Purpose -Laser sintering kinetics and part reliability are critically dependent on the melt viscosity of materials, including polyamide 12 (PA-12). The purpose of this paper is to characterise the viscosity of PA-12 powders using alternative scientific methods: constrained boundary flows (capillary rheometry) and rotational rheometry. Design / methodology / approach -Various PA-12 powders were selected and characterised by both techniques. Measurement of molecular weight was also carried out to interpret the viscosity data. Findings -Results demonstrate conventional pseudoplastic flow in all PA-12 materials. Zero-shear viscosity has been quantified by rotational rheometry; a notable observation is the striking difference between virgin / used PA-12. This is interpreted in terms of molecular weight and chain structure modifications, arising from polycondensation of PA-12 held at the bed temperature during laser sintering. Research limitations / implications -Accurate zero-shear viscosity data provide scope for use in predictive computational models for laser sintering processes. Careful sample preparation and equipment operation are critical prerequisites for accurate rheological characterisation of PA-12 powders. Practical implications -Differences in flow behaviour and molecular structure allow prediction and deeper understanding of process-property relationships in laser sintering, giving potential for further optimisation of material specification and in-process machine parameter control. Originality / value -This is believed to be the first time that techniques other than MFR have been reported to measure the viscosity of PA-12 in a laser sintering context, noting the effects of pre-drying and molecular weight, then predicting differences between virgin / used powders in practical sintering behaviour.
Rigid poly(viny1 chloride) (PVC) sheets were stretched uniaxially (at constant width), equally biaxially, and unequally biaxially to various draw ratios. Tensile properties, density, and birefringence of the stretched sheets were measured, and their wide angle X-ray diffraction traces recorded. Comparison of results showed the highest crystallite and overall orientation and density in the uniaxial samples, and lowest values for the equal biaxial samples. Drawing resulted in the alignment of some existing crystallites in the plane of the film, together with the formation of new mesomorphous structures. Changes in tensile strength were attributed to overall orientation.
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