差示扫描量热法
成核
结晶
再结晶(地质)
材料科学
战术性
聚合物结晶
光学显微镜
球晶(高分子物理)
部分熔融
聚合物
大气温度范围
结晶学
高分子化学
热力学
扫描电子显微镜
化学
复合材料
聚合
物理
生物
古生物学
地幔(地质学)
地球物理学
作者
B. Fillon,J. C. Wittmann,Bernard Lotz,A. Thierry
标识
DOI:10.1002/polb.1993.090311013
摘要
Abstract The crystallization behavior after partial or complete melting of the α phase of iPP is examined by combined differential scanning calorimetry (DSC) and optical microscopy: calorimetric results are directly correlated with corresponding morphologies of microtome sections of DSC samples. On partial melting at various temperatures (hereafter referred to as T s ) located in a narrow range (4°C) below and near T m , the number of nuclei increases (as in classical self‐nucleation experiments), by several orders of magnitude; on subsequent cooling, the crystallization peak is shifted by up to 25°C. After partial melting in the lower part of the T s range and recrystallization, the polymers display a prominent morphology “memory effect” whereby a phantom pattern of the initial spherulite morphology is maintained. After partial melting in the upper part of the T s range the initial morphology is erased and self‐nucleation affects only the total number of nuclei. The present experimental procedures make it possible to define, under “standard” conditions, the crystallization range of the polymer and in particular, the maximum crystallization temperature achievable when “ideally” nucleated. © John Wiley & Sons, Inc.
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