首页> 外文期刊>Macromolecules >Structural regularization in the crystallization process from the glass or melt of poly(l-lactic acid) viewed from the temperature-dependent and time-resolved measurements of FTIR and wide-angle/small-angle X-ray scatterings
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Structural regularization in the crystallization process from the glass or melt of poly(l-lactic acid) viewed from the temperature-dependent and time-resolved measurements of FTIR and wide-angle/small-angle X-ray scatterings

机译:从FTIR和广角/小角X射线散射的温度相关和时间分辨的测量结果来看,从玻璃或聚(l-乳酸)的熔融物中结晶过程中的结构规则化

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Structural evolution has been traced in the crystallization process of poly(l-lactic acid) (PLLA) from the melt or from the glass by measuring the FTIR spectra, wide-angle X-ray diffraction (WAXD), and small-angle X-ray scattering (SAXS) patterns as functions of temperature or time. Using the infrared bands characteristic of the melt, mesomorphic phase (mesophase) and crystalline phase as well as the WAXD 200/110 and 0010 reflections and the SAXS long-period peak, the regularization processes were analyzed systematically from the different points of view. In the case of cold-crystallization from the glass, the mesophase was found to regularize into the disordered α (α′ or δ) form in the temperature region from just above the glass transition point (Tg, 70 °C) to 120 °C, whereas it changed to the regular α form in the higher temperature region. On the other hand, in the melt-crystallization process, the crystallization to the α or δ form occurred not directly from the melt but via the mesophase from the melt. In this way the isothermal crystallizations from the glass and from the melt were found to occur always with the first appearance of the mesophase from the amorphous phase followed by the transition to the crystalline α or δ phase. The 2-dimenisonal X-ray diffraction diagram was analyzed to investigate the structure of the oriented mesophase, in which the conformationally disordered (10/3) helical chains are gathered together with low correlation to form a small domain of about 30 ? (c axis) × 20 ? (lateral direction) size. In the cold crystallization process, these small domains of the mesophase grew larger to form the domains of the δ form of 75 × 100 ? size, attendant with the imperfect conformational regularization as well as the disorder in relative height between the neighboring domains. By increasing the temperature furthermore, the δ form transforms to the α form consisting of the more tightly packed chains of regular conformation in the domain of about 170 × 300 ? size. In this way, the thermally induced regularization of PLLA was found to occur in a complicated manner: from the glass to the mesophase, to the δ form and to the α form in the cold crystallization phenomenon of the melt-quenched sample, while it occurs from the melt to the mesophase and to the α or δ form in the cooling process from the melt.
机译:通过测量FTIR光谱,广角X射线衍射(WAXD)和小角度X-射线,可以从熔体或玻璃的聚(1-乳酸)(PLLA)结晶过程中追溯结构演变。光线散射(SAXS)模式作为温度或时间的函数。利用熔体,同晶相(中间相)和结晶相以及WAXD 200/110和0010反射以及SAXS长周期峰的红外波段特征,从不同的角度系统地分析了正则化过程。在玻璃冷结晶的情况下,发现中间相在刚好高于玻璃化转变点(Tg,70°C)到120°C的温度区域内规则化为无序α(α'或δ)形式。 ,而在较高温度区域它变成规则的α形式。另一方面,在熔融结晶过程中,结晶成α或δ形式的结晶不直接从熔体中发生,而是经由熔体的中间相发生。以这种方式,发现从玻璃和从熔体的等温结晶总是在中间相从非晶相首先出现,然后过渡到结晶α或δ相时发生。分析了二维的X射线衍射图,研究了定向中间相的结构,其中构象无序的(10/3)螺旋链以低相关性聚集在一起,形成一个约30?的小区域。 (c轴)×20? (横向)尺寸。在冷结晶过程中,中间相的这些小区域逐渐变大,形成75×100?大小,伴随着不完善的构象正则化以及相邻域之间相对高度的混乱。通过进一步升高温度,δ形式转变为α形式,该α形式由在170×300?左右的区域中规则排列的更紧密堆积的链组成。尺寸。以这种方式,发现了热致的PLLA正则化过程以复杂的方式发生:在熔融淬火样品的冷结晶现象中,从玻璃到中间相,从δ形式到α形式同时发生。从熔体到中间相,再到冷却过程中的α或δ。

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