Comparação entre duas teorias para a determinação da tensão interfacial pelo método de fibra quebrante Comparison between two theories for determination of interfacial tension with the breaking thread method

A tensão interfacial entre polímeros fundidos é um fator chave para a predição da morfologia de blendas poliméricas. Neste trabalho, as teorias de Tomotika e Tjahjadi et al. para medir tensão interfacial entre polímeros fundidos usando o método de fibra quebrante são avaliadas e comparadas. Em particular, foram testadas ambas as teorias para o par de polímeros PP/PS à temperatura de 200 &deg;C. O valor médio de tensão interfacial calculado usando a teoria de Tomotika foi de 5,88 mN/m, e usando a teoria de Tjahjadi et al. foi de 5,66 mN/m.<br>Interfacial tension between molten polymers is a key factor that helps predicting the morphology of polymer blends. In this work, the theories of Tomotika and Tjahjadi et al. to measure interfacial tension between molten polymers using the breaking thread method are evaluated and compared. In particular, both theories were tested for PP/PS polymer pair at temperature of 200 &deg;C. The average values of interfacial tension calculated using Tomotika&acute;s theory and Tjahjadi et al.&acute;s theory are 5.88 mN/m and 5.66 mN/m, respectively

Influence of water content, time, and temperature on the rheological behavior of polyethylene terephtalate

International audienc

Estudo do efeito do tipo de polipropileno na fotodegradação da blenda polipropileno/poliestireno de alto impacto Influence of the type of polypropylene on the photodegradation of blends of polypropylene/high impact polystyrene

Este trabalho visa avaliar a influência do tipo de polipropileno no comportamento da blenda polipropileno/poliestireno de alto impacto (PP/HIPS) quando exposta à radiação UV. Foram usados uma resina virgem de PP (PPv) e outra reprocessada (PPrep). Inicialmente, avaliou-se o comportamento individual dos componentes da blenda, HIPS, PPv e PPrep, quando submetidos à radiação UV por até 15 semanas de exposição. As técnicas de caracterização utilizadas para monitorar o desempenho tanto das resinas individualmente quanto das blendas submetidas à radiação UV foram: propriedades mecânicas (tração e impacto), medidas de índice de fluidez (MFI), análise térmica (DSC), espectroscopia no infravermelho (FTIR) e microscopia eletrônica de varredura (MEV). A partir dos resultados com essas técnicas verificou-se que o PPv foi a resina mais afetada pela radiação e consequentemente as blendas preparadas com esse PP também foram mais sensíveis à fotodegradação do que as demais. Em termos de fotoestabilização este resultado mostra-se interessante, já que as blendas PP/HIPS preparadas com uma resina previamente degradada necessitariam de menores teores de aditivos do que esse mesmo tipo de blenda preparada com resina virgem.The influence from the type of polypropylene on the photodegradation resistance of blends of polypropylene/high impact polystyrene (PP/HIPS) was studied. A virgin polypropylene (PPv) and another sample that suffered prior thermo-mechanical degradation (PPrep) were used. All materials, components of the blends and blends were exposed to UV radiation for up to 15 weeks. They were characterized as a function of time of UV exposure using differential scanning calorimetry (DSC), infrared spectroscopy (FTIR) and scanning electron microscopy (SEM). The mechanical (tensile and impact) properties and melt flow indexes of the materials were also evaluated. The experimental results revealed that PPv resin and its blends were more sensitive to UV radiation than PPrep and its blends. In terms of photostabilization this finding is very interesting, since PP/HIPS blends prepared with a previously degraded polyolefin would require smaller amounts of additives than the same kind of blends prepared with virgin resin

Photodegradation of Thermodegraded Polypropylene/High-Impact Polystyrene Blends: Mechanical Properties

The influence of the addition of high-impact polystyrene (HIPS) on polypropylene (PP) photodegradation was studied with blends obtained by extrusion with and without styrene-butadiene-styrene (SBS) copolymer (10 wt % with respect to the dispersed phase). The concentrations of HIPS ranged from 10 to 30 wt %. The blends and pure materials were exposed for periods of up to 15 weeks of UV irradiation; their mechanical properties (tensile and impact), fracture surface, and melt flow indices were monitored. After 3 weeks of UV exposure, all of the materials presented mechanical properties of the same order of magnitude. However, for times of exposure greater than 3 weeks, an increasing concentration of HIPS resulted in a better photostability of PP. These results were explained in light of morphological observations. This increase of photostability was even greater when SBS was added to the blends. It was more difficult to measure the melt flow index of the binary PP/HIPS blends than that of PP for low concentrations of HIPS; this was most likely due to energy transfer between the blend domains during photodegradation. This phenomenon was not observed for the ternary blends. (C) 2010 Wiley Periodicals, Inc. J Appl Polym Sci 120: 770-779, 2011FAPESP Fundacao de Amparo a Pesquisa do Estado de Sao PauloCAPES Coordenação de Aperfeiçoamento de Pessoal de Nível SuperiorCNPq Conselho Nacional de Desenvolvimento Cientifico e Tecnologic

