Iwata Tadahisa, Fujita Masahiro, Aoyagi Yoshihiro, Doi Yoshiharu, Fujisawa Tetsuro
Polymer Chemistry Laboratory, RIKEN Institute, 2-1 Hirosawa, Wako-shi, Saitama 351-0198, Japan.
Biomacromolecules. 2005 May-Jun;6(3):1803-9. doi: 10.1021/bm050152s.
Uniaxially oriented films with high tensile strength were processed from ultrahigh-molecular-weight poly[(R)-3-hydroxybutyrate] (P(3HB)) by a method combining hot-drawing near the melting point of the polymer and two-step-drawing at room temperature. In a two-step-drawn and subsequently annealed film, P(3HB) molecular chains fall into two states: 2/1 helix (alpha-form) and planar zigzag (beta-form) conformations. The mechanism for generating the beta-form during two-step-drawing was investigated by time-resolved synchrotron wide- and small-angle X-ray scattering measurements (WAXD and SAXS), together with the measurement of stress-strain curves. It was found that the improvement of mechanical properties is due to not only the orientation of molecular chains but also the generation of the beta-form during the drawing. The crystal and molecular structures of the alpha-form remained unchanged until the yield point of the stress-strain curve. At the yield point, the long period obtained from SAXS doubled and a new reflection indicative of the beta-form was observed on the equatorial line in WAXD. The intensity of the reflection from the beta-form increased with an increase in the two-step-drawing ratio at room temperature. The SAXS pattern changed from a two-point reflection along the meridian to a cross pattern with streaking on the equatorial line, demonstrating the close alignment of shish-kebab structures. The reflection intensity, crystal orientation and crystal size of the alpha-form decreased during two-step-drawing. Based on these results, the beta-form is mainly introduced from the orientation of free molecular chains in the amorphous regions between alpha-form lamellar crystals, but the structural transformation of molecular chains also occurs from the alpha-form to the beta-form at the deformed lamellar crystals.
通过将聚合物熔点附近的热拉伸与室温下的两步拉伸相结合的方法,由超高分子量聚(R)-3-羟基丁酸酯制备了具有高拉伸强度的单轴取向薄膜。在两步拉伸并随后退火的薄膜中,P(3HB)分子链呈现两种状态:2/1螺旋(α-型)和平面锯齿(β-型)构象。通过时间分辨同步加速器广角和小角X射线散射测量(WAXD和SAXS)以及应力-应变曲线测量,研究了两步拉伸过程中β-型产生的机理。结果发现,力学性能的提高不仅归因于分子链的取向,还归因于拉伸过程中β-型的产生。α-型的晶体和分子结构在应力-应变曲线的屈服点之前保持不变。在屈服点,SAXS得到的长周期加倍,并且在WAXD的赤道线上观察到一个指示β-型的新反射。β-型反射的强度随着室温下两步拉伸比的增加而增加。SAXS图案从沿子午线的两点反射变为赤道线上有条纹的十字图案,表明串晶结构紧密排列。在两步拉伸过程中,α-型的反射强度、晶体取向和晶体尺寸减小。基于这些结果,β-型主要是由α-型片晶之间非晶区域中自由分子链的取向引入的,但分子链的结构转变也发生在变形的片晶处从α-型转变为β-型。