Khoury F
J Res Natl Bur Stand A Phys Chem. 1966 Jan-Feb;70A(1):29-61. doi: 10.6028/jres.070A.006.
Polypropylene can be crystallized in the form of monoclinic (Natta) spherulites from moderately concentrated solutions of the polymer in different solvents. A study is presented involving both optical and electron microscopy which has led to the characterization of the unusual structure and morphology of the dendritic precursor crystals from which such spherulites evolve, as well as the manner in which these precursors degenerate progressively into spherulites. The shape of the above mentioned polypropylene dendrites approximates that of a rectangular parallelepiped (reference axes , where ≈ 1.1 and > 2z). These dendrites consist of a dense but not compact network of monolayer chain-folded lamellar branches which traverse the dendrite with respect to its rectangular cross section, the fold surfaces of the individual lamellar branches (i.e., those faces which the constituent molecules in each branch fold back and forth) being normal to the cross section. Electron diffraction data indicate that the orientation of the -crystallographic axis is unique throughout the cross-hatched array of lamellar branches and is parallel to , the latter axis corresponding to the direction of slowest growth of the dendrite as a whole as well as its constituent branches. It has also been deduced on the basis of the above features coupled with electron diffraction data and consideration of two different but plausible model twinned dendrites that the fold surfaces of the lamellar branches are (001) and that the angle between the -crystallographic axis in intercrossing branches is circa 80°. The possible origin of this unusual mode of twinning, which involves an 80° change in the orientation of the chain axes in offspring branches from that in parent branches, is briefly presented. The process of evolution of monoclinic polypropylene spherulites from the unusually twinned dendritic crystal precursors is contrasted with the evolution of spherulites in other polymers; furthermore, the relevance of the observations presented in this study to an understanding of the origin of the previously reported atypical fine structures exhibited by monoclinic spherulites of polypropylene crystallized from the melt, is discussed.
聚丙烯可以从其在不同溶剂中的适度浓溶液中以单斜(纳塔)球晶的形式结晶。本文介绍了一项涉及光学显微镜和电子显微镜的研究,该研究对这类球晶所源自的树枝状前驱晶体的异常结构和形态进行了表征,同时也研究了这些前驱体逐渐演变成球晶的方式。上述聚丙烯树枝状晶体的形状近似于长方体(参考轴 ,其中 ≈ 1.1 且 > 2z)。这些树枝状晶体由单层链折叠片层分支构成的致密但不紧密的网络组成,这些片层分支相对于树枝状晶体的矩形横截面横穿树枝状晶体,各个片层分支的折叠面(即每个分支中组成分子来回折叠的那些面)垂直于横截面。电子衍射数据表明,在整个交叉排列的片层分支阵列中,-晶轴的取向是唯一的,并且与 平行,后一轴对应于整个树枝状晶体及其组成分支生长最慢的方向。基于上述特征以及电子衍射数据,并考虑两种不同但合理的孪晶树枝状晶体模型,还推断出片层分支的折叠面为(001),并且交叉分支中 -晶轴之间的夹角约为80°。简要介绍了这种不寻常孪晶模式的可能起源,该模式涉及子代分支中链轴方向相对于亲代分支有80°的变化。将单斜聚丙烯球晶从异常孪晶树枝状晶体前驱体的演化过程与其他聚合物中球晶的演化过程进行了对比;此外,还讨论了本研究中所呈现的观察结果与理解先前报道的从熔体中结晶的聚丙烯单斜球晶所表现出的非典型精细结构起源的相关性。