. O software ESAWIN, o banco de dados de espectros atômicos e iônicos do NIST e algoritmo desenvolvido em ambiente MATLAB® foram utilizados para aquisição e tratamento dos dados. A avaliação da topografia das crateras nas placas dos polímeros foi feita por perfilometria e microscopia eletrônica de varredura, que proporcionaram informações úteis para a caracterização das crateras. As massas removidas das placas de polietileno de alta densidade e de polipropileno foram calculadas a partir dos volumes das crateras obtidos pelas análises perfilométricas. A taxa de repetição e número de pulsos do laser tiveram efeitos marcantes na ablação dos polímeros, e as principais causas foram atribuídas ao grau de cristalinidade, à temperatura de fusão cristalina (Tm) e à temperatura de transição vítrea (Tg). Os resultados desta tese indicaram que diâmetros de focalização da ordem de 600 \'mü\'m e fluências entre 50 e 85 J cm-2 podem ser recomendados para análises de PEAD e PP por LIBS com laser de Nd:YAG@1064 nm (pulsos de 5 ns) e taxa de repetição de 10Hz. Nessas condições, as curvas de calibração obtidas apresentaram boa correlação. Identificaram-se três amostras contaminadas por Cd, Cr e Pb dentre 60 embalagens plásticas analisadas. A comparação dos resultados obtidos por LIBS e ICP OES apresentou concordâncias e algumas diferenças significativas (teste t ao nível de 95% de probabilidade) que foram associadas a efeitos de matriz observados na análise dos polímeros por LIBS / LIBS is an optical emission spectroscopy technique that employs a laser for micro sampling and induction of a plasma for determination of chemical elements in a sample. In this work, LIBS was evaluated for the analysis of plastic packaging produced with high density polyethylene (HDPE) and polypropylene (PP). Plates of these polymers with different concentrations of Cd, Cr and Pb were prepared for evaluating the effects of laser repetition rate, number of pulses, fluence and laser focusing as well as for building the analytical calibration curves. The LIBS system was designed by using a Q-Switch Nd:YAG laser operating at 1064 nm (5 ns, 360 mJ/pulse) and the emission signals were collected by lenses into an optical fiber coupled to a high-resolution echelle spectrometer equipped with ICCD. Instrumental parameters consisted of 10 accumulated laser pulses, 2 \'mü\'s delay time and 6 \'mü\'s integration time gate. Software ESAWIN, NIST atomic database and an algorithm develop in MATLAB® were used for acquisition and data processing. The evaluation of topographical features of craters on the plates of the polymers was carried out by perfilometry and scanning electron microscopy, and provides useful information for the characterization of the craters. The mass removal of HDPE and PP were calculated using craters volume obtained in perfilometric analysis. The repetition rate and number of laser pulses affect the ablation process in polymers. Moreover, the main properties of polymers that affect the ablation are degree of crystallinity, crystalline melting temperature (Tm) and glass transition temperature (Tg). The results indicated that laser focusing of 610 \'mü\'m and fluences between 50 and 85 J cm-2 can be indicated for LIBS analysis of HDPE and PP with Nd:YAG@1064 nm, 5 ns and 10 Hz. Under these conditions the calibration curves obtained presented good correlations and 3 samples containing Cd, Cr and Pb were identified from 60 samples from the local market. LIBS results compared well with ICP OES but some data presented significant differences by applying a t-test at 95 % confidence level, which were mainly associated to matrix effects observed in the analysis of polymers by LIBS