High efficiency, high quality x-ray optic based on ellipsoidally bent highly oriented pyrolytic graphite crystal for ultrafast x-ray diffraction experiments

2005 ◽  
Vol 44 (24) ◽  
pp. 5069 ◽  
Author(s):  
I. Uschmann ◽  
U. Nothelle ◽  
E. Förster ◽  
V. Arkadiev ◽  
N. Langhoff ◽  
...  
1973 ◽  
Vol 27 (6) ◽  
pp. 454-456 ◽  
Author(s):  
H. L. Kestenbaum

We report x-ray diffraction measurements from highly oriented pyrolytic graphite over the energy range 2 to 8 keV. The measured reflectivity exhibits an energy dependence which closely follows that predicted for an ideally imperfect graphite crystal, although the reflectivity itself is a factor of 1.5 less than the calculated value.


1986 ◽  
Vol 19 (3) ◽  
pp. 200-201 ◽  
Author(s):  
T. H. Metzger

The measurement of the mean-square thermal displacement 〈u 2〉 of carbon atoms in highly oriented pyrolytic graphite (HOPG) in the hexagonal c direction is reported. Energy-dispersive X-ray diffraction (EDXD) has been used to study the integrated intensity of all Bragg reflections 004 through 0′0′14 as a function of temperature. It is demonstrated that the correction of the Bragg intensities due to thermal diffuse scattering contributions is very important for HOPG, when EDXD is used. The Debye temperature ΘD = 554 (30) K is obtained.


2005 ◽  
Vol 38 (2) ◽  
pp. 361-367 ◽  
Author(s):  
Anjana Asthana ◽  
Yoshio Matsui ◽  
Makoto Yasuda ◽  
Koji Kimoto ◽  
Tadao Iwata ◽  
...  

Light and heavy neutron-irradiation damage of highly oriented pyrolytic graphite (HOPG) crystals was examined by means of X-ray diffraction and high-resolution high-voltage transmission electron microscopy (TEM). From the X-ray data analysis, it was found that there is an average increase of about 3% in thec-axis lattice parameter of the unit cell of graphite for lightly neutron-irradiated HOPG. However, thec-axis lattice parameter could not be estimated from the HOPG sample having the highest dose of neutron irradiation under the present investigation, because the X-ray profile was highly asymmetrical. This increase in thec-axis lattice parameter is attributed to lattice expansion due to the static displacement of atoms after neutron irradiation. Local structure analysis by TEM shows that the 0002 lattice spacing for the above-mentioned HOPG samples has been increased by up to 10% as a result of the neutron irradiation. This increase inc-axis lattice spacing can be ascribed to the fragmentation of the crystal lattice into nanocrystallites, breaking and bending of the 0002 straight lattice fringes, appearance of dislocation loops, and extra interstitial planes within the fragmented nanocrystallites. All these changes are a result of the static displacement of atoms after neutron irradiation.


Author(s):  
Koji INAKA ◽  
Saori ICHIMIZU ◽  
Izumi YOSHIZAKI ◽  
Kiyohito KIHIRA ◽  
Elena G. LAVRENKO ◽  
...  

A series of space experiments aboard the International Space Station (ISS) associated with high-quality Protein Crystal Growth (PCG) in microgravity conditions can be considered as a unique and one of the best examples of fruitful collaboration between Japanese and Russian scientists and engineers in space, which includes also other ISS International Partners. X-ray diffraction is still the most powerful tool to determine the protein three dimensional structure necessary for Structure based drug design (SBDD). The major purpose of the experiment is to grow high quality protein crystals in microgravity for X-ray diffraction on Earth. Within one and a half decade, Japan and Russia have established an efficient process over PCG in space to support latest developments over drug design and structural biology. One of the keys for success of the experiment lies in how precisely pre-launch preparations are made. Japanese party provides flight equipment for crystallization and ensures the required environment to support the experiment aboard of the ISS’s Kibo module, and also mainly takes part of the experiment ground support such as protein sample characterization, purification, crystallization screening, and solution optimization for microgravity experiment. Russian party is responsible for integration of the flight items equipped with proteins and precipitants on board Russian transportation space vehicles (Soyuz or Progress), for delivery them at the ISS, transfer to Kibo module, and returning the experiments’ results back on Earth aboard Soyuz manned capsule. Due to close cooperation of the parties and solid organizational structure, samples can be launched at the ISS every half a year if the ground preparation goes smoothly. The samples are crystallized using counter diffusion method at 20 degree C for 1–2.5 months. After samples return, the crystals are carefully taken out from the capillary, and frozen for X-ray diffraction at SPring8 facility in Japan. Extensive support of researchers from both countries is also a part of this process. The paper analyses details of the PCG experiment scheme, unique and reliable technology of its execution, and contains examples of the application. Key words: International Space Station, Protein crystals, Microgravity, International collaboration.


Author(s):  
Anatoly A. Udovenko ◽  
Alexander A. Karabtsov ◽  
Natalia M. Laptash

A classical elpasolite-type structure is considered with respect to dynamically disordered ammonium fluoro-(oxofluoro-)metallates. Single-crystal X-ray diffraction data from high quality (NH4)3HfF7 and (NH4)3Ti(O2)F5 samples enabled the refinement of the ligand and cationic positions in the cubic Fm \bar 3 m (Z = 4) structure. Electron-density atomic profiles show that the ligand atoms are distributed in a mixed (split) position instead of 24e. One of the ammonium groups is disordered near 8c so that its central atom (N1) forms a tetrahedron with vertexes in 32f. However, a center of another group (N2) remains in the 4b site, whereas its H atoms (H2) occupy the 96k positions instead of 24e and, together with the H3 atom in the 32f position, they form eight spatial orientations of the ammonium group. It is a common feature of all ammonium fluoroelpasolites with orientational disorder of structural units of a dynamic nature.


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