Abstract

AbstractPoly(trimethylene terephthalate) (PTT) and cationic dyeable poly(trimethylene terephthalate) (CD‐PTT) were extruded (in the proportions of 80:20, 60:40, 40:60, and 20:80) from one melt twin‐screw extruder to prepare four PTT/CD‐PTT polyblended fibers. The molar ratio of 5‐sodium sulfonate dimethyl isophthalate (5‐SSDMI) for CD‐PTT polymer was 2%. This study investigated the thermal and mechanical properties of PTT/CD‐PTT polyblended fibers using gel permeation chromatograph, differential scanning calorimetry (DSC), thermogravimetric analysis, potentiometer, a rheometer, the density gradient, wide‐angle X‐ray diffraction, extension stress–strain measurement, and scanning electron microscope (SEM). Melting behavior of PTT/CD‐PTT polyblended polymers exhibited positive‐deviation blends, and the blend of PTT/CD‐PTT between 60:40 and 40:60 showed a maximum value of the melt viscosity. Experimental results from the DSC indicated that PTT and CD‐PTT molecules formed a miscible system. The tenacity of PTT/CD‐PTT polyblended fibers declined as the 5‐SSDMI content increased. Crystallinities and densities of PTT/CD‐PTT polyblended fibers were also found decrease as the 5‐SSDMI content increased. The surface of PTT/CD‐PTT polyblended fibers exhibited a uniform morphology, from the SEM observation. It indicated that PTT and CD‐PTT polymers were identified to be a miscible system. Though there is a good interfacial adhesion between PTT and CD‐PTT polymer, the mechanical properties of PTT/CD‐PTT ployblended fibers were largely affected by the 5‐SSDMI content. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 1008–1013, 2006

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