Crystallization study of poly(etheretherketone)/poly(etherimide) blends by real-time small-angle x-ray scattering

被引:9
|
作者
Hsiao, BS [1 ]
Verma, RK [1 ]
Sauer, BB [1 ]
机构
[1] Dupont Co, Cent Res & Dev, Expt Stn, Wilmington, DE 19880 USA
来源
关键词
poly(ether ether ketone); PEEK; poly(ether imide); Ultem (R); blends; lamellae; crystals; stacks; fibrils; crystallization; SAXS; synchrotron x-ray;
D O I
10.1080/00222349808220478
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Morphological changes during isothermal melt crystallization in poly(aryl ether ether ketone) (PEEK)/poly(ether imide) (PEI, Ultem(R) 1000) blends were monitored via real-time small-angle x-ray scattering (SAXS) using synchrotron radiation. SAXS data were analyzed using a novel combination of correlation and interface distribution functions to determine the lamellar crystal thicknesses l(c) and interlamellar noncrystalline or "amorphous" layer thicknesses l(a). The higher glass transition noncrystalline PEI component slows the PEEK crystallization substantially, but l(a) (about 40 Angstrom) and l(c) (about 85 Angstrom) are independent of crystallization time and blend composition. This is consistent with the known independence of melting temperature with blend composition. These results indicate that PEEK crystallizes in densely crystalline lamellar stacks through all stages of primary crystallization, and that the noncrystalline PEI is almost entirely excluded from the stacks at all times during spherulitic growth. The rate of increase in scattering invariant is found to be reduced during spherulite impingement due to spatial limitations.
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页码:365 / 374
页数:10
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