Influence of Water Content, Time, and Temperature on the Rheological Behavior of Polyethylene Terephtalate

In this work, the main factors affecting the rheological behavior of polyethylene terephtalate (PET) in the linear viscoelastic regime (water content, time delay before test, duration of experiment, and temperature) were accessed. Small amplitude oscillatory shear tests were performed after different time delays ranging from 300 to 5000 s for samples with water contents ranging from 0.02 to 0.45 wt %. Time sweep tests were carried out for different durations to explain the changes undergone by PET before and during small amplitude oscillatory shear measurements. Immediately after the time sweep tests, the PET samples were removed from the rheometer, analyzed by differential scanning calorimetry and their molar mass was obtained by viscometry analysis. It was shown that for all the samples, the delay before test and residence time within the rheometer (i.e. duration of experiment) result in structural changes of the PET samples, such as increase or decrease of molar mass, broadening of molar mass distribution, and branching phenomena. (C) 2010 Wiley Periodicals, Inc. J Appl Polym Sci 116: 3525-3533, 2010FAPESPCNPqCAPE

Clay-containing block copolymer nanocomposites with aligned morphology prepared by extrusion

Clay-containing nanocomposites of polystyrene-b-poly(ethylene-co-butylene)-b-polystyrene (SEBS) copolymers having cylindrical domains were obtained by melt extrusion using a tape die. One type of sample (SEBS-MA) had maleic anhydride attached to the middle block. Two types of organoclays were added, namely Cloisite 20A and Cloisite 30B. Small angle X-ray scattering and transmission electron microscopy (TEM) analyses showed that the addition of 20A clay to SEBS and SEBS-MA resulted in nanocomposites with intercalated and partially exfoliated structures, respectively. The addition of 30B clay to SEBS and SEBS-MA promoted the formation of composites containing relatively large micron-sized and partially exfoliated clay particles, respectively. Our TEM analysis revealed that clay particles embedded in SEBS are preferably in contact with the polystyrene cylindrical domains, while in SEBS-MA they are in contact with the maleated matrix. The extrusion processing promoted alignment of the axes of the polystyrene cylinders along the extrusion direction in all samples, and the basal planes of the clay particles were mostly parallel to the main external surfaces of the extruded tapes632184194CONSELHO NACIONAL DE DESENVOLVIMENTO CIENTÍFICO E TECNOLÓGICO - CNPQCOORDENAÇÃO DE APERFEIÇOAMENTO DE PESSOAL DE NÍVEL SUPERIOR - CAPESFUNDAÇÃO DE AMPARO À PESQUISA DO ESTADO DE SÃO PAULO - FAPES

Comparação entre o método da gota pendente e o método da gota girante para medida da tensão interfacial entre polímeros Comparison between the pendant drop and spinning drop method to measure interfacial tension between polymers

Dois instrumentos, um deles baseado no princípio da gota pendente e o outro baseado no método da gota girante, para medir a tensão interfacial entre polímeros, são apresentados e comparados aqui. Com ambos instrumentos foi possível visualizar a gota de polímero "on line". Os instrumentos mostraram-se complementares quanto às suas áreas de aplicação. O método da gota pendente deve ser usado quando as quantidades de polímero são limitadas ou quando o polímero mais denso é opaco. O método da gota girante deve ser usado quando a degradação térmica pode ser um problema ou quando o polímero menos denso é opaco.<br>In this paper two apparatuses, one based on the principle of the pendant drop method and one based on the principle of the spinning drop are presented and compared. With both apparatuses it was possible to view the drop in real time and calculate the interfacial tension on-line. The two equipments were shown to be complementary in their use. The pendant drop method should be used when there are limited quantities of polymer and/or the denser polymer is opaque. The spinning drop method should be used when thermal degradation could be a problem and/or when the lighter polymer is opaque