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基于广角X射线散射技术的竹材纤维素晶型研究 被引量:2

Study of Crystal Structures of Cellulose in Bamboo Using Wide Angle X-ray Scattering Technique
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摘要 纤维素Ⅰ是自然界中纤维素晶体的主要存在形式,它具有三斜晶体结构的I_α和单斜晶体结构的I_β。为进一步研究竹材中的纤维素晶型,利用同步辐射广角X射线散射(SR—WAXS)技术对毛竹竹壁纤维素晶型进行了初步研究,通过已知的纤维素晶胞模型计算晶面间距并预测衍射峰的峰位,再根据实验所得的实际峰位,判定竹材中纤维素的晶型。结果表明,竹材的衍射峰位与纤维素I_α的理论计算值相近,证明竹材中的纤维素I_β是绝大多数甚至是唯一品型。相比核磁共振技术而言,利用同步辐射广角X射线散射研究竹材中纤维素晶型是一个较为简单的方法。 Cellulose I is the main existence form of cellulose crystal in nature,which consists of two different crystal structures which are marked as cellulose Iα and Iβ.In order to obtain a better and more comprehensive understanding of crystal forms of native cellulose in bamboo culm,Synchrotron Wide Angle X-ray Scattering(SR-WAXS) was used to investigate cellulose polymorphy.The interplanar spacing was calculated and the peak position of the diffraction peaks was predicated through the existed cellulose cell model.And then the crystal structures of cellulose were determined by actual peak position.According to the results,the cellulose Iβ model is in good agreement with experimental values from SR-WAXS peaks,so authors of this paper confirm that the cellulose Iβ is dominant or the unique crystalline structure in bamboo culm.To this extent,it is much convenient to use SR-WAXS to study crystal structures of cellulose than NMR(Nuclear Magnetic Resonance).
出处 《林产工业》 北大核心 2016年第12期8-10,30,共4页 China Forest Products Industry
基金 国家自然科学基金面上项目“竹纤维细胞壁多层构造的理化表征”(31370563) 留学回国科研启动基金“医用生物可降解高分子共混物的降解及原位拉伸同步辐射SAXS/WAXS研究”(教外司留[2014]1685)
关键词 竹材 纤维素晶型 广角X射线散射 Bamboo Cellulose polymorphs Wide Angle X-ray Scattering
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  • 1王越平,高绪珊,耿丽,张晓丹.天然竹纤维与几种纤维素纤维的性能测试与比较[J].针织工业,2005(11):58-60. 被引量:12
  • 2VanderHart D L, Atalla R H. Studies of microstructure in native cellulose using solid-state ^13C NMR[J].Macromoleeules, 1984, 17:1465-1472.
  • 3Newman R H, Hemmingson J A. Determination of the degree of cellulose crystallinity in wood by carbon-13 nuclear magnetic resonance spectroscopy[J]. Holzforschung, 1990, 44:351-355.
  • 4Heux L, Dinand E, Vignon M R. Structural aspects of ultrathin cellulose microfibrils followed by ^13C CP- MAS NMR[J]. Carbohydrate Polymer, 1999, 40:115-124.
  • 5Segal L, Creely L, Martin A E. An empirical method for estimating the degree of crystallinity of native cellulose using X-ray diffractometer[J]. Textiles Research Journal, 1959, 29: 786-794.
  • 6Gumuskaya E, Usta M, Kirci H. The effects of various pulping conditions on crystalline structure of cellulose in cotton linters[J]. Polymer Degradadation Stability, 2003, 81: 559-564.
  • 7Yakunin N A, Zavadskii A E. Effect of damping on the supramolecular structure of cotton cellulose[J]. Fiber Chemistry, 2004, 36: 463-466.
  • 8Foeher B, Palma M. Structural differences between nOn-wood plant celluloses: evidence from solid state NMR, vibrational spectroscopy and X-ray diffractometry[J]. Industrial Crops and Products, 2001, 13: 193-208.
  • 9Tang L C, Hon D N S, Pan S H. Evaluation of microcrystalline cellulose. 1. Changes in ultrastructural eharaeteristics during preliminary acid hydrolysis[J]. Journal of Applied Polymer Science, 1996, 59: 483-488.
  • 10Wada M, Okano T, Sugiyama J. Allomorphs of native crystalline cellulose I evaluated by two equatodaldspacings[J]. Journal of Wood Science, 2001, 47(2): 124-28.

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