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不同晶相草酸钙晶体的选区电子衍射和X射线衍射比较分析

Comparative Analysis on Various Calcium Oxalate Hydrates by SAED and XRD

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【作者】 郑辉欧阳健明段荔

【Author】 ZHENG Hui~1, OUYANG Jian-ming~(1,2), DUAN Li~1(1.Institute of Biomineralization and Lithiasis Research, Jinan University, Guangzhou 510632, China;2.State Key Laboratory of Rare Earth Materials Chemistry and Applications, Peking University, Beijing 100871, China)

【机构】 暨南大学生物矿化与结石病防治研究所暨南大学生物矿化与结石病防治研究所 广州510632广州510632北京大学稀土材料化学及应用国家重点实验室北京100871

【摘要】 在卵磷脂-水脂质体中制备了一水草酸钙(COM)、二水草酸钙(COD)和三水草酸钙(COT)。并对它们分别进行了透射电镜(TEM)、选区电子衍射分析(SAED)和X射线衍射(XRD)分析。TEM结果表明,COM、COD和COT均为泡状,粒径约80~150nm。将SAED结果与XRD结果对比分析,发现将SAED图谱指标化后所得的衍射数据与XRD的特征峰值基本相符,但在相对强度上存在差别。本实验结果表明,将TEM、SAED和XRD技术联合分析纳米级草酸钙晶体,不但可以观察纳米级草酸钙的形貌,而且能对其晶相、单晶和多晶等进行深入的了解。

【Abstract】 Calcium oxalate monohydrate (COM), dihydrate (COD) and trihydrate (COT) prepared in Lecithin-water liposomes were characterized by transmission electron microscope (TEM), selected area electron diffraction (SAED) and X-ray powder diffraction (XRD), respectively. TEM results show that the COM, COD and COT crystals grown in vesicles are nanoparticles with a diameter of about 80-150 nm. Compared the results of SAED with that of XRD, the characteristic diffraction peaks of the three calcium oxalate hydrates in XRD patterns were in agreement with the diffraction data of their corresponding SAED after indexing. But the relative intensity is different. The results of this work show that if combined the results obtained by TEM, SAED and XRD, not only the morphology of calcium oxalate nanoparticles could be observed, but also their phase composition, monocrystalline and polycrystalline structure, etc. could be obtained.

【基金】 广州市重点科技项目(2001-Z-123-01);国家自然科学基金(No.20471024);国家自然科学基金重点项目(No.20031010);北京大学稀土材料化学及应用国家重点实验室开放基金资助
  • 【文献出处】 人工晶体学报 ,Journal of Synthetic Crystals , 编辑部邮箱 ,2005年04期
  • 【分类号】O73
  • 【被引频次】5
  • 【下载频次】789
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