射线分析显示化合物1和2的晶体结构均由分子间氢键和-弱相互作用堆积而成的二维层状结构。
The X-ray analysis reveals that the crystal structures of compounds 1 and 2 are two-dimensional layer structures through intramolecular hydrogen bonding and -? stacking.
在水热条件下合成了一种新型超分子化合物，通过元素分析、红外光谱、热重分析和X射线单晶衍射方法确定了其晶体结构。
A new supramolecular compound has been synthesized under hydrothermal conditions and characterized by element analysis, IR, TG analysis and single-crystal X-ray diffraction.
利用X射线衍射分析方法，对湿压磁场成型的永磁铁氧体生坯晶体取向度进行了研究。
Degree of preferred orientation of hard Sr ferrite compacts molded with magnetic field was studied by X ray diffraction analysis.
用X射线单晶衍射分析法测定了该配合物的晶体结构。
The crystal structure was determined by X ray single crystal diffraction analysis.
并通过元素分析及X-射线单晶衍射法，测定了该化合物的晶体结构。
The crystal structure of the compound has been determined by elemental analysis and X-ray single-crystal diffraction.
本文用衍生物合成、降解反应、红外光谱、核磁共振谱及x -射线衍射晶体分析法研究了它的化学结构。
Its structure has been studied through a series of chemical synthesis, preparation of derivatives, degradations and IR analyses, and ultimately determined by X-ray diffraction.
射线粉末衍射（XRD）分析表明，复合掺杂没有改变晶体的六方单相层状结构。
The results of X-ray diffraction (XRD) analysis show that it remains a well-layered structure with single phase of hexagonal after composite doping.
再次，通过采用X射线衍射、红外光谱、拉曼光谱、吸收光谱和荧光光谱等方法分析了晶体的结构与性能；
Thirdly, analyzing crystal structure and character by X-ray diffraction, infra-red spectrum, Raman spectrum, absorption spectrum and fluorescence spectrum.
X 射线晶体结构分析与TG DTA分析表明，镍铁与镁铁水滑石晶体两者结构相似，但热稳定性存在一定差异。
Their heat stability difference were compared by X-ray crystal structural analysis and TG-DTA analysis. The results showed a similar crystal structure and different heat stability.
研究人员利用X射线衍射晶体分析法比较不同的结构来确定差异，弄清楚了细菌移除重金属毒物的机制。
The researchers used X-ray crystallography to compare the various structures, identify the differences and understand the mechanism that removes heavy-metal toxins from cells.
借助热分析和X-射线衍射分析讨论了色料的合成过程和晶体结构。
The synthetic process and the crystal structure of stain, with the aid of thermal analysis and X ray diffraction studies, were discussed.
用X-射线单晶衍射分析确定了其晶体结构。
The crystal structure of the complex was determined by X-ray single diffraction.
利用X射线双晶衍射分析了晶体的完整性。
The lattice perfection of the InAs single crystal is studied with X-ray diffraction.
射线衍射、扫描电镜分析表明，水溶性P2O5存在降低了碳酸钙晶型由球霞石向方解石转变的速率，并使碳酸钙晶体晶习变坏。
The results obtained from XRD and SEM indicate that water-soluble P2O5 in gypsum reduces the rate of transformation from vaterite to calcite and makes crystalline grains smaller and irregular.
当X射线在晶体中通过并从原子上反弹时，他们留下衍射图案，可用其分析得到该蛋白三维形状。
As the x-rays pass through and bounce off of atoms in the crystal, they leave a diffraction pattern, which can then be analyzed to determine the three-dimensional shape of the protein.
这种方法使用了纽约布鲁克黑文的国家同步加速器光源产生的强大的X射线，以分析用TIGAR酶的样本生长出来的晶体。
The process involved using intensive X-ray light produced at the National Synchroton Light Source in Brookhaven, N. Y. , to analyze crystals grown from samples of the TIGAR enzyme.
经x射线衍射分析，纯钛表面经阳极氧化处理后，其表面生成了一层非晶态的氧化钛薄膜，并且钛晶体的各个表面沿不同结晶方向的腐蚀速率不相同。
XRD results indicate that amorphous titanium oxide film is formed on the surface after anodic oxidation, and corrosion rates of titanium crystal vary along different crystalline orientation.
并且通过IR、TGA、荧光光谱分析和X -射线单晶衍射对晶体结构和性质进行了表征和研究。
And by IR, TGA, fluorescence spectroscopy and X-ray diffraction on the crystal structure and properties were characterized and studied.
射线分析表明，改性后该石墨晶体中三方石墨的含量增高。
The X ray diffraction (XRD) results showed that the rhombohedral phase fraction of natural graphite increased after being coated.
通过元素分析、 红外光谱和氢核磁共振谱对其结构进行了表征。用X-射线单晶衍射测定了该化合物的晶体结构。
The crystal structure has been determined by X ray single crystal diffraction, showing a distorted trigonal bipyramidal configuration with five coordination for the central tin atom.
利用X射线衍射仪、扫描电子显微镜和荧光分光光度计对样品的晶体结构和光学性质进行了分析。
The structural and optical characteristics were studied by X-ray diffraction, scanning electron microscopy and Photoluminescence spectrum.
利用核磁共振仪、扩展X射线吸收精细结构分析、透射电镜对溶胶中的锐钛矿晶体进行深入分析，并考察了锐钛矿晶体的光催化活性。
Nuclear magnetic resonance (NMR) imaging, X-ray absorption fine structure (XAFS) analysis, transmission electron microscope (TEM), and photocatalytic property testing were carried out.
经X射线衍射分析证实，铁核的大小为15纳米，在SPIO纳米颗粒中形成了Fe3O4晶体。
The iron core size was 15 nm and the formation of Fe(3)O(4) crystal in SPIO nanoparticles was confirmed by X-ray diffraction (XRD) analysis.
用光学显微镜、电子扫描显微镜、能谱及X射线衍射分析，比较详细地观察了各种掺杂物和温度对氧化铝晶体形貌的影响。
Effects of different dopants and sintering temperature on the morphology of alumina crystallites were observed in detail by using light scattering observation apparatus, SEM, EDX and XRD.
用光学显微镜、电子扫描显微镜、能谱及X射线衍射分析，比较详细地观察了各种掺杂物和温度对氧化铝晶体形貌的影响。
Effects of different dopants and sintering temperature on the morphology of alumina crystallites were observed in detail by using light scattering observation apparatus, SEM, EDX and XRD.
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