Gan Zhihua, Kuwabara Kazuhiro, Abe Hideki, Iwata Tadahisa, Doi Yoshiharu
SORST Group of Japan Science and Technology Corporation, Polymer Chemistry Laboratory, RIKEN Institute, 2-1 Hirosawa, Wako-shi, Saitama 351-0198, Japan.
Biomacromolecules. 2004 Mar-Apr;5(2):371-8. doi: 10.1021/bm0343850.
Polymorphism phenomenon of melt-crystallized poly(butylene adipate) (PBA) has been studied by wide-angle X-ray diffraction (WAXD), small-angle X-ray scattering (SAXS), and differential scanning calorimetry (DSC). It has been found that the isothermal crystallization leads to the formation of PBA polymorphic crystals, simply by changing the crystallization temperature. The PBA alpha crystal, beta crystal, and the mixture of two crystal forms grow at the crystallization temperatures above 32 degrees C, below 27 degrees C, and between these two temperatures, respectively. The relationship between PBA polymorphism and melting behaviors has been analyzed by the assignments of multiple melting peaks. Accordingly, the equilibrium melting temperatures Tm degrees of both alpha and beta crystals were determined by Hoffman-Weeks and Gibbs-Thomson equations for the purpose of understanding the structural metastability. The Tm degrees of the PBA alpha crystal was found to be higher than that of the beta crystal, indicating that the PBA alpha crystal form is a structurally stable phase and that the beta crystal form is a metastable phase. The analysis of growth kinetics of PBA polymorphic crystals indicates that the metastable PBA beta crystal is indeed the kinetically preferential result. Based on the thermal and kinetic results, the phenomenon of stability inversion with crystal size in melt-crystallized PBA was recognized, in terms of the growth mechanisms of PBA alpha and beta crystals and the transformation of beta to alpha crystals. The PBA beta --> alpha crystal transformation takes place at a sufficiently high annealing temperature, and the transformation has been evident to be a solid-solid-phase transition process accompanied by the thickening of lamellar crystals. The molecular motion of polymer chains in both crystalline and amorphous phases has been discussed to understand the thickening and phase transformation behaviors.
通过广角X射线衍射(WAXD)、小角X射线散射(SAXS)和差示扫描量热法(DSC)研究了熔融结晶聚己二酸丁二醇酯(PBA)的多晶型现象。研究发现,通过改变结晶温度,等温结晶会导致PBA多晶型晶体的形成。PBA的α晶体、β晶体以及两种晶型的混合物分别在高于32℃、低于27℃以及这两个温度之间的结晶温度下生长。通过对多个熔融峰的归属分析了PBA多晶型与熔融行为之间的关系。因此,为了理解结构亚稳性,利用霍夫曼-韦克斯方程和吉布斯-汤姆逊方程确定了α和β晶体的平衡熔融温度Tm°。发现PBAα晶体的Tm°高于β晶体,这表明PBAα晶型是结构稳定相,而β晶型是亚稳相。PBA多晶型晶体生长动力学分析表明,亚稳的PBAβ晶体确实是动力学上优先的结果。基于热学和动力学结果,从PBAα和β晶体的生长机制以及β向α晶体的转变方面,认识到了熔融结晶PBA中晶体尺寸稳定性反转的现象。PBAβ→α晶体转变在足够高的退火温度下发生,并且该转变显然是一个伴随着片晶增厚的固-固相变过程。讨论了结晶相和非晶相中聚合物链的分子运动,以理解增厚和相变行为。