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《Composite Interfaces》2013,20(5-6):347-359
Scanning electron microscopy (SEM), polarized light microscopy (PLM), and transmission electron microscopy (TEM) techniques have been used to characterize the normal surface and flank surface microstructure of a polyacrylonitrile (PAN)-based carbon fiber reinforced chemical vapor infiltrated (CVI) matrix carbon–carbon composite. Optical and SEM results indicate that the CVI deposit consists of two structures: an isotropic phase is present in the fiber bundle-bundle junctions and a second highly oriented lamellar structure is present in the intrabundle matrix. TEM shows that matrix platelets are highly parallel to the fiber axis and the crystallites of the matrix near the fiber surface exhibit better alignment than those farther away from fibers. 相似文献
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《Composite Interfaces》2013,20(3-4):365-378
The influence of the uniformity of geometric fiber arrangement on the fracture behavior was investigated for unidirectional fiber-reinforced composites from both experimental and analytic viewpoints. Two types of mini-composites, composed of 20 carbon fibers and epoxy resin, were prepared using our original method to control the fiber arrangement in experiments: one type had uniform fiber arrangement and the other non-uniform. The tensile tests of these mini-composites showed that the fracture pattern was quite different between the two types of mini-composites, although the difference in the tensile fracture load between them was minimal. A Monte Carlo simulation of the fracture process was carried out using the modified shear lag analysis. The simulation results, showing that the non-uniform fiber arrangement accelerates the crack growth towards the matrix-rich part, accounted for the difference in fracture patterns due to the fiber arrangement. 相似文献
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Jun-tingXu Bo-taoLi Zhi-qiangFan 《高分子科学》2004,(3):279-287
The fractions of one metallocene-based (mPE) and one conventional (znPE) ethylene-butene copolymer eluted at 80-82℃ from temperature rising elution fractionation were selected for DSC and time-resolved small angle X-ray scattering (SAXS) and wide angle X-ray scattering (WAXS) characterization. The DSC and WAXS results show that two crystal structures exist in both mPE and znPE: structure A with higher melting temperature and structure B with lower melting temperature. It was found that original znPE (s-znPE) contains more highly ordered structure A than original mPE (s-mPE) in spite of the higher comonomer content of znPE. Another structure C is also identified because of higher crystallinity measured by WAXS than by DSC and is attributed to the interfacial region. The SAXS data were analyzed with correlation function and two maxima were observed in s-mPE and s-znPE, in agreement with the conclusion of two crystal populations drawn from DSC and WAXS results. These two crystal populatiorts have close long periods in s-mPE, but very different long periods in s-znPE. In contrast, freshly crystallized mPE and znPE (f-mPE and f-znPE) contain only a single crystal population with a broader distribution of long period 相似文献
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