首页> 外文期刊>Polymer: The International Journal for the Science and Technology of Polymers >Small-angle X-ray scattering studies on melting and recrystallization behaviors of poly(oxyethylene) crystallites in poly(D,L-lactide)/ poly(oxyethylene) blends
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Small-angle X-ray scattering studies on melting and recrystallization behaviors of poly(oxyethylene) crystallites in poly(D,L-lactide)/ poly(oxyethylene) blends

机译:小角X射线散射研究聚(D,L-丙交酯)/聚(氧乙烯)共混物中聚(氧乙烯)微晶的熔融和重结晶行为

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摘要

Direct determination of the discrete distribution for crystalline lamellar thickness has been performed for poly(D,L-lactic acid)/poly(oxyethylene) (PDLLA/PEG) blends by conducting small-angle X-ray scattering (SAXS) measurements using synchrotron radiation. The PDLLA used was an random (racemic) copolymer of bio-based poly(L-lactic acid) (PLLA) and poly(D-lactic acid) (PDLA) with the lactide monomer ratio of L:D = 50:50. It is known that PLA is miscible with PEG in the amorphous state. In the current paper, we report comprehensive results on structural analyses of PDLLA/PEG blends in the course of heating and cooling process using SAXS to elucidate the change in the thickness distribution of the lamellae. As a consequence, it was found that the distribution of the lamellar thickness moves toward the larger value (in other words, lamellar thickening) as temperature approaches the melting point. Typically, the thickness distribution was dispersed in the range of 10-20 nm at room temperature and it changed toward 40 nm in the vicinity of the melting temperature. To the best of our knowledge, this is the first report of direct determination of the discrete distribution for the crystalline lamellar thickness and their in-situ changes in the course of the lamellar thickening process. As a result, the lamellar thickening was found to occur at much lower temperature for the blend samples with 10% and 20% of PDLLA contents as compared to the PEG 100% sample. This phenomenon can be ascribed to the melting point depression owing to the miscibility between PEG and PDLLA. Thereby, thinner lamellae were melted and thicker ones appeared at much lower temperature for the blends than for the PEG 100% sample. As for the average repeating distance (long period) of the lamellar stacks, an abrupt increase similar to the critical divergence was observed (from 25 nm to 50 nm) in the heating process. Not only for the melting behavior but also in the course of recrystallization, change in the lamellar-thickness distribution was uncovered, which shows strong hysteresis depending on what temperature the sample was cooled down from.
机译:对于聚(D,L-乳酸)/聚(氧化乙烯)(PDLLA / PEG)共混物,已经通过使用同步加速器辐射进行小角度X射线散射(SAXS)测量来直接确定晶体层状厚度的离散分布。所用的PDLLA是生物基聚(L-乳酸)(PLLA)和聚(D-乳酸)(PDLA)的无规(外消旋)共聚物,丙交酯单体比例为L:D = 50:50。已知PLA与无定形的PEG可混溶。在当前的论文中,我们报告了在使用SAXS进行加热和冷却过程中PDLLA / PEG共混物结构分析的综合结果,以阐明薄片厚度分布的变化。结果,发现随着温度接近熔点,层状厚度的分布向较大的值移动(换言之,层状增厚)。通常,厚度分布在室温下分散在10-20nm的范围内,并且在熔融温度附近朝40nm变化。据我们所知,这是第一个直接确定晶体层状厚度及其在层状增稠过程中原位变化的离散分布的报告。结果,与PEG 100%样品相比,发现具有10%和20%PDLLA含量的共混物样品在更低的温度下发生层状增稠。该现象可归因于由于PEG与PDLLA之间的可混溶性而导致的熔点降低。因此,与PEG 100%样品相比,掺混物的薄片变薄了,而掺混物出现的温度却低得多。至于层状叠层的平均重复距离(长周期),在加热过程中观察到与临界发散相似的突然增加(从25nm至50nm)。不仅对于熔融行为,而且在重结晶过程中,均未发现层状厚度分布的变化,这取决于样品从什么温度冷却而显示出强的滞后性。

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