4.6 Article

Dual Types of Spherulites in Poly(octamethylene terephthalate) Confined in Thin-Film Growth

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LANGMUIR
卷 24, 期 20, 页码 11880-11888

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AMER CHEMICAL SOC
DOI: 10.1021/la802192w

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  1. National Science Council (NSC) of Taiwan [94 2216 E006 003]

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Spherulite morphology and growth kinetics of poly(octamethylene terephthalate) (POT), cast on single-side glass or confined between two slides in thin-film forms, were characterized using polarized versus nonpolarized optical microscopy, scanning electron microscopy (SEM), and wide-angle X-ray (WAXD) analysis. POT can simultaneously display solely one type of spherulite or dual types of spherulites (double-ring-banded and ringless ones), depending on T-c or T-max imposed. Fractions of these two types depend on T-c when quenched from a fixed T-max = 160 degrees C. At lower T-c's, POT exhibits higher crystallization rates leading to higher fractions of ringless spherulites; at higher T-c's, POT exhibits lower crystallization rates leading to ring-banded spherulites. At intermediate to high T-c's where the growth kinetics of POT could be monitored, the ring-band type dominates and the fraction of ringless spherulites is insignificantly small. Both ringless and ring-banded spherulites can be seen in regime III (T-c = 70-110 degrees C) with fractions of ringless type of spherulites decreasing with temperature. Thus, growth kinetics for POT was mainly focused on the regime of ring-banded spherulites. In regime III, the ring-band pattern is more orderly concentric with smaller inter-ring spacing (1-2 mu m) for lower T-c's but intermediately larger spacing (3-5 mu m) for higher T-c's. The orderly lamellar orientation in the ring-bands in contrast with the inter-ring valley region is discussed. In regime II (115 degrees C and above), the ring-band pattern is first distorted to highly zigzag irregularity at higher T-c's and then eventually disappears at extremely high T-c, with the lamellar crystals eventually turning dendritic with no rings. Apparently, the types of spherulites in polymers are more influenced by the growth rates as determined by T-c and slightly less by T-max, but not by the substrate surface nucleation.

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