scholarly journals Development of a Novel Time-Resolved Synchrotron-Radiation X-ray Diffraction Measurement System for In Situ Observation of Crystal Structure in Aqueous Solution during Chemical Reaction: Application to the Anion-Exchange Reaction of a Layered Double Hydroxide from Chloride to Nitrate

2019 ◽  
Vol 92 (12) ◽  
pp. 1986-1992 ◽  
Author(s):  
Ryo Sasai ◽  
Takuya Fujimura ◽  
Nobuhiko Onda ◽  
Yu-to Nakayashiki ◽  
Hidenobu Sumiyoshi ◽  
...  
2014 ◽  
Vol 70 (a1) ◽  
pp. C1138-C1138
Author(s):  
Chiaki Tsuboi ◽  
Kazuki Aburaya ◽  
Shingo Higuchi ◽  
Fumiko Kimura ◽  
Masataka Maeyama ◽  
...  

We have developed magnetically oriented microcrystal array (MOMA) technique that enables single crystal X-ray diffraction analyses from microcrystalline powder. In this method, microcrystals suspended in a UV-curable monomer matrix are there-dimensionally aligned by special rotating magnetic field, followed by consolidation of the matrix by photopolymerization. From thus achieved MOMAs, we have been succeeded in crystal structure analysis for some substances [1, 2]. Though MOMA method is an effective technique, it has some problems as follows: in a MOMA, the alignment is deteriorated during the consolidation process. In addition, the sample microcrystals cannot be recovered from a MOMA. To overcome these problems, we performed an in-situ X-ray diffraction measurement using a three-dimensional magnetically oriented microcrystal suspension (3D MOMS) of L-alanine. An experimental setting of the in-situ X-ray measurement of MOMS is schematically shown in the figure. L-alanine microcrystal suspension was poured into a glass capillary and placed on the rotating unit equipped with a pair of neodymium magnets. Rotating X-ray chopper with 10°-slits was placed between the collimator and the suspension. By using this chopper, it was possible to expose the X-ray only when the rotating MOMS makes a specific direction with respect to the impinging X-ray. This has the same effect as the omega oscillation in conventional single crystal measurement. A total of 22 XRD images of 10° increments from 0° to 220° were obtained. The data set was processed by using conventional software to obtain three-dimensional molecular structure of L-alanine. The structure is in good agreement with that reported for the single crystal. R1 and wR2 were 6.53 and 17.4 %, respectively. RMSD value between the determined molecular structure and the reported one was 0.0045 Å. From this result, we conclude that this method can be effective and practical to be used widely for crystal structure analyses.


Cryobiology ◽  
2009 ◽  
Vol 59 (3) ◽  
pp. 405 ◽  
Author(s):  
Hiroko Ando ◽  
Satoshi Takeya ◽  
Yoshinori Kawagoe ◽  
Yoshio Makino ◽  
Toru Suzuki ◽  
...  

2011 ◽  
Vol 172-174 ◽  
pp. 1255-1260
Author(s):  
Hidenori Terasaki ◽  
Zhang Shouyuan ◽  
Yu Ichi Komizo

A hybrid in-situ observation system has been developed to study the phase transformation behaviour simultaneously in both real and reciprocal lattice space. This paper presents the development of the observation system. Furthermore, as an example of the application of our developed system, martensitic transformation of Cr–Ni steel along a designed thermal cycle was in-situ tracked with the developed system. As a result of analysing the time-resolved X-ray diffraction data for the observed target, our system could directly detect the effect of transformation strain on austenite during martensitic transformation.


2015 ◽  
Vol 44 (4) ◽  
pp. 434-436 ◽  
Author(s):  
Koji Maruyama ◽  
Hiroyuki Kagi ◽  
Toru Inoue ◽  
Hiroaki Ohfuji ◽  
Toru Yoshino

2007 ◽  
Vol 93 (2) ◽  
pp. 138-144 ◽  
Author(s):  
Mitsuharu YONEMURA ◽  
Takahiro OSUKI ◽  
Hidenori TERASAKI ◽  
Yuichi KOMIZO ◽  
Masugu SATO ◽  
...  

2012 ◽  
Vol 512-515 ◽  
pp. 1511-1515
Author(s):  
Chun Lin Zhao ◽  
Li Xing ◽  
Xiao Hong Liang ◽  
Jun Hui Xiang ◽  
Fu Shi Zhang ◽  
...  

Cadmium sulfide (CdS) nanocrystals (NCs) were self-assembled and in-situ immobilized on the dithiocarbamate (DTCs)-functionalized polyethylene glycol terephthalate (PET) substrates between the organic (carbon disulfide diffused in n-hexane) –aqueous (ethylenediamine and Cd2+ dissolved in water) interface at room temperature. Powder X-ray diffraction measurement revealed the hexagonal structure of CdS nanocrystals. Morphological studies performed by scanning electron microscopy (SEM) and high-resolution transmission electron microscope (HRTEM) showed the island-like structure of CdS nanocrystals on PET substrates, as well as energy-dispersive X-ray spectroscopy (EDS) confirmed the stoichiometries of CdS nanocrystals. The optical properties of DTCs modified CdS nanocrystals were thoroughly investigated by ultraviolet-visible absorption spectroscopy (UV-vis) and fluorescence spectroscopy. The as-prepared DTCs present intrinsic hydrophobicity and strong affinity for CdS nanocrystals.


Carbon ◽  
2015 ◽  
Vol 87 ◽  
pp. 246-256 ◽  
Author(s):  
Périne Landois ◽  
Mathieu Pinault ◽  
Stéphan Rouzière ◽  
Dominique Porterat ◽  
Cristian Mocuta ◽  
...  

2001 ◽  
Vol 15 (18) ◽  
pp. 2491-2497 ◽  
Author(s):  
J. L. ZHU ◽  
L. C. CHEN ◽  
R. C. YU ◽  
F. Y. LI ◽  
J. LIU ◽  
...  

In situ high pressure energy dispersive X-ray diffraction measurements on layered perovskite-like manganate Ca 3 Mn 2 O 7 under pressures up to 35 GPa have been performed by using diamond anvil cell with synchrotron radiation. The results show that the structure of layered perovskite-like manganate Ca 3 Mn 2 O 7 is unstable under pressure due to the easy compression of NaCl-type blocks. The structure of Ca 3 Mn 2 O 7 underwent two phase transitions under pressures in the range of 0~35 GPa. One was at about 1.3 GPa with the crystal structure changing from tetragonal to orthorhombic. The other was at about 9.5 GPa with the crystal structure changing from orthorhombic back to another tetragonal.


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