Nishiyama Yoshiharu, Wada Masahisa, Hanson B Leif, Langan Paul
Centre de Recherches sur les Macromolécules, Végétales-CNRS, Joseph Fourier University of Grenoble, BP 53, 38041 Grenoble Cedex 9, France.
Cellulose (Lond). 2010 Jun;17(4):735-745. doi: 10.1007/s10570-010-9415-9.
Structural changes during the treatment of films of highly crystalline microfibers of Cladophora cellulose with ethylenediamine (EDA) have been studied by time-resolved X-ray microprobe diffraction methods. As EDA penetrates the sample and converts cellulose I to EDA-cellulose I, the measured profile widths of reflections reveal changes in the shapes and average dimensions of cellulose I and EDA-cellulose I crystals. The (200) direction of cellulose I is most resistant to EDA penetration, with EDA penetrating most effectively at the hydrophilic edges of the hydrogen bonded sheets of cellulose chains. Most of the cellulose chains in the initial crystals of cellulose I are incorporated into crystals of EDA-cellulose I. The size of the emerging EDA-cellulose I crystals is limited to about half of their size in cellulose I, most likely due to strains introduced by the penetration of EDA molecules. There is no evidence of any gradual structural transition from cellulose I to EDA-cellulose I involving a continuously changing intermediate phase. Rather, the results point to a rapid transition to EDA-cellulose I in regions of the microfibrils that have been penetrated by EDA.
利用时间分辨X射线微探针衍射方法研究了用乙二胺(EDA)处理的刚毛藻纤维素高结晶微纤丝薄膜在处理过程中的结构变化。随着EDA渗透到样品中并将纤维素I转化为EDA - 纤维素I,所测量的反射峰宽揭示了纤维素I和EDA - 纤维素I晶体的形状和平均尺寸的变化。纤维素I的(200)方向对EDA渗透最具抗性,EDA在纤维素链氢键片层的亲水性边缘处渗透最有效。纤维素I初始晶体中的大多数纤维素链被并入EDA - 纤维素I晶体中。新形成的EDA - 纤维素I晶体的尺寸限制在其在纤维素I中尺寸的约一半左右,这很可能是由于EDA分子渗透引入的应变所致。没有证据表明从纤维素I到EDA - 纤维素I存在任何涉及连续变化中间相的逐渐结构转变。相反,结果表明在微纤丝中已被EDA渗透的区域中迅速转变为EDA - 纤维素I